Variant report

Variant	rs58410126
Chromosome Location	chr22:33017527-33017528
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:33014781..33017660-chr22:33019637..33021375,2	MCF-7	breast:
2	chr22:33013961..33016702-chr22:33017273..33018854,2	MCF-7	breast:
3	chr22:33016718..33020351-chr22:33021844..33025503,4	K562	blood:
4	chr22:33015941..33022634-chr22:33022783..33027992,6	MCF-7	breast:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs16990831	0.80[EUR][1000 genomes]
rs16990849	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16990857	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16990872	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2858223	0.89[ASN][1000 genomes]
rs3827336	0.80[AFR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5754173	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58228617	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58291507	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67485432	0.83[ASN][1000 genomes]
rs73154363	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73154365	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73154374	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9609608	0.84[ASN][1000 genomes]
rs9621513	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055541	chr22:33006967-33101138	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv2762119	chr22:33006967-33101150	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1061824	chr22:33013014-33101138	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33012400-33017600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr22:33012400-33017800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr22:33012400-33018400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr22:33012800-33017600	Enhancers	HepG2	liver
5	chr22:33014200-33017800	Weak transcription	Brain Anterior Caudate	brain
6	chr22:33014200-33022200	Weak transcription	Small Intestine	intestine
7	chr22:33014400-33019800	Weak transcription	Brain Angular Gyrus	brain
8	chr22:33014600-33017600	Weak transcription	Brain Hippocampus Middle	brain
9	chr22:33014600-33017600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr22:33014800-33017600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr22:33015000-33019800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr22:33015200-33017600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr22:33015800-33017600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr22:33015800-33017800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr22:33016000-33017600	Weak transcription	K562	blood
16	chr22:33016000-33020000	Weak transcription	Liver	Liver
17	chr22:33017000-33017600	Enhancers	Stomach Smooth Muscle	stomach
18	chr22:33017000-33017800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr22:33017000-33017800	Enhancers	Adipose Nuclei	Adipose
20	chr22:33017000-33017800	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr22:33017000-33017800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
22	chr22:33017000-33018000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr22:33017000-33018000	Enhancers	Hela-S3	cervix
24	chr22:33017000-33018200	Enhancers	Fetal Muscle Trunk	muscle
25	chr22:33017000-33018600	Enhancers	Lung	lung
26	chr22:33017000-33019600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr22:33017000-33020200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr22:33017000-33020600	Enhancers	Fetal Kidney	kidney
29	chr22:33017000-33021000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr22:33017000-33021000	Enhancers	Fetal Muscle Leg	muscle
31	chr22:33017000-33021000	Enhancers	Fetal Stomach	stomach
32	chr22:33017000-33022600	Enhancers	Fetal Lung	lung
33	chr22:33017000-33022600	Enhancers	Right Atrium	heart
34	chr22:33017000-33025800	Enhancers	Left Ventricle	heart
35	chr22:33017000-33025800	Enhancers	Spleen	Spleen
36	chr22:33017000-33027200	Enhancers	Placenta	Placenta
37	chr22:33017200-33018000	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr22:33017200-33019000	Enhancers	Fetal Thymus	thymus
39	chr22:33017200-33020600	Enhancers	Colon Smooth Muscle	Colon
40	chr22:33017200-33020800	Enhancers	Ovary	ovary
41	chr22:33017400-33017800	Enhancers	Psoas Muscle	Psoas
42	chr22:33017400-33018000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr22:33017400-33018000	Enhancers	Brain Cingulate Gyrus	brain
44	chr22:33017400-33018000	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr22:33017400-33018000	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr22:33017400-33018200	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr22:33017400-33018400	Enhancers	Stomach Mucosa	stomach
48	chr22:33017400-33019000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr22:33017400-33019600	Enhancers	Fetal Intestine Large	intestine
50	chr22:33017400-33020000	Enhancers	Fetal Heart	heart

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