Variant report

Variant	rs28370010
Chromosome Location	chr1:223901210-223901211
allele	A/G
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:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:223900680..223901441-chr10:134145170..134146133,2	Hela-S3	cervix:
2	chr1:223900203..223902153-chr1:223927273..223928993,2	K562	blood:
3	chr1:223899719..223901460-chr1:224517221..224519970,2	K562	blood:
4	chr1:223898558..223902080-chr1:223957242..223958839,3	K562	blood:
5	chr1:223900571..223903093-chr1:223940555..223942413,2	K562	blood:
6	chr1:223887434..223890501-chr1:223901110..223904266,3	K562	blood:
7	chr1:223900402..223903093-chr1:223939885..223943104,3	K562	blood:
8	chr1:223900439..223903816-chr1:223918326..223920507,3	MCF-7	breast:
9	chr1:223900176..223902216-chr1:223970691..223973184,2	MCF-7	breast:
10	chr1:223897577..223900459-chr1:223900975..223902562,2	MCF-7	breast:
11	chr1:223897551..223903480-chr1:224031634..224036730,7	K562	blood:
12	chr1:223885961..223896993-chr1:223898177..223910405,32	MCF-7	breast:
13	chr1:155022792..155023626-chr1:223900625..223901256,2	Hela-S3	cervix:
14	chr1:223899719..223902673-chr1:224516675..224518721,2	K562	blood:
15	chr1:223898558..223902031-chr1:223957339..223960421,3	K562	blood:
16	chr1:223900092..223902158-chr1:223929992..223931627,2	K562	blood:
17	chr1:223897059..223902247-chr1:223935403..223939761,6	K562	blood:
18	chr1:223900420..223902460-chr1:224007560..224009954,2	K562	blood:
19	chr1:223900203..223901722-chr1:223926667..223928773,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000165752	Chromatin interaction
ENSG00000143514	Chromatin interaction
ENSG00000143748	Chromatin interaction
ENSG00000162909	Chromatin interaction
ENSG00000143537	Chromatin interaction
ENSG00000148814	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs12048989	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832681	chr1:223698048-224002691	Strong transcription Active TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	esv3361888	chr1:223725597-224114846	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1007380	chr1:223834380-224042190	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv535310	chr1:223834380-224042190	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	esv34082	chr1:223851018-224144509	Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv873213	chr1:223885843-223924236	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
7	esv3344542	chr1:223899354-223901902	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223899400-223901400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
2	chr1:223899600-223901400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
3	chr1:223899600-223901800	Active TSS	Gastric	stomach
4	chr1:223899600-223901800	Active TSS	HSMMtube	muscle
5	chr1:223899800-223901400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:223899800-223901400	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr1:223899800-223901400	Active TSS	Left Ventricle	heart
8	chr1:223899800-223901400	Active TSS	Psoas Muscle	Psoas
9	chr1:223899800-223901400	Bivalent/Poised TSS	HepG2	liver
10	chr1:223899800-223901600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:223899800-223901600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
12	chr1:223899800-223901600	Active TSS	Fetal Kidney	kidney
13	chr1:223899800-223901800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:223899800-223901800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:223899800-223901800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
16	chr1:223899800-223901800	Active TSS	Aorta	Aorta
17	chr1:223899800-223902000	Active TSS	Breast Myoepithelial Primary Cells	Breast
18	chr1:223899800-223902000	Active TSS	Esophagus	oesophagus
19	chr1:223900000-223901400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:223900000-223901400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:223900000-223901400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:223900000-223901400	Active TSS	Muscle Satellite Cultured Cells	--
23	chr1:223900000-223901400	Active TSS	Brain Substantia Nigra	brain
24	chr1:223900000-223901400	Active TSS	Fetal Intestine Large	intestine
25	chr1:223900000-223901400	Active TSS	Lung	lung
26	chr1:223900000-223901400	Active TSS	Right Ventricle	heart
27	chr1:223900000-223901400	Active TSS	Stomach Mucosa	stomach
28	chr1:223900000-223901400	Active TSS	A549	lung
29	chr1:223900000-223901400	Active TSS	NHDF-Ad	bronchial
30	chr1:223900000-223901400	Active TSS	NHLF	lung
31	chr1:223900000-223901400	Active TSS	Osteobl	bone
32	chr1:223900000-223901600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:223900000-223901600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:223900000-223901600	Active TSS	HMEC	breast
35	chr1:223900000-223901600	Active TSS	HSMM	muscle
36	chr1:223900000-223901600	Active TSS	NH-A	brain
37	chr1:223900000-223901600	Active TSS	NHEK	skin
38	chr1:223900000-223901800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:223900200-223901400	Active TSS	Placenta Amnion	Placenta Amnion
40	chr1:223900200-223901400	Active TSS	Sigmoid Colon	Sigmoid Colon
41	chr1:223900400-223901400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr1:223900400-223901600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:223900600-223901400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr1:223900600-223901400	Active TSS	Right Atrium	heart
45	chr1:223900600-223901800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr1:223900600-223901800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:223900800-223901400	Flanking Active TSS	Liver	Liver
48	chr1:223900800-223901400	Flanking Active TSS	GM12878-XiMat	blood
49	chr1:223900800-223901600	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr1:223900800-223901600	Flanking Active TSS	Primary T cells from cord blood	blood

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