Variant report

Variant	rs129303
Chromosome Location	chr22:33158361-33158362
allele	C/T
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:32920308-32927723..22:33154607-33167707	H1-hESC	embryonic stem cell:	embryo
2	22:32578360-32590642..22:33154607-33167707	K562	blood:
3	22:32342898-32343477..22:33154607-33167707	Hela-S3	cervix:
4	22:32764253-32784733..22:33154607-33167707	K562	blood:
5	22:32053085-32061138..22:33154607-33167707	K562	blood:
6	22:33154607-33167707..22:33262063-33266567	Hela-S3	cervix:
7	22:33154607-33167707..22:33339333-33353583	Hela-S3	cervix:
8	22:32292186-32294405..22:33154607-33167707	K562	blood:
9	22:32594665-32606395..22:33154607-33167707	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
ENSG00000241878	Chromatin interaction
ENSG00000205853	Chromatin interaction
ENSG00000232218	Chromatin interaction
ENSG00000185666	Chromatin interaction
ENSG00000241954	Chromatin interaction
ENSG00000230736	Chromatin interaction
ENSG00000128245	Chromatin interaction
ENSG00000100150	Chromatin interaction
ENSG00000254127	Chromatin interaction
ENSG00000128253	Chromatin interaction
ENSG00000243519	Chromatin interaction
ENSG00000242082	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1018791	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs129305	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs130526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs130527	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs130528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs130529	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs135151	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs135153	0.81[AMR][1000 genomes]
rs73156461	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064719	chr22:33028891-33159636	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33151000-33175400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr22:33155000-33161400	Enhancers	Right Atrium	heart
3	chr22:33156200-33158800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr22:33156200-33158800	Enhancers	Left Ventricle	heart
5	chr22:33156200-33158800	Enhancers	Lung	lung
6	chr22:33156200-33158800	Enhancers	HSMMtube	muscle
7	chr22:33156200-33160600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr22:33156200-33161400	Enhancers	Adipose Nuclei	Adipose
9	chr22:33156400-33158400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr22:33156400-33158400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
11	chr22:33156400-33158400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
12	chr22:33156400-33158800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr22:33156400-33158800	Enhancers	Osteobl	bone
14	chr22:33156400-33159000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr22:33156400-33160200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr22:33156400-33161600	Enhancers	Spleen	Spleen
17	chr22:33156600-33158400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr22:33156600-33158400	Enhancers	Primary hematopoietic stem cells	blood
19	chr22:33156600-33158400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr22:33156600-33158400	Enhancers	HepG2	liver
21	chr22:33156600-33158800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr22:33156800-33158400	Flanking Active TSS	Hela-S3	cervix
23	chr22:33157000-33158400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr22:33157000-33158400	Enhancers	NH-A	brain
25	chr22:33157200-33159600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr22:33157200-33160400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr22:33157400-33158400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr22:33157400-33158800	Enhancers	Gastric	stomach
29	chr22:33157400-33159000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr22:33157600-33158600	Enhancers	Fetal Muscle Trunk	muscle
31	chr22:33157600-33158600	Weak transcription	Placenta	Placenta
32	chr22:33157600-33158800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr22:33157600-33158800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr22:33157600-33160400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr22:33157600-33160400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr22:33157800-33159600	Weak transcription	Fetal Thymus	thymus
37	chr22:33157800-33160200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr22:33157800-33160200	Weak transcription	Fetal Kidney	kidney
39	chr22:33157800-33160200	Weak transcription	Fetal Lung	lung
40	chr22:33157800-33160400	Weak transcription	NHDF-Ad	bronchial
41	chr22:33158000-33158400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr22:33158000-33158400	Enhancers	Pancreas	Pancrea
43	chr22:33158000-33158800	Enhancers	HSMM	muscle
44	chr22:33158000-33159000	Enhancers	Right Ventricle	heart
45	chr22:33158200-33159400	Weak transcription	Psoas Muscle	Psoas
46	chr22:33158200-33159800	Weak transcription	Fetal Stomach	stomach
47	chr22:33158200-33160200	Weak transcription	NHLF	lung
48	chr22:33158200-33160400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr22:33158200-33160400	Weak transcription	Esophagus	oesophagus
50	chr22:33158200-33160600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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