Variant report

Variant	rs61732672
Chromosome Location	chr12:1740554-1740555
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:1703157..1705505-chr12:1739226..1741204,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000171823	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529398	chr12:941915-1741311	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1042863	chr12:1163817-1902302	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv541345	chr12:1163817-1902302	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv898584	chr12:1607390-1783251	Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv826180	chr12:1614395-1759431	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv826181	chr12:1619798-1754941	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv832304	chr12:1710249-1868642	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
8	nsv898587	chr12:1732295-1756642	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
9	nsv898588	chr12:1736314-1755960	Bivalent Enhancer Enhancers Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
10	nsv556994	chr12:1737309-1743843	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv898589	chr12:1738111-1755654	Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
12	nsv898590	chr12:1740171-1757743	Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1733000-1744000	Weak transcription	K562	blood
2	chr12:1737600-1740600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
3	chr12:1737800-1740600	Enhancers	Spleen	Spleen
4	chr12:1737800-1740800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr12:1737800-1740800	Bivalent Enhancer	Fetal Lung	lung
6	chr12:1738400-1740600	Enhancers	Lung	lung
7	chr12:1738600-1740600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
8	chr12:1738600-1740600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:1738600-1740600	Active TSS	Colon Smooth Muscle	Colon
10	chr12:1738600-1740800	Flanking Active TSS	Brain Germinal Matrix	brain
11	chr12:1738800-1740600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
12	chr12:1738800-1740600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:1738800-1740600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
14	chr12:1739000-1740600	Bivalent/Poised TSS	Thymus	Thymus
15	chr12:1739400-1740600	Bivalent Enhancer	Fetal Thymus	thymus
16	chr12:1739600-1740600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
17	chr12:1739600-1740600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:1739600-1740600	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr12:1739600-1740600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
20	chr12:1739600-1740600	Bivalent Enhancer	HepG2	liver
21	chr12:1739800-1740600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr12:1739800-1740600	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
23	chr12:1739800-1740600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
24	chr12:1739800-1740600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr12:1739800-1740600	Enhancers	Placenta Amnion	Placenta Amnion
26	chr12:1739800-1740800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:1739800-1740800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
28	chr12:1739800-1740800	Enhancers	HSMM	muscle
29	chr12:1739800-1740800	Enhancers	NH-A	brain
30	chr12:1739800-1741400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:1739800-1742000	Weak transcription	Right Atrium	heart
32	chr12:1739800-1753800	Weak transcription	Esophagus	oesophagus
33	chr12:1740000-1740600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr12:1740000-1740600	Enhancers	Brain Angular Gyrus	brain
35	chr12:1740000-1740600	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr12:1740000-1740800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
37	chr12:1740000-1740800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr12:1740000-1740800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr12:1740000-1740800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:1740000-1740800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr12:1740000-1740800	Bivalent Enhancer	Fetal Heart	heart
42	chr12:1740000-1740800	Bivalent Enhancer	Placenta	Placenta
43	chr12:1740000-1740800	Bivalent Enhancer	Fetal Stomach	stomach
44	chr12:1740000-1740800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
45	chr12:1740000-1741000	Bivalent Enhancer	Fetal Intestine Large	intestine
46	chr12:1740000-1741200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
47	chr12:1740000-1741200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
48	chr12:1740000-1741400	Weak transcription	Liver	Liver
49	chr12:1740000-1744000	Weak transcription	Aorta	Aorta
50	chr12:1740000-1748800	Weak transcription	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links