Variant report

Variant	rs62148507
Chromosome Location	chr2:86974689-86974690
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	chr2:86850136..86852379-chr2:86973884..86976847,2	K562	blood:

Variant related genes	Relation type
ENSG00000249884	Chromatin interaction
ENSG00000239305	Chromatin interaction

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

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532724	chr2:86622295-87086407	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer 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 target site	45 gene(s)	inside rSNPs	diseases
2	nsv10063	chr2:86940988-87084360	Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1002420	chr2:86948835-87172715	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv874472	chr2:86961252-87071474	Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv1008817	chr2:86970406-87172715	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	esv14382	chr2:86972214-87174121	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv997982	chr2:86972834-87105864	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv1007746	chr2:86972834-87172715	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
9	nsv521780	chr2:86974318-86994719	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv458585	chr2:86974318-87108211	Flanking Active TSS Genic enhancers Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv582373	chr2:86974318-87108211	Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
12	nsv1007307	chr2:86974563-87055214	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
13	nsv535809	chr2:86974563-87055214	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86949000-86979600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr2:86962200-86975400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr2:86962200-86977000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:86965200-86978800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr2:86966800-86977200	Weak transcription	Osteobl	bone
6	chr2:86968600-86974800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:86968600-86993000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:86968600-86997600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr2:86968800-86975000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr2:86968800-86977000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr2:86968800-86977000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr2:86968800-86978600	Weak transcription	Placenta	Placenta
13	chr2:86968800-86980400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:86969200-86975000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr2:86969200-86977400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr2:86969200-86986400	Strong transcription	Fetal Thymus	thymus
17	chr2:86969200-86997800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:86969400-86979000	Weak transcription	Ovary	ovary
19	chr2:86969400-86984400	Weak transcription	Fetal Heart	heart
20	chr2:86969400-86997800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr2:86969600-86977200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr2:86969600-86995400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:86969600-86995400	Weak transcription	Esophagus	oesophagus
24	chr2:86969800-86975000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:86969800-86975000	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr2:86969800-86977200	Weak transcription	Fetal Kidney	kidney
27	chr2:86969800-86978600	Weak transcription	HSMM	muscle
28	chr2:86970000-86974800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr2:86970000-86974800	Weak transcription	HMEC	breast
30	chr2:86970000-86976000	Weak transcription	Hela-S3	cervix
31	chr2:86970000-86979800	Weak transcription	Colonic Mucosa	Colon
32	chr2:86970000-86980200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:86970000-87002000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr2:86970200-86974800	Strong transcription	Primary B cells from peripheral blood	blood
35	chr2:86970200-86974800	Strong transcription	Dnd41	blood
36	chr2:86970200-86976800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr2:86970400-86975200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr2:86970400-86980600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr2:86970400-86995400	Weak transcription	Aorta	Aorta
40	chr2:86970800-86975000	Weak transcription	NH-A	brain
41	chr2:86971000-86975000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr2:86971000-86975000	Weak transcription	Fetal Brain Male	brain
43	chr2:86971400-86974800	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr2:86971400-86976000	Weak transcription	Brain Germinal Matrix	brain
45	chr2:86971600-86976600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:86971600-86977000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr2:86971600-86993000	Weak transcription	Lung	lung
48	chr2:86971800-86975000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:86972000-86974800	Weak transcription	Adipose Nuclei	Adipose
50	chr2:86972000-86975400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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