Variant report

Variant	rs7792998
Chromosome Location	chr7:78218883-78218884
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10258158	1.00[EUR][1000 genomes]
rs10485908	0.80[ASN][1000 genomes]
rs11981895	1.00[EUR][1000 genomes]
rs2215932	1.00[EUR][1000 genomes]
rs6974517	1.00[EUR][1000 genomes]
rs73378221	1.00[ASN][1000 genomes]
rs73378222	1.00[ASN][1000 genomes]
rs7800480	1.00[ASN][1000 genomes]
rs7812172	1.00[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	nsv1022764	chr7:77911072-78316607	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78209000-78219000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:78209800-78219600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:78210600-78219400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:78216800-78223200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr7:78217200-78219000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:78217600-78219800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr7:78218000-78220800	Weak transcription	Left Ventricle	heart
8	chr7:78218000-78222000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr7:78218000-78223400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:78218200-78223000	Weak transcription	Brain Substantia Nigra	brain
11	chr7:78218200-78223200	Weak transcription	Fetal Heart	heart
12	chr7:78218200-78223400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr7:78218200-78223400	Weak transcription	Brain Angular Gyrus	brain
14	chr7:78218200-78223400	Weak transcription	Brain Hippocampus Middle	brain
15	chr7:78218400-78224400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr7:78218800-78219000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:78218800-78223400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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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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