Variant report

Variant	nsv1037298
Chromosome Location	chr9:72085974-72118434
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	chr9:72109731-72109931	K562	blood:	n/a	n/a
2	BHLHE40	chr9:72089795-72090335	GM12878	blood:	n/a	n/a
3	CEBPB	chr9:72086809-72086957	HepG2	liver:	n/a	chr9:72086839-72086850 chr9:72086837-72086848 chr9:72086837-72086850
4	CTCF	chr9:72106347-72106437	Lung_OC	lung:	n/a	n/a
5	CTCF	chr9:72091968-72092033	HepG2	liver:	n/a	n/a
6	CTCF	chr9:72110540-72110690	A549	lung:	n/a	chr9:72110556-72110574
7	CTCF	chr9:72092014-72092027	MCF-7	breast:	n/a	n/a
8	CTCF	chr9:72091880-72092030	MCF-7	breast:	n/a	n/a
9	CTCF	chr9:72091953-72092043	MCF-7	breast:	n/a	n/a
10	CTCF	chr9:72089523-72089557	Lung_OC	lung:	n/a	n/a
11	CTCF	chr9:72091968-72092057	A549	lung:	n/a	n/a
12	E2F6	chr9:72091544-72092120	H1-hESC	embryonic stem cell:	n/a	n/a
13	EBF1	chr9:72112364-72112592	GM12878	blood:	n/a	chr9:72112535-72112544 chr9:72112534-72112544 chr9:72112533-72112546 chr9:72112533-72112544
14	EBF1	chr9:72089882-72090243	GM12878	blood:	n/a	n/a
15	EP300	chr9:72089847-72090204	GM12878	blood:	n/a	chr9:72090060-72090076
16	EP300	chr9:72091026-72091146	GM12878	blood:	n/a	n/a
17	EP300	chr9:72089781-72090161	GM12878	blood:	n/a	chr9:72090060-72090076
18	EP300	chr9:72089801-72090204	GM12878	blood:	n/a	chr9:72090060-72090076
19	FOS	chr9:72086358-72086899	MCF10A-Er-Src	breast:	n/a	chr9:72086534-72086544 chr9:72086533-72086545 chr9:72086534-72086544 chr9:72086535-72086542 chr9:72086534-72086544 chr9:72086533-72086544 chr9:72086535-72086543 chr9:72086535-72086543
20	FOS	chr9:72117786-72118367	MCF10A-Er-Src	breast:	n/a	chr9:72118116-72118125 chr9:72118115-72118127 chr9:72118117-72118126 chr9:72118116-72118126 chr9:72118115-72118126 chr9:72118118-72118125 chr9:72118089-72118101 chr9:72118116-72118126
21	FOS	chr9:72117672-72118530	MCF10A-Er-Src	breast:	n/a	chr9:72118116-72118125 chr9:72118115-72118127 chr9:72118117-72118126 chr9:72118116-72118126 chr9:72118115-72118126 chr9:72118118-72118125 chr9:72118089-72118101 chr9:72118116-72118126
22	FOS	chr9:72100441-72100748	MCF10A-Er-Src	breast:	n/a	chr9:72100489-72100498 chr9:72100595-72100605 chr9:72100596-72100603 chr9:72100595-72100604 chr9:72100596-72100605
23	FOS	chr9:72086359-72086721	MCF10A-Er-Src	breast:	n/a	chr9:72086534-72086544 chr9:72086533-72086545 chr9:72086534-72086544 chr9:72086535-72086542 chr9:72086534-72086544 chr9:72086533-72086544 chr9:72086535-72086543 chr9:72086535-72086543
24	FOS	chr9:72086364-72086895	MCF10A-Er-Src	breast:	n/a	chr9:72086534-72086544 chr9:72086533-72086545 chr9:72086534-72086544 chr9:72086535-72086542 chr9:72086534-72086544 chr9:72086533-72086544 chr9:72086535-72086543 chr9:72086535-72086543
25	FOS	chr9:72117841-72118332	HUVEC	blood vessel:	n/a	chr9:72118116-72118125 chr9:72118115-72118127 chr9:72118117-72118126 chr9:72118116-72118126 chr9:72118115-72118126 chr9:72118118-72118125 chr9:72118089-72118101 chr9:72118116-72118126
26	FOS	chr9:72100425-72100753	MCF10A-Er-Src	breast:	n/a	chr9:72100489-72100498 chr9:72100595-72100605 chr9:72100596-72100603 chr9:72100595-72100604 chr9:72100596-72100605
27	FOS	chr9:72086314-72086725	HUVEC	blood vessel:	n/a	chr9:72086534-72086544 chr9:72086533-72086545 chr9:72086534-72086544 chr9:72086535-72086542 chr9:72086534-72086544 chr9:72086533-72086544 chr9:72086535-72086543 chr9:72086535-72086543
28	FOS	chr9:72117945-72118277	MCF10A-Er-Src	breast:	n/a	chr9:72118116-72118125 chr9:72118115-72118127 chr9:72118117-72118126 chr9:72118116-72118126 chr9:72118115-72118126 chr9:72118118-72118125 chr9:72118089-72118101 chr9:72118116-72118126
29	FOS	chr9:72117950-72118283	MCF10A-Er-Src	breast:	n/a	chr9:72118116-72118125 chr9:72118115-72118127 chr9:72118117-72118126 chr9:72118116-72118126 chr9:72118115-72118126 chr9:72118118-72118125 chr9:72118089-72118101 chr9:72118116-72118126
