Variant report

Variant	nsv432626
Chromosome Location	chr4:131837395-132602395
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1936)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1936 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:131963666-131963672	K562	blood:	n/a	n/a
2	ATF2	chr4:132534989-132535386	GM12878	blood:	n/a	n/a
3	ATF2	chr4:132347383-132348003	GM12878	blood:	n/a	n/a
4	ATF2	chr4:132230758-132231240	GM12878	blood:	n/a	n/a
5	ATF2	chr4:132347459-132347932	GM12878	blood:	n/a	n/a
6	ATF2	chr4:132468655-132469308	GM12878	blood:	n/a	n/a
7	ATF3	chr4:132179544-132179772	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:132391549-132391886	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:132237834-132237865	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:132142159-132142343	K562	blood:	n/a	n/a
11	BACH1	chr4:132391570-132391880	K562	blood:	n/a	n/a
12	BACH1	chr4:132150946-132150962	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:132164565-132164579	K562	blood:	n/a	n/a
14	BATF	chr4:132347469-132347900	GM12878	blood:	n/a	n/a
15	BATF	chr4:132230807-132231142	GM12878	blood:	n/a	chr4:132230925-132230936
16	BATF	chr4:132269461-132269747	GM12878	blood:	n/a	n/a
17	BATF	chr4:132579445-132580058	GM12878	blood:	n/a	n/a
18	BATF	chr4:132230793-132231130	GM12878	blood:	n/a	chr4:132230925-132230936
19	BATF	chr4:132468793-132469303	GM12878	blood:	n/a	n/a
20	BATF	chr4:132269393-132269798	GM12878	blood:	n/a	n/a
21	BATF	chr4:132469892-132470158	GM12878	blood:	n/a	chr4:132470014-132470025 chr4:132469980-132469991
22	BATF	chr4:132237297-132237506	GM12878	blood:	n/a	chr4:132237434-132237445
23	BATF	chr4:132579714-132580021	GM12878	blood:	n/a	n/a
24	BATF	chr4:132347572-132347877	GM12878	blood:	n/a	n/a
25	BATF	chr4:132584050-132584633	GM12878	blood:	n/a	n/a
26	BATF	chr4:132584215-132584596	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:132347576-132347893	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:132584212-132584619	GM12878	blood:	n/a	n/a
29	BCL11A	chr4:132178410-132178696	GM12878	blood:	n/a	n/a
30	BCL11A	chr4:132469009-132469193	GM12878	blood:	n/a	n/a
31	BCL11A	chr4:132579505-132580074	GM12878	blood:	n/a	n/a
32	BCL11A	chr4:132347442-132347953	GM12878	blood:	n/a	n/a
33	BCL11A	chr4:132230818-132231127	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:132584240-132584512	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:132178348-132178643	GM12878	blood:	n/a	chr4:132178369-132178378
36	BCL11A	chr4:132468778-132469283	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:132579674-132579989	GM12878	blood:	n/a	n/a
38	BCL3	chr4:132347488-132347811	GM12878	blood:	n/a	n/a
39	BCLAF1	chr4:132468685-132469223	GM12878	blood:	n/a	n/a
40	BCLAF1	chr4:132347460-132347821	GM12878	blood:	n/a	n/a
41	BCLAF1	chr4:132347567-132347910	GM12878	blood:	n/a	n/a
42	BHLHE40	chr4:132534939-132535181	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:132468935-132469065	GM12878	blood:	n/a	n/a
44	BHLHE40	chr4:132369178-132369366	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:132347604-132347811	GM12878	blood:	n/a	n/a
46	BHLHE40	chr4:132128800-132129079	HepG2	liver:	n/a	n/a
47	BHLHE40	chr4:132178402-132178703	GM12878	blood:	n/a	n/a
48	BRCA1	chr4:132082475-132082658	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr4:132417524-132417687	K562	blood:	n/a	n/a
50	CBX3	chr4:132209558-132210022	HCT-116	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132300589-132300639	U87	brain:	n/a
2	chr4:132300589-132300639	AG09309	skin:	n/a
3	chr4:132273830-132273880	NHDF-neo	bronchial:	n/a
4	chr4:132273830-132273880	MCF10A-Er-Src	breast:	n/a
5	chr4:132273830-132273880	HMEC	breast:	n/a
6	chr4:132300589-132300639	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:132300589-132300639	HNPCEpiC	eye:	n/a
8	chr4:132300589-132300639	AoSMC	blood vessel:	n/a
9	chr4:132300589-132300639	HCM	heart:	n/a
10	chr4:132300589-132300639	PrEC	prostate:	n/a
11	chr4:132300589-132300639	LNCaP	prostate:	n/a
12	chr4:132273830-132273880	AG04450	lung:	fetal
13	chr4:132300589-132300639	BJ	skin:	n/a
14	chr4:132300589-132300639	PANC-1	pancreas:	n/a
15	chr4:132273830-132273880	A549	lung:	n/a
16	chr4:132300589-132300639	HCT-116	colon:	n/a
17	chr4:132300589-132300639	HIPEpiC	eye:	n/a
18	chr4:132300589-132300639	T-47D	breast:	n/a
19	chr4:132273830-132273880	U87	brain:	n/a
20	chr4:132273830-132273880	SKMC	muscle:	n/a
21	chr4:132300589-132300639	GM19239	blood:	n/a
22	chr4:132273830-132273880	AG09309	skin:	n/a
23	chr4:132300589-132300639	GM12878	blood:	n/a
24	chr4:132273830-132273880	SAEC	small airway:	n/a
25	chr4:132300589-132300639	NHDF-neo	bronchial:	n/a
26	chr4:132273830-132273880	RPTEC	kidney:	n/a
27	chr4:132273830-132273880	HCF	heart:	n/a
28	chr4:132300589-132300639	GM12891	blood:	n/a
29	chr4:132273830-132273880	HNPCEpiC	eye:	n/a
30	chr4:132273830-132273880	GM12892	blood:	n/a
31	chr4:132300589-132300639	HRPEpiC	eye:	n/a
32	chr4:132273830-132273880	HRCEpiC	kidney:	n/a
33	chr4:132273830-132273880	Hepatocyte	liver:	n/a
34	chr4:132273830-132273880	HAEpiC	amniotic membrane:	n/a
35	chr4:132273830-132273880	PANC-1	pancreas:	n/a
36	chr4:132273830-132273880	HCM	heart:	n/a
37	chr4:132273830-132273880	GM19239	blood:	n/a
38	chr4:132273830-132273880	HUVEC	blood vessel:	n/a
39	chr4:132273830-132273880	NH-A	brain:	n/a
40	chr4:132273830-132273880	H1-hESC	embryonic stem cell:	embryo
41	chr4:132273830-132273880	ProgFib	skin:	n/a
42	chr4:132300589-132300639	NH-A	brain:	n/a
43	chr4:132300589-132300639	HRE	kidney:	n/a
44	chr4:132300589-132300639	HAEpiC	amniotic membrane:	n/a
45	chr4:132300589-132300639	SKMC	muscle:	n/a
46	chr4:132273830-132273880	HRE	kidney:	n/a
47	chr4:132300589-132300639	AG04450	lung:	fetal
48	chr4:132273830-132273880	GM12891	blood:	n/a
49	chr4:132273830-132273880	Hela-S3	cervix:	n/a
