Variant report

Variant	rs16900989
Chromosome Location	chr6:160516757-160516758
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:160516728-160516780	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
IGF2R	TF binding region

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12202113	1.00[AMR][1000 genomes]
rs16888665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16891138	0.82[YRI][hapmap]
rs2777355	1.00[YRI][hapmap]
rs3777402	1.00[YRI][hapmap]
rs6413491	1.00[YRI][hapmap]
rs8191872	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758089	chr6:160372244-161234665	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2759484	chr6:160372244-161234665	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv35098	chr6:160422589-161070870	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	esv2757197	chr6:160432331-161070870	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv818463	chr6:160435569-161025547	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:160444200-160521600	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr6:160453000-160534600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:160455800-160532000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:160459600-160519200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:160460800-160520200	Strong transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:160460800-160520200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:160464400-160519800	Strong transcription	Lung	lung
8	chr6:160464600-160531800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr6:160465600-160530800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:160466000-160521000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:160474200-160519600	Strong transcription	Cortex derived primary cultured neurospheres	brain
12	chr6:160474200-160519800	Strong transcription	Fetal Stomach	stomach
13	chr6:160474400-160520600	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr6:160477200-160531200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:160477200-160531400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:160485800-160522800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr6:160487600-160520000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:160487600-160530800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr6:160487800-160519200	Strong transcription	Esophagus	oesophagus
20	chr6:160487800-160519400	Strong transcription	Gastric	stomach
21	chr6:160487800-160519800	Strong transcription	Ovary	ovary
22	chr6:160487800-160519800	Strong transcription	Pancreas	Pancrea
23	chr6:160487800-160520200	Strong transcription	Adipose Nuclei	Adipose
24	chr6:160490200-160531400	Strong transcription	Dnd41	blood
25	chr6:160490400-160521200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr6:160490600-160519800	Strong transcription	Spleen	Spleen
27	chr6:160490600-160521000	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr6:160490600-160521200	Strong transcription	Thymus	Thymus
29	chr6:160490800-160521400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr6:160491000-160518200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr6:160491000-160519600	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr6:160491200-160517800	Weak transcription	HUVEC	blood vessel
33	chr6:160491200-160519200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr6:160491200-160520200	Strong transcription	Primary T cells from cord blood	blood
35	chr6:160491200-160520400	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr6:160491200-160531400	Strong transcription	Fetal Thymus	thymus
37	chr6:160492000-160528800	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr6:160492600-160521200	Strong transcription	Primary B cells from cord blood	blood
39	chr6:160498400-160519200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr6:160498800-160520200	Strong transcription	Primary B cells from peripheral blood	blood
41	chr6:160499600-160522200	Weak transcription	Fetal Heart	heart
42	chr6:160501400-160522000	Weak transcription	Psoas Muscle	Psoas
43	chr6:160501400-160522400	Weak transcription	Primary hematopoietic stem cells	blood
44	chr6:160501600-160520200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr6:160501600-160527000	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr6:160502200-160521800	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr6:160502600-160520600	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr6:160503400-160518000	Strong transcription	Brain Anterior Caudate	brain
49	chr6:160503800-160520400	Strong transcription	GM12878-XiMat	blood
50	chr6:160504200-160521000	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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