Variant report

Variant	nsv461282
Chromosome Location	chr4:19035608-19304946
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	ATF2	chr4:19197235-19197676	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:19137800-19138204	GM12878	blood:	n/a	n/a
3	ATF2	chr4:19197286-19197699	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:19137962-19138101	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:19134974-19135295	A549	lung:	n/a	chr4:19135127-19135138
6	CEBPB	chr4:19196878-19197790	H1-hESC	embryonic stem cell:	n/a	chr4:19197052-19197065
7	CEBPB	chr4:19226069-19226374	Hela-S3	cervix:	n/a	chr4:19226205-19226216
8	CEBPB	chr4:19143247-19143482	IMR90	lung:	n/a	chr4:19143358-19143369 chr4:19143357-19143370 chr4:19143357-19143368
9	CEBPB	chr4:19146661-19146739	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:19197001-19197141	IMR90	lung:	n/a	chr4:19197052-19197065
11	CEBPB	chr4:19288115-19288116	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:19187049-19187517	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:19265137-19265337	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:19134971-19135274	K562	blood:	n/a	chr4:19135127-19135138
15	CEBPB	chr4:19147727-19148019	IMR90	lung:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
16	CEBPB	chr4:19149012-19149189	HepG2	liver:	n/a	chr4:19149089-19149098 chr4:19149087-19149098
17	CEBPB	chr4:19286887-19287044	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:19226066-19226394	HepG2	liver:	n/a	chr4:19226205-19226216
19	CEBPB	chr4:19122665-19122865	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:19132498-19132945	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:19226059-19226306	K562	blood:	n/a	chr4:19226205-19226216
22	CEBPB	chr4:19219629-19219706	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:19148249-19148491	IMR90	lung:	n/a	chr4:19148352-19148363
24	CEBPB	chr4:19147696-19148020	H1-hESC	embryonic stem cell:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
25	CEBPB	chr4:19115665-19115921	HepG2	liver:	n/a	chr4:19115855-19115866 chr4:19115855-19115866 chr4:19115691-19115704
26	CEBPB	chr4:19147718-19148107	ECC-1	luminal epithelium:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879
27	CEBPB	chr4:19143246-19143469	HepG2	liver:	n/a	chr4:19143358-19143369 chr4:19143357-19143370 chr4:19143357-19143368
28	CEBPB	chr4:19147751-19148518	HepG2	liver:	n/a	chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147868-19147877 chr4:19147866-19147879 chr4:19148352-19148363
29	CEBPB	chr4:19303235-19303482	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:19134973-19135293	H1-hESC	embryonic stem cell:	n/a	chr4:19135127-19135138
31	CEBPB	chr4:19226065-19226352	H1-hESC	embryonic stem cell:	n/a	chr4:19226205-19226216
32	CEBPB	chr4:19134953-19135308	HepG2	liver:	n/a	chr4:19135127-19135138
33	CEBPB	chr4:19185777-19186242	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr4:19226085-19226381	IMR90	lung:	n/a	chr4:19226205-19226216
35	CEBPB	chr4:19115771-19115787	K562	blood:	n/a	n/a
36	CEBPB	chr4:19134958-19135299	IMR90	lung:	n/a	chr4:19135127-19135138
37	CEBPB	chr4:19303074-19303531	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:19123587-19124188	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:19148242-19148497	Hela-S3	cervix:	n/a	chr4:19148352-19148363
40	CHD2	chr4:19197288-19197935	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr4:19197218-19197812	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTBP2	chr4:19197170-19197696	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:19112084-19112256	K562	blood:	n/a	n/a
44	CTCF	chr4:19226300-19226450	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr4:19226460-19226610	GM12873	blood:	n/a	n/a
46	CTCF	chr4:19226558-19226563	LNCaP	prostate:	n/a	n/a
47	CTCF	chr4:19226520-19226670	BJ	skin:	n/a	chr4:19226642-19226650 chr4:19226638-19226654 chr4:19226639-19226660 chr4:19226637-19226655
48	CTCF	chr4:19093300-19093450	HVMF	connective:	n/a	n/a
49	CTCF	chr4:19226540-19226690	GM12865	blood:	n/a	chr4:19226642-19226650 chr4:19226638-19226654 chr4:19226639-19226660 chr4:19226637-19226655
50	CTCF	chr4:19226020-19226170	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:19134792-19134842	GM12878	blood:	n/a
2	chr4:19134792-19134842	HEEpiC	esophagus:	n/a
3	chr4:19134792-19134842	GM12878	blood:	n/a
4	chr4:19134792-19134842	HEEpiC	esophagus:	n/a
5	chr4:19197380-19197430	Jurkat	blood:	n/a
6	chr4:19197380-19197430	NHDF-neo	bronchial:	n/a
7	chr4:19197380-19197430	HRPEpiC	eye:	n/a
8	chr4:19134792-19134842	HCT-116	colon:	n/a
9	chr4:19197380-19197430	AG09309	skin:	n/a
10	chr4:19134792-19134842	Jurkat	blood:	n/a
11	chr4:19197380-19197430	H1-hESC	embryonic stem cell:	embryo
12	chr4:19197380-19197430	HAEpiC	amniotic membrane:	n/a
13	chr4:19134792-19134842	HRE	kidney:	n/a
14	chr4:19134792-19134842	HCM	heart:	n/a
15	chr4:19134792-19134842	GM19239	blood:	n/a
16	chr4:19134792-19134842	HNPCEpiC	eye:	n/a
17	chr4:19134792-19134842	ProgFib	skin:	n/a