50	chr4:132273830-132273880	MCF-7	breast:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:52859439..52860286-chr4:132071047..132072003,2	MCF-7	breast:
2	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
3	chr4:132050225..132052503-chr4:132053839..132055546,2	MCF-7	breast:
4	chr4:131991641..131994380-chr4:131997829..132000348,2	MCF-7	breast:
5	chr4:88902738..88903615-chr4:132032553..132033450,2	MCF-7	breast:
6	chr4:131891594..131894034-chr4:131900622..131902132,2	K562	blood:
7	chr10:15257912..15258445-chr4:132538874..132539729,2	MCF-7	breast:
8	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
9	chr4:131991641..131994380-chr4:131997829..132000348,2	MCF-7	breast:
10	chr4:132495865..132498860-chr4:132534309..132536542,2	K562	blood:
11	chr4:131891594..131894034-chr4:131900622..131902132,2	K562	blood:
12	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
13	chr4:131949917..131952007-chr4:131958103..131960574,2	K562	blood:
14	chr4:132387674..132388400-chr4:132565905..132566424,2	MCF-7	breast:
15	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
16	chr4:132564996..132567264-chr4:132571046..132573271,2	K562	blood:
17	chr4:132387674..132388400-chr4:132565905..132566424,2	MCF-7	breast:
18	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
19	chr4:132564996..132567264-chr4:132571046..132573271,2	K562	blood:
20	chr4:3075352..3076921-chr4:131867632..131869317,2	MCF-7	breast:
21	chr4:132050225..132052503-chr4:132053839..132055546,2	MCF-7	breast:
22	chr4:132409731..132412260-chr4:132416731..132419042,2	K562	blood:
23	chr4:132012841..132013396-chr4:132565892..132566443,2	MCF-7	breast:
24	chr4:132409731..132412260-chr4:132416731..132419042,2	K562	blood:
25	chr4:132122573..132124807-chr4:132127097..132129962,3	MCF-7	breast:
26	chr4:132122573..132124807-chr4:132127097..132129962,3	MCF-7	breast:
27	chr15:72524014..72524697-chr4:131897075..131897575,2	Hela-S3	cervix:
28	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
29	chr4:131949917..131952007-chr4:131958103..131960574,2	K562	blood:
30	chr4:132495865..132498860-chr4:132534309..132536542,2	K562	blood:
31	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
32	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
33	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
34	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
35	chr4:132012841..132013396-chr4:132565892..132566443,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-7	chr4:132448385-132448443	NONHSAT098311
2	lnc-PCDH10-7	chr4:132462296-132462552	ENSG00000250102.1
3	lnc-PCDH10-7	chr4:132448385-132448443	ENSG00000250102.1
4	lnc-PCDH10-7	chr4:132300925-132301522	NONHSAT098311
5	lnc-PCDH10-7	chr4:132301168-132301496	ENSG00000250102.1
6	lnc-PCDH10-7	chr4:132444075-132444163	ENSG00000250102.1
7	lnc-PCDH10-7	chr4:132407112-132407229	ENSG00000250102.1
8	lnc-PCDH10-17	chr4:132461436-132461644	NONHSAT098315
9	lnc-PCDH10-7	chr4:132448385-132448443	ENSG00000250102.1
10	lnc-PCDH10-7	chr4:132449215-132449276	NONHSAT098311
11	lnc-PCDH10-7	chr4:132449215-132449276	ENSG00000250102.1

No data

Variant related genes	Relation type
ENSG00000248715	TF binding region
RNU6-224P	TF binding region
ENSG00000250102	TF binding region
ENSG00000250213	TF binding region
ENSG00000248715	CpG island
RNU6-224P	CpG island
ENSG00000250102	CpG island
ENSG00000250213	CpG island
ENSG00000067225	chromatin interactions
ENSG00000197386	chromatin interactions
ENSG00000251075	chromatin interactions

Extended variants
information (count: 6398 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:6398 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531758039	chr4:131856616-131856617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534686590	chr4:131856619-131856620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376823260	chr4:131856678-131856679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141248121	chr4:131856681-131856682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537234300	chr4:131856696-131856697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545478590	chr4:131856702-131856703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573858816	chr4:131856711-131856712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542593372	chr4:131856713-131856714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559667585	chr4:131856781-131856782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573176192	chr4:131856787-131856788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188657869	chr4:131856866-131856867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565046769	chr4:131856932-131856933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77913138	chr4:131856973-131856974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544397091	chr4:131857026-131857027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7658306	chr4:131857035-131857036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376235953	chr4:131857037-131857038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540399334	chr4:131857050-131857051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530404651	chr4:131857139-131857140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191334759	chr4:131857151-131857152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182145133	chr4:131857152-131857153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528085023	chr4:131857172-131857173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146064031	chr4:131857173-131857174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73850191	chr4:131857185-131857186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538060892	chr4:131857254-131857255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571362936	chr4:131857318-131857319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547791973	chr4:131857412-131857413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35248656	