Variant report

Variant	rs73237160
Chromosome Location	chr4:15539453-15539454
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16892063	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs16892095	0.89[AFR][1000 genomes]
rs16892131	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4698396	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4698397	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs73235029	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73235033	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs73237156	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3448986	chr4:14928802-15805558	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv2757923	chr4:15444617-15749520	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv2759227	chr4:15444617-15749520	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15487400-15570400	Weak transcription	Psoas Muscle	Psoas
2	chr4:15490400-15539600	Weak transcription	Esophagus	oesophagus
3	chr4:15495600-15559400	Weak transcription	HSMMtube	muscle
4	chr4:15502800-15549200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr4:15502800-15577600	Weak transcription	Right Ventricle	heart
6	chr4:15508200-15556400	Weak transcription	Colonic Mucosa	Colon
7	chr4:15508800-15545800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:15509200-15564400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr4:15509600-15553400	Weak transcription	HepG2	liver
10	chr4:15512000-15580000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr4:15513000-15562400	Weak transcription	Primary B cells from cord blood	blood
12	chr4:15515400-15545200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:15516000-15545600	Weak transcription	Fetal Thymus	thymus
14	chr4:15517800-15551600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr4:15517800-15593600	Weak transcription	HUVEC	blood vessel
16	chr4:15519400-15539600	Weak transcription	Gastric	stomach
17	chr4:15519800-15539600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr4:15520000-15572400	Weak transcription	Small Intestine	intestine
19	chr4:15520400-15544200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr4:15520600-15544400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr4:15520600-15544600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr4:15520600-15545200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr4:15520600-15553400	Weak transcription	A549	lung
24	chr4:15520800-15539800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:15520800-15545000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr4:15521800-15539600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr4:15522200-15544600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr4:15526000-15558200	Weak transcription	Spleen	Spleen
29	chr4:15527600-15539600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:15530200-15556600	Weak transcription	HSMM	muscle
31	chr4:15530600-15540000	Weak transcription	NHDF-Ad	bronchial
32	chr4:15530800-15554600	Weak transcription	Placenta	Placenta
33	chr4:15530800-15554600	Weak transcription	NH-A	brain
34	chr4:15531000-15539600	Weak transcription	Aorta	Aorta
35	chr4:15531000-15539800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:15531200-15545200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr4:15531600-15548600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr4:15533000-15554800	Weak transcription	Fetal Brain Male	brain
39	chr4:15537000-15540400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr4:15537200-15540200	Strong transcription	Brain Hippocampus Middle	brain
41	chr4:15537200-15565000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr4:15537400-15540400	Strong transcription	Adipose Nuclei	Adipose
43	chr4:15537400-15540400	Strong transcription	Fetal Kidney	kidney
44	chr4:15537400-15540600	Strong transcription	Fetal Stomach	stomach
45	chr4:15537400-15542600	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr4:15537400-15621000	Weak transcription	Hela-S3	cervix
47	chr4:15537800-15549000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr4:15538000-15539600	Weak transcription	Thymus	Thymus
49	chr4:15538000-15540200	Strong transcription	Liver	Liver
50	chr4:15538000-15540400	Strong transcription	Cortex derived primary cultured neurospheres	brain

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