Variant report

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12055836	0.89[AMR][1000 genomes]
rs12662995	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3777569	0.89[AMR][1000 genomes]
rs3777570	0.89[AMR][1000 genomes]
rs3777574	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3777575	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3777576	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3777577	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3777578	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3798266	0.94[ASN][1000 genomes]
rs3822886	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3822887	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6907979	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9395137	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs946226	0.89[AMR][1000 genomes]
rs949678	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][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	nsv532024	chr6:45475088-45982640	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv517891	chr6:45899823-45915088	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45881200-45908000	Weak transcription	Duodenum Mucosa	Duodenum
2	chr6:45886800-45910600	Weak transcription	Psoas Muscle	Psoas
3	chr6:45895400-45910800	Weak transcription	Placenta	Placenta
4	chr6:45898600-45914600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr6:45898600-45916800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr6:45898800-45911000	Weak transcription	Adipose Nuclei	Adipose
7	chr6:45898800-45919200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr6:45899000-45910600	Weak transcription	Fetal Heart	heart
9	chr6:45899200-45910000	Strong transcription	Fetal Intestine Small	intestine
10	chr6:45899800-45908000	Weak transcription	Lung	lung
11	chr6:45901800-45907800	Weak transcription	Right Ventricle	heart
12	chr6:45903000-45917200	Strong transcription	Fetal Intestine Large	intestine
13	chr6:45903400-45914400	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr6:45904800-45906600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr6:45904800-45907200	Weak transcription	Colonic Mucosa	Colon
16	chr6:45904800-45907800	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr6:45905000-45911800	Strong transcription	Rectal Mucosa Donor 29	rectum
18	chr6:45905400-45908800	Weak transcription	Spleen	Spleen
19	chr6:45905400-45909600	Strong transcription	Skeletal Muscle Female	skeletal muscle
20	chr6:45905800-45906800	Genic enhancers	Left Ventricle	heart

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