Variant report

Variant	nsv831523
Chromosome Location	chr9:18592398-18753451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:567)
CpG islands
(count:244)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:18669020-18669356	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:18705112-18705234	K562	blood:	n/a	n/a
3	ARID3A	chr9:18622195-18622391	HepG2	liver:	n/a	n/a
4	BACH1	chr9:18708496-18708726	H1-hESC	embryonic stem cell:	n/a	chr9:18708633-18708647
5	BACH1	chr9:18606813-18606827	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr9:18658837-18659489	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr9:18650195-18650502	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr9:18658575-18659425	IMR90	lung:	n/a	chr9:18659245-18659262
9	CEBPB	chr9:18632838-18633486	IMR90	lung:	n/a	n/a
10	CEBPB	chr9:18658554-18659633	Hela-S3	cervix:	n/a	chr9:18659245-18659262
11	CEBPB	chr9:18669029-18669318	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:18607910-18608198	HepG2	liver:	n/a	chr9:18608045-18608056
13	CEBPB	chr9:18744024-18744386	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:18607924-18608166	IMR90	lung:	n/a	chr9:18608045-18608056
15	CEBPB	chr9:18668980-18669271	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr9:18668962-18669337	MCF-7	breast:	n/a	n/a
17	CEBPB	chr9:18707138-18707487	HepG2	liver:	n/a	chr9:18707297-18707314
18	CEBPB	chr9:18707301-18707356	K562	blood:	n/a	n/a
19	CEBPB	chr9:18666502-18666830	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:18632787-18632970	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:18707184-18707437	IMR90	lung:	n/a	chr9:18707297-18707314
22	CEBPB	chr9:18607894-18608148	A549	lung:	n/a	chr9:18608045-18608056
23	CEBPB	chr9:18631227-18631419	K562	blood:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
24	CEBPB	chr9:18699795-18700171	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr9:18631153-18631463	HepG2	liver:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
26	CEBPB	chr9:18631140-18631424	IMR90	lung:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
27	CEBPB	chr9:18707230-18707376	A549	lung:	n/a	chr9:18707297-18707314
28	CEBPB	chr9:18597002-18597198	A549	lung:	n/a	chr9:18597079-18597090
29	CEBPB	chr9:18638458-18639249	IMR90	lung:	n/a	n/a
30	CEBPB	chr9:18607360-18607559	HepG2	liver:	n/a	chr9:18607503-18607516 chr9:18607502-18607519 chr9:18607503-18607516 chr9:18607504-18607515 chr9:18607503-18607516 chr9:18607503-18607514
31	CEBPB	chr9:18596902-18597284	Hela-S3	cervix:	n/a	chr9:18597079-18597090
32	CEBPB	chr9:18631285-18631331	A549	lung:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
33	CEBPB	chr9:18596985-18597185	HepG2	liver:	n/a	chr9:18597079-18597090
34	CEBPB	chr9:18596902-18597290	IMR90	lung:	n/a	chr9:18597079-18597090
35	CHD1	chr9:18606430-18606432	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr9:18707401-18707405	HepG2	liver:	n/a	n/a
37	CHD2	chr9:18662583-18662584	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr9:18626180-18626330	HEK293	kidney:	n/a	n/a
39	CTCF	chr9:18703160-18703310	AoAF	blood vessel:	n/a	chr9:18703274-18703292
40	CTCF	chr9:18626214-18626391	LNCaP	prostate:	n/a	n/a
41	CTCF	chr9:18626160-18626310	HRE	kidney:	n/a	n/a
42	CTCF	chr9:18626240-18626390	NHEK	skin:	n/a	n/a
43	CTCF	chr9:18617200-18617350	GM12867	blood:	n/a	n/a
44	CTCF	chr9:18667080-18667230	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr9:18752659-18752701	GM10248	blood:	n/a	n/a
46	CTCF	chr9:18703180-18703330	AG09319	gingival:	n/a	chr9:18703274-18703292
47	CTCF	chr9:18626205-18626366	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr9:18672920-18673070	GM12867	blood:	n/a	n/a
