Variant report

Variant	rs7306450
Chromosome Location	chr12:62901534-62901535
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	chr12:62897832..62899888-chr12:62900613..62903392,2	K562	blood:
2	chr12:62901029..62903305-chr12:62910983..62913530,2	MCF-7	breast:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17098035	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56079604	0.93[AFR][1000 genomes]
rs61035483	0.87[AFR][1000 genomes]
rs7302924	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095811	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095819	0.87[AFR][1000 genomes]
rs74095831	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74098031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74098033	0.93[AFR][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	nsv530690	chr12:62678463-62999462	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv899158	chr12:62783967-62937259	Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv899159	chr12:62783967-62945245	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv821671	chr12:62794304-63007964	Strong transcription ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv469418	chr12:62893199-62959137	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
6	nsv559156	chr12:62893199-62959137	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62861800-62902200	Weak transcription	Fetal Kidney	kidney
2	chr12:62863200-62901800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr12:62863200-62937400	Weak transcription	Pancreas	Pancrea
4	chr12:62863400-62902000	Weak transcription	HUVEC	blood vessel
5	chr12:62863400-62911000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr12:62863600-62926400	Weak transcription	Colon Smooth Muscle	Colon
7	chr12:62864000-62901600	Weak transcription	Lung	lung
8	chr12:62864000-62901600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr12:62864000-62906200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:62866200-62906200	Weak transcription	Aorta	Aorta
11	chr12:62866600-62906200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:62866600-62912400	Weak transcription	NHLF	lung
13	chr12:62866600-62953200	Weak transcription	Psoas Muscle	Psoas
14	chr12:62869000-62904400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr12:62871000-62910800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr12:62871800-62926200	Weak transcription	Fetal Brain Male	brain
17	chr12:62872600-62901600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr12:62874600-62917400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr12:62876000-62902000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr12:62876000-62905800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr12:62876000-62937400	Weak transcription	Gastric	stomach
22	chr12:62876200-62913000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr12:62876400-62902000	Weak transcription	Brain Anterior Caudate	brain
24	chr12:62877800-62906200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr12:62879000-62912000	Weak transcription	Brain Angular Gyrus	brain
26	chr12:62879800-62901800	Weak transcription	HepG2	liver
27	chr12:62886000-62902000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr12:62886000-62911200	Weak transcription	Brain Substantia Nigra	brain
29	chr12:62888400-62904400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr12:62888800-62906400	Weak transcription	Right Ventricle	heart
31	chr12:62889200-62949600	Weak transcription	Small Intestine	intestine
32	chr12:62890600-62901600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr12:62890600-62901600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr12:62891000-62904400	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr12:62891800-62904800	Weak transcription	HSMMtube	muscle
36	chr12:62892200-62904400	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr12:62892800-62911200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:62893800-62905000	Strong transcription	Primary B cells from peripheral blood	blood
39	chr12:62894200-62903600	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr12:62894200-62904000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr12:62894400-62926200	Weak transcription	NH-A	brain
42	chr12:62895200-62903200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr12:62895200-62905200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:62895200-62906200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr12:62895400-62906200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr12:62895800-62903400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr12:62895800-62906200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:62896200-62902400	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr12:62896200-62904600	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr12:62896400-62903000	Strong transcription	Primary T cells from cord blood	blood

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