Variant report

Variant	rs12021634
Chromosome Location	chr1:175096910-175096911
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	chr1:175091685..175094091-chr1:175094460..175097259,2	K562	blood:

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12022593	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2269652	0.85[EUR][1000 genomes];1.00[ASN][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	nsv825487	chr1:175031609-175113572	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv508648	chr1:175056387-175121913	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175084800-175097000	Weak transcription	Gastric	stomach
2	chr1:175086400-175099600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:175091200-175098600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:175094000-175100000	Enhancers	Liver	Liver
5	chr1:175094400-175098400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr1:175094400-175098800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:175095600-175098200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:175095600-175098200	Enhancers	Lung	lung
9	chr1:175095600-175099600	Enhancers	Fetal Lung	lung
10	chr1:175095600-175099800	Enhancers	Placenta	Placenta
11	chr1:175095600-175099800	Enhancers	Right Atrium	heart
12	chr1:175095600-175100400	Enhancers	Fetal Stomach	stomach
13	chr1:175095800-175097000	Weak transcription	Left Ventricle	heart
14	chr1:175095800-175102600	Enhancers	Stomach Smooth Muscle	stomach
15	chr1:175096000-175097000	Weak transcription	Adipose Nuclei	Adipose
16	chr1:175096200-175097200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:175096200-175097400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr1:175096200-175097400	Enhancers	Stomach Mucosa	stomach
19	chr1:175096400-175102600	Enhancers	Colon Smooth Muscle	Colon
20	chr1:175096600-175098000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:175096600-175099400	Enhancers	Spleen	Spleen
22	chr1:175096600-175099800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr1:175096800-175097000	Enhancers	Primary hematopoietic stem cells	blood
24	chr1:175096800-175097000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:175096800-175097000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr1:175096800-175097000	Enhancers	GM12878-XiMat	blood
27	chr1:175096800-175097400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:175096800-175098000	Enhancers	Right Ventricle	heart
29	chr1:175096800-175098200	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr1:175096800-175098200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr1:175096800-175098800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr1:175096800-175100000	Enhancers	Fetal Muscle Leg	muscle

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