Variant report

Variant	rs16866416
Chromosome Location	chr2:179479741-179479742
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	chr2:179478723..179480906-chr2:179482461..179485170,2	K562	blood:

Variant related genes	Relation type
ENSG00000237298	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10164753	1.00[CHD][hapmap];0.89[GIH][hapmap];0.94[LWK][hapmap];0.92[MEX][hapmap];0.91[MKK][hapmap];0.83[AMR][1000 genomes]
rs10176708	0.84[EUR][1000 genomes]
rs10179811	0.84[EUR][1000 genomes]
rs10183237	1.00[CHD][hapmap];0.84[EUR][1000 genomes]
rs10183361	0.85[CHD][hapmap];0.84[EUR][1000 genomes]
rs10203085	0.84[EUR][1000 genomes]
rs10204913	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10221760	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10497517	1.00[CHD][hapmap];0.89[GIH][hapmap]
rs11888217	0.83[CHD][hapmap];0.84[GIH][hapmap];0.84[EUR][1000 genomes]
rs11895382	0.83[CHD][hapmap];0.84[MEX][hapmap]
rs11897366	1.00[CHD][hapmap];0.89[GIH][hapmap]
rs13398235	1.00[CHD][hapmap];0.84[EUR][1000 genomes]
rs13398590	1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13417645	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13421990	0.84[MEX][hapmap]
rs16866425	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16866473	0.84[EUR][1000 genomes]
rs1864243	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2366752	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2366753	1.00[CHD][hapmap];0.88[GIH][hapmap];0.85[EUR][1000 genomes]
rs28378468	0.89[EUR][1000 genomes]
rs28710392	0.81[AMR][1000 genomes]
rs28715837	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4893852	1.00[CHD][hapmap];0.84[EUR][1000 genomes]
rs4893853	0.83[CHD][hapmap];0.84[MEX][hapmap]
rs4894034	1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6732060	1.00[CHD][hapmap];0.89[GIH][hapmap]
rs6735083	0.81[AMR][1000 genomes]
rs747122	1.00[CHD][hapmap];0.85[GIH][hapmap]
rs7590037	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7606485	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9808036	1.00[CHD][hapmap];0.85[GIH][hapmap];0.92[MEX][hapmap];0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834468	chr2:179351116-179533625	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv2757841	chr2:179409072-179608242	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv2759103	chr2:179409072-179608242	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1000642	chr2:179438866-179503211	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179388800-179495800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:179408000-179503000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:179430800-179480000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr2:179438400-179518200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:179440600-179494000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr2:179440600-179505200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:179441400-179498800	Weak transcription	Brain Anterior Caudate	brain
8	chr2:179441600-179495000	Weak transcription	Fetal Intestine Small	intestine
9	chr2:179442000-179484200	Weak transcription	Colonic Mucosa	Colon
10	chr2:179442800-179492000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr2:179442800-179493400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:179444800-179484400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr2:179450000-179482400	Weak transcription	Small Intestine	intestine
14	chr2:179460800-179480200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:179461800-179480400	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr2:179461800-179484000	Weak transcription	Fetal Brain Male	brain
17	chr2:179463800-179492000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:179464600-179497400	Weak transcription	GM12878-XiMat	blood
19	chr2:179464800-179481600	Weak transcription	Dnd41	blood
20	chr2:179465600-179483600	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr2:179465800-179481000	Weak transcription	Colon Smooth Muscle	Colon
22	chr2:179465800-179483200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:179466200-179480400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:179466200-179484600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:179467000-179480200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:179467200-179481800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:179468000-179486800	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr2:179468400-179484200	Strong transcription	HSMMtube	muscle
29	chr2:179468400-179486600	Strong transcription	Fetal Muscle Leg	muscle
30	chr2:179468400-179489200	Strong transcription	Left Ventricle	heart
31	chr2:179468400-179490400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr2:179468600-179480200	Strong transcription	Primary B cells from peripheral blood	blood
33	chr2:179468600-179480400	Strong transcription	Pancreas	Pancrea
34	chr2:179468600-179484600	Strong transcription	Right Ventricle	heart
35	chr2:179468600-179486400	Strong transcription	Primary B cells from cord blood	blood
36	chr2:179468600-179486400	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr2:179468600-179486400	Strong transcription	Fetal Muscle Trunk	muscle
38	chr2:179468600-179489600	Strong transcription	Primary T cells from cord blood	blood
39	chr2:179468600-179490000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr2:179470000-179480800	Weak transcription	Fetal Stomach	stomach
41	chr2:179470000-179481800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr2:179470000-179482600	Weak transcription	Gastric	stomach
43	chr2:179470000-179489800	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr2:179470200-179480000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr2:179470400-179482000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr2:179471400-179483800	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr2:179471800-179483400	Strong transcription	Primary hematopoietic stem cells	blood
48	chr2:179471800-179483400	Strong transcription	Fetal Intestine Large	intestine
49	chr2:179472400-179502600	Weak transcription	Brain Substantia Nigra	brain
50	chr2:179472800-179489400	Strong transcription	Primary T helper cells PMA-I stimulated	--

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