Variant report

Variant	nsv967276
Chromosome Location	chr4:615881-624526
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:1099)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:86 , 50 per page) page: 1 2

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	CEBPB	chr4:623849-624084	HepG2	liver:	n/a	chr4:623964-623975
3	CHD2	chr4:621316-621357	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr4:618839-618975	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr4:616620-616750	Fibrobl	skin:	n/a	n/a
6	CTCF	chr4:618840-618990	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr4:618699-619112	K562	blood:	n/a	chr4:618772-618785 chr4:618786-618794
8	CTCF	chr4:618840-618990	HepG2	liver:	n/a	n/a
9	CTCF	chr4:618820-618970	K562	blood:	n/a	n/a
10	CTCF	chr4:618754-619011	K562	blood:	n/a	chr4:618772-618785 chr4:618786-618794
11	CTCF	chr4:618891-618972	K562	blood:	n/a	n/a
12	CTCF	chr4:618780-618930	WERI-Rb-1	eye:	n/a	chr4:618786-618794
13	CTCF	chr4:618869-618959	HepG2	liver:	n/a	n/a
14	CTCF	chr4:618820-618970	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr4:618974-618975	K562	blood:	n/a	n/a
16	CTCF	chr4:618740-618890	HRE	kidney:	n/a	chr4:618772-618785 chr4:618786-618794
17	CTCF	chr4:618768-619128	H1-hESC	embryonic stem cell:	n/a	chr4:618772-618785 chr4:618786-618794
18	CTCF	chr4:623120-623270	GM12874	blood:	n/a	chr4:623175-623193
19	CTCF	chr4:618794-618986	K562	blood:	n/a	n/a
20	CTCF	chr4:618840-618990	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr4:619920-620070	WERI-Rb-1	eye:	n/a	chr4:620031-620044
22	CTCF	chr4:618880-619030	HRE	kidney:	n/a	n/a
23	CTCF	chr4:618735-619001	H1-hESC	embryonic stem cell:	n/a	chr4:618772-618785 chr4:618786-618794
24	CTCF	chr4:618860-619010	HepG2	liver:	n/a	n/a
25	CTCF	chr4:618826-619035	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr4:618912-618944	MCF-7	breast:	n/a	n/a
27	EBF1	chr4:619019-619131	GM12878	blood:	n/a	chr4:619099-619110
28	EGR1	chr4:619186-619431	K562	blood:	n/a	n/a
29	EGR1	chr4:616278-616796	GM12878	blood:	n/a	n/a
30	EGR1	chr4:619143-619455	K562	blood:	n/a	n/a
31	ELF1	chr4:621072-621300	K562	blood:	n/a	n/a
32	ESR1	chr4:618978-619401	ECC-1	luminal epithelium:	n/a	n/a
33	GABPA	chr4:618744-619078	H1-hESC	embryonic stem cell:	n/a	n/a
34	HMGN3	chr4:620665-620704	K562	blood:	n/a	n/a
35	MAFK	chr4:619042-619412	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAX	chr4:618140-618245	NB4	blood:	n/a	n/a
37	MAX	chr4:618837-619779	ECC-1	luminal epithelium:	n/a	n/a
38	MAX	chr4:618870-619756	ECC-1	luminal epithelium:	n/a	n/a
39	MYC	chr4:618289-618301	MCF-7	breast:	n/a	n/a
40	NFIC	chr4:618843-619815	ECC-1	luminal epithelium:	n/a	n/a
41	NFIC	chr4:618808-619891	ECC-1	luminal epithelium:	n/a	n/a
42	PAX5	chr4:618902-619295	GM12878	blood:	n/a	chr4:619149-619167 chr4:619151-619168
43	PAX5	chr4:618920-619278	GM12878	blood:	n/a	chr4:619149-619167 chr4:619151-619168
44	PAX5	chr4:618889-619257	GM12892	blood:	n/a	chr4:619149-619167 chr4:619151-619168
45	PAX5	chr4:618801-619359	GM12878	blood:	n/a	chr4:619149-619167 chr4:619151-619168
