Variant report

Variant	rs2747492
Chromosome Location	chr6:15132949-15132950
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:15132794..15134906-chr6:15135026..15137692,3	K562	blood:
2	chr6:15131659..15133367-chr6:15138303..15139913,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10949273	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12524376	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12524746	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16876121	0.86[EUR][1000 genomes]
rs1739085	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1739086	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1739087	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1770339	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1770340	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1980528	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2474109	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2474110	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2474111	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2474112	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2486914	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2486915	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2486916	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2486917	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2747489	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2747494	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2747506	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2747507	1.00[CEU][hapmap];0.86[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2791609	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2791610	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2791623	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2791624	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2791625	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2994318	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35821948	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs55930114	0.83[EUR][1000 genomes]
rs66616859	0.86[ASN][1000 genomes]
rs73724749	0.88[EUR][1000 genomes]
rs73724750	0.88[EUR][1000 genomes]
rs9464751	0.88[EUR][1000 genomes]
rs9464752	0.88[EUR][1000 genomes]
rs9476742	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9476749	0.88[EUR][1000 genomes]
rs9476750	0.88[EUR][1000 genomes]
rs9476751	0.83[EUR][1000 genomes]
rs9476752	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs9476753	1.00[CEU][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830593	chr6:15049636-15244190	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1016007	chr6:15099585-15159098	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv2762580	chr6:15105917-15159110	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15130200-15136400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr6:15130400-15133400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr6:15130400-15135400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:15130400-15136400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr6:15130600-15133000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:15130600-15133400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:15130600-15136400	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr6:15130800-15133200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:15130800-15136600	Weak transcription	GM12878-XiMat	blood
10	chr6:15131600-15133800	Enhancers	Fetal Stomach	stomach
11	chr6:15131800-15135000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:15132000-15133000	Enhancers	NH-A	brain
13	chr6:15132000-15133400	Enhancers	K562	blood
14	chr6:15132000-15134000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:15132000-15134200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr6:15132000-15134400	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr6:15132400-15133200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:15132400-15133600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:15132400-15133600	Weak transcription	Esophagus	oesophagus
20	chr6:15132400-15134000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr6:15132400-15135200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:15132600-15133000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:15132600-15133000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr6:15132600-15133600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:15132600-15135800	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr6:15132800-15133000	Enhancers	Muscle Satellite Cultured Cells	--
27	chr6:15132800-15133000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr6:15132800-15133200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr6:15132800-15133600	Active TSS	A549	lung
30	chr6:15132800-15133600	Flanking Active TSS	HMEC	breast
31	chr6:15132800-15134000	Flanking Active TSS	NHEK	skin

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