Variant report

Variant	rs61523733
Chromosome Location	chr8:11300643-11300644
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11294217..11296027-chr8:11297947..11300867,2	MCF-7	breast:
2	chr8:11280386..11282841-chr8:11298445..11301046,2	MCF-7	breast:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs4585709	0.83[ASN][1000 genomes]
rs4841531	0.84[ASN][1000 genomes]
rs60532605	0.83[ASN][1000 genomes]
rs61069759	1.00[EUR][1000 genomes]
rs73544596	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7844316	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv1022525	chr8:11066191-11309356	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv539474	chr8:11066191-11309356	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS 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 target site	19 gene(s)	inside rSNPs	diseases
6	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv470183	chr8:11236975-11307118	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv465465	chr8:11245064-11307118	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv610275	chr8:11245064-11307118	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv522860	chr8:11253879-11330364	Bivalent/Poised TSS Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv890357	chr8:11286146-11330364	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1030756	chr8:11292073-11332782	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1022074	chr8:11292256-11394526	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11280600-11308800	Weak transcription	Primary B cells from cord blood	blood
2	chr8:11286200-11306400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr8:11287800-11313600	Weak transcription	Right Atrium	heart
4	chr8:11289800-11305800	Weak transcription	Osteobl	bone
5	chr8:11291600-11303800	Weak transcription	Brain Angular Gyrus	brain
6	chr8:11291800-11300800	Weak transcription	NHEK	skin
7	chr8:11292400-11313000	Weak transcription	Pancreas	Pancrea
8	chr8:11292600-11302200	Weak transcription	Lung	lung
9	chr8:11296200-11305800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr8:11296200-11319200	Enhancers	Fetal Thymus	thymus
11	chr8:11296400-11301800	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr8:11297600-11301200	Enhancers	Brain Cingulate Gyrus	brain
13	chr8:11298200-11305800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:11298200-11306000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:11298200-11306000	Weak transcription	Fetal Heart	heart
16	chr8:11298400-11306000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:11298400-11306000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr8:11298800-11300800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:11298800-11308600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr8:11299200-11306000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr8:11299400-11306600	Enhancers	Stomach Mucosa	stomach
22	chr8:11299600-11301800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:11299600-11301800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr8:11299800-11304600	Enhancers	Thymus	Thymus
25	chr8:11300000-11301400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:11300200-11301000	Weak transcription	Brain Anterior Caudate	brain
27	chr8:11300200-11301200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr8:11300200-11301600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:11300400-11301200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr8:11300400-11301200	Enhancers	Esophagus	oesophagus
31	chr8:11300600-11301000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:11300600-11301000	Weak transcription	Brain Substantia Nigra	brain
33	chr8:11300600-11301000	Active TSS	Placenta	Placenta
34	chr8:11300600-11301200	Enhancers	Gastric	stomach
35	chr8:11300600-11301400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:11300600-11301400	Enhancers	GM12878-XiMat	blood
37	chr8:11300600-11303200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:11300600-11305800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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