Variant report

Variant	rs59126262
Chromosome Location	chr6:74009995-74009996
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:74008749..74010443-chr6:74018010..74020997,3	MCF-7	breast:
2	6:73927031-73938730..6:74000304-74012200	K562	blood:
3	6:74000304-74012200..6:74062967-74076046	GM12878	blood:
4	chr6:74008984..74013407-chr6:74017731..74021238,5	K562	blood:
5	chr6:74008167..74010358-chr6:74012095..74014040,2	K562	blood:
6	6:74000304-74012200..6:74160392-74184826	K562	blood:
7	6:74000304-74012200..6:74078047-74099067	H1-hESC	embryonic stem cell:	embryo
8	chr6:74009555..74011702-chr6:74018026..74021147,3	MCF-7	breast:
9	6:74000304-74012200..6:74099986-74112890	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
ENSG00000203908	Chromatin interaction
ENSG00000080007	Chromatin interaction
ENSG00000235174	Chromatin interaction
ENSG00000256980	Chromatin interaction
ENSG00000135314	Chromatin interaction
ENSG00000203909	Chromatin interaction
ENSG00000164430	Chromatin interaction
ENSG00000203907	Chromatin interaction
ENSG00000207023	Chromatin interaction
ENSG00000135297	Chromatin interaction
ENSG00000224221	Chromatin interaction
ENSG00000238464	Chromatin interaction
ENSG00000231332	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12203691	0.89[ASN][1000 genomes]
rs4706535	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4706536	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4708043	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56846430	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57140549	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57209376	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57385669	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58345476	0.93[ASN][1000 genomes]
rs58356246	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59378494	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59747599	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60119590	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61123006	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61584268	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61594993	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61633633	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72945999	0.81[ASN][1000 genomes]
rs73462509	0.80[AFR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73462517	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73462537	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73462545	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73462547	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7382737	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7762937	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

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	esv3410973	chr6:73716033-74419545	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73973600-74018600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:73973600-74018600	Weak transcription	A549	lung
3	chr6:73973600-74018800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:73974000-74018400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr6:73983800-74018600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:73984400-74018600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:73989000-74017200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:73992400-74013200	Weak transcription	GM12878-XiMat	blood
9	chr6:73994200-74018600	Weak transcription	Stomach Mucosa	stomach
10	chr6:73996000-74015800	Weak transcription	Hela-S3	cervix
11	chr6:74001000-74017200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:74002000-74013000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr6:74005200-74018600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr6:74006000-74011200	Strong transcription	Dnd41	blood
15	chr6:74007400-74010600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr6:74007800-74010000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:74007800-74017400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr6:74008400-74012600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr6:74008400-74013200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:74008600-74010000	Enhancers	Fetal Heart	heart
21	chr6:74008800-74010000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:74008800-74010000	Active TSS	Brain Angular Gyrus	brain
23	chr6:74008800-74018400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr6:74009000-74018400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr6:74009400-74010000	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr6:74009400-74017200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:74009400-74017200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:74009400-74017200	Weak transcription	Fetal Thymus	thymus
29	chr6:74009400-74017200	Weak transcription	Pancreas	Pancrea
30	chr6:74009400-74017400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr6:74009400-74018400	Weak transcription	Fetal Lung	lung
32	chr6:74009400-74019000	Weak transcription	Right Atrium	heart
33	chr6:74009600-74010000	Strong transcription	Thymus	Thymus
34	chr6:74009600-74010200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:74009600-74011800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr6:74009600-74012200	Weak transcription	NHDF-Ad	bronchial
37	chr6:74009600-74013000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:74009600-74016000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:74009600-74016000	Weak transcription	Fetal Brain Male	brain
40	chr6:74009600-74017200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr6:74009600-74017400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr6:74009600-74017400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:74009600-74017400	Weak transcription	Osteobl	bone
44	chr6:74009600-74018600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr6:74009600-74018600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr6:74009600-74018600	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr6:74009600-74018600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:74009600-74018600	Weak transcription	NHLF	lung
49	chr6:74009800-74010000	Enhancers	Fetal Intestine Large	intestine
50	chr6:74009800-74010000	Enhancers	Fetal Intestine Small	intestine

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