Variant report

Variant	rs576004316
Chromosome Location	chr1:70604594-70604595
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv531879	chr1:70386455-70644617	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1005397	chr1:70598803-70634585	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	esv1796744	chr1:70604106-70621290	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	esv1798518	chr1:70604106-70723347	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	esv1797140	chr1:70604106-70724622	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70596800-70609200	Weak transcription	Liver	Liver
2	chr1:70599000-70606000	Weak transcription	Osteobl	bone
3	chr1:70599000-70606600	Weak transcription	K562	blood
4	chr1:70599000-70609600	Weak transcription	GM12878-XiMat	blood
5	chr1:70600200-70605600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:70600200-70606000	Weak transcription	Aorta	Aorta
7	chr1:70600400-70604600	Weak transcription	Fetal Brain Female	brain
8	chr1:70600400-70605200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr1:70600400-70605600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:70600400-70605800	Weak transcription	NHDF-Ad	bronchial
11	chr1:70600600-70605200	Weak transcription	Brain Germinal Matrix	brain
12	chr1:70600600-70605200	Weak transcription	Fetal Heart	heart
13	chr1:70601000-70615400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:70601000-70643200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr1:70601200-70605400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:70601200-70606000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr1:70601200-70606200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr1:70601200-70652000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:70601800-70605200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr1:70603000-70605200	Weak transcription	Psoas Muscle	Psoas
21	chr1:70603000-70614800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:70603400-70605000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr1:70603400-70648800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:70603600-70604800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:70603600-70605200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr1:70604400-70605000	Enhancers	Fetal Brain Male	brain

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