Variant report

Variant	esv3407157
Chromosome Location	chr9:140409531-140414029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:140413661-140413862	K562	blood:	n/a	n/a
2	ATF3	chr9:140412120-140413744	K562	blood:	n/a	n/a
3	ATF3	chr9:140411303-140411539	K562	blood:	n/a	n/a
4	ATF3	chr9:140411269-140411670	K562	blood:	n/a	n/a
5	BHLHE40	chr9:140413599-140414372	K562	blood:	n/a	n/a
6	CBX3	chr9:140413277-140413859	K562	blood:	n/a	n/a
7	CEBPB	chr9:140413585-140413601	A549	lung:	n/a	n/a
8	CEBPB	chr9:140413462-140413696	IMR90	lung:	n/a	chr9:140413648-140413656
9	E2F6	chr9:140409360-140409804	H1-hESC	embryonic stem cell:	n/a	chr9:140409523-140409535
10	E2F6	chr9:140409424-140409597	K562	blood:	n/a	chr9:140409523-140409535
11	E2F6	chr9:140409356-140409652	H1-hESC	embryonic stem cell:	n/a	chr9:140409523-140409535
12	E2F6	chr9:140413628-140413831	K562	blood:	n/a	n/a
13	EGR1	chr9:140409862-140410029	K562	blood:	n/a	n/a
14	EP300	chr9:140411532-140412646	GM12878	blood:	n/a	n/a
15	ESR1	chr9:140408300-140409532	T-47D	breast:	n/a	n/a
16	FOS	chr9:140413497-140413820	MCF10A-Er-Src	breast:	n/a	chr9:140413722-140413734 chr9:140413722-140413733 chr9:140413727-140413734 chr9:140413723-140413733 chr9:140413619-140413629 chr9:140413723-140413732
17	FOS	chr9:140413458-140413879	MCF10A-Er-Src	breast:	n/a	chr9:140413722-140413734 chr9:140413722-140413733 chr9:140413727-140413734 chr9:140413723-140413733 chr9:140413619-140413629 chr9:140413723-140413732
18	FOS	chr9:140413566-140413839	MCF10A-Er-Src	breast:	n/a	chr9:140413722-140413734 chr9:140413722-140413733 chr9:140413727-140413734 chr9:140413723-140413733 chr9:140413619-140413629 chr9:140413723-140413732
19	FOS	chr9:140413566-140413772	MCF10A-Er-Src	breast:	n/a	chr9:140413722-140413734 chr9:140413722-140413733 chr9:140413727-140413734 chr9:140413723-140413733 chr9:140413619-140413629 chr9:140413723-140413732
20	FOSL1	chr9:140413505-140414000	K562	blood:	n/a	chr9:140413722-140413734 chr9:140413722-140413733 chr9:140413722-140413733 chr9:140413727-140413734 chr9:140413723-140413733 chr9:140413619-140413629 chr9:140413723-140413732
21	FOSL1	chr9:140413595-140413890	K562	blood:	n/a	chr9:140413722-140413734 chr9:140413722-140413733 chr9:140413722-140413733 chr9:140413727-140413734 chr9:140413723-140413733 chr9:140413619-140413629 chr9:140413723-140413732
22	FOSL2	chr9:140411448-140412672	HepG2	liver:	n/a	n/a
23	GABPA	chr9:140411788-140412321	Hela-S3	cervix:	n/a	n/a
24	GABPA	chr9:140412432-140412576	Hela-S3	cervix:	n/a	n/a
25	GABPA	chr9:140411555-140411766	Hela-S3	cervix:	n/a	n/a
26	GABPA	chr9:140411377-140413301	Hela-S3	cervix:	n/a	n/a
27	GABPA	chr9:140409816-140410090	H1-hESC	embryonic stem cell:	n/a	n/a
28	GATA2	chr9:140411388-140412266	K562	blood:	n/a	n/a
29	HEY1	chr9:140411460-140412407	K562	blood:	n/a	n/a
30	IRF4	chr9:140411382-140412729	GM12878	blood:	n/a	n/a
31	JUND	chr9:140413572-140413909	K562	blood:	n/a	chr9:140413722-140413734 chr9:140413722-140413733 chr9:140413727-140413734 chr9:140413723-140413733 chr9:140413619-140413629 chr9:140413723-140413732
32	JUND	chr9:140413612-140413788	HepG2	liver:	n/a	chr9:140413722-140413734 chr9:140413722-140413733 chr9:140413727-140413734 chr9:140413723-140413733 chr9:140413619-140413629 chr9:140413723-140413732
33	MAX	chr9:140409371-140409767	H1-hESC	embryonic stem cell:	n/a	chr9:140409704-140409713 chr9:140409702-140409711 chr9:140409703-140409710
34	MAX	chr9:140413531-140414243	K562	blood:	n/a	chr9:140413724-140413733
35	MAX	chr9:140409370-140409667	K562	blood:	n/a	n/a
36	MAX	chr9:140409386-140409792	A549	lung:	n/a	chr9:140409704-140409713 chr9:140409702-140409711 chr9:140409703-140409710
37	MAX	chr9:140409403-140409700	H1-hESC	embryonic stem cell:	n/a	n/a
38	MAX	chr9:140409322-140409821	MCF-7	breast:	n/a	chr9:140409704-140409713 chr9:140409702-140409711 chr9:140409703-140409710
39	MEF2A	chr9:140413455-140413788	K562	blood:	n/a	chr9:140413653-140413667 chr9:140413652-140413667 chr9:140413654-140413665 chr9:140413653-140413668 chr9:140413652-140413667 chr9:140413655-140413666 chr9:140413651-140413667 chr9:140413655-140413664 chr9:140413648-140413669 chr9:140413724-140413732 chr9:140413652-140413668 chr9:140413648-140413669
