Variant report

Variant	rs7152150
Chromosome Location	chr14:103886611-103886612
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:103878753..103883496-chr14:103884428..103888484,4	MCF-7	breast:
2	chr14:103885868..103889537-chr14:103891147..103894147,4	K562	blood:
3	chr14:103878188..103883188-chr14:103884541..103889590,5	MCF-7	breast:
4	chr14:103883876..103886732-chr14:103888841..103890509,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000244691	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10137098	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10146340	1.00[AMR][1000 genomes]
rs10149270	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10151139	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11621406	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs11625988	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12887238	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951393	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2065014	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2065020	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2145858	0.86[AFR][1000 genomes]
rs2180992	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2403175	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2403181	0.84[AFR][1000 genomes]
rs2756130	0.82[AFR][1000 genomes]
rs2756131	0.82[AFR][1000 genomes]
rs2756137	0.82[AFR][1000 genomes]
rs2765050	0.80[AFR][1000 genomes]
rs2765053	0.82[AFR][1000 genomes]
rs34721082	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4900576	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4906326	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4906328	0.88[AFR][1000 genomes]
rs6575987	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6575989	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6575990	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6575993	0.88[AFR][1000 genomes]
rs7146717	0.82[AFR][1000 genomes]
rs7149291	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7153380	0.88[AFR][1000 genomes]
rs8003497	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8014010	0.90[AFR][1000 genomes]
rs911556	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049747	chr14:103126148-103955984	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	113 gene(s)	inside rSNPs	diseases
2	nsv534254	chr14:103470073-104023906	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
3	nsv9168	chr14:103531729-103913306	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103862000-103919400	Weak transcription	Colonic Mucosa	Colon
2	chr14:103874600-103900800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr14:103875200-103888200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr14:103875200-103889200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr14:103875200-103893600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr14:103875400-103887400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr14:103875400-103888600	Weak transcription	Gastric	stomach
8	chr14:103875400-103889600	Weak transcription	Colon Smooth Muscle	Colon
9	chr14:103875400-103892200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr14:103875400-103893600	Weak transcription	Brain Germinal Matrix	brain
11	chr14:103875600-103893800	Weak transcription	Fetal Heart	heart
12	chr14:103875600-103894000	Weak transcription	Fetal Brain Male	brain
13	chr14:103875800-103889800	Weak transcription	Lung	lung
14	chr14:103876800-103887800	Weak transcription	Pancreas	Pancrea
15	chr14:103879000-103892800	Weak transcription	Spleen	Spleen
16	chr14:103879000-103895200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr14:103879000-103914200	Weak transcription	Esophagus	oesophagus
18	chr14:103879000-103941400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:103879200-103887200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr14:103879600-103889400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr14:103879800-103887400	Weak transcription	HepG2	liver
22	chr14:103880400-103894200	Weak transcription	Liver	Liver
23	chr14:103880400-103904600	Weak transcription	Fetal Kidney	kidney
24	chr14:103881000-103887000	Weak transcription	Thymus	Thymus
25	chr14:103881000-103889200	Weak transcription	Stomach Smooth Muscle	stomach
26	chr14:103881000-103890600	Weak transcription	Fetal Muscle Trunk	muscle
27	chr14:103881000-103900600	Weak transcription	Placenta	Placenta
28	chr14:103882000-103887200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr14:103882600-103886800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr14:103883000-103894400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:103883200-103892800	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr14:103883200-103893800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr14:103883400-103887400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr14:103883400-103889200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr14:103883400-103889800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr14:103883400-103889800	Weak transcription	Fetal Intestine Large	intestine
37	chr14:103883400-103892800	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr14:103883400-103893600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr14:103883400-103900000	Weak transcription	Fetal Thymus	thymus
40	chr14:103883600-103887200	Weak transcription	Right Atrium	heart
41	chr14:103883600-103887200	Weak transcription	Dnd41	blood
42	chr14:103883600-103888000	Weak transcription	Fetal Muscle Leg	muscle
43	chr14:103883600-103888800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr14:103883600-103889200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr14:103883600-103889200	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr14:103883600-103889800	Weak transcription	Fetal Lung	lung
47	chr14:103883600-103889800	Weak transcription	Fetal Stomach	stomach
48	chr14:103883600-103892600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr14:103883600-103892800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr14:103883600-103894000	Weak transcription	Fetal Brain Female	brain

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