Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:37544738..37547399-chr6:37555553..37558096,2	MCF-7	breast:
2	chr6:37556006..37559631-chr6:37561589..37564141,4	K562	blood:

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

rs_ID	r²[population]
rs11751582	0.86[ASN][1000 genomes]
rs11752518	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11752560	0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11753180	0.97[ASN][1000 genomes]
rs11754348	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11755524	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11755639	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11758637	0.83[ASN][1000 genomes]
rs11758741	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs2051073	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34388013	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34529589	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs34989139	0.86[ASN][1000 genomes]
rs35084219	0.86[ASN][1000 genomes]
rs35288154	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs35416456	0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6925759	0.97[ASN][1000 genomes]
rs71569382	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71569383	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs71569384	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752124	chr6:37416219-37680622	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37552000-37556800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:37552600-37558600	Enhancers	Fetal Brain Male	brain
3	chr6:37553400-37559400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:37555000-37556800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:37555200-37556800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:37555400-37556800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:37555400-37556800	Enhancers	Brain Germinal Matrix	brain
8	chr6:37556000-37556800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:37556000-37556800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr6:37556200-37556800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:37556200-37556800	Enhancers	Fetal Brain Female	brain
12	chr6:37556400-37556800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:37556600-37556800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
14	chr6:37556600-37556800	Enhancers	HMEC	breast
15	chr6:37556600-37557600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:37556600-37561800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:37556600-37562000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr6:37556600-37567600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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