Variant report

Variant	rs6451304
Chromosome Location	chr5:36618403-36618404
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1030239	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.86[MEX][hapmap];0.82[YRI][hapmap];0.95[ASN][1000 genomes]
rs10941306	0.89[YRI][hapmap]
rs1862638	0.80[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1864213	0.86[YRI][hapmap]
rs1864214	0.83[ASW][hapmap];0.86[YRI][hapmap]
rs372171	0.86[CHB][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs3733810	1.00[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs3776566	0.93[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs3776567	0.86[CHB][hapmap];0.92[JPT][hapmap];0.81[YRI][hapmap];0.82[ASN][1000 genomes]
rs3776568	0.86[CHB][hapmap];0.83[JPT][hapmap];0.82[ASN][1000 genomes]
rs432268	0.86[CHB][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs442867	0.80[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492319	chr5:36570707-37061019	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv830263	chr5:36576504-36755093	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36608800-36639600	Weak transcription	Esophagus	oesophagus
2	chr5:36609400-36619200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:36609400-36619800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr5:36610600-36629800	Weak transcription	NHDF-Ad	bronchial
5	chr5:36611000-36633600	Weak transcription	Brain Germinal Matrix	brain
6	chr5:36611200-36630000	Weak transcription	Right Ventricle	heart
7	chr5:36612200-36623400	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr5:36612400-36619200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
9	chr5:36613200-36620200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr5:36613400-36618800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr5:36613600-36618600	Weak transcription	NHEK	skin
12	chr5:36613600-36618800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:36613600-36619000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr5:36613600-36624400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:36614000-36624000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr5:36614000-36629600	Weak transcription	Fetal Muscle Leg	muscle
17	chr5:36614200-36619000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:36614400-36619000	Weak transcription	Hela-S3	cervix
19	chr5:36614600-36619400	Enhancers	Fetal Heart	heart
20	chr5:36614800-36618600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:36614800-36621400	Weak transcription	Brain Angular Gyrus	brain
22	chr5:36615000-36624000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr5:36615000-36629600	Weak transcription	Fetal Muscle Trunk	muscle
24	chr5:36615200-36618600	Weak transcription	HMEC	breast
25	chr5:36615200-36621800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr5:36615200-36624200	Weak transcription	HSMM	muscle
27	chr5:36615200-36627600	Weak transcription	Adipose Nuclei	Adipose
28	chr5:36615400-36621800	Weak transcription	Brain Substantia Nigra	brain
29	chr5:36615400-36630000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:36615400-36630200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:36615800-36619000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr5:36615800-36629800	Weak transcription	Placenta	Placenta
33	chr5:36616000-36624000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr5:36616400-36620800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr5:36616800-36619000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr5:36616800-36620600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:36616800-36651200	Weak transcription	Psoas Muscle	Psoas
38	chr5:36617000-36620800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr5:36617200-36619200	Weak transcription	Left Ventricle	heart
40	chr5:36617200-36620800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr5:36617800-36618800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr5:36617800-36619200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr5:36617800-36620600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr5:36618000-36618800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:36618000-36619000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:36618000-36619200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:36618000-36620600	Enhancers	Brain Hippocampus Middle	brain
48	chr5:36618200-36618800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr5:36618200-36619000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr5:36618200-36619600	Enhancers	Brain Anterior Caudate	brain

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