Variant report

Variant	rs9411203
Chromosome Location	chr9:71815392-71815393
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr9:71814940-71815427	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr9:71815254-71815423	HepG2	liver:	n/a	n/a
3	CTCF	chr9:71815091-71815439	MCF-7	breast:	n/a	n/a
4	CEBPB	chr9:71815046-71815401	IMR90	lung:	n/a	n/a
5	MYC	chr9:71815372-71815412	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr9:71815320-71815470	GM12869	blood:	n/a	n/a
7	POLR2A	chr9:71815382-71815456	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71813787..71816021-chr9:71816458..71819040,2	K562	blood:
2	chr9:71733939..71735989-chr9:71814942..71816605,2	MCF-7	breast:
3	chr9:71812890..71815440-chr9:71822433..71824150,2	MCF-7	breast:
4	chr9:71814337..71816203-chr9:71818025..71821433,3	MCF-7	breast:

No data

Variant related genes	Relation type
TJP2	TF binding region
ENSG00000119139	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10156634	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10156651	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10735653	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10781434	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10781435	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11791970	1.00[ASN][1000 genomes]
rs12551317	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12551566	1.00[ASN][1000 genomes]
rs12553945	1.00[ASN][1000 genomes]
rs12555245	1.00[ASN][1000 genomes]
rs2498437	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2993817	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2993822	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3002381	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34774441	1.00[ASN][1000 genomes]
rs41277913	1.00[ASN][1000 genomes]
rs4567104	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4745625	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4745626	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4745627	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62567098	1.00[ASN][1000 genomes]
rs62567099	1.00[ASN][1000 genomes]
rs6560586	0.88[EUR][1000 genomes]
rs6560593	0.81[AMR][1000 genomes]
rs7020849	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7030890	0.88[EUR][1000 genomes]
rs7875573	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9411187	1.00[ASN][1000 genomes]
rs9411202	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	nsv893416	chr9:71597840-71888601	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised 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	21 gene(s)	inside rSNPs	diseases
14	nsv1040539	chr9:71600042-71844108	Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
15	nsv540149	chr9:71600042-71844108	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
16	nsv949664	chr9:71607398-71842391	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv948708	chr9:71632265-71842391	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv817209	chr9:71675454-71829412	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
19	nsv817406	chr9:71675454-72179318	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
20	nsv893427	chr9:71762766-71858517	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71790400-71832200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr9:71790400-71835600	Weak transcription	Colonic Mucosa	Colon
3	chr9:71797200-71832000	Weak transcription	Esophagus	oesophagus
4	chr9:71804000-71831800	Weak transcription	Aorta	Aorta
5	chr9:71805000-71817000	Enhancers	Brain Substantia Nigra	brain
6	chr9:71805200-71815400	Enhancers	Fetal Heart	heart
7	chr9:71805400-71817000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr9:71806600-71816200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr9:71806600-71819000	Weak transcription	Fetal Kidney	kidney
10	chr9:71807400-71832200	Weak transcription	Primary T cells from cord blood	blood
11	chr9:71807800-71842800	Weak transcription	Small Intestine	intestine
12	chr9:71808000-71819200	Weak transcription	NHLF	lung
13	chr9:71808200-71816200	Weak transcription	Duodenum Mucosa	Duodenum
14	chr9:71808200-71819000	Weak transcription	Fetal Stomach	stomach
15	chr9:71808200-71819200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr9:71809000-71816600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr9:71810400-71832400	Weak transcription	GM12878-XiMat	blood
18	chr9:71810600-71818800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr9:71811000-71817200	Enhancers	Brain Hippocampus Middle	brain
20	chr9:71811000-71819000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:71811200-71822400	Weak transcription	Pancreas	Pancrea
22	chr9:71811600-71815800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr9:71811600-71819400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr9:71812200-71815400	Enhancers	K562	blood
25	chr9:71812400-71817000	Genic enhancers	HepG2	liver
26	chr9:71812600-71815600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr9:71812600-71815600	Enhancers	Right Ventricle	heart
28	chr9:71812600-71816400	Enhancers	Left Ventricle	heart
29	chr9:71812800-71815600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr9:71812800-71815800	Enhancers	Liver	Liver
31	chr9:71813000-71819000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr9:71813200-71815400	Enhancers	Stomach Mucosa	stomach
33	chr9:71813200-71815600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr9:71813400-71815600	Enhancers	Ovary	ovary
35	chr9:71813400-71819000	Weak transcription	Placenta	Placenta
36	chr9:71813600-71815600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr9:71813600-71819200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr9:71813800-71818800	Weak transcription	Brain Anterior Caudate	brain
39	chr9:71814000-71816000	Enhancers	Brain Cingulate Gyrus	brain
40	chr9:71814000-71818800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:71814200-71815400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr9:71814200-71815400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr9:71814200-71815400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr9:71814200-71815600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr9:71814200-71815600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:71814200-71815800	Enhancers	Primary T cells fromperipheralblood	blood
47	chr9:71814200-71816000	Enhancers	Brain Angular Gyrus	brain
48	chr9:71814200-71816000	Strong transcription	Fetal Intestine Small	intestine
49	chr9:71814200-71816600	Enhancers	Lung	lung
50	chr9:71814400-71815400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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