Variant report

Variant	rs72953021
Chromosome Location	chr4:152998651-152998652
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1385784	1.00[AMR][1000 genomes]
rs17028462	1.00[AMR][1000 genomes]
rs55943229	1.00[AMR][1000 genomes]
rs58239760	1.00[AMR][1000 genomes]
rs61484042	1.00[AMR][1000 genomes]
rs72953008	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72953014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72953090	1.00[AMR][1000 genomes]
rs72953091	1.00[AMR][1000 genomes]
rs72953095	1.00[AMR][1000 genomes]
rs73865606	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:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152983800-153000800	Enhancers	Fetal Thymus	thymus
2	chr4:152985200-153000000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr4:152989400-153000400	Enhancers	Thymus	Thymus
4	chr4:152990400-153000000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr4:152994600-152998800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:152995400-153000600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:152995400-153000800	Enhancers	Primary T cells from cord blood	blood
8	chr4:152996000-153000000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr4:152996600-153002800	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr4:152996800-153000600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:152997400-153011800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr4:152997600-152998800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr4:152997600-153003400	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr4:152998000-152999400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr4:152998400-152999000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr4:152998400-152999400	Enhancers	Primary T cells fromperipheralblood	blood
17	chr4:152998600-152998800	Transcr. at gene 5' and 3'	Dnd41	blood
18	chr4:152998600-152999000	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr4:152998600-153001000	Enhancers	Primary T helper memory cells from peripheral blood 2	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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