Variant report

Variant	rs67025912
Chromosome Location	chr2:55087540-55087541
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:55087086..55089357-chr2:55090408..55092933,2	K562	blood:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12713280	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12713281	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12713283	0.90[ASN][1000 genomes]
rs13390007	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1347816	0.95[ASN][1000 genomes]
rs35459932	0.90[ASN][1000 genomes]
rs4613325	0.85[ASN][1000 genomes]
rs6545451	0.93[ASN][1000 genomes]
rs6756000	0.97[ASN][1000 genomes]
rs7588455	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33638	chr2:54765256-55109455	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1005449	chr2:54938633-55129503	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv457930	chr2:55073428-55091029	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv582028	chr2:55073428-55091029	Enhancers Flanking Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1796192	chr2:55081033-55110969	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55066800-55088800	Weak transcription	Brain Substantia Nigra	brain
2	chr2:55068400-55096200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr2:55068400-55109000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr2:55068600-55122400	Weak transcription	Brain Anterior Caudate	brain
5	chr2:55072600-55091600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:55073400-55093800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr2:55078000-55087600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:55078800-55106800	Weak transcription	Brain Angular Gyrus	brain
9	chr2:55081400-55122400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr2:55084400-55088800	Enhancers	HSMMtube	muscle
11	chr2:55084800-55088400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:55084800-55088400	Enhancers	Fetal Muscle Leg	muscle
13	chr2:55085400-55088200	Enhancers	NHDF-Ad	bronchial
14	chr2:55086000-55088600	Enhancers	HSMM	muscle
15	chr2:55086400-55090400	Weak transcription	Liver	Liver
16	chr2:55086600-55088000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:55087000-55087800	Enhancers	Placenta	Placenta
18	chr2:55087000-55088000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:55087000-55088000	Enhancers	Psoas Muscle	Psoas
20	chr2:55087000-55088200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:55087000-55088200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:55087000-55088200	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr2:55087000-55088200	Enhancers	NHEK	skin
24	chr2:55087000-55088400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr2:55087000-55088400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr2:55087000-55088400	Enhancers	Osteobl	bone
27	chr2:55087000-55088600	Enhancers	Muscle Satellite Cultured Cells	--
28	chr2:55087000-55098600	Weak transcription	HepG2	liver
29	chr2:55087200-55087800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr2:55087200-55088000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr2:55087200-55088000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:55087200-55088000	Enhancers	NHLF	lung
33	chr2:55087400-55087800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr2:55087400-55087800	Flanking Active TSS	A549	lung
35	chr2:55087400-55088000	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr2:55087400-55088200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr2:55087400-55088400	Enhancers	NH-A	brain

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