Variant report

Variant	rs12318187
Chromosome Location	chr12:51447145-51447146
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:51447052-51447339	K562	blood:	n/a	n/a
2	POLR2A	chr12:51447078-51447393	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:51446371..51449109-chr12:51475954..51477544,3	K562	blood:
2	chr12:51446671..51449109-chr12:51475852..51477454,2	K562	blood:
3	chr12:51440271..51447226-chr12:51475135..51479930,16	MCF-7	breast:
4	chr12:51445541..51448064-chr12:51474329..51477358,3	MCF-7	breast:

Variant related genes	Relation type
LETMD1	TF binding region
ENSG00000110925	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10082984	1.00[AMR][1000 genomes]
rs11169699	1.00[AMR][1000 genomes]
rs12297361	1.00[AMR][1000 genomes]
rs12304202	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12304653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12305543	1.00[AMR][1000 genomes]
rs12307922	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12311001	1.00[AMR][1000 genomes]
rs12312957	1.00[AMR][1000 genomes]
rs12316887	1.00[AMR][1000 genomes]
rs12317077	1.00[AMR][1000 genomes]
rs12317980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12318042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12318936	1.00[AMR][1000 genomes]
rs12322602	0.83[AFR][1000 genomes]
rs17216086	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3414501	chr12:51174503-51534707	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	esv34039	chr12:51326702-51671911	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 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	chr12:51442800-51448200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:51442800-51449000	Weak transcription	Aorta	Aorta
3	chr12:51442800-51449800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:51442800-51450000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:51442800-51452800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:51442800-51470200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr12:51443000-51448200	Weak transcription	Gastric	stomach
8	chr12:51443000-51453200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:51443200-51447200	Weak transcription	Ovary	ovary
10	chr12:51443200-51447600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr12:51443200-51449600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:51443400-51447200	Weak transcription	Pancreas	Pancrea
13	chr12:51443400-51447400	Weak transcription	HSMM	muscle
14	chr12:51443400-51447600	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr12:51443400-51448200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr12:51443400-51448200	Weak transcription	Esophagus	oesophagus
17	chr12:51443400-51449200	Weak transcription	Right Ventricle	heart
18	chr12:51443400-51452600	Weak transcription	Stomach Mucosa	stomach
19	chr12:51443400-51476000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:51443600-51447200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr12:51443600-51447400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr12:51443600-51447400	Weak transcription	Primary B cells from cord blood	blood
23	chr12:51443600-51447600	Weak transcription	Rectal Smooth Muscle	rectum
24	chr12:51443600-51447800	Weak transcription	Brain Angular Gyrus	brain
25	chr12:51443600-51448600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr12:51443600-51451600	Weak transcription	Colonic Mucosa	Colon
27	chr12:51443600-51451800	Weak transcription	Small Intestine	intestine
28	chr12:51443600-51452600	Weak transcription	Psoas Muscle	Psoas
29	chr12:51443600-51457400	Weak transcription	Fetal Brain Male	brain
30	chr12:51443600-51459600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr12:51443600-51462800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr12:51443800-51447400	Weak transcription	Fetal Lung	lung
33	chr12:51443800-51447800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr12:51443800-51448000	Weak transcription	NHLF	lung
35	chr12:51443800-51449000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr12:51443800-51455600	Weak transcription	Fetal Heart	heart
37	chr12:51443800-51462600	Strong transcription	A549	lung
38	chr12:51444000-51449600	Weak transcription	HUVEC	blood vessel
39	chr12:51444200-51447200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr12:51444200-51448200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr12:51444200-51452400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:51444200-51454800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr12:51444200-51463200	Strong transcription	Placenta	Placenta
44	chr12:51444200-51465000	Strong transcription	Fetal Muscle Leg	muscle
45	chr12:51444200-51465400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr12:51444200-51465600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr12:51444200-51470400	Strong transcription	Fetal Stomach	stomach
48	chr12:51444400-51462800	Strong transcription	Duodenum Mucosa	Duodenum
49	chr12:51444400-51464800	Strong transcription	Fetal Muscle Trunk	muscle
50	chr12:51444600-51455600	Strong transcription	Fetal Intestine Small	intestine

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