Variant report

Variant	rs1801449
Chromosome Location	chr15:42681199-42681200
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:42679543..42681444-chr15:42683292..42685260,2	K562	blood:
2	chr15:42679521..42681202-chr15:42684595..42687043,2	MCF-7	breast:
3	chr15:42559733..42563310-chr15:42678634..42681534,3	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10518763	0.82[CEU][hapmap]
rs1659215	0.82[CEU][hapmap]
rs16973053	1.00[CEU][hapmap]
rs16973054	0.82[CEU][hapmap]
rs16973059	0.82[CEU][hapmap]
rs16973089	0.82[CEU][hapmap]
rs16973091	0.82[CEU][hapmap]
rs16973093	0.82[CEU][hapmap]
rs16973095	0.82[CEU][hapmap]
rs16973096	0.82[CEU][hapmap]
rs16973097	0.82[CEU][hapmap]
rs16973107	0.82[CEU][hapmap]
rs16973109	0.82[CEU][hapmap]
rs16973132	0.82[CEU][hapmap]
rs16973137	0.82[CEU][hapmap]
rs16973148	0.82[CEU][hapmap]
rs16973153	0.82[CEU][hapmap]
rs16973171	0.82[CEU][hapmap]
rs16973174	0.82[CEU][hapmap]
rs16973175	0.82[CEU][hapmap]
rs1712391	0.82[CEU][hapmap]
rs1712407	0.82[CEU][hapmap]
rs17695121	0.82[CEU][hapmap]
rs2412704	0.82[CEU][hapmap]
rs28364347	0.82[CEU][hapmap]
rs4344713	0.82[CEU][hapmap]
rs635919	0.82[CEU][hapmap]
rs685521	0.82[CEU][hapmap]
rs7164437	0.82[CEU][hapmap]
rs7164874	0.82[CEU][hapmap]
rs7178901	0.82[CEU][hapmap]
rs7182797	0.82[CEU][hapmap]
rs8037100	0.82[CEU][hapmap]
rs8038153	0.82[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 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	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
5	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
6	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
7	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:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42652800-42684400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr15:42653200-42691600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr15:42656800-42693400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr15:42656800-42697800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:42663000-42691400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:42672400-42688800	Weak transcription	Esophagus	oesophagus
7	chr15:42673400-42691800	Weak transcription	Primary T cells from cord blood	blood
8	chr15:42674000-42694400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr15:42674600-42682600	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr15:42674600-42684400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr15:42675200-42683600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr15:42675200-42684800	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr15:42675200-42702800	Weak transcription	Colon Smooth Muscle	Colon
14	chr15:42675600-42691600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr15:42676200-42682400	Strong transcription	Liver	Liver
16	chr15:42676800-42693200	Weak transcription	Fetal Stomach	stomach
17	chr15:42677000-42693400	Weak transcription	GM12878-XiMat	blood
18	chr15:42677200-42684000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr15:42677400-42687800	Weak transcription	Brain Substantia Nigra	brain
20	chr15:42677600-42689000	Weak transcription	Right Ventricle	heart
21	chr15:42677800-42682600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr15:42678200-42688000	Weak transcription	Brain Hippocampus Middle	brain
23	chr15:42678400-42681600	Weak transcription	HepG2	liver
24	chr15:42678400-42682200	Weak transcription	Fetal Intestine Large	intestine
25	chr15:42678400-42687400	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr15:42678600-42691200	Weak transcription	Gastric	stomach
27	chr15:42678600-42706800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr15:42678800-42684600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr15:42678800-42691600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr15:42678800-42694000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr15:42678800-42702800	Weak transcription	NHLF	lung
32	chr15:42679000-42681200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr15:42679000-42683600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:42679000-42684400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr15:42679000-42687400	Weak transcription	Spleen	Spleen
36	chr15:42679000-42691400	Weak transcription	Thymus	Thymus
37	chr15:42679000-42706800	Weak transcription	Right Atrium	heart
38	chr15:42679200-42681200	Weak transcription	Psoas Muscle	Psoas
39	chr15:42679200-42681400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr15:42679200-42681600	Weak transcription	Fetal Intestine Small	intestine
41	chr15:42679200-42681800	Genic enhancers	Skeletal Muscle Male	skeletal muscle
42	chr15:42679200-42691600	Weak transcription	Brain Anterior Caudate	brain
43	chr15:42679200-42694000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr15:42679600-42681800	Weak transcription	K562	blood
45	chr15:42679600-42691400	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr15:42679800-42681200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr15:42680000-42682000	Enhancers	Adipose Nuclei	Adipose
48	chr15:42680000-42684600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:42680000-42693200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr15:42680200-42681800	Weak transcription	Aorta	Aorta

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