30	FOS	chr9:72100508-72100705	MCF10A-Er-Src	breast:	n/a	chr9:72100595-72100604 chr9:72100596-72100605 chr9:72100595-72100605 chr9:72100596-72100603
31	FOS	chr9:72100421-72100761	MCF10A-Er-Src	breast:	n/a	chr9:72100489-72100498 chr9:72100595-72100605 chr9:72100596-72100603 chr9:72100595-72100604 chr9:72100596-72100605
32	FOS	chr9:72086368-72086728	MCF10A-Er-Src	breast:	n/a	chr9:72086534-72086544 chr9:72086533-72086545 chr9:72086534-72086544 chr9:72086535-72086542 chr9:72086534-72086544 chr9:72086533-72086544 chr9:72086535-72086543 chr9:72086535-72086543
33	FOSL2	chr9:72100406-72100792	MCF-7	breast:	n/a	chr9:72100489-72100498 chr9:72100595-72100605 chr9:72100596-72100603 chr9:72100595-72100604 chr9:72100596-72100605
34	FOSL2	chr9:72100485-72100773	MCF-7	breast:	n/a	chr9:72100489-72100498 chr9:72100595-72100605 chr9:72100596-72100603 chr9:72100595-72100604 chr9:72100596-72100605
35	FOSL2	chr9:72100394-72100775	HepG2	liver:	n/a	chr9:72100489-72100498 chr9:72100595-72100605 chr9:72100596-72100603 chr9:72100595-72100604 chr9:72100596-72100605
36	FOSL2	chr9:72086259-72086774	SK-N-SH	brain:	n/a	chr9:72086534-72086544 chr9:72086533-72086545 chr9:72086534-72086544 chr9:72086535-72086542 chr9:72086534-72086544 chr9:72086535-72086543 chr9:72086535-72086543
37	FOSL2	chr9:72117887-72118418	SK-N-SH	brain:	n/a	chr9:72118116-72118125 chr9:72118115-72118127 chr9:72118117-72118126 chr9:72118116-72118126 chr9:72118118-72118125 chr9:72118089-72118101 chr9:72118116-72118126
38	FOXA1	chr9:72092324-72092607	HepG2	liver:	n/a	n/a
39	FOXA2	chr9:72092091-72092834	A549	lung:	n/a	n/a
40	FOXA2	chr9:72092189-72092715	A549	lung:	n/a	n/a
41	GATA2	chr9:72087144-72087721	SH-SY5Y	brain:	n/a	chr9:72087371-72087378 chr9:72087371-72087378 chr9:72087371-72087378 chr9:72087369-72087379
42	GATA2	chr9:72116953-72117211	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr9:72100444-72100709	MCF-7	breast:	n/a	n/a
44	HEY1	chr9:72092356-72092543	K562	blood:	n/a	n/a
45	HEY1	chr9:72092307-72092528	K562	blood:	n/a	n/a
46	JUN	chr9:72087054-72087189	H1-hESC	embryonic stem cell:	n/a	n/a
47	JUN	chr9:72117829-72118311	HUVEC	blood vessel:	n/a	chr9:72118116-72118125 chr9:72118115-72118127 chr9:72118117-72118126 chr9:72118116-72118126 chr9:72118118-72118125 chr9:72118089-72118101 chr9:72118116-72118126
48	JUN	chr9:72086367-72086696	HUVEC	blood vessel:	n/a	chr9:72086534-72086544 chr9:72086533-72086545 chr9:72086534-72086544 chr9:72086535-72086542 chr9:72086534-72086544 chr9:72086535-72086543 chr9:72086535-72086543
49	JUN	chr9:72109200-72109450	HepG2	liver:	n/a	chr9:72109317-72109330
50	JUN	chr9:72107957-72108045	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:72098374..72100350-chr9:72107226..72109233,2	MCF-7	breast:
2	chr9:72098374..72100350-chr9:72107226..72109233,2	MCF-7	breast:
3	chr9:72089155..72091732-chr9:72106824..72109478,2	MCF-7	breast:
4	chr9:72099255..72100862-chr9:72117750..72119500,2	MCF-7	breast:
5	chr9:72113417..72115409-chr9:72425666..72428097,2	K562	blood:
6	chr9:72108434..72110396-chr9:72113331..72115330,2	MCF-7	breast:
7	chr9:72098831..72100503-chr9:72120147..72122522,2	MCF-7	breast:
8	chr9:72086703..72089641-chr9:72090516..72093121,4	MCF-7	breast:
9	chr9:72089279..72091764-chr9:72373318..72374835,2	MCF-7	breast:
10	chr9:72088172..72090177-chr9:72119590..72122551,2	MCF-7	breast:
11	chr9:72108434..72110396-chr9:72113331..72115330,2	MCF-7	breast:
12	chr9:72089155..72091732-chr9:72106824..72109478,2	MCF-7	breast:
13	chr9:72099255..72100862-chr9:72117750..72119500,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM189A2-1	chr9:72109203-72109429	ENSG00000229312.1
2	lnc-FAM189A2-1	chr9:72089179-72089268	ENSG00000229312.2
3	lnc-FAM189A2-1	chr9:72109203-72109429	ENSG00000229312.2
4	lnc-FAM189A2-1	chr9:72087382-72087506	ENSG00000229312.2
5	lnc-FAM189A2-1	chr9:72089179-72089269	ENSG00000229312.1
6	lnc-FAM189A2-1	chr9:72087382-72087506	ENSG00000229312.1

Variant related genes	Relation type
ENSG00000229312	TF binding region
