Variant report

Variant	rs11072803
Chromosome Location	chr15:79077878-79077879
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11072804	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11072806	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11631955	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11632102	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11634042	0.81[AMR][1000 genomes]
rs11634450	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11638321	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11639044	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11856536	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11858210	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12050525	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12592721	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12899147	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12903203	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1825087	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1994016	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2277545	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2277546	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28610385	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2904220	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3825807	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4886592	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4887113	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7173267	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7177699	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv977739	chr15:79062099-79080757	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	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:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79054000-79083200	Weak transcription	Fetal Intestine Small	intestine
2	chr15:79058000-79090000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr15:79060800-79078600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr15:79061000-79078000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr15:79061000-79078800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr15:79061000-79078800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr15:79061000-79080000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr15:79061600-79080400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr15:79062200-79080200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr15:79063800-79078600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:79069000-79080000	Weak transcription	Osteobl	bone
12	chr15:79069200-79090200	Weak transcription	NHDF-Ad	bronchial
13	chr15:79071200-79078800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr15:79071200-79079800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:79071200-79080200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr15:79071400-79078000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr15:79071400-79078400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr15:79071400-79078600	Weak transcription	Fetal Brain Female	brain
19	chr15:79071400-79080200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr15:79072000-79080000	Weak transcription	NHLF	lung
21	chr15:79072000-79096600	Weak transcription	Brain Substantia Nigra	brain
22	chr15:79072000-79096800	Weak transcription	Colon Smooth Muscle	Colon
23	chr15:79072200-79078000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr15:79072200-79078000	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr15:79072200-79078200	Weak transcription	Fetal Stomach	stomach
26	chr15:79072200-79078600	Weak transcription	Ovary	ovary
27	chr15:79072200-79080200	Weak transcription	Lung	lung
28	chr15:79072200-79082000	Weak transcription	Right Atrium	heart
29	chr15:79072800-79078400	Weak transcription	HUVEC	blood vessel
30	chr15:79072800-79078800	Weak transcription	Stomach Smooth Muscle	stomach
31	chr15:79072800-79080000	Weak transcription	Aorta	Aorta
32	chr15:79072800-79082000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:79072800-79089800	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr15:79072800-79102400	Weak transcription	Fetal Kidney	kidney
35	chr15:79073800-79080200	Weak transcription	Spleen	Spleen
36	chr15:79074000-79078800	Weak transcription	Left Ventricle	heart
37	chr15:79074200-79078600	Weak transcription	Fetal Muscle Trunk	muscle
38	chr15:79074200-79080200	Weak transcription	Right Ventricle	heart
39	chr15:79074400-79078000	Weak transcription	HSMM	muscle
40	chr15:79074600-79078000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr15:79074800-79083000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr15:79075600-79082200	Weak transcription	Fetal Brain Male	brain
43	chr15:79075800-79078000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr15:79076400-79090400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr15:79076400-79090400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr15:79076400-79090800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr15:79076800-79078600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr15:79077200-79078600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr15:79077200-79080200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr15:79077200-79081400	Strong transcription	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links