Variant report

Variant	rs13378711
Chromosome Location	chr13:111096645-111096646
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:48286253..48286993-chr13:111096495..111097274,2	MCF-7	breast:
2	chr13:110874131..110875670-chr13:111096283..111097578,7	MCF-7	breast:
3	chr13:111064379..111065184-chr13:111096354..111096894,3	MCF-7	breast:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10161944	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12184943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13378248	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72657930	1.00[AFR][1000 genomes]
rs7988186	0.85[AMR][1000 genomes]
rs9583494	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9583495	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9583496	0.85[AMR][1000 genomes]
rs9588163	0.85[AMR][1000 genomes]
rs9588164	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9588165	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1038914	chr13:110860219-111190104	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1046423	chr13:110936104-111286607	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	esv2751128	chr13:111040798-111132490	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv901008	chr13:111089573-111126501	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv430604	chr13:111095999-111156999	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111068000-111107000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:111070200-111108400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr13:111078200-111099000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr13:111078200-111136800	Weak transcription	Colonic Mucosa	Colon
5	chr13:111079200-111097600	Weak transcription	Fetal Brain Female	brain
6	chr13:111083600-111110000	Weak transcription	Esophagus	oesophagus
7	chr13:111084200-111106400	Weak transcription	Liver	Liver
8	chr13:111084400-111100000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr13:111084800-111098800	Strong transcription	Fetal Stomach	stomach
10	chr13:111086000-111105800	Strong transcription	Adipose Nuclei	Adipose
11	chr13:111087400-111099400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr13:111087400-111099600	Weak transcription	Pancreas	Pancrea
13	chr13:111088000-111107800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr13:111089400-111100000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr13:111091000-111098200	Weak transcription	Gastric	stomach
16	chr13:111091000-111108400	Weak transcription	Brain Angular Gyrus	brain
17	chr13:111092400-111098400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr13:111092600-111099400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr13:111092600-111099400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr13:111093600-111097000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr13:111093600-111098200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr13:111093600-111098600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr13:111093800-111099400	Weak transcription	Fetal Lung	lung
24	chr13:111093800-111099600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr13:111093800-111101400	Genic enhancers	NH-A	brain
26	chr13:111093800-111108200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr13:111094000-111097600	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr13:111094000-111097800	Weak transcription	HSMMtube	muscle
29	chr13:111094000-111102000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr13:111094000-111102200	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr13:111094200-111097600	Weak transcription	Lung	lung
32	chr13:111094200-111098200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:111094600-111096800	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr13:111094600-111096800	Enhancers	Hela-S3	cervix
35	chr13:111094600-111097000	Enhancers	NHLF	lung
36	chr13:111094600-111099600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr13:111094800-111097000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr13:111094800-111097000	Genic enhancers	Osteobl	bone
39	chr13:111094800-111097600	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr13:111094800-111099400	Enhancers	HMEC	breast
41	chr13:111094800-111099600	Strong transcription	Placenta	Placenta
42	chr13:111094800-111108200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr13:111095000-111101600	Genic enhancers	HSMM	muscle
44	chr13:111095000-111108400	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr13:111095200-111096800	Genic enhancers	Stomach Smooth Muscle	stomach
46	chr13:111095200-111097000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr13:111095200-111097200	Enhancers	Colon Smooth Muscle	Colon
48	chr13:111095200-111098000	Enhancers	NHEK	skin
49	chr13:111095200-111099400	Weak transcription	Fetal Kidney	kidney
50	chr13:111095400-111096800	Enhancers	Fetal Heart	heart

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