Variant report

Variant	rs1149804
Chromosome Location	chr12:26127228-26127229
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10505990	0.81[JPT][hapmap]
rs10842643	0.88[CHB][hapmap];0.87[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10842644	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10842653	0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11048360	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11048372	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11048376	0.80[GIH][hapmap];0.87[MEX][hapmap];0.82[MKK][hapmap]
rs11048378	0.82[CHB][hapmap];0.90[JPT][hapmap];0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11048379	0.82[CHB][hapmap];0.90[JPT][hapmap];0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11048380	0.82[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11048381	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11048382	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11048383	0.82[AMR][1000 genomes]
rs11048384	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1120064	0.88[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes]
rs11561207	0.81[AMR][1000 genomes]
rs12227689	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12578169	0.90[JPT][hapmap]
rs12812752	0.81[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12813641	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12818478	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12831248	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1390326	0.90[JPT][hapmap]
rs1691889	1.00[CEU][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16929784	0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16929817	0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16929830	0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs16929846	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16929940	0.90[JPT][hapmap]
rs16929945	0.90[JPT][hapmap]
rs16929950	0.90[JPT][hapmap]
rs16929958	0.90[JPT][hapmap]
rs2055180	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs2132317	0.82[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2279680	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2343201	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2643941	0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs34595529	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35924984	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3803009	0.88[CHB][hapmap];0.87[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs61622173	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6487525	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs706524	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs706526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs706531	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs706532	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs706533	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs706538	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7132590	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7134721	0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7298162	0.88[CHB][hapmap];0.90[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7953171	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7963603	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs829837	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs829987	0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs853656	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	esv2758300	chr12:25992331-26161116	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	esv2759886	chr12:25992331-26161116	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv898931	chr12:26123345-26192936	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26113400-26128800	Weak transcription	HSMM	muscle
2	chr12:26114000-26128000	Weak transcription	Fetal Intestine Small	intestine
3	chr12:26115000-26127800	Weak transcription	Fetal Kidney	kidney
4	chr12:26117200-26130200	Weak transcription	Fetal Heart	heart
5	chr12:26117600-26150000	Weak transcription	Hela-S3	cervix
6	chr12:26118400-26131600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr12:26119600-26130200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:26120000-26127400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr12:26121000-26131600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr12:26121200-26129600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:26122400-26128200	Enhancers	Osteobl	bone
12	chr12:26123400-26129400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:26123800-26128800	Weak transcription	Spleen	Spleen
14	chr12:26123800-26129000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr12:26123800-26129200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr12:26123800-26134000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:26123800-26134200	Weak transcription	Gastric	stomach
18	chr12:26123800-26137200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr12:26124200-26129400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr12:26124400-26128800	Weak transcription	Esophagus	oesophagus
21	chr12:26124400-26128800	Enhancers	NHDF-Ad	bronchial
22	chr12:26124400-26138000	Weak transcription	Fetal Intestine Large	intestine
23	chr12:26124800-26127600	Weak transcription	HUVEC	blood vessel
24	chr12:26124800-26129200	Enhancers	Colon Smooth Muscle	Colon
25	chr12:26124800-26130800	Weak transcription	Fetal Lung	lung
26	chr12:26125000-26128600	Weak transcription	Adipose Nuclei	Adipose
27	chr12:26125000-26129000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:26125000-26130800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:26125000-26138600	Weak transcription	Pancreas	Pancrea
30	chr12:26125200-26128000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:26125800-26129000	Enhancers	Brain Hippocampus Middle	brain
32	chr12:26125800-26129600	Enhancers	Right Atrium	heart
33	chr12:26126000-26127600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr12:26126200-26127400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr12:26126200-26127800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr12:26126200-26128000	Weak transcription	NH-A	brain
37	chr12:26126200-26128200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr12:26126400-26127400	Enhancers	Psoas Muscle	Psoas
39	chr12:26126400-26128200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:26126400-26129200	Weak transcription	NHLF	lung
41	chr12:26126400-26132200	Weak transcription	HMEC	breast
42	chr12:26126600-26127600	Weak transcription	Brain Anterior Caudate	brain
43	chr12:26126600-26127600	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr12:26126600-26128800	Weak transcription	Brain Cingulate Gyrus	brain
45	chr12:26126600-26129000	Enhancers	Stomach Smooth Muscle	stomach
46	chr12:26126800-26127600	Weak transcription	Right Ventricle	heart
47	chr12:26126800-26127800	Weak transcription	Brain Substantia Nigra	brain
48	chr12:26126800-26128000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr12:26126800-26128600	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr12:26126800-26128600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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