Variant report

Variant	rs585406
Chromosome Location	chr1:10559598-10559599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:10552588..10555183-chr1:10557797..10560030,2	MCF-7	breast:
2	chr1:10515344..10518157-chr1:10557483..10560138,2	MCF-7	breast:
3	chr1:10531903..10534239-chr1:10558821..10560390,2	K562	blood:
4	chr1:10548374..10550861-chr1:10557856..10560546,2	K562	blood:

Variant related genes	Relation type
ENSG00000160049	Chromatin interaction
ENSG00000142655	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11121579	0.84[EUR][1000 genomes]
rs12073943	0.82[EUR][1000 genomes]
rs12565133	0.82[EUR][1000 genomes]
rs2186949	0.87[EUR][1000 genomes]
rs655271	0.82[EUR][1000 genomes]
rs663864	0.84[EUR][1000 genomes]
rs670666	0.84[EUR][1000 genomes]
rs673254	0.84[EUR][1000 genomes]
rs684016	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757722	chr1:10238070-10582554	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv2758920	chr1:10238070-10582554	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv817370	chr1:10305470-10697150	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1008021	chr1:10363794-10802633	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv2764192	chr1:10383734-10594186	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1003498	chr1:10445928-10607351	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv998731	chr1:10464176-10607351	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv2521	chr1:10553530-10598171	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10553000-10567200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:10554800-10568600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:10555200-10567400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:10555200-10567400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr1:10555200-10567400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:10555200-10568400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:10555200-10568600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:10555200-10570000	Weak transcription	Aorta	Aorta
9	chr1:10555400-10567200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr1:10555400-10567400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr1:10555600-10560800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr1:10555600-10561000	Weak transcription	Brain Hippocampus Middle	brain
13	chr1:10555600-10564200	Weak transcription	HUVEC	blood vessel
14	chr1:10555600-10567400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr1:10555600-10567400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr1:10555600-10567400	Weak transcription	A549	lung
17	chr1:10555600-10567600	Weak transcription	NH-A	brain
18	chr1:10555600-10567800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:10555600-10567800	Weak transcription	HSMM	muscle
20	chr1:10555600-10567800	Weak transcription	NHDF-Ad	bronchial
21	chr1:10555600-10568600	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:10555600-10568600	Weak transcription	Pancreas	Pancrea
23	chr1:10555600-10568600	Weak transcription	HSMMtube	muscle
24	chr1:10555600-10570400	Weak transcription	Brain Substantia Nigra	brain
25	chr1:10555600-10570400	Weak transcription	Rectal Smooth Muscle	rectum
26	chr1:10555600-10570600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr1:10555800-10564400	Weak transcription	Placenta	Placenta
28	chr1:10555800-10564400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr1:10555800-10567200	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr1:10555800-10567400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr1:10555800-10567400	Weak transcription	Osteobl	bone
32	chr1:10555800-10567800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:10555800-10567800	Weak transcription	Fetal Lung	lung
34	chr1:10555800-10568600	Weak transcription	Esophagus	oesophagus
35	chr1:10555800-10569600	Weak transcription	Colonic Mucosa	Colon
36	chr1:10555800-10570400	Weak transcription	Brain Anterior Caudate	brain
37	chr1:10556000-10560000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:10556000-10560000	Weak transcription	Thymus	Thymus
39	chr1:10556000-10561000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr1:10556000-10567200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr1:10556000-10567400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr1:10556000-10569400	Weak transcription	Fetal Brain Female	brain
43	chr1:10556000-10570200	Weak transcription	Brain Angular Gyrus	brain
44	chr1:10556400-10564600	Weak transcription	Gastric	stomach
45	chr1:10556400-10567200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr1:10556400-10567400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:10556400-10567800	Weak transcription	Hela-S3	cervix
48	chr1:10556400-10570200	Weak transcription	Fetal Kidney	kidney
49	chr1:10556600-10562000	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr1:10556600-10564200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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