Variant report

Variant	rs28619538
Chromosome Location	chr8:120793332-120793333
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:120792905..120795655-chr8:120801527..120803030,2	K562	blood:
2	chr8:120786484..120788471-chr8:120793020..120795080,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10086597	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10089043	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10090726	0.82[AFR][1000 genomes]
rs10095185	0.89[AFR][1000 genomes]
rs10095406	0.89[AFR][1000 genomes]
rs10097203	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10097757	0.95[AFR][1000 genomes]
rs10098362	0.89[AFR][1000 genomes]
rs10099163	0.98[AFR][1000 genomes]
rs10101842	0.82[AFR][1000 genomes]
rs10102508	0.98[AFR][1000 genomes]
rs10104449	0.91[AFR][1000 genomes]
rs10105858	0.85[AFR][1000 genomes]
rs10109941	0.80[AFR][1000 genomes]
rs12334592	0.98[AFR][1000 genomes]
rs16892935	1.00[EUR][1000 genomes]
rs16893011	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16893021	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16893034	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28502370	0.89[AFR][1000 genomes]
rs28517862	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28529634	0.80[AFR][1000 genomes]
rs28636993	0.85[AFR][1000 genomes]
rs28684724	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28735236	0.98[AFR][1000 genomes]
rs28852781	0.89[AFR][1000 genomes]
rs6980897	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6984913	0.89[AFR][1000 genomes]
rs6990166	0.82[AFR][1000 genomes]
rs6998771	0.84[AFR][1000 genomes]
rs7010646	0.84[AFR][1000 genomes]
rs7833422	0.80[AFR][1000 genomes]
rs9693192	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534028	chr8:120348940-120906079	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv949368	chr8:120568034-121019872	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1021071	chr8:120589963-120968317	Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
5	nsv465789	chr8:120636850-120994394	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv612111	chr8:120636850-120994394	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv427826	chr8:120642181-120953395	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120742600-120812800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:120744000-120814600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:120744400-120824400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr8:120760600-120804600	Weak transcription	Psoas Muscle	Psoas
5	chr8:120761600-120800800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr8:120767200-120807400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr8:120773600-120795000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr8:120776400-120797800	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr8:120780400-120801200	Weak transcription	Brain Substantia Nigra	brain
10	chr8:120781000-120807000	Weak transcription	Brain Angular Gyrus	brain
11	chr8:120781000-120813800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr8:120781200-120795000	Weak transcription	NHEK	skin
13	chr8:120781200-120795600	Weak transcription	HMEC	breast
14	chr8:120781200-120796400	Weak transcription	Pancreas	Pancrea
15	chr8:120781200-120801000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr8:120781200-120801400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr8:120781200-120804400	Weak transcription	Spleen	Spleen
18	chr8:120781200-120804600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr8:120781200-120807000	Weak transcription	Colon Smooth Muscle	Colon
20	chr8:120781200-120807800	Weak transcription	NHLF	lung
21	chr8:120781200-120812800	Weak transcription	Colonic Mucosa	Colon
22	chr8:120781200-120829400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:120781400-120794000	Weak transcription	Ovary	ovary
24	chr8:120781400-120802800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr8:120781400-120803000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:120781400-120804400	Weak transcription	Esophagus	oesophagus
27	chr8:120781400-120804600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:120781400-120804800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr8:120781400-120805000	Weak transcription	Gastric	stomach
30	chr8:120781400-120812800	Weak transcription	Right Ventricle	heart
31	chr8:120781400-120813800	Weak transcription	Aorta	Aorta
32	chr8:120781600-120812800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr8:120781600-120844200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr8:120782800-120797400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr8:120782800-120797800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr8:120782800-120799000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:120783800-120804400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:120785200-120812000	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr8:120785200-120812600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr8:120785600-120797400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:120785600-120797400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:120785600-120810600	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr8:120785800-120797000	Strong transcription	Liver	Liver
44	chr8:120785800-120808800	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr8:120785800-120810400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr8:120786000-120797400	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr8:120786200-120794000	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr8:120786200-120797000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr8:120786400-120798800	Strong transcription	HUES48 Cell Line	embryonic stem cell
50	chr8:120786400-120799000	Strong transcription	Dnd41	blood

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