Variant report

Variant	rs16828693
Chromosome Location	chr2:149258834-149258835
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:149257990..149260894-chr2:149265586..149267154,2	K562	blood:
2	chr2:149257941..149260096-chr2:149261087..149264018,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10928398	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12619515	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12620213	0.93[JPT][hapmap]
rs13032758	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1404183	0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs1404184	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16828672	0.93[JPT][hapmap]
rs16828691	0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs73003524	0.84[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	esv2753542	chr2:149004714-149268503	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1012275	chr2:149031668-149316793	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2751831	chr2:149151358-150105603	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv1000101	chr2:149165813-149361220	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv868861	chr2:149198443-149434604	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv917109	chr2:149198443-149948302	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
7	nsv1004663	chr2:149214090-149373061	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv2762913	chr2:149249683-149345487	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:149227200-149259200	Weak transcription	Right Ventricle	heart
2	chr2:149227600-149259200	Weak transcription	Gastric	stomach
3	chr2:149227800-149259200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr2:149228000-149259200	Weak transcription	Pancreas	Pancrea
5	chr2:149244200-149261400	Weak transcription	Small Intestine	intestine
6	chr2:149245400-149266800	Weak transcription	Thymus	Thymus
7	chr2:149246000-149261200	Weak transcription	Fetal Heart	heart
8	chr2:149247000-149266400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr2:149247200-149266200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr2:149247400-149259200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr2:149247600-149291000	Weak transcription	Spleen	Spleen
12	chr2:149247800-149266400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr2:149247800-149266800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr2:149247800-149266800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr2:149248000-149266800	Weak transcription	Brain Angular Gyrus	brain
16	chr2:149248200-149259000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:149248200-149266800	Weak transcription	Brain Hippocampus Middle	brain
18	chr2:149248400-149266600	Weak transcription	Colon Smooth Muscle	Colon
19	chr2:149248400-149266600	Weak transcription	Fetal Brain Male	brain
20	chr2:149248400-149266800	Weak transcription	Fetal Brain Female	brain
21	chr2:149248600-149259000	Weak transcription	Ovary	ovary
22	chr2:149248600-149259200	Weak transcription	Adipose Nuclei	Adipose
23	chr2:149248600-149259200	Weak transcription	Aorta	Aorta
24	chr2:149248600-149266400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:149248600-149266800	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr2:149248600-149266800	Weak transcription	Brain Anterior Caudate	brain
27	chr2:149248600-149266800	Weak transcription	Stomach Smooth Muscle	stomach
28	chr2:149248600-149266800	Weak transcription	HSMM	muscle
29	chr2:149248600-149266800	Weak transcription	HSMMtube	muscle
30	chr2:149248600-149267000	Weak transcription	Fetal Muscle Leg	muscle
31	chr2:149248800-149259600	Weak transcription	Fetal Intestine Small	intestine
32	chr2:149248800-149265600	Weak transcription	Fetal Lung	lung
33	chr2:149248800-149266800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr2:149248800-149266800	Weak transcription	Fetal Intestine Large	intestine
35	chr2:149248800-149266800	Weak transcription	Fetal Stomach	stomach
36	chr2:149248800-149266800	Weak transcription	Left Ventricle	heart
37	chr2:149248800-149267000	Weak transcription	Fetal Muscle Trunk	muscle
38	chr2:149248800-149269600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr2:149248800-149276800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:149248800-149284600	Weak transcription	Lung	lung
41	chr2:149249200-149266800	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr2:149251200-149266600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:149251200-149266800	Weak transcription	NH-A	brain
44	chr2:149251600-149259200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:149252200-149266800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:149252800-149264000	Weak transcription	GM12878-XiMat	blood
47	chr2:149252800-149266800	Weak transcription	Primary hematopoietic stem cells	blood
48	chr2:149254000-149266400	Weak transcription	Primary T cells from cord blood	blood
49	chr2:149254200-149266800	Weak transcription	Primary B cells from cord blood	blood
50	chr2:149254400-149259200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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