40	MYC	chr9:140410958-140411258	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr9:140413596-140413757	MCF10A-Er-Src	breast:	n/a	chr9:140413724-140413733
42	PAX5	chr9:140411433-140412459	GM12878	blood:	n/a	n/a
43	PAX5	chr9:140411321-140412549	GM12878	blood:	n/a	n/a
44	POU2F2	chr9:140411302-140413573	GM12891	blood:	n/a	n/a
45	POU2F2	chr9:140411493-140411769	GM12878	blood:	n/a	n/a
46	POU2F2	chr9:140411830-140412178	GM12878	blood:	n/a	n/a
47	POU2F2	chr9:140412302-140412471	GM12878	blood:	n/a	n/a
48	POU2F2	chr9:140411330-140413470	GM12891	blood:	n/a	n/a
49	POU2F2	chr9:140411309-140413607	GM12878	blood:	n/a	n/a
50	RCOR1	chr9:140413678-140413732	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140409915-140409965	NT2-D1	testis:	n/a
2	chr9:140409915-140409965	HCPEpiC	choroid plexus:	n/a
3	chr9:140409915-140409965	SKMC	muscle:	n/a
4	chr9:140409915-140409965	Hela-S3	cervix:	n/a
5	chr9:140409915-140409965	AG04449	skin:	fetal
6	chr9:140409915-140409965	HPAEpiC	pulmonary alveolar:	n/a
7	chr9:140409915-140409965	ovcar-3	ovarian:	n/a
8	chr9:140409915-140409965	HCF	heart:	n/a
9	chr9:140409915-140409965	ECC-1	luminal epithelium:	n/a
10	chr9:140409915-140409965	BJ	skin:	n/a
11	chr9:140409915-140409965	Jurkat	blood:	n/a
12	chr9:140409915-140409965	H1-hESC	embryonic stem cell:	embryo
13	chr9:140409915-140409965	GM12891	blood:	n/a
14	chr9:140409915-140409965	SK-N-MC	brain:	n/a
15	chr9:140409915-140409965	RPTEC	kidney:	n/a
16	chr9:140409915-140409965	AG09309	skin:	n/a
17	chr9:140409915-140409965	CMK	blood:	n/a
18	chr9:140409915-140409965	HEEpiC	esophagus:	n/a
19	chr9:140409915-140409965	HEK293	kidney:	embryo
20	chr9:140409915-140409965	MCF-7	breast:	n/a
21	chr9:140409915-140409965	Hepatocyte	liver:	n/a
22	chr9:140409915-140409965	GM19239	blood:	n/a
23	chr9:140409915-140409965	GM06990	blood:	n/a
24	chr9:140409915-140409965	IMR90	lung:	fetal
25	chr9:140409915-140409965	LNCaP	prostate:	n/a
26	chr9:140409915-140409965	HRE	kidney:	n/a
27	chr9:140409915-140409965	SK-N-SH_RA	brain:	n/a
28	chr9:140409915-140409965	HUVEC	blood vessel:	n/a
29	chr9:140409915-140409965	MCF10A-Er-Src	breast:	n/a
30	chr9:140409915-140409965	AG04450	lung:	fetal
31	chr9:140409915-140409965	HIPEpiC	eye:	n/a
32	chr9:140409915-140409965	Caco-2	colon:	n/a
33	chr9:140409915-140409965	GM12878	blood:	n/a
34	chr9:140409915-140409965	HNPCEpiC	eye:	n/a
35	chr9:140409915-140409965	GM12892	blood:	n/a
36	chr9:140409915-140409965	HCT-116	colon:	n/a
37	chr9:140409915-140409965	PFSK-1	brain:	n/a
38	chr9:140409915-140409965	NH-A	brain:	n/a
39	chr9:140409915-140409965	HRPEpiC	eye:	n/a
40	chr9:140409915-140409965	NHDF-neo	bronchial:	n/a
41	chr9:140409915-140409965	A549	lung:	n/a
42	chr9:140409915-140409965	PANC-1	pancreas:	n/a
43	chr9:140409915-140409965	K562	blood:	n/a
44	chr9:140409915-140409965	AG10803	skin:	n/a
45	chr9:140409915-140409965	T-47D	breast:	n/a
46	chr9:140409915-140409965	HepG2	liver:	n/a
47	chr9:140409915-140409965	HL-60	blood:	n/a
48	chr9:140409915-140409965	AoSMC	blood vessel:	n/a
49	chr9:140409915-140409965	PrEC	prostate:	n/a
50	chr9:140409915-140409965	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:140407045..140410269-chr9:140412474..140414794,3	MCF-7	breast:
2	chr9:140189647..140191629-chr9:140408835..140411014,2	MCF-7	breast:
3	chr9:140192004..140196032-chr9:140413457..140417425,3	MCF-7	breast:
4	chr9:140352304..140355788-chr9:140405232..140410099,5	MCF-7	breast:
5	chr9:140332776..140334313-chr9:140412829..140415749,2	MCF-7	breast:
6	chr9:140413558..140415139-chr9:140438109..140439773,2	MCF-7	breast:
7	chr9:140386446..140388269-chr9:140413186..140415741,2	K562	blood:
8	chr9:140412465..140415104-chr9:140500104..140501750,2	MCF-7	breast:
9	chr9:140199124..140201769-chr9:140410590..140413646,3	K562	blood:
10	chr9:140385602..140387946-chr9:140412336..140414686,2	K562	blood:
11	chr9:140412905..140414820-chr9:140475554..140478292,2	K562	blood:
12	chr9:140352371..140354173-chr9:140410410..140412850,2	MCF-7	breast:
13	chr9:140408886..140411394-chr9:140412638..140414476,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR85-1	chr9:140412889-140412899	NONHSAT135734
2	lnc-WDR85-1	chr9:140411319-140412418	NONHSAT135734

Variant related genes	Relation type
PNPLA7	TF binding region
