Variant report

Variant	rs870858
Chromosome Location	chr2:33501320-33501321
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:33169785..33172664-chr2:33500827..33503324,2	K562	blood:

Variant related genes	Relation type
ENSG00000206951	Chromatin interaction
ENSG00000049323	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11883651	0.96[CEU][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12468099	1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13034772	0.81[ASN][1000 genomes]
rs1453845	0.83[CEU][hapmap]
rs17581939	0.92[CHB][hapmap];0.94[JPT][hapmap];0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2123769	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3731575	0.92[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs3769531	0.87[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3769535	0.92[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3816479	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6756709	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998167	chr2:33074313-33541100	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv535623	chr2:33074313-33541100	Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1005435	chr2:33136117-33747159	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
4	nsv535624	chr2:33136117-33747159	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
5	nsv873791	chr2:33489975-33586776	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33472000-33516600	Weak transcription	Psoas Muscle	Psoas
2	chr2:33487000-33509800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:33487800-33502400	Weak transcription	Brain Anterior Caudate	brain
4	chr2:33490600-33515600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr2:33491800-33502000	Weak transcription	Brain Angular Gyrus	brain
6	chr2:33491800-33504400	Weak transcription	Colonic Mucosa	Colon
7	chr2:33492000-33515800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr2:33492200-33516600	Weak transcription	Brain Hippocampus Middle	brain
9	chr2:33492200-33516600	Weak transcription	Brain Substantia Nigra	brain
10	chr2:33492400-33501800	Weak transcription	Lung	lung
11	chr2:33492400-33502000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr2:33492400-33502000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr2:33492400-33502000	Weak transcription	Spleen	Spleen
14	chr2:33492400-33547400	Weak transcription	Fetal Intestine Small	intestine
15	chr2:33492600-33502000	Weak transcription	Ovary	ovary
16	chr2:33492600-33508400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:33493400-33502000	Weak transcription	Fetal Brain Male	brain
18	chr2:33493600-33515200	Weak transcription	Fetal Lung	lung
19	chr2:33493800-33503400	Weak transcription	Fetal Brain Female	brain
20	chr2:33493800-33515400	Weak transcription	Colon Smooth Muscle	Colon
21	chr2:33494000-33502000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr2:33494200-33506200	Weak transcription	Fetal Heart	heart
23	chr2:33494200-33516000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr2:33494200-33516200	Weak transcription	Fetal Kidney	kidney
25	chr2:33494600-33515200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr2:33497800-33503400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:33499200-33508000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:33499400-33502400	Strong transcription	Liver	Liver
29	chr2:33499600-33501400	Strong transcription	Left Ventricle	heart
30	chr2:33499600-33502200	Strong transcription	Aorta	Aorta
31	chr2:33499800-33501400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:33499800-33501600	Genic enhancers	NH-A	brain
33	chr2:33499800-33502400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr2:33500000-33502200	Strong transcription	Fetal Stomach	stomach
35	chr2:33500000-33502400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr2:33500200-33501600	Enhancers	HUVEC	blood vessel
37	chr2:33500200-33504800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:33500400-33502400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:33500400-33502600	Genic enhancers	Muscle Satellite Cultured Cells	--
40	chr2:33500800-33501400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr2:33500800-33501400	Flanking Active TSS	A549	lung
42	chr2:33500800-33501400	Genic enhancers	K562	blood
43	chr2:33500800-33501400	Enhancers	NHDF-Ad	bronchial
44	chr2:33500800-33501800	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr2:33500800-33502000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:33500800-33502400	Enhancers	Esophagus	oesophagus
47	chr2:33500800-33502400	Genic enhancers	Osteobl	bone
48	chr2:33500800-33502600	Genic enhancers	Fetal Muscle Leg	muscle
49	chr2:33500800-33503800	Genic enhancers	Cortex derived primary cultured neurospheres	brain
50	chr2:33501000-33501400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain

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