Variant report

Variant	rs3918385
Chromosome Location	chr3:46398911-46398912
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs3176763	1.00[GIH][hapmap]
rs3918370	1.00[GIH][hapmap]
rs3918379	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3918384	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41372645	1.00[AMR][1000 genomes]
rs41391847	1.00[AMR][1000 genomes]
rs41411547	1.00[AMR][1000 genomes]
rs41418945	0.90[AFR][1000 genomes]
rs41445746	1.00[AMR][1000 genomes]
rs41466044	0.90[AFR][1000 genomes]
rs41482046	1.00[AMR][1000 genomes]
rs41498544	1.00[AMR][1000 genomes]
rs5742906	1.00[GIH][hapmap]
rs7652954	1.00[GIH][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	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats 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	esv3323840	chr3:46352348-46497196	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3389382	chr3:46352798-46496696	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46392400-46402600	Weak transcription	Spleen	Spleen
2	chr3:46394400-46401200	Weak transcription	Brain Substantia Nigra	brain
3	chr3:46395800-46404200	Weak transcription	Right Atrium	heart
4	chr3:46396000-46401000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr3:46396000-46422000	Weak transcription	Lung	lung
6	chr3:46396400-46400800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr3:46396400-46401000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr3:46396800-46401000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr3:46397000-46400800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr3:46397000-46401000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:46397200-46401000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr3:46397400-46400600	Weak transcription	Primary B cells from cord blood	blood
13	chr3:46397800-46399200	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr3:46397800-46399800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr3:46397800-46400800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr3:46397800-46401000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:46397800-46401000	Weak transcription	Fetal Thymus	thymus
18	chr3:46398000-46401000	Weak transcription	Duodenum Mucosa	Duodenum
19	chr3:46398000-46401600	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr3:46398000-46404200	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr3:46398200-46399200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr3:46398200-46399400	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr3:46398200-46400600	Weak transcription	Fetal Stomach	stomach
24	chr3:46398400-46400400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr3:46398400-46401000	Weak transcription	Primary B cells from peripheral blood	blood
26	chr3:46398400-46401400	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood
27	chr3:46398400-46402000	Weak transcription	Colonic Mucosa	Colon
28	chr3:46398600-46399400	Weak transcription	GM12878-XiMat	blood
29	chr3:46398600-46400400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr3:46398600-46402800	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
31	chr3:46398800-46399000	Enhancers	Brain Germinal Matrix	brain
32	chr3:46398800-46399600	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr3:46398800-46399800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr3:46398800-46402000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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