Variant report

Variant	rs74015236
Chromosome Location	chr15:51227473-51227474
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:51224967..51227623-chr15:51229522..51232521,3	K562	blood:
2	chr15:51199999..51202298-chr15:51226903..51228842,2	K562	blood:
3	chr15:51191862..51194538-chr15:51226502..51228724,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000081014	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs16963979	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28865017	1.00[AMR][1000 genomes]
rs55683982	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55735813	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55742119	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55763666	1.00[AMR][1000 genomes]
rs55912100	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55920356	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55940433	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55973448	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56010315	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56017509	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56046825	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56049414	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56056949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56121717	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56222335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56273151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56283133	1.00[AMR][1000 genomes]
rs56289716	1.00[AMR][1000 genomes]
rs56374503	1.00[AMR][1000 genomes]
rs56813592	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57221782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57305511	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57322405	0.86[AFR][1000 genomes]
rs57499524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57831362	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57949904	1.00[AMR][1000 genomes]
rs58651255	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59067851	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59155793	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59364110	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59681404	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59843670	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59865784	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60037205	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60253924	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60297574	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60700183	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60775199	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61106666	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61698311	1.00[AMR][1000 genomes]
rs6493467	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7171301	1.00[AMR][1000 genomes]
rs7174066	1.00[AMR][1000 genomes]
rs7175547	1.00[AMR][1000 genomes]
rs74012820	1.00[AMR][1000 genomes]
rs74012821	1.00[AMR][1000 genomes]
rs74013114	1.00[AMR][1000 genomes]
rs74013115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74013125	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74013127	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74013128	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74013130	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74013132	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74013134	0.86[AFR][1000 genomes]
rs74013136	0.86[AFR][1000 genomes]
rs74015214	1.00[AMR][1000 genomes]
rs74015215	1.00[AMR][1000 genomes]
rs74015226	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015228	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015229	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015230	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015232	1.00[AMR][1000 genomes]
rs74015235	1.00[AFR][1000 genomes];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	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
5	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
6	nsv529339	chr15:51048579-51270372	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
7	nsv428636	chr15:51154834-51298044	Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
8	nsv569403	chr15:51191421-51304373	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv1038778	chr15:51196641-51356728	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	nsv904214	chr15:51204364-51535192	Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51201600-51243200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:51201600-51245000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:51201800-51230600	Weak transcription	K562	blood
4	chr15:51201800-51242800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr15:51201800-51248400	Weak transcription	Colonic Mucosa	Colon
6	chr15:51201800-51271600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr15:51202600-51236800	Weak transcription	Small Intestine	intestine
8	chr15:51202600-51241800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr15:51202600-51242800	Weak transcription	Gastric	stomach
10	chr15:51202800-51230400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr15:51202800-51243400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr15:51203000-51230400	Weak transcription	Colon Smooth Muscle	Colon
13	chr15:51203200-51242200	Weak transcription	Brain Substantia Nigra	brain
14	chr15:51203200-51242800	Weak transcription	Lung	lung
15	chr15:51203400-51242400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr15:51204000-51231200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr15:51204200-51231200	Strong transcription	Placenta	Placenta
18	chr15:51204600-51229000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr15:51204800-51243000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr15:51205600-51242800	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr15:51205800-51249000	Weak transcription	Fetal Brain Male	brain
22	chr15:51205800-51254400	Weak transcription	Fetal Heart	heart
23	chr15:51208000-51250400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr15:51208400-51242200	Weak transcription	Fetal Kidney	kidney
25	chr15:51210400-51243000	Weak transcription	Brain Angular Gyrus	brain
26	chr15:51210600-51298400	Weak transcription	Stomach Mucosa	stomach
27	chr15:51212200-51230600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr15:51213000-51242800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr15:51213200-51245400	Weak transcription	Psoas Muscle	Psoas
30	chr15:51213600-51243400	Weak transcription	Pancreas	Pancrea
31	chr15:51213800-51247600	Weak transcription	Aorta	Aorta
32	chr15:51214600-51230200	Weak transcription	Spleen	Spleen
33	chr15:51214600-51236800	Weak transcription	Rectal Smooth Muscle	rectum
34	chr15:51214600-51247800	Weak transcription	Esophagus	oesophagus
35	chr15:51214800-51230400	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr15:51217200-51231000	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr15:51217600-51230400	Weak transcription	Fetal Lung	lung
38	chr15:51218000-51230400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr15:51219200-51228400	Strong transcription	HSMM	muscle
40	chr15:51219200-51230400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr15:51219800-51229800	Weak transcription	Thymus	Thymus
42	chr15:51219800-51230400	Weak transcription	Brain Germinal Matrix	brain
43	chr15:51219800-51243000	Weak transcription	Brain Hippocampus Middle	brain
44	chr15:51220000-51242200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr15:51220200-51234200	Weak transcription	Ovary	ovary
46	chr15:51220200-51236800	Weak transcription	Right Ventricle	heart
47	chr15:51220200-51243000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr15:51220400-51231800	Weak transcription	NHLF	lung
49	chr15:51220800-51227600	Weak transcription	NHEK	skin
50	chr15:51220800-51230000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links