Variant report

Variant	rs73586910
Chromosome Location	chr6:144628770-144628771
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs2179337	0.83[AMR][1000 genomes]
rs2179338	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2179339	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59084029	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60083419	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60318438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6912024	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6912336	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585069	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585072	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585080	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585083	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585088	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585090	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585093	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585099	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73585102	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73586908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73586913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73591120	0.85[AMR][1000 genomes]
rs7745952	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7761266	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830831	chr6:144501371-144649509	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv830832	chr6:144572378-144759023	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2422260	chr6:144574591-144731630	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1031253	chr6:144599055-144883013	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv538461	chr6:144599055-144883013	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144608600-144629800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:144608600-144631400	Weak transcription	Colonic Mucosa	Colon
3	chr6:144609200-144641600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr6:144609600-144628800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:144609600-144629000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:144609600-144629800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr6:144615400-144630200	Weak transcription	Hela-S3	cervix
8	chr6:144616400-144648000	Weak transcription	NHEK	skin
9	chr6:144617200-144629400	Weak transcription	Placenta	Placenta
10	chr6:144617200-144636400	Weak transcription	A549	lung
11	chr6:144617400-144628800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:144617400-144629000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr6:144617400-144630200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:144617400-144632800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr6:144617600-144629000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr6:144617600-144629800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr6:144617800-144629800	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr6:144618200-144629400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:144618200-144629800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:144618200-144630200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr6:144618200-144630200	Weak transcription	HUVEC	blood vessel
22	chr6:144618400-144628800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr6:144618400-144630000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:144619200-144629400	Weak transcription	Fetal Lung	lung
25	chr6:144619200-144634600	Weak transcription	Colon Smooth Muscle	Colon
26	chr6:144619600-144629800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:144619600-144629800	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr6:144619600-144630000	Weak transcription	NHDF-Ad	bronchial
29	chr6:144619800-144629000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr6:144619800-144629400	Weak transcription	Fetal Intestine Small	intestine
31	chr6:144619800-144629600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr6:144619800-144631800	Weak transcription	Fetal Heart	heart
33	chr6:144619800-144634600	Weak transcription	Brain Hippocampus Middle	brain
34	chr6:144620000-144629600	Weak transcription	Dnd41	blood
35	chr6:144620200-144628800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:144620400-144629800	Weak transcription	Fetal Intestine Large	intestine
37	chr6:144622400-144637000	Genic enhancers	HepG2	liver
38	chr6:144622600-144628800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:144623400-144629200	Weak transcription	Fetal Muscle Trunk	muscle
40	chr6:144623400-144629600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:144623400-144629600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr6:144623600-144629000	Weak transcription	Fetal Stomach	stomach
43	chr6:144624200-144629200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:144624200-144632000	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr6:144624200-144641400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr6:144624200-144641600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:144624400-144629200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:144624400-144648000	Weak transcription	HMEC	breast
49	chr6:144625800-144629200	Weak transcription	Fetal Kidney	kidney
50	chr6:144625800-144632600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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