Variant report

Variant	rs572266379
Chromosome Location	chr11:47353593-47353594
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:47346954..47348985-chr11:47352662..47354542,2	MCF-7	breast:
2	chr11:47290102..47294520-chr11:47352678..47355861,4	K562	blood:
3	chr11:47291226..47293092-chr11:47352052..47354178,2	K562	blood:
4	chr11:47352349..47353915-chr11:47361681..47363878,2	MCF-7	breast:
5	chr11:47350500..47353711-chr11:47353800..47358007,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000110514	Chromatin interaction
ENSG00000256746	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv897323	chr11:47182926-47460306	Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv917316	chr11:47232210-47448882	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
3	esv3330173	chr11:47289256-47450681	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
4	esv3416377	chr11:47289276-47450651	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
5	nsv832141	chr11:47333180-47520993	Flanking Active TSS Genic enhancers Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	nsv554209	chr11:47353498-47364127	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47294600-47355200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr11:47296000-47353600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr11:47324200-47354600	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr11:47326000-47353600	Strong transcription	Fetal Stomach	stomach
5	chr11:47338800-47356200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr11:47342800-47353600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:47343200-47370600	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr11:47347800-47354000	Weak transcription	HSMM	muscle
9	chr11:47347800-47354800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr11:47348000-47358200	Weak transcription	K562	blood
11	chr11:47348600-47355000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr11:47349800-47354000	Genic enhancers	Fetal Muscle Trunk	muscle
13	chr11:47350400-47356800	Genic enhancers	Right Ventricle	heart
14	chr11:47350800-47354400	Genic enhancers	Left Ventricle	heart
15	chr11:47350800-47357400	Weak transcription	HepG2	liver
16	chr11:47351000-47354000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr11:47351000-47355800	Enhancers	Fetal Heart	heart
18	chr11:47351200-47353800	Weak transcription	Fetal Lung	lung
19	chr11:47351200-47353800	Enhancers	Stomach Mucosa	stomach
20	chr11:47351200-47354200	Weak transcription	Osteobl	bone
21	chr11:47351200-47354600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:47351400-47354800	Weak transcription	Brain Angular Gyrus	brain
23	chr11:47351400-47358800	Weak transcription	Aorta	Aorta
24	chr11:47351400-47375600	Weak transcription	Primary B cells from cord blood	blood
25	chr11:47351600-47358400	Weak transcription	A549	lung
26	chr11:47351600-47358600	Weak transcription	Hela-S3	cervix
27	chr11:47351800-47354000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr11:47352000-47353600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr11:47352000-47354200	Weak transcription	Primary T cells from cord blood	blood
30	chr11:47352000-47354200	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr11:47352000-47354200	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr11:47352200-47353800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr11:47352200-47354000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr11:47352200-47354600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:47352200-47355400	Weak transcription	Fetal Brain Female	brain
36	chr11:47352400-47353600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr11:47352400-47353600	Weak transcription	Right Atrium	heart
38	chr11:47352400-47353800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr11:47352400-47354000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr11:47352400-47354000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr11:47352400-47354000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr11:47352400-47354000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr11:47352400-47354000	Weak transcription	Dnd41	blood
44	chr11:47352400-47354200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr11:47352400-47354200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr11:47352400-47354200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr11:47352400-47354200	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr11:47352400-47354200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:47352400-47354200	Enhancers	Colonic Mucosa	Colon
50	chr11:47352400-47354200	Weak transcription	Ovary	ovary

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