Variant report

Variant	rs73655814
Chromosome Location	chr9:115940047-115940048
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:115932248..115934923-chr9:115939803..115942130,2	MCF-7	breast:
2	chr9:115938881..115940407-chr9:115956072..115958715,2	MCF-7	breast:
3	chr9:115935268..115937947-chr9:115939386..115941079,2	K562	blood:
4	chr9:115938010..115940553-chr9:115943307..115944894,2	MCF-7	breast:
5	chr9:115929834..115932137-chr9:115938047..115940360,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10114293	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10117100	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10118727	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10118914	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10123301	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981672	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981682	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1133618	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1133619	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1133620	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12339424	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12344443	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16912536	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16927031	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28790397	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28790632	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28830537	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28887481	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28891677	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4333682	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4378033	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4407968	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4490910	0.84[EUR][1000 genomes]
rs4548256	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5015972	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55660432	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7029139	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7029228	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7029472	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7030027	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7033282	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7034425	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7035169	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7038133	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73550301	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73552213	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73655844	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73655845	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7852613	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7865445	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7865584	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7865650	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7866432	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7874583	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9722731	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758198	chr9:115240454-116002951	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759710	chr9:115240454-116002951	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription 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	71 gene(s)	inside rSNPs	diseases
4	nsv1035406	chr9:115883978-116003980	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv540201	chr9:115883978-116003980	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv1042663	chr9:115920158-116167140	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
7	nsv893744	chr9:115934852-116170227	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs73655814	FKBP15	cis	brain	BrainEAC

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115917800-115949400	Strong transcription	Placenta	Placenta
2	chr9:115918400-115947200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr9:115919200-115950800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr9:115919400-115950800	Strong transcription	Primary T cells from cord blood	blood
5	chr9:115919400-115954200	Strong transcription	Fetal Intestine Large	intestine
6	chr9:115919600-115940200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr9:115920000-115942400	Strong transcription	Duodenum Mucosa	Duodenum
8	chr9:115920000-115950200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr9:115920000-115951400	Strong transcription	Fetal Muscle Trunk	muscle
10	chr9:115920000-115970200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:115920000-115973400	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr9:115920200-115956600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr9:115920400-115973400	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr9:115920600-115941600	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr9:115920800-115966400	Strong transcription	Dnd41	blood
16	chr9:115920800-115975000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr9:115921800-115951000	Strong transcription	Fetal Thymus	thymus
18	chr9:115922400-115942000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr9:115922800-115956400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr9:115923000-115942200	Strong transcription	GM12878-XiMat	blood
21	chr9:115923000-115956200	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr9:115923200-115940800	Strong transcription	NHEK	skin
23	chr9:115923400-115941800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr9:115923400-115976400	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr9:115923600-115953600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr9:115923800-115950600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr9:115923800-115951600	Strong transcription	HepG2	liver
28	chr9:115924000-115965800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr9:115924200-115969600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:115925200-115940800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr9:115926000-115956200	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr9:115926400-115941200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr9:115926600-115951000	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr9:115927200-115953600	Strong transcription	Fetal Lung	lung
35	chr9:115927600-115940400	Strong transcription	HSMM	muscle
36	chr9:115927600-115941200	Strong transcription	Cortex derived primary cultured neurospheres	brain
37	chr9:115927600-115949400	Strong transcription	Adipose Nuclei	Adipose
38	chr9:115927600-115973400	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr9:115927800-115940200	Strong transcription	Muscle Satellite Cultured Cells	--
40	chr9:115927800-115951000	Strong transcription	Duodenum Smooth Muscle	Duodenum
41	chr9:115928000-115940200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr9:115929200-115941400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:115929400-115951400	Strong transcription	Liver	Liver
44	chr9:115929800-115950000	Strong transcription	Primary hematopoietic stem cells	blood
45	chr9:115931800-115946600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr9:115932000-115945000	Weak transcription	Stomach Mucosa	stomach
47	chr9:115932200-115942200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:115932200-115945000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr9:115933400-115944200	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr9:115935200-115940400	Strong transcription	Primary B cells from peripheral blood	blood

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