Variant report

Variant	rs62128614
Chromosome Location	chr2:10706259-10706260
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:10706246..10708825-chr2:10732569..10734672,2	MCF-7	breast:
2	chr2:10699769..10703142-chr2:10704473..10707229,3	K562	blood:
3	chr2:10704742..10707402-chr2:10805825..10808809,2	K562	blood:
4	chr2:10601253..10603779-chr2:10706014..10708775,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12474784	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12479122	1.00[AFR][1000 genomes]
rs35587360	0.83[EUR][1000 genomes]
rs3821195	1.00[AFR][1000 genomes]
rs4669591	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs58932234	0.85[ASN][1000 genomes]
rs62127224	1.00[AFR][1000 genomes]
rs62128596	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6718912	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6736915	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7570690	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][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	nsv1007185	chr2:10540386-10791743	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv833370	chr2:10625149-10785402	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1009897	chr2:10627248-10751468	Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	esv3457339	chr2:10702380-10706604	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv3457338	chr2:10702420-10706592	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv3457340	chr2:10702450-10706544	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv3457342	chr2:10702450-10706544	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv828330	chr2:10702518-10706354	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10688200-10708800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:10689200-10710600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:10692200-10709600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:10693000-10708800	Weak transcription	NHEK	skin
5	chr2:10694200-10710000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr2:10696000-10709200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:10696000-10710200	Weak transcription	Left Ventricle	heart
8	chr2:10696600-10710000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:10697600-10708800	Weak transcription	Thymus	Thymus
10	chr2:10698000-10709000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr2:10698200-10709000	Weak transcription	Dnd41	blood
12	chr2:10698200-10709800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr2:10698600-10736600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:10698800-10709200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr2:10698800-10710400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr2:10699000-10707400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:10699000-10709000	Weak transcription	Esophagus	oesophagus
18	chr2:10699000-10709400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:10699000-10709800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr2:10699200-10708800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr2:10699200-10709200	Weak transcription	Liver	Liver
22	chr2:10699400-10709000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr2:10699400-10711000	Weak transcription	GM12878-XiMat	blood
24	chr2:10699400-10716200	Weak transcription	Fetal Brain Male	brain
25	chr2:10699600-10709000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:10700400-10708800	Weak transcription	Fetal Intestine Large	intestine
27	chr2:10700800-10708800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr2:10700800-10709800	Weak transcription	Placenta	Placenta
29	chr2:10700800-10710200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:10700800-10710400	Weak transcription	Fetal Brain Female	brain
31	chr2:10701000-10709600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr2:10701400-10709200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:10701400-10710200	Weak transcription	Colon Smooth Muscle	Colon
34	chr2:10701600-10709000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr2:10701800-10708600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr2:10701800-10708600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr2:10701800-10708800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr2:10701800-10710000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:10702000-10706400	Weak transcription	Fetal Intestine Small	intestine
40	chr2:10702000-10708600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr2:10702000-10709000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr2:10702000-10709200	Weak transcription	Right Ventricle	heart
43	chr2:10702000-10710200	Weak transcription	Ovary	ovary
44	chr2:10702000-10710200	Weak transcription	Right Atrium	heart
45	chr2:10702000-10715800	Weak transcription	Hela-S3	cervix
46	chr2:10702000-10717400	Weak transcription	Psoas Muscle	Psoas
47	chr2:10702200-10706400	Weak transcription	Fetal Muscle Trunk	muscle
48	chr2:10702200-10710400	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr2:10702200-10713800	Weak transcription	K562	blood
50	chr2:10703400-10710200	Weak transcription	Primary hematopoietic stem cells	blood

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