Variant report

Variant	rs2837058
Chromosome Location	chr21:40891422-40891423
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:40890342..40891575-chr21:41084640..41085747,7	MCF-7	breast:
2	chr21:40889961..40891928-chr21:40983982..40986182,2	MCF-7	breast:
3	chr21:40815529..40818322-chr21:40890161..40892801,2	MCF-7	breast:
4	chr21:40889185..40892036-chr21:40982501..40984839,2	MCF-7	breast:
5	chr21:40891069..40892721-chr21:40900987..40902576,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000157578	Chromatin interaction
ENSG00000184809	Chromatin interaction
ENSG00000185437	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11088480	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1522	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs16997635	1.00[CEU][hapmap]
rs16997780	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2037668	1.00[YRI][hapmap]
rs2091242	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2091243	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2103152	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837056	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837057	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837060	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837061	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837062	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837064	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837065	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837066	1.00[CEU][hapmap];0.89[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2837067	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs57239120	0.94[EUR][1000 genomes]
rs7281425	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs7281794	0.98[EUR][1000 genomes]
rs7282142	0.94[EUR][1000 genomes]
rs7283949	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs8130969	0.94[EUR][1000 genomes]
rs8131078	0.94[EUR][1000 genomes]
rs8133147	0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059868	chr21:40711535-41043291	Active TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv1061454	chr21:40757973-41265404	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1062088	chr21:40838027-40919253	Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2756754	chr21:40857523-40966156	Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv2758820	chr21:40857523-40966156	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	esv34779	chr21:40884871-40977473	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40836400-40894800	Weak transcription	Right Ventricle	heart
2	chr21:40848200-40895600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr21:40875800-40895200	Weak transcription	Brain Substantia Nigra	brain
4	chr21:40875800-40898600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr21:40876400-40894600	Weak transcription	Gastric	stomach
6	chr21:40876400-40897400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr21:40877400-40899600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr21:40880200-40899800	Weak transcription	Fetal Muscle Leg	muscle
9	chr21:40887400-40895200	Weak transcription	Liver	Liver
10	chr21:40888000-40894800	Weak transcription	Aorta	Aorta
11	chr21:40888200-40895400	Weak transcription	Fetal Brain Male	brain
12	chr21:40888200-40907400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr21:40888400-40895200	Weak transcription	Brain Anterior Caudate	brain
14	chr21:40890200-40891600	Enhancers	Stomach Mucosa	stomach
15	chr21:40890200-40897400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr21:40890400-40892000	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr21:40890600-40891600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr21:40890600-40891800	Enhancers	Fetal Heart	heart
19	chr21:40890800-40895200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr21:40890800-40895600	Weak transcription	Adipose Nuclei	Adipose
21	chr21:40891000-40891600	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr21:40891000-40891600	Enhancers	Pancreas	Pancrea
23	chr21:40891000-40895400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr21:40891000-40895400	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr21:40891000-40895600	Weak transcription	Brain Hippocampus Middle	brain
26	chr21:40891200-40894800	Weak transcription	Duodenum Mucosa	Duodenum
27	chr21:40891400-40891600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr21:40891400-40892000	Enhancers	Left Ventricle	heart
29	chr21:40891400-40892000	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr21:40891400-40894600	Weak transcription	Rectal Mucosa Donor 31	rectum

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