46	PAX5	chr4:618994-619252	GM12878	blood:	n/a	chr4:619149-619167 chr4:619151-619168
47	POLR2A	chr4:618266-618268	Gliobla	brain:	n/a	n/a
48	POLR2A	chr4:616435-616471	MCF-7	breast:	n/a	n/a
49	POLR2A	chr4:616389-616718	Gliobla	brain:	n/a	n/a
50	POLR2A	chr4:618266-618309	MCF-7	breast:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:619162-619212	MCF-7	breast:	n/a
2	chr4:619162-619212	MCF-7	breast:	n/a
3	chr4:622887-622937	PFSK-1	brain:	n/a
4	chr4:618549-618599	AG09309	skin:	n/a
5	chr4:622887-622937	AG10803	skin:	n/a
6	chr4:619162-619212	AoSMC	blood vessel:	n/a
7	chr4:619375-619425	LNCaP	prostate:	n/a
8	chr4:621306-621356	IMR90	lung:	fetal
9	chr4:619314-619364	AG09309	skin:	n/a
10	chr4:621306-621356	BE2_C	brain:	n/a
11	chr4:619659-619709	NB4	blood:	n/a
12	chr4:619272-619322	HEEpiC	esophagus:	n/a
13	chr4:618753-618803	Hela-S3	cervix:	n/a
14	chr4:621306-621356	HUVEC	blood vessel:	n/a
15	chr4:618114-618164	PrEC	prostate:	n/a
16	chr4:619375-619425	PANC-1	pancreas:	n/a
17	chr4:619659-619709	PANC-1	pancreas:	n/a
18	chr4:619167-619217	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:619392-619442	HMEC	breast:	n/a
20	chr4:619167-619217	NHBE	bronchial:	n/a
21	chr4:619162-619212	AG09309	skin:	n/a
22	chr4:619392-619442	GM12891	blood:	n/a
23	chr4:618204-618254	HCF	heart:	n/a
24	chr4:621306-621356	Jurkat	blood:	n/a
25	chr4:619375-619425	GM06990	blood:	n/a
26	chr4:618753-618803	A549	lung:	n/a
27	chr4:619272-619322	NT2-D1	testis:	n/a
28	chr4:616584-616634	Hepatocyte	liver:	n/a
29	chr4:616584-616634	LNCaP	prostate:	n/a
30	chr4:619635-619685	HepG2	liver:	n/a
31	chr4:619375-619425	AG09319	gingival:	n/a
32	chr4:622887-622937	ProgFib	skin:	n/a
33	chr4:619272-619322	CMK	blood:	n/a
34	chr4:618332-618382	A549	lung:	n/a
35	chr4:618114-618164	GM19239	blood:	n/a
36	chr4:622887-622937	AoSMC	blood vessel:	n/a
37	chr4:619314-619364	AG04450	lung:	fetal
38	chr4:619375-619425	HRCEpiC	kidney:	n/a
39	chr4:619167-619217	HepG2	liver:	n/a
40	chr4:618114-618164	HCT-116	colon:	n/a
41	chr4:619167-619217	GM12891	blood:	n/a
42	chr4:618549-618599	HEEpiC	esophagus:	n/a
43	chr4:618114-618164	HAEpiC	amniotic membrane:	n/a
44	chr4:619659-619709	HL-60	blood:	n/a
45	chr4:618497-618547	Hepatocyte	liver:	n/a
46	chr4:616584-616634	AG09319	gingival:	n/a
47	chr4:622887-622937	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:619314-619364	SK-N-SH	brain:	n/a
49	chr4:619375-619425	PrEC	prostate:	n/a
50	chr4:619272-619322	BE2_C	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:619437..623881-chr4:666212..669300,4	MCF-7	breast:
2	chr4:613849..616261-chr4:650426..653017,2	K562	blood:
3	chr4:619501..622132-chr4:622263..626030,4	MCF-7	breast:
4	chr4:623895..625703-chr4:641254..643295,2	K562	blood:
5	chr4:615876..617771-chr4:628086..630978,3	K562	blood:
6	chr4:492359..493966-chr4:619634..621403,2	K562	blood:
7	chr4:619501..622132-chr4:622263..626030,4	MCF-7	breast:
8	chr4:624127..625792-chr4:659574..661910,2	K562	blood:
9	chr4:615679..617414-chr4:667788..669338,2	MCF-7	breast:

