Variant report

Variant	rs13419918
Chromosome Location	chr2:64333527-64333528
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:64325352..64327561-chr2:64332535..64335174,2	K562	blood:
2	chr2:64331549..64334048-chr2:64335542..64337218,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10165165	0.81[ASN][1000 genomes]
rs10169847	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10170224	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10175483	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10176596	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs10183513	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10185776	0.85[YRI][hapmap]
rs10186108	0.85[YRI][hapmap]
rs10191854	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10192104	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10192378	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10201191	0.80[AMR][1000 genomes]
rs10204631	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10496106	0.81[YRI][hapmap]
rs13385515	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13408188	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13412068	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13418461	0.81[ASN][1000 genomes]
rs13428357	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2017834	0.84[YRI][hapmap]
rs28757314	0.81[ASN][1000 genomes]
rs28798530	0.81[ASN][1000 genomes]
rs3731962	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3755112	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56028117	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56301411	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60338887	0.93[ASN][1000 genomes]
rs60882934	1.00[ASN][1000 genomes]
rs714672	0.81[YRI][hapmap]
rs7579828	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531376	chr2:64094322-64521876	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1013132	chr2:64235175-64631084	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	esv2757803	chr2:64253005-64539556	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	esv2759055	chr2:64253005-64539556	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv428396	chr2:64253005-64539556	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	esv34698	chr2:64312142-64521366	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	esv34955	chr2:64312182-64521290	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
8	nsv834243	chr2:64316514-64476935	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:64313200-64341800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:64317200-64335600	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr2:64318200-64333600	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr2:64318400-64335600	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:64318800-64336400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:64320400-64339200	Weak transcription	NHLF	lung
7	chr2:64322200-64336200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:64322400-64336000	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:64322800-64335800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr2:64323400-64334000	Weak transcription	Esophagus	oesophagus
11	chr2:64323400-64341400	Weak transcription	Aorta	Aorta
12	chr2:64323600-64336000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:64323600-64336000	Weak transcription	Brain Angular Gyrus	brain
14	chr2:64323600-64336000	Weak transcription	Psoas Muscle	Psoas
15	chr2:64323600-64341800	Weak transcription	Right Ventricle	heart
16	chr2:64323600-64364400	Weak transcription	Fetal Brain Male	brain
17	chr2:64323800-64341000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr2:64323800-64341600	Weak transcription	Gastric	stomach
19	chr2:64323800-64341600	Weak transcription	K562	blood
20	chr2:64324000-64336000	Weak transcription	Dnd41	blood
21	chr2:64324000-64341200	Weak transcription	HSMM	muscle
22	chr2:64324000-64341600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr2:64324400-64335800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr2:64324400-64335800	Weak transcription	Brain Substantia Nigra	brain
25	chr2:64324400-64336000	Weak transcription	Ovary	ovary
26	chr2:64324400-64336000	Weak transcription	Spleen	Spleen
27	chr2:64324400-64338200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:64324400-64341600	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr2:64324400-64344800	Weak transcription	HSMMtube	muscle
30	chr2:64325000-64341600	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr2:64325600-64333600	Weak transcription	Brain Hippocampus Middle	brain
32	chr2:64328800-64336000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr2:64329000-64338800	Weak transcription	Fetal Lung	lung
34	chr2:64329000-64342800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:64329200-64335600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:64329200-64341000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:64329400-64336000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr2:64329600-64334400	Strong transcription	Fetal Muscle Trunk	muscle
39	chr2:64329800-64335000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr2:64329800-64336000	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr2:64329800-64340200	Genic enhancers	GM12878-XiMat	blood
42	chr2:64330000-64336200	Strong transcription	Primary B cells from peripheral blood	blood
43	chr2:64330200-64335000	Strong transcription	Adipose Nuclei	Adipose
44	chr2:64330200-64336000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
45	chr2:64330400-64334000	Enhancers	Fetal Intestine Small	intestine
46	chr2:64330400-64335200	Strong transcription	Placenta	Placenta
47	chr2:64330400-64336000	Weak transcription	Lung	lung
48	chr2:64330600-64334800	Strong transcription	Primary B cells from cord blood	blood
49	chr2:64330600-64335000	Enhancers	Small Intestine	intestine
50	chr2:64330600-64335600	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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