Variant report

Variant	rs10106062
Chromosome Location	chr8:66977625-66977626
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:66976835..66977882-chr8:67333673..67334537,6	MCF-7	breast:
2	chr8:66975090..66978056-chr8:67341293..67343047,2	MCF-7	breast:
3	chr8:66971479..66974707-chr8:66974890..66977947,4	K562	blood:
4	chr8:66976852..66977966-chr8:67088847..67090142,11	MCF-7	breast:
5	chr8:66976931..66977680-chr8:67340745..67341286,2	K562	blood:
6	chr8:66977395..66977951-chr8:66988398..66989060,2	K562	blood:
7	chr8:66977023..66977851-chr8:67088772..67089376,4	K562	blood:

Variant related genes	Relation type
ENSG00000246145	Chromatin interaction
ENSG00000179041	Chromatin interaction
ENSG00000147576	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10090752	1.00[EUR][1000 genomes]
rs10091688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10093753	1.00[EUR][1000 genomes]
rs10095531	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10096043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10099780	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10107052	1.00[EUR][1000 genomes]
rs10108405	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10110227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10113256	1.00[EUR][1000 genomes]
rs13439700	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16932461	0.83[AFR][1000 genomes]
rs16932465	0.83[AFR][1000 genomes]
rs16932468	0.83[AFR][1000 genomes]
rs28364014	1.00[EUR][1000 genomes]
rs28482448	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28491110	0.83[AFR][1000 genomes]
rs28577932	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28623751	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28690794	1.00[EUR][1000 genomes]
rs28702525	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28705810	1.00[EUR][1000 genomes]
rs28770228	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28855126	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28871963	1.00[EUR][1000 genomes]
rs28873428	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57754344	1.00[EUR][1000 genomes]
rs7003229	1.00[EUR][1000 genomes]
rs73244947	1.00[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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv3414665	chr8:66936816-67381935	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66975200-66977800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr8:66975600-66977800	Enhancers	NHDF-Ad	bronchial
3	chr8:66975800-66977800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:66975800-66977800	Enhancers	Dnd41	blood
5	chr8:66975800-66977800	Enhancers	HMEC	breast
6	chr8:66975800-66977800	Enhancers	NHLF	lung
7	chr8:66976000-66977800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:66976200-66977800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:66976200-66977800	Enhancers	Colon Smooth Muscle	Colon
10	chr8:66976200-66977800	Enhancers	A549	lung
11	chr8:66976200-66978000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr8:66976200-66978000	Enhancers	HSMM	muscle
13	chr8:66976200-66978000	Enhancers	HSMMtube	muscle
14	chr8:66976400-66978000	Enhancers	Fetal Muscle Leg	muscle
15	chr8:66976800-66977800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:66976800-66977800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr8:66977200-66979600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr8:66977400-66977800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:66977400-66977800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:66977400-66977800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr8:66977400-66977800	Enhancers	Liver	Liver
22	chr8:66977400-66977800	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr8:66977400-66978200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr8:66977600-66977800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:66977600-66977800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr8:66977600-66988200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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