Variant report

Variant	rs553597627
Chromosome Location	chr10:38697762-38697763
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF37A-3	chr10:38697731-38697862	ENSG00000225119.2

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	nsv427860	chr10:38588021-38818835	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv895034	chr10:38632352-38743545	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2764202	chr10:38641508-39076221	Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1048953	chr10:38645824-39074038	Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv428230	chr10:38652001-38818835	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2757379	chr10:38677023-38978680	Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	esv2759744	chr10:38677023-39154935	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv947860	chr10:38678275-38747483	Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv895035	chr10:38678941-38739427	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv895036	chr10:38678941-38741100	Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv895037	chr10:38678941-38741777	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv895038	chr10:38678941-38890240	ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv1036840	chr10:38682579-39074038	ZNF genes & repeats Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv540569	chr10:38689167-38769822	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases
15	esv16395	chr10:38693709-38772324	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv821215	chr10:38693709-38772324	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	nsv540570	chr10:38696654-38728292	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv540571	chr10:38696654-38743406	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv540572	chr10:38696654-38769822	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases
20	nsv1052697	chr10:38696664-39030136	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
21	nsv1043781	chr10:38696664-39074038	ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38691800-38698000	Weak transcription	Spleen	Spleen
2	chr10:38692200-38741000	Weak transcription	Aorta	Aorta
3	chr10:38692400-38739600	Weak transcription	Gastric	stomach
4	chr10:38692600-38698000	Weak transcription	Ovary	ovary
5	chr10:38692600-38699400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr10:38692600-38716400	Weak transcription	Primary T cells from cord blood	blood
7	chr10:38692600-38736800	Weak transcription	Pancreas	Pancrea
8	chr10:38692600-38737200	Weak transcription	Esophagus	oesophagus
9	chr10:38692800-38698000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:38692800-38698000	Weak transcription	Lung	lung
11	chr10:38692800-38699800	Weak transcription	Fetal Stomach	stomach
12	chr10:38692800-38700000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr10:38692800-38700200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr10:38692800-38701800	Weak transcription	Fetal Intestine Small	intestine
15	chr10:38692800-38703200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:38692800-38709200	Weak transcription	Adipose Nuclei	Adipose
17	chr10:38692800-38714600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:38692800-38728800	Weak transcription	Brain Substantia Nigra	brain
19	chr10:38692800-38736800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr10:38692800-38736800	Weak transcription	Brain Anterior Caudate	brain
21	chr10:38692800-38736800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr10:38692800-38737200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr10:38692800-38737200	Weak transcription	Brain Hippocampus Middle	brain
24	chr10:38692800-38737400	Weak transcription	Fetal Intestine Large	intestine
25	chr10:38692800-38737600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr10:38692800-38741200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr10:38693000-38698000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr10:38693000-38698000	Weak transcription	Left Ventricle	heart
29	chr10:38693000-38700000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr10:38693000-38700200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr10:38693000-38714000	Weak transcription	Right Ventricle	heart
32	chr10:38693000-38716000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr10:38693000-38736800	Weak transcription	Stomach Smooth Muscle	stomach
34	chr10:38693000-38737200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:38693000-38737200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr10:38693000-38737200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr10:38693000-38737200	Weak transcription	Fetal Muscle Leg	muscle
38	chr10:38693000-38737400	Weak transcription	Placenta	Placenta
39	chr10:38693000-38739200	Weak transcription	Primary B cells from peripheral blood	blood
40	chr10:38693200-38698000	Weak transcription	Fetal Muscle Trunk	muscle
41	chr10:38693200-38699800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr10:38697200-38700600	Strong transcription	Liver	Liver

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