Variant report

Variant	rs71434756
Chromosome Location	chr13:30329391-30329392
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs12859613	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12868469	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12869325	0.91[AMR][1000 genomes]
rs1327643	0.88[EUR][1000 genomes]
rs2031280	0.88[EUR][1000 genomes]
rs34114731	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34129219	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34317115	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34726132	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34837672	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34943308	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35042630	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35158864	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35177317	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35452290	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35520191	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35727212	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35735441	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35849390	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35889915	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35933528	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4335642	0.81[EUR][1000 genomes]
rs4385989	0.88[EUR][1000 genomes]
rs4611301	0.88[EUR][1000 genomes]
rs4769024	0.88[EUR][1000 genomes]
rs71434755	0.86[AFR][1000 genomes]
rs71434759	0.85[EUR][1000 genomes]
rs71434760	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71434762	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71434763	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71434764	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs71434765	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs71434766	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8000607	0.88[EUR][1000 genomes]
rs8000887	0.84[EUR][1000 genomes]
rs8001330	0.88[EUR][1000 genomes]
rs9314977	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899961	chr13:30226924-30407273	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3520592	chr13:30243601-30648554	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv3520593	chr13:30243601-30648554	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30317600-30335800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:30324600-30340400	Weak transcription	Adipose Nuclei	Adipose
3	chr13:30326600-30343200	Weak transcription	Spleen	Spleen
4	chr13:30328400-30337200	Weak transcription	Osteobl	bone
5	chr13:30328400-30340600	Weak transcription	NHLF	lung
6	chr13:30328600-30330800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr13:30328600-30333000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:30328600-30337200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr13:30328600-30341200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr13:30328800-30337200	Weak transcription	NHDF-Ad	bronchial
11	chr13:30328800-30337400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr13:30328800-30340400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr13:30328800-30340400	Weak transcription	Brain Hippocampus Middle	brain
14	chr13:30328800-30340800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr13:30328800-30347800	Weak transcription	Fetal Kidney	kidney
16	chr13:30328800-30351800	Weak transcription	NH-A	brain
17	chr13:30328800-30352600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr13:30329000-30332800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr13:30329000-30335800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr13:30329200-30332800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr13:30329200-30332800	Weak transcription	HepG2	liver
22	chr13:30329200-30335400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr13:30329200-30338000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr13:30329200-30340000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr13:30329200-30340600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:30329200-30351200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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