Variant report

Variant	rs3918848
Chromosome Location	chr13:110665253-110665254
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	chr13:110651700..110653449-chr13:110664832..110667633,2	K562	blood:
2	chr13:110658379..110661796-chr13:110663475..110666715,3	MCF-7	breast:

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049593	chr13:110615494-110725945	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv1842097	chr13:110644990-110680944	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv901004	chr13:110653666-110682916	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv11075	chr13:110663770-110667708	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv14637	chr13:110664264-110665673	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv826798	chr13:110664799-110665288	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv826799	chr13:110664799-110665425	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv826800	chr13:110664799-110665626	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv826801	chr13:110664864-110665425	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv826802	chr13:110664904-110665425	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110659200-110669800	Weak transcription	Pancreas	Pancrea
2	chr13:110661000-110666800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:110661200-110669400	Enhancers	HSMM	muscle
4	chr13:110662200-110666000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr13:110662600-110666400	Enhancers	HMEC	breast
6	chr13:110662600-110668600	Enhancers	HSMMtube	muscle
7	chr13:110662800-110666200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr13:110662800-110671000	Enhancers	NHEK	skin
9	chr13:110663000-110665800	Enhancers	NHLF	lung
10	chr13:110663000-110666200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:110663200-110667000	Weak transcription	Left Ventricle	heart
12	chr13:110663400-110665600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr13:110663400-110665600	Enhancers	NHDF-Ad	bronchial
14	chr13:110663400-110666800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr13:110663400-110666800	Weak transcription	Fetal Heart	heart
16	chr13:110663400-110667000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr13:110663400-110670600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr13:110664000-110665400	Enhancers	HUVEC	blood vessel
19	chr13:110664000-110665600	Enhancers	Placenta Amnion	Placenta Amnion
20	chr13:110664000-110665800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr13:110664000-110665800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr13:110664000-110665800	Enhancers	Hela-S3	cervix
23	chr13:110664000-110666400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:110664200-110665800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr13:110664600-110665400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr13:110664600-110665800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr13:110664600-110665800	Enhancers	NH-A	brain
28	chr13:110664600-110666000	Enhancers	Osteobl	bone
29	chr13:110664800-110665600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr13:110664800-110668600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr13:110665000-110665600	Flanking Active TSS	A549	lung
32	chr13:110665000-110665800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr13:110665200-110665400	Enhancers	Muscle Satellite Cultured Cells	--

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