Variant report

Variant	nsv593205
Chromosome Location	chr4:601791-623629
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:253)
CpG islands
(count:1222)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:618888-618908	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr4:602536-602846	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:602695-602895	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:604800-604810	HepG2	liver:	n/a	n/a
5	CBX3	chr4:603198-603614	K562	blood:	n/a	n/a
6	CBX3	chr4:603130-603735	K562	blood:	n/a	n/a
7	CEBPB	chr4:604276-604867	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:612293-612435	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:604404-604612	A549	lung:	n/a	n/a
10	CEBPB	chr4:604302-604754	MCF-7	breast:	n/a	n/a
11	CEBPB	chr4:604217-604731	MCF-7	breast:	n/a	n/a
12	CEBPD	chr4:603182-603551	K562	blood:	n/a	n/a
13	CEBPD	chr4:603158-603680	K562	blood:	n/a	n/a
14	CHD2	chr4:604382-604828	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr4:621316-621357	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr4:618839-618975	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr4:618735-619001	H1-hESC	embryonic stem cell:	n/a	chr4:618772-618785 chr4:618786-618794
18	CTCF	chr4:618860-619010	HepG2	liver:	n/a	n/a
19	CTCF	chr4:618699-619112	K562	blood:	n/a	chr4:618772-618785 chr4:618786-618794
20	CTCF	chr4:604740-604890	NHEK	skin:	n/a	n/a
21	CTCF	chr4:604740-604890	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:604768-604996	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:604800-604950	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr4:604600-604750	SAEC	small airway:	n/a	n/a
25	CTCF	chr4:604700-604850	RPTEC	kidney:	n/a	n/a
26	CTCF	chr4:618820-618970	K562	blood:	n/a	n/a
27	CTCF	chr4:604758-604833	Fibrobl	skin:	n/a	n/a
28	CTCF	chr4:604360-604510	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr4:603640-603790	WERI-Rb-1	eye:	n/a	chr4:603650-603663
30	CTCF	chr4:604660-604810	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:618754-619011	K562	blood:	n/a	chr4:618772-618785 chr4:618786-618794
32	CTCF	chr4:604713-604971	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:618974-618975	K562	blood:	n/a	n/a
34	CTCF	chr4:603700-603850	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr4:604680-604830	HEK293	kidney:	n/a	n/a
36	CTCF	chr4:618840-618990	HepG2	liver:	n/a	n/a
37	CTCF	chr4:616620-616750	Fibrobl	skin:	n/a	n/a
38	CTCF	chr4:604725-604987	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:618820-618970	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr4:618840-618990	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:604695-604905	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr4:618869-618959	HepG2	liver:	n/a	n/a
43	CTCF	chr4:604660-604810	HMEC	breast:	n/a	n/a
44	CTCF	chr4:618740-618890	HRE	kidney:	n/a	chr4:618772-618785 chr4:618786-618794
45	CTCF	chr4:604780-604930	NHEK	skin:	n/a	n/a
46	CTCF	chr4:618891-618972	K562	blood:	n/a	n/a
47	CTCF	chr4:604720-604870	HMEC	breast:	n/a	n/a
48	CTCF	chr4:618768-619128	H1-hESC	embryonic stem cell:	n/a	chr4:618772-618785 chr4:618786-618794
49	CTCF	chr4:618880-619030	HRE	kidney:	n/a	n/a
50	CTCF	chr4:619920-620070	WERI-Rb-1	eye:	n/a	chr4:620031-620044

