Variant report

Variant	rs10033770
Chromosome Location	chr4:152923519-152923520
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10030608	1.00[AMR][1000 genomes]
rs17028060	1.00[AMR][1000 genomes]
rs28391448	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28704615	0.90[AFR][1000 genomes];1.00[AMR][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	nsv432644	chr4:152635395-153023402	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv880341	chr4:152861685-153110256	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv931416	chr4:152877808-153440553	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152915200-152930200	Weak transcription	Right Atrium	heart
2	chr4:152915600-152924200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr4:152915600-152924200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr4:152915800-152924200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr4:152916000-152924400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr4:152919000-152925200	Weak transcription	Gastric	stomach
7	chr4:152919200-152924200	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr4:152919600-152930200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr4:152919800-152930200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:152920400-152925800	Weak transcription	Fetal Heart	heart
11	chr4:152920400-152928200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr4:152921400-152931600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr4:152921800-152927400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	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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