Variant report

Variant	rs13021215
Chromosome Location	chr2:55422454-55422455
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:55421052..55423867-chr2:55459760..55462720,2	K562	blood:

Variant related genes	Relation type
ENSG00000143947	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10172326	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10197309	0.81[EUR][1000 genomes]
rs1133181	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1133182	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11679663	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11685292	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12616435	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12619400	0.80[ASN][1000 genomes]
rs12621144	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13012766	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13013134	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13019355	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13023235	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13417057	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs14026	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2164714	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2576710	0.83[AMR][1000 genomes]
rs2576724	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2864818	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34054131	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34564471	0.88[ASN][1000 genomes]
rs35026006	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35161040	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35890669	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3762509	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3935223	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4420737	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4671241	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4671242	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4672024	0.88[ASN][1000 genomes]
rs4672026	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4672027	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56095114	0.95[ASN][1000 genomes]
rs56339196	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6545474	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6545475	0.83[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs6545478	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6714830	0.82[ASN][1000 genomes]
rs6759911	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7595134	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010438	chr2:55373562-55450144	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv522016	chr2:55404794-55560298	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13021215	FLJ31438	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55395600-55422800	Weak transcription	Ovary	ovary
2	chr2:55395600-55427000	Weak transcription	Left Ventricle	heart
3	chr2:55395800-55427000	Weak transcription	Aorta	Aorta
4	chr2:55397200-55450000	Weak transcription	NH-A	brain
5	chr2:55397400-55423000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:55399600-55423000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr2:55402600-55423200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:55402800-55450000	Weak transcription	NHDF-Ad	bronchial
9	chr2:55403200-55423800	Weak transcription	Osteobl	bone
10	chr2:55403200-55426800	Weak transcription	Colon Smooth Muscle	Colon
11	chr2:55403200-55431800	Weak transcription	Fetal Brain Male	brain
12	chr2:55403400-55423000	Weak transcription	NHEK	skin
13	chr2:55404200-55423000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:55405400-55423000	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr2:55406800-55423000	Weak transcription	Lung	lung
16	chr2:55408600-55423000	Weak transcription	Pancreas	Pancrea
17	chr2:55408800-55423600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr2:55409000-55423000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr2:55409200-55425800	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr2:55410000-55424000	Weak transcription	Fetal Thymus	thymus
21	chr2:55410600-55422800	Weak transcription	HepG2	liver
22	chr2:55411200-55427000	Weak transcription	Primary B cells from cord blood	blood
23	chr2:55412200-55423000	Weak transcription	Dnd41	blood
24	chr2:55412600-55423000	Weak transcription	Thymus	Thymus
25	chr2:55412800-55428200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:55413000-55427000	Weak transcription	Brain Angular Gyrus	brain
27	chr2:55413600-55427000	Weak transcription	Fetal Lung	lung
28	chr2:55414600-55427000	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr2:55414800-55423200	Weak transcription	Spleen	Spleen
30	chr2:55415400-55450000	Weak transcription	GM12878-XiMat	blood
31	chr2:55415600-55423000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:55416000-55426800	Weak transcription	Fetal Kidney	kidney
33	chr2:55416000-55428400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr2:55416200-55428800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr2:55416800-55423000	Weak transcription	Esophagus	oesophagus
36	chr2:55416800-55450000	Weak transcription	Rectal Smooth Muscle	rectum
37	chr2:55417200-55422800	Weak transcription	Primary T cells from cord blood	blood
38	chr2:55417400-55423600	Weak transcription	Brain Germinal Matrix	brain
39	chr2:55417400-55450200	Weak transcription	Placenta	Placenta
40	chr2:55417800-55439200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:55417800-55450000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:55418000-55423200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr2:55418400-55433600	Weak transcription	Brain Anterior Caudate	brain
44	chr2:55419200-55423000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:55419200-55427000	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr2:55419200-55429600	Weak transcription	Fetal Intestine Large	intestine
47	chr2:55419400-55423000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:55419400-55434400	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr2:55419600-55431800	Weak transcription	Fetal Heart	heart
50	chr2:55419800-55423400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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