Variant report

Variant	rs11783096
Chromosome Location	chr8:59799585-59799586
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10098381	0.88[CEU][hapmap]
rs10504273	0.88[CEU][hapmap]
rs10504275	0.88[CEU][hapmap]
rs1105608	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs11777659	0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs11778333	0.86[CEU][hapmap]
rs11779544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11782466	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11784073	0.85[CEU][hapmap]
rs11784291	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13252116	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs13256007	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs13258467	0.94[EUR][1000 genomes]
rs13259869	0.87[EUR][1000 genomes]
rs13262426	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13273148	0.81[ASN][1000 genomes]
rs16924199	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16924207	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16924213	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs16924253	0.94[EUR][1000 genomes]
rs16924314	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[ASN][1000 genomes]
rs17232126	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs17232411	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs17241424	0.88[CEU][hapmap]
rs17298221	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs17301816	1.00[CEU][hapmap]
rs34130829	0.97[ASN][1000 genomes]
rs34434301	0.87[EUR][1000 genomes]
rs402443	1.00[CHB][hapmap]
rs6984848	1.00[CEU][hapmap]
rs6988646	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6996574	0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs71521434	0.94[ASN][1000 genomes]
rs71521437	0.81[EUR][1000 genomes]
rs7815098	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs7823862	1.00[CEU][hapmap]

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	nsv890938	chr8:59355053-59809785	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv890940	chr8:59785412-59809785	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59764200-59806400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:59771400-59811000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr8:59773400-59808200	Weak transcription	Thymus	Thymus
4	chr8:59782200-59800200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr8:59788200-59803400	Weak transcription	Gastric	stomach
6	chr8:59790600-59804000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:59790800-59800400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr8:59790800-59811200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr8:59791400-59811000	Weak transcription	Brain Angular Gyrus	brain
10	chr8:59794200-59820000	Weak transcription	Fetal Intestine Large	intestine
11	chr8:59794800-59800200	Weak transcription	Primary T cells from cord blood	blood
12	chr8:59794800-59804000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr8:59794800-59811000	Weak transcription	Duodenum Mucosa	Duodenum
14	chr8:59795000-59805600	Weak transcription	Colon Smooth Muscle	Colon
15	chr8:59795400-59800200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:59795400-59800400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr8:59795600-59801800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr8:59795600-59803400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr8:59797200-59801800	Weak transcription	NHDF-Ad	bronchial
20	chr8:59797400-59800600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:59798000-59801000	Strong transcription	Dnd41	blood
22	chr8:59798600-59802000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr8:59798800-59800400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr8:59798800-59800400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:59798800-59803200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr8:59799000-59801400	Weak transcription	Osteobl	bone
27	chr8:59799000-59801800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr8:59799000-59803400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:59799000-59804200	Weak transcription	HSMM	muscle
30	chr8:59799000-59804600	Weak transcription	Fetal Thymus	thymus
31	chr8:59799200-59801400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:59799200-59801800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr8:59799400-59801600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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