Variant report

Variant	rs28551010
Chromosome Location	chr4:79845213-79845214
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:79844612..79846577-chr4:79849709..79851536,2	K562	blood:
2	chr4:79836564..79840244-chr4:79843893..79846943,5	K562	blood:

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10009008	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17003468	0.87[AMR][1000 genomes]
rs6534086	0.81[AFR][1000 genomes]
rs6854586	0.92[AFR][1000 genomes];1.00[AMR][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	nsv879504	chr4:79759796-79874275	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv829979	chr4:79819168-80019159	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1000907	chr4:79838948-80224764	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79779800-79858200	Weak transcription	Fetal Brain Male	brain
2	chr4:79794200-79850000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:79794200-79859600	Weak transcription	Colonic Mucosa	Colon
4	chr4:79794400-79850000	Weak transcription	Pancreas	Pancrea
5	chr4:79794800-79850200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr4:79794800-79858000	Weak transcription	HepG2	liver
7	chr4:79799200-79858000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr4:79814600-79859600	Weak transcription	Fetal Kidney	kidney
9	chr4:79815200-79845400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr4:79815800-79846600	Weak transcription	Colon Smooth Muscle	Colon
11	chr4:79816000-79848200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:79816200-79848600	Weak transcription	Fetal Lung	lung
13	chr4:79816200-79858400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr4:79827400-79858000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr4:79827400-79858000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr4:79829000-79859200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr4:79830200-79850000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr4:79830200-79859200	Weak transcription	Hela-S3	cervix
19	chr4:79831000-79850000	Weak transcription	Gastric	stomach
20	chr4:79831200-79858000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr4:79831400-79856600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr4:79833000-79849800	Weak transcription	Fetal Stomach	stomach
23	chr4:79833000-79850000	Weak transcription	Lung	lung
24	chr4:79833000-79850000	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr4:79833000-79850000	Weak transcription	Spleen	Spleen
26	chr4:79833000-79850000	Weak transcription	HSMMtube	muscle
27	chr4:79833000-79859800	Weak transcription	Esophagus	oesophagus
28	chr4:79833000-79859800	Weak transcription	Right Ventricle	heart
29	chr4:79833200-79846600	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr4:79833200-79847000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:79833200-79847000	Weak transcription	HMEC	breast
32	chr4:79833200-79847400	Weak transcription	Brain Anterior Caudate	brain
33	chr4:79833200-79848600	Weak transcription	Aorta	Aorta
34	chr4:79833200-79848600	Weak transcription	Brain Hippocampus Middle	brain
35	chr4:79833200-79849800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:79833200-79849800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:79833200-79849800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr4:79833200-79849800	Weak transcription	Ovary	ovary
39	chr4:79833200-79850000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr4:79833200-79853400	Weak transcription	NHLF	lung
41	chr4:79833200-79859000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:79833200-79859600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:79833400-79856800	Weak transcription	GM12878-XiMat	blood
44	chr4:79833600-79847000	Weak transcription	Fetal Muscle Trunk	muscle
45	chr4:79833600-79849000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:79833600-79849800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr4:79833600-79858000	Weak transcription	Brain Substantia Nigra	brain
48	chr4:79833600-79859000	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr4:79833600-79859800	Weak transcription	Placenta	Placenta
50	chr4:79833800-79846600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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