Variant report

Variant	rs10506881
Chromosome Location	chr12:83324054-83324055
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1023967	0.82[TSI][hapmap]
rs10746260	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10778915	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10778917	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10862533	0.82[TSI][hapmap]
rs1625996	0.93[YRI][hapmap];0.85[AFR][1000 genomes]
rs1796297	0.85[LWK][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes]
rs7296753	0.82[TSI][hapmap]
rs7307017	0.89[YRI][hapmap];0.86[AFR][1000 genomes]
rs7316631	1.00[CEU][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7975374	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs892539	0.82[TSI][hapmap]

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	esv2758315	chr12:83101045-83357621	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv2759911	chr12:83101045-83357621	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	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

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83279000-83336400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr12:83293200-83324200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:83305800-83336800	Weak transcription	Fetal Stomach	stomach
4	chr12:83307200-83324200	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr12:83307800-83336800	Weak transcription	Fetal Lung	lung
6	chr12:83313800-83324200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:83316600-83328800	Weak transcription	Pancreas	Pancrea
8	chr12:83316800-83324200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:83317000-83325200	Weak transcription	Colon Smooth Muscle	Colon
10	chr12:83318800-83324600	Weak transcription	Brain Substantia Nigra	brain
11	chr12:83318800-83325200	Weak transcription	Brain Angular Gyrus	brain
12	chr12:83319400-83325000	Weak transcription	Left Ventricle	heart
13	chr12:83321000-83324200	Weak transcription	Brain Hippocampus Middle	brain
14	chr12:83321000-83324200	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr12:83321400-83324200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr12:83321600-83325400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr12:83322000-83325200	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr12:83322000-83325400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr12:83322200-83327200	Weak transcription	Fetal Muscle Leg	muscle
20	chr12:83322600-83325400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr12:83322800-83327200	Weak transcription	Fetal Muscle Trunk	muscle
22	chr12:83323200-83328000	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr12:83323400-83329600	Weak transcription	Fetal Brain Male	brain
24	chr12:83323600-83334400	Weak transcription	Fetal Heart	heart
25	chr12:83323800-83326600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:83324000-83325200	Enhancers	Placenta Amnion	Placenta Amnion

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links