Variant report

Variant	rs2901988
Chromosome Location	chr10:98112603-98112604
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1923705	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2861573	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7073904	0.87[YRI][hapmap];1.00[AMR][1000 genomes]
rs7908144	0.83[AFR][1000 genomes];1.00[AMR][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	esv3413353	chr10:98039370-98561524	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active 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	45 gene(s)	inside rSNPs	diseases
2	nsv831950	chr10:98080972-98245434	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98105000-98113200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr10:98106200-98113000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr10:98106200-98126000	Weak transcription	Aorta	Aorta
4	chr10:98109600-98113000	Weak transcription	Thymus	Thymus
5	chr10:98110800-98114200	Enhancers	Brain Angular Gyrus	brain
6	chr10:98111200-98114200	Enhancers	Fetal Intestine Small	intestine
7	chr10:98111400-98112800	Enhancers	Liver	Liver
8	chr10:98111400-98113200	Enhancers	Brain Hippocampus Middle	brain
9	chr10:98111800-98114000	Enhancers	Fetal Intestine Large	intestine
10	chr10:98112200-98113200	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr10:98112400-98113800	Enhancers	Brain Substantia Nigra	brain
12	chr10:98112400-98114000	Enhancers	Duodenum Mucosa	Duodenum
13	chr10:98112600-98112800	Enhancers	Pancreas	Pancrea
14	chr10:98112600-98113000	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr10:98112600-98113200	Enhancers	Brain Cingulate Gyrus	brain
16	chr10:98112600-98114000	Enhancers	Brain Anterior Caudate	brain

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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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