Variant report

Variant	rs11853646
Chromosome Location	chr15:34147309-34147310
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10438378	1.00[CEU][hapmap]
rs10519889	0.85[CEU][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]
rs11629862	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11855356	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs12899100	0.82[CEU][hapmap]
rs16958202	0.85[CEU][hapmap];0.93[EUR][1000 genomes]
rs16958222	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs16958228	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs16958235	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs16958242	0.88[EUR][1000 genomes]
rs16958247	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs16958281	1.00[CEU][hapmap];0.85[TSI][hapmap];0.83[EUR][1000 genomes]
rs16958299	1.00[CEU][hapmap]
rs41279232	0.86[EUR][1000 genomes]
rs55688824	0.86[EUR][1000 genomes]
rs55726623	0.86[EUR][1000 genomes]
rs55786211	0.86[EUR][1000 genomes]
rs55803898	0.86[EUR][1000 genomes]
rs55846435	0.86[EUR][1000 genomes]
rs55980511	0.86[EUR][1000 genomes]
rs56090340	0.86[EUR][1000 genomes]
rs56258848	0.86[EUR][1000 genomes]
rs56385459	0.86[EUR][1000 genomes]
rs57308544	0.93[EUR][1000 genomes]
rs60933918	0.93[EUR][1000 genomes]
rs61027076	0.88[EUR][1000 genomes]
rs6495271	1.00[CEU][hapmap]
rs6495303	0.92[GIH][hapmap]
rs6495305	0.90[EUR][1000 genomes]
rs7165072	0.93[EUR][1000 genomes]
rs7170693	0.82[CEU][hapmap];0.93[EUR][1000 genomes]
rs7172406	0.96[GIH][hapmap]
rs7176081	1.00[CEU][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]
rs7177269	0.85[CEU][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]
rs7177889	0.93[EUR][1000 genomes]
rs73372076	0.86[EUR][1000 genomes]
rs73375714	0.88[EUR][1000 genomes]
rs73375717	0.88[EUR][1000 genomes]
rs9302282	0.85[TSI][hapmap];0.93[EUR][1000 genomes]
rs9302283	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv456789	chr15:34034421-34426618	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv568920	chr15:34034421-34426618	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv471235	chr15:34035529-34421951	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv568921	chr15:34046635-34247622	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1044844	chr15:34065524-34296829	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34090600-34151800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr15:34091800-34151000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr15:34114400-34149400	Weak transcription	Fetal Stomach	stomach
4	chr15:34121400-34158400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr15:34124400-34148600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr15:34124400-34151200	Weak transcription	Brain Hippocampus Middle	brain
7	chr15:34127800-34147800	Weak transcription	Colon Smooth Muscle	Colon
8	chr15:34129800-34151600	Weak transcription	Fetal Brain Female	brain
9	chr15:34130000-34151000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr15:34130800-34151200	Weak transcription	Aorta	Aorta
11	chr15:34130800-34158600	Weak transcription	Brain Germinal Matrix	brain
12	chr15:34137400-34164200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr15:34138000-34148200	Weak transcription	Spleen	Spleen
14	chr15:34138600-34151600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:34139800-34156400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr15:34139800-34164200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr15:34141600-34149400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr15:34142400-34168600	Weak transcription	Esophagus	oesophagus
19	chr15:34143000-34165000	Weak transcription	Psoas Muscle	Psoas
20	chr15:34143400-34160400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr15:34143600-34164200	Weak transcription	Brain Angular Gyrus	brain
22	chr15:34143800-34156200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr15:34144400-34151000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr15:34144600-34151600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr15:34145000-34152200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr15:34145000-34152200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr15:34145000-34158200	Weak transcription	Gastric	stomach
28	chr15:34145000-34161200	Weak transcription	Small Intestine	intestine
29	chr15:34145200-34151000	Weak transcription	Placenta	Placenta
30	chr15:34145200-34152200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr15:34145200-34152200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr15:34145200-34152200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr15:34145200-34152200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr15:34145200-34152200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr15:34145200-34152200	Weak transcription	HMEC	breast
36	chr15:34145400-34149800	Weak transcription	HSMMtube	muscle
37	chr15:34145400-34152200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr15:34145400-34152200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr15:34145400-34152800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr15:34145400-34156600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr15:34145600-34151200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr15:34145600-34154200	Strong transcription	Fetal Muscle Leg	muscle
43	chr15:34145600-34158200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr15:34145600-34158600	Weak transcription	HSMM	muscle
45	chr15:34145800-34148400	Weak transcription	NHDF-Ad	bronchial
46	chr15:34145800-34150800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr15:34145800-34152800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr15:34145800-34152800	Weak transcription	Osteobl	bone
49	chr15:34145800-34153000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr15:34145800-34158400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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