Variant report

Variant	rs58932972
Chromosome Location	chr12:12524148-12524149
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:12523614..12525450-chr12:12713286..12715120,2	MCF-7	breast:
2	chr12:12522631..12525556-chr12:12525783..12528472,2	MCF-7	breast:
3	chr12:12517934..12520693-chr12:12524024..12526072,2	MCF-7	breast:
4	chr12:12510200..12513346-chr12:12523638..12526361,3	K562	blood:
5	chr12:12508565..12513346-chr12:12518905..12526361,9	K562	blood:

Variant related genes	Relation type
ENSG00000205791	Chromatin interaction
ENSG00000111266	Chromatin interaction
ENSG00000165714	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs55794458	1.00[AFR][1000 genomes]
rs7137659	1.00[EUR][1000 genomes]
rs7303326	0.84[AFR][1000 genomes]
rs74062518	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7966625	1.00[AFR][1000 genomes]
rs7976922	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949003	chr12:11938229-12618690	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv898808	chr12:12463407-12549503	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv1036040	chr12:12506839-12541869	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1037542	chr12:12506839-12542868	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv1045637	chr12:12506839-12546747	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	esv1812889	chr12:12510842-12593406	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
7	nsv1052243	chr12:12512726-12541869	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv1051597	chr12:12513364-12541869	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv557584	chr12:12514203-12541869	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv818893	chr12:12515184-12541869	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv1042425	chr12:12519319-12540455	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
12	nsv1050133	chr12:12519319-12541869	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
13	nsv1049869	chr12:12519319-12542868	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
14	nsv1047762	chr12:12520906-12541869	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12510800-12527400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:12510800-12528200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:12511200-12525800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr12:12511400-12532600	Weak transcription	Fetal Lung	lung
5	chr12:12511400-12532800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr12:12511400-12535000	Weak transcription	Esophagus	oesophagus
7	chr12:12511400-12537800	Weak transcription	HSMMtube	muscle
8	chr12:12511400-12540600	Weak transcription	HSMM	muscle
9	chr12:12511600-12530200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr12:12511600-12532800	Weak transcription	Osteobl	bone
11	chr12:12511600-12540000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr12:12511600-12550600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr12:12511800-12526200	Weak transcription	Liver	Liver
14	chr12:12511800-12526800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr12:12511800-12532600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:12512000-12525200	Weak transcription	Fetal Thymus	thymus
17	chr12:12512000-12532600	Weak transcription	Colon Smooth Muscle	Colon
18	chr12:12512000-12545000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:12512200-12525800	Weak transcription	Fetal Intestine Large	intestine
20	chr12:12512200-12526000	Weak transcription	Small Intestine	intestine
21	chr12:12512200-12529800	Weak transcription	Fetal Kidney	kidney
22	chr12:12512200-12540400	Weak transcription	HMEC	breast
23	chr12:12512400-12525600	Weak transcription	HepG2	liver
24	chr12:12512400-12526400	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr12:12512400-12540600	Weak transcription	Psoas Muscle	Psoas
26	chr12:12512800-12525800	Weak transcription	K562	blood
27	chr12:12512800-12532600	Weak transcription	Hela-S3	cervix
28	chr12:12513000-12532600	Weak transcription	GM12878-XiMat	blood
29	chr12:12513200-12532400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr12:12516200-12537600	Weak transcription	Dnd41	blood
31	chr12:12516400-12529800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr12:12516400-12535200	Weak transcription	Lung	lung
33	chr12:12516400-12540000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:12516600-12525000	Weak transcription	Fetal Muscle Leg	muscle
35	chr12:12517800-12525800	Weak transcription	Pancreas	Pancrea
36	chr12:12518200-12525000	Weak transcription	Fetal Muscle Trunk	muscle
37	chr12:12518200-12531800	Weak transcription	Fetal Brain Female	brain
38	chr12:12519200-12524200	Weak transcription	Fetal Intestine Small	intestine
39	chr12:12519200-12529800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr12:12519200-12531400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr12:12519200-12532200	Weak transcription	Placenta	Placenta
42	chr12:12519200-12532600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr12:12519200-12549800	Weak transcription	Aorta	Aorta
44	chr12:12519400-12525000	Weak transcription	Fetal Stomach	stomach
45	chr12:12519400-12525200	Weak transcription	Brain Germinal Matrix	brain
46	chr12:12519400-12525200	Weak transcription	Stomach Smooth Muscle	stomach
47	chr12:12519400-12532600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:12519400-12537400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr12:12519600-12540400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:12519800-12537600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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