Variant report

Variant	rs6506942
Chromosome Location	chr18:29406757-29406758
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	chr18:29406625..29408228-chr18:29410273..29412352,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs7226494	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7227330	1.00[AMR][1000 genomes]
rs7228390	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7234585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7234891	1.00[AFR][1000 genomes]
rs7238380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8082921	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9675374	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9965789	1.00[AMR][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	nsv1059078	chr18:29225522-29454980	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv543675	chr18:29225522-29454980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv431975	chr18:29311034-29527902	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv1057229	chr18:29335175-29514265	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv2247	chr18:29370842-29415712	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29394400-29418200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr18:29399400-29407800	Weak transcription	Placenta	Placenta
3	chr18:29399600-29409000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr18:29399800-29408800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr18:29399800-29409400	Weak transcription	HSMMtube	muscle
6	chr18:29400200-29415600	Weak transcription	Brain Angular Gyrus	brain
7	chr18:29401000-29409400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr18:29401600-29408600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr18:29401800-29407400	Weak transcription	Fetal Intestine Small	intestine
10	chr18:29401800-29407800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr18:29401800-29409000	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr18:29401800-29409400	Weak transcription	HUVEC	blood vessel
13	chr18:29402000-29406800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr18:29402000-29407000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr18:29402000-29408600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr18:29402000-29408600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr18:29402000-29408800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr18:29402000-29408800	Weak transcription	Left Ventricle	heart
19	chr18:29402000-29409200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr18:29402000-29409400	Weak transcription	Fetal Lung	lung
21	chr18:29402000-29415400	Weak transcription	Right Ventricle	heart
22	chr18:29402200-29408600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr18:29402200-29408600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr18:29402200-29408800	Weak transcription	Adipose Nuclei	Adipose
25	chr18:29402200-29408800	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr18:29402200-29408800	Weak transcription	Fetal Intestine Large	intestine
27	chr18:29402200-29409000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr18:29402200-29409200	Weak transcription	HepG2	liver
29	chr18:29402200-29409400	Weak transcription	Gastric	stomach
30	chr18:29402200-29414600	Weak transcription	Fetal Heart	heart
31	chr18:29402200-29417200	Weak transcription	Pancreas	Pancrea
32	chr18:29402400-29408800	Weak transcription	K562	blood
33	chr18:29402400-29415400	Weak transcription	Ovary	ovary
34	chr18:29402800-29409400	Weak transcription	Lung	lung
35	chr18:29403600-29408800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr18:29403800-29409200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr18:29404800-29407400	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr18:29404800-29407400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr18:29405200-29413600	Weak transcription	Fetal Stomach	stomach
40	chr18:29405400-29407200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr18:29405400-29408800	Weak transcription	Liver	Liver
42	chr18:29405400-29415200	Weak transcription	Small Intestine	intestine
43	chr18:29405600-29406800	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr18:29405600-29407200	Weak transcription	Primary T cells from cord blood	blood
45	chr18:29405600-29409400	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr18:29405600-29412600	Weak transcription	Brain Hippocampus Middle	brain
47	chr18:29405600-29414800	Weak transcription	NH-A	brain
48	chr18:29405600-29481800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr18:29405800-29407400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr18:29405800-29407400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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