Variant report

Variant	rs73857549
Chromosome Location	chr4:158925955-158925956
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:158921420..158925394-chr4:158925624..158927441,3	MCF-7	breast:
2	chr4:158923730..158926268-chr4:158927220..158929131,2	MCF-7	breast:
3	chr4:158924817..158927091-chr4:158928943..158930898,2	MCF-7	breast:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11936729	1.00[AMR][1000 genomes]
rs11944517	1.00[AMR][1000 genomes]
rs11945640	1.00[AMR][1000 genomes]
rs11946222	1.00[AMR][1000 genomes]
rs55788430	1.00[AMR][1000 genomes]
rs56033321	1.00[AMR][1000 genomes]
rs56167625	1.00[AMR][1000 genomes]
rs56754638	1.00[AMR][1000 genomes]
rs57754015	1.00[AMR][1000 genomes]
rs58547264	1.00[AMR][1000 genomes]
rs58624740	1.00[AMR][1000 genomes]
rs59234905	1.00[AMR][1000 genomes]
rs72967842	1.00[AMR][1000 genomes]
rs72971730	1.00[AMR][1000 genomes]
rs73857535	1.00[AMR][1000 genomes]
rs73857540	1.00[AMR][1000 genomes]
rs73857576	1.00[AMR][1000 genomes]
rs73857581	1.00[AMR][1000 genomes]
rs73857583	1.00[AMR][1000 genomes]
rs73857587	1.00[AMR][1000 genomes]
rs73857590	1.00[AMR][1000 genomes]
rs73857591	1.00[AMR][1000 genomes]
rs73857593	1.00[AMR][1000 genomes]
rs73857598	1.00[AMR][1000 genomes]
rs7655528	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993476	chr4:158550643-159202015	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1030124	chr4:158758675-159251140	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv881288	chr4:158891733-159028080	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:158913800-158928200	Weak transcription	HSMM	muscle
2	chr4:158913800-158930000	Weak transcription	Right Atrium	heart
3	chr4:158917800-158926400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr4:158922600-158930000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr4:158922800-158926000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:158922800-158929200	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr4:158923200-158928400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:158923600-158927800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:158923800-158926200	Weak transcription	Fetal Heart	heart
10	chr4:158923800-158926600	Weak transcription	HUVEC	blood vessel
11	chr4:158923800-158929800	Weak transcription	Left Ventricle	heart
12	chr4:158923800-158939400	Weak transcription	HepG2	liver
13	chr4:158924600-158927800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr4:158924800-158926600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr4:158924800-158927800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr4:158925400-158927200	Enhancers	Ovary	ovary
17	chr4:158925400-158930200	Enhancers	Rectal Smooth Muscle	rectum
18	chr4:158925600-158927800	Weak transcription	Brain Substantia Nigra	brain
19	chr4:158925600-158928000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:158925600-158928000	Enhancers	Adipose Nuclei	Adipose
21	chr4:158925600-158930600	Enhancers	Colon Smooth Muscle	Colon
22	chr4:158925800-158927800	Enhancers	Fetal Stomach	stomach
23	chr4:158925800-158928000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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