Variant report

Variant	rs11632102
Chromosome Location	chr15:79086057-79086058
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11072803	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11072804	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11072806	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11631955	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634042	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11634450	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11638321	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11639044	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11856536	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11856953	0.84[ASN][1000 genomes]
rs11858210	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12050525	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12592721	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12899147	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12903203	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12907065	0.92[ASN][1000 genomes]
rs12913260	0.82[AMR][1000 genomes]
rs1825087	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1994016	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2277545	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2277546	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28610385	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2904220	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3825807	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4389112	0.84[ASN][1000 genomes]
rs4886592	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4887113	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66925868	0.84[ASN][1000 genomes]
rs7173267	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7177699	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72749206	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917303	chr15:78491050-79205255	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
2	nsv904431	chr15:79006442-79155088	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv33573	chr15:79053484-79293881	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904432	chr15:79066932-79175813	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79058000-79090000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr15:79069200-79090200	Weak transcription	NHDF-Ad	bronchial
3	chr15:79072000-79096600	Weak transcription	Brain Substantia Nigra	brain
4	chr15:79072000-79096800	Weak transcription	Colon Smooth Muscle	Colon
5	chr15:79072800-79089800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr15:79072800-79102400	Weak transcription	Fetal Kidney	kidney
7	chr15:79076400-79090400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr15:79076400-79090400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr15:79076400-79090800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:79077200-79089800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr15:79077200-79096600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:79077400-79089000	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr15:79077600-79087800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr15:79077800-79090600	Strong transcription	Brain Germinal Matrix	brain
15	chr15:79078000-79089400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr15:79078200-79093200	Strong transcription	Fetal Stomach	stomach
17	chr15:79078400-79091800	Weak transcription	Gastric	stomach
18	chr15:79078600-79089800	Weak transcription	HMEC	breast
19	chr15:79078600-79090600	Strong transcription	Fetal Brain Female	brain
20	chr15:79079000-79089600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr15:79079400-79091000	Weak transcription	HUVEC	blood vessel
22	chr15:79079600-79090600	Weak transcription	NH-A	brain
23	chr15:79080400-79096200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr15:79080600-79087400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr15:79080600-79087400	Weak transcription	Osteobl	bone
26	chr15:79080800-79089400	Weak transcription	NHLF	lung
27	chr15:79080800-79095200	Weak transcription	Fetal Intestine Large	intestine
28	chr15:79081000-79088600	Weak transcription	Placenta	Placenta
29	chr15:79082000-79088000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:79082400-79087800	Weak transcription	Lung	lung
31	chr15:79082600-79089800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr15:79082800-79087400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr15:79082800-79096200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr15:79082800-79102200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr15:79083000-79087200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr15:79083200-79102000	Weak transcription	Fetal Heart	heart
37	chr15:79083400-79086600	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr15:79083600-79087400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr15:79083600-79087600	Weak transcription	Ovary	ovary
40	chr15:79083600-79089600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr15:79083800-79087800	Weak transcription	Fetal Intestine Small	intestine
42	chr15:79083800-79102400	Weak transcription	Aorta	Aorta
43	chr15:79084000-79086200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr15:79084000-79087400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr15:79084000-79087400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr15:79084000-79087400	Weak transcription	Adipose Nuclei	Adipose
47	chr15:79084000-79087600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:79084200-79086200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr15:79084200-79087000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr15:79084200-79087600	Weak transcription	H1 Cell Line	embryonic stem cell

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