Variant report

Variant	rs1941711
Chromosome Location	chr11:58893935-58893936
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050013	chr11:58394598-59221090	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv948365	chr11:58515163-59156405	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	esv2758272	chr11:58700092-59008673	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv2759830	chr11:58700092-59008673	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	esv2757447	chr11:58746238-58906018	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
6	nsv975329	chr11:58767290-58907813	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv430388	chr11:58769524-58925824	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
8	nsv468578	chr11:58790628-58901763	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv555147	chr11:58790628-58901763	Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv975190	chr11:58893580-58903375	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58875200-58909600	Weak transcription	Stomach Mucosa	stomach
2	chr11:58875400-58909600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr11:58880800-58894800	ZNF genes & repeats	Dnd41	blood
4	chr11:58881600-58903600	Weak transcription	Hela-S3	cervix
5	chr11:58884000-58894800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:58886000-58898800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:58886600-58898600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:58886800-58898400	Weak transcription	Osteobl	bone
9	chr11:58886800-58898800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr11:58886800-58901200	Weak transcription	NHLF	lung
11	chr11:58886800-58903400	Weak transcription	NHEK	skin
12	chr11:58887000-58899000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:58887000-58899000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr11:58887800-58894600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr11:58888400-58899400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr11:58889800-58894600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr11:58890000-58894600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr11:58890200-58894200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:58890600-58894400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
20	chr11:58890800-58894000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr11:58890800-58894400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
22	chr11:58890800-58894600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr11:58891000-58894400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:58891400-58899200	Weak transcription	Left Ventricle	heart
25	chr11:58891600-58894000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
26	chr11:58891600-58894400	Strong transcription	HMEC	breast
27	chr11:58891800-58894400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr11:58891800-58894600	ZNF genes & repeats	Primary B cells from cord blood	blood
29	chr11:58892000-58894400	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr11:58892200-58894000	ZNF genes & repeats	A549	lung
31	chr11:58892200-58899200	Weak transcription	Small Intestine	intestine
32	chr11:58892800-58898000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr11:58893200-58894600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:58893200-58899000	Weak transcription	Thymus	Thymus
35	chr11:58893400-58897600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:58893400-58898000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:58893600-58894400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr11:58893600-58898800	Weak transcription	Duodenum Mucosa	Duodenum
39	chr11:58893600-58898800	Weak transcription	Fetal Thymus	thymus
40	chr11:58893600-58899000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr11:58893600-58899000	Weak transcription	Fetal Intestine Large	intestine
42	chr11:58893600-58902200	Weak transcription	HSMM	muscle
43	chr11:58893800-58896200	Weak transcription	Primary T cells from cord blood	blood
44	chr11:58893800-58898000	Weak transcription	Primary hematopoietic stem cells	blood
45	chr11:58893800-58898800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr11:58893800-58901800	Weak transcription	NHDF-Ad	bronchial
47	chr11:58893800-58903400	Weak transcription	HUVEC	blood vessel
48	chr11:58893800-58909600	Weak transcription	Fetal Brain Male	brain

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