Variant report

Variant	rs1805728
Chromosome Location	chr12:9097234-9097235
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	USF2	chr12:9096938-9097248	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr12:9097135-9097262	H1-hESC	embryonic stem cell:	n/a	n/a
3	USF1	chr12:9096872-9097360	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr12:9091005-9097565	H1-hESC	embryonic stem cell:	n/a	n/a
5	USF1	chr12:9096939-9097277	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr12:9096017-9097308	K562	blood:	n/a	n/a
7	MYC	chr12:9096950-9097300	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9085152..9087931-chr12:9094994..9098809,4	K562	blood:
2	chr12:9085152..9087425-chr12:9095080..9098809,3	K562	blood:
3	chr12:9065799..9067529-chr12:9095135..9097465,2	MCF-7	breast:
4	chr12:9096830..9100498-chr12:9102068..9104762,4	K562	blood:

No data

Variant related genes	Relation type
M6PR	TF binding region
ENSG00000139187	Chromatin interaction
ENSG00000111752	Chromatin interaction
ENSG00000003056	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10842665	0.81[CEU][hapmap];0.80[EUR][1000 genomes]
rs11048208	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11048241	0.87[EUR][1000 genomes]
rs11048353	0.80[EUR][1000 genomes]
rs11048369	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11494758	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11834163	1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs12371962	0.85[EUR][1000 genomes]
rs1805726	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805729	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1805730	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805731	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805734	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1805738	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1805776	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3026261	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4140911	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs887783	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[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	nsv832327	chr12:9081779-9246220	Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9068200-9100000	Weak transcription	Stomach Mucosa	stomach
2	chr12:9071400-9099400	Strong transcription	HUES48 Cell Line	embryonic stem cell
3	chr12:9071600-9100000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:9073800-9099800	Strong transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:9087000-9101200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr12:9091000-9099000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:9091600-9101200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:9093600-9099200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:9093600-9099200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr12:9093600-9099600	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr12:9093800-9098400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr12:9093800-9098800	Strong transcription	Primary T cells from cord blood	blood
13	chr12:9093800-9099000	Strong transcription	Fetal Intestine Large	intestine
14	chr12:9093800-9099200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr12:9093800-9099200	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr12:9093800-9099200	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr12:9093800-9099200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr12:9093800-9099200	Strong transcription	Fetal Thymus	thymus
19	chr12:9093800-9099400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:9093800-9099400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr12:9093800-9099400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:9093800-9099400	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr12:9093800-9099600	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr12:9093800-9099600	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr12:9093800-9099600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:9093800-9099600	Strong transcription	Fetal Muscle Trunk	muscle
27	chr12:9093800-9099600	Strong transcription	A549	lung
28	chr12:9093800-9099800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr12:9094000-9098000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr12:9094000-9098200	Strong transcription	Right Ventricle	heart
31	chr12:9094000-9098200	Strong transcription	Skeletal Muscle Male	skeletal muscle
32	chr12:9094000-9098200	Strong transcription	HUVEC	blood vessel
33	chr12:9094000-9098400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr12:9094000-9098400	Strong transcription	Brain Substantia Nigra	brain
35	chr12:9094000-9098600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
36	chr12:9094000-9098600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:9094000-9098600	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr12:9094000-9098600	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr12:9094000-9098600	Strong transcription	HMEC	breast
40	chr12:9094000-9098600	Strong transcription	NHDF-Ad	bronchial
41	chr12:9094000-9098800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
42	chr12:9094000-9098800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:9094000-9098800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr12:9094000-9098800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr12:9094000-9098800	Strong transcription	Primary T helper cells PMA-I stimulated	--
46	chr12:9094000-9098800	Strong transcription	Brain Anterior Caudate	brain
47	chr12:9094000-9098800	Strong transcription	GM12878-XiMat	blood
48	chr12:9094000-9099000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr12:9094000-9099000	Strong transcription	Primary B cells from peripheral blood	blood
50	chr12:9094000-9099000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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