18	chr4:19134792-19134842	RPTEC	kidney:	n/a
19	chr4:19134792-19134842	BJ	skin:	n/a
20	chr4:19197380-19197430	HMEC	breast:	n/a
21	chr4:19197380-19197430	ECC-1	luminal epithelium:	n/a
22	chr4:19197380-19197430	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:19197380-19197430	BE2_C	brain:	n/a
24	chr4:19197380-19197430	HCPEpiC	choroid plexus:	n/a
25	chr4:19197380-19197430	HCF	heart:	n/a
26	chr4:19197380-19197430	SK-N-SH	brain:	n/a
27	chr4:19197380-19197430	SKMC	muscle:	n/a
28	chr4:19134792-19134842	AG09319	gingival:	n/a
29	chr4:19197380-19197430	GM12892	blood:	n/a
30	chr4:19197380-19197430	PrEC	prostate:	n/a
31	chr4:19134792-19134842	PFSK-1	brain:	n/a
32	chr4:19134792-19134842	HRCEpiC	kidney:	n/a
33	chr4:19197380-19197430	SAEC	small airway:	n/a
34	chr4:19134792-19134842	NH-A	brain:	n/a
35	chr4:19197380-19197430	NB4	blood:	n/a
36	chr4:19134792-19134842	A549	lung:	n/a
37	chr4:19197380-19197430	MCF-7	breast:	n/a
38	chr4:19134792-19134842	HCPEpiC	choroid plexus:	n/a
39	chr4:19197380-19197430	GM12891	blood:	n/a
40	chr4:19134792-19134842	HL-60	blood:	n/a
41	chr4:19197380-19197430	RPTEC	kidney:	n/a
42	chr4:19197380-19197430	NT2-D1	testis:	n/a
43	chr4:19197380-19197430	PFSK-1	brain:	n/a
44	chr4:19134792-19134842	SK-N-MC	brain:	n/a
45	chr4:19197380-19197430	T-47D	breast:	n/a
46	chr4:19197380-19197430	SK-N-SH_RA	brain:	n/a
47	chr4:19197380-19197430	HCM	heart:	n/a
48	chr4:19134792-19134842	NB4	blood:	n/a
49	chr4:19134792-19134842	Hela-S3	cervix:	n/a
50	chr4:19134792-19134842	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:19258834..19261386-chr4:19628228..19629933,2	K562	blood:
2	chr4:19118666..19120200-chr4:19121807..19124671,2	K562	blood:
3	chr4:19078847..19080844-chr4:19084174..19086115,2	MCF-7	breast:
4	chr4:19118666..19120200-chr4:19121807..19124671,2	K562	blood:
5	chr4:19078847..19080844-chr4:19084174..19086115,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LCORL-2	chr4:19173958-19174149	ENSG00000248238

Variant related genes	Relation type
RNA5SP157	TF binding region
RNA5SP157	CpG island

Extended variants
information (count: 4118 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:4118 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10001989	chr4:19035608-19035609	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150601926	chr4:19035625-19035626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569651695	chr4:19035637-19035638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536599226	chr4:19035667-19035668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555636198	chr4:19035740-19035741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192019215	chr4:19035745-19035746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184259888	chr4:19035829-19035830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs33978564	chr4:19035868-19035869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs57909704	chr4:19035882-19035883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs714614	chr4:19035888-19035889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138647414	chr4:19035949-19035950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577393757	chr4:19036002-19036003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149313841	chr4:19036010-19036011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563596771	chr4:19036032-19036033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188791410	chr4:19036053-19036054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542702107	chr4:19036070-19036071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527269795	chr4:19036084-19036085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561326767	chr4:19036112-19036113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144557766	chr4:19036126-19036127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35466660	chr4:19036128-19036129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547293873	chr4:19036157-19036158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550038201	chr4:19036162-19036163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551513934	chr4:19036215-19036216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs207343	chr4:19036305-19036306	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537144301	chr4:19036308-19036309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376832584	chr4:19036316-19036317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548742724	chr4:19036329-19036330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551902190	chr4:19036342-19036343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570351738	chr4:19036359-19036360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534628800	chr4:19036407-19036408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181207933	chr4:19036408-19036409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148447535	chr4:19036453-19036454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538400224	chr4:19036458-19036459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557117090	