Variant report

Variant	rs569825707
Chromosome Location	chr11:76389178-76389179
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	chr11:76309665..76310190-chr11:76388826..76389418,2	MCF-7	breast:
2	chr11:76387901..76389837-chr11:76392060..76394666,2	K562	blood:

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	nsv1043912	chr11:76301316-76439095	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1039451	chr11:76301316-76440221	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv1810781	chr11:76311021-76464814	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1047069	chr11:76367686-76420813	Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	esv1850014	chr11:76384895-76464814	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv39437	chr11:76388349-76396423	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76384400-76391800	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr11:76384400-76412800	Weak transcription	Right Atrium	heart
3	chr11:76385400-76390200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:76385400-76391600	Weak transcription	Right Ventricle	heart
5	chr11:76386200-76389600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr11:76386200-76389600	Enhancers	GM12878-XiMat	blood
7	chr11:76387000-76389400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr11:76387000-76390600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:76387200-76389200	Enhancers	Fetal Thymus	thymus
10	chr11:76387200-76390200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr11:76387400-76389200	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr11:76387400-76390200	Enhancers	Primary hematopoietic stem cells	blood
13	chr11:76387800-76389200	Enhancers	HSMMtube	muscle
14	chr11:76388000-76389200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:76388000-76389200	Enhancers	Fetal Muscle Leg	muscle
16	chr11:76388200-76389200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr11:76388200-76389400	Enhancers	Stomach Smooth Muscle	stomach
18	chr11:76388200-76389800	Enhancers	Duodenum Mucosa	Duodenum
19	chr11:76388200-76390000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr11:76388400-76391600	Weak transcription	Pancreas	Pancrea
21	chr11:76388400-76392200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr11:76388600-76389200	Enhancers	Spleen	Spleen
23	chr11:76388600-76391600	Weak transcription	Fetal Heart	heart
24	chr11:76388800-76389200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:76388800-76389600	Bivalent Enhancer	Fetal Stomach	stomach
26	chr11:76388800-76390000	Enhancers	Primary B cells from cord blood	blood
27	chr11:76388800-76391400	Weak transcription	Placenta	Placenta
28	chr11:76388800-76391800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:76389000-76389200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr11:76389000-76389200	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr11:76389000-76391400	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr11:76389000-76391600	Weak transcription	Adipose Nuclei	Adipose
33	chr11:76389000-76391800	Weak transcription	Colon Smooth Muscle	Colon

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