Variant report

Variant	rs38140
Chromosome Location	chr7:20059955-20059956
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITGB8-9	chr7:20057492-20064037	NONHSAT119404

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12533874	0.93[EUR][1000 genomes]
rs38128	0.82[EUR][1000 genomes]
rs38130	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs38131	0.82[EUR][1000 genomes]
rs38132	0.82[EUR][1000 genomes]
rs38134	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs38135	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs38139	0.82[EUR][1000 genomes]
rs38143	0.89[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs38144	0.89[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs38145	0.86[AFR][1000 genomes]
rs38148	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs38150	0.82[EUR][1000 genomes]
rs38151	0.82[EUR][1000 genomes]
rs38152	0.82[EUR][1000 genomes]
rs38153	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs38156	0.82[EUR][1000 genomes]
rs38158	0.82[EUR][1000 genomes]
rs38160	0.82[EUR][1000 genomes]
rs62455467	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033223	chr7:19682192-20461375	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv538795	chr7:19682192-20461375	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1027445	chr7:19947297-20211733	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv887830	chr7:19970584-20114589	Enhancers Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1027849	chr7:20003094-20084998	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2762658	chr7:20023224-20127561	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1023992	chr7:20053816-20104675	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:20058000-20060800	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr7:20058200-20060400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr7:20058800-20060200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr7:20058800-20060400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr7:20058800-20060600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:20058800-20062400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr7:20058800-20062800	Enhancers	Primary B cells from cord blood	blood
8	chr7:20059000-20060400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:20059200-20060000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:20059200-20060000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr7:20059200-20060000	Flanking Active TSS	GM12878-XiMat	blood
12	chr7:20059200-20060200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr7:20059200-20060600	Enhancers	Primary B cells from peripheral blood	blood
14	chr7:20059400-20060000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:20059400-20060200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr7:20059400-20060400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:20059400-20062000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr7:20059600-20060000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr7:20059600-20060400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:20059800-20060200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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