Variant report

Variant	rs1848486
Chromosome Location	chr5:90314905-90314906
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	chr5:90314128..90316238-chr5:90320139..90322345,2	K562	blood:
2	chr5:90313237..90315031-chr5:90316021..90318044,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10942624	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12186662	0.84[ASN][1000 genomes]
rs13179479	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13180409	0.95[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1819073	0.91[CEU][hapmap];0.95[CHB][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1819074	0.91[CEU][hapmap];0.95[CHB][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1828177	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs1828178	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs1848487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1852734	0.95[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1858070	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2010355	0.82[YRI][hapmap]
rs2048217	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs2367186	0.90[ASN][1000 genomes]
rs2367274	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2463775	1.00[CEU][hapmap];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2662278	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2662279	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2662280	0.95[CEU][hapmap];0.82[JPT][hapmap];0.90[EUR][1000 genomes]
rs2662281	0.99[ASN][1000 genomes]
rs2662282	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2662283	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2662284	0.96[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2697543	0.95[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2697544	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2697546	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28875340	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4254936	0.96[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4454077	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6452930	0.96[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6452934	0.96[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6865615	0.91[CEU][hapmap];0.95[CHB][hapmap]
rs689544	1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs7706034	0.91[CEU][hapmap];0.95[CHB][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7719311	0.96[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7723511	0.96[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7733230	0.91[CEU][hapmap];0.95[CHB][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs937920	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs998788	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv882369	chr5:90275825-90344149	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90308600-90318400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:90308800-90316000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:90309800-90323200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:90312800-90315000	Enhancers	Fetal Intestine Small	intestine
5	chr5:90313200-90315200	Enhancers	Fetal Lung	lung
6	chr5:90313200-90315400	Enhancers	Colon Smooth Muscle	Colon
7	chr5:90313200-90315400	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr5:90313200-90318200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr5:90313400-90315400	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr5:90313400-90318400	Weak transcription	A549	lung
11	chr5:90313400-90321600	Weak transcription	Liver	Liver
12	chr5:90313600-90321400	Weak transcription	Small Intestine	intestine
13	chr5:90313800-90320000	Weak transcription	Adipose Nuclei	Adipose
14	chr5:90314000-90319200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr5:90314200-90315200	Enhancers	Stomach Mucosa	stomach
16	chr5:90314200-90316200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr5:90314200-90319800	Weak transcription	Fetal Stomach	stomach
18	chr5:90314200-90320800	Weak transcription	Fetal Intestine Large	intestine
19	chr5:90314400-90315000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr5:90314400-90315200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:90314400-90316200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:90314400-90317400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr5:90314400-90318400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr5:90314800-90315000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:90314800-90315000	Enhancers	Psoas Muscle	Psoas
26	chr5:90314800-90315200	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr5:90314800-90316000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr5:90314800-90316000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:90314800-90316600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr5:90314800-90316800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:90314800-90323200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr5:90314800-90327000	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links