Variant report

Variant	rs11140199
Chromosome Location	chr9:86273428-86273429
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:86264014..86266194-chr9:86272774..86275597,2	MCF-7	breast:
2	chr9:86272259..86273802-chr9:86274538..86277129,2	K562	blood:
3	chr9:86272972..86276734-chr9:86321182..86324221,4	K562	blood:
4	chr9:86271855..86273661-chr9:86280180..86281686,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000254473	Chromatin interaction
ENSG00000135018	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11140178	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11140179	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11140182	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11140183	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11140191	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11140192	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11140197	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11140203	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11140215	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11140217	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11140219	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11140225	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11140228	1.00[EUR][1000 genomes]
rs11140229	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11140230	0.92[EUR][1000 genomes]
rs11140235	1.00[EUR][1000 genomes]
rs11140238	1.00[CEU][hapmap]
rs11140248	1.00[EUR][1000 genomes]
rs11140250	1.00[EUR][1000 genomes]
rs11140252	1.00[EUR][1000 genomes]
rs11140254	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11140257	1.00[EUR][1000 genomes]
rs11140258	1.00[EUR][1000 genomes]
rs11140266	0.92[EUR][1000 genomes]
rs11140269	0.85[EUR][1000 genomes]
rs11140270	0.85[EUR][1000 genomes]
rs11559387	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs11560627	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12235151	0.92[EUR][1000 genomes]
rs12235969	1.00[CEU][hapmap]
rs12236455	0.92[EUR][1000 genomes]
rs12236743	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12237262	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12237555	1.00[EUR][1000 genomes]
rs12238365	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12238575	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2282221	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2282222	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2780985	1.00[CHB][hapmap]
rs28627139	1.00[EUR][1000 genomes]
rs28655802	0.86[EUR][1000 genomes]
rs3763626	1.00[EUR][1000 genomes];1.00[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	nsv893512	chr9:86022215-86323309	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers 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	29 gene(s)	inside rSNPs	diseases
2	nsv1044639	chr9:86252505-86412041	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86244800-86278800	Weak transcription	Spleen	Spleen
2	chr9:86244800-86285800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:86252800-86294000	Weak transcription	Small Intestine	intestine
4	chr9:86260600-86300400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr9:86260800-86281400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:86261000-86280200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:86263400-86298800	Strong transcription	Fetal Thymus	thymus
8	chr9:86264400-86280200	Strong transcription	Fetal Muscle Leg	muscle
9	chr9:86264600-86280200	Strong transcription	Adipose Nuclei	Adipose
10	chr9:86264600-86280400	Strong transcription	Fetal Muscle Trunk	muscle
11	chr9:86264600-86280600	Strong transcription	Stomach Smooth Muscle	stomach
12	chr9:86264600-86281400	Strong transcription	HSMMtube	muscle
13	chr9:86264600-86284200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr9:86264600-86284400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:86264600-86297000	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr9:86264800-86279400	Strong transcription	Primary T cells from cord blood	blood
17	chr9:86264800-86280200	Strong transcription	Primary B cells from peripheral blood	blood
18	chr9:86264800-86280200	Strong transcription	Duodenum Mucosa	Duodenum
19	chr9:86264800-86280200	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr9:86264800-86281800	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr9:86264800-86294600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr9:86264800-86295600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:86264800-86298200	Strong transcription	Dnd41	blood
24	chr9:86264800-86300200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr9:86265000-86274000	Strong transcription	Fetal Intestine Large	intestine
26	chr9:86265000-86280000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr9:86265000-86280800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr9:86265000-86282000	Strong transcription	Placenta	Placenta
29	chr9:86265000-86284400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:86265000-86295200	Strong transcription	HSMM	muscle
31	chr9:86265000-86296800	Strong transcription	Liver	Liver
32	chr9:86265000-86298800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr9:86265200-86281400	Strong transcription	NH-A	brain
34	chr9:86265400-86274600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr9:86265400-86285800	Weak transcription	Gastric	stomach
36	chr9:86265600-86277600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:86266000-86281600	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr9:86266000-86283600	Strong transcription	NHDF-Ad	bronchial
39	chr9:86266200-86280600	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr9:86266200-86296000	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr9:86266400-86279800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr9:86266400-86281800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr9:86266400-86298800	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr9:86267000-86274400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr9:86267000-86277600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:86267000-86282200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr9:86267000-86292000	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr9:86267000-86293800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr9:86267200-86276000	Weak transcription	Brain Hippocampus Middle	brain
50	chr9:86267400-86273800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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