Variant report

Variant	rs10205569
Chromosome Location	chr2:187520366-187520367
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:187517214..187519461-chr2:187519500..187521687,2	K562	blood:
2	chr2:187519814..187522484-chr2:187522890..187524533,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10195983	1.00[AFR][1000 genomes]
rs13413716	1.00[YRI][hapmap]
rs16828299	1.00[AMR][1000 genomes]
rs2122176	1.00[YRI][hapmap]
rs2594700	1.00[YRI][hapmap]
rs2595381	1.00[YRI][hapmap]
rs2682849	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2682851	1.00[YRI][hapmap]
rs2682871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682875	1.00[YRI][hapmap]
rs2682876	1.00[AFR][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	esv2757844	chr2:187332780-187580547	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh 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	13 gene(s)	inside rSNPs	diseases
2	esv2759107	chr2:187332780-187580547	Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187456200-187533000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr2:187456800-187534400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr2:187457200-187533800	Weak transcription	Spleen	Spleen
4	chr2:187458000-187529000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr2:187464800-187536200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr2:187465800-187529200	Weak transcription	Dnd41	blood
7	chr2:187466800-187533200	Weak transcription	Colonic Mucosa	Colon
8	chr2:187467200-187528600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr2:187471600-187521000	Weak transcription	Aorta	Aorta
10	chr2:187476800-187536200	Weak transcription	Fetal Brain Male	brain
11	chr2:187482200-187533800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr2:187482800-187527800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr2:187482800-187533200	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr2:187482800-187533600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr2:187482800-187533800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:187482800-187533800	Weak transcription	Psoas Muscle	Psoas
17	chr2:187486600-187531400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:187489400-187534400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:187493800-187529200	Weak transcription	Brain Substantia Nigra	brain
20	chr2:187494200-187529200	Weak transcription	Brain Germinal Matrix	brain
21	chr2:187494200-187535800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:187494800-187531800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr2:187495000-187534400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr2:187501000-187548400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:187502800-187533000	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr2:187503400-187545000	Weak transcription	Hela-S3	cervix
27	chr2:187504200-187529400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr2:187505400-187522200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:187505400-187533400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr2:187505600-187527600	Weak transcription	Fetal Heart	heart
31	chr2:187505800-187528800	Weak transcription	Stomach Mucosa	stomach
32	chr2:187506600-187529600	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr2:187506600-187533400	Weak transcription	NHLF	lung
34	chr2:187506600-187537000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr2:187507200-187529200	Weak transcription	Fetal Brain Female	brain
36	chr2:187507400-187529000	Weak transcription	Primary T cells from cord blood	blood
37	chr2:187507800-187529200	Weak transcription	GM12878-XiMat	blood
38	chr2:187507800-187546600	Weak transcription	Small Intestine	intestine
39	chr2:187508000-187529200	Weak transcription	NHEK	skin
40	chr2:187508600-187521200	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr2:187509000-187521000	Weak transcription	Fetal Lung	lung
42	chr2:187509000-187521400	Weak transcription	Esophagus	oesophagus
43	chr2:187509800-187521000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:187509800-187521000	Weak transcription	Fetal Thymus	thymus
45	chr2:187510200-187521400	Weak transcription	Colon Smooth Muscle	Colon
46	chr2:187510200-187529200	Weak transcription	Pancreas	Pancrea
47	chr2:187510400-187521000	Weak transcription	Fetal Muscle Leg	muscle
48	chr2:187510800-187535000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr2:187511200-187536200	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr2:187511400-187546600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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