Variant report

Variant	rs6865426
Chromosome Location	chr5:79398709-79398710
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:79397094..79398973-chr5:79550751..79553647,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164300	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11738548	0.97[EUR][1000 genomes]
rs11738550	0.97[EUR][1000 genomes]
rs11750846	0.97[EUR][1000 genomes]
rs16877496	0.80[AMR][1000 genomes]
rs62363993	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6453502	0.92[EUR][1000 genomes]
rs7704169	0.93[CEU][hapmap];0.97[EUR][1000 genomes]
rs7708735	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7718534	0.98[EUR][1000 genomes]
rs7722374	0.97[EUR][1000 genomes]

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	nsv432748	chr5:79300434-79577760	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv598744	chr5:79388745-79423347	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv462219	chr5:79398394-79402236	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv598745	chr5:79398394-79402236	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv462220	chr5:79398394-79402443	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv598746	chr5:79398394-79402443	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 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	chr5:79379400-79400600	Weak transcription	Left Ventricle	heart
2	chr5:79388000-79405000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr5:79389400-79412200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr5:79389800-79411800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr5:79390000-79401200	Weak transcription	Pancreas	Pancrea
6	chr5:79390600-79405400	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr5:79390800-79402000	Weak transcription	Right Atrium	heart
8	chr5:79393400-79410800	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr5:79393600-79399000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr5:79393800-79405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:79395200-79399200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr5:79395200-79401800	Weak transcription	Fetal Muscle Leg	muscle
13	chr5:79395800-79400400	Weak transcription	HepG2	liver
14	chr5:79396000-79406200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:79397400-79404000	Enhancers	Fetal Thymus	thymus
16	chr5:79397600-79402000	Enhancers	Primary T cells from cord blood	blood
17	chr5:79397600-79402400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr5:79397800-79403000	Enhancers	Thymus	Thymus
19	chr5:79398000-79402800	Enhancers	Fetal Heart	heart
20	chr5:79398400-79399800	Enhancers	Primary T cells fromperipheralblood	blood
21	chr5:79398400-79403000	Enhancers	Dnd41	blood
22	chr5:79398600-79398800	Enhancers	Esophagus	oesophagus
23	chr5:79398600-79405600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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