Variant report

Variant	rs7181688
Chromosome Location	chr15:42747695-42747696
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs1062038	0.92[CHB][hapmap];0.90[ASN][1000 genomes]
rs10775126	0.83[CHB][hapmap]
rs10851409	0.81[CHB][hapmap]
rs11070370	0.81[CHB][hapmap]
rs1139100	0.90[ASN][1000 genomes]
rs11631983	0.83[CHB][hapmap]
rs12101559	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12441700	0.81[CHB][hapmap]
rs12442040	1.00[ASN][1000 genomes]
rs12442046	1.00[ASN][1000 genomes]
rs1359003	0.81[CHB][hapmap]
rs1359004	0.83[CHB][hapmap]
rs1659212	0.83[CHB][hapmap]
rs1659213	0.91[CHB][hapmap]
rs1659218	0.91[CHB][hapmap]
rs1659219	0.90[CHB][hapmap]
rs1659222	0.90[CHB][hapmap]
rs1678992	0.91[CHB][hapmap]
rs1678993	0.91[CHB][hapmap]
rs16973261	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16973265	0.93[JPT][hapmap];0.84[ASN][1000 genomes]
rs2289295	0.83[CHB][hapmap]
rs2412715	0.82[ASN][1000 genomes]
rs2918459	0.83[CHB][hapmap]
rs2918460	0.91[CHB][hapmap]
rs2918461	0.81[CHB][hapmap]
rs3742996	0.83[AMR][1000 genomes]
rs3742997	0.97[ASN][1000 genomes]
rs3743006	0.81[CHB][hapmap]
rs4329897	0.83[CHB][hapmap]
rs4923940	0.83[CHB][hapmap]
rs4924645	0.83[CHB][hapmap]
rs4924653	0.82[CHB][hapmap]
rs4924658	0.83[CHB][hapmap]
rs4924676	0.90[ASN][1000 genomes]
rs4924677	0.83[AMR][1000 genomes]
rs4924679	0.80[AMR][1000 genomes]
rs4924680	0.80[AMR][1000 genomes]
rs4924682	0.82[AMR][1000 genomes]
rs57502147	0.90[ASN][1000 genomes]
rs57734638	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58567518	0.83[AMR][1000 genomes]
rs59091866	0.80[AMR][1000 genomes]
rs59206762	0.80[AMR][1000 genomes]
rs59414917	0.80[AMR][1000 genomes]
rs59908459	0.80[AMR][1000 genomes]
rs60328984	0.85[AMR][1000 genomes]
rs60569090	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61071861	0.88[ASN][1000 genomes]
rs61115119	1.00[ASN][1000 genomes]
rs6493027	0.82[CHB][hapmap]
rs7163986	0.81[CHB][hapmap];0.81[ASN][1000 genomes]
rs7166604	0.90[ASN][1000 genomes]
rs7166785	0.83[CHB][hapmap]
rs7168709	0.83[CHB][hapmap]
rs7169521	0.90[ASN][1000 genomes]
rs7169615	0.82[ASN][1000 genomes]
rs7169767	0.82[AMR][1000 genomes]
rs7171201	0.85[AMR][1000 genomes]
rs7179709	0.91[CHB][hapmap]
rs7180315	0.83[AMR][1000 genomes]
rs7181742	0.81[CHB][hapmap]
rs7183015	0.82[CHB][hapmap]
rs7183546	0.81[CHB][hapmap]
rs751572	0.81[CHB][hapmap]
rs8024113	0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs8024732	0.81[CHB][hapmap]
rs8026817	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8027283	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8031315	0.81[CHB][hapmap]
rs8036255	0.80[AMR][1000 genomes]
rs8036544	0.84[ASN][1000 genomes]
rs8036596	0.81[CHB][hapmap]
rs8037020	0.81[CHB][hapmap]
rs934876	0.85[AMR][1000 genomes]
rs9920921	0.81[CHB][hapmap]

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	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
4	nsv832986	chr15:42587825-42753664	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv832987	chr15:42627447-42792348	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers 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	28 gene(s)	inside rSNPs	diseases
6	esv3334708	chr15:42664344-42827738	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr15:42694600-42750600	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr15:42701200-42766600	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr15:42702200-42750200	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr15:42705800-42749200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr15:42711800-42749200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr15:42720400-42759200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr15:42733400-42748000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr15:42737200-42764800	Weak transcription	A549	lung
9	chr15:42740800-42749200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr15:42742600-42749200	Weak transcription	Pancreas	Pancrea
11	chr15:42743200-42750200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr15:42743800-42749400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr15:42744000-42747800	Weak transcription	Psoas Muscle	Psoas
14	chr15:42744000-42748400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr15:42744000-42749000	Weak transcription	Brain Angular Gyrus	brain
16	chr15:42744000-42749200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:42744000-42749200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr15:42744000-42749200	Weak transcription	Esophagus	oesophagus
19	chr15:42744000-42757400	Weak transcription	Gastric	stomach
20	chr15:42744000-42757600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr15:42744200-42747800	Weak transcription	NHLF	lung
22	chr15:42744200-42748000	Weak transcription	Adipose Nuclei	Adipose
23	chr15:42744200-42748400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr15:42744200-42748400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:42744200-42748400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:42744200-42748600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr15:42744200-42748600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr15:42744200-42748600	Weak transcription	Brain Hippocampus Middle	brain
29	chr15:42744200-42748800	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr15:42744200-42748800	Weak transcription	HUVEC	blood vessel
31	chr15:42744200-42748800	Weak transcription	NH-A	brain
32	chr15:42744200-42749000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr15:42744200-42749000	Weak transcription	Brain Anterior Caudate	brain
34	chr15:42744200-42749000	Weak transcription	Brain Germinal Matrix	brain
35	chr15:42744200-42749000	Weak transcription	Brain Substantia Nigra	brain
36	chr15:42744200-42749200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr15:42744200-42749200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr15:42744200-42749200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr15:42744200-42749200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr15:42744200-42749200	Weak transcription	Colonic Mucosa	Colon
41	chr15:42744200-42749200	Weak transcription	Lung	lung
42	chr15:42744200-42749400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr15:42744200-42749400	Weak transcription	Liver	Liver
44	chr15:42744200-42749400	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr15:42744200-42749600	Weak transcription	Fetal Brain Female	brain
46	chr15:42744200-42749800	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr15:42744200-42749800	Weak transcription	Thymus	Thymus
48	chr15:42744200-42750400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr15:42744200-42753400	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr15:42744200-42754000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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