APBA1	TF binding region
ENSG00000229312	chromatin interactions

Extended variants
information (count: 1131 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575281345	chr9:72086013-72086014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146000858	chr9:72086043-72086044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111403332	chr9:72086045-72086046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557867725	chr9:72086067-72086068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189678861	chr9:72086074-72086075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540445825	chr9:72086095-72086096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4744900	chr9:72086114-72086115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561797596	chr9:72086137-72086138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74584038	chr9:72086141-72086142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs76597739	chr9:72086337-72086338	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs562461944	chr9:72086366-72086367	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs532997600	chr9:72086376-72086377	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs545108403	chr9:72086380-72086381	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs148657012	chr9:72086385-72086386	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs528649328	chr9:72086401-72086402	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs547182728	chr9:72086413-72086414	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs1761287	chr9:72086415-72086416	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142879371	chr9:72086456-72086457	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs550904281	chr9:72086488-72086489	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs181019194	chr9:72086491-72086492	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs199523531	chr9:72086584-72086585	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs375570385	chr9:72086620-72086621	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs539479097	chr9:72086679-72086680	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs557804292	chr9:72086702-72086703	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs566973404	chr9:72086728-72086729	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs111671754	chr9:72086741-72086742	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs533707063	chr9:72086811-72086812	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs555540080	chr9:72086820-72086821	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs368834446	chr9:72086850-72086851	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs573797452	chr9:72086873-72086874	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs78183309	chr9:72086874-72086875	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs150650283	chr9:72086901-72086902	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs111680038	chr9:72086957-72086958	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs565974628	chr9:72086976-72086977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs959613	chr9:72087039-72087040	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs959612	chr9:72087066-72087067	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs139755033	chr9:72087085-72087086	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs554971087	chr9:72087157-72087158	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs187208580	chr9:72087194-72087195	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs4744901	chr9:72087236-72087237	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs118169897	chr9:72087238-72087239	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs560074068	chr9:72087260-72087261	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs562299163	chr9:72087305-72087306	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs192003392	