Variant report

Variant	rs73732013
Chromosome Location	chr6:36820683-36820684
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36818424..36822217-chr6:36952499..36954853,3	K562	blood:
2	chr6:36815130..36818530-chr6:36818954..36823604,5	K562	blood:
3	chr6:36818402..36820845-chr6:36839633..36841729,2	K562	blood:
4	chr6:36819964..36824038-chr6:36826260..36830015,5	MCF-7	breast:
5	chr6:36819191..36821393-chr6:36826640..36829329,2	MCF-7	breast:
6	chr6:36811312..36813099-chr6:36818892..36821190,2	MCF-7	breast:
7	chr6:36820493..36822217-chr6:36952499..36954085,2	K562	blood:
8	chr6:36819209..36822564-chr6:36824095..36826600,3	K562	blood:
9	chr6:36733851..36734590-chr6:36820298..36821123,2	K562	blood:
10	chr6:36742135..36744958-chr6:36819478..36821110,2	K562	blood:
11	chr6:36818579..36822639-chr6:36835896..36837920,3	K562	blood:
12	chr6:36816699..36818320-chr6:36819945..36822001,2	MCF-7	breast:
13	chr6:36818907..36820999-chr6:36822300..36824076,3	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPIL1-1	chr6:36819837-36822439	NONHSAT112236

No data

Variant related genes	Relation type
ENSG00000198663	Chromatin interaction
ENSG00000137409	Chromatin interaction
ENSG00000137168	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1008027	0.87[EUR][1000 genomes]
rs13193599	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13193613	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16889199	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34433592	0.81[AFR][1000 genomes]
rs6930737	0.87[EUR][1000 genomes]
rs729659	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023171	chr6:36686935-36880899	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv538202	chr6:36686935-36880899	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv1033261	chr6:36687424-36837315	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv5262	chr6:36799329-36826210	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1030015	chr6:36818510-37104446	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36809000-36823000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr6:36811400-36823200	Weak transcription	Esophagus	oesophagus
3	chr6:36813200-36821200	Weak transcription	Brain Hippocampus Middle	brain
4	chr6:36813200-36823200	Weak transcription	Brain Substantia Nigra	brain
5	chr6:36816600-36823000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:36816800-36821800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr6:36817000-36821400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:36817000-36823200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:36817000-36826200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:36817000-36841400	Weak transcription	Colonic Mucosa	Colon
11	chr6:36817200-36821200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:36817200-36823200	Weak transcription	Gastric	stomach
13	chr6:36817200-36823200	Weak transcription	Pancreas	Pancrea
14	chr6:36817200-36823600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:36817200-36830200	Weak transcription	Fetal Lung	lung
16	chr6:36817200-36833400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr6:36817200-36841200	Weak transcription	Fetal Brain Male	brain
18	chr6:36817200-36842000	Weak transcription	Stomach Mucosa	stomach
19	chr6:36817400-36820800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr6:36817400-36821400	Enhancers	Fetal Heart	heart
21	chr6:36817600-36821000	Weak transcription	Fetal Intestine Large	intestine
22	chr6:36817600-36821200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:36817600-36822400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:36818000-36821400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr6:36818000-36821400	Enhancers	Left Ventricle	heart
26	chr6:36818000-36822800	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr6:36818000-36824800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr6:36818200-36822200	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr6:36818400-36821000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr6:36818400-36821600	Enhancers	Colon Smooth Muscle	Colon
31	chr6:36818400-36821800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:36818600-36821600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:36818600-36822200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:36818800-36820800	Enhancers	NHLF	lung
35	chr6:36818800-36821400	Enhancers	HSMM	muscle
36	chr6:36818800-36821800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr6:36818800-36821800	Enhancers	Osteobl	bone
38	chr6:36818800-36822400	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr6:36819000-36820800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr6:36819000-36822000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr6:36819000-36823000	Weak transcription	Lung	lung
42	chr6:36819000-36830000	Weak transcription	Fetal Kidney	kidney
43	chr6:36819000-36840400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr6:36819200-36821200	Enhancers	Aorta	Aorta
45	chr6:36819200-36821400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr6:36819200-36821800	Enhancers	HSMMtube	muscle
47	chr6:36819200-36821800	Enhancers	NHDF-Ad	bronchial
48	chr6:36819200-36822200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr6:36819200-36822200	Enhancers	Psoas Muscle	Psoas
50	chr6:36819200-36823200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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