chr4:19036488-19036489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144058276	chr4:19036495-19036496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369717481	chr4:19036498-19036499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184519853	chr4:19036505-19036506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573248859	chr4:19036507-19036508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189451582	chr4:19036510-19036511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145963898	chr4:19036528-19036529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs16898010	chr4:19036546-19036547	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs550936866	chr4:19036593-19036594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139832877	chr4:19036601-19036602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13434706	chr4:19036646-19036647	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs143161023	chr4:19036677-19036678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35673318	chr4:19036693-19036694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566943824	chr4:19036723-19036724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570192342	chr4:19036767-19036768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76421740	chr4:19036806-19036807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370346415	chr4:19036852-19036853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19032000-19037600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:19032600-19036000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr4:19035600-19035800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:19035600-19035800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:19035600-19035800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:19035600-19036400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:19035800-19036200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:19035800-19036400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:19036000-19036800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr4:19036200-19036800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:19036400-19036800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:19036400-19039800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:19036800-19038000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:19037600-19037800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr4:19037600-19038000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr4:19037800-19038000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:19038000-19038200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:19038000-19039600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr4:19039600-19040200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:19039800-19040200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:19039800-19040200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr4:19040200-19041000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr4:19041000-19041600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr4:19043000-19043200	ZNF genes & repeats	Pancreas	Pancrea
25	chr4:19048800-19049200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:19048800-19049600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:19049200-19052800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:19049600-19056200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:19052600-19054000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:19052600-19054000	Enhancers	Fetal Kidney	kidney
31	chr4:19052800-19054000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:19052800-19054200	Enhancers	Fetal Lung	lung
33	chr4:19053000-19054000	Enhancers	Colon Smooth Muscle	Colon
34	chr4:19053000-19054200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr4:19053200-19053800	Enhancers	Fetal Stomach	stomach
36	chr4:19053400-19053800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:19053400-19053800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:19053400-19054000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:19053400-19054000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr4:19053400-19054000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr4:19053600-19054000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:19053600-19054000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:19053600-19054000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:19053600-19054000	Enhancers	Brain Germinal Matrix	brain
45	chr4:19053600-19054200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr4:19053800-19054200	Enhancers	Fetal Brain Male	brain
47	chr4:19054000-19054600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:19054000-19056200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:19054000-19056400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:19054200-19056400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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