Variant report

Variant	rs933861
Chromosome Location	chr15:52967110-52967111
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:52966230..52968677-chr15:52969167..52971307,2	K562	blood:
2	chr15:52965949..52968646-chr15:53025332..53028243,3	MCF-7	breast:
3	chr15:52966884..52967402-chr2:185577216..185577716,2	MCF-7	breast:
4	chr15:52966586..52968208-chr15:53018199..53019999,2	MCF-7	breast:
5	chr15:52855349..52864927-chr15:52966670..52972620,15	MCF-7	breast:
6	chr15:52942408..52952117-chr15:52965431..52973600,32	MCF-7	breast:
7	chr15:52966022..52968187-chr15:52971881..52974523,2	K562	blood:
8	chr15:52964942..52967730-chr15:52969807..52971860,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000047346	Chromatin interaction
ENSG00000128989	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs17708373	0.80[ASN][1000 genomes]
rs2414172	0.95[ASN][1000 genomes]
rs35689765	0.95[ASN][1000 genomes]
rs3751613	0.95[ASN][1000 genomes]
rs59336405	0.87[ASN][1000 genomes]
rs59360599	0.94[ASN][1000 genomes]
rs59808396	0.98[ASN][1000 genomes]
rs59920981	0.87[ASN][1000 genomes]
rs59997215	0.87[ASN][1000 genomes]
rs60200908	0.86[ASN][1000 genomes]
rs61021982	0.93[ASN][1000 genomes]
rs7182896	0.90[ASN][1000 genomes]
rs72623993	0.85[ASN][1000 genomes]
rs72623994	0.88[ASN][1000 genomes]
rs72623995	0.93[ASN][1000 genomes]
rs72623996	0.92[ASN][1000 genomes]
rs72623997	0.87[ASN][1000 genomes]
rs72623998	0.95[ASN][1000 genomes]
rs72623999	0.90[ASN][1000 genomes]
rs72624000	0.89[ASN][1000 genomes]
rs877974	0.95[ASN][1000 genomes]
rs877975	0.98[ASN][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	nsv471245	chr15:52607262-53187165	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv1041421	chr15:52661342-53148286	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv833006	chr15:52825954-53040462	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv457140	chr15:52901433-52968746	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1049534	chr15:52903314-53022926	Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52871800-52967600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr15:52944400-52969600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr15:52944400-52970200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:52944600-52969800	Weak transcription	Fetal Brain Male	brain
5	chr15:52945000-52968600	Weak transcription	HepG2	liver
6	chr15:52946000-52968200	Weak transcription	Fetal Heart	heart
7	chr15:52946000-52968600	Weak transcription	Stomach Mucosa	stomach
8	chr15:52950400-52969400	Weak transcription	A549	lung
9	chr15:52950800-52968400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr15:52951000-52970200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:52952000-52967400	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr15:52952000-52968000	Strong transcription	Fetal Thymus	thymus
13	chr15:52952200-52967800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr15:52953200-52967800	Weak transcription	Fetal Intestine Small	intestine
15	chr15:52957400-52967400	Weak transcription	Right Atrium	heart
16	chr15:52957400-52970000	Weak transcription	Colonic Mucosa	Colon
17	chr15:52957400-52970000	Weak transcription	Lung	lung
18	chr15:52959200-52967200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr15:52960000-52969000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr15:52960400-52967600	Weak transcription	Ovary	ovary
21	chr15:52960400-52969600	Weak transcription	HMEC	breast
22	chr15:52960600-52969400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:52960600-52969400	Weak transcription	NHEK	skin
24	chr15:52960600-52970000	Weak transcription	Small Intestine	intestine
25	chr15:52961600-52969000	Strong transcription	Osteobl	bone
26	chr15:52962000-52967600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr15:52962200-52967800	Strong transcription	Fetal Lung	lung
28	chr15:52962200-52967800	Strong transcription	NH-A	brain
29	chr15:52962200-52969800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr15:52962400-52969400	Weak transcription	Fetal Stomach	stomach
31	chr15:52962600-52967800	Weak transcription	Pancreas	Pancrea
32	chr15:52962600-52968600	Weak transcription	Rectal Smooth Muscle	rectum
33	chr15:52962600-52969800	Weak transcription	Right Ventricle	heart
34	chr15:52962600-52970200	Weak transcription	Gastric	stomach
35	chr15:52962600-52970400	Weak transcription	Spleen	Spleen
36	chr15:52962800-52969400	Weak transcription	Aorta	Aorta
37	chr15:52963000-52969600	Weak transcription	NHLF	lung
38	chr15:52963000-52970000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr15:52963200-52967400	Weak transcription	Fetal Muscle Trunk	muscle
40	chr15:52963600-52968800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
41	chr15:52963800-52967200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr15:52964000-52969000	Weak transcription	Stomach Smooth Muscle	stomach
43	chr15:52964200-52968600	Weak transcription	Fetal Kidney	kidney
44	chr15:52964400-52967800	Weak transcription	Psoas Muscle	Psoas
45	chr15:52964600-52969400	Weak transcription	Thymus	Thymus
46	chr15:52964600-52969800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr15:52964600-52970000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:52965000-52967600	Strong transcription	HSMM	muscle
49	chr15:52965000-52968800	Genic enhancers	Primary B cells from cord blood	blood
50	chr15:52965000-52969000	Genic enhancers	Primary T helper cells fromperipheralblood	blood

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