Variant report

Variant	rs60636837
Chromosome Location	chr1:151129328-151129329
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151116657..151121305-chr1:151127749..151129795,4	K562	blood:
2	chr1:150994233..150997009-chr1:151128495..151131109,2	MCF-7	breast:
3	chr1:121484816..121485357-chr1:151129317..151130198,2	NB4	blood:
4	chr1:151042151..151045476-chr1:151127754..151130933,3	MCF-7	breast:
5	chr1:151128359..151130289-chr1:151160585..151164269,3	K562	blood:
6	chr1:150997070..150998682-chr1:151128410..151130437,2	K562	blood:
7	chr1:151041073..151043333-chr1:151126816..151129566,2	K562	blood:
8	chr1:151128133..151130862-chr1:151227086..151228869,2	MCF-7	breast:
9	chr1:151114895..151122057-chr1:151125026..151130825,9	MCF-7	breast:
10	chr1:151117604..151120749-chr1:151128246..151131666,4	MCF-7	breast:
11	chr1:150980779..150982400-chr1:151127994..151130267,2	MCF-7	breast:
12	chr1:151128026..151130888-chr1:151138043..151140258,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000200759	Chromatin interaction
ENSG00000159352	Chromatin interaction
ENSG00000143363	Chromatin interaction
ENSG00000143434	Chromatin interaction
ENSG00000163155	Chromatin interaction
ENSG00000143458	Chromatin interaction
ENSG00000143409	Chromatin interaction
ENSG00000163159	Chromatin interaction
ENSG00000197622	Chromatin interaction
ENSG00000163156	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs41299635	1.00[AMR][1000 genomes]
rs41310891	1.00[AMR][1000 genomes]
rs55716130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55935377	1.00[AMR][1000 genomes]
rs57330524	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58618837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58763463	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59737164	1.00[AMR][1000 genomes]
rs60865304	1.00[AMR][1000 genomes]
rs74125051	1.00[AMR][1000 genomes]
rs74125053	1.00[AMR][1000 genomes]
rs74125059	1.00[AMR][1000 genomes]
rs74125062	1.00[AMR][1000 genomes]
rs74125063	1.00[AMR][1000 genomes]
rs74125065	1.00[AMR][1000 genomes]
rs74125077	1.00[AMR][1000 genomes]
rs74125079	1.00[AMR][1000 genomes]
rs74125080	1.00[AMR][1000 genomes]
rs74125087	1.00[AMR][1000 genomes]
rs74125088	1.00[AMR][1000 genomes]
rs74125093	1.00[AMR][1000 genomes]
rs74127505	1.00[AMR][1000 genomes]
rs74127506	1.00[AMR][1000 genomes]
rs74127513	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127514	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127515	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127528	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127529	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127530	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127531	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127535	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127536	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127537	0.82[AFR][1000 genomes]
rs74127539	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74127540	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001897	chr1:150743271-151241600	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv535158	chr1:150743271-151241600	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
3	nsv522840	chr1:150933723-151347746	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
4	nsv916272	chr1:150961809-151557253	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
5	nsv831559	chr1:151109459-151239921	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
6	nsv831570	chr1:151129020-151281778	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	106 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151120000-151130800	Weak transcription	Pancreas	Pancrea
2	chr1:151120000-151131200	Weak transcription	Ovary	ovary
3	chr1:151120000-151131400	Weak transcription	NH-A	brain
4	chr1:151120000-151131400	Weak transcription	NHLF	lung
5	chr1:151120200-151129400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:151120200-151129400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr1:151120200-151129400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:151120200-151129400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:151120200-151129600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:151120200-151129800	Weak transcription	Fetal Lung	lung
11	chr1:151120200-151130800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:151120200-151131000	Weak transcription	Osteobl	bone
13	chr1:151120200-151131200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:151120200-151132000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:151120200-151132000	Weak transcription	NHDF-Ad	bronchial
16	chr1:151120400-151129400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr1:151120400-151129600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:151120400-151129800	Weak transcription	Fetal Brain Male	brain
19	chr1:151120400-151130200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:151120400-151131600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:151120400-151133200	Weak transcription	Psoas Muscle	Psoas
22	chr1:151120600-151129400	Weak transcription	Fetal Kidney	kidney
23	chr1:151120600-151129800	Weak transcription	Brain Angular Gyrus	brain
24	chr1:151120600-151130800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:151120600-151132000	Weak transcription	HSMMtube	muscle
26	chr1:151125000-151132800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr1:151127000-151130000	Enhancers	HUVEC	blood vessel
28	chr1:151127200-151134600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:151127400-151134800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:151127600-151129600	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr1:151127600-151131200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:151127600-151132800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr1:151128000-151129400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr1:151128200-151130800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:151128400-151131000	Weak transcription	Right Ventricle	heart
36	chr1:151128400-151136800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr1:151128600-151129400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
38	chr1:151128600-151129600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr1:151128600-151129600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
40	chr1:151128600-151130400	Flanking Active TSS	Primary B cells from peripheral blood	blood
41	chr1:151128600-151130600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:151128600-151130600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr1:151128600-151131000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:151128600-151131200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr1:151128600-151131200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:151128800-151129400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr1:151128800-151129400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
48	chr1:151128800-151129600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr1:151128800-151129600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr1:151128800-151129800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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