Variant report

Variant	rs13183472
Chromosome Location	chr5:112450178-112450179
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	chr5:112421011..112422798-chr5:112448533..112450483,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10040400	0.93[EUR][1000 genomes]
rs10478110	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs11241191	0.85[EUR][1000 genomes]
rs11241192	0.88[EUR][1000 genomes]
rs11241193	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs11749995	0.80[AFR][1000 genomes]
rs11953203	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs11960706	0.87[CEU][hapmap];0.84[EUR][1000 genomes]
rs12109548	0.85[CEU][hapmap]
rs12187718	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12187866	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12188482	0.95[EUR][1000 genomes]
rs12517185	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs12517187	0.88[EUR][1000 genomes]
rs12523053	0.84[EUR][1000 genomes]
rs13156718	0.81[CEU][hapmap];0.82[EUR][1000 genomes]
rs13168126	0.84[CEU][hapmap]
rs13170088	0.91[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs13173830	0.86[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs13174483	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs13179421	0.96[EUR][1000 genomes]
rs13183116	0.84[CEU][hapmap]
rs13183638	0.92[CEU][hapmap];0.96[EUR][1000 genomes]
rs13184187	0.96[EUR][1000 genomes]
rs13190424	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs36041392	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3922585	0.84[CEU][hapmap];0.88[JPT][hapmap];0.80[YRI][hapmap];0.93[AFR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4705543	0.81[CEU][hapmap];0.82[EUR][1000 genomes]
rs4705546	0.91[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4705778	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4705779	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4705782	0.88[CEU][hapmap];0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62374710	0.88[EUR][1000 genomes]
rs6594682	0.85[EUR][1000 genomes]
rs6860460	0.88[CEU][hapmap]
rs6883605	0.84[CEU][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap];0.91[AFR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7700271	0.88[EUR][1000 genomes]
rs7704382	0.86[EUR][1000 genomes]
rs7707142	0.88[EUR][1000 genomes]
rs7731180	0.88[EUR][1000 genomes]
rs9326877	0.87[EUR][1000 genomes]
rs9326878	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs9326879	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs9885385	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018344	chr5:112390951-112458853	Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv599396	chr5:112408944-112853189	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112384000-112453000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr5:112426600-112453000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr5:112426800-112450200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:112426800-112450600	Weak transcription	Primary T cells from cord blood	blood
5	chr5:112426800-112450600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:112426800-112453800	Weak transcription	HSMMtube	muscle
7	chr5:112427000-112453800	Weak transcription	Fetal Kidney	kidney
8	chr5:112431200-112461600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr5:112432200-112450200	Weak transcription	Spleen	Spleen
10	chr5:112432200-112454600	Weak transcription	Pancreas	Pancrea
11	chr5:112434000-112459200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr5:112437800-112454400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr5:112438000-112450600	Weak transcription	Aorta	Aorta
14	chr5:112438000-112454200	Weak transcription	Psoas Muscle	Psoas
15	chr5:112438200-112450200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr5:112438200-112452800	Weak transcription	Brain Anterior Caudate	brain
17	chr5:112439600-112454600	Weak transcription	Esophagus	oesophagus
18	chr5:112439800-112452600	Weak transcription	Fetal Lung	lung
19	chr5:112440200-112454200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr5:112442800-112452600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr5:112446400-112450200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr5:112448600-112455000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:112448800-112450400	Weak transcription	Left Ventricle	heart
24	chr5:112448800-112454400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:112448800-112455200	Weak transcription	HUVEC	blood vessel
26	chr5:112449000-112450200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:112449000-112452800	Weak transcription	Right Ventricle	heart
28	chr5:112449000-112452800	Weak transcription	HMEC	breast
29	chr5:112449000-112452800	Weak transcription	NHEK	skin
30	chr5:112449000-112453000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:112449000-112453600	Weak transcription	Right Atrium	heart
32	chr5:112449200-112450200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr5:112449200-112452200	Weak transcription	Fetal Heart	heart
34	chr5:112449400-112452600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr5:112449800-112451600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr5:112449800-112454200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:112450000-112450200	Enhancers	Duodenum Mucosa	Duodenum
38	chr5:112450000-112450800	ZNF genes & repeats	Fetal Muscle Leg	muscle
39	chr5:112450000-112450800	ZNF genes & repeats	Fetal Stomach	stomach
40	chr5:112450000-112451000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr5:112450000-112451000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr5:112450000-112451000	ZNF genes & repeats	Adipose Nuclei	Adipose
43	chr5:112450000-112451000	ZNF genes & repeats	Lung	lung
44	chr5:112450000-112451000	Strong transcription	Ovary	ovary
45	chr5:112450000-112451400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr5:112450000-112451800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr5:112450000-112452200	Strong transcription	Liver	Liver
48	chr5:112450000-112454600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:112450000-112459200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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