Variant report

Variant	rs7941789
Chromosome Location	chr11:108614424-108614425
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:108612671..108614669-chr11:108618122..108620015,2	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs17108652	1.00[AMR][1000 genomes]
rs2250385	1.00[AMR][1000 genomes]
rs2553759	1.00[AMR][1000 genomes]
rs60625914	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60861863	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7110445	1.00[AMR][1000 genomes]
rs7930190	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7932521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7950532	1.00[AMR][1000 genomes]
rs898973	1.00[AMR][1000 genomes]
rs970163	1.00[AMR][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	nsv1052254	chr11:108122683-108845008	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv541164	chr11:108122683-108845008	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv898386	chr11:108409442-108831875	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv898388	chr11:108440814-108724639	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv832264	chr11:108449613-108623720	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108581600-108626600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr11:108581800-108616200	Weak transcription	Esophagus	oesophagus
3	chr11:108592000-108620000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr11:108594200-108615400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr11:108594400-108625400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr11:108596400-108621000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr11:108603600-108617600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:108604600-108616000	Weak transcription	Right Atrium	heart
9	chr11:108604600-108625600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr11:108604600-108625800	Weak transcription	Primary T cells from cord blood	blood
11	chr11:108604800-108627800	Weak transcription	Left Ventricle	heart
12	chr11:108605200-108614800	Weak transcription	A549	lung
13	chr11:108605200-108618400	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr11:108605400-108625400	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr11:108605800-108622800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr11:108605800-108663800	Weak transcription	K562	blood
17	chr11:108606000-108627400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:108607600-108614800	Weak transcription	Ovary	ovary
19	chr11:108607600-108622000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr11:108607600-108644600	Weak transcription	Aorta	Aorta
21	chr11:108607800-108628200	Weak transcription	Liver	Liver
22	chr11:108611000-108625400	Weak transcription	NHLF	lung
23	chr11:108612200-108627400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr11:108612600-108617000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:108612600-108622400	Weak transcription	Primary B cells from peripheral blood	blood
26	chr11:108612600-108626600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:108612800-108630200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr11:108614400-108614600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:108614400-108614600	Enhancers	Pancreas	Pancrea
30	chr11:108614400-108614600	Enhancers	Right Ventricle	heart
31	chr11:108614400-108614600	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr11:108614400-108614600	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr11:108614400-108614800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:108614400-108615000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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