49	CTCF	chr9:18626160-18626310	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr9:18703360-18703510	NHDF-neo	bronchial:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18622331-18622381	SKMC	muscle:	n/a
2	chr9:18727406-18727456	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:18622331-18622381	U87	brain:	n/a
4	chr9:18605667-18605717	LNCaP	prostate:	n/a
5	chr9:18622331-18622381	SK-N-SH	brain:	n/a
6	chr9:18706865-18706915	GM12892	blood:	n/a
7	chr9:18706865-18706915	SKMC	muscle:	n/a
8	chr9:18727406-18727456	A549	lung:	n/a
9	chr9:18727406-18727456	PFSK-1	brain:	n/a
10	chr9:18727406-18727456	GM12892	blood:	n/a
11	chr9:18727406-18727456	T-47D	breast:	n/a
12	chr9:18605667-18605717	HNPCEpiC	eye:	n/a
13	chr9:18727406-18727456	LNCaP	prostate:	n/a
14	chr9:18622331-18622381	GM12892	blood:	n/a
15	chr9:18706865-18706915	LNCaP	prostate:	n/a
16	chr9:18605667-18605717	RPTEC	kidney:	n/a
17	chr9:18605667-18605717	GM12892	blood:	n/a
18	chr9:18727406-18727456	H1-hESC	embryonic stem cell:	embryo
19	chr9:18706865-18706915	HRPEpiC	eye:	n/a
20	chr9:18727406-18727456	U87	brain:	n/a
21	chr9:18727406-18727456	IMR90	lung:	fetal
22	chr9:18727406-18727456	Jurkat	blood:	n/a
23	chr9:18622331-18622381	SAEC	small airway:	n/a
24	chr9:18622331-18622381	ovcar-3	ovarian:	n/a
25	chr9:18605667-18605717	HL-60	blood:	n/a
26	chr9:18605667-18605717	PANC-1	pancreas:	n/a
27	chr9:18727406-18727456	GM19239	blood:	n/a
28	chr9:18706865-18706915	GM12878	blood:	n/a
29	chr9:18706865-18706915	MCF10A-Er-Src	breast:	n/a
30	chr9:18727406-18727456	HepG2	liver:	n/a
31	chr9:18706865-18706915	HCF	heart:	n/a
32	chr9:18622331-18622381	HEEpiC	esophagus:	n/a
33	chr9:18706865-18706915	RPTEC	kidney:	n/a
34	chr9:18605667-18605717	NHDF-neo	bronchial:	n/a
35	chr9:18727406-18727456	Hepatocyte	liver:	n/a
36	chr9:18706865-18706915	AG09309	skin:	n/a
37	chr9:18727406-18727456	AG04450	lung:	fetal
38	chr9:18727406-18727456	PANC-1	pancreas:	n/a
39	chr9:18727406-18727456	HEK293	kidney:	embryo
40	chr9:18706865-18706915	NB4	blood:	n/a
41	chr9:18706865-18706915	IMR90	lung:	fetal
42	chr9:18605667-18605717	GM12878	blood:	n/a
43	chr9:18622331-18622381	NH-A	brain:	n/a
44	chr9:18622331-18622381	HCM	heart:	n/a
45	chr9:18706865-18706915	HNPCEpiC	eye:	n/a
46	chr9:18605667-18605717	HAEpiC	amniotic membrane:	n/a
47	chr9:18622331-18622381	NB4	blood:	n/a
48	chr9:18706865-18706915	HRE	kidney:	n/a
49	chr9:18622331-18622381	HMEC	breast:	n/a
50	chr9:18727406-18727456	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:18733967..18736858-chr9:18739933..18741976,3	MCF-7	breast:
2	chr9:18745157..18747160-chr9:18747921..18750231,2	MCF-7	breast:
3	chr9:18725510..18728390-chr9:18733590..18735848,2	MCF-7	breast:
4	chr9:18705469..18707872-chr9:18709248..18712015,2	MCF-7	breast:
5	chr9:18745157..18747160-chr9:18747921..18750231,2	MCF-7	breast:
6	chr8:61562599..61565494-chr9:18702295..18704681,2	MCF-7	breast:
7	chr9:18725510..18728390-chr9:18733590..18735848,2	MCF-7	breast:
8	chr21:39358274..39359037-chr9:18704805..18705621,2	MCF-7	breast:
9	chr9:18722180..18723810-chr9:18726997..18728852,2	K562	blood:
10	chr9:18734493..18736072-chr9:18736528..18738186,2	MCF-7	breast:
11	chr9:18662167..18665769-chr9:18669383..18672936,3	MCF-7	breast:
12	chr9:18722180..18723810-chr9:18726997..18728852,2	K562	blood:
13	chr9:18662167..18665769-chr9:18669383..18672936,3	MCF-7	breast:
14	chr2:126575127..126575844-chr9:18665491..18666183,2	MCF-7	breast:
15	chr9:18734493..18736072-chr9:18736528..18738186,2	MCF-7	breast:
16	chr9:18733967..18736858-chr9:18739933..18741976,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM154A-3	chr9:18717972-18718524	NONHSAT130313
2	lnc-RRAGA-3	chr9:18651145-18651448	NONHSAT130312

