Variant report

Variant	rs874277
Chromosome Location	chr6:167117839-167117840
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	MAX	chr6:167117559-167118199	H1-hESC	embryonic stem cell:	n/a	chr6:167117846-167117855 chr6:167117874-167117884
2	MAX	chr6:167117729-167118039	NB4	blood:	n/a	chr6:167117846-167117855 chr6:167117874-167117884
3	MAX	chr6:167117634-167118110	H1-hESC	embryonic stem cell:	n/a	chr6:167117846-167117855 chr6:167117874-167117884
4	CEBPB	chr6:167117703-167118012	H1-hESC	embryonic stem cell:	n/a	n/a
5	POU5F1	chr6:167117497-167118084	H1-hESC	embryonic stem cell:	n/a	chr6:167117501-167117515
6	MAX	chr6:167117600-167118099	H1-hESC	embryonic stem cell:	n/a	chr6:167117846-167117855 chr6:167117874-167117884
7	TCF12	chr6:167117594-167118047	H1-hESC	embryonic stem cell:	n/a	chr6:167117804-167117811
8	GTF2F1	chr6:167117797-167117995	H1-hESC	embryonic stem cell:	n/a	n/a
9	TCF12	chr6:167117632-167117938	H1-hESC	embryonic stem cell:	n/a	chr6:167117804-167117811
10	E2F6	chr6:167117503-167118315	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
ENSG00000235008	TF binding region

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11754784	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11966441	0.84[EUR][1000 genomes]
rs12660310	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12660333	0.83[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2345259	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3734603	0.83[CEU][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs4709127	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs61513772	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6456104	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs6456105	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6456106	0.93[CEU][hapmap]
rs66549668	0.83[EUR][1000 genomes]
rs66759203	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67900389	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs68131305	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6928848	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6929068	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7738343	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7742383	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7766655	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs874276	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9366049	0.81[CHB][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv605260	chr6:166984094-167455139	Enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
4	nsv432984	chr6:167018915-167181613	Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1020888	chr6:167059455-167136562	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv538540	chr6:167059455-167136562	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv2754464	chr6:167059528-167130749	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv482478	chr6:167071366-167265821	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1019381	chr6:167090236-167558598	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
10	nsv538541	chr6:167090236-167558598	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
11	nsv1022866	chr6:167108740-167345629	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers 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	10 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	chr6:167115000-167120800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr6:167115200-167120400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:167115400-167118400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:167115800-167118000	Enhancers	H1 Cell Line	embryonic stem cell
5	chr6:167116000-167118000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:167116000-167118400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:167116000-167118400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr6:167116400-167118000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:167116400-167118000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr6:167117200-167118000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr6:167117400-167120200	Weak transcription	Brain Anterior Caudate	brain
12	chr6:167117600-167118000	Enhancers	Fetal Brain Male	brain
13	chr6:167117600-167118200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr6:167117600-167118200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:167117800-167118000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
16	chr6:167117800-167118200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr6:167117800-167118800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
18	chr6:167117800-167119000	Enhancers	Fetal Brain Female	brain
19	chr6:167117800-167119000	Enhancers	Pancreas	Pancrea

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