PNPLA7	CpG island
ENSG00000130653	chromatin interactions
ENSG00000260996	chromatin interactions
ENSG00000165802	chromatin interactions
ENSG00000197070	chromatin interactions

Extended variants
information (count: 240 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:240 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530666372	chr9:140409534-140409535	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544195442	chr9:140409538-140409539	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs149338533	chr9:140409554-140409555	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs529704568	chr9:140409555-140409556	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546548551	chr9:140409572-140409573	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs377054254	chr9:140409604-140409605	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs371689080	chr9:140409665-140409666	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs843967	chr9:140409726-140409727	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs368059013	chr9:140409727-140409728	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs567254715	chr9:140409735-140409736	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569006707	chr9:140409739-140409740	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs537901338	chr9:140409766-140409767	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375993394	chr9:140409814-140409815	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs367807807	chr9:140409818-140409819	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201315398	chr9:140409837-140409838	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs371745534	chr9:140409841-140409842	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs140581167	chr9:140409842-140409843	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs375373628	chr9:140409853-140409854	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369435624	chr9:140409864-140409865	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs145715625	chr9:140409865-140409866	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs3750379	chr9:140409877-140409878	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs112737127	chr9:140409882-140409883	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs3750378	chr9:140409891-140409892	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs144167030	chr9:140409908-140409909	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs143346074	chr9:140409915-140409916	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs7470764	chr9:140409948-140409949	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs369622448	chr9:140409952-140409953	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147499925	chr9:140409953-140409954	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371479812	chr9:140409957-140409958	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375185516	chr9:140409967-140409968	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs552958298	chr9:140409983-140409984	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs561057616	chr9:140409985-140409986	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs574328549	chr9:140409988-140409989	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs112246271	chr9:140409993-140409994	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs200451754	chr9:140409997-140409998	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs532319723	chr9:140409998-140409999	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs565495466	chr9:140410009-140410010	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs552055887	chr9:140410038-140410039	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs562299972	chr9:140410062-140410063	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs531548278	chr9:140410076-140410077	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs547928208	chr9:140410077-140410078	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs561122936	chr9:140410087-140410088	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs533925088	chr9:140410089-140410090	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs530264983	chr9:140410091-140410092	