Variant report

Variant	rs117962157
Chromosome Location	chr14:66346877-66346878
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2014B16.3.1-3	chr14:66346310-66347788	NONHSAT037399

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
2	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	nsv1045000	chr14:66010886-66372518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1042671	chr14:66010886-66399888	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv817409	chr14:66220075-66990168	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv564953	chr14:66287921-67046960	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv1050485	chr14:66308283-67109270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
9	nsv832820	chr14:66310846-66362845	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv530775	chr14:66316836-67079049	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
11	nsv530793	chr14:66317036-67078908	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
12	nsv1046455	chr14:66345369-66848234	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
13	nsv974348	chr14:66346539-66347039	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66343200-66347000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
2	chr14:66343600-66347000	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr14:66343600-66348000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr14:66344000-66347200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr14:66344200-66347800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr14:66344600-66347000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr14:66344600-66347600	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr14:66345000-66347600	Enhancers	Fetal Thymus	thymus
9	chr14:66345200-66347800	Enhancers	NHDF-Ad	bronchial
10	chr14:66345800-66347800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr14:66345800-66348000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr14:66346000-66347000	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr14:66346000-66347800	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr14:66346000-66347800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr14:66346200-66347000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr14:66346200-66347200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr14:66346200-66347200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr14:66346200-66347600	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr14:66346400-66347000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:66346400-66347000	Enhancers	Primary hematopoietic stem cells	blood
21	chr14:66346400-66347000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr14:66346400-66347200	Enhancers	Primary T cells fromperipheralblood	blood
23	chr14:66346400-66347400	Weak transcription	Primary T cells from cord blood	blood
24	chr14:66346600-66348000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr14:66346800-66347000	Enhancers	Esophagus	oesophagus
26	chr14:66346800-66347200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr14:66346800-66347200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr14:66346800-66347200	Flanking Active TSS	Dnd41	blood
29	chr14:66346800-66347800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr14:66346800-66348400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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