Variant report

Variant	rs55749071
Chromosome Location	chr12:31837150-31837151
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11830639	1.00[AMR][1000 genomes]
rs11831623	1.00[AMR][1000 genomes]
rs11832803	1.00[AMR][1000 genomes]
rs11832825	1.00[AMR][1000 genomes]
rs11833397	1.00[AMR][1000 genomes]
rs11833865	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11834122	1.00[AMR][1000 genomes]
rs11835079	1.00[AMR][1000 genomes]
rs11835928	1.00[AMR][1000 genomes]
rs35548973	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55698487	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55702366	1.00[AMR][1000 genomes]
rs55704003	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55717538	1.00[AMR][1000 genomes]
rs56010814	1.00[AMR][1000 genomes]
rs56122817	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56131645	1.00[AMR][1000 genomes]
rs56224974	1.00[AMR][1000 genomes]
rs56348448	1.00[AMR][1000 genomes]
rs56410922	1.00[AMR][1000 genomes]
rs56947635	1.00[AMR][1000 genomes]
rs58644649	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58672841	1.00[AMR][1000 genomes]
rs59530163	1.00[AMR][1000 genomes]
rs59834841	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59956729	1.00[AMR][1000 genomes]
rs60374609	1.00[AMR][1000 genomes]
rs60557264	1.00[AMR][1000 genomes]
rs60663805	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60680259	1.00[AMR][1000 genomes]
rs60942371	1.00[AMR][1000 genomes]
rs60971872	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61373187	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61398234	1.00[AMR][1000 genomes]
rs61593882	1.00[AMR][1000 genomes]
rs74085127	1.00[AMR][1000 genomes]
rs74085129	1.00[AMR][1000 genomes]
rs74085131	1.00[AMR][1000 genomes]
rs74085134	1.00[AMR][1000 genomes]
rs74085139	1.00[AMR][1000 genomes]
rs74085141	1.00[AMR][1000 genomes]
rs74085142	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74085158	1.00[AMR][1000 genomes]
rs74085160	1.00[AMR][1000 genomes]
rs74085162	1.00[AMR][1000 genomes]
rs74085164	1.00[AMR][1000 genomes]
rs74085165	1.00[AMR][1000 genomes]
rs74085166	1.00[AMR][1000 genomes]
rs74085167	1.00[AMR][1000 genomes]
rs74085168	1.00[AMR][1000 genomes]
rs74085193	1.00[AMR][1000 genomes]
rs74085194	1.00[AMR][1000 genomes]
rs74085196	1.00[AMR][1000 genomes]
rs74085198	1.00[AMR][1000 genomes]
rs74085199	1.00[AMR][1000 genomes]
rs74085201	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760267	chr12:31626732-31909908	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS 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	34 gene(s)	inside rSNPs	diseases
2	nsv1043010	chr12:31798446-32143151	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv541446	chr12:31798446-32143151	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers 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 target site	41 gene(s)	inside rSNPs	diseases
4	esv3432694	chr12:31801467-32109828	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv898966	chr12:31810126-31944985	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent/Poised 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	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31815200-31840600	Weak transcription	Pancreas	Pancrea
2	chr12:31817400-31850400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr12:31822400-31840600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr12:31822600-31862000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr12:31822600-31874200	Weak transcription	Right Ventricle	heart
6	chr12:31827000-31871800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:31827400-31855000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:31835000-31837200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
9	chr12:31835000-31839200	ZNF genes & repeats	Fetal Thymus	thymus
10	chr12:31835200-31837200	ZNF genes & repeats	Primary T cells from cord blood	blood
11	chr12:31835200-31837200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
12	chr12:31835200-31837600	ZNF genes & repeats	Liver	Liver
13	chr12:31835200-31838000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
14	chr12:31835200-31838200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
15	chr12:31835200-31838600	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
16	chr12:31835200-31838600	ZNF genes & repeats	Fetal Stomach	stomach
17	chr12:31835400-31837200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
18	chr12:31835400-31839000	ZNF genes & repeats	Primary B cells from cord blood	blood
19	chr12:31835400-31839200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:31835400-31841800	ZNF genes & repeats	Fetal Intestine Small	intestine
21	chr12:31835600-31837200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:31835600-31837200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:31835600-31837200	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
24	chr12:31835600-31837200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
25	chr12:31835600-31837200	ZNF genes & repeats	Fetal Brain Female	brain
26	chr12:31835600-31837200	ZNF genes & repeats	Fetal Lung	lung
27	chr12:31835600-31837200	ZNF genes & repeats	Dnd41	blood
28	chr12:31835600-31837400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr12:31835600-31837600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr12:31835600-31837800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
31	chr12:31835600-31841600	Strong transcription	Thymus	Thymus
32	chr12:31835600-31860200	Weak transcription	Fetal Kidney	kidney
33	chr12:31835800-31854800	Weak transcription	K562	blood
34	chr12:31836000-31837200	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
35	chr12:31836000-31837800	ZNF genes & repeats	Ovary	ovary
36	chr12:31836000-31842600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr12:31836000-31857600	Weak transcription	A549	lung
38	chr12:31836200-31837200	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
39	chr12:31836200-31837200	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr12:31836200-31837400	Weak transcription	Left Ventricle	heart
41	chr12:31836200-31837600	Strong transcription	Brain Angular Gyrus	brain
42	chr12:31836200-31838400	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr12:31836200-31840800	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr12:31836400-31837200	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
45	chr12:31836400-31837200	ZNF genes & repeats	Adipose Nuclei	Adipose
46	chr12:31836400-31837200	Strong transcription	Brain Substantia Nigra	brain
47	chr12:31836400-31838200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr12:31836400-31838200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
49	chr12:31836400-31840000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:31836600-31837200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links