Variant report

Variant	rs3892497
Chromosome Location	chr11:120411267-120411268
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:120400831..120403773-chr11:120408682..120411578,3	K562	blood:
2	chr11:120400831..120403773-chr11:120408317..120411578,3	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11599940	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11600436	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11601826	0.85[AMR][1000 genomes]
rs11602075	0.82[AMR][1000 genomes]
rs11602493	0.83[EUR][1000 genomes]
rs11603180	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11824600	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11827023	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1573789	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17311310	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17311317	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17311324	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4297478	0.84[AMR][1000 genomes]
rs4500499	0.82[EUR][1000 genomes]
rs4561221	0.85[AMR][1000 genomes]
rs4936521	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4938818	0.82[EUR][1000 genomes]
rs61900897	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61900900	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73000621	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1051115	chr11:120376808-120446434	Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1036388	chr11:120395104-120427135	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1054301	chr11:120396485-120465800	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1053749	chr11:120398643-120417586	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1035499	chr11:120398643-120446434	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1049494	chr11:120400115-120453381	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv1052932	chr11:120406628-120442955	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120398600-120417200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:120403800-120417000	Weak transcription	Right Atrium	heart
3	chr11:120403800-120418800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:120403800-120418800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:120404000-120411800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:120404200-120411600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr11:120409200-120411800	Enhancers	HSMMtube	muscle
8	chr11:120409200-120412400	Enhancers	Primary B cells from peripheral blood	blood
9	chr11:120409800-120414600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr11:120410000-120411600	Weak transcription	Fetal Muscle Leg	muscle
11	chr11:120410000-120412600	Enhancers	Fetal Intestine Small	intestine
12	chr11:120410200-120411600	Weak transcription	Fetal Lung	lung
13	chr11:120410200-120411600	Enhancers	HepG2	liver
14	chr11:120410200-120412600	Enhancers	Fetal Intestine Large	intestine
15	chr11:120410400-120411600	Weak transcription	Fetal Kidney	kidney
16	chr11:120410600-120411800	Enhancers	NH-A	brain
17	chr11:120410600-120412400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:120410800-120411400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr11:120410800-120412000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr11:120411000-120411800	Weak transcription	Fetal Heart	heart
21	chr11:120411000-120411800	Weak transcription	HSMM	muscle
22	chr11:120411000-120416800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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