Variant report

Variant	rs6740836
Chromosome Location	chr2:58457705-58457706
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	chr2:58457454..58459312-chr2:58461373..58464013,3	K562	blood:
2	chr2:58455073..58459456-chr2:58466641..58469255,4	K562	blood:

Variant related genes	Relation type
ENSG00000273063	Chromatin interaction
ENSG00000115392	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10165760	0.89[AMR][1000 genomes]
rs10182762	0.89[AMR][1000 genomes]
rs1025755	0.89[AMR][1000 genomes]
rs11883874	0.84[YRI][hapmap];0.89[AMR][1000 genomes]
rs11891477	0.89[AMR][1000 genomes]
rs11892302	0.89[AMR][1000 genomes]
rs11900900	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11903212	0.86[YRI][hapmap];0.87[AFR][1000 genomes]
rs13397947	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13405281	0.89[AMR][1000 genomes]
rs13410500	0.87[YRI][hapmap];0.89[AMR][1000 genomes]
rs13422760	0.85[AFR][1000 genomes]
rs1371213	0.89[AMR][1000 genomes]
rs1404459	0.87[AFR][1000 genomes]
rs1404460	0.86[YRI][hapmap];0.87[AFR][1000 genomes]
rs2165103	0.86[YRI][hapmap];0.89[AMR][1000 genomes]
rs2312486	0.89[AMR][1000 genomes]
rs34335951	0.86[AFR][1000 genomes]
rs57112138	0.89[AMR][1000 genomes]
rs58470176	0.89[AMR][1000 genomes]
rs60364084	0.89[AMR][1000 genomes]
rs6709533	0.84[AFR][1000 genomes]
rs6740373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6742445	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs716758	0.89[AMR][1000 genomes]
rs72948876	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72951042	0.89[AMR][1000 genomes]
rs72951048	0.89[AMR][1000 genomes]
rs72951056	0.89[AMR][1000 genomes]
rs7340170	0.83[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7590976	0.81[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7597069	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9309303	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs9973345	0.89[AMR][1000 genomes]
rs9973928	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999042	chr2:58326123-58530903	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv535734	chr2:58326123-58530903	ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1007527	chr2:58386271-58477536	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv535735	chr2:58386271-58477536	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:58391000-58467000	Weak transcription	HMEC	breast
2	chr2:58414000-58461400	Weak transcription	NHEK	skin
3	chr2:58416600-58467200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:58432000-58466400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr2:58437000-58460200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:58437200-58459000	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr2:58438600-58466400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr2:58439000-58467400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr2:58440000-58465000	Weak transcription	Fetal Brain Male	brain
10	chr2:58440000-58467400	Weak transcription	Primary B cells from peripheral blood	blood
11	chr2:58440600-58462000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:58440600-58467400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr2:58441000-58458200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:58443400-58460400	Weak transcription	Brain Germinal Matrix	brain
15	chr2:58443600-58462200	Weak transcription	Brain Substantia Nigra	brain
16	chr2:58444200-58466200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr2:58448800-58464800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr2:58449400-58462400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:58450000-58466200	Weak transcription	HUVEC	blood vessel
20	chr2:58451000-58458000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr2:58452000-58467400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr2:58452000-58467400	Weak transcription	NHLF	lung
23	chr2:58452200-58459000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr2:58452600-58460600	Weak transcription	Brain Hippocampus Middle	brain
25	chr2:58453200-58458400	Weak transcription	Colon Smooth Muscle	Colon
26	chr2:58453800-58467400	Weak transcription	NHDF-Ad	bronchial
27	chr2:58454600-58457800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:58454600-58466800	Weak transcription	HSMM	muscle
29	chr2:58454800-58458000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr2:58454800-58458600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr2:58454800-58460600	Weak transcription	Small Intestine	intestine
32	chr2:58454800-58462000	Weak transcription	K562	blood
33	chr2:58454800-58464400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:58454800-58464800	Weak transcription	Fetal Brain Female	brain
35	chr2:58454800-58466200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr2:58454800-58466400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr2:58454800-58467400	Weak transcription	Primary B cells from cord blood	blood
38	chr2:58454800-58467400	Weak transcription	Fetal Thymus	thymus
39	chr2:58454800-58467400	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr2:58454800-58467400	Weak transcription	Stomach Smooth Muscle	stomach
41	chr2:58454800-58467400	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr2:58455000-58458000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr2:58455000-58458000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr2:58455000-58458200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:58455000-58458200	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr2:58455000-58458200	Weak transcription	Esophagus	oesophagus
47	chr2:58455000-58458200	Weak transcription	Fetal Muscle Trunk	muscle
48	chr2:58455000-58459400	Weak transcription	Aorta	Aorta
49	chr2:58455000-58459600	Weak transcription	Fetal Intestine Large	intestine
50	chr2:58455000-58460400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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