Variant report

Variant	rs200569273
Chromosome Location	chr11:3879484-3879485
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:3868931..3871708-chr11:3879201..3881695,3	K562	blood:
2	chr11:3851375..3853538-chr11:3878671..3880501,2	K562	blood:
3	chr11:3853294..3855023-chr11:3877821..3880627,2	K562	blood:
4	chr11:3876409..3878027-chr11:3879355..3881248,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000177105	Chromatin interaction
ENSG00000263421	Chromatin interaction
ENSG00000167323	Chromatin interaction
ENSG00000228661	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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	nsv1049560	chr11:3678259-3980746	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv540907	chr11:3678259-3980746	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' 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	32 gene(s)	inside rSNPs	diseases
3	nsv1052744	chr11:3739162-4017601	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv1047025	chr11:3750969-4017601	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	esv1803195	chr11:3806490-3924156	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv1046065	chr11:3808818-4049150	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv540909	chr11:3808818-4049150	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
8	nsv1046325	chr11:3856201-3895148	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
9	nsv1039059	chr11:3856201-3909415	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
10	nsv540910	chr11:3856201-3909415	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
11	nsv1051580	chr11:3856201-3924216	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
12	nsv1043265	chr11:3856201-3926407	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
13	nsv896894	chr11:3859856-3888234	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
14	nsv869701	chr11:3879297-3973762	Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
15	esv1955529	chr11:3879484-3879485	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3877200-3879600	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr11:3877200-3881200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr11:3877400-3879800	Flanking Active TSS	Primary hematopoietic stem cells	blood
4	chr11:3877400-3881200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
5	chr11:3877400-3881200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr11:3877400-3881400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
7	chr11:3877400-3882600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
8	chr11:3877600-3881200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:3877600-3881400	Flanking Active TSS	Fetal Thymus	thymus
10	chr11:3877600-3883800	Flanking Active TSS	Primary T cells from cord blood	blood
11	chr11:3877800-3879600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
12	chr11:3877800-3881200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr11:3877800-3881200	Flanking Active TSS	Dnd41	blood
14	chr11:3878000-3880200	Active TSS	Brain Inferior Temporal Lobe	brain
15	chr11:3878000-3881200	Enhancers	Brain Germinal Matrix	brain
16	chr11:3878000-3881200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr11:3878000-3881400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr11:3878000-3882400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr11:3878000-3883000	Weak transcription	Fetal Intestine Large	intestine
20	chr11:3878000-3883200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
21	chr11:3878000-3883200	Enhancers	Fetal Heart	heart
22	chr11:3878200-3879600	Weak transcription	Brain Substantia Nigra	brain
23	chr11:3878200-3879800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr11:3878200-3880000	Weak transcription	HSMMtube	muscle
25	chr11:3878200-3880400	Active TSS	Fetal Muscle Trunk	muscle
26	chr11:3878200-3880400	Enhancers	Small Intestine	intestine
27	chr11:3878200-3880400	Weak transcription	NH-A	brain
28	chr11:3878200-3880600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:3878200-3880600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:3878200-3880600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:3878200-3880600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr11:3878200-3880600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:3878200-3880600	Enhancers	Brain Cingulate Gyrus	brain
34	chr11:3878200-3880600	Enhancers	Stomach Mucosa	stomach
35	chr11:3878200-3880600	Weak transcription	HSMM	muscle
36	chr11:3878200-3881000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr11:3878200-3881200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:3878200-3881200	Enhancers	Placenta	Placenta
39	chr11:3878200-3881200	Enhancers	Gastric	stomach
40	chr11:3878200-3881200	Enhancers	Pancreas	Pancrea
41	chr11:3878200-3881200	Enhancers	Spleen	Spleen
42	chr11:3878200-3886800	Weak transcription	NHLF	lung
43	chr11:3878400-3879600	Enhancers	Brain Angular Gyrus	brain
44	chr11:3878400-3879600	Flanking Active TSS	Psoas Muscle	Psoas
45	chr11:3878400-3880000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
46	chr11:3878400-3880200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:3878400-3880400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr11:3878400-3880600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr11:3878400-3880600	Enhancers	Fetal Stomach	stomach
50	chr11:3878400-3881200	Enhancers	NHDF-Ad	bronchial

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