Variant report

Variant	rs191098818
Chromosome Location	chr17:33827489-33827490
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055936	chr17:33327166-33884184	Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
2	nsv543317	chr17:33327166-33884184	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer 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 target site	112 gene(s)	inside rSNPs	diseases
3	nsv534371	chr17:33456878-34094068	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv960581	chr17:33827264-33841554	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33823000-33830400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr17:33823400-33828200	Genic enhancers	Primary T cells fromperipheralblood	blood
3	chr17:33823400-33835600	Weak transcription	GM12878-XiMat	blood
4	chr17:33823800-33828600	Weak transcription	Pancreas	Pancrea
5	chr17:33824200-33834800	Weak transcription	Spleen	Spleen
6	chr17:33824400-33827600	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr17:33824800-33829000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr17:33825000-33828800	Strong transcription	Dnd41	blood
9	chr17:33825400-33827600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr17:33826200-33835000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr17:33826400-33828800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr17:33826400-33835000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr17:33826800-33827800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr17:33826800-33832200	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr17:33827000-33828000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr17:33827000-33829000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr17:33827000-33840000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr17:33827200-33828000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr17:33827200-33828000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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