Variant report

Variant	rs62285381
Chromosome Location	chr3:195806641-195806642
allele	C/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:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195752724..195755222-chr3:195806059..195808616,2	K562	blood:
2	chr3:195806486..195808572-chr3:195852578..195854905,2	MCF-7	breast:
3	chr3:195796379..195810322-chr3:195910077..195926320,43	MCF-7	breast:
4	chr3:195781523..195783440-chr3:195805045..195807096,2	K562	blood:
5	chr3:195793504..195812987-chr3:195901613..195938073,113	K562	blood:
6	chr3:195805990..195808883-chr3:195933159..195936246,3	K562	blood:
7	chr3:195781940..195789641-chr3:195805045..195810311,11	K562	blood:
8	chr13:92000244..92002396-chr3:195806622..195808883,2	K562	blood:
9	chr3:195806495..195808059-chr3:195895549..195897513,2	MCF-7	breast:
10	chr3:195804323..195810515-chr3:195865435..195874009,30	K562	blood:
11	chr3:195804970..195807492-chr3:195930599..195932477,2	K562	blood:
12	chr3:195806535..195810385-chr3:195863612..195875110,36	K562	blood:
13	chr3:195793504..195812415-chr3:195915832..195927942,46	K562	blood:

No data

Variant related genes	Relation type
ENSG00000163958	Chromatin interaction
ENSG00000072274	Chromatin interaction
ENSG00000224652	Chromatin interaction
ENSG00000222335	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1004860	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1004992	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12487702	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12490842	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12491771	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12493933	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2300779	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34906439	0.96[ASN][1000 genomes]
rs3761716	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3804138	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3804141	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3827556	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3933	0.96[ASN][1000 genomes]
rs406271	0.92[ASN][1000 genomes]
rs41259844	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41297523	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs41298087	0.96[ASN][1000 genomes]
rs41298097	0.96[ASN][1000 genomes]
rs41299394	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41300427	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41301353	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs419059	0.92[ASN][1000 genomes]
rs492288	0.96[ASN][1000 genomes]
rs492349	0.96[ASN][1000 genomes]
rs539816	0.96[ASN][1000 genomes]
rs557527	0.96[ASN][1000 genomes]
rs570	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60148746	0.90[ASN][1000 genomes]
rs62284053	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62285382	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62285387	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62285392	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62285393	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6763092	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7645812	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759213	chr3:195102787-196071593	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv428102	chr3:195201080-195829426	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv428430	chr3:195201080-195829426	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
4	esv2757913	chr3:195379484-196071593	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
5	nsv1010395	chr3:195641908-195848264	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	nsv532213	chr3:195643944-196063636	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer 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	87 gene(s)	inside rSNPs	diseases
7	esv1820982	chr3:195651349-195835519	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
8	nsv997797	chr3:195658360-196212958	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
9	nsv878170	chr3:195677895-195871388	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
10	nsv878171	chr3:195677895-195959924	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv1008512	chr3:195709662-195974936	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
12	nsv1002584	chr3:195734933-195910772	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
13	nsv432543	chr3:195746690-196015690	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
14	nsv878172	chr3:195751853-195831098	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
15	nsv532214	chr3:195762648-195916068	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
16	nsv1002065	chr3:195769609-195877692	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv1009105	chr3:195769609-195984388	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
18	nsv524410	chr3:195776240-195816195	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
19	nsv461130	chr3:195776240-195907653	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
20	nsv593069	chr3:195776240-195907653	Flanking Active TSS Weak transcription 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	50 gene(s)	inside rSNPs	diseases
21	nsv1005558	chr3:195789462-195919077	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking 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	49 gene(s)	inside rSNPs	diseases
22	nsv536890	chr3:195789462-195919077	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195785200-195807400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr3:195792800-195807400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:195794200-195807800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:195798200-195807400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr3:195799000-195807000	Weak transcription	Fetal Brain Male	brain
6	chr3:195799400-195807000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr3:195800800-195807400	Weak transcription	Fetal Kidney	kidney
8	chr3:195800800-195807600	Weak transcription	Aorta	Aorta
9	chr3:195801000-195807400	Weak transcription	HSMM	muscle
10	chr3:195801200-195807400	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr3:195801600-195807400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr3:195802000-195807400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr3:195802400-195806800	Weak transcription	A549	lung
14	chr3:195802400-195807200	Weak transcription	NHLF	lung
15	chr3:195802400-195807400	Weak transcription	Fetal Lung	lung
16	chr3:195802400-195807400	Weak transcription	NH-A	brain
17	chr3:195802400-195807400	Weak transcription	NHDF-Ad	bronchial
18	chr3:195802400-195807600	Weak transcription	HSMMtube	muscle
19	chr3:195802600-195806800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:195802800-195806800	Weak transcription	Brain Angular Gyrus	brain
21	chr3:195802800-195807000	Weak transcription	Colonic Mucosa	Colon
22	chr3:195802800-195807200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr3:195802800-195807200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr3:195802800-195807200	Weak transcription	Ovary	ovary
25	chr3:195802800-195807400	Weak transcription	Esophagus	oesophagus
26	chr3:195803000-195806800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:195803000-195807200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:195803000-195807200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:195803400-195806800	Weak transcription	Brain Hippocampus Middle	brain
30	chr3:195803400-195807000	Weak transcription	Fetal Muscle Trunk	muscle
31	chr3:195803400-195807200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr3:195803400-195807400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:195803400-195807400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:195803400-195807400	Weak transcription	HUVEC	blood vessel
35	chr3:195803400-195807400	Weak transcription	Osteobl	bone
36	chr3:195803600-195807200	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr3:195803600-195807400	Weak transcription	Lung	lung
38	chr3:195803800-195806800	Weak transcription	Fetal Stomach	stomach
39	chr3:195804000-195806800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr3:195804000-195806800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr3:195804000-195806800	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr3:195804000-195807200	Weak transcription	Rectal Smooth Muscle	rectum
43	chr3:195804000-195807400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:195804000-195807400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr3:195804200-195806800	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr3:195804600-195807000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
47	chr3:195804800-195806800	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr3:195804800-195807600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr3:195805600-195807000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr3:195805600-195807400	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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