Variant report

Variant	rs61930799
Chromosome Location	chr12:44936784-44936785
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10880649	0.96[ASN][1000 genomes]
rs10880650	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10880651	0.98[ASN][1000 genomes]
rs11182530	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11182531	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1493748	0.96[ASN][1000 genomes]
rs1552860	0.96[ASN][1000 genomes]
rs1901556	0.98[ASN][1000 genomes]
rs1908179	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2198338	0.93[ASN][1000 genomes]
rs2218986	0.91[ASN][1000 genomes]
rs2859835	0.99[ASN][1000 genomes]
rs4768555	0.96[ASN][1000 genomes]
rs4768556	0.96[ASN][1000 genomes]
rs7953009	0.96[ASN][1000 genomes]
rs7953156	0.96[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44909200-44939800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr12:44918600-44972000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:44924400-44939800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr12:44924800-44939800	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr12:44932400-44937200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr12:44935800-44937400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:44936200-44937400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr12:44936200-44937600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:44936200-44938400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:44936400-44936800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:44936600-44936800	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr12:44936600-44937600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr12:44936600-44944400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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