Variant report

Variant	rs10003345
Chromosome Location	chr4:153003757-153003758
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10013460	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10013642	1.00[AMR][1000 genomes]
rs10025820	1.00[AMR][1000 genomes]
rs10032430	1.00[AMR][1000 genomes]
rs1425400	1.00[AMR][1000 genomes]
rs1425401	1.00[AMR][1000 genomes]
rs28562808	1.00[AMR][1000 genomes]
rs28585419	1.00[AMR][1000 genomes]
rs28603056	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28640127	1.00[AMR][1000 genomes]
rs28681446	1.00[AMR][1000 genomes]
rs72953023	1.00[AMR][1000 genomes]
rs9999071	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:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152997400-153011800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:152998800-153003800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr4:153001200-153008800	Enhancers	Thymus	Thymus
4	chr4:153002600-153010400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr4:153002800-153004000	Enhancers	Dnd41	blood
6	chr4:153002800-153006000	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr4:153003000-153006000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr4:153003200-153006000	Weak transcription	Primary T cells from cord blood	blood
9	chr4:153003200-153007200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr4:153003200-153009600	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr4:153003200-153013800	Enhancers	Fetal Thymus	thymus
12	chr4:153003400-153003800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr4:153003600-153003800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr4:153003600-153006200	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr4:153003600-153009600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr4:153003600-153014000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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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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