Variant report

Variant	rs73661779
Chromosome Location	chr8:6339923-6339924
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:6339705..6342364-chr8:6348069..6350911,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs58739616	0.87[AFR][1000 genomes]
rs58946561	0.87[AFR][1000 genomes]
rs73661770	0.87[AFR][1000 genomes]
rs73661771	0.92[AFR][1000 genomes]
rs73661773	0.92[AFR][1000 genomes]
rs73661777	0.92[AFR][1000 genomes]
rs73661778	0.96[AFR][1000 genomes]
rs73661781	0.87[AFR][1000 genomes]
rs73661783	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890034	chr8:5926632-6427868	Enhancers Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1021175	chr8:5965453-6880364	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1027682	chr8:6018123-6920312	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	esv3506199	chr8:6116693-6536592	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
5	esv3506200	chr8:6116693-6536592	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS 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	11 gene(s)	inside rSNPs	diseases
6	nsv482828	chr8:6182711-6355710	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv890055	chr8:6237397-6351252	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv933282	chr8:6261036-6440592	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS 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	8 gene(s)	inside rSNPs	diseases
9	nsv1015981	chr8:6286575-6578450	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
10	nsv1027313	chr8:6286575-6920312	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
11	nsv890056	chr8:6314486-6343727	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv890057	chr8:6317165-6427868	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv1025860	chr8:6328628-6360743	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv890058	chr8:6329510-6367302	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6287600-6344400	Weak transcription	Small Intestine	intestine
2	chr8:6303200-6340000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr8:6304400-6360200	Weak transcription	Esophagus	oesophagus
4	chr8:6308000-6372600	Weak transcription	HMEC	breast
5	chr8:6316400-6345600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr8:6317800-6380200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr8:6321800-6342000	Weak transcription	Aorta	Aorta
8	chr8:6321800-6343800	Weak transcription	Hela-S3	cervix
9	chr8:6322000-6340000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:6322000-6346800	Weak transcription	Colon Smooth Muscle	Colon
11	chr8:6323400-6340200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:6323400-6342000	Weak transcription	NHEK	skin
13	chr8:6325800-6374400	Weak transcription	K562	blood
14	chr8:6326000-6340000	Weak transcription	Pancreas	Pancrea
15	chr8:6331400-6345600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:6333000-6342000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr8:6335000-6344200	Weak transcription	NHLF	lung
18	chr8:6335000-6345200	Weak transcription	Ovary	ovary
19	chr8:6335400-6341200	Weak transcription	Fetal Lung	lung
20	chr8:6335600-6344400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:6336000-6340000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr8:6336800-6340000	Weak transcription	HUVEC	blood vessel
23	chr8:6336800-6377600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr8:6337000-6342200	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr8:6337000-6342400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr8:6337600-6340400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr8:6337800-6342200	Strong transcription	Lung	lung
28	chr8:6337800-6342400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr8:6337800-6347600	Strong transcription	Primary T cells from cord blood	blood
30	chr8:6338000-6340800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr8:6338000-6342400	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr8:6338000-6342400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr8:6338000-6342600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:6338000-6343600	Strong transcription	GM12878-XiMat	blood
35	chr8:6338200-6340000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr8:6338200-6340200	Strong transcription	Fetal Intestine Small	intestine
37	chr8:6338200-6340400	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr8:6338200-6340400	Strong transcription	Left Ventricle	heart
39	chr8:6338200-6340600	Strong transcription	Liver	Liver
40	chr8:6338200-6340600	Strong transcription	Fetal Muscle Trunk	muscle
41	chr8:6338200-6340800	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr8:6338200-6341000	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr8:6338200-6341000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr8:6338200-6341000	Strong transcription	Brain Hippocampus Middle	brain
45	chr8:6338200-6341000	Strong transcription	Duodenum Mucosa	Duodenum
46	chr8:6338200-6341000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr8:6338200-6341200	Strong transcription	Primary B cells from cord blood	blood
48	chr8:6338200-6341800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr8:6338200-6342000	Strong transcription	Primary B cells from peripheral blood	blood
50	chr8:6338200-6342400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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