Variant report

Variant	rs4741394
Chromosome Location	chr9:14537386-14537387
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10756572	0.81[JPT][hapmap]
rs7020007	0.91[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029491	chr9:14033607-14942373	Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv915804	chr9:14182608-14903050	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv916811	chr9:14210978-14542068	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv831517	chr9:14512924-14738206	Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv892604	chr9:14519301-14559910	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14532200-14538400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr9:14532800-14541200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:14534400-14538400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr9:14534600-14541200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:14534800-14537600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr9:14534800-14541200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr9:14535000-14538400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr9:14535000-14538400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:14535400-14541200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:14535400-14541200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr9:14535400-14541600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr9:14535400-14542200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:14536200-14537400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:14536600-14537600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr9:14537000-14539200	Enhancers	K562	blood
16	chr9:14537000-14541200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr9:14537200-14537800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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