Variant report

Variant	rs73855951
Chromosome Location	chr3:113303955-113303956
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1486896	1.00[AMR][1000 genomes]
rs2399482	1.00[AMR][1000 genomes]
rs3856722	1.00[AMR][1000 genomes]
rs56167882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56843844	0.80[AFR][1000 genomes]
rs56985546	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58329399	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59848630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59888133	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59925484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61299722	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6782872	1.00[AMR][1000 genomes]
rs73855954	0.80[AFR][1000 genomes]
rs73855956	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv1004000	chr3:113116778-113513899	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv877349	chr3:113208224-113323787	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
4	nsv877350	chr3:113208224-113332235	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113280200-113321600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:113280400-113304000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:113280600-113314800	Weak transcription	Spleen	Spleen
4	chr3:113285200-113329800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr3:113285200-113343400	Weak transcription	Small Intestine	intestine
6	chr3:113286000-113316800	Weak transcription	Brain Angular Gyrus	brain
7	chr3:113294400-113321600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr3:113294800-113304200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr3:113296800-113324200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr3:113297400-113315600	Strong transcription	GM12878-XiMat	blood
11	chr3:113297800-113308000	Strong transcription	Primary T cells from cord blood	blood
12	chr3:113298800-113309400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr3:113298800-113315200	Strong transcription	Primary B cells from peripheral blood	blood
14	chr3:113299400-113308000	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr3:113299400-113315400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:113299600-113306400	Weak transcription	Primary hematopoietic stem cells	blood
17	chr3:113299600-113309400	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr3:113300800-113308800	Weak transcription	Thymus	Thymus
19	chr3:113302000-113308200	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr3:113302200-113305400	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr3:113302200-113308400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr3:113302200-113309400	Strong transcription	Primary B cells from cord blood	blood
23	chr3:113302400-113304600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr3:113302400-113306000	Strong transcription	Primary T killer memory cells from peripheral blood	blood
25	chr3:113302600-113304200	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr3:113302600-113305000	Strong transcription	Fetal Thymus	thymus
27	chr3:113302800-113304800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
28	chr3:113302800-113305400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr3:113303000-113304000	Weak transcription	HepG2	liver
30	chr3:113303400-113308200	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr3:113303600-113305400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:113303600-113305600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr3:113303600-113308400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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