Variant report

Variant	rs190004606
Chromosome Location	chr14:67933744-67933745
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv1045518	chr14:67529049-67959582	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv456331	chr14:67732861-68103780	Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv564961	chr14:67732861-68103780	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv470651	chr14:67732861-68113293	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv902066	chr14:67873128-68103780	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv1048046	chr14:67932876-67958467	Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67927800-67935400	Enhancers	Fetal Thymus	thymus
2	chr14:67928200-67935200	Enhancers	Thymus	Thymus
3	chr14:67928600-67934400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr14:67928800-67933800	Weak transcription	Fetal Intestine Large	intestine
5	chr14:67928800-67946600	Weak transcription	Pancreas	Pancrea
6	chr14:67929000-67934000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr14:67929200-67933800	Weak transcription	Fetal Intestine Small	intestine
8	chr14:67929600-67942600	Weak transcription	Lung	lung
9	chr14:67929800-67938600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr14:67930200-67934000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr14:67930400-67935400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr14:67931200-67939600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr14:67931400-67939000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:67931800-67938600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr14:67932000-67934000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr14:67932000-67934200	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr14:67932000-67939600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr14:67932200-67933800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr14:67932200-67934200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr14:67932400-67933800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr14:67932400-67934000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr14:67932600-67934000	Enhancers	Duodenum Mucosa	Duodenum
23	chr14:67932600-67934400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr14:67932800-67933800	Weak transcription	Placenta	Placenta
25	chr14:67932800-67934000	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr14:67932800-67937600	Weak transcription	Primary T cells from cord blood	blood
27	chr14:67932800-67939200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr14:67932800-67940000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:67933000-67954400	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr14:67933200-67934000	Enhancers	Small Intestine	intestine
31	chr14:67933200-67939400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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