Variant report

Variant	rs73423541
Chromosome Location	chr15:57814234-57814235
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1280393	1.00[AMR][1000 genomes]
rs1280394	1.00[AMR][1000 genomes]
rs1290244	1.00[EUR][1000 genomes]
rs1540397	1.00[EUR][1000 genomes]
rs16953334	1.00[EUR][1000 genomes]
rs16977546	1.00[EUR][1000 genomes]
rs16977553	1.00[EUR][1000 genomes]
rs16977555	1.00[EUR][1000 genomes]
rs16977563	1.00[EUR][1000 genomes]
rs16977581	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16977583	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16977584	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16977600	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1834487	1.00[EUR][1000 genomes]
rs1946357	1.00[EUR][1000 genomes]
rs2098891	1.00[EUR][1000 genomes]
rs28540249	1.00[EUR][1000 genomes]
rs28547400	1.00[EUR][1000 genomes]
rs28707698	1.00[EUR][1000 genomes]
rs55782827	1.00[EUR][1000 genomes]
rs56091272	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56179101	1.00[EUR][1000 genomes]
rs56810932	1.00[EUR][1000 genomes]
rs58764014	1.00[EUR][1000 genomes]
rs60234362	1.00[EUR][1000 genomes]
rs60767381	1.00[EUR][1000 genomes]
rs60973024	1.00[EUR][1000 genomes]
rs7167118	1.00[EUR][1000 genomes]
rs7168720	1.00[AMR][1000 genomes]
rs7174185	1.00[EUR][1000 genomes]
rs7174359	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7181645	1.00[EUR][1000 genomes]
rs73421833	1.00[EUR][1000 genomes]
rs73421838	1.00[EUR][1000 genomes]
rs73421863	1.00[EUR][1000 genomes]
rs73421865	1.00[EUR][1000 genomes]
rs73421901	1.00[EUR][1000 genomes]
rs73423507	1.00[EUR][1000 genomes]
rs73423512	1.00[EUR][1000 genomes]
rs73423518	1.00[EUR][1000 genomes]
rs73423522	1.00[EUR][1000 genomes]
rs73423555	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73423558	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73423560	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73423562	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73423566	1.00[EUR][1000 genomes]
rs73423591	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74016229	1.00[EUR][1000 genomes]
rs74016236	1.00[EUR][1000 genomes]
rs74018224	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs933839	1.00[EUR][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	nsv1045611	chr15:57350965-58070807	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1054547	chr15:57600488-57977659	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv833022	chr15:57657412-57830112	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv904255	chr15:57790436-57907574	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr15:57797000-57827200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:57801800-57819000	Weak transcription	Esophagus	oesophagus
3	chr15:57802000-57819600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr15:57802600-57846600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr15:57802800-57822600	Weak transcription	Brain Hippocampus Middle	brain
6	chr15:57803000-57818800	Weak transcription	Fetal Intestine Large	intestine
7	chr15:57803200-57819400	Weak transcription	Ovary	ovary
8	chr15:57803200-57842800	Weak transcription	Aorta	Aorta
9	chr15:57807000-57816200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr15:57807000-57818400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr15:57808400-57817200	Strong transcription	H1 Cell Line	embryonic stem cell
12	chr15:57808600-57817200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr15:57808600-57817800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
14	chr15:57808800-57818000	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr15:57808800-57818000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr15:57808800-57818200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:57809000-57817200	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr15:57809400-57816600	Weak transcription	Fetal Muscle Leg	muscle
19	chr15:57809800-57815600	Weak transcription	Lung	lung
20	chr15:57810000-57814400	Weak transcription	Fetal Lung	lung
21	chr15:57810400-57814400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr15:57811000-57814400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr15:57811000-57816400	Weak transcription	Placenta	Placenta
24	chr15:57811000-57827800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr15:57811200-57815400	Weak transcription	HepG2	liver
26	chr15:57811200-57819400	Weak transcription	Fetal Intestine Small	intestine
27	chr15:57811600-57817200	Weak transcription	HUVEC	blood vessel
28	chr15:57812400-57819400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr15:57812600-57815200	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr15:57813200-57816000	Enhancers	Fetal Heart	heart
31	chr15:57813600-57814800	Enhancers	Pancreas	Pancrea
32	chr15:57813800-57814600	Enhancers	Brain Cingulate Gyrus	brain
33	chr15:57813800-57814600	Enhancers	Brain Substantia Nigra	brain
34	chr15:57813800-57814800	Enhancers	Left Ventricle	heart
35	chr15:57813800-57815200	Enhancers	Colon Smooth Muscle	Colon
36	chr15:57813800-57816400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr15:57813800-57817200	Strong transcription	Fetal Stomach	stomach
38	chr15:57814000-57814400	Enhancers	Rectal Smooth Muscle	rectum
39	chr15:57814000-57814800	Enhancers	Brain Angular Gyrus	brain
40	chr15:57814000-57815200	Enhancers	Stomach Smooth Muscle	stomach
41	chr15:57814000-57815400	Enhancers	Fetal Kidney	kidney
42	chr15:57814200-57814600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr15:57814200-57814600	Genic enhancers	Liver	Liver
44	chr15:57814200-57814800	Enhancers	Brain Anterior Caudate	brain
45	chr15:57814200-57814800	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr15:57814200-57814800	Enhancers	Right Atrium	heart
47	chr15:57814200-57815000	Enhancers	Stomach Mucosa	stomach
48	chr15:57814200-57815400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr15:57814200-57816400	Weak transcription	Gastric	stomach

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