Variant report

Variant	rs2486916
Chromosome Location	chr6:15131267-15131268
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:15130172..15131963-chr6:15134360..15137201,2	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	0.93[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	0.96[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	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2486915	0.96[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]
rs2747492	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2747494	0.86[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	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	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2791624	0.91[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	0.96[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	0.88[EUR][1000 genomes]
rs9476753	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:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15116400-15132000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:15130200-15132000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:15130200-15136400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:15130400-15131600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:15130400-15132000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:15130400-15132000	Weak transcription	Esophagus	oesophagus
7	chr6:15130400-15133400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:15130400-15135400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:15130400-15136400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr6:15130600-15131800	Weak transcription	Fetal Kidney	kidney
11	chr6:15130600-15132000	Weak transcription	K562	blood
12	chr6:15130600-15132000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr6:15130600-15133000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr6:15130600-15133400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:15130600-15136400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr6:15130800-15133200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr6:15130800-15136600	Weak transcription	GM12878-XiMat	blood
18	chr6:15131000-15132000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr6:15131200-15132000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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