Variant report

Variant	rs2758863
Chromosome Location	chr6:39239477-39239478
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:39193484..39195491-chr6:39238843..39241224,2	K562	blood:
2	chr6:39238194..39240550-chr6:39241911..39243898,2	K562	blood:
3	chr6:39239173..39241787-chr6:39269864..39271484,2	MCF-7	breast:
4	chr6:39173237..39177206-chr6:39236026..39240576,5	MCF-7	breast:
5	chr6:39235849..39239507-chr6:39267408..39272188,7	MCF-7	breast:
6	chr6:39233505..39239976-chr6:39262109..39267318,6	MCF-7	breast:
7	chr6:39237190..39240116-chr6:39261691..39264000,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12191604	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12191756	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12198547	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12198665	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2253582	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2758864	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2758865	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2758866	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2758867	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2758868	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2758869	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2758871	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2758872	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2758874	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2815019	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815020	0.85[ASN][1000 genomes]
rs2815024	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815025	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815026	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815028	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815029	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815030	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2815031	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815032	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815035	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815036	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815037	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815038	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2815039	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2815040	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2815041	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2815042	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2815044	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2815045	0.81[ASN][1000 genomes]
rs34170020	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34343201	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830644	chr6:39116530-39325980	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1022974	chr6:39120271-39277553	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv830645	chr6:39227601-39408310	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:39232000-39239800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr6:39233600-39240200	Enhancers	Placenta	Placenta
3	chr6:39236000-39241200	Weak transcription	Colonic Mucosa	Colon
4	chr6:39236000-39241400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr6:39236600-39241000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:39236800-39239800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:39236800-39240000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:39236800-39240000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr6:39237000-39239800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:39237000-39240000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:39237200-39239600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr6:39237200-39240200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr6:39237800-39240000	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr6:39237800-39241200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:39238200-39241400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr6:39238400-39243200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr6:39238600-39243000	Weak transcription	Spleen	Spleen
18	chr6:39239000-39241200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr6:39239400-39241200	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr6:39239400-39242600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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