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs547852444	chr9:140410116-140410117	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571160227	chr9:140410131-140410132	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs191878497	chr9:140410153-140410154	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11137387	chr9:140410267-140410268	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs11137388	chr9:140410268-140410269	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs11137390	chr9:140410298-140410299	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140376800-140444000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:140377000-140437000	Weak transcription	Left Ventricle	heart
3	chr9:140377200-140420200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr9:140388400-140425200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr9:140392000-140425800	Weak transcription	Primary T cells from cord blood	blood
6	chr9:140393000-140417800	Weak transcription	Fetal Brain Female	brain
7	chr9:140393000-140429400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr9:140394000-140419800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr9:140394000-140429200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr9:140394800-140415600	Weak transcription	Brain Angular Gyrus	brain
11	chr9:140395000-140414000	Weak transcription	Brain Substantia Nigra	brain
12	chr9:140396400-140429200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr9:140401400-140413600	Weak transcription	Gastric	stomach
14	chr9:140404000-140413400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr9:140404200-140413800	Weak transcription	Primary B cells from cord blood	blood
16	chr9:140404200-140414000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr9:140404200-140414000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr9:140404200-140415000	Weak transcription	HSMMtube	muscle
19	chr9:140404200-140415600	Weak transcription	Brain Hippocampus Middle	brain
20	chr9:140404200-140420000	Weak transcription	Brain Anterior Caudate	brain
21	chr9:140404200-140429200	Weak transcription	Aorta	Aorta
22	chr9:140404400-140415600	Weak transcription	Lung	lung
23	chr9:140406000-140413800	Weak transcription	Fetal Intestine Small	intestine
24	chr9:140406800-140420000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr9:140407000-140413600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr9:140407000-140414000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr9:140407200-140413400	Weak transcription	K562	blood
28	chr9:140407200-140414000	Weak transcription	Liver	Liver
29	chr9:140407200-140414000	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr9:140408600-140410000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr9:140408600-140410600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr9:140408600-140410600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr9:140408600-140413800	Weak transcription	Colonic Mucosa	Colon
34	chr9:140408600-140444400	Weak transcription	Esophagus	oesophagus
35	chr9:140409000-140413400	Weak transcription	Osteobl	bone
36	chr9:140409200-140410000	Enhancers	Stomach Mucosa	stomach
37	chr9:140409200-140410200	Strong transcription	Right Ventricle	heart
38	chr9:140409200-140410800	Strong transcription	Ovary	ovary
39	chr9:140409400-140409800	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr9:140409400-140410000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr9:140409400-140410000	Strong transcription	Adipose Nuclei	Adipose
42	chr9:140409400-140410000	Strong transcription	Fetal Stomach	stomach
43	chr9:140409400-140410000	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr9:140409400-140410000	Active TSS	Spleen	Spleen
45	chr9:140409400-140410200	Strong transcription	Pancreas	Pancrea
46	chr9:140409400-140410400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr9:140409400-140411000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr9:140409600-140409800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr9:140409800-140410200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr9:140409800-140420000	Weak transcription	Rectal Mucosa Donor 31	rectum

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