Variant report

Variant	rs575743585
Chromosome Location	chr10:45880051-45880052
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895105	chr10:45636867-45928822	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv430166	chr10:45668894-46148794	Bivalent Enhancer Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv993428	chr10:45742877-46224333	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active 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	19 gene(s)	inside rSNPs	diseases
4	nsv895107	chr10:45850300-45953767	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv466910	chr10:45878908-45898356	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv550715	chr10:45878908-45898356	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv895108	chr10:45878908-46224333	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45870600-45891200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:45870800-45880400	Weak transcription	Esophagus	oesophagus
3	chr10:45871400-45904600	Weak transcription	Gastric	stomach
4	chr10:45871600-45894000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr10:45872200-45883800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr10:45875800-45891200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr10:45876000-45899200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr10:45876800-45884000	Strong transcription	Spleen	Spleen
9	chr10:45876800-45884400	Strong transcription	Primary B cells from peripheral blood	blood
10	chr10:45877000-45880800	Genic enhancers	Primary monocytes fromperipheralblood	blood
11	chr10:45877000-45882800	Weak transcription	Brain Hippocampus Middle	brain
12	chr10:45877000-45891000	Weak transcription	Thymus	Thymus
13	chr10:45877800-45884200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr10:45878800-45880200	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr10:45878800-45880200	Enhancers	Adipose Nuclei	Adipose
16	chr10:45878800-45880200	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
17	chr10:45878800-45891400	Weak transcription	Pancreas	Pancrea
18	chr10:45879000-45880200	Genic enhancers	Primary B cells from cord blood	blood
19	chr10:45879000-45880200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr10:45879000-45883000	Weak transcription	Fetal Intestine Small	intestine
21	chr10:45879200-45891400	Weak transcription	Placenta	Placenta
22	chr10:45879600-45880200	Enhancers	Primary hematopoietic stem cells	blood
23	chr10:45879800-45881200	Weak transcription	Lung	lung
24	chr10:45880000-45880200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr10:45880000-45880800	Weak transcription	GM12878-XiMat	blood
26	chr10:45880000-45883600	Genic enhancers	Primary neutrophils fromperipheralblood	blood

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