Variant report

Variant	rs28924699
Chromosome Location	chr8:107762078-107762079
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:107750673..107753111-chr8:107761641..107763838,2	K562	blood:

Variant related genes	Relation type
ENSG00000164830	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1080966	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13257240	0.83[AMR][1000 genomes]
rs16875042	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16875077	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17258979	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2035514	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28921377	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28921399	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28921400	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28921407	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28924682	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28924693	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3739323	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56171452	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57273012	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57378512	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57400955	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73699979	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73699980	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73699981	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73699996	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73699998	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7831263	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7843781	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831419	chr8:107624709-107827801	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1032991	chr8:107756661-107819035	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107719600-107762400	Weak transcription	Lung	lung
2	chr8:107719600-107765600	Weak transcription	Colonic Mucosa	Colon
3	chr8:107719600-107775200	Weak transcription	Gastric	stomach
4	chr8:107719600-107777800	Weak transcription	Esophagus	oesophagus
5	chr8:107739000-107775200	Weak transcription	A549	lung
6	chr8:107740000-107775200	Weak transcription	Ovary	ovary
7	chr8:107740200-107767400	Weak transcription	K562	blood
8	chr8:107740200-107783800	Weak transcription	Fetal Brain Male	brain
9	chr8:107740800-107775200	Weak transcription	Brain Substantia Nigra	brain
10	chr8:107741000-107768200	Weak transcription	Brain Germinal Matrix	brain
11	chr8:107747000-107768000	Weak transcription	Small Intestine	intestine
12	chr8:107749200-107765000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr8:107749400-107775200	Weak transcription	HMEC	breast
14	chr8:107751000-107764800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr8:107751600-107763000	Weak transcription	HSMMtube	muscle
16	chr8:107753000-107762800	Weak transcription	Aorta	Aorta
17	chr8:107753200-107771400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr8:107753600-107763600	Weak transcription	Colon Smooth Muscle	Colon
19	chr8:107753600-107777400	Weak transcription	HUVEC	blood vessel
20	chr8:107753800-107775200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr8:107754200-107775200	Weak transcription	Pancreas	Pancrea
22	chr8:107754400-107766400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:107754800-107775200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr8:107755200-107764600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:107755200-107772000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr8:107755400-107771600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr8:107755600-107763600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr8:107755800-107763000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr8:107755800-107771200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr8:107755800-107777800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr8:107756000-107775000	Weak transcription	Fetal Heart	heart
32	chr8:107756400-107766800	Weak transcription	Primary T cells from cord blood	blood
33	chr8:107756400-107767000	Weak transcription	Rectal Smooth Muscle	rectum
34	chr8:107756400-107772400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr8:107756400-107775000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:107756400-107777800	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr8:107756600-107763000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr8:107756600-107763400	Weak transcription	Liver	Liver
39	chr8:107756600-107763600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:107756600-107763600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr8:107756600-107763600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr8:107756600-107764000	Weak transcription	Fetal Lung	lung
43	chr8:107756600-107765400	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr8:107756600-107765400	Weak transcription	Dnd41	blood
45	chr8:107756600-107769800	Weak transcription	Brain Hippocampus Middle	brain
46	chr8:107756600-107771200	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr8:107756600-107772000	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr8:107756600-107772200	Weak transcription	Primary hematopoietic stem cells	blood
49	chr8:107756600-107772400	Weak transcription	Left Ventricle	heart
50	chr8:107756600-107772800	Weak transcription	Primary T cells fromperipheralblood	blood

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