Variant report

Variant	rs7291935
Chromosome Location	chr22:33026842-33026843
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:33015941..33022634-chr22:33022783..33027992,6	MCF-7	breast:
2	chr22:32953953..32955561-chr22:33025472..33027182,2	MCF-7	breast:
3	22:32920308-32927723..22:33024278-33030812	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000185666	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12166424	1.00[CEU][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13340088	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13340089	1.00[CEU][hapmap];0.95[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16990867	0.95[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28373783	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs55771461	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55904255	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56315097	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58007110	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58659637	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7284915	0.96[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7290002	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7290248	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7291390	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73881769	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs8140105	1.00[CEU][hapmap];0.95[YRI][hapmap];0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8140208	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9619279	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs9619282	1.00[CEU][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9619285	1.00[CEU][hapmap]
rs9621511	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9621512	1.00[CEU][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
4	nsv459875	chr22:33025180-33097662	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv588896	chr22:33025180-33097662	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33017000-33027200	Enhancers	Placenta	Placenta
2	chr22:33020600-33030200	Weak transcription	Colon Smooth Muscle	Colon
3	chr22:33022200-33027000	Enhancers	Fetal Stomach	stomach
4	chr22:33023600-33028800	Enhancers	Primary hematopoietic stem cells	blood
5	chr22:33025000-33027200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr22:33025000-33028400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr22:33025000-33028800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr22:33025200-33030200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr22:33025200-33030200	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr22:33025400-33033200	Weak transcription	Fetal Kidney	kidney
11	chr22:33025600-33027800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr22:33025600-33028000	Weak transcription	Lung	lung
13	chr22:33025600-33030200	Weak transcription	Right Atrium	heart
14	chr22:33025800-33027600	Weak transcription	HepG2	liver
15	chr22:33025800-33027800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr22:33025800-33028000	Weak transcription	Adipose Nuclei	Adipose
17	chr22:33025800-33028000	Weak transcription	Fetal Muscle Trunk	muscle
18	chr22:33025800-33028000	Weak transcription	Left Ventricle	heart
19	chr22:33025800-33028200	Weak transcription	Fetal Muscle Leg	muscle
20	chr22:33025800-33028200	Weak transcription	Spleen	Spleen
21	chr22:33026000-33029400	Enhancers	Fetal Thymus	thymus
22	chr22:33026400-33028000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr22:33026600-33027000	Enhancers	Thymus	Thymus
24	chr22:33026600-33027400	Enhancers	GM12878-XiMat	blood
25	chr22:33026800-33027000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr22:33026800-33027000	Enhancers	Fetal Lung	lung
27	chr22:33026800-33027200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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