Variant report

Variant	rs74074443
Chromosome Location	chr12:32323380-32323381
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12304056	1.00[AMR][1000 genomes]
rs12304066	1.00[AMR][1000 genomes]
rs161972	1.00[AMR][1000 genomes]
rs16919377	1.00[AMR][1000 genomes]
rs55802552	1.00[AMR][1000 genomes]
rs57735320	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58039881	1.00[AMR][1000 genomes]
rs58186216	1.00[AMR][1000 genomes]
rs59313683	1.00[AMR][1000 genomes]
rs59549999	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60994230	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7294637	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7295834	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74072003	1.00[AMR][1000 genomes]
rs74072005	1.00[AMR][1000 genomes]
rs74072006	1.00[AMR][1000 genomes]
rs74074440	1.00[AMR][1000 genomes]
rs74074445	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74074446	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7957620	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7957784	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7958620	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3363806	chr12:31872264-32410283	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3508621	chr12:31872654-32410593	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers 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
3	esv3508622	chr12:31872654-32410593	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv983498	chr12:32153446-32388092	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv898969	chr12:32224948-32375677	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv558171	chr12:32287259-32559693	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription 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	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32269000-32340200	Weak transcription	Dnd41	blood
2	chr12:32287800-32328400	Weak transcription	Aorta	Aorta
3	chr12:32293600-32323600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:32293600-32369200	Weak transcription	Thymus	Thymus
5	chr12:32299400-32334800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:32299600-32346200	Weak transcription	Primary B cells from peripheral blood	blood
7	chr12:32300200-32336600	Weak transcription	A549	lung
8	chr12:32303000-32336600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr12:32309400-32324000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr12:32309400-32325000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:32309400-32353400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr12:32309600-32336400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:32309600-32346000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:32309600-32351400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr12:32309600-32352200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr12:32309800-32336400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:32309800-32336600	Weak transcription	HMEC	breast
18	chr12:32310800-32323400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr12:32313200-32325600	Weak transcription	Ovary	ovary
20	chr12:32313200-32336600	Weak transcription	NH-A	brain
21	chr12:32313400-32331400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr12:32313400-32369400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr12:32313600-32324000	Weak transcription	HSMMtube	muscle
24	chr12:32313600-32325600	Weak transcription	Osteobl	bone
25	chr12:32315000-32333000	Weak transcription	Right Atrium	heart
26	chr12:32315400-32346000	Weak transcription	Primary B cells from cord blood	blood
27	chr12:32315600-32336600	Weak transcription	HSMM	muscle
28	chr12:32316400-32334600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr12:32318000-32327800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr12:32319800-32330800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr12:32319800-32331200	Weak transcription	Fetal Brain Female	brain
32	chr12:32319800-32340400	Weak transcription	Fetal Intestine Small	intestine
33	chr12:32319800-32343600	Weak transcription	Primary hematopoietic stem cells	blood
34	chr12:32321400-32326000	Weak transcription	Fetal Stomach	stomach
35	chr12:32321600-32331600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:32321800-32323600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr12:32322800-32324000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr12:32323000-32324000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr12:32323000-32324000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr12:32323000-32324200	Enhancers	Fetal Heart	heart
41	chr12:32323000-32325400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr12:32323000-32325600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:32323000-32325800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr12:32323200-32324000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr12:32323200-32325800	Enhancers	H1 Cell Line	embryonic stem cell

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