Variant report

Variant	rs11615313
Chromosome Location	chr12:33019436-33019437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1046116	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11611761	0.90[EUR][1000 genomes]
rs11612954	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11615926	0.92[ASN][1000 genomes]
rs11616075	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12099507	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17543624	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17543896	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2168207	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34634865	0.85[ASN][1000 genomes]
rs60549952	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7302486	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7302979	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7313522	0.87[EUR][1000 genomes]
rs73303664	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7963225	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7975559	0.85[EUR][1000 genomes];1.00[ASN][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	nsv530421	chr12:32825335-33465991	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1054440	chr12:32872999-33150460	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv532334	chr12:32884789-33034791	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv976595	chr12:33010536-33021896	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1035900	chr12:33010643-33079667	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv541458	chr12:33010643-33079667	Strong transcription Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32941800-33033400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr12:32943800-33026800	Weak transcription	Fetal Kidney	kidney
3	chr12:32972000-33029000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:32974200-33030400	Weak transcription	Right Ventricle	heart
5	chr12:32975800-33020000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:32993000-33030400	Weak transcription	Colonic Mucosa	Colon
7	chr12:32997800-33044400	Weak transcription	Hela-S3	cervix
8	chr12:32997800-33046000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr12:33000400-33020000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr12:33003200-33022800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr12:33003800-33030400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr12:33004000-33020000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr12:33004000-33020000	Weak transcription	HepG2	liver
14	chr12:33004000-33020200	Weak transcription	Fetal Intestine Large	intestine
15	chr12:33004000-33030400	Weak transcription	Gastric	stomach
16	chr12:33004200-33028800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr12:33004400-33019600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr12:33008200-33019600	Weak transcription	Duodenum Mucosa	Duodenum
19	chr12:33008200-33019800	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr12:33011800-33021800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr12:33012000-33020000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr12:33012000-33029000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr12:33012000-33031000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr12:33013200-33020000	Weak transcription	Left Ventricle	heart
25	chr12:33013400-33019600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr12:33013600-33019600	Weak transcription	HMEC	breast
27	chr12:33013800-33020200	Weak transcription	Pancreas	Pancrea
28	chr12:33014600-33022800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:33014800-33030400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr12:33014800-33041200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr12:33015000-33019600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr12:33015600-33023200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:33016000-33022200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr12:33016400-33021600	Weak transcription	NHEK	skin
35	chr12:33017000-33030400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr12:33017000-33030600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr12:33018000-33020400	Weak transcription	Fetal Heart	heart
38	chr12:33018200-33022200	Strong transcription	Fetal Intestine Small	intestine
39	chr12:33018400-33029200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:33018600-33026000	Weak transcription	Esophagus	oesophagus
41	chr12:33019000-33019600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr12:33019000-33021600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr12:33019200-33023800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr12:33019200-33027400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:33019400-33021800	Weak transcription	Fetal Stomach	stomach
46	chr12:33019400-33022200	Strong transcription	Liver	Liver
47	chr12:33019400-33022200	Strong transcription	Placenta	Placenta
48	chr12:33019400-33022800	Strong transcription	Rectal Mucosa Donor 31	rectum

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