Variant report

Variant	rs1996981
Chromosome Location	chr7:150129726-150129727
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr7:150129270-150129908	K562	blood:	n/a	chr7:150129715-150129726 chr7:150129717-150129724 chr7:150129405-150129415 chr7:150129716-150129725 chr7:150129418-150129427 chr7:150129716-150129726
2	MAX	chr7:150129321-150129769	K562	blood:	n/a	chr7:150129715-150129726 chr7:150129717-150129724 chr7:150129405-150129415 chr7:150129716-150129725 chr7:150129418-150129427 chr7:150129716-150129726
3	RCOR1	chr7:150129280-150129745	K562	blood:	n/a	n/a
4	BHLHE40	chr7:150129459-150129780	K562	blood:	n/a	n/a
5	MAFK	chr7:150129165-150129957	K562	blood:	n/a	n/a
6	MAFF	chr7:150129322-150129893	K562	blood:	n/a	n/a
7	CUX1	chr7:150128919-150129769	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150124983..150127260-chr7:150127633..150130251,3	MCF-7	breast:
2	chr7:150099718..150102062-chr7:150129624..150131770,3	K562	blood:
3	chr7:150064404..150066708-chr7:150128401..150130893,2	MCF-7	breast:

Variant related genes	Relation type
LINC00996	TF binding region
ENSG00000196456	Chromatin interaction
ENSG00000214022	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10257386	0.93[YRI][hapmap]
rs10271549	0.96[YRI][hapmap]
rs10275627	1.00[CEU][hapmap]
rs10952256	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12333724	1.00[ASN][1000 genomes]
rs12703063	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12703068	1.00[CEU][hapmap]
rs1524335	1.00[ASN][1000 genomes]
rs1880315	1.00[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2030681	1.00[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2030682	1.00[ASN][1000 genomes]
rs2888634	1.00[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4725894	1.00[CEU][hapmap]
rs4725899	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6944824	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6960284	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6960822	1.00[ASN][1000 genomes]
rs6962146	1.00[ASN][1000 genomes]
rs6970196	1.00[CEU][hapmap]
rs6973612	1.00[CEU][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	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
6	esv1819714	chr7:150055837-150154944	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150104400-150131600	Weak transcription	Right Atrium	heart
2	chr7:150110200-150142200	Weak transcription	Gastric	stomach
3	chr7:150126000-150130200	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr7:150126400-150130000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr7:150126400-150130200	Weak transcription	Pancreas	Pancrea
6	chr7:150126400-150130800	Weak transcription	Esophagus	oesophagus
7	chr7:150126600-150130200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr7:150126600-150132600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr7:150126600-150148000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:150126800-150129800	Weak transcription	Fetal Thymus	thymus
11	chr7:150126800-150130200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:150127000-150130000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:150127000-150130800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr7:150127800-150131000	Weak transcription	Colonic Mucosa	Colon
15	chr7:150127800-150138800	Weak transcription	Spleen	Spleen
16	chr7:150128600-150130400	Enhancers	K562	blood
17	chr7:150129000-150130000	Enhancers	GM12878-XiMat	blood
18	chr7:150129000-150130600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:150129200-150132600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:150129400-150130400	Enhancers	Primary hematopoietic stem cells short term culture	blood

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