Variant report

Variant	rs7595405
Chromosome Location	chr2:144715912-144715913
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:144709222..144711643-chr2:144714685..144716340,2	K562	blood:

Variant related genes	Relation type
ENSG00000121964	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16823383	1.00[AMR][1000 genomes]
rs16823387	1.00[AMR][1000 genomes]
rs16823389	1.00[AMR][1000 genomes]
rs16823390	1.00[AMR][1000 genomes]
rs16823396	1.00[AMR][1000 genomes]
rs6727568	0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7559704	1.00[AMR][1000 genomes]
rs7565007	1.00[AMR][1000 genomes]
rs7578419	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532755	chr2:144631279-145270874	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1006344	chr2:144657716-145334899	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv535951	chr2:144657716-145334899	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv1067624	chr2:144657717-145425705	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv531413	chr2:144657717-145425705	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:144696600-144717800	Weak transcription	Fetal Muscle Leg	muscle
2	chr2:144699600-144730400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr2:144700800-144719600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr2:144704600-144728800	Weak transcription	Spleen	Spleen
5	chr2:144704800-144719200	Weak transcription	Primary B cells from cord blood	blood
6	chr2:144704800-144730800	Weak transcription	Left Ventricle	heart
7	chr2:144705000-144717800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:144711400-144717600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:144713400-144719600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:144713600-144717800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:144713600-144717800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr2:144713600-144717800	Weak transcription	NHEK	skin
13	chr2:144713600-144719600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:144713600-144719800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:144713600-144721000	Weak transcription	Fetal Lung	lung
16	chr2:144713600-144723400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:144713600-144780000	Weak transcription	HSMMtube	muscle
18	chr2:144713800-144717600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr2:144713800-144717600	Weak transcription	NHDF-Ad	bronchial
20	chr2:144713800-144717800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr2:144713800-144719800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr2:144713800-144725200	Weak transcription	Brain Hippocampus Middle	brain
23	chr2:144714800-144725000	Weak transcription	Psoas Muscle	Psoas
24	chr2:144715200-144717600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr2:144715800-144720200	Weak transcription	Fetal Brain Male	brain

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