chr4:131857431-131857432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551028808	chr4:131857443-131857444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537173442	chr4:131857459-131857460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557179509	chr4:131857476-131857477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567901162	chr4:131857499-131857500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536522193	chr4:131857515-131857516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552992946	chr4:131857516-131857517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138119996	chr4:131857543-131857544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544990159	chr4:131857583-131857584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187106288	chr4:131857592-131857593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575311734	chr4:131857633-131857634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35162821	chr4:131857654-131857655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571523106	chr4:131857662-131857663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374702359	chr4:131857672-131857673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538910383	chr4:131857722-131857723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530413511	chr4:131857733-131857734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141966711	chr4:131857746-131857747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146288940	chr4:131857789-131857790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560615425	chr4:131857799-131857800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139318034	chr4:131857811-131857812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369075577	chr4:131857936-131857937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370140395	chr4:131857942-131857943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551375788	chr4:131857943-131857944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571299624	chr4:131857952-131857953	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
Bipolar disorder	19114987	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:131856600-131856800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:131856600-131857800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:131856800-131857600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:131857600-131858400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:131885200-131885800	Active TSS	Fetal Heart	heart
6	chr4:131885800-131887600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:131886400-131887200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:131887200-131890200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:131890400-131890600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:131894200-131894600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:131894200-131894600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:131894200-131894600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:131906200-131907600	Enhancers	HUVEC	blood vessel
14	chr4:131906600-131906800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr4:131906600-131907000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr4:131906600-131907000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:131915200-131915600	Enhancers	Fetal Kidney	kidney
18	chr4:131916600-131917600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr4:131918200-131918400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:131918600-131919400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:131918800-131919200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:131919000-131919800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:131919800-131923400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:131922200-131924000	Enhancers	HUVEC	blood vessel
25	chr4:131922600-131924200	Enhancers	NHEK	skin
26	chr4:131923400-131924000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:131931400-131932800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:131932000-131933000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:131932000-131933600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr4:131932800-131933600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:131933000-131933400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr4:131933400-131933600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:131933400-131933600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:131933400-131933800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr4:131933400-131933800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr4:131933400-131933800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr4:131933400-131933800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:131933400-131935200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:131933400-131935400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
40	chr4:131933400-131935800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:131933600-131934000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
42	chr4:131933600-131934800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:131933600-131935000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr4:131933600-131935000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:131933800-131934800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr4:131933800-131934800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr4:131933800-131935000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr4:131933800-131935000	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr4:131934400-131935200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
50	chr4:131934800-131935000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links