Variant report

Variant	rs1152905
Chromosome Location	chr12:66620283-66620284
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:66619417..66622573-chr12:66625034..66628303,3	MCF-7	breast:
2	chr12:66613438..66616221-chr12:66619493..66621113,2	K562	blood:
3	chr12:66561837..66563807-chr12:66619260..66621917,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000155957	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10506476	1.00[EUR][1000 genomes]
rs10506477	1.00[EUR][1000 genomes]
rs1058981	1.00[EUR][1000 genomes]
rs11176027	1.00[EUR][1000 genomes]
rs1152910	1.00[EUR][1000 genomes]
rs1168738	1.00[EUR][1000 genomes]
rs1168740	1.00[EUR][1000 genomes]
rs1168741	1.00[EUR][1000 genomes]
rs1168746	1.00[EUR][1000 genomes]
rs1168764	1.00[EUR][1000 genomes]
rs1168767	1.00[EUR][1000 genomes]
rs1168773	1.00[EUR][1000 genomes]
rs1179916	1.00[EUR][1000 genomes]
rs12099497	1.00[EUR][1000 genomes]
rs1617632	1.00[EUR][1000 genomes]
rs17102069	1.00[EUR][1000 genomes]
rs17102109	1.00[EUR][1000 genomes]
rs17102115	1.00[EUR][1000 genomes]
rs1797400	1.00[EUR][1000 genomes]
rs1946750	1.00[EUR][1000 genomes]
rs6581665	1.00[EUR][1000 genomes]
rs7307987	1.00[EUR][1000 genomes]
rs7487759	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052503	chr12:66293898-67269495	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv541515	chr12:66293898-67269495	Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv899216	chr12:66563835-66716844	Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv541517	chr12:66576953-66639823	ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66583800-66623400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:66589600-66623400	Weak transcription	Spleen	Spleen
3	chr12:66592400-66628400	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr12:66597600-66623400	Weak transcription	Aorta	Aorta
5	chr12:66604400-66628800	Weak transcription	Right Ventricle	heart
6	chr12:66605200-66628800	Weak transcription	Psoas Muscle	Psoas
7	chr12:66605400-66628200	Weak transcription	NHDF-Ad	bronchial
8	chr12:66606800-66623000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr12:66606800-66625800	Weak transcription	Fetal Muscle Leg	muscle
10	chr12:66608800-66628800	Weak transcription	Gastric	stomach
11	chr12:66609000-66628800	Weak transcription	Left Ventricle	heart
12	chr12:66609200-66628800	Weak transcription	Colonic Mucosa	Colon
13	chr12:66609200-66629000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr12:66609400-66626200	Weak transcription	Small Intestine	intestine
15	chr12:66610000-66628800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr12:66611600-66627600	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr12:66612000-66626600	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr12:66612200-66628000	Weak transcription	Placenta	Placenta
19	chr12:66612400-66628200	Weak transcription	Primary B cells from cord blood	blood
20	chr12:66612600-66628000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr12:66613400-66628400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:66614000-66621800	Weak transcription	Adipose Nuclei	Adipose
23	chr12:66614200-66627200	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr12:66614200-66628000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:66614400-66622600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr12:66615600-66643400	Weak transcription	Stomach Mucosa	stomach
27	chr12:66616800-66626600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:66618000-66626600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr12:66618400-66626600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr12:66618800-66620600	Strong transcription	Primary hematopoietic stem cells	blood
31	chr12:66618800-66628600	Weak transcription	Brain Hippocampus Middle	brain
32	chr12:66618800-66628800	Weak transcription	Fetal Stomach	stomach
33	chr12:66619200-66628400	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr12:66620000-66621000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr12:66620000-66621400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr12:66620200-66621200	Strong transcription	Lung	lung
37	chr12:66620200-66625800	Weak transcription	Liver	Liver
38	chr12:66620200-66626600	Strong transcription	Fetal Lung	lung

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