Variant report

Variant	rs377052596
Chromosome Location	chr1:221956787-221956788
allele	-/T
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	nsv469786	chr1:221855871-222040335	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv482867	chr1:221855871-222040335	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1002463	chr1:221863355-222095773	Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv535302	chr1:221863355-222095773	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv1007092	chr1:221883491-221958279	Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv535303	chr1:221883491-221958279	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv873201	chr1:221956626-222007535	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221948800-221958200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:221949400-221958000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr1:221949800-221958200	Enhancers	Primary T cells fromperipheralblood	blood
4	chr1:221950000-221956800	Enhancers	Fetal Thymus	thymus
5	chr1:221951800-221958000	Enhancers	Primary B cells from cord blood	blood
6	chr1:221952000-221958000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr1:221953200-221958000	Enhancers	GM12878-XiMat	blood
8	chr1:221954000-221966400	Weak transcription	Spleen	Spleen
9	chr1:221954600-221956800	Enhancers	Thymus	Thymus
10	chr1:221955200-221956800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:221955200-221958000	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr1:221955400-221956800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:221955400-221958000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr1:221955600-221956800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:221955600-221958200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr1:221955600-221958400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:221955800-221956800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr1:221955800-221958000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr1:221955800-221958200	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr1:221956000-221956800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:221956000-221956800	Enhancers	Brain Hippocampus Middle	brain
22	chr1:221956000-221958200	Enhancers	Primary B cells from peripheral blood	blood
23	chr1:221956000-221958200	Enhancers	Primary hematopoietic stem cells	blood
24	chr1:221956000-221958200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr1:221956200-221957000	Enhancers	Brain Anterior Caudate	brain
26	chr1:221956200-221958000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:221956200-221958200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr1:221956200-221958600	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr1:221956200-221960000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:221956400-221957200	Weak transcription	Adipose Nuclei	Adipose
31	chr1:221956400-221957400	Weak transcription	Brain Substantia Nigra	brain
32	chr1:221956400-221958000	Flanking Active TSS	Dnd41	blood
33	chr1:221956600-221957400	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr1:221956600-221957400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr1:221956600-221957800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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