Variant report

Variant	rs756690
Chromosome Location	chr9:136549043-136549044
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:136546579..136549426-chr9:136551457..136554920,3	K562	blood:
2	chr9:136547609..136549609-chr9:136554134..136556211,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DBH-3	chr9:136548433-136550559	NONHSAT135337

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1076149	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs129889	0.83[CHB][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs129891	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs129892	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs129893	0.95[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs129894	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs129895	0.95[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs129896	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs129897	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs129898	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs129899	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs129900	1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs129901	0.96[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap]
rs129903	0.91[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs129904	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs129905	0.96[CHB][hapmap];0.82[JPT][hapmap];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs129906	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs129907	0.81[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs129939	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs129948	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs129951	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs129957	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1548362	0.96[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1548363	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2073816	0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs2073817	0.87[CHB][hapmap];0.86[ASN][1000 genomes]
rs2502734	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2502736	0.82[ASN][1000 genomes]
rs2519071	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2519072	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2519120	0.90[CEU][hapmap];0.85[CHB][hapmap];0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2519126	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2519129	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2519130	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2519131	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2797820	0.95[CHB][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2797823	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2797829	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2797830	0.96[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2797831	0.96[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap]
rs2797832	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35138178	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4744533	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs730007	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs733149	0.96[CHB][hapmap];0.86[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs756682	1.00[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs756687	0.96[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs756691	0.96[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs886016	0.95[CHB][hapmap];0.85[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894081	chr9:136227260-136678954	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv894086	chr9:136281753-136657960	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
3	nsv530972	chr9:136324358-136643044	Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
4	nsv870051	chr9:136459745-136656889	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv894106	chr9:136489539-136566959	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv894107	chr9:136494566-136579589	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv894108	chr9:136507473-136617292	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv894111	chr9:136522985-136563926	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv894112	chr9:136528721-136571089	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1049434	chr9:136529766-136618314	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	esv1793889	chr9:136533509-136581419	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1049281	chr9:136535471-136617805	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv894113	chr9:136538798-136586367	Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv894114	chr9:136538798-136779153	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv428546	chr9:136541745-136720872	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136524800-136555600	Weak transcription	HSMM	muscle
2	chr9:136525000-136556800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr9:136530800-136561000	Weak transcription	Gastric	stomach
4	chr9:136540200-136549200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr9:136541600-136551000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr9:136544200-136549400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr9:136545400-136559600	Weak transcription	Fetal Heart	heart
8	chr9:136545600-136557800	Weak transcription	Ovary	ovary
9	chr9:136545600-136567600	Weak transcription	Colon Smooth Muscle	Colon
10	chr9:136546200-136550600	Enhancers	Fetal Muscle Leg	muscle
11	chr9:136546400-136549400	Enhancers	Fetal Thymus	thymus
12	chr9:136546600-136549200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr9:136546600-136551400	Strong transcription	HepG2	liver
14	chr9:136547400-136549600	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr9:136547400-136550000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr9:136547600-136549400	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr9:136547600-136550000	Enhancers	Duodenum Mucosa	Duodenum
18	chr9:136547600-136551000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr9:136548000-136549400	Enhancers	Primary B cells from peripheral blood	blood
20	chr9:136548000-136549600	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr9:136548000-136550000	Bivalent Enhancer	Placenta	Placenta
22	chr9:136548200-136549200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
23	chr9:136548200-136549200	Enhancers	Left Ventricle	heart
24	chr9:136548200-136549400	Enhancers	Brain Substantia Nigra	brain
25	chr9:136548200-136549600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
26	chr9:136548200-136549600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr9:136548200-136549600	Bivalent Enhancer	Adipose Nuclei	Adipose
28	chr9:136548200-136549600	Enhancers	Colonic Mucosa	Colon
29	chr9:136548200-136549600	Enhancers	Spleen	Spleen
30	chr9:136548200-136549800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr9:136548200-136550000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr9:136548200-136550000	Enhancers	Fetal Intestine Small	intestine
33	chr9:136548200-136550000	Enhancers	Fetal Lung	lung
34	chr9:136548200-136550000	Enhancers	Right Ventricle	heart
35	chr9:136548200-136550200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr9:136548200-136550200	Enhancers	Lung	lung
37	chr9:136548200-136550200	Enhancers	Right Atrium	heart
38	chr9:136548200-136550400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr9:136548200-136550600	Genic enhancers	Fetal Stomach	stomach
40	chr9:136548200-136550800	Enhancers	Brain Germinal Matrix	brain
41	chr9:136548200-136552200	Enhancers	Brain Cingulate Gyrus	brain
42	chr9:136548400-136549200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr9:136548400-136549200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr9:136548400-136549400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr9:136548400-136549400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
46	chr9:136548400-136549400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr9:136548400-136549400	Enhancers	Brain Angular Gyrus	brain
48	chr9:136548400-136549400	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr9:136548400-136549400	Enhancers	Fetal Intestine Large	intestine
50	chr9:136548400-136549400	Enhancers	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links