Variant report

Variant	rs11211257
Chromosome Location	chr1:46581933-46581934
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:46578598..46585447-chr1:46594467..46599717,10	K562	blood:
2	chr1:46577072..46584318-chr1:46595242..46600133,10	K562	blood:
3	chr1:46580648..46582998-chr1:46586284..46587905,2	K562	blood:
4	chr1:46579933..46582318-chr1:46586882..46588511,2	MCF-7	breast:
5	chr1:46580670..46583258-chr1:46587444..46589652,3	K562	blood:

Variant related genes	Relation type
ENSG00000117461	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1085240	0.85[ASN][1000 genomes]
rs12090501	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1473840	0.80[ASN][1000 genomes]
rs1588663	0.90[ASN][1000 genomes]
rs1612419	0.90[ASN][1000 genomes]
rs1613296	0.90[ASN][1000 genomes]
rs1707302	0.81[ASN][1000 genomes]
rs1707303	0.91[ASN][1000 genomes]
rs1707317	0.85[ASN][1000 genomes]
rs1707322	0.85[ASN][1000 genomes]
rs1707337	0.85[ASN][1000 genomes]
rs1707338	0.85[ASN][1000 genomes]
rs1707339	0.84[ASN][1000 genomes]
rs1768800	0.90[ASN][1000 genomes]
rs1768801	0.90[ASN][1000 genomes]
rs1768802	0.90[ASN][1000 genomes]
rs1768807	0.85[ASN][1000 genomes]
rs1768815	0.85[ASN][1000 genomes]
rs1768817	0.84[ASN][1000 genomes]
rs1768818	0.84[ASN][1000 genomes]
rs2297883	0.85[ASN][1000 genomes]
rs2458400	0.85[ASN][1000 genomes]
rs4660341	0.92[ASN][1000 genomes]
rs7538978	0.84[ASN][1000 genomes]
rs785463	0.85[ASN][1000 genomes]
rs785465	0.85[ASN][1000 genomes]
rs785466	0.85[ASN][1000 genomes]
rs785467	0.85[ASN][1000 genomes]
rs785468	0.85[ASN][1000 genomes]
rs785469	0.85[ASN][1000 genomes]
rs785470	0.85[ASN][1000 genomes]
rs785483	0.93[ASN][1000 genomes]
rs785484	0.96[ASN][1000 genomes]
rs785486	0.96[ASN][1000 genomes]
rs785490	0.96[ASN][1000 genomes]
rs785493	0.96[ASN][1000 genomes]
rs785496	0.96[ASN][1000 genomes]
rs785497	0.96[ASN][1000 genomes]
rs785499	0.92[ASN][1000 genomes]
rs785500	0.90[ASN][1000 genomes]
rs785501	0.85[ASN][1000 genomes]
rs785504	0.91[ASN][1000 genomes]
rs785506	0.87[ASN][1000 genomes]
rs785507	0.87[ASN][1000 genomes]
rs785510	0.85[ASN][1000 genomes]
rs785512	0.85[ASN][1000 genomes]
rs785516	0.93[ASN][1000 genomes]
rs785517	0.96[ASN][1000 genomes]
rs785518	0.87[ASN][1000 genomes]
rs785519	0.96[ASN][1000 genomes]
rs796773	0.94[ASN][1000 genomes]
rs814168	0.88[ASN][1000 genomes]
rs9429186	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
2	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
3	nsv871928	chr1:46024701-46609736	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
4	nsv1003517	chr1:46244432-46609881	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1005189	chr1:46335186-46949309	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
6	nsv534946	chr1:46335186-46949309	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
7	esv2761743	chr1:46339858-47026743	Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
8	nsv1000557	chr1:46383876-46591182	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	esv2754420	chr1:46461580-46635180	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
10	nsv1006747	chr1:46476089-46655484	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv534947	chr1:46476089-46655484	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
12	nsv1012418	chr1:46544842-46619890	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
13	nsv534948	chr1:46544842-46619890	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
14	nsv1006530	chr1:46544842-46655484	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
15	nsv534949	chr1:46544842-46655484	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 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	chr1:46540400-46595200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:46541200-46595800	Weak transcription	Fetal Intestine Small	intestine
3	chr1:46562400-46595800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr1:46565600-46593200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:46566800-46594000	Weak transcription	Thymus	Thymus
6	chr1:46567800-46595200	Weak transcription	Primary T cells from cord blood	blood
7	chr1:46574000-46595200	Weak transcription	HSMM	muscle
8	chr1:46576000-46583400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:46576000-46594200	Weak transcription	HMEC	breast
10	chr1:46576600-46592000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:46576800-46593200	Weak transcription	Hela-S3	cervix
12	chr1:46577200-46583200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:46577200-46583400	Weak transcription	Lung	lung
14	chr1:46577200-46593800	Weak transcription	Right Ventricle	heart
15	chr1:46579800-46594400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:46580200-46582000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:46580200-46583200	Weak transcription	HepG2	liver
18	chr1:46580400-46593400	Weak transcription	Right Atrium	heart
19	chr1:46580600-46582800	Weak transcription	Psoas Muscle	Psoas
20	chr1:46581000-46593800	Weak transcription	Brain Germinal Matrix	brain
21	chr1:46581200-46582000	Enhancers	K562	blood
22	chr1:46581200-46592000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:46581400-46589200	Weak transcription	Adipose Nuclei	Adipose
24	chr1:46581600-46582000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:46581600-46582200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:46581600-46584400	Weak transcription	Fetal Heart	heart
27	chr1:46581800-46582000	Genic enhancers	Left Ventricle	heart
28	chr1:46581800-46584000	Weak transcription	GM12878-XiMat	blood
29	chr1:46581800-46593400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:46581800-46595200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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