Variant report

Variant	rs555695017
Chromosome Location	chr11:104950985-104950986
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv468862	chr11:104774014-105243371	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv556218	chr11:104774014-105243371	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	esv3385159	chr11:104786549-105051555	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv1044970	chr11:104809246-105225032	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv541160	chr11:104809246-105225032	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
8	esv2757475	chr11:104895876-104979717	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	esv2759863	chr11:104895876-104979717	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv470	chr11:104916361-104961230	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	n/a
11	nsv1042388	chr11:104934347-104988325	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island	4 gene(s)	inside rSNPs	diseases
12	esv2756562	chr11:104937371-104981568	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region CpG island	4 gene(s)	inside rSNPs	diseases
13	esv3450730	chr11:104938956-104968986	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
14	nsv1040275	chr11:104939029-104988325	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island	4 gene(s)	inside rSNPs	diseases
15	nsv818863	chr11:104940204-104960997	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	n/a
16	nsv8871	chr11:104941750-104973508	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island	4 gene(s)	inside rSNPs	diseases
17	esv33277	chr11:104944762-104969485	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
18	nsv1054109	chr11:104948117-104976058	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island	3 gene(s)	inside rSNPs	diseases
19	nsv949337	chr11:104950007-105510193	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
20	nsv1049355	chr11:104950412-104972518	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island	3 gene(s)	inside rSNPs	diseases
21	nsv442241	chr11:104950424-104972558	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island	3 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	chr11:104948000-104953200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:104949200-104951000	Weak transcription	Adipose Nuclei	Adipose
3	chr11:104950200-104951000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:104950200-104953400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr11:104950400-104951200	Enhancers	Small Intestine	intestine
6	chr11:104950400-104951400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr11:104950400-104951800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr11:104950400-104952000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr11:104950400-104952200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:104950600-104951000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:104950600-104951800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:104950600-104951800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:104950600-104952400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr11:104950600-104953800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr11:104950800-104951000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr11:104950800-104951000	Enhancers	H9 Cell Line	embryonic stem cell
17	chr11:104950800-104951000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr11:104950800-104951000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr11:104950800-104951000	Enhancers	Duodenum Mucosa	Duodenum
20	chr11:104950800-104951000	Weak transcription	Right Atrium	heart
21	chr11:104950800-104951200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
22	chr11:104950800-104951200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr11:104950800-104951200	Enhancers	Fetal Intestine Large	intestine
24	chr11:104950800-104951200	Enhancers	NHEK	skin
25	chr11:104950800-104951400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:104950800-104951600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:104950800-104951600	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr11:104950800-104951600	Active TSS	Rectal Mucosa Donor 29	rectum
29	chr11:104950800-104951800	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr11:104950800-104951800	Enhancers	Dnd41	blood
31	chr11:104950800-104951800	Enhancers	HUVEC	blood vessel
32	chr11:104950800-104952200	Enhancers	Fetal Intestine Small	intestine
33	chr11:104950800-104953000	Enhancers	HUES6 Cell Line	embryonic stem cell

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