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:618114-618164	HNPCEpiC	eye:	n/a
2	chr4:619865-619915	HL-60	blood:	n/a
3	chr4:618114-618164	HNPCEpiC	eye:	n/a
4	chr4:619865-619915	HL-60	blood:	n/a
5	chr4:614552-614602	ProgFib	skin:	n/a
6	chr4:618549-618599	AG09319	gingival:	n/a
7	chr4:619659-619709	NB4	blood:	n/a
8	chr4:619375-619425	NHDF-neo	bronchial:	n/a
9	chr4:618332-618382	NHDF-neo	bronchial:	n/a
10	chr4:619272-619322	GM12878	blood:	n/a
11	chr4:614552-614602	HCT-116	colon:	n/a
12	chr4:621306-621356	LNCaP	prostate:	n/a
13	chr4:619314-619364	LNCaP	prostate:	n/a
14	chr4:619375-619425	Hela-S3	cervix:	n/a
15	chr4:619635-619685	AoSMC	blood vessel:	n/a
16	chr4:622887-622937	Hela-S3	cervix:	n/a
17	chr4:622887-622937	HRE	kidney:	n/a
18	chr4:619659-619709	H1-hESC	embryonic stem cell:	embryo
19	chr4:619272-619322	HCM	heart:	n/a
20	chr4:619314-619364	ovcar-3	ovarian:	n/a
21	chr4:619635-619685	HAEpiC	amniotic membrane:	n/a
22	chr4:614752-614802	HL-60	blood:	n/a
23	chr4:614752-614802	HRCEpiC	kidney:	n/a
24	chr4:618549-618599	AG10803	skin:	n/a
25	chr4:619167-619217	AG04449	skin:	fetal
26	chr4:616584-616634	NH-A	brain:	n/a
27	chr4:616584-616634	NT2-D1	testis:	n/a
28	chr4:619375-619425	HNPCEpiC	eye:	n/a
29	chr4:619865-619915	SK-N-MC	brain:	n/a
30	chr4:619272-619322	AG09309	skin:	n/a
31	chr4:618549-618599	HRPEpiC	eye:	n/a
32	chr4:618549-618599	K562	blood:	n/a
33	chr4:619314-619364	NHDF-neo	bronchial:	n/a
34	chr4:619272-619322	SAEC	small airway:	n/a
35	chr4:618332-618382	LNCaP	prostate:	n/a
36	chr4:614552-614602	PANC-1	pancreas:	n/a
37	chr4:614752-614802	PrEC	prostate:	n/a
38	chr4:622887-622937	RPTEC	kidney:	n/a
39	chr4:618497-618547	NB4	blood:	n/a
40	chr4:618753-618803	MCF10A-Er-Src	breast:	n/a
41	chr4:619659-619709	HAEpiC	amniotic membrane:	n/a
42	chr4:619635-619685	Jurkat	blood:	n/a
43	chr4:614552-614602	NT2-D1	testis:	n/a
44	chr4:618114-618164	SAEC	small airway:	n/a
45	chr4:622887-622937	PFSK-1	brain:	n/a
46	chr4:618114-618164	Hepatocyte	liver:	n/a
47	chr4:619659-619709	AG10803	skin:	n/a
48	chr4:618497-618547	PrEC	prostate:	n/a
49	chr4:618332-618382	RPTEC	kidney:	n/a
50	chr4:618497-618547	Hepatocyte	liver:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:611669..613220-chr4:626593..629173,2	MCF-7	breast:
2	chr4:599560..602481-chr4:609054..611964,2	K562	blood:
3	chr4:608874..610845-chr4:663421..664979,2	K562	blood:
4	chr4:604354..606441-chr4:673757..676151,2	MCF-7	breast:
5	chr4:619501..622132-chr4:622263..626030,4	MCF-7	breast:
6	chr4:606087..607621-chr4:663295..666195,2	MCF-7	breast:
7	chr4:608593..612078-chr4:666747..670592,3	MCF-7	breast:
8	chr4:601870..605072-chr4:605774..608100,3	MCF-7	breast:
9	chr4:605044..607670-chr4:680554..683532,2	MCF-7	breast:
10	chr4:602970..606601-chr4:666119..669923,8	MCF-7	breast:
11	chr4:604637..608287-chr4:609936..613205,3	K562	blood:
12	chr4:610434..612539-chr4:674484..677455,3	MCF-7	breast:
13	chr4:595274..598065-chr4:602440..604215,2	K562	blood:
14	chr4:603212..604817-chr4:605106..607499,2	K562	blood:
15	chr4:608907..613151-chr4:666337..671528,7	MCF-7	breast:
16	chr4:613849..616261-chr4:650426..653017,2	K562	blood:
17	chr4:604595..606902-chr4:659011..661677,2	MCF-7	breast:
18	chr4:615876..617771-chr4:628086..630978,3	K562	blood:
19	chr4:604637..608287-chr4:609936..613205,3	K562	blood:
20	chr4:492359..493966-chr4:619634..621403,2	K562	blood:
21	chr1:115298950..115300909-chr4:600171..602025,2	MCF-7	breast:
22	chr4:601870..605072-chr4:605774..608100,3	MCF-7	breast:
23	chr4:603737..606534-chr4:610162..613022,2	MCF-7	breast:
24	chr4:603212..604817-chr4:605106..607499,2	K562	blood:
25	chr4:619501..622132-chr4:622263..626030,4	MCF-7	breast:
26	chr4:603305..603835-chr8:30391968..30392468,2	NB4	blood:
27	chr4:615679..617414-chr4:667788..669338,2	MCF-7	breast:
28	chr4:599560..602481-chr4:609054..611964,2	K562	blood:
29	chr4:594354..601823-chr4:659072..674169,20	MCF-7	breast:
30	chr4:619437..623881-chr4:666212..669300,4	MCF-7	breast:
31	chr4:603737..606534-chr4:610162..613022,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE6B-1	chr4:611511-611754	XLOC_003411
2	lnc-PDE6B-1	chr4:601762-601867	l_2578_chr4:572257-601867_testes
3	lnc-PDE6B-1	chr4:611511-611793	NONHSAT094580