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ADAMTSL1	hsa-miR-132-3p	chr9:18684803-18684824
2	ADAMTSL1	hsa-miR-25-3p	chr9:18681248-18681269
3	ADAMTSL1	hsa-miR-25-3p	chr9:18681336-18681357

Variant related genes	Relation type
RN7SKP258	TF binding region
ADAMTSL1	TF binding region
ENSG00000236857	TF binding region
RN7SKP258	CpG island
ADAMTSL1	CpG island
ENSG00000236857	CpG island
ENSG00000178031	chromatin interactions

Extended variants
information (count: 7461 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:7461 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577079457	chr9:18592406-18592407	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564931061	chr9:18592446-18592447	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138143908	chr9:18592452-18592453	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545529727	chr9:18592466-18592467	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141074781	chr9:18592470-18592471	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144782000	chr9:18592477-18592478	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549360972	chr9:18592501-18592502	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567980897	chr9:18592511-18592512	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148259267	chr9:18592535-18592536	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550396377	chr9:18592543-18592544	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571738496	chr9:18592558-18592559	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186764924	chr9:18592566-18592567	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115401709	chr9:18592598-18592599	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565403620	chr9:18592600-18592601	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112981400	chr9:18592613-18592614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141254354	chr9:18592617-18592618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150754319	chr9:18592621-18592622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10963656	chr9:18592622-18592623	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs558778150	chr9:18592624-18592625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541899405	chr9:18592640-18592641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34178821	chr9:18592663-18592664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577117006	chr9:18592677-18592678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541202361	chr9:18592728-18592729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189696271	chr9:18592776-18592777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563695974	chr9:18592834-18592835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs137971263	chr9:18592841-18592842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143434106	chr9:18592845-18592846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552210608	chr9:18592937-18592938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561120421	chr9:18592952-18592953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532072387	chr9:18592954-18592955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550216609	chr9:18592996-18592997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182597335	chr9:18593003-18593004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117204544	chr9:18593013-18593014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528632272	chr9:18593020-18593021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547569853	chr9:18593028-18593029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370820804	chr9:18593067-18593068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535940619	chr9:18593080-18593081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147129409	chr9:18593111-18593112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140192147	chr9:18593160-18593161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537006417	chr9:18593165-18593166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77821616	chr9:18593198-18593199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201440590	chr9:18593222-18593223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577172026	chr9:18593223-18593224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548467953	chr9:18593275-18593276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553179674	chr9:18593278-18593279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572617284	chr9:18593301-18593302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145710446	chr9:18593304-18593305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561391728	chr9:18593308-18593309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576362439	chr9:18593313-18593314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144383846	chr9:18593322-18593323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Myelofibrosis	22110671	CNVD
Autism	20841430	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1505 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18569800-18601000	Weak transcription	NHLF	lung
2	chr9:18583800-18595000	Weak transcription	Fetal Stomach	stomach
3	chr9:18584000-18603200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:18584200-18594800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:18584800-18595600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:18588600-18605600	Weak transcription	NH-A	brain
7	chr9:18590000-18592400	Strong transcription	Osteobl	bone
8	chr9:18590600-18592600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:18591200-18592600	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
10	chr9:18591200-18592600	Strong transcription	HSMM	muscle
11	chr9:18591400-18592800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:18591600-18592400	Strong transcription	NHDF-Ad	bronchial
13	chr9:18591800-18592600	Strong transcription	Aorta	Aorta
14	chr9:18592000-18595400	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr9:18592200-18593200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:18592200-18595400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr9:18592200-18595400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:18592200-18596800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:18592400-18594800	Weak transcription	Osteobl	bone
20	chr9:18592400-18595200	Weak transcription	NHDF-Ad	bronchial
21	chr9:18592600-18594800	Weak transcription	HSMM	muscle
22	chr9:18592600-18595200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:18592600-18596600	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr9:18592600-18605800	Weak transcription	Aorta	Aorta
25	chr9:18593200-18594800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:18594200-18605800	Weak transcription	HSMMtube	muscle
27	chr9:18594800-18595200	Strong transcription	Osteobl	bone
28	chr9:18594800-18595400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:18594800-18595400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr9:18594800-18595400	ZNF genes & repeats	HSMM	muscle
31	chr9:18594800-18596000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr9:18595000-18595400	Enhancers	HMEC	breast
33	chr9:18595000-18595600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr9:18595000-18595800	ZNF genes & repeats	Fetal Stomach	stomach
35	chr9:18595000-18596000	Enhancers	Fetal Muscle Leg	muscle
36	chr9:18595200-18595400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr9:18595200-18595400	Enhancers	Gastric	stomach
38	chr9:18595200-18595400	Genic enhancers	Osteobl	bone
39	chr9:18595200-18595600	Enhancers	NHDF-Ad	bronchial
40	chr9:18595200-18599000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:18595400-18595600	Weak transcription	HSMM	muscle
42	chr9:18595400-18595800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:18595400-18595800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr9:18595400-18595800	Enhancers	Right Ventricle	heart
45	chr9:18595400-18596000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:18595400-18596000	Enhancers	Fetal Muscle Trunk	muscle
47	chr9:18595400-18596200	Enhancers	Stomach Smooth Muscle	stomach
48	chr9:18595400-18598200	Enhancers	Osteobl	bone
49	chr9:18595400-18602400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:18595600-18595800	Enhancers	Brain Germinal Matrix	brain

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