Variant report

Variant	rs534022908
Chromosome Location	chr11:85890261-85890262
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:85888440..85890283-chr11:85910710..85912765,2	K562	blood:
2	chr11:85861500..85864478-chr11:85889998..85891794,2	K562	blood:

Variant related genes	Relation type
ENSG00000200877	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050948	chr11:85756325-85968665	Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv541117	chr11:85756325-85968665	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv832223	chr11:85845315-86015957	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	esv2757460	chr11:85869944-85905513	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv2759846	chr11:85869944-85905513	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1040400	chr11:85883303-85898809	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv1043422	chr11:85883840-85898809	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv1049658	chr11:85885461-85898809	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv1049881	chr11:85885684-85898809	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
10	nsv555645	chr11:85886994-85898770	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	esv2760233	chr11:85887957-85899812	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
12	nsv8851	chr11:85888397-85899580	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
13	esv999880	chr11:85888638-85902307	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
14	esv3471552	chr11:85888769-85899564	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
15	esv3471563	chr11:85888947-85899377	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
16	esv999639	chr11:85889185-85898814	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
17	esv992965	chr11:85889435-85899023	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
18	nsv514637	chr11:85889632-85898584	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
19	esv988186	chr11:85889658-85898821	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
20	esv2421379	chr11:85889658-85898821	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
21	nsv442624	chr11:85889658-85898821	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85882600-85890800	Enhancers	Placenta	Placenta
2	chr11:85882600-85891600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr11:85883200-85891400	Weak transcription	Thymus	Thymus
4	chr11:85883800-85890400	Enhancers	Placenta Amnion	Placenta Amnion
5	chr11:85883800-85890800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:85885200-85895200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:85886000-85890800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr11:85886000-85891600	Weak transcription	Brain Substantia Nigra	brain
9	chr11:85886000-85891600	Weak transcription	Fetal Thymus	thymus
10	chr11:85886000-85894000	Weak transcription	Esophagus	oesophagus
11	chr11:85886000-85894000	Weak transcription	Pancreas	Pancrea
12	chr11:85886000-85903000	Weak transcription	Brain Cingulate Gyrus	brain
13	chr11:85886200-85890400	Weak transcription	Lung	lung
14	chr11:85886200-85893800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr11:85886800-85894000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr11:85887000-85890400	Weak transcription	Fetal Muscle Leg	muscle
17	chr11:85887000-85891600	Weak transcription	Brain Angular Gyrus	brain
18	chr11:85887000-85892800	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr11:85887000-85894000	Weak transcription	Right Atrium	heart
20	chr11:85887200-85894200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr11:85887200-85898000	Weak transcription	Brain Anterior Caudate	brain
22	chr11:85887600-85891400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr11:85887800-85892400	Enhancers	Adipose Nuclei	Adipose
24	chr11:85887800-85893800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr11:85888000-85891400	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr11:85888000-85893400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:85888000-85894000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:85888200-85890400	Weak transcription	Liver	Liver
29	chr11:85888200-85890400	Weak transcription	HepG2	liver
30	chr11:85888600-85893400	Weak transcription	Fetal Intestine Large	intestine
31	chr11:85888800-85893000	Weak transcription	Fetal Intestine Small	intestine
32	chr11:85888800-85893400	Weak transcription	HMEC	breast
33	chr11:85888800-85893600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:85888800-85893800	Enhancers	K562	blood
35	chr11:85888800-85894000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:85888800-85894000	Weak transcription	A549	lung
37	chr11:85888800-85894000	Weak transcription	GM12878-XiMat	blood
38	chr11:85888800-85894000	Enhancers	Hela-S3	cervix
39	chr11:85888800-85894200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr11:85888800-85894200	Weak transcription	Brain Hippocampus Middle	brain
41	chr11:85888800-85894200	Weak transcription	Spleen	Spleen
42	chr11:85888800-85895600	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr11:85888800-85896400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr11:85889000-85895800	Weak transcription	Psoas Muscle	Psoas
45	chr11:85889400-85891000	Enhancers	Osteobl	bone
46	chr11:85889400-85895200	Enhancers	Primary hematopoietic stem cells	blood
47	chr11:85889600-85890800	Enhancers	NHDF-Ad	bronchial
48	chr11:85889800-85890400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:85889800-85890600	Enhancers	Small Intestine	intestine
50	chr11:85889800-85891200	Weak transcription	Primary B cells from cord blood	blood

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