Variant report

Variant	rs10182993
Chromosome Location	chr2:153214934-153214935
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10166701	1.00[ASN][1000 genomes]
rs10181910	1.00[ASN][1000 genomes]
rs10188437	1.00[ASN][1000 genomes]
rs12693278	1.00[ASN][1000 genomes]
rs13382381	1.00[ASN][1000 genomes]
rs13386095	1.00[ASN][1000 genomes]
rs13394982	1.00[ASN][1000 genomes]
rs13401202	1.00[ASN][1000 genomes]
rs13408985	1.00[ASN][1000 genomes]
rs13420003	1.00[ASN][1000 genomes]
rs28581765	1.00[ASN][1000 genomes]
rs35406869	1.00[ASN][1000 genomes]
rs6726207	1.00[ASN][1000 genomes]
rs6742020	1.00[ASN][1000 genomes]
rs6742139	1.00[ASN][1000 genomes]
rs6753703	1.00[ASN][1000 genomes]
rs7590270	1.00[ASN][1000 genomes]
rs7600978	1.00[ASN][1000 genomes]
rs7604840	1.00[ASN][1000 genomes]
rs9288079	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834419	chr2:153179420-153381476	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1005012	chr2:153206764-153273886	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv3693435	chr2:153210444-153219178	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:153194200-153224400	Weak transcription	Aorta	Aorta
2	chr2:153196000-153224800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:153200400-153215200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr2:153200600-153225600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:153200800-153215800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:153200800-153222000	Weak transcription	Placenta	Placenta
7	chr2:153200800-153225800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:153201600-153216000	Weak transcription	Fetal Lung	lung
9	chr2:153202400-153219800	Weak transcription	Hela-S3	cervix
10	chr2:153202400-153225600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:153203000-153223800	Weak transcription	Fetal Stomach	stomach
12	chr2:153203000-153233000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:153205200-153216000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:153205400-153223800	Weak transcription	HMEC	breast
15	chr2:153206800-153215600	Weak transcription	Pancreas	Pancrea
16	chr2:153206800-153240800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:153207000-153223200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:153207600-153246400	Weak transcription	Fetal Intestine Small	intestine
19	chr2:153209400-153237000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:153209800-153225200	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr2:153210800-153223200	Weak transcription	Ovary	ovary
22	chr2:153211000-153223200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:153212000-153216000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:153212000-153218200	Weak transcription	NH-A	brain
25	chr2:153212000-153223600	Weak transcription	NHEK	skin
26	chr2:153212000-153224200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr2:153212400-153215800	Weak transcription	A549	lung
28	chr2:153212400-153216000	Weak transcription	Osteobl	bone
29	chr2:153212400-153218000	Weak transcription	Brain Anterior Caudate	brain
30	chr2:153212400-153224200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:153212600-153215800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr2:153212600-153216200	Weak transcription	Brain Substantia Nigra	brain
33	chr2:153212800-153215200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr2:153212800-153215800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr2:153212800-153219400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr2:153212800-153225600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr2:153213400-153216200	Weak transcription	Brain Hippocampus Middle	brain
38	chr2:153213400-153219400	Weak transcription	Brain Angular Gyrus	brain
39	chr2:153213400-153221600	Weak transcription	Psoas Muscle	Psoas
40	chr2:153214600-153215000	Active TSS	Gastric	stomach
41	chr2:153214600-153215000	Strong transcription	Left Ventricle	heart
42	chr2:153214800-153215800	Enhancers	HepG2	liver
43	chr2:153214800-153223800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr2:153214800-153227600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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