Variant report

Variant	rs33976205
Chromosome Location	chr14:55373670-55373671
allele	-/AA
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	nsv530042	chr14:55208170-55386966	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv932970	chr14:55326559-55532749	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	esv3358123	chr14:55359251-55378030	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	n/a
4	nsv68444	chr14:55373670-55373671	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55370200-55374600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr14:55370200-55374800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr14:55370200-55376800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr14:55370400-55374400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr14:55370400-55374600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr14:55370400-55374600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr14:55370400-55374600	Weak transcription	Dnd41	blood
8	chr14:55370400-55374800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr14:55370400-55374800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:55370600-55374600	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr14:55370600-55388600	Weak transcription	HepG2	liver
12	chr14:55372200-55373800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:55372200-55374600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr14:55372200-55374800	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr14:55373200-55374400	Weak transcription	GM12878-XiMat	blood
16	chr14:55373600-55373800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:55373600-55374000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived

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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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