Variant report

Variant	rs17038293
Chromosome Location	chr12:106628396-106628397
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:106626541..106632087-chr12:106638755..106642966,8	MCF-7	breast:
2	chr12:106627619..106631130-chr12:106633186..106636182,4	MCF-7	breast:
3	chr12:106628053..106629764-chr12:106751194..106753543,2	K562	blood:
4	chr12:106626663..106628634-chr12:106673414..106675622,2	MCF-7	breast:
5	chr12:106627724..106631160-chr12:106750781..106752959,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000013503	Chromatin interaction
ENSG00000258355	Chromatin interaction
ENSG00000136026	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11834258	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs15040	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7132695	0.97[AFR][1000 genomes];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	esv1830730	chr12:106621530-106642222	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	esv1839947	chr12:106622186-106642064	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	esv1797996	chr12:106622186-106642222	Genic enhancers Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106618000-106632000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr12:106618000-106632200	Weak transcription	Psoas Muscle	Psoas
3	chr12:106618600-106630600	Weak transcription	Ovary	ovary
4	chr12:106618600-106632200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr12:106620800-106630400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:106621200-106632000	Weak transcription	Brain Hippocampus Middle	brain
7	chr12:106621200-106632600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr12:106621400-106630200	Weak transcription	NHLF	lung
9	chr12:106621400-106632600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr12:106621400-106638200	Weak transcription	Primary hematopoietic stem cells	blood
11	chr12:106621600-106630400	Weak transcription	HSMM	muscle
12	chr12:106621600-106630600	Weak transcription	Liver	Liver
13	chr12:106621600-106630600	Weak transcription	A549	lung
14	chr12:106621600-106631400	Weak transcription	Adipose Nuclei	Adipose
15	chr12:106621600-106631800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr12:106621600-106632600	Weak transcription	Colonic Mucosa	Colon
17	chr12:106621600-106632800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr12:106621800-106628600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr12:106621800-106629200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr12:106621800-106629600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:106621800-106629800	Weak transcription	Stomach Mucosa	stomach
22	chr12:106621800-106630400	Weak transcription	Fetal Lung	lung
23	chr12:106621800-106630600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr12:106621800-106630600	Weak transcription	Spleen	Spleen
25	chr12:106621800-106631800	Weak transcription	Gastric	stomach
26	chr12:106621800-106631800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr12:106621800-106632800	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr12:106622000-106629000	Weak transcription	Fetal Heart	heart
29	chr12:106622000-106629200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:106622000-106630000	Weak transcription	Brain Germinal Matrix	brain
31	chr12:106622000-106630600	Weak transcription	Lung	lung
32	chr12:106622000-106632200	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr12:106622200-106632000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr12:106622200-106639000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr12:106622200-106639600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr12:106622400-106632200	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr12:106622400-106632800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr12:106624400-106633000	Weak transcription	Aorta	Aorta
39	chr12:106625000-106631800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr12:106625200-106629000	Weak transcription	Fetal Muscle Trunk	muscle
41	chr12:106625200-106629600	Weak transcription	Fetal Muscle Leg	muscle
42	chr12:106625200-106631800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr12:106625200-106631800	Weak transcription	Placenta	Placenta
44	chr12:106625200-106632600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr12:106625200-106636800	Weak transcription	Right Atrium	heart
46	chr12:106625200-106640800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr12:106625400-106630200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr12:106625400-106632600	Weak transcription	Right Ventricle	heart
49	chr12:106625400-106632600	Weak transcription	HepG2	liver
50	chr12:106625600-106630600	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links