Variant report

Variant	rs1015343
Chromosome Location	chr7:138353187-138353188
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:5)

rs_ID	r²[population]
rs11770967	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17160449	0.80[EUR][1000 genomes]
rs28601695	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7796576	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7809600	0.83[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030956	chr7:138163169-138579519	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138349800-138355000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:138350000-138353200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:138350200-138353600	Weak transcription	Colonic Mucosa	Colon
4	chr7:138350200-138354800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:138350400-138354000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:138351000-138353800	Enhancers	H9 Cell Line	embryonic stem cell
7	chr7:138351000-138354600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr7:138351800-138353200	Weak transcription	HepG2	liver
9	chr7:138351800-138358200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr7:138351800-138369200	Weak transcription	Hela-S3	cervix
11	chr7:138352200-138353800	Weak transcription	Fetal Intestine Large	intestine
12	chr7:138352600-138353400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:138352600-138354000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:138352600-138354400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr7:138352800-138354000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr7:138352800-138354000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:138352800-138355400	Enhancers	Placenta	Placenta
18	chr7:138353000-138353200	Enhancers	HUES48 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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