No data

Variant related genes	Relation type
PDE6B	TF binding region
PDE6B	CpG island
ENSG00000182903	chromatin interactions
ENSG00000169020	chromatin interactions
ENSG00000215375	chromatin interactions
ENSG00000174227	chromatin interactions

Extended variants
information (count: 484 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565128810	chr4:615922-615923	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs77105558	chr4:615946-615947	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs6827034	chr4:616002-616003	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs115259166	chr4:616035-616036	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs377381812	chr4:616098-616099	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535942067	chr4:616113-616114	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs540440490	chr4:616127-616128	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs547855005	chr4:616230-616231	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs182081714	chr4:616241-616242	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534852293	chr4:616242-616243	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs141406900	chr4:616285-616286	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs386670411	chr4:616309-616310	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs150593059	chr4:616320-616321	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs529200863	chr4:616323-616324	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs544548497	chr4:616330-616331	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs539359611	chr4:616336-616337	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs557063731	chr4:616339-616340	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs375045700	chr4:616343-616344	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs575624028	chr4:616356-616357	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs146714615	chr4:616374-616375	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs542671074	chr4:616412-616413	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs72600023	chr4:616418-616419	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs71636503	chr4:616419-616420	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs72501955	chr4:616420-616421	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs373758323	chr4:616431-616432	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs573378570	chr4:616448-616449	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs199884893	chr4:616451-616452	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566566017	chr4:616466-616467	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs540424428	chr4:616507-616508	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs527434686	chr4:616535-616536	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369673574	chr4:616542-616543	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs550430842	chr4:616552-616553	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs532286770	chr4:616585-616586	Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs201751868	chr4:616588-616589	Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs111827885	chr4:616608-616609	Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs551796904	chr4:616625-616626	Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs34143738	chr4:616642-616643	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs563644618	chr4:616652-616653	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs562664550	chr4:616667-616668	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs559564896	chr4:616676-616677	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369487529	chr4:616678-616679	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs566073613	chr4:616685-616686	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs529659618	chr4:616694-616695	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs199760753	chr4:616701-616702	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs117188514	chr4:616735-616736	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs372222774	chr4:616747-616748	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs71602484	chr4:616748-616749	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539627965	chr4:616752-616753	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs193012819	chr4:616754-616755	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs368255756	chr4:616760-616761	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	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:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:612400-616200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:615600-617600	Enhancers	Brain Hippocampus Middle	brain
3	chr4:615800-618200	Enhancers	Brain Substantia Nigra	brain
4	chr4:616000-617400	Enhancers	Brain Cingulate Gyrus	brain
5	chr4:616200-617000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr4:616200-617400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr4:616200-618200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:616200-618400	Enhancers	Brain Angular Gyrus	brain
9	chr4:616600-617000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:616600-617000	Enhancers	Brain Anterior Caudate	brain
11	chr4:616800-624200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr4:617000-617200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:617000-617600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:617000-618200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr4:617200-618200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:617200-619800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:617400-617600	Bivalent Enhancer	Placenta	Placenta
18	chr4:617400-617800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:617600-619600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:617600-619800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr4:617600-620000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr4:617600-620200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:617600-620200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:617800-618200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr4:618000-618400	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr4:618000-619800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:618200-618400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr4:618200-618400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:618200-618400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr4:618200-618800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:618200-618800	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:618200-619200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr4:618200-619200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:618200-619200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:618200-619200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr4:618200-619600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:618200-619600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:618400-619200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:618400-619200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr4:618600-619200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:618800-620000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr4:619000-619400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr4:619200-620200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr4:619200-624000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:619600-620000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:619600-626000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:619800-621400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:620000-621200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr4:620000-622800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:620200-620400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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