Variant report

Variant	esv3418296
Chromosome Location	chr4:616802-619150
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:68)
CpG islands
(count:367)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:68 , 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	CHD2	chr4:618839-618975	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr4:618840-618990	SK-N-SH_RA	brain:	n/a	n/a
4	CTCF	chr4:618768-619128	H1-hESC	embryonic stem cell:	n/a	chr4:618772-618785 chr4:618786-618794
5	CTCF	chr4:618840-618990	HepG2	liver:	n/a	n/a
6	CTCF	chr4:618891-618972	K562	blood:	n/a	n/a
7	CTCF	chr4:618880-619030	HRE	kidney:	n/a	n/a
8	CTCF	chr4:618820-618970	HRPEpiC	eye:	n/a	n/a
9	CTCF	chr4:618912-618944	MCF-7	breast:	n/a	n/a
10	CTCF	chr4:618826-619035	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr4:618974-618975	K562	blood:	n/a	n/a
12	CTCF	chr4:618860-619010	HepG2	liver:	n/a	n/a
13	CTCF	chr4:618820-618970	K562	blood:	n/a	n/a
14	CTCF	chr4:618754-619011	K562	blood:	n/a	chr4:618772-618785 chr4:618786-618794
15	CTCF	chr4:618735-619001	H1-hESC	embryonic stem cell:	n/a	chr4:618772-618785 chr4:618786-618794
16	CTCF	chr4:618740-618890	HRE	kidney:	n/a	chr4:618772-618785 chr4:618786-618794
17	CTCF	chr4:618869-618959	HepG2	liver:	n/a	n/a
18	CTCF	chr4:618780-618930	WERI-Rb-1	eye:	n/a	chr4:618786-618794
19	CTCF	chr4:618794-618986	K562	blood:	n/a	n/a
20	CTCF	chr4:618840-618990	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr4:618699-619112	K562	blood:	n/a	chr4:618772-618785 chr4:618786-618794
22	EBF1	chr4:619019-619131	GM12878	blood:	n/a	chr4:619099-619110
23	EGR1	chr4:619143-619455	K562	blood:	n/a	n/a
24	ESR1	chr4:618978-619401	ECC-1	luminal epithelium:	n/a	n/a
25	GABPA	chr4:618744-619078	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAFK	chr4:619042-619412	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAX	chr4:618870-619756	ECC-1	luminal epithelium:	n/a	n/a
28	MAX	chr4:618837-619779	ECC-1	luminal epithelium:	n/a	n/a
29	MAX	chr4:618140-618245	NB4	blood:	n/a	n/a
30	MYC	chr4:618289-618301	MCF-7	breast:	n/a	n/a
31	NFIC	chr4:618843-619815	ECC-1	luminal epithelium:	n/a	n/a
32	NFIC	chr4:618808-619891	ECC-1	luminal epithelium:	n/a	n/a
33	PAX5	chr4:618920-619278	GM12878	blood:	n/a	chr4:619149-619167 chr4:619151-619168
34	PAX5	chr4:618994-619252	GM12878	blood:	n/a	chr4:619149-619167 chr4:619151-619168
35	PAX5	chr4:618902-619295	GM12878	blood:	n/a	chr4:619149-619167 chr4:619151-619168
36	PAX5	chr4:618801-619359	GM12878	blood:	n/a	chr4:619149-619167 chr4:619151-619168
37	PAX5	chr4:618889-619257	GM12892	blood:	n/a	chr4:619149-619167 chr4:619151-619168
38	POLR2A	chr4:619076-619309	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr4:618995-619579	ECC-1	luminal epithelium:	n/a	n/a
40	POLR2A	chr4:618266-618309	MCF-7	breast:	n/a	n/a
41	POLR2A	chr4:618221-618244	Gliobla	brain:	n/a	n/a
42	POLR2A	chr4:618266-618268	Gliobla	brain:	n/a	n/a
43	RAD21	chr4:618808-618948	K562	blood:	n/a	chr4:618876-618889
44	RAD21	chr4:618773-618967	HepG2	liver:	n/a	chr4:618876-618889
45	RAD21	chr4:618720-619097	H1-hESC	embryonic stem cell:	n/a	chr4:618876-618889
46	RAD21	chr4:618634-619203	H1-hESC	embryonic stem cell:	n/a	chr4:618876-618889
47	RAD21	chr4:618706-619143	H1-hESC	embryonic stem cell:	n/a	chr4:618876-618889
48	RAD21	chr4:618745-618922	HepG2	liver:	n/a	chr4:618876-618889
49	SIN3A	chr4:618849-618898	H1-hESC	embryonic stem cell:	n/a	n/a
50	SUZ12	chr4:616422-616865	H1-hESC	embryonic stem cell:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:618204-618254	HIPEpiC	eye:	n/a
2	chr4:618204-618254	HIPEpiC	eye:	n/a
3	chr4:618497-618547	HCT-116	colon:	n/a
4	chr4:618497-618547	GM19239	blood:	n/a
5	chr4:618549-618599	NT2-D1	testis:	n/a
6	chr4:618549-618599	AG09319	gingival:	n/a
7	chr4:618204-618254	BE2_C	brain:	n/a
8	chr4:618497-618547	NHDF-neo	bronchial:	n/a
9	chr4:618332-618382	A549	lung:	n/a
10	chr4:618114-618164	MCF-7	breast:	n/a
11	chr4:618114-618164	Hepatocyte	liver:	n/a
12	chr4:618753-618803	BJ	skin:	n/a
13	chr4:618332-618382	MCF10A-Er-Src	breast:	n/a
14	chr4:618753-618803	H1-hESC	embryonic stem cell:	embryo
15	chr4:618204-618254	HEK293	kidney:	embryo
16	chr4:618332-618382	LNCaP	prostate:	n/a
17	chr4:618549-618599	SKMC	muscle:	n/a
18	chr4:618332-618382	NHBE	bronchial:	n/a
19	chr4:618549-618599	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:618497-618547	PrEC	prostate:	n/a
21	chr4:618549-618599	SAEC	small airway:	n/a
22	chr4:618332-618382	HL-60	blood:	n/a
23	chr4:618204-618254	AG10803	skin:	n/a
24	chr4:618549-618599	HEK293	kidney:	embryo
25	chr4:618204-618254	HepG2	liver:	n/a
26	chr4:618204-618254	SAEC	small airway:	n/a
27	chr4:618332-618382	HRPEpiC	eye:	n/a
28	chr4:618753-618803	AoSMC	blood vessel:	n/a
29	chr4:618332-618382	HRE	kidney:	n/a
30	chr4:618114-618164	NT2-D1	testis:	n/a
31	chr4:618753-618803	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:618332-618382	GM12891	blood:	n/a
33	chr4:618497-618547	AG09309	skin:	n/a
34	chr4:618204-618254	GM12891	blood:	n/a
35	chr4:618549-618599	MCF10A-Er-Src	breast:	n/a
36	chr4:618332-618382	BJ	skin:	n/a
37	chr4:618753-618803	HCF	heart:	n/a
38	chr4:618204-618254	SKMC	muscle:	n/a
39	chr4:618549-618599	HCPEpiC	choroid plexus:	n/a
40	chr4:618332-618382	HUVEC	blood vessel:	n/a
41	chr4:618497-618547	GM06990	blood:	n/a
42	chr4:618332-618382	SK-N-SH	brain:	n/a
43	chr4:618497-618547	AG04450	lung:	fetal
44	chr4:618497-618547	CMK	blood:	n/a
45	chr4:618753-618803	NH-A	brain:	n/a
46	chr4:618549-618599	PrEC	prostate:	n/a
47	chr4:618114-618164	SKMC	muscle:	n/a
48	chr4:618497-618547	HCM	heart:	n/a
49	chr4:618549-618599	T-47D	breast:	n/a
50	chr4:618549-618599	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:615679..617414-chr4:667788..669338,2	MCF-7	breast:
2	chr4:615876..617771-chr4:628086..630978,3	K562	blood:

No data

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

Extended variants
information (count: 122 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:122 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs67376373	chr4:616824-616825	Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112670697	chr4:616830-616831	Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs536601810	chr4:616838-616839	Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs555047716	chr4:616850-616851	Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs143007729	chr4:616920-616921	Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs540761317	chr4:616943-616944	Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs570506541	chr4:616959-616960	Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs558761234	chr4:616995-616996	Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs576939255	chr4:617006-617007	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534710004	chr4:617014-617015	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs544093443	chr4:617028-617029	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs185882056	chr4:617048-617049	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs562763320	chr4:617064-617065	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs529951512	chr4:617072-617073	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs541424720	chr4:617129-617130	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs78556176	chr4:617149-617150	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs543192024	chr4:617169-617170	Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs527369953	chr4:617210-617211	Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs551882162	chr4:617224-617225	Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs188348458	chr4:617236-617237	Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs151331770	chr4:617261-617262	Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs550895921	chr4:617262-617263	Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573917545	chr4:617267-617268	Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs112892700	chr4:617283-617284	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs112383336	chr4:617299-617300	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370454304	chr4:617300-617301	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544485113	chr4:617325-617326	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs116046412	chr4:617329-617330	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs554983432	chr4:617338-617339	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113717999	chr4:617354-617355	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73056559	chr4:617357-617358	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs193190106	chr4:617383-617384	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577278263	chr4:617392-617393	Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs75541215	chr4:617427-617428	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs13147797	chr4:617469-617470	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs574667770	chr4:617471-617472	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs112008573	chr4:617546-617547	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs559698659	chr4:617550-617551	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs527267119	chr4:617563-617564	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs544999685	chr4:617566-617567	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs559938019	chr4:617583-617584	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs140578825	chr4:617595-617596	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs73219277	chr4:617618-617619	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs531351791	chr4:617620-617621	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs551144677	chr4:617621-617622	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs569382277	chr4:617629-617630	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs530393873	chr4:617725-617726	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs115113507	chr4:617747-617748	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs567185814	chr4:617837-617838	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs13107358	chr4:617843-617844	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:41 , 50 per page) page: 1

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

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