Variant report

Variant	rs60064859
Chromosome Location	chr5:80412107-80412108
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs13340388	1.00[EUR][1000 genomes]
rs13361744	1.00[EUR][1000 genomes]
rs34039392	1.00[EUR][1000 genomes]
rs56157507	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58071944	1.00[EUR][1000 genomes]
rs59441376	1.00[EUR][1000 genomes]
rs59626246	1.00[EUR][1000 genomes]
rs59719994	1.00[EUR][1000 genomes]
rs61194622	1.00[EUR][1000 genomes]
rs61629530	1.00[EUR][1000 genomes]
rs6870928	1.00[EUR][1000 genomes]
rs73128867	1.00[EUR][1000 genomes]
rs73766146	1.00[EUR][1000 genomes]
rs73766153	1.00[EUR][1000 genomes]
rs73766159	1.00[EUR][1000 genomes]
rs73766199	1.00[EUR][1000 genomes]
rs73768003	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9293834	1.00[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	nsv1024844	chr5:79862428-80860430	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv830360	chr5:80283278-80446040	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv882232	chr5:80393949-80436584	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80375000-80422600	Weak transcription	Left Ventricle	heart
2	chr5:80383200-80413600	Weak transcription	Ovary	ovary
3	chr5:80383400-80414800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr5:80383400-80421600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr5:80383600-80412600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr5:80394000-80417000	Weak transcription	NHLF	lung
7	chr5:80401000-80417600	Weak transcription	Brain Angular Gyrus	brain
8	chr5:80401600-80413400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr5:80401600-80421400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr5:80401800-80420200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr5:80401800-80420600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr5:80404400-80417600	Weak transcription	Brain Anterior Caudate	brain
13	chr5:80404800-80428200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr5:80406200-80417400	Weak transcription	Fetal Intestine Small	intestine
15	chr5:80406400-80412400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:80406400-80415600	Weak transcription	Spleen	Spleen
17	chr5:80406600-80417800	Strong transcription	Primary T cells from cord blood	blood
18	chr5:80406800-80417400	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr5:80407000-80428000	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr5:80408400-80415600	Strong transcription	HepG2	liver
21	chr5:80408400-80418400	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr5:80408800-80426400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:80409800-80422600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr5:80410200-80413800	Weak transcription	Brain Hippocampus Middle	brain
25	chr5:80410200-80417800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr5:80410600-80412400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr5:80410600-80414600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr5:80410600-80416800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr5:80410600-80419600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr5:80410600-80421600	Weak transcription	Brain Substantia Nigra	brain
31	chr5:80410600-80432400	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr5:80410600-80446600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr5:80410800-80413400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr5:80410800-80413600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr5:80410800-80416000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr5:80411200-80427800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr5:80411600-80412200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr5:80411800-80413800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr5:80411800-80421800	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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