Variant report

Variant	rs10985279
Chromosome Location	chr9:100930947-100930948
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:100929714..100931731-chr9:100933494..100935958,2	K562	blood:
2	chr9:100927949..100931625-chr9:100946011..100949394,3	K562	blood:
3	chr9:100930925..100932866-chr9:100942560..100944463,2	K562	blood:
4	chr9:100930862..100931822-chr9:101025607..101026459,2	K562	blood:
5	chr9:100930069..100933063-chr9:100933663..100936506,3	MCF-7	breast:
6	chr9:100921877..100926007-chr9:100929067..100934621,5	K562	blood:
7	chr9:100930731..100932939-chr9:100939830..100941779,2	K562	blood:
8	chr9:100881024..100882919-chr9:100930055..100932510,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000106785	Chromatin interaction
ENSG00000106789	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10818540	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10818581	1.00[YRI][hapmap]
rs10985266	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.90[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10985302	1.00[CEU][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16914196	1.00[YRI][hapmap]
rs17690174	1.00[YRI][hapmap]
rs2417733	0.82[CHD][hapmap]
rs3758261	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3758262	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3780456	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7023194	0.92[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7032570	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7035365	1.00[YRI][hapmap]
rs7847003	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7868004	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482635	chr9:100775549-100953239	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv893613	chr9:100885779-100943397	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1053729	chr9:100909554-100997718	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv520067	chr9:100927161-100978542	Genic enhancers Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100896000-100931000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr9:100898400-100931200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:100909400-100933600	Weak transcription	Colonic Mucosa	Colon
4	chr9:100914600-100931000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr9:100917600-100933400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:100919600-100932200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr9:100920000-100931000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr9:100920400-100942200	Weak transcription	Primary T cells from cord blood	blood
9	chr9:100921800-100935200	Weak transcription	Lung	lung
10	chr9:100922400-100933600	Weak transcription	Gastric	stomach
11	chr9:100924600-100939000	Enhancers	Duodenum Mucosa	Duodenum
12	chr9:100924800-100931600	Weak transcription	Right Atrium	heart
13	chr9:100924800-100935000	Enhancers	Fetal Intestine Large	intestine
14	chr9:100925200-100931200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr9:100926200-100932000	Weak transcription	Esophagus	oesophagus
16	chr9:100926200-100935000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr9:100926800-100934800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr9:100927000-100936800	Weak transcription	Thymus	Thymus
19	chr9:100927200-100931200	Weak transcription	Fetal Thymus	thymus
20	chr9:100928200-100933000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr9:100929000-100932600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr9:100929200-100931000	Weak transcription	Small Intestine	intestine
23	chr9:100929800-100932400	Enhancers	Stomach Mucosa	stomach
24	chr9:100929800-100935800	Enhancers	K562	blood
25	chr9:100930200-100932800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr9:100930400-100931000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr9:100930400-100931200	Enhancers	HepG2	liver
28	chr9:100930400-100932400	Enhancers	HMEC	breast
29	chr9:100930400-100933800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr9:100930600-100931000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr9:100930600-100932200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr9:100930600-100932200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr9:100930600-100932200	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr9:100930600-100932400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr9:100930600-100932400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr9:100930600-100932600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr9:100930600-100932600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr9:100930600-100932600	Enhancers	GM12878-XiMat	blood
39	chr9:100930600-100932800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr9:100930600-100932800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr9:100930600-100933200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr9:100930600-100933800	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr9:100930800-100931000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr9:100930800-100931200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr9:100930800-100931400	Enhancers	Spleen	Spleen
46	chr9:100930800-100932000	Enhancers	Primary B cells from cord blood	blood
47	chr9:100930800-100932000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr9:100930800-100932200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr9:100930800-100932200	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr9:100930800-100932400	Enhancers	Primary T helper naive cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links