Variant report

Variant	rs16924208
Chromosome Location	chr8:59805558-59805559
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:59801933..59804319-chr8:59804381..59806631,2	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10504268	0.89[CEU][hapmap];1.00[GIH][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16924195	1.00[ASW][hapmap];0.88[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.88[TSI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17231026	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17232203	0.89[CEU][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17233300	0.89[CEU][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17296738	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17297508	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2218684	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62508361	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62508363	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72649495	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72651303	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72651304	0.98[AMR][1000 genomes];0.97[EUR][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	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:30 , 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	chr8:59790800-59811200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr8:59791400-59811000	Weak transcription	Brain Angular Gyrus	brain
6	chr8:59794200-59820000	Weak transcription	Fetal Intestine Large	intestine
7	chr8:59794800-59811000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr8:59795000-59805600	Weak transcription	Colon Smooth Muscle	Colon
9	chr8:59800600-59809800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:59800800-59809600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:59800800-59810600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr8:59800800-59811000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr8:59801000-59808000	Weak transcription	Dnd41	blood
14	chr8:59801400-59811000	Weak transcription	Primary T cells from cord blood	blood
15	chr8:59801800-59805600	Enhancers	NHDF-Ad	bronchial
16	chr8:59802200-59810800	Weak transcription	HUVEC	blood vessel
17	chr8:59802800-59826600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr8:59804200-59811000	Weak transcription	Gastric	stomach
19	chr8:59804400-59806000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr8:59804600-59806000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr8:59804600-59806600	Strong transcription	Fetal Thymus	thymus
22	chr8:59804800-59806200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr8:59805000-59812200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr8:59805000-59815200	Weak transcription	Fetal Heart	heart
25	chr8:59805200-59815600	Weak transcription	Fetal Stomach	stomach
26	chr8:59805400-59808000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr8:59805400-59808200	Weak transcription	Osteobl	bone
28	chr8:59805400-59808400	Weak transcription	Fetal Brain Male	brain
29	chr8:59805400-59810600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr8:59805400-59826800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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