Variant report

Variant	nsv893439
Chromosome Location	chr9:72500956-72568962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:913)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:72547942-72548142	HepG2	liver:	n/a	n/a
2	ATF1	chr9:72551434-72551710	K562	blood:	n/a	n/a
3	ATF3	chr9:72561761-72562186	HCT-116	colon:	n/a	n/a
4	ATF3	chr9:72551440-72551684	K562	blood:	n/a	n/a
5	ATF3	chr9:72561686-72562065	K562	blood:	n/a	n/a
6	ATF3	chr9:72561624-72562128	HCT-116	colon:	n/a	n/a
7	BACH1	chr9:72514740-72514755	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr9:72540793-72540973	GM12878	blood:	n/a	n/a
9	BRCA1	chr9:72546453-72546462	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr9:72513598-72514297	HCT-116	colon:	n/a	n/a
11	CBX3	chr9:72561650-72562184	HCT-116	colon:	n/a	n/a
12	CBX3	chr9:72561555-72562148	HCT-116	colon:	n/a	n/a
13	CBX3	chr9:72548472-72548697	K562	blood:	n/a	n/a
14	CEBPB	chr9:72544106-72544301	IMR90	lung:	n/a	chr9:72544208-72544219
15	CEBPB	chr9:72552432-72552778	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:72561755-72562059	K562	blood:	n/a	chr9:72561929-72561940
17	CEBPB	chr9:72509814-72509856	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:72504152-72504319	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:72544196-72544220	H1-hESC	embryonic stem cell:	n/a	chr9:72544208-72544219
20	CEBPB	chr9:72564251-72564632	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:72561495-72562305	HCT-116	colon:	n/a	chr9:72561929-72561940
22	CEBPB	chr9:72505957-72506205	A549	lung:	n/a	chr9:72506059-72506070
23	CEBPB	chr9:72561610-72562125	Hela-S3	cervix:	n/a	chr9:72561929-72561940
24	CEBPB	chr9:72534818-72535045	HepG2	liver:	n/a	chr9:72534986-72534997
25	CEBPB	chr9:72553184-72553382	A549	lung:	n/a	n/a
26	CEBPB	chr9:72513639-72514234	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:72551252-72551687	IMR90	lung:	n/a	n/a
28	CEBPB	chr9:72513524-72514336	HCT-116	colon:	n/a	n/a
29	CEBPB	chr9:72526659-72526834	A549	lung:	n/a	n/a
30	CEBPB	chr9:72534905-72535124	K562	blood:	n/a	chr9:72534986-72534997
31	CEBPB	chr9:72561682-72562077	A549	lung:	n/a	chr9:72561929-72561940
32	CEBPB	chr9:72505931-72506206	HepG2	liver:	n/a	chr9:72506059-72506070
33	CEBPB	chr9:72561798-72562067	HepG2	liver:	n/a	chr9:72561929-72561940
34	CEBPB	chr9:72513117-72513260	H1-hESC	embryonic stem cell:	n/a	chr9:72513179-72513192
35	CEBPB	chr9:72513030-72513315	HepG2	liver:	n/a	chr9:72513289-72513300 chr9:72513179-72513192
36	CEBPB	chr9:72544067-72544275	A549	lung:	n/a	chr9:72544208-72544219
37	CEBPB	chr9:72552499-72552748	A549	lung:	n/a	n/a
38	CEBPB	chr9:72513039-72513361	IMR90	lung:	n/a	chr9:72513289-72513300 chr9:72513179-72513192
39	CEBPB	chr9:72561616-72562248	HCT-116	colon:	n/a	chr9:72561929-72561940
40	CEBPB	chr9:72544172-72544225	HepG2	liver:	n/a	chr9:72544208-72544219
41	CEBPB	chr9:72560547-72561073	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:72513027-72513373	Hela-S3	cervix:	n/a	chr9:72513289-72513300 chr9:72513179-72513192
43	CEBPB	chr9:72513618-72514318	A549	lung:	n/a	n/a
44	CEBPB	chr9:72561597-72562165	A549	lung:	n/a	chr9:72561929-72561940
45	CEBPB	chr9:72546261-72546424	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr9:72561631-72562122	IMR90	lung:	n/a	chr9:72561929-72561940
47	CEBPB	chr9:72561701-72562037	K562	blood:	n/a	chr9:72561929-72561940
48	CEBPB	chr9:72560624-72560843	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr9:72561727-72562130	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr9:72529145-72529292	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72560940-72560990	GM12878	blood:	n/a
