Variant report

Variant	rs4744375
Chromosome Location	chr9:97561914-97561915
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:97561245..97563934-chr9:97767178..97770063,2	MCF-7	breast:
2	chr9:97559408..97562110-chr9:97687505..97689946,2	MCF-7	breast:
3	chr9:97558473..97564935-chr9:97678907..97687123,11	MCF-7	breast:

Variant related genes	Relation type
ENSG00000148120	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10217143	0.80[EUR][1000 genomes]
rs10739982	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10739983	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10761351	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10821390	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10821392	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10821393	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10821398	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10821404	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10993344	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11788697	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1867102	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2031698	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4743969	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4744386	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7022894	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7027708	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7847277	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7848139	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893596	chr9:97321172-97598966	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97523400-97563800	Weak transcription	Fetal Kidney	kidney
2	chr9:97530200-97563000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr9:97531600-97563000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:97531600-97563000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:97545400-97567200	Weak transcription	Small Intestine	intestine
6	chr9:97545800-97562200	Weak transcription	Ovary	ovary
7	chr9:97545800-97562200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr9:97545800-97563000	Weak transcription	Adipose Nuclei	Adipose
9	chr9:97545800-97563000	Weak transcription	Gastric	stomach
10	chr9:97545800-97563000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:97545800-97563000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr9:97545800-97563200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:97545800-97567000	Weak transcription	Fetal Brain Female	brain
14	chr9:97546000-97562400	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr9:97548000-97563000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr9:97548200-97562200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr9:97548200-97563600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr9:97548200-97564800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr9:97548400-97563200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr9:97548600-97570400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr9:97549200-97567800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr9:97549600-97562600	Weak transcription	Fetal Thymus	thymus
23	chr9:97549600-97562800	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr9:97550200-97571200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr9:97551400-97562200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr9:97551400-97563000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:97553400-97563000	Weak transcription	Dnd41	blood
28	chr9:97555000-97563000	Weak transcription	Left Ventricle	heart
29	chr9:97555000-97563200	Weak transcription	Right Ventricle	heart
30	chr9:97555200-97562200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr9:97555200-97562200	Weak transcription	HSMMtube	muscle
32	chr9:97555200-97562600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:97555200-97563000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr9:97555200-97563000	Weak transcription	Lung	lung
35	chr9:97555200-97563000	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr9:97555400-97563000	Weak transcription	Spleen	Spleen
37	chr9:97555800-97563000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:97556400-97562600	Weak transcription	Brain Angular Gyrus	brain
39	chr9:97556400-97562600	Weak transcription	Brain Germinal Matrix	brain
40	chr9:97556600-97563000	Weak transcription	Fetal Stomach	stomach
41	chr9:97556600-97563400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr9:97556800-97575800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr9:97557000-97562200	Weak transcription	Brain Substantia Nigra	brain
44	chr9:97557000-97563200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr9:97557200-97563000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr9:97557400-97563000	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr9:97557400-97566800	Weak transcription	Fetal Brain Male	brain
48	chr9:97557400-97567400	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr9:97557600-97562000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:97557600-97562400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links