Variant report

Variant	rs10515374
Chromosome Location	chr5:106980183-106980184
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	chr5:106966022..106967957-chr5:106979262..106981193,2	MCF-7	breast:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10043284	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10043302	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10044934	1.00[ASN][1000 genomes]
rs12110095	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12514246	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12519552	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12519591	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12520660	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12522223	1.00[ASN][1000 genomes]
rs17160227	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs58880008	1.00[ASN][1000 genomes]
rs6881619	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6888194	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6897852	1.00[JPT][hapmap]
rs6898202	1.00[JPT][hapmap]
rs755966	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7726649	1.00[ASN][1000 genomes]
rs7732162	0.94[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs957662	1.00[ASN][1000 genomes]
rs9986282	1.00[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106942400-106981600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:106969600-106988600	Weak transcription	Fetal Stomach	stomach
3	chr5:106970200-106985600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:106972200-106986000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:106972600-106981800	Weak transcription	HMEC	breast
6	chr5:106972800-106983400	Weak transcription	Fetal Lung	lung
7	chr5:106973200-106981600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr5:106973400-106982000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:106976600-106981400	Weak transcription	Fetal Heart	heart
10	chr5:106976600-106981800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr5:106976600-106984600	Weak transcription	A549	lung
12	chr5:106976600-106987200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:106976600-106991600	Weak transcription	Left Ventricle	heart
14	chr5:106977800-106981200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr5:106978800-106980800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:106979200-106985800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr5:106979400-106985600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:106979400-106988600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:106980000-106981200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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