Variant report

Variant	rs11054675
Chromosome Location	chr12:12241338-12241339
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10845472	0.84[ASN][1000 genomes]
rs10845474	0.84[ASN][1000 genomes]
rs11054673	0.84[ASN][1000 genomes]
rs11054674	0.84[ASN][1000 genomes]
rs11054676	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11054677	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11054678	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11054680	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2287155	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73053308	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7962856	0.84[ASN][1000 genomes]
rs7972500	0.84[ASN][1000 genomes]
rs7973469	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949003	chr12:11938229-12618690	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv975623	chr12:12238184-12243964	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv557583	chr12:12238317-12253591	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12225000-12255000	Weak transcription	Small Intestine	intestine
2	chr12:12226600-12245000	Weak transcription	Fetal Brain Male	brain
3	chr12:12232800-12257000	Weak transcription	HSMMtube	muscle
4	chr12:12234800-12259600	Weak transcription	Aorta	Aorta
5	chr12:12235200-12242000	Weak transcription	NHLF	lung
6	chr12:12235400-12243600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr12:12235400-12244600	Weak transcription	Colonic Mucosa	Colon
8	chr12:12235400-12245000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr12:12235400-12245200	Weak transcription	Pancreas	Pancrea
10	chr12:12235400-12260200	Weak transcription	Gastric	stomach
11	chr12:12235400-12260800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr12:12235400-12278800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr12:12237400-12259800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr12:12238000-12245000	Strong transcription	Duodenum Mucosa	Duodenum
15	chr12:12238600-12241800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:12238600-12242000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:12239200-12241800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr12:12239400-12241800	Enhancers	HepG2	liver
19	chr12:12239600-12241400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:12239600-12249200	Strong transcription	Fetal Intestine Small	intestine
21	chr12:12240000-12242000	Strong transcription	Rectal Mucosa Donor 31	rectum
22	chr12:12240200-12241800	Strong transcription	Fetal Stomach	stomach
23	chr12:12240200-12241800	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr12:12240200-12242200	Strong transcription	Fetal Intestine Large	intestine
25	chr12:12240400-12244200	Weak transcription	Fetal Lung	lung
26	chr12:12240400-12254200	Weak transcription	Stomach Mucosa	stomach
27	chr12:12240600-12241600	Weak transcription	Fetal Muscle Leg	muscle
28	chr12:12240600-12245400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:12240600-12245400	Weak transcription	Brain Germinal Matrix	brain
30	chr12:12240600-12256800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr12:12240800-12241400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr12:12240800-12241400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:12240800-12241400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr12:12241000-12241800	Weak transcription	Brain Anterior Caudate	brain
35	chr12:12241000-12242000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:12241000-12242000	Strong transcription	Rectal Mucosa Donor 29	rectum
37	chr12:12241000-12244200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr12:12241000-12244200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:12241000-12250200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:12241000-12260600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr12:12241000-12273400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr12:12241200-12241600	Active TSS	Adipose Nuclei	Adipose
43	chr12:12241200-12245000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr12:12241200-12245600	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr12:12241200-12245600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr12:12241200-12256800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr12:12241200-12261000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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