Variant report

Variant	rs2620903
Chromosome Location	chr10:50010214-50010215
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr10:50010200-50010350	GM12864	blood:	n/a	n/a
2	POLR2A	chr10:50010148-50010282	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
WDFY4	TF binding region

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

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1904603	0.80[EUR][1000 genomes]
rs2127590	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2170132	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663035	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2663044	0.80[ASN][1000 genomes]
rs2663053	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2928393	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2928401	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2940704	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4838648	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6537576	0.80[ASN][1000 genomes]
rs726786	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831865	chr10:49994254-50164239	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50001000-50012800	Weak transcription	Right Ventricle	heart
2	chr10:50004000-50011000	Weak transcription	Lung	lung
3	chr10:50005200-50026800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:50005400-50011000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr10:50006600-50010400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr10:50006600-50010800	Genic enhancers	GM12878-XiMat	blood
7	chr10:50007000-50012800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr10:50007200-50014600	Weak transcription	NHLF	lung
9	chr10:50007200-50017200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr10:50007600-50013000	Enhancers	Primary T cells fromperipheralblood	blood
11	chr10:50008200-50010400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr10:50008200-50012400	Enhancers	Primary T cells from cord blood	blood
13	chr10:50008200-50012600	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr10:50008200-50013600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr10:50008200-50015000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr10:50008400-50010400	Enhancers	Spleen	Spleen
17	chr10:50008400-50013600	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr10:50008600-50013000	Weak transcription	Right Atrium	heart
19	chr10:50008600-50013200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr10:50009000-50010800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr10:50009000-50013600	Genic enhancers	Primary B cells from peripheral blood	blood
22	chr10:50009200-50015200	Genic enhancers	Primary B cells from cord blood	blood
23	chr10:50009400-50013200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr10:50009600-50010400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:50009600-50010400	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr10:50009600-50011200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr10:50009600-50011400	Weak transcription	Dnd41	blood
28	chr10:50009600-50012800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr10:50009600-50012800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr10:50009600-50013200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr10:50009600-50014800	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr10:50009600-50028000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr10:50009800-50010800	Weak transcription	Fetal Thymus	thymus
34	chr10:50009800-50011200	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr10:50009800-50011200	Weak transcription	Fetal Muscle Leg	muscle
36	chr10:50009800-50012000	Weak transcription	Primary hematopoietic stem cells	blood
37	chr10:50009800-50012200	Weak transcription	Brain Cingulate Gyrus	brain
38	chr10:50009800-50012800	Weak transcription	NHEK	skin
39	chr10:50009800-50013000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:50010000-50011600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr10:50010000-50012000	Weak transcription	Left Ventricle	heart
42	chr10:50010000-50012400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr10:50010000-50012800	Weak transcription	Adipose Nuclei	Adipose

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