2	chr9:72560940-72560990	H1-hESC	embryonic stem cell:	embryo
3	chr9:72560940-72560990	BE2_C	brain:	n/a
4	chr9:72514243-72514293	IMR90	lung:	fetal
5	chr9:72514243-72514293	HCT-116	colon:	n/a
6	chr9:72514243-72514293	NH-A	brain:	n/a
7	chr9:72560940-72560990	HPAEpiC	pulmonary alveolar:	n/a
8	chr9:72514243-72514293	PANC-1	pancreas:	n/a
9	chr9:72560940-72560990	RPTEC	kidney:	n/a
10	chr9:72514243-72514293	HCM	heart:	n/a
11	chr9:72514243-72514293	HNPCEpiC	eye:	n/a
12	chr9:72514243-72514293	HRE	kidney:	n/a
13	chr9:72560940-72560990	LNCaP	prostate:	n/a
14	chr9:72514243-72514293	HEEpiC	esophagus:	n/a
15	chr9:72560940-72560990	NH-A	brain:	n/a
16	chr9:72560940-72560990	AG04450	lung:	fetal
17	chr9:72514243-72514293	U87	brain:	n/a
18	chr9:72560940-72560990	HCPEpiC	choroid plexus:	n/a
19	chr9:72560940-72560990	HNPCEpiC	eye:	n/a
20	chr9:72560940-72560990	AoSMC	blood vessel:	n/a
21	chr9:72560940-72560990	AG09319	gingival:	n/a
22	chr9:72560940-72560990	GM06990	blood:	n/a
23	chr9:72514243-72514293	MCF-7	breast:	n/a
24	chr9:72560940-72560990	Caco-2	colon:	n/a
25	chr9:72514243-72514293	K562	blood:	n/a
26	chr9:72514243-72514293	NHBE	bronchial:	n/a
27	chr9:72560940-72560990	SK-N-SH_RA	brain:	n/a
28	chr9:72514243-72514293	HepG2	liver:	n/a
29	chr9:72560940-72560990	NHBE	bronchial:	n/a
30	chr9:72560940-72560990	SAEC	small airway:	n/a
31	chr9:72560940-72560990	HCF	heart:	n/a
32	chr9:72514243-72514293	Hepatocyte	liver:	n/a
33	chr9:72514243-72514293	HCF	heart:	n/a
34	chr9:72514243-72514293	GM12878	blood:	n/a
35	chr9:72514243-72514293	NB4	blood:	n/a
36	chr9:72514243-72514293	Caco-2	colon:	n/a
37	chr9:72560940-72560990	HMEC	breast:	n/a
38	chr9:72560940-72560990	Jurkat	blood:	n/a
39	chr9:72560940-72560990	PFSK-1	brain:	n/a
40	chr9:72560940-72560990	NHDF-neo	bronchial:	n/a
41	chr9:72514243-72514293	GM12891	blood:	n/a
42	chr9:72560940-72560990	PrEC	prostate:	n/a
43	chr9:72514243-72514293	SK-N-SH	brain:	n/a
44	chr9:72514243-72514293	BJ	skin:	n/a
45	chr9:72560940-72560990	NT2-D1	testis:	n/a
46	chr9:72514243-72514293	AG10803	skin:	n/a
47	chr9:72514243-72514293	RPTEC	kidney:	n/a
48	chr9:72514243-72514293	HEK293	kidney:	embryo
49	chr9:72560940-72560990	AG10803	skin:	n/a
50	chr9:72514243-72514293	HL-60	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:72533081..72534901-chr9:72537488..72539273,2	MCF-7	breast:
2	chr9:72371606..72373829-chr9:72533135..72535747,2	MCF-7	breast:
3	chr9:72552090..72553965-chr9:72554095..72555858,2	K562	blood:
4	chr9:72554296..72556311-chr9:72558075..72560208,2	K562	blood:
5	chr9:72513695..72515625-chr9:72515816..72518282,2	K562	blood:
6	chr9:72505375..72507864-chr9:72508984..72510952,2	K562	blood:
7	chr9:72533081..72534901-chr9:72537488..72539273,2	MCF-7	breast:
8	chr9:72554296..72556311-chr9:72558075..72560208,2	K562	blood:
9	chr9:72480266..72482674-chr9:72527396..72529225,2	K562	blood:
10	chr9:72513695..72515625-chr9:72515816..72518282,2	K562	blood:
11	chr9:72373598..72376289-chr9:72500894..72503778,2	K562	blood:
12	chr9:72512582..72514126-chr9:72872792..72874503,2	MCF-7	breast:
13	chr9:72505375..72507864-chr9:72508984..72510952,2	K562	blood:
14	chr9:72287397..72288112-chr9:72533825..72535064,5	MCF-7	breast:
15	chr9:72287443..72288006-chr9:72547582..72548391,2	K562	blood:
16	chr9:72552090..72553965-chr9:72554095..72555858,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAMDC2-3	chr9:72501754-72501811	NONHSAT131791
2	lnc-MAMDC2-3	chr9:72520870-72521143	NONHSAT131791

