Variant report

Variant	rs60568951
Chromosome Location	chr6:36914264-36914265
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs2145435	0.89[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs2145436	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2180778	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57336743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58088068	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60607208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60875770	0.86[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs62406494	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7740320	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7753241	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7759265	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030015	chr6:36818510-37104446	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv916833	chr6:36826524-37029833	Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36892800-36915600	Weak transcription	Pancreas	Pancrea
2	chr6:36896200-36915400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr6:36898600-36922200	Weak transcription	Right Atrium	heart
4	chr6:36908000-36915200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr6:36910800-36916000	Weak transcription	Hela-S3	cervix
6	chr6:36912600-36915000	Weak transcription	Primary B cells from cord blood	blood
7	chr6:36912600-36915400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:36912800-36914600	Weak transcription	Brain Anterior Caudate	brain
9	chr6:36912800-36915200	Weak transcription	Primary B cells from peripheral blood	blood
10	chr6:36913200-36917000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr6:36913800-36916000	Enhancers	Fetal Thymus	thymus
12	chr6:36914000-36915400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr6:36914000-36915800	Enhancers	Thymus	Thymus
14	chr6:36914200-36914600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:36914200-36915400	Enhancers	Brain Substantia Nigra	brain
16	chr6:36914200-36915800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr6:36914200-36916600	Enhancers	Primary T cells from cord blood	blood
18	chr6:36914200-36916600	Enhancers	Dnd41	blood
19	chr6:36914200-36916800	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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

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