Variant report

Variant	rs1474506
Chromosome Location	chr8:91334044-91334045
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10101254	0.80[EUR][1000 genomes]
rs10956586	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10956589	0.80[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10956590	0.80[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11778822	0.81[EUR][1000 genomes]
rs12542159	0.88[ASN][1000 genomes]
rs12548764	0.81[ASN][1000 genomes]
rs12550585	0.81[EUR][1000 genomes]
rs12679551	0.81[EUR][1000 genomes]
rs13263139	0.80[ASN][1000 genomes]
rs16904359	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1989936	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2107072	0.80[EUR][1000 genomes]
rs2214416	0.81[EUR][1000 genomes]
rs28546857	0.80[EUR][1000 genomes]
rs2879345	0.81[EUR][1000 genomes]
rs4081549	0.81[EUR][1000 genomes]
rs4527927	0.84[JPT][hapmap]
rs4576466	0.83[JPT][hapmap]
rs4734447	0.82[ASN][1000 genomes]
rs4735420	0.80[EUR][1000 genomes]
rs4735609	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6470999	0.83[JPT][hapmap]
rs7009723	0.83[JPT][hapmap]
rs7014679	0.84[JPT][hapmap]
rs726619	0.82[EUR][1000 genomes]
rs726620	0.81[EUR][1000 genomes]
rs727099	0.85[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7813747	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7814038	0.82[EUR][1000 genomes]
rs7824559	0.82[EUR][1000 genomes]
rs7824692	0.82[EUR][1000 genomes]
rs7825774	0.82[EUR][1000 genomes]
rs7845926	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91314800-91341200	Weak transcription	K562	blood
2	chr8:91330600-91343800	Weak transcription	Ovary	ovary
3	chr8:91331400-91336600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:91332600-91334400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:91332800-91334400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:91333200-91334600	Enhancers	Pancreas	Pancrea
7	chr8:91333600-91334200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:91333600-91334200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:91333600-91334400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr8:91333600-91336400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:91333800-91334200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:91333800-91336400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr8:91333800-91336400	Weak transcription	HUVEC	blood vessel
14	chr8:91334000-91336200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr8:91334000-91336400	Weak transcription	Dnd41	blood
16	chr8:91334000-91336600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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