Variant report

Variant	rs73430290
Chromosome Location	chr6:53724010-53724011
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:53719967..53722619-chr6:53723859..53726928,3	MCF-7	breast:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs56044016	0.82[AFR][1000 genomes]
rs56093057	1.00[AFR][1000 genomes]
rs60637604	0.92[AFR][1000 genomes]
rs6933638	0.92[AFR][1000 genomes]
rs73430206	0.92[AFR][1000 genomes]
rs73430273	1.00[AFR][1000 genomes]
rs73430278	1.00[AFR][1000 genomes]
rs73430284	1.00[AFR][1000 genomes]
rs73430291	0.92[AFR][1000 genomes]
rs73430293	1.00[AFR][1000 genomes]
rs73430295	0.96[AFR][1000 genomes]
rs73430297	0.96[AFR][1000 genomes]
rs73430300	1.00[AFR][1000 genomes]
rs73741372	1.00[AFR][1000 genomes]
rs7770003	0.82[AFR][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	nsv1034955	chr6:53447607-53931055	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1021506	chr6:53600338-53770482	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv830664	chr6:53698021-53825270	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53695000-53743200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:53703200-53726400	Weak transcription	Fetal Stomach	stomach
3	chr6:53703800-53727600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr6:53709800-53762200	Weak transcription	Primary B cells from cord blood	blood
5	chr6:53717800-53731800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:53719800-53727600	Enhancers	Brain Substantia Nigra	brain
7	chr6:53719800-53727800	Enhancers	Brain Hippocampus Middle	brain
8	chr6:53719800-53747800	Weak transcription	Primary T cells from cord blood	blood
9	chr6:53720000-53724400	Enhancers	Brain Anterior Caudate	brain
10	chr6:53720000-53727600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:53720600-53741400	Weak transcription	Dnd41	blood
12	chr6:53720800-53736600	Weak transcription	Fetal Thymus	thymus
13	chr6:53721200-53726200	Weak transcription	Fetal Intestine Small	intestine
14	chr6:53721200-53726400	Weak transcription	Fetal Intestine Large	intestine
15	chr6:53721200-53726600	Weak transcription	Rectal Smooth Muscle	rectum
16	chr6:53721200-53726800	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr6:53721400-53724200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:53721600-53728000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:53721800-53725600	Weak transcription	Aorta	Aorta
20	chr6:53721800-53726800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr6:53722000-53725000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr6:53722000-53748200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr6:53722400-53724400	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr6:53722400-53725400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr6:53722600-53725000	Enhancers	HUVEC	blood vessel
26	chr6:53722600-53725400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:53722600-53725600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr6:53722600-53725600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr6:53722800-53726200	Weak transcription	HepG2	liver
30	chr6:53722800-53726400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr6:53723000-53725400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr6:53723000-53725600	Weak transcription	Lung	lung
33	chr6:53723000-53726200	Weak transcription	HSMMtube	muscle
34	chr6:53723000-53727000	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr6:53723000-53727200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr6:53723000-53727200	Enhancers	Brain Angular Gyrus	brain
37	chr6:53723000-53728000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:53723000-53728000	Weak transcription	Pancreas	Pancrea
39	chr6:53723000-53728000	Weak transcription	Right Atrium	heart
40	chr6:53723200-53725400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:53723200-53725600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr6:53723200-53725600	Weak transcription	Colon Smooth Muscle	Colon
43	chr6:53723200-53725800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:53723400-53726000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:53723400-53726000	Weak transcription	HMEC	breast
46	chr6:53723400-53726000	Weak transcription	NHEK	skin
47	chr6:53723400-53726400	Weak transcription	Esophagus	oesophagus
48	chr6:53723400-53736800	Weak transcription	Stomach Mucosa	stomach
49	chr6:53724000-53724200	Enhancers	Brain Germinal Matrix	brain
50	chr6:53724000-53724600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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