Variant report

Variant	rs12306337
Chromosome Location	chr12:8821407-8821408
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIMKLB-2	chr12:8821225-8821607	ENSG00000255829.1
2	lnc-RIMKLB-2	chr12:8821229-8821576	ENSG00000255829.1

rs_ID	r²[population]
rs10128818	1.00[JPT][hapmap]
rs10505736	1.00[JPT][hapmap]
rs11046858	1.00[JPT][hapmap]
rs11046887	1.00[JPT][hapmap]
rs11046900	1.00[JPT][hapmap]
rs11047042	1.00[JPT][hapmap]
rs11612882	1.00[JPT][hapmap]
rs11616092	1.00[JPT][hapmap]
rs12297411	1.00[JPT][hapmap]
rs12299640	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12302099	1.00[JPT][hapmap]
rs12303273	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs12306245	1.00[JPT][hapmap]
rs12307610	1.00[JPT][hapmap]
rs12311263	1.00[JPT][hapmap]
rs12311861	1.00[JPT][hapmap]
rs12312128	1.00[JPT][hapmap]
rs12314360	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12314822	1.00[JPT][hapmap]
rs12318215	1.00[JPT][hapmap]
rs12385824	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12822141	1.00[ASN][1000 genomes]
rs12824174	1.00[ASN][1000 genomes]
rs1476902	1.00[JPT][hapmap]
rs16917739	1.00[JPT][hapmap]
rs16917746	1.00[JPT][hapmap]
rs2159889	1.00[JPT][hapmap]
rs2377491	1.00[ASN][1000 genomes]
rs28372697	0.82[ASN][1000 genomes]
rs57541397	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58333563	0.90[ASN][1000 genomes]
rs58503001	0.90[ASN][1000 genomes]
rs58544193	0.90[ASN][1000 genomes]
rs58860639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59480189	0.83[AMR][1000 genomes]
rs6487313	1.00[JPT][hapmap]
rs6487333	1.00[JPT][hapmap]
rs6487347	1.00[JPT][hapmap]
rs6487354	1.00[JPT][hapmap]
rs7132012	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7139182	1.00[JPT][hapmap]
rs71447528	1.00[ASN][1000 genomes]
rs7303757	1.00[JPT][hapmap]
rs7316051	1.00[JPT][hapmap]
rs7960582	1.00[JPT][hapmap]
rs7968935	1.00[JPT][hapmap]
rs7977372	1.00[JPT][hapmap]

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8811800-8829600	Weak transcription	Thymus	Thymus
2	chr12:8814400-8823400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:8818600-8822200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr12:8819600-8822000	Enhancers	Primary B cells from peripheral blood	blood
5	chr12:8819600-8822000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:8819800-8822000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr12:8819800-8822000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:8821000-8822000	Enhancers	Primary hematopoietic stem cells	blood
9	chr12:8821200-8821600	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr12:8821200-8821800	Enhancers	Fetal Muscle Leg	muscle
11	chr12:8821400-8822000	Active TSS	Brain Anterior Caudate	brain
12	chr12:8821400-8822200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr12:8821400-8824600	Weak transcription	Adipose Nuclei	Adipose

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