chr9:72087379-72087380	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs550843231	chr9:72087403-72087404	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs144666942	chr9:72087437-72087438	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs371702339	chr9:72087530-72087531	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs533123853	chr9:72087587-72087588	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs551368808	chr9:72087620-72087621	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs147874630	chr9:72087696-72087697	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72077200-72086800	Weak transcription	Fetal Brain Male	brain
2	chr9:72079000-72086400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:72079000-72091600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:72079200-72086200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:72080400-72089400	Weak transcription	Fetal Thymus	thymus
6	chr9:72081200-72087000	Weak transcription	Fetal Muscle Trunk	muscle
7	chr9:72081600-72090600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr9:72081800-72086200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr9:72082000-72091000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:72082200-72090600	Weak transcription	Fetal Lung	lung
11	chr9:72082200-72091000	Weak transcription	Fetal Stomach	stomach
12	chr9:72082400-72090200	Weak transcription	Spleen	Spleen
13	chr9:72082400-72091200	Weak transcription	Brain Hippocampus Middle	brain
14	chr9:72082600-72086600	Weak transcription	Fetal Brain Female	brain
15	chr9:72082800-72088000	Enhancers	Liver	Liver
16	chr9:72082800-72091000	Weak transcription	Esophagus	oesophagus
17	chr9:72082800-72091400	Weak transcription	Brain Germinal Matrix	brain
18	chr9:72083000-72087800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr9:72083000-72088200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr9:72083000-72089800	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr9:72083000-72091000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr9:72083200-72086200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr9:72083200-72087200	Weak transcription	Brain Angular Gyrus	brain
24	chr9:72084200-72086400	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr9:72084400-72086000	Enhancers	Fetal Intestine Small	intestine
26	chr9:72084400-72086200	Enhancers	Fetal Intestine Large	intestine
27	chr9:72084400-72087000	Enhancers	Stomach Mucosa	stomach
28	chr9:72084400-72087600	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr9:72085000-72086000	Enhancers	HepG2	liver
30	chr9:72085000-72086800	Enhancers	Duodenum Mucosa	Duodenum
31	chr9:72085200-72086200	Enhancers	A549	lung
32	chr9:72085400-72086000	Strong transcription	Aorta	Aorta
33	chr9:72085600-72086000	Enhancers	Gastric	stomach
34	chr9:72085600-72086000	Enhancers	Left Ventricle	heart
35	chr9:72085600-72086200	Enhancers	Colonic Mucosa	Colon
36	chr9:72085600-72086400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:72085600-72086400	Enhancers	Brain Anterior Caudate	brain
38	chr9:72085600-72087600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr9:72085600-72088000	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr9:72085800-72086000	Enhancers	Brain Substantia Nigra	brain
41	chr9:72085800-72086000	Enhancers	Fetal Muscle Leg	muscle
42	chr9:72085800-72086000	Enhancers	Ovary	ovary
43	chr9:72085800-72086000	Enhancers	Pancreas	Pancrea
44	chr9:72085800-72087200	Enhancers	HUVEC	blood vessel
45	chr9:72086000-72086400	Enhancers	Small Intestine	intestine
46	chr9:72086000-72087000	Weak transcription	Fetal Intestine Small	intestine
47	chr9:72086000-72088800	Weak transcription	Aorta	Aorta
48	chr9:72086000-72089000	Weak transcription	Ovary	ovary
49	chr9:72086000-72089400	Weak transcription	Pancreas	Pancrea
50	chr9:72086000-72090000	Weak transcription	Gastric	stomach

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