Variant report

Variant	rs4745451
Chromosome Location	chr9:71597314-71597315
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:71589348..71591998-chr9:71596121..71599178,3	K562	blood:
2	chr9:71584135..71587170-chr9:71595047..71597666,3	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10114872	0.84[CHD][hapmap];0.82[GIH][hapmap]
rs10115155	0.88[EUR][1000 genomes]
rs10117043	0.82[CHD][hapmap];0.91[GIH][hapmap]
rs10117198	0.82[GIH][hapmap]
rs10124169	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10746974	0.82[GIH][hapmap]
rs10746979	0.95[CEU][hapmap];0.84[CHD][hapmap];0.94[GIH][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes]
rs10781264	0.80[CEU][hapmap]
rs10781283	0.95[CEU][hapmap];0.83[TSI][hapmap];0.82[EUR][1000 genomes]
rs10781293	0.90[CEU][hapmap];0.86[EUR][1000 genomes]
rs10869487	0.85[CEU][hapmap]
rs10869541	0.85[CEU][hapmap];0.80[TSI][hapmap]
rs10869574	0.95[CEU][hapmap]
rs10869610	1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs11143802	0.89[CEU][hapmap]
rs11144476	0.95[CEU][hapmap];0.80[CHD][hapmap];0.89[GIH][hapmap]
rs12337140	0.82[CEU][hapmap];0.86[EUR][1000 genomes]
rs12349586	0.88[CEU][hapmap];0.85[GIH][hapmap]
rs12379823	0.91[GIH][hapmap];0.81[MEX][hapmap]
rs2027205	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs2152649	0.90[CEU][hapmap];0.80[TSI][hapmap];0.81[EUR][1000 genomes]
rs2309384	0.88[EUR][1000 genomes]
rs6560420	0.95[CEU][hapmap]
rs6560444	0.95[CEU][hapmap];0.83[TSI][hapmap];0.82[EUR][1000 genomes]
rs7018692	0.95[CEU][hapmap];0.88[GIH][hapmap];0.83[TSI][hapmap]
rs7020192	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7021212	0.90[CEU][hapmap];0.82[EUR][1000 genomes]
rs7031059	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7040120	0.85[GIH][hapmap]
rs7048167	0.92[ASN][1000 genomes]
rs756326	0.84[EUR][1000 genomes]
rs7852633	0.89[CEU][hapmap]
rs7853501	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs7867240	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422258	chr9:71234845-71663340	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv1017903	chr9:71276951-71690579	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1051723	chr9:71398713-71971285	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1053402	chr9:71399722-71819949	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
5	nsv540146	chr9:71399722-71819949	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv1043689	chr9:71399922-71800338	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	nsv540147	chr9:71399922-71800338	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS 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	27 gene(s)	inside rSNPs	diseases
8	nsv1047540	chr9:71401918-71803639	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
9	nsv931684	chr9:71417110-71957723	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	nsv1049175	chr9:71418242-71986910	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	nsv466393	chr9:71453443-71704827	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv614547	chr9:71453443-71704827	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
13	nsv1035823	chr9:71465139-71901672	Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
14	nsv466396	chr9:71471912-71935577	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
15	nsv614548	chr9:71471912-71935577	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
16	nsv614549	chr9:71506459-71659280	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
17	nsv1051798	chr9:71511805-71792032	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
18	nsv1035477	chr9:71511927-71959487	Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
19	esv1833433	chr9:71544920-71598165	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
20	nsv466397	chr9:71574757-71843023	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
21	nsv614550	chr9:71574757-71843023	Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
22	nsv1050692	chr9:71578494-71843023	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4745451	FAM108B1	cis	cerebellum	SCAN
rs4745451	PGM5	cis	cerebellum	SCAN

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71590800-71597400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr9:71590800-71606400	Weak transcription	Stomach Mucosa	stomach
3	chr9:71592000-71598000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:71593000-71597800	Enhancers	K562	blood
5	chr9:71593600-71606200	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr9:71594600-71597400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:71594600-71597400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr9:71594600-71597400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr9:71594600-71597400	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr9:71594800-71598000	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:71594800-71628400	Weak transcription	Spleen	Spleen
12	chr9:71595000-71598400	Enhancers	Colon Smooth Muscle	Colon
13	chr9:71595000-71600600	Weak transcription	Primary B cells from cord blood	blood
14	chr9:71595200-71598000	Weak transcription	Right Ventricle	heart
15	chr9:71595200-71598600	Weak transcription	Fetal Intestine Large	intestine
16	chr9:71595200-71606400	Weak transcription	Lung	lung
17	chr9:71595200-71628000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:71595200-71631600	Weak transcription	Gastric	stomach
19	chr9:71595400-71599800	Weak transcription	Fetal Intestine Small	intestine
20	chr9:71595400-71600400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr9:71595600-71597800	Weak transcription	HepG2	liver
22	chr9:71595600-71598000	Weak transcription	Fetal Brain Male	brain
23	chr9:71595600-71598600	Weak transcription	Right Atrium	heart
24	chr9:71595800-71626200	Weak transcription	Colonic Mucosa	Colon
25	chr9:71596200-71597800	Enhancers	Fetal Heart	heart
26	chr9:71596200-71598600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr9:71596200-71612200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:71596600-71597400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr9:71596600-71597400	Enhancers	Psoas Muscle	Psoas
30	chr9:71596800-71597400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr9:71596800-71599000	Enhancers	Left Ventricle	heart
32	chr9:71596800-71599400	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr9:71597000-71597400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:71597000-71597400	Enhancers	Fetal Stomach	stomach
35	chr9:71597000-71599400	Enhancers	Brain Germinal Matrix	brain
36	chr9:71597000-71609200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr9:71597200-71597600	Enhancers	GM12878-XiMat	blood
38	chr9:71597200-71598200	Weak transcription	Fetal Kidney	kidney
39	chr9:71597200-71598200	Weak transcription	Pancreas	Pancrea
40	chr9:71597200-71598200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr9:71597200-71598200	Enhancers	Rectal Smooth Muscle	rectum
42	chr9:71597200-71599000	Enhancers	Primary hematopoietic stem cells	blood
43	chr9:71597200-71600200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr9:71597200-71605800	Weak transcription	Primary B cells from peripheral blood	blood
45	chr9:71597200-71606000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr9:71597200-71613000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr9:71597200-71626000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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