Variant report

Variant	rs28364385
Chromosome Location	chr15:42675990-42675991
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:42672860..42675186-chr15:42675250..42677559,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs16973182	0.89[AFR][1000 genomes]
rs16973184	0.89[AFR][1000 genomes]
rs16973188	0.89[AFR][1000 genomes]
rs16973200	0.80[AFR][1000 genomes]
rs16973206	0.91[AFR][1000 genomes]
rs17593	0.91[AFR][1000 genomes]
rs28364383	0.89[AFR][1000 genomes]
rs28364399	0.80[AFR][1000 genomes]
rs4307925	0.89[AFR][1000 genomes]
rs4486855	0.89[AFR][1000 genomes]
rs4516202	0.89[AFR][1000 genomes]
rs7167683	0.93[AFR][1000 genomes]
rs7174880	0.85[AFR][1000 genomes]
rs8024452	0.89[AFR][1000 genomes]
rs8033734	0.89[AFR][1000 genomes]
rs8033882	0.89[AFR][1000 genomes]
rs8033960	0.89[AFR][1000 genomes]
rs8038771	0.89[AFR][1000 genomes]
rs8038967	0.89[AFR][1000 genomes]
rs8039470	0.89[AFR][1000 genomes]
rs8040129	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
4	nsv904133	chr15:42528982-42681057	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	nsv832986	chr15:42587825-42753664	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv832987	chr15:42627447-42792348	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	nsv932995	chr15:42640015-42704121	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	esv3334708	chr15:42664344-42827738	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42645600-42677800	Weak transcription	Spleen	Spleen
2	chr15:42646000-42678600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr15:42647800-42678200	Weak transcription	Ovary	ovary
4	chr15:42652800-42684400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr15:42653200-42691600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr15:42654200-42677800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr15:42656000-42678800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr15:42656800-42693400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr15:42656800-42697800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr15:42657200-42678800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr15:42659600-42676800	Weak transcription	Lung	lung
12	chr15:42663000-42691400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr15:42663200-42678400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr15:42666600-42676800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr15:42666600-42676800	Weak transcription	Fetal Muscle Leg	muscle
16	chr15:42666600-42676800	Weak transcription	Left Ventricle	heart
17	chr15:42666800-42676800	Weak transcription	Fetal Muscle Trunk	muscle
18	chr15:42670200-42676800	Weak transcription	Primary B cells from cord blood	blood
19	chr15:42670400-42676200	Weak transcription	Liver	Liver
20	chr15:42672400-42688800	Weak transcription	Esophagus	oesophagus
21	chr15:42673400-42691800	Weak transcription	Primary T cells from cord blood	blood
22	chr15:42673600-42676200	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr15:42673800-42676800	Weak transcription	Brain Substantia Nigra	brain
24	chr15:42673800-42678000	Weak transcription	Fetal Intestine Small	intestine
25	chr15:42673800-42678200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr15:42674000-42694400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr15:42674200-42676400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr15:42674600-42678200	Weak transcription	Aorta	Aorta
29	chr15:42674600-42682600	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr15:42674600-42684400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr15:42674800-42678400	Weak transcription	Brain Anterior Caudate	brain
32	chr15:42675200-42676800	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr15:42675200-42676800	Weak transcription	Adipose Nuclei	Adipose
34	chr15:42675200-42677800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
35	chr15:42675200-42683600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr15:42675200-42684800	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr15:42675200-42702800	Weak transcription	Colon Smooth Muscle	Colon
38	chr15:42675600-42676400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr15:42675600-42676600	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr15:42675600-42691600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr15:42675800-42676400	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr15:42675800-42678800	Weak transcription	Brain Angular Gyrus	brain

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