Variant report

Variant	rs16924207
Chromosome Location	chr8:59803436-59803437
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	chr8:59801544..59803959-chr8:59811921..59813443,2	K562	blood:
2	chr8:59801933..59804319-chr8:59804381..59806631,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10098381	0.88[CEU][hapmap]
rs10504273	0.88[CEU][hapmap]
rs10504275	0.88[CEU][hapmap]
rs1105608	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs11777659	0.88[CEU][hapmap];1.00[CHB][hapmap];0.97[ASN][1000 genomes]
rs11778333	0.87[CEU][hapmap]
rs11779544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11782466	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11783096	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11784073	0.85[CEU][hapmap]
rs11784291	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13252116	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13256007	1.00[CHB][hapmap];0.97[ASN][1000 genomes]
rs13258467	0.98[EUR][1000 genomes]
rs13259869	0.83[EUR][1000 genomes]
rs13262426	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13273148	0.83[ASN][1000 genomes]
rs16924199	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];0.93[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16924253	0.98[EUR][1000 genomes]
rs16924314	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs17232126	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs17232411	1.00[CHB][hapmap];0.97[ASN][1000 genomes]
rs17241424	0.88[CEU][hapmap]
rs17298221	1.00[CHB][hapmap];0.97[ASN][1000 genomes]
rs17301816	1.00[CEU][hapmap]
rs34130829	1.00[ASN][1000 genomes]
rs34434301	0.83[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];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6996574	0.88[CEU][hapmap];1.00[CHB][hapmap];0.97[ASN][1000 genomes]
rs71521434	0.97[ASN][1000 genomes]
rs7815098	1.00[CHB][hapmap];0.97[ASN][1000 genomes]
rs7823862	1.00[CEU][hapmap]

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	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
3	nsv526468	chr8:59799820-59813809	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:35 , 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	chr8:59790600-59804000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:59790800-59811200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr8:59791400-59811000	Weak transcription	Brain Angular Gyrus	brain
7	chr8:59794200-59820000	Weak transcription	Fetal Intestine Large	intestine
8	chr8:59794800-59804000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:59794800-59811000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr8:59795000-59805600	Weak transcription	Colon Smooth Muscle	Colon
11	chr8:59799000-59804200	Weak transcription	HSMM	muscle
12	chr8:59799000-59804600	Weak transcription	Fetal Thymus	thymus
13	chr8:59800600-59809800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr8:59800800-59809600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr8:59800800-59810600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr8:59800800-59811000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr8:59801000-59808000	Weak transcription	Dnd41	blood
18	chr8:59801400-59805400	Enhancers	Osteobl	bone
19	chr8:59801400-59811000	Weak transcription	Primary T cells from cord blood	blood
20	chr8:59801800-59805600	Enhancers	NHDF-Ad	bronchial
21	chr8:59802200-59810800	Weak transcription	HUVEC	blood vessel
22	chr8:59802800-59804000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr8:59802800-59804800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr8:59802800-59826600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr8:59803000-59804600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr8:59803000-59804800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr8:59803000-59805000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr8:59803000-59805400	Enhancers	Fetal Brain Male	brain
29	chr8:59803200-59803600	Enhancers	Placenta	Placenta
30	chr8:59803200-59805400	Enhancers	Placenta Amnion	Placenta Amnion
31	chr8:59803400-59803600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr8:59803400-59803600	Enhancers	Gastric	stomach
33	chr8:59803400-59805000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:59803400-59805400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr8:59803400-59805400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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