Variant report

Variant	rs72913331
Chromosome Location	chr2:189358367-189358368
allele	A/G/T
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:2)

rs_ID	r²[population]
rs72907642	1.00[AFR][1000 genomes]
rs72909506	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534341	chr2:189200405-189368467	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv584055	chr2:189266823-189493686	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv834489	chr2:189329027-189494224	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv1003974	chr2:189331760-189827814	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv533110	chr2:189354436-189462552	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 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	chr2:189329200-189399000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:189334600-189367600	Weak transcription	Fetal Lung	lung
3	chr2:189338600-189360600	Weak transcription	Ovary	ovary
4	chr2:189341200-189358800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:189344000-189358400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:189344000-189370200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr2:189344200-189390400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:189348400-189358400	Weak transcription	Placenta	Placenta
9	chr2:189353000-189366400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr2:189355800-189382400	Weak transcription	Gastric	stomach
11	chr2:189356000-189370800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:189356400-189370000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:189356400-189371200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr2:189356400-189373600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr2:189356800-189362600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr2:189356800-189371000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr2:189357000-189370000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr2:189357800-189371000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr2:189358200-189359200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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