Variant report

Variant	rs568313431
Chromosome Location	chr13:47689802-47689803
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	chr13:47687158..47689535-chr13:47689573..47691245,2	MCF-7	breast:
2	chr13:47687420..47689651-chr13:47689739..47691291,2	K562	blood:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3394678	chr13:47678184-48039379	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv2483982	chr13:47688819-47690364	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv5610	chr13:47689217-47690055	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2244372	chr13:47689296-47689989	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3510119	chr13:47689365-47689879	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3497643	chr13:47689382-47689900	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3497646	chr13:47689388-47689873	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3497644	chr13:47689390-47689844	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3497647	chr13:47689402-47689845	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3497648	chr13:47689404-47689824	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3510086	chr13:47689412-47689857	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3510130	chr13:47689417-47689858	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3497645	chr13:47689420-47689842	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3510097	chr13:47689424-47689815	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3368759	chr13:47689440-47689812	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv4875	chr13:47689447-47689929	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3497649	chr13:47689477-47689805	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3510141	chr13:47689477-47689805	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:47683800-47695200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:47685800-47694800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr13:47686600-47695200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr13:47687400-47693400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr13:47687600-47691800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr13:47688200-47690000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr13:47688200-47691800	Weak transcription	K562	blood
8	chr13:47688200-47695800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr13:47688400-47693200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr13:47688600-47691400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr13:47688600-47691800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr13:47688600-47692600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr13:47688600-47693400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr13:47688600-47694000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr13:47688600-47694600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr13:47688600-47694600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr13:47688800-47693200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr13:47688800-47695600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr13:47689000-47691400	Weak transcription	Osteobl	bone
20	chr13:47689000-47691600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr13:47689200-47690000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr13:47689200-47691200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr13:47689200-47691200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr13:47689200-47691800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr13:47689200-47693200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr13:47689600-47690000	Weak transcription	NHDF-Ad	bronchial

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