Variant report

Variant	rs35137237
Chromosome Location	chr12:83404060-83404061
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1655594	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1655595	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8181714	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv469490	chr12:83089431-83507269	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv559542	chr12:83089431-83507269	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv832472	chr12:83248283-83419753	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
5	nsv559557	chr12:83334204-83453620	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
6	nsv1047239	chr12:83362299-83444855	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83358400-83409200	Weak transcription	Brain Angular Gyrus	brain
2	chr12:83358600-83409400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr12:83375600-83405600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr12:83377600-83409400	Weak transcription	Brain Hippocampus Middle	brain
5	chr12:83377800-83410200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr12:83378400-83409600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:83378800-83409000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr12:83380000-83409200	Weak transcription	Gastric	stomach
9	chr12:83386000-83404200	Weak transcription	Colon Smooth Muscle	Colon
10	chr12:83390200-83409200	Weak transcription	Pancreas	Pancrea
11	chr12:83392200-83409000	Weak transcription	Stomach Mucosa	stomach
12	chr12:83398000-83409000	Weak transcription	Brain Substantia Nigra	brain
13	chr12:83398000-83409000	Weak transcription	Fetal Heart	heart
14	chr12:83398400-83409600	Weak transcription	Brain Anterior Caudate	brain
15	chr12:83398800-83405800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:83399800-83409400	Weak transcription	Fetal Brain Male	brain
17	chr12:83400200-83409400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr12:83401600-83404800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:83401600-83405400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
20	chr12:83402000-83404800	Strong transcription	Fetal Lung	lung
21	chr12:83402200-83405200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr12:83402400-83404800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
23	chr12:83402400-83405400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr12:83402600-83405600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:83402600-83405600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
26	chr12:83402800-83405200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr12:83403000-83404400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
28	chr12:83403000-83405200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
29	chr12:83403200-83404600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
30	chr12:83403400-83404400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:83403400-83404400	ZNF genes & repeats	Fetal Muscle Trunk	muscle
32	chr12:83403400-83404400	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
33	chr12:83403400-83404800	ZNF genes & repeats	Fetal Muscle Leg	muscle
34	chr12:83403400-83405400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr12:83403600-83404200	ZNF genes & repeats	Colonic Mucosa	Colon
36	chr12:83403600-83404400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:83403600-83404400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
38	chr12:83403600-83404400	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
39	chr12:83403600-83404400	ZNF genes & repeats	Esophagus	oesophagus
40	chr12:83403600-83404400	ZNF genes & repeats	Fetal Stomach	stomach
41	chr12:83403600-83404600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr12:83403600-83404600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
43	chr12:83403600-83404600	ZNF genes & repeats	Stomach Smooth Muscle	stomach
44	chr12:83403600-83405000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:83403800-83404600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr12:83403800-83404600	ZNF genes & repeats	Fetal Kidney	kidney
47	chr12:83403800-83405200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
48	chr12:83404000-83404400	Strong transcription	Placenta Amnion	Placenta Amnion

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links