Variant report

Variant	rs6671078
Chromosome Location	chr1:93439652-93439653
allele	G/T
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	STAT3	chr1:93439637-93439702	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
RNU6-970P	TF binding region

Extended variants
information (count: 36 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10747454	0.86[ASN][1000 genomes]
rs10874752	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11164848	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11164849	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11164850	0.86[ASN][1000 genomes]
rs11164851	0.86[ASN][1000 genomes]
rs11164854	0.84[ASN][1000 genomes]
rs12092304	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12133990	0.83[ASN][1000 genomes]
rs12144226	0.88[ASN][1000 genomes]
rs12747275	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1678784	0.84[ASN][1000 genomes]
rs28561471	0.86[ASN][1000 genomes]
rs4515797	0.88[ASN][1000 genomes]
rs4847386	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4847389	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs514235	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs521428	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs534409	0.88[ASN][1000 genomes]
rs567613	0.86[ASN][1000 genomes]
rs594527	0.86[ASN][1000 genomes]
rs606344	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs619784	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs641462	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs660870	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs663112	0.81[ASN][1000 genomes]
rs6671268	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6681240	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6681345	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7517539	0.88[ASN][1000 genomes]
rs7524934	0.81[ASN][1000 genomes]
rs753391	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs770883	0.81[ASN][1000 genomes]
rs770884	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs945630	0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008602	chr1:93176811-93640808	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6671078	MTF2	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93428400-93445800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr1:93433200-93445000	Enhancers	Primary B cells from cord blood	blood
3	chr1:93434200-93445600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr1:93435400-93440600	Enhancers	Primary B cells from peripheral blood	blood
5	chr1:93436200-93441800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:93436600-93440600	Weak transcription	Pancreas	Pancrea
7	chr1:93437000-93441800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr1:93437600-93441400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr1:93437800-93439800	Enhancers	Primary T cells from cord blood	blood
10	chr1:93438000-93441800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:93438000-93443600	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr1:93438200-93443400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr1:93438600-93440000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr1:93438800-93439800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:93438800-93440600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr1:93438800-93446000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:93439000-93444400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:93439200-93440400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr1:93439400-93440400	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr1:93439400-93440600	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr1:93439400-93441600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:93439400-93446400	Weak transcription	Thymus	Thymus
23	chr1:93439600-93440400	Enhancers	GM12878-XiMat	blood
24	chr1:93439600-93440600	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr1:93439600-93440600	Weak transcription	Dnd41	blood
26	chr1:93439600-93441200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr1:93439600-93441200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr1:93439600-93441200	Weak transcription	K562	blood
29	chr1:93439600-93443000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr1:93439600-93445600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr1:93439600-93446000	Weak transcription	Fetal Thymus	thymus
32	chr1:93439600-93446400	Weak transcription	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links