Variant report

Variant	rs150880128
Chromosome Location	chr3:59974769-59974770
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	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014983	chr3:59884024-60558331	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv590387	chr3:59890976-60481459	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv876838	chr3:59952152-59999690	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv590388	chr3:59957252-60018326	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv965380	chr3:59970574-59976399	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
7	esv3410955	chr3:59974588-59974906	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:59967400-59993000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr3:59968000-59986600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr3:59968400-59982600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr3:59972000-59977000	Weak transcription	Dnd41	blood
5	chr3:59972800-59974800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr3:59972800-59976800	Enhancers	Primary T cells from cord blood	blood
7	chr3:59972800-59980400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr3:59972800-59983600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr3:59973000-59975600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr3:59973000-59975800	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr3:59973200-59976200	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr3:59973200-59977800	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr3:59974200-59983000	Enhancers	Fetal Thymus	thymus
14	chr3:59974400-59975000	Enhancers	Primary hematopoietic stem cells	blood
15	chr3:59974400-59975200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr3:59974400-59983000	Enhancers	Thymus	Thymus
17	chr3:59974600-59975000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:59974600-59975200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr3:59974600-59975400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr3:59974600-59976000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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