Variant report

Variant	rs376147432
Chromosome Location	chr3:177366773-177366774
allele	A/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	esv2752972	chr3:176924298-177425298	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv931055	chr3:177229521-177889872	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv514189	chr3:177294490-177383578	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv4131	chr3:177366549-177399301	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island 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	chr3:177360600-177369600	Weak transcription	Fetal Brain Female	brain
2	chr3:177360800-177367000	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr3:177360800-177367200	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr3:177361000-177369800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr3:177361400-177367200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr3:177363000-177369600	Weak transcription	Fetal Kidney	kidney
7	chr3:177363400-177366800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr3:177363600-177366800	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr3:177363800-177366800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr3:177363800-177367000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr3:177364400-177367000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr3:177364600-177367200	Enhancers	Primary T cells fromperipheralblood	blood
13	chr3:177364600-177367200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr3:177364800-177369800	Weak transcription	Colon Smooth Muscle	Colon
15	chr3:177364800-177370800	Weak transcription	Psoas Muscle	Psoas
16	chr3:177365800-177370800	Weak transcription	Aorta	Aorta
17	chr3:177366000-177367200	Enhancers	Dnd41	blood
18	chr3:177366000-177368000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr3:177366000-177369800	Weak transcription	Primary hematopoietic stem cells short term culture	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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