Variant report

Variant	rs2033261
Chromosome Location	chr5:89754102-89754103
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:89752607..89755470-chr5:89857714..89859860,2	MCF-7	breast:
2	chr5:89749257..89756333-chr5:89766701..89771382,10	K562	blood:
3	chr5:89704413..89707772-chr5:89751873..89754605,3	K562	blood:
4	chr5:89752454..89759037-chr5:89767298..89771861,10	MCF-7	breast:
5	chr5:89752466..89754308-chr5:89769045..89771515,2	K562	blood:
6	chr5:89752385..89754792-chr5:89760288..89762882,3	MCF-7	breast:
7	chr5:89748881..89751681-chr5:89752674..89755420,2	K562	blood:
8	chr5:89742653..89745217-chr5:89752023..89754805,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000113356	Chromatin interaction
ENSG00000153140	Chromatin interaction
ENSG00000176055	Chromatin interaction
ENSG00000255647	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs2162986	1.00[GIH][hapmap]
rs6862171	1.00[CHB][hapmap];1.00[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021142	chr5:89102893-89897826	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers 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 miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv537804	chr5:89102893-89897826	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv917025	chr5:89208994-89855436	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
7	nsv518131	chr5:89748142-89781594	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases
8	nsv882364	chr5:89748142-89808531	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89734600-89769000	Weak transcription	Pancreas	Pancrea
2	chr5:89736400-89754400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:89736400-89767600	Weak transcription	Hela-S3	cervix
4	chr5:89736400-89768400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:89737600-89757000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:89743800-89767800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr5:89744200-89759000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:89744400-89768600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr5:89745400-89765800	Weak transcription	A549	lung
10	chr5:89746400-89765200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr5:89747400-89768600	Weak transcription	NHDF-Ad	bronchial
12	chr5:89747600-89760200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:89748000-89768400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr5:89748200-89757400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr5:89748200-89759600	Weak transcription	Primary T cells from cord blood	blood
16	chr5:89748400-89768600	Weak transcription	Adipose Nuclei	Adipose
17	chr5:89748600-89754400	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr5:89748600-89768200	Weak transcription	Osteobl	bone
19	chr5:89749000-89754400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:89749200-89768400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr5:89749200-89768800	Weak transcription	Brain Germinal Matrix	brain
22	chr5:89749200-89768800	Weak transcription	Ovary	ovary
23	chr5:89749200-89769000	Weak transcription	Left Ventricle	heart
24	chr5:89749400-89767600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr5:89749400-89768600	Weak transcription	Fetal Intestine Large	intestine
26	chr5:89749800-89768600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr5:89750000-89754800	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr5:89750200-89756600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr5:89750200-89768800	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr5:89750600-89755000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr5:89750600-89759000	Weak transcription	Lung	lung
32	chr5:89750600-89763800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr5:89750800-89760200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr5:89750800-89768800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr5:89751200-89755200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr5:89751200-89758600	Weak transcription	Fetal Brain Female	brain
37	chr5:89751200-89766600	Weak transcription	Fetal Muscle Trunk	muscle
38	chr5:89751200-89769000	Weak transcription	Spleen	Spleen
39	chr5:89751400-89754200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr5:89751400-89754800	Weak transcription	Primary B cells from cord blood	blood
41	chr5:89751600-89754400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr5:89751600-89767600	Weak transcription	Brain Anterior Caudate	brain
43	chr5:89751800-89767600	Weak transcription	Fetal Intestine Small	intestine
44	chr5:89752000-89759800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:89752000-89760000	Weak transcription	Fetal Stomach	stomach
46	chr5:89752000-89769200	Weak transcription	Small Intestine	intestine
47	chr5:89752200-89757800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr5:89752200-89768400	Weak transcription	Stomach Smooth Muscle	stomach
49	chr5:89752200-89768800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:89752600-89758000	Weak transcription	Liver	Liver

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