Variant report

Variant	rs73885122
Chromosome Location	chr22:33260055-33260056
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr22:33240885-33261662	ProgFib	skin:	n/a	n/a
2	POLR2A	chr22:33259646-33262120	U87	brain:	n/a	n/a
3	POLR2A	chr22:33259540-33260439	U87	brain:	n/a	n/a
4	POLR2A	chr22:33259130-33262120	U87	brain:	n/a	n/a
5	POLR2A	chr22:33254453-33260989	IMR90	lung:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	22:32750950-32761732..22:33253287-33262063	Hela-S3	cervix:
2	chr22:33257978..33261996-chr22:33266633..33269916,3	K562	blood:
3	22:32544939-32549151..22:33253287-33262063	Hela-S3	cervix:
4	22:32868055-32872511..22:33253287-33262063	Hela-S3	cervix:
5	22:31961151-31976153..22:33253287-33262063	K562	blood:
6	22:32920308-32927723..22:33253287-33262063	Hela-S3	cervix:
7	chr22:33196558..33199719-chr22:33257750..33262273,4	MCF-7	breast:
8	chr22:33258265..33260703-chr22:33277216..33279656,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000183531	TF binding region
ENSG00000185666	Chromatin interaction
ENSG00000198089	Chromatin interaction
ENSG00000205853	Chromatin interaction
ENSG00000100225	Chromatin interaction
ENSG00000100234	Chromatin interaction
ENSG00000205856	Chromatin interaction
ENSG00000128276	Chromatin interaction
ENSG00000271093	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs16991252	1.00[AMR][1000 genomes]
rs16991417	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16991442	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35396081	1.00[AMR][1000 genomes]
rs55843131	1.00[AMR][1000 genomes]
rs56283234	1.00[AMR][1000 genomes]
rs57139579	1.00[AMR][1000 genomes]
rs57490118	1.00[AMR][1000 genomes]
rs57620882	1.00[AMR][1000 genomes]
rs57966112	1.00[AMR][1000 genomes]
rs58329553	0.89[AFR][1000 genomes]
rs58394026	1.00[AMR][1000 genomes]
rs58627239	1.00[AMR][1000 genomes]
rs58709981	1.00[AMR][1000 genomes]
rs5998647	1.00[AMR][1000 genomes]
rs60903857	1.00[AMR][1000 genomes]
rs73881787	1.00[AMR][1000 genomes]
rs73881794	1.00[AMR][1000 genomes]
rs73881795	1.00[AMR][1000 genomes]
rs73881801	1.00[AMR][1000 genomes]
rs73881903	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73881907	1.00[AMR][1000 genomes]
rs73885104	1.00[AMR][1000 genomes]
rs73885107	1.00[AMR][1000 genomes]
rs73885108	1.00[AMR][1000 genomes]
rs73885115	1.00[AMR][1000 genomes]
rs73885117	1.00[AMR][1000 genomes]
rs8142286	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9619287	1.00[AMR][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	nsv3599	chr22:33230106-33274789	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1059368	chr22:33249121-33268782	Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33227000-33272400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr22:33237400-33282200	Weak transcription	Fetal Brain Female	brain
3	chr22:33243400-33260200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr22:33244200-33262000	Weak transcription	Brain Germinal Matrix	brain
5	chr22:33245600-33265000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr22:33245800-33264800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr22:33247800-33260200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr22:33249800-33262800	Weak transcription	Brain Angular Gyrus	brain
9	chr22:33255200-33263800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr22:33255800-33262000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr22:33256000-33262200	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr22:33256000-33263800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr22:33256000-33265200	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr22:33256200-33264800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr22:33256400-33264400	Weak transcription	Brain Hippocampus Middle	brain
16	chr22:33256400-33269400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr22:33256800-33264800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr22:33257200-33262200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr22:33257600-33261400	Weak transcription	Gastric	stomach
20	chr22:33257800-33260400	Weak transcription	NH-A	brain
21	chr22:33257800-33261000	Weak transcription	NHLF	lung
22	chr22:33257800-33261200	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr22:33257800-33264200	Weak transcription	NHDF-Ad	bronchial
24	chr22:33257800-33269600	Weak transcription	Fetal Intestine Small	intestine
25	chr22:33257800-33270000	Weak transcription	Fetal Intestine Large	intestine
26	chr22:33257800-33282000	Weak transcription	HepG2	liver
27	chr22:33258000-33262400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr22:33258200-33260400	Enhancers	Fetal Heart	heart
29	chr22:33258200-33266600	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr22:33258400-33260200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr22:33258400-33260200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr22:33258400-33260200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr22:33258400-33260800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr22:33258400-33261600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr22:33258400-33262800	Weak transcription	Spleen	Spleen
36	chr22:33258400-33266800	Weak transcription	Aorta	Aorta
37	chr22:33258400-33267200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr22:33258600-33260400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr22:33258600-33260400	Weak transcription	Adipose Nuclei	Adipose
40	chr22:33258600-33260800	Weak transcription	HMEC	breast
41	chr22:33258800-33260600	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr22:33258800-33260600	Weak transcription	HSMM	muscle
43	chr22:33258800-33260800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr22:33258800-33261400	Enhancers	Placenta	Placenta
45	chr22:33258800-33261600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr22:33258800-33261800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr22:33258800-33262200	Weak transcription	Osteobl	bone
48	chr22:33259000-33260800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr22:33259000-33265800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr22:33259000-33270800	Weak transcription	Fetal Lung	lung

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