Variant report

Variant	rs7299842
Chromosome Location	chr12:122492313-122492314
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:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:122491959..122492866-chr12:122516568..122517309,2	MCF-7	breast:
2	chr12:122492257..122492931-chr12:122607541..122608235,2	MCF-7	breast:
3	chr12:122491264..122492772-chr12:122613226..122615522,2	MCF-7	breast:
4	chr12:122491891..122492950-chr12:122675163..122676073,7	K562	blood:
5	chr12:122491977..122492787-chr14:22328270..22328892,2	MCF-7	breast:
6	chr12:122491384..122494042-chr12:122494209..122496970,2	MCF-7	breast:
7	chr12:122491823..122494895-chr12:122496656..122499239,3	K562	blood:
8	chr12:122491890..122493016-chr12:122610733..122612779,17	MCF-7	breast:
9	chr12:122487474..122489659-chr12:122490996..122492915,2	MCF-7	breast:
10	chr12:122492019..122492888-chr12:122608485..122609005,2	MCF-7	breast:
11	chr12:122491927..122492922-chr12:122675234..122675854,3	MCF-7	breast:
12	chr12:122492288..122492924-chr12:122675554..122676136,3	MCF-7	breast:
13	chr12:122492209..122492850-chr12:122621521..122622107,2	MCF-7	breast:
14	chr12:122491108..122493990-chr12:122605278..122608052,2	K562	blood:
15	chr12:122491967..122493498-chr12:122607388..122608388,14	K562	blood:
16	chr12:122491216..122493323-chr12:122496696..122498393,2	K562	blood:
17	chr12:122491929..122492972-chr12:122611006..122612751,16	MCF-7	breast:
18	chr12:122491907..122493455-chr12:122607305..122608643,21	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000175727	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10770189	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10840645	0.91[ASN][1000 genomes]
rs11835818	0.82[CHB][hapmap];0.90[JPT][hapmap];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12230227	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12812519	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1316787	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1880030	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1976859	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2280573	0.85[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2280574	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28629903	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28691281	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28759327	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34739240	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35159488	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7137049	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529868	chr12:121956483-122944265	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	173 gene(s)	inside rSNPs	diseases
2	nsv916686	chr12:122240149-122714056	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
3	esv34001	chr12:122298737-122521637	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv899569	chr12:122478728-122630909	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv527450	chr12:122481290-122676531	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS 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:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122461600-122492400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr12:122462000-122492400	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr12:122462400-122500000	Weak transcription	Hela-S3	cervix
4	chr12:122466200-122500800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr12:122467800-122500000	Strong transcription	Thymus	Thymus
6	chr12:122467800-122500200	Strong transcription	Dnd41	blood
7	chr12:122468200-122492800	Weak transcription	NHDF-Ad	bronchial
8	chr12:122470000-122492400	Strong transcription	Fetal Thymus	thymus
9	chr12:122470000-122492400	Weak transcription	K562	blood
10	chr12:122472000-122507200	Weak transcription	Fetal Brain Male	brain
11	chr12:122473600-122492800	Weak transcription	Esophagus	oesophagus
12	chr12:122474000-122496800	Weak transcription	HMEC	breast
13	chr12:122474400-122496600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr12:122474400-122500600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:122474600-122492400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr12:122475200-122501400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr12:122479200-122493200	Weak transcription	Gastric	stomach
18	chr12:122479400-122492400	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr12:122479400-122500600	Weak transcription	Small Intestine	intestine
20	chr12:122482800-122492400	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr12:122483600-122492800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr12:122483600-122500200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:122483800-122492800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr12:122484400-122492600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr12:122484600-122492400	Weak transcription	Colonic Mucosa	Colon
26	chr12:122484600-122492400	Weak transcription	Duodenum Mucosa	Duodenum
27	chr12:122484600-122493000	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr12:122484800-122492600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr12:122484800-122492600	Weak transcription	NHEK	skin
30	chr12:122484800-122493000	Weak transcription	Brain Hippocampus Middle	brain
31	chr12:122484800-122495200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr12:122485000-122492800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr12:122485000-122494200	Weak transcription	Brain Angular Gyrus	brain
34	chr12:122486000-122492800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr12:122486600-122492600	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr12:122487800-122492600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr12:122488000-122492600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:122488000-122492800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr12:122488000-122493400	Weak transcription	Fetal Kidney	kidney
40	chr12:122488000-122500600	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr12:122488600-122492400	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr12:122488600-122493000	Weak transcription	Primary B cells from cord blood	blood
43	chr12:122488800-122492800	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr12:122488800-122493000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr12:122489000-122492600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:122489200-122492400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:122489400-122492600	Weak transcription	Primary T cells from cord blood	blood
48	chr12:122489400-122492600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr12:122489400-122492800	Weak transcription	Brain Cingulate Gyrus	brain
50	chr12:122489400-122493000	Weak transcription	Aorta	Aorta

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