Variant report

Variant	rs74037660
Chromosome Location	chr14:25259015-25259016
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17106989	1.00[AMR][1000 genomes]
rs17109209	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	nsv1041336	chr14:24726564-25527319	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542000	chr14:24726564-25527319	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv901504	chr14:25184210-25646203	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv901505	chr14:25237268-25360584	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1046542	chr14:25244806-25267208	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1045403	chr14:25249822-25271815	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv564063	chr14:25253343-25262952	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv564064	chr14:25257780-25262886	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25255400-25261800	Enhancers	Fetal Lung	lung
2	chr14:25258000-25259200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr14:25258200-25259200	Enhancers	Colon Smooth Muscle	Colon
4	chr14:25258200-25259200	Enhancers	Duodenum Mucosa	Duodenum
5	chr14:25258200-25259200	Enhancers	Fetal Muscle Leg	muscle
6	chr14:25258200-25259200	Enhancers	Fetal Stomach	stomach
7	chr14:25258200-25259200	Enhancers	Left Ventricle	heart
8	chr14:25258200-25259800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr14:25258400-25259200	Enhancers	Adipose Nuclei	Adipose
10	chr14:25258400-25259200	Enhancers	Right Ventricle	heart
11	chr14:25258400-25259200	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr14:25258400-25260000	Enhancers	Stomach Mucosa	stomach
13	chr14:25258600-25259400	Enhancers	Fetal Intestine Large	intestine
14	chr14:25258600-25259800	Bivalent Enhancer	HepG2	liver
15	chr14:25259000-25263800	Weak transcription	Fetal Brain Male	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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