Variant report

Variant	rs11973583
Chromosome Location	chr7:26358318-26358319
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:26347459..26349895-chr7:26355478..26358331,2	MCF-7	breast:
2	chr7:26237797..26240269-chr7:26356166..26359044,2	MCF-7	breast:
3	chr7:26353571..26356318-chr7:26357830..26359410,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10251329	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10279116	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10499574	0.81[CEU][hapmap]
rs2893245	1.00[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4722590	0.81[CEU][hapmap]
rs6461926	0.96[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6976271	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7786623	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7794280	0.96[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][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	nsv1021308	chr7:26116605-26419720	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv1018971	chr7:26161228-26380361	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv1029596	chr7:26302739-26737913	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv538804	chr7:26302739-26737913	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	esv2761313	chr7:26340970-26389772	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26335200-26386400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:26345600-26386200	Weak transcription	Thymus	Thymus
3	chr7:26345800-26375600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr7:26346000-26368200	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr7:26346000-26373800	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr7:26346800-26360600	Weak transcription	Fetal Thymus	thymus
7	chr7:26347800-26358600	Weak transcription	Adipose Nuclei	Adipose
8	chr7:26349800-26360400	Weak transcription	HepG2	liver
9	chr7:26349800-26360600	Weak transcription	Primary T cells from cord blood	blood
10	chr7:26351400-26360600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr7:26353600-26358600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:26353600-26368000	Weak transcription	Spleen	Spleen
13	chr7:26354600-26359200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr7:26354800-26358600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:26354800-26358600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:26355200-26358600	Weak transcription	GM12878-XiMat	blood
17	chr7:26355400-26360800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:26356400-26358400	Strong transcription	Primary hematopoietic stem cells	blood
19	chr7:26356600-26361400	Weak transcription	Pancreas	Pancrea
20	chr7:26356800-26358600	Weak transcription	Primary B cells from cord blood	blood
21	chr7:26357800-26358600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr7:26358000-26359800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:26358200-26359000	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr7:26358200-26359200	Enhancers	Liver	Liver
25	chr7:26358200-26359400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr7:26358200-26359800	Enhancers	Primary B cells from peripheral blood	blood

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