Variant report

Variant	rs545426372
Chromosome Location	chr11:66843631-66843632
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:66842897..66845460-chr16:20741423..20744346,2	MCF-7	breast:
2	chr11:66795520..66800243-chr11:66842447..66847308,8	MCF-7	breast:
3	chr11:66622562..66624128-chr11:66843340..66844958,2	MCF-7	breast:
4	chr11:66843398..66845458-chr11:66847926..66850776,2	MCF-7	breast:
5	chr11:66836812..66842156-chr11:66842651..66845856,9	MCF-7	breast:
6	chr11:66788209..66792754-chr11:66842062..66847594,9	MCF-7	breast:
7	chr11:66821776..66823454-chr11:66841539..66844484,2	K562	blood:
8	chr11:66843110..66845610-chr11:67055483..67057190,2	K562	blood:
9	chr11:66797798..66801949-chr11:66843586..66847456,4	MCF-7	breast:
10	chr11:66748815..66755953-chr11:66843606..66849844,15	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000173621	Chromatin interaction
ENSG00000173227	Chromatin interaction
ENSG00000172932	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv555226	chr11:66579572-66845362	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
3	nsv532287	chr11:66784014-67023899	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	esv3470874	chr11:66842691-66845080	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	esv3470885	chr11:66842691-66845080	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	esv11382	chr11:66843375-66844907	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv555241	chr11:66843402-66844860	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	nsv555242	chr11:66843454-66844084	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv555243	chr11:66843454-66844860	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv555244	chr11:66843507-66844808	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv555245	chr11:66843610-66844189	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66825200-66849200	Weak transcription	Colon Smooth Muscle	Colon
2	chr11:66825400-66849400	Weak transcription	Ovary	ovary
3	chr11:66828000-66845600	Weak transcription	Osteobl	bone
4	chr11:66831400-66844600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:66839200-66845000	Weak transcription	Gastric	stomach
6	chr11:66839400-66844600	Weak transcription	Stomach Mucosa	stomach
7	chr11:66839400-66844800	Weak transcription	A549	lung
8	chr11:66839400-66845200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:66839400-66845800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr11:66839400-66849400	Weak transcription	Lung	lung
11	chr11:66839400-66849400	Weak transcription	Right Atrium	heart
12	chr11:66839400-66849400	Weak transcription	Right Ventricle	heart
13	chr11:66839600-66844600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr11:66839800-66844000	Strong transcription	Placenta	Placenta
15	chr11:66840200-66844800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:66840200-66845800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:66840400-66843800	Weak transcription	HMEC	breast
18	chr11:66840400-66845200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr11:66840400-66845800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr11:66841000-66844600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:66841000-66844600	Weak transcription	NHEK	skin
22	chr11:66841000-66844800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr11:66841200-66843800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:66841800-66845000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr11:66842200-66844000	Weak transcription	K562	blood
26	chr11:66842200-66844600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:66842200-66844800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr11:66842200-66846000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr11:66842400-66844600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:66843200-66843800	Enhancers	HepG2	liver
31	chr11:66843200-66844000	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr11:66843200-66844200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr11:66843400-66844000	Enhancers	Pancreas	Pancrea
34	chr11:66843400-66844200	Enhancers	Liver	Liver
35	chr11:66843400-66844600	Enhancers	Hela-S3	cervix
36	chr11:66843400-66846600	Enhancers	Fetal Intestine Large	intestine
37	chr11:66843400-66846600	Enhancers	GM12878-XiMat	blood
38	chr11:66843400-66846800	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr11:66843600-66843800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr11:66843600-66843800	Flanking Active TSS	Esophagus	oesophagus
41	chr11:66843600-66843800	Enhancers	Fetal Muscle Trunk	muscle
42	chr11:66843600-66844600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr11:66843600-66847000	Enhancers	Fetal Intestine Small	intestine

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