Variant report

Variant	rs12151587
Chromosome Location	chr2:171836895-171836896
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10515934	0.86[ASN][1000 genomes]
rs10803853	0.81[ASN][1000 genomes]
rs10803854	0.86[ASN][1000 genomes]
rs10930448	0.86[ASN][1000 genomes]
rs10930449	0.86[ASN][1000 genomes]
rs12471930	0.86[ASN][1000 genomes]
rs12612871	0.86[ASN][1000 genomes]
rs12996518	0.86[ASN][1000 genomes]
rs13000898	0.89[ASN][1000 genomes]
rs13015226	0.81[ASN][1000 genomes]
rs13026662	0.92[ASN][1000 genomes]
rs13028857	0.81[ASN][1000 genomes]
rs13035460	0.81[ASN][1000 genomes]
rs1529391	0.86[ASN][1000 genomes]
rs16859066	0.86[ASN][1000 genomes]
rs17281735	0.86[ASN][1000 genomes]
rs2114738	0.92[ASN][1000 genomes]
rs2557799	0.92[ASN][1000 genomes]
rs34005022	0.81[ASN][1000 genomes]
rs34342928	0.83[ASN][1000 genomes]
rs34911788	0.81[ASN][1000 genomes]
rs35123411	0.86[ASN][1000 genomes]
rs35890547	0.86[ASN][1000 genomes]
rs35987434	0.92[ASN][1000 genomes]
rs3755125	0.81[ASN][1000 genomes]
rs3770440	0.86[ASN][1000 genomes]
rs3770441	0.81[ASN][1000 genomes]
rs4668355	0.86[ASN][1000 genomes]
rs6433267	0.81[ASN][1000 genomes]
rs6714164	0.81[ASN][1000 genomes]
rs6714300	0.86[ASN][1000 genomes]
rs6715386	0.81[ASN][1000 genomes]
rs6724493	0.81[ASN][1000 genomes]
rs6729847	0.81[ASN][1000 genomes]
rs6742797	0.86[ASN][1000 genomes]
rs71415229	0.81[ASN][1000 genomes]
rs71415232	0.86[ASN][1000 genomes]
rs731693	0.86[ASN][1000 genomes]
rs73976229	0.86[ASN][1000 genomes]
rs7570701	0.86[ASN][1000 genomes]
rs965518	0.92[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431801	chr2:171721493-171966493	ZNF genes & repeats Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12151587	TLK1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:171830400-171842200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:171830600-171902800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr2:171830800-171839800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:171830800-171891400	Weak transcription	Spleen	Spleen
5	chr2:171831000-171838600	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:171831000-171840000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr2:171831000-171847600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr2:171831000-171850000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr2:171831200-171838200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr2:171831200-171840400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:171831200-171843200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:171831200-171845400	Weak transcription	HMEC	breast
13	chr2:171831200-171845800	Weak transcription	Osteobl	bone
14	chr2:171831200-171847000	Weak transcription	A549	lung
15	chr2:171831200-171857400	Weak transcription	HSMMtube	muscle
16	chr2:171831400-171849400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:171831400-171857000	Weak transcription	NHEK	skin
18	chr2:171831400-171879200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr2:171831400-171916200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:171831600-171840000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr2:171832000-171844800	Weak transcription	GM12878-XiMat	blood
22	chr2:171832200-171838200	Weak transcription	K562	blood
23	chr2:171832600-171839000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr2:171832600-171846000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr2:171832600-171852200	Weak transcription	Fetal Intestine Small	intestine
26	chr2:171833000-171848800	Weak transcription	HepG2	liver
27	chr2:171833400-171837400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr2:171835600-171843400	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr2:171836600-171844800	Weak transcription	Primary T cells from cord blood	blood

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