Variant report

Variant	rs16835352
Chromosome Location	chr1:153463037-153463038
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153445167..153447773-chr1:153461159..153464090,2	MCF-7	breast:
2	chr1:153371450..153373306-chr1:153462974..153465949,3	MCF-7	breast:
3	chr1:153323483..153340048-chr1:153448254..153469845,61	MCF-7	breast:
4	chr1:153362845..153364948-chr1:153461555..153463988,2	MCF-7	breast:
5	chr1:153434339..153436072-chr1:153461738..153464674,2	MCF-7	breast:
6	chr1:153452726..153455263-chr1:153460858..153463511,2	MCF-7	breast:
7	chr1:153320974..153341807-chr1:153456098..153486349,81	MCF-7	breast:
8	chr1:153354527..153358677-chr1:153460629..153464225,4	MCF-7	breast:
9	chr1:153449114..153453479-chr1:153459428..153463150,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000163218	Chromatin interaction
ENSG00000143546	Chromatin interaction
ENSG00000163220	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs16835344	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16835349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2986203	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2986204	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2986205	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2986207	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3006432	1.00[AMR][1000 genomes]
rs3014830	1.00[AMR][1000 genomes]
rs3014844	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3014852	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3118476	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58408424	1.00[AMR][1000 genomes]
rs60387319	1.00[AMR][1000 genomes]
rs73022422	1.00[AMR][1000 genomes]
rs73022487	1.00[AMR][1000 genomes]
rs73022488	1.00[AMR][1000 genomes]
rs73022493	1.00[AMR][1000 genomes]
rs73022495	1.00[AMR][1000 genomes]
rs73024403	1.00[AMR][1000 genomes]
rs73024405	1.00[AMR][1000 genomes]
rs73024413	1.00[AMR][1000 genomes]
rs73024414	1.00[AMR][1000 genomes]
rs73024423	1.00[AMR][1000 genomes]
rs9003	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010488	chr1:152901263-153670972	Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
2	nsv535171	chr1:152901263-153670972	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv533877	chr1:152923645-153468131	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	nsv1002705	chr1:153307852-153525589	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
5	nsv831603	chr1:153405842-153576143	Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	148 gene(s)	inside rSNPs	diseases
6	nsv1007306	chr1:153413827-153541798	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153451000-153467400	Weak transcription	Ovary	ovary
2	chr1:153457200-153465800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:153459000-153467800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:153460600-153464400	Enhancers	Fetal Heart	heart
5	chr1:153461000-153464400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr1:153461000-153465000	Enhancers	Fetal Muscle Leg	muscle
7	chr1:153461200-153463400	Enhancers	Fetal Brain Male	brain
8	chr1:153461200-153464000	Enhancers	Lung	lung
9	chr1:153461200-153464400	Enhancers	Fetal Muscle Trunk	muscle
10	chr1:153461200-153464400	Enhancers	Rectal Smooth Muscle	rectum
11	chr1:153461600-153463800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr1:153461600-153467600	Weak transcription	Psoas Muscle	Psoas
13	chr1:153462000-153463800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr1:153462000-153464400	Enhancers	Esophagus	oesophagus
15	chr1:153462200-153463800	Enhancers	NH-A	brain
16	chr1:153462200-153464000	Enhancers	Brain Angular Gyrus	brain
17	chr1:153462200-153464600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:153462200-153464600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:153462400-153463400	Weak transcription	Aorta	Aorta
20	chr1:153462400-153464400	Enhancers	NHLF	lung
21	chr1:153462600-153463200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr1:153462600-153463200	Enhancers	HSMM	muscle
23	chr1:153462600-153463400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr1:153462600-153463400	Enhancers	Pancreas	Pancrea
25	chr1:153462600-153463400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr1:153462600-153463400	Enhancers	Stomach Mucosa	stomach
27	chr1:153462600-153463400	Flanking Active TSS	NHEK	skin
28	chr1:153462600-153463600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr1:153462600-153463600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:153462600-153463600	Enhancers	Brain Anterior Caudate	brain
31	chr1:153462600-153463600	Enhancers	Brain Cingulate Gyrus	brain
32	chr1:153462600-153463600	Enhancers	A549	lung
33	chr1:153462600-153463800	Flanking Active TSS	Hela-S3	cervix
34	chr1:153462600-153464200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr1:153462600-153464200	Enhancers	Adipose Nuclei	Adipose
36	chr1:153462600-153464200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr1:153462600-153464400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:153462600-153464400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:153462600-153464400	Enhancers	Colon Smooth Muscle	Colon
40	chr1:153462800-153463400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:153462800-153463400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
42	chr1:153462800-153463400	Enhancers	Brain Substantia Nigra	brain
43	chr1:153462800-153463600	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr1:153462800-153463600	Enhancers	Placenta Amnion	Placenta Amnion
45	chr1:153462800-153463800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:153462800-153463800	Enhancers	Fetal Stomach	stomach
47	chr1:153462800-153463800	Weak transcription	Left Ventricle	heart
48	chr1:153462800-153464000	Enhancers	Fetal Lung	lung
49	chr1:153462800-153464200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:153462800-153464200	Enhancers	Stomach Smooth Muscle	stomach

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