Variant report

Variant	rs73063169
Chromosome Location	chr3:194924933-194924934
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:194909256..194910883-chr3:194924062..194925968,2	K562	blood:
2	chr3:194902302..194904530-chr3:194924527..194926708,2	K562	blood:
3	chr3:194916402..194919849-chr3:194924223..194926668,3	MCF-7	breast:
4	chr3:194924474..194927698-chr3:194929012..194931458,3	K562	blood:
5	chr3:194924290..194926220-chr3:194926449..194928088,2	K562	blood:
6	chr3:194909256..194911400-chr3:194924468..194926175,2	K562	blood:

Variant related genes	Relation type
ENSG00000173950	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs57287670	0.91[AFR][1000 genomes]
rs58699597	0.91[AFR][1000 genomes]
rs59208268	0.87[AFR][1000 genomes]
rs61022222	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007697	chr3:194554814-195009930	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv536873	chr3:194554814-195009930	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
3	nsv1009796	chr3:194737333-195124248	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
4	nsv1012592	chr3:194814446-194931562	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers 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	13 gene(s)	inside rSNPs	diseases
5	nsv536875	chr3:194814446-194931562	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1001492	chr3:194814990-194935397	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv461126	chr3:194817484-194961888	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
8	nsv592981	chr3:194817484-194961888	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
9	nsv461127	chr3:194833940-194934634	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
10	nsv592982	chr3:194833940-194934634	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
11	nsv1014826	chr3:194834615-195631793	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
12	nsv536876	chr3:194834615-195631793	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
13	nsv533904	chr3:194868329-195438728	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
14	nsv1009120	chr3:194874494-194974672	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv1010168	chr3:194874494-195135790	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
16	nsv536877	chr3:194874494-195135790	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking 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	21 gene(s)	inside rSNPs	diseases
17	nsv997956	chr3:194879534-195087539	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv536878	chr3:194879534-195087539	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
19	esv1832781	chr3:194902818-195528226	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
20	nsv432508	chr3:194916131-195478861	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194916600-194929000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr3:194917200-194925200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:194917200-194925200	Weak transcription	Esophagus	oesophagus
4	chr3:194917200-194927800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:194917600-194929400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:194917600-194930600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr3:194917800-194925200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr3:194917800-194925200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:194917800-194930400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr3:194918800-194945000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr3:194919400-194925000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr3:194919400-194925400	Weak transcription	HSMMtube	muscle
13	chr3:194919400-194945200	Weak transcription	Thymus	Thymus
14	chr3:194919600-194925000	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr3:194919600-194925200	Weak transcription	Stomach Mucosa	stomach
16	chr3:194919600-194925400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr3:194919800-194925000	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr3:194919800-194925000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr3:194919800-194925200	Weak transcription	Small Intestine	intestine
20	chr3:194919800-194926000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr3:194920000-194925200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr3:194920000-194925200	Weak transcription	Gastric	stomach
23	chr3:194920000-194925400	Weak transcription	Liver	Liver
24	chr3:194920000-194927800	Weak transcription	Pancreas	Pancrea
25	chr3:194920000-194930800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr3:194921000-194925200	Weak transcription	Fetal Intestine Small	intestine
27	chr3:194921000-194941600	Weak transcription	Primary T cells from cord blood	blood
28	chr3:194922600-194925400	Weak transcription	HepG2	liver
29	chr3:194923400-194925200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr3:194923600-194925200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:194923600-194925800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr3:194924000-194925000	Enhancers	Fetal Lung	lung
33	chr3:194924000-194925400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:194924000-194925400	Enhancers	NHDF-Ad	bronchial
35	chr3:194924000-194925800	Enhancers	NHLF	lung
36	chr3:194924000-194926000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr3:194924000-194926400	Enhancers	Fetal Stomach	stomach
38	chr3:194924200-194925200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:194924200-194925200	Enhancers	K562	blood
40	chr3:194924200-194925400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr3:194924200-194925400	Enhancers	GM12878-XiMat	blood
42	chr3:194924200-194925400	Enhancers	NH-A	brain
43	chr3:194924200-194925600	Enhancers	HUVEC	blood vessel
44	chr3:194924200-194925800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr3:194924200-194925800	Enhancers	Lung	lung
46	chr3:194924200-194926400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:194924200-194926400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr3:194924200-194926400	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr3:194924200-194926400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr3:194924200-194926400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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