Variant report

Variant	rs1498608
Chromosome Location	chr5:58343067-58343068
allele	A/T
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:6)

rs_ID	r²[population]
rs10940640	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs1353747	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1553113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16889126	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17777413	0.84[EUR][1000 genomes]
rs2968010	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2830363	chr5:57893949-58555491	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv830312	chr5:58191579-58382226	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv830313	chr5:58273724-58421098	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv1032308	chr5:58312468-58371239	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr5:58336000-58343600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:58336200-58375600	Weak transcription	Left Ventricle	heart
3	chr5:58336600-58348000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:58336600-58351800	Weak transcription	Fetal Intestine Small	intestine
5	chr5:58336600-58358000	Weak transcription	Fetal Intestine Large	intestine
6	chr5:58336600-58358000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr5:58337400-58359000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr5:58338200-58347600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:58338400-58350200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr5:58338800-58351800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:58338800-58359200	Weak transcription	Fetal Muscle Leg	muscle
12	chr5:58338800-58362000	Weak transcription	Gastric	stomach
13	chr5:58339000-58345000	Weak transcription	Fetal Lung	lung
14	chr5:58339000-58351600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:58339000-58365200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr5:58340600-58359000	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr5:58342400-58343600	Weak transcription	Hela-S3	cervix
18	chr5:58342600-58343600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:58342600-58344800	Enhancers	A549	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
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