No data

Variant related genes	Relation type
PDE6B	TF binding region
PDE6B	CpG island
ENSG00000182903	chromatin interactions
ENSG00000215375	chromatin interactions
ENSG00000169020	chromatin interactions
ENSG00000169026	chromatin interactions
ENSG00000009307	chromatin interactions
ENSG00000174227	chromatin interactions
C5orf41	miRNA target sites

Extended variants
information (count: 1057 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1057 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10015198	chr4:601791-601792	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565837170	chr4:601846-601847	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs113543599	chr4:601890-601891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112281856	chr4:601898-601899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs564309936	chr4:601905-601906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531507269	chr4:601916-601917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549708182	chr4:601943-601944	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs567704934	chr4:601994-601995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs191774911	chr4:602043-602044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554398646	chr4:602071-602072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376586275	chr4:602107-602108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575943718	chr4:602119-602120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537219859	chr4:602125-602126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547009006	chr4:602172-602173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565603222	chr4:602181-602182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181441967	chr4:602222-602223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143511054	chr4:602258-602259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528794214	chr4:602268-602269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571071596	chr4:602269-602270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538529125	chr4:602280-602281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148002764	chr4:602284-602285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141636140	chr4:602293-602294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535815223	chr4:602308-602309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554147733	chr4:602338-602339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572403089	chr4:602340-602341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372082034	chr4:602371-602372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374593051	chr4:602425-602426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386670409	chr4:602426-602427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80091832	chr4:602427-602428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76593560	chr4:602428-602429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77178257	chr4:602429-602430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71614937	chr4:602432-602433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546945675	chr4:602437-602438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559301303	chr4:602452-602453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374336613	chr4:602493-602494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142291422	chr4:602523-602524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35566788	chr4:602538-602539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536990546	chr4:602592-602593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373494953	chr4:602660-602661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185929796	chr4:602670-602671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189952008	chr4:602697-602698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550413880	chr4:602724-602725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568731971	chr4:602731-602732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536159832	chr4:602739-602740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182541525	chr4:602755-602756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572445378	chr4:602757-602758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539538721	chr4:602767-602768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558127942	chr4:602787-602788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568427673	chr4:602795-602796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186078860	chr4:602834-602835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	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	chr4:593600-605800	Weak transcription	Right Atrium	heart
2	chr4:594800-604200	Weak transcription	Brain Anterior Caudate	brain
3	chr4:603400-605200	Enhancers	Hela-S3	cervix
4	chr4:603600-605200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:603600-606600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr4:603800-605000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:604000-604200	Enhancers	HSMMtube	muscle
8	chr4:604000-604600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:604000-605000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:604000-605200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:604000-605200	Enhancers	HMEC	breast
12	chr4:604200-604400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:604200-604400	Enhancers	Brain Anterior Caudate	brain
14	chr4:604200-604600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr4:604200-604600	Enhancers	Fetal Intestine Large	intestine
16	chr4:604200-605000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:604200-605000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:604200-605000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:604200-605000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr4:604200-605000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr4:604200-605000	Enhancers	HSMM	muscle
22	chr4:604200-605000	Enhancers	NHEK	skin
23	chr4:604200-605200	Bivalent Enhancer	Placenta	Placenta
24	chr4:604200-605800	Enhancers	Duodenum Mucosa	Duodenum
25	chr4:604200-606000	Enhancers	Esophagus	oesophagus
26	chr4:604400-604800	Enhancers	Brain Hippocampus Middle	brain
27	chr4:604400-605000	Enhancers	Osteobl	bone
28	chr4:604400-605200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:604600-605000	Bivalent Enhancer	Fetal Intestine Large	intestine
30	chr4:604800-605000	Enhancers	HSMMtube	muscle
31	chr4:605000-610400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:605200-611400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:605400-607200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr4:605800-606000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
35	chr4:605800-606600	Strong transcription	Right Atrium	heart
36	chr4:606400-607200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:606600-608200	Weak transcription	Right Atrium	heart
38	chr4:610200-611000	Enhancers	Fetal Brain Male	brain
39	chr4:610400-612600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:610600-612200	Enhancers	Placenta Amnion	Placenta Amnion
41	chr4:610600-612400	Enhancers	Placenta	Placenta
42	chr4:611200-611800	Bivalent Enhancer	NHEK	skin
43	chr4:611200-612000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr4:611200-612000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:611400-612400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:612400-616200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:615600-617600	Enhancers	Brain Hippocampus Middle	brain
48	chr4:615800-618200	Enhancers	Brain Substantia Nigra	brain
49	chr4:616000-617400	Enhancers	Brain Cingulate Gyrus	brain
50	chr4:616200-617000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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