Variant report

Variant	rs16903740
Chromosome Location	chr5:14937733-14937734
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	chr5:14937263..14940130-chr5:14945612..14948261,3	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs16903737	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018187	chr5:14385164-15127103	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv830212	chr5:14784197-14966683	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv530221	chr5:14859687-15364470	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
4	nsv432717	chr5:14887400-15126500	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv1017579	chr5:14888997-15194335	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv597261	chr5:14913369-14962587	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv881238	chr5:14917813-14950952	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	nsv881343	chr5:14917813-14956699	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv881445	chr5:14917813-14960920	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv881333	chr5:14924458-14962587	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14936200-14937800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr5:14936200-14938000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:14936400-14939400	Enhancers	Adipose Nuclei	Adipose
4	chr5:14936800-14937800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:14936800-14937800	Enhancers	HUVEC	blood vessel
6	chr5:14936800-14938000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:14936800-14938600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:14937000-14938000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:14937200-14937800	Enhancers	Duodenum Mucosa	Duodenum
10	chr5:14937200-14937800	Enhancers	Fetal Intestine Large	intestine
11	chr5:14937200-14937800	Enhancers	Stomach Mucosa	stomach
12	chr5:14937200-14937800	Enhancers	Hela-S3	cervix
13	chr5:14937400-14937800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:14937400-14937800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
15	chr5:14937400-14937800	Enhancers	NH-A	brain
16	chr5:14937600-14937800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:14937600-14937800	Enhancers	Primary T cells fromperipheralblood	blood
18	chr5:14937600-14937800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr5:14937600-14937800	Enhancers	Small Intestine	intestine
20	chr5:14937600-14938000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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