Variant report

Variant	rs73411707
Chromosome Location	chr12:122120267-122120268
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:121937416..121938308-chr12:122120124..122120655,4	K562	blood:
2	chr12:121989434..121989957-chr12:122119628..122120622,2	MCF-7	breast:
3	chr12:122120133..122122587-chr12:122231814..122234462,2	K562	blood:
4	chr12:121916414..121917326-chr12:122119708..122120635,3	K562	blood:
5	chr12:121990152..121991135-chr12:122119277..122120606,4	K562	blood:
6	chr12:121903995..121905837-chr12:122120190..122123061,2	MCF-7	breast:
7	chr12:121937349..121938292-chr12:122119734..122120626,3	MCF-7	breast:
8	chr12:122119277..122120923-chr12:122122798..122124808,2	K562	blood:
9	chr12:121990167..121991233-chr12:122119689..122120628,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000139725	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs28477684	1.00[AMR][1000 genomes]
rs60282131	1.00[AMR][1000 genomes]
rs73411715	1.00[AMR][1000 genomes]
rs73411716	1.00[AMR][1000 genomes]
rs73411766	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053272	chr12:121956483-122132477	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	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
3	nsv1040169	chr12:122096825-122209555	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122111400-122124200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr12:122111400-122124400	Weak transcription	Brain Anterior Caudate	brain
3	chr12:122111400-122124800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:122111600-122124600	Weak transcription	Fetal Kidney	kidney
5	chr12:122117000-122125800	Weak transcription	K562	blood
6	chr12:122117200-122123800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:122117200-122125000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr12:122117400-122123600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr12:122117600-122120800	Weak transcription	HepG2	liver
10	chr12:122117600-122124200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr12:122117600-122124800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:122117800-122124200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr12:122117800-122124800	Weak transcription	Brain Substantia Nigra	brain
14	chr12:122118000-122124200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:122118000-122125000	Weak transcription	Brain Germinal Matrix	brain
16	chr12:122118600-122124200	Weak transcription	Placenta	Placenta
17	chr12:122118800-122124400	Weak transcription	Brain Hippocampus Middle	brain
18	chr12:122119600-122120400	Enhancers	Primary B cells from peripheral blood	blood
19	chr12:122119600-122120400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:122119600-122120600	Enhancers	Primary T cells fromperipheralblood	blood
21	chr12:122119600-122120600	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr12:122119800-122120400	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr12:122119800-122120600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr12:122119800-122121000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr12:122120000-122120400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr12:122120000-122120400	Enhancers	Fetal Thymus	thymus
27	chr12:122120000-122124200	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr12:122120200-122120600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr12:122120200-122120600	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr12:122120200-122124200	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr12:122120200-122124200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:122120200-122124400	Weak transcription	Hela-S3	cervix
33	chr12:122120200-122125000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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