Variant report

Variant	rs73334142
Chromosome Location	chr14:45409009-45409010
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKBP3-7	chr14:45407755-45409773	NONHSAT036628

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs73334123	1.00[AFR][1000 genomes]
rs73334134	1.00[AFR][1000 genomes]
rs73348989	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869289	chr14:44752382-45447415	Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv901832	chr14:44847444-45415597	Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv1047886	chr14:45189653-45543182	Strong transcription Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv542079	chr14:45189653-45543182	Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv901841	chr14:45198196-45719643	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh 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	66 gene(s)	inside rSNPs	diseases
6	nsv1053437	chr14:45232269-45424222	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	esv1795667	chr14:45361680-45721052	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
8	esv1794986	chr14:45368685-45650813	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
9	nsv1042585	chr14:45401506-45497907	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45391200-45411000	Weak transcription	HSMM	muscle
2	chr14:45391200-45413000	Weak transcription	HUVEC	blood vessel
3	chr14:45394200-45413800	Weak transcription	HepG2	liver
4	chr14:45395200-45412400	Weak transcription	Brain Anterior Caudate	brain
5	chr14:45395200-45413800	Weak transcription	Fetal Brain Male	brain
6	chr14:45395400-45414400	Weak transcription	NH-A	brain
7	chr14:45395600-45416200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr14:45396200-45428400	Weak transcription	HMEC	breast
9	chr14:45396600-45414200	Weak transcription	Ovary	ovary
10	chr14:45396600-45416400	Weak transcription	Psoas Muscle	Psoas
11	chr14:45396800-45413000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr14:45396800-45414200	Weak transcription	Fetal Heart	heart
13	chr14:45397000-45414200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:45397000-45417000	Weak transcription	Stomach Mucosa	stomach
15	chr14:45397800-45409400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr14:45397800-45414200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr14:45398400-45414400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr14:45401000-45414200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr14:45401400-45411200	Weak transcription	NHDF-Ad	bronchial
20	chr14:45401800-45411200	Weak transcription	Brain Substantia Nigra	brain
21	chr14:45402000-45430000	Weak transcription	Colonic Mucosa	Colon
22	chr14:45402200-45409200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr14:45402400-45414400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr14:45403200-45410600	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr14:45403200-45415400	Strong transcription	Dnd41	blood
26	chr14:45403400-45410400	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr14:45403800-45409200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr14:45404200-45409400	Strong transcription	Primary T cells from cord blood	blood
29	chr14:45405000-45414200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr14:45405200-45414200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr14:45405400-45416800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr14:45405600-45410400	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr14:45405600-45411400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr14:45405600-45415200	Strong transcription	Fetal Lung	lung
35	chr14:45405600-45417200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr14:45405800-45409400	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr14:45405800-45410600	Strong transcription	Fetal Intestine Large	intestine
38	chr14:45405800-45412000	Strong transcription	Liver	Liver
39	chr14:45405800-45416600	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr14:45406000-45410600	Strong transcription	Primary B cells from peripheral blood	blood
41	chr14:45406400-45409600	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr14:45406600-45409600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr14:45406600-45410400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr14:45406600-45410600	Strong transcription	Primary B cells from cord blood	blood
45	chr14:45406600-45414200	Weak transcription	NHEK	skin
46	chr14:45406800-45409200	Strong transcription	Thymus	Thymus
47	chr14:45406800-45409200	Strong transcription	Osteobl	bone
48	chr14:45406800-45409400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr14:45406800-45409400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:45406800-45409400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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