Variant report

Variant	rs10280874
Chromosome Location	chr7:16626655-16626656
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:10)

rs_ID	r²[population]
rs10247772	0.80[ASN][1000 genomes]
rs10269268	0.82[CHB][hapmap];0.81[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10273896	0.82[CHB][hapmap];0.81[JPT][hapmap];0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10274133	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs13228317	0.82[CHB][hapmap]
rs6973195	0.82[EUR][1000 genomes]
rs7796550	0.82[CHB][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs7796676	0.82[CHB][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs7801358	0.80[ASN][1000 genomes]
rs7802116	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised 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	56 gene(s)	inside rSNPs	diseases
2	nsv1028125	chr7:16529160-16847225	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv830912	chr7:16623196-16791974	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16622200-16635000	Weak transcription	K562	blood
2	chr7:16624000-16645600	Weak transcription	Gastric	stomach
3	chr7:16626000-16638000	Weak transcription	Fetal Stomach	stomach
4	chr7:16626200-16627000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:16626200-16627400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:16626200-16627800	Enhancers	Fetal Brain Female	brain
7	chr7:16626200-16627800	Enhancers	Fetal Muscle Leg	muscle
8	chr7:16626400-16627000	Enhancers	Fetal Muscle Trunk	muscle
9	chr7:16626400-16627400	Weak transcription	Adipose Nuclei	Adipose
10	chr7:16626400-16628600	Enhancers	Fetal Brain Male	brain
11	chr7:16626400-16639400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:16626600-16627400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:16626600-16627400	Weak transcription	Right Ventricle	heart
14	chr7:16626600-16637800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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