Variant report

Variant	rs2815334
Chromosome Location	chr1:77816367-77816368
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:77813619..77816574-chr1:78468319..78470340,2	K562	blood:

Variant related genes	Relation type
ENSG00000273338	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1353727	1.00[MEX][hapmap]
rs1453974	1.00[MEX][hapmap]
rs1869468	1.00[MEX][hapmap]
rs2602939	1.00[MEX][hapmap]
rs2647491	1.00[MEX][hapmap]
rs2803144	1.00[MEX][hapmap]
rs2803149	1.00[MEX][hapmap]
rs2815331	1.00[MEX][hapmap]
rs3112830	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005183	chr1:77728990-77949309	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv535010	chr1:77728990-77949309	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv932557	chr1:77730247-77958687	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1003714	chr1:77756861-77949309	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv470719	chr1:77774413-78269207	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv546591	chr1:77774413-78269207	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77789000-77831200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:77795000-77836400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr1:77801000-77825800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:77803400-77839200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:77809000-77819200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr1:77813000-77816600	Enhancers	NHDF-Ad	bronchial
7	chr1:77813600-77819800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr1:77813800-77819400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr1:77813800-77820600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr1:77813800-77820600	Weak transcription	NHLF	lung
11	chr1:77813800-77834200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:77814000-77820800	Weak transcription	HSMMtube	muscle
13	chr1:77814400-77816400	Enhancers	Brain Hippocampus Middle	brain
14	chr1:77814400-77819200	Weak transcription	Primary T cells from cord blood	blood
15	chr1:77814400-77835600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr1:77814600-77817000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:77814600-77820400	Weak transcription	Osteobl	bone
18	chr1:77814800-77816800	Strong transcription	HSMM	muscle
19	chr1:77815000-77820200	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr1:77815200-77816400	Enhancers	Brain Cingulate Gyrus	brain
21	chr1:77815200-77816400	Enhancers	Brain Substantia Nigra	brain
22	chr1:77815800-77816400	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr1:77815800-77816400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr1:77816000-77816400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:77816000-77816400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:77816000-77816600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr1:77816000-77824000	Weak transcription	Brain Anterior Caudate	brain
28	chr1:77816200-77819200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:77816200-77819600	Weak transcription	Brain Angular Gyrus	brain
30	chr1:77816200-77825800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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