Variant report

Variant	rs3099996
Chromosome Location	chr2:39068165-39068166
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:39064983..39068575-chr2:39101517..39104346,3	MCF-7	breast:
2	chr2:39067403..39069873-chr2:39082049..39084866,2	K562	blood:
3	chr2:39060938..39063167-chr2:39068142..39070499,2	K562	blood:

Variant related genes	Relation type
ENSG00000188010	Chromatin interaction
ENSG00000163214	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10165289	1.00[EUR][1000 genomes]
rs10166557	1.00[EUR][1000 genomes]
rs10173380	1.00[EUR][1000 genomes]
rs10173563	1.00[EUR][1000 genomes]
rs10180775	1.00[EUR][1000 genomes]
rs10186448	1.00[EUR][1000 genomes]
rs10186842	1.00[EUR][1000 genomes]
rs10194533	1.00[EUR][1000 genomes]
rs10202876	1.00[EUR][1000 genomes]
rs10495882	1.00[EUR][1000 genomes]
rs12329307	1.00[EUR][1000 genomes]
rs13382974	1.00[EUR][1000 genomes]
rs13395448	1.00[EUR][1000 genomes]
rs13396461	1.00[EUR][1000 genomes]
rs13399254	1.00[EUR][1000 genomes]
rs13409776	1.00[EUR][1000 genomes]
rs13420732	1.00[EUR][1000 genomes]
rs13421894	1.00[EUR][1000 genomes]
rs1451278	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17023037	1.00[EUR][1000 genomes]
rs17023042	1.00[EUR][1000 genomes]
rs17023045	1.00[EUR][1000 genomes]
rs17023148	1.00[EUR][1000 genomes]
rs17023149	1.00[EUR][1000 genomes]
rs17023214	1.00[EUR][1000 genomes]
rs17023241	1.00[EUR][1000 genomes]
rs17425982	1.00[EUR][1000 genomes]
rs1901290	1.00[EUR][1000 genomes]
rs2044853	0.87[AFR][1000 genomes]
rs2218850	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2373466	1.00[EUR][1000 genomes]
rs2373472	1.00[EUR][1000 genomes]
rs28473018	1.00[EUR][1000 genomes]
rs28499207	1.00[EUR][1000 genomes]
rs3099938	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3099953	1.00[EUR][1000 genomes]
rs3099973	1.00[EUR][1000 genomes]
rs3099986	1.00[EUR][1000 genomes]
rs3099997	1.00[EUR][1000 genomes]
rs3112145	1.00[EUR][1000 genomes]
rs3112146	1.00[EUR][1000 genomes]
rs3112148	1.00[EUR][1000 genomes]
rs3112155	1.00[EUR][1000 genomes]
rs3112157	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3112158	1.00[EUR][1000 genomes]
rs3112160	1.00[EUR][1000 genomes]
rs3112164	1.00[EUR][1000 genomes]
rs3112169	1.00[AMR][1000 genomes]
rs3112174	1.00[EUR][1000 genomes]
rs3112177	1.00[EUR][1000 genomes]
rs60703378	1.00[EUR][1000 genomes]
rs6737680	1.00[EUR][1000 genomes]
rs6751306	1.00[EUR][1000 genomes]
rs6753426	1.00[EUR][1000 genomes]
rs72916836	1.00[EUR][1000 genomes]
rs72916860	1.00[EUR][1000 genomes]
rs72918710	1.00[EUR][1000 genomes]
rs7565814	1.00[EUR][1000 genomes]
rs7582586	1.00[EUR][1000 genomes]
rs7599990	1.00[EUR][1000 genomes]
rs9646968	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916059	chr2:38332341-39119398	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	143 gene(s)	inside rSNPs	diseases
2	nsv9646	chr2:38358311-39082189	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
3	nsv2692	chr2:39065768-39111871	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39006400-39085600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr2:39026600-39079800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:39030600-39088200	Weak transcription	Fetal Heart	heart
4	chr2:39032800-39072800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr2:39038800-39095600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:39038800-39102200	Weak transcription	Gastric	stomach
7	chr2:39039000-39085400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:39039000-39090000	Weak transcription	Esophagus	oesophagus
9	chr2:39039000-39101200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr2:39039000-39102000	Weak transcription	Colonic Mucosa	Colon
11	chr2:39040000-39069000	Strong transcription	Fetal Muscle Leg	muscle
12	chr2:39042800-39080600	Weak transcription	Small Intestine	intestine
13	chr2:39043600-39079800	Weak transcription	Right Ventricle	heart
14	chr2:39046000-39073200	Weak transcription	Pancreas	Pancrea
15	chr2:39046200-39070200	Weak transcription	NHLF	lung
16	chr2:39050400-39072800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:39050400-39079800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr2:39050400-39079800	Weak transcription	Spleen	Spleen
19	chr2:39050400-39088000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr2:39051000-39068600	Weak transcription	HMEC	breast
21	chr2:39052200-39068600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr2:39053200-39068600	Weak transcription	Brain Substantia Nigra	brain
23	chr2:39053200-39069600	Weak transcription	HUVEC	blood vessel
24	chr2:39053800-39068200	Weak transcription	HSMM	muscle
25	chr2:39053800-39068400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr2:39053800-39068600	Weak transcription	Aorta	Aorta
27	chr2:39053800-39068800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr2:39053800-39080200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr2:39053800-39080600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr2:39054200-39076400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:39055000-39080000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr2:39055200-39068800	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr2:39055200-39085600	Weak transcription	Psoas Muscle	Psoas
34	chr2:39055600-39071600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:39055600-39073200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr2:39055600-39080000	Weak transcription	NH-A	brain
37	chr2:39055600-39080600	Weak transcription	Hela-S3	cervix
38	chr2:39055600-39080600	Weak transcription	K562	blood
39	chr2:39055800-39071200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr2:39057000-39086200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:39057200-39071400	Strong transcription	Fetal Muscle Trunk	muscle
42	chr2:39058000-39068400	Weak transcription	Brain Angular Gyrus	brain
43	chr2:39058000-39087800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr2:39060000-39080000	Weak transcription	Lung	lung
45	chr2:39060200-39075400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:39061200-39073400	Strong transcription	Fetal Intestine Large	intestine
47	chr2:39061800-39068200	Strong transcription	Fetal Stomach	stomach
48	chr2:39062400-39083400	Weak transcription	NHEK	skin
49	chr2:39063200-39068600	Weak transcription	Fetal Kidney	kidney
50	chr2:39063400-39070200	Weak transcription	Brain Cingulate Gyrus	brain

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