No data

Variant related genes	Relation type
RN7SL570P	TF binding region
RN7SL570P	CpG island
ENSG00000268364	chromatin interactions
ENSG00000198887	chromatin interactions
ENSG00000261447	chromatin interactions
ENSG00000188647	chromatin interactions

Extended variants
information (count: 2280 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2280 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10868234	chr9:72500956-72500957	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558741339	chr9:72500957-72500958	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs577045467	chr9:72500960-72500961	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs139098318	chr9:72500965-72500966	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs145082891	chr9:72500999-72501000	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs182596290	chr9:72501037-72501038	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541858112	chr9:72501042-72501043	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs563339538	chr9:72501079-72501080	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs185089322	chr9:72501116-72501117	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs573014913	chr9:72501124-72501125	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565509035	chr9:72501132-72501133	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs140285810	chr9:72501145-72501146	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375672966	chr9:72501157-72501158	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs201016314	chr9:72501160-72501161	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373011704	chr9:72501172-72501173	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs566252650	chr9:72501185-72501186	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144550527	chr9:72501191-72501192	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548198512	chr9:72501207-72501208	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs72723254	chr9:72501264-72501265	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs376210066	chr9:72501313-72501314	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs148895536	chr9:72501347-72501348	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs578238353	chr9:72501352-72501353	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs4258059	chr9:72501377-72501378	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs10435948	chr9:72501445-72501446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs4744948	chr9:72501455-72501456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs74640881	chr9:72501459-72501460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs4744949	chr9:72501492-72501493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs4237236	chr9:72501591-72501592	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs541819488	chr9:72501660-72501661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs557024283	chr9:72501661-72501662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542871095	chr9:72501682-72501683	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs4407955	chr9:72501698-72501699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs369519722	chr9:72501712-72501713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564029894	chr9:72501721-72501722	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369800889	chr9:72501723-72501724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201193659	chr9:72501738-72501739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541280576	chr9:72501760-72501761	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs144962381	chr9:72501768-72501769	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs138837310	chr9:72501775-72501776	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs142028833	chr9:72501780-72501781	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs181590821	chr9:72501791-72501792	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs372834896	chr9:72501792-72501793	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs377248041	chr9:72501826-72501827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs201215177	chr9:72501827-72501828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143557522	chr9:72501875-72501876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs150972567	chr9:72501920-72501921	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs4548246	chr9:72501962-72501963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545041721	chr9:72501983-72501984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564831439	chr9:72501987-72501988	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs537354009	chr9:72502019-72502020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Autism	21484199	CNVD
Breast cancer	22737080	CNVD
Malignant peripheral nerve sheath tumor	22811580	CNVD
Leprosy	22719964	CNVD
Primary ovarian insufficiency	22879975	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72498400-72506800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:72499200-72501200	Enhancers	Psoas Muscle	Psoas
3	chr9:72499200-72501600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:72499200-72501800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr9:72499200-72502200	Enhancers	HMEC	breast
6	chr9:72499400-72505400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr9:72499800-72501600	Enhancers	Hela-S3	cervix
8	chr9:72499800-72501600	Enhancers	HUVEC	blood vessel
9	chr9:72499800-72501600	Enhancers	NHEK	skin
10	chr9:72500000-72501200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:72500000-72501200	Enhancers	Liver	Liver
12	chr9:72500200-72501000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr9:72500200-72501000	Enhancers	Osteobl	bone
14	chr9:72500200-72501200	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr9:72500200-72501200	Enhancers	HSMM	muscle
16	chr9:72500400-72501000	Enhancers	Brain Cingulate Gyrus	brain
17	chr9:72500400-72501000	Enhancers	Brain Hippocampus Middle	brain
18	chr9:72500400-72501000	Enhancers	NH-A	brain
19	chr9:72500400-72501200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:72500400-72501200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:72500400-72501200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr9:72500400-72501200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr9:72500400-72501200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr9:72500400-72501200	Enhancers	Brain Anterior Caudate	brain
25	chr9:72500400-72501600	Enhancers	Brain Angular Gyrus	brain
26	chr9:72500600-72501000	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr9:72500600-72501000	Flanking Active TSS	A549	lung
28	chr9:72500600-72501200	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr9:72500600-72501400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:72500600-72501400	Enhancers	Fetal Heart	heart
31	chr9:72500600-72501600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:72500600-72508000	Weak transcription	Right Ventricle	heart
33	chr9:72500800-72509400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:72500800-72512800	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr9:72501000-72501200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr9:72501000-72501400	Flanking Active TSS	Brain Cingulate Gyrus	brain
37	chr9:72501000-72501400	Flanking Active TSS	Brain Hippocampus Middle	brain
38	chr9:72501000-72501400	Enhancers	A549	lung
39	chr9:72501000-72509400	Weak transcription	Osteobl	bone
40	chr9:72501200-72501600	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr9:72501200-72506600	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr9:72501200-72507200	Weak transcription	Psoas Muscle	Psoas
43	chr9:72501200-72508200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr9:72501200-72509600	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr9:72501200-72512600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr9:72501400-72501600	Enhancers	Brain Hippocampus Middle	brain
47	chr9:72501400-72501800	Enhancers	Brain Cingulate Gyrus	brain
48	chr9:72501400-72504000	Weak transcription	A549	lung
49	chr9:72501400-72505600	Weak transcription	Fetal Heart	heart
50	chr9:72501600-72504200	Weak transcription	Hela-S3	cervix

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