Variant report

Variant	rs572302566
Chromosome Location	chr2:178482222-178482223
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:178480859..178483355-chr2:178499342..178501117,2	K562	blood:
2	chr2:178415963..178418015-chr2:178480825..178484170,3	K562	blood:

Variant related genes	Relation type
ENSG00000196659	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999086	chr2:178262348-178773585	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv536055	chr2:178262348-178773585	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh 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	14 gene(s)	inside rSNPs	diseases
3	nsv583688	chr2:178427640-178540293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv583689	chr2:178468008-178509820	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	esv1815823	chr2:178479149-178489902	Active TSS Enhancers Weak transcription Flanking Active TSS 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 target site	8 gene(s)	inside rSNPs	diseases
6	nsv961914	chr2:178481282-178483895	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178462800-178482800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:178464200-178482600	Weak transcription	Psoas Muscle	Psoas
3	chr2:178464200-178482600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr2:178464600-178482400	Weak transcription	Colon Smooth Muscle	Colon
5	chr2:178468400-178482800	Weak transcription	Fetal Brain Male	brain
6	chr2:178471800-178482600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr2:178476400-178482800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:178476800-178482600	Weak transcription	HepG2	liver
9	chr2:178477400-178482600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr2:178477600-178482600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr2:178477800-178482400	Weak transcription	Brain Substantia Nigra	brain
12	chr2:178477800-178482800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr2:178477800-178482800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr2:178479600-178482600	Weak transcription	HSMM	muscle
15	chr2:178480000-178482600	Weak transcription	K562	blood
16	chr2:178480000-178482800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:178481200-178482600	Weak transcription	Brain Angular Gyrus	brain
18	chr2:178481200-178482600	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr2:178481200-178482600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr2:178481200-178482600	Weak transcription	Left Ventricle	heart
21	chr2:178481200-178482600	Weak transcription	Ovary	ovary
22	chr2:178481200-178482600	Weak transcription	Pancreas	Pancrea
23	chr2:178481200-178482600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr2:178481200-178482600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr2:178481200-178482800	Weak transcription	Gastric	stomach
26	chr2:178481200-178482800	Weak transcription	Right Atrium	heart
27	chr2:178481200-178482800	Weak transcription	GM12878-XiMat	blood
28	chr2:178481400-178482600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:178481400-178482600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr2:178481400-178482600	Weak transcription	Fetal Lung	lung
31	chr2:178481400-178482600	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr2:178481600-178482600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:178481600-178482600	Weak transcription	Fetal Heart	heart
34	chr2:178481600-178482800	Weak transcription	Fetal Kidney	kidney
35	chr2:178481800-178482800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr2:178482200-178482600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr2:178482200-178482800	Enhancers	Right Ventricle	heart

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