Variant report

Variant	rs1655612
Chromosome Location	chr12:83372701-83372702
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10746262	0.94[EUR][1000 genomes]
rs10778918	0.92[EUR][1000 genomes]
rs10778921	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1434425	0.88[CEU][hapmap];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1655611	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1682567	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1682575	0.88[CEU][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1682579	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1682580	0.89[CEU][hapmap];0.98[EUR][1000 genomes]
rs1682606	0.94[EUR][1000 genomes]
rs1682607	0.82[EUR][1000 genomes]
rs1682608	0.94[EUR][1000 genomes]
rs1796150	0.90[EUR][1000 genomes]
rs1796157	1.00[CEU][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1796161	0.94[EUR][1000 genomes]
rs1796162	0.94[EUR][1000 genomes]
rs1796166	0.90[EUR][1000 genomes]
rs1796167	0.82[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1796168	0.94[EUR][1000 genomes]
rs1796178	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs1796187	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1796296	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1796300	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1821444	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1972801	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2046417	0.89[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2062357	0.94[EUR][1000 genomes]
rs2403025	1.00[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2403026	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2707753	0.94[EUR][1000 genomes]
rs2707754	0.94[EUR][1000 genomes]
rs2707760	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs2708000	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4882531	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6539697	0.94[EUR][1000 genomes]
rs7297707	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs7299175	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7303058	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7953974	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv469490	chr12:83089431-83507269	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv559542	chr12:83089431-83507269	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv832472	chr12:83248283-83419753	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
5	nsv559557	chr12:83334204-83453620	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
6	nsv469495	chr12:83339933-83374779	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	nsv559558	chr12:83339933-83374779	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	nsv1047239	chr12:83362299-83444855	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83347000-83379600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:83349400-83374600	Weak transcription	Colon Smooth Muscle	Colon
3	chr12:83356200-83379400	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr12:83356400-83381600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr12:83356600-83381400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr12:83357800-83389600	Weak transcription	Fetal Intestine Large	intestine
7	chr12:83358000-83389600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr12:83358400-83397600	Weak transcription	Brain Anterior Caudate	brain
9	chr12:83358400-83409200	Weak transcription	Brain Angular Gyrus	brain
10	chr12:83358600-83379400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:83358600-83394200	Weak transcription	Fetal Muscle Leg	muscle
12	chr12:83358600-83399600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr12:83358600-83409400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr12:83362000-83382200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:83364200-83379600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:83367000-83379400	Weak transcription	Brain Cingulate Gyrus	brain
17	chr12:83367400-83391800	Weak transcription	Small Intestine	intestine
18	chr12:83367600-83379400	Weak transcription	Brain Substantia Nigra	brain
19	chr12:83368800-83373200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:83368800-83379600	Weak transcription	Fetal Lung	lung
21	chr12:83368800-83386800	Weak transcription	Fetal Stomach	stomach
22	chr12:83368800-83393800	Weak transcription	Fetal Muscle Trunk	muscle
23	chr12:83368800-83399200	Weak transcription	Esophagus	oesophagus
24	chr12:83369000-83379000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:83369000-83379000	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr12:83369200-83379400	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr12:83369400-83373400	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr12:83371600-83379600	Weak transcription	Gastric	stomach
29	chr12:83372400-83372800	Enhancers	Pancreatic Islets	Pancreatic Islet

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