Variant report

Variant	rs57160874
Chromosome Location	chr12:45805697-45805698
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12578638	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs17095779	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17095781	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17095835	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17095858	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17095860	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17095861	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17095862	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17095884	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17095890	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17095914	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17121366	0.91[ASN][1000 genomes]
rs3803177	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs41338444	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4512918	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57056104	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57455310	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58028140	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58152224	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58213849	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58282976	0.91[AFR][1000 genomes]
rs58940403	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60688397	1.00[AFR][1000 genomes]
rs60794282	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61276164	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61351713	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61484865	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74081808	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74081818	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74081821	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9788104	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050923	chr12:45581310-45808289	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45744800-45809200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:45752200-45809200	Weak transcription	Small Intestine	intestine
3	chr12:45759200-45822600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr12:45764400-45821000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr12:45764600-45815400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr12:45772600-45815400	Weak transcription	K562	blood
7	chr12:45774800-45811400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr12:45780400-45829800	Weak transcription	Brain Anterior Caudate	brain
9	chr12:45783200-45818800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr12:45783400-45826400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:45786200-45806200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:45786200-45809200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:45786400-45806200	Weak transcription	Esophagus	oesophagus
14	chr12:45786600-45806000	Weak transcription	Ovary	ovary
15	chr12:45786600-45827000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:45792000-45828600	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr12:45792600-45822600	Weak transcription	Colonic Mucosa	Colon
18	chr12:45792600-45827000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr12:45792800-45811800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr12:45793000-45827600	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr12:45794200-45807400	Strong transcription	A549	lung
22	chr12:45794200-45823200	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr12:45794400-45807400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:45794600-45806800	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr12:45794600-45809200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr12:45794600-45812200	Weak transcription	Fetal Brain Male	brain
27	chr12:45794800-45807600	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr12:45795000-45812200	Weak transcription	Fetal Brain Female	brain
29	chr12:45795200-45808000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:45795200-45813200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:45795200-45817800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr12:45795400-45813400	Strong transcription	Dnd41	blood
33	chr12:45795600-45807000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr12:45795600-45807600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr12:45795600-45825600	Strong transcription	Fetal Intestine Large	intestine
36	chr12:45795800-45806800	Strong transcription	Placenta	Placenta
37	chr12:45795800-45808200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr12:45796000-45807400	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr12:45796000-45812400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:45796400-45812200	Weak transcription	Hela-S3	cervix
41	chr12:45796400-45829600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr12:45796600-45808000	Strong transcription	GM12878-XiMat	blood
43	chr12:45796600-45828400	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr12:45796600-45828600	Weak transcription	Brain Substantia Nigra	brain
45	chr12:45796600-45828800	Weak transcription	Brain Angular Gyrus	brain
46	chr12:45797600-45819200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr12:45798600-45806600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr12:45799800-45807200	Strong transcription	Primary hematopoietic stem cells	blood
49	chr12:45799800-45807600	Strong transcription	Stomach Smooth Muscle	stomach
50	chr12:45799800-45808000	Strong transcription	Duodenum Mucosa	Duodenum

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