Variant report

Variant	nsv822768
Chromosome Location	chr4:147556986-147562654
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:227)
CpG islands
(count:1160)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:227 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:147558227-147558300	HepG2	liver:	n/a	n/a
2	ATF2	chr4:147558048-147558348	H1-hESC	embryonic stem cell:	n/a	chr4:147558317-147558331
3	BHLHE40	chr4:147558034-147558061	K562	blood:	n/a	n/a
4	CHD1	chr4:147560154-147560352	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr4:147561612-147561851	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr4:147559720-147560281	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr4:147561608-147561962	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr4:147561500-147562057	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr4:147559162-147562308	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr4:147557997-147558703	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr4:147558180-147558330	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr4:147558340-147558490	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr4:147558140-147558290	SAEC	small airway:	n/a	n/a
14	CTCF	chr4:147558174-147558329	MCF-7	breast:	n/a	n/a
15	CTCF	chr4:147558160-147558310	HCM	heart:	n/a	n/a
16	CTCF	chr4:147558190-147558299	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:147558160-147558310	HPF	lung:	n/a	n/a
18	CTCF	chr4:147558200-147558350	HFF	foreskin:	n/a	n/a
19	CTCF	chr4:147558100-147558380	IMR90	lung:	n/a	n/a
20	CTCF	chr4:147558140-147558290	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr4:147558220-147558370	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr4:147558160-147558310	AG04450	lung:	n/a	n/a
23	CTCF	chr4:147558160-147558310	SAEC	small airway:	n/a	n/a
24	CTCF	chr4:147558140-147558290	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr4:147558160-147558310	HRE	kidney:	n/a	n/a
26	CTCF	chr4:147558160-147558310	AG10803	skin:	n/a	n/a
27	CTCF	chr4:147558210-147558306	ProgFib	skin:	n/a	n/a
28	CTCF	chr4:147558120-147558270	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr4:147558169-147558310	GM12891	blood:	n/a	n/a
30	CTCF	chr4:147558190-147558294	GM19238	blood:	n/a	n/a
31	CTCF	chr4:147558140-147558290	HepG2	liver:	n/a	n/a
32	CTCF	chr4:147558140-147558290	AG09309	skin:	n/a	n/a
33	CTCF	chr4:147558210-147558315	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr4:147558420-147558570	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr4:147558120-147558270	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr4:147558180-147558330	BJ	skin:	n/a	n/a
37	CTCF	chr4:147558182-147558303	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:147558180-147558330	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr4:147558180-147558330	NHEK	skin:	n/a	n/a
40	CTCF	chr4:147560180-147560330	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr4:147558200-147558350	RPTEC	kidney:	n/a	n/a
42	CTCF	chr4:147558140-147558290	HMF	breast:	n/a	n/a
43	CTCF	chr4:147558140-147558290	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr4:147558171-147558330	LNCaP	prostate:	n/a	n/a
45	CTCF	chr4:147558120-147558270	HRE	kidney:	n/a	n/a
46	CTCF	chr4:147558160-147558310	AG04449	skin:	n/a	n/a
47	CTCF	chr4:147558160-147558310	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr4:147560280-147560430	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr4:147558180-147558330	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:147558160-147558310	AoAF	blood vessel:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:147559648-147559698	NB4	blood:	n/a
2	chr4:147559648-147559698	NB4	blood:	n/a
3	chr4:147558239-147558289	GM12892	blood:	n/a
4	chr4:147559423-147559473	K562	blood:	n/a
5	chr4:147558544-147558594	GM12892	blood:	n/a
6	chr4:147557859-147557909	HRPEpiC	eye:	n/a
7	chr4:147561775-147561825	NH-A	brain:	n/a
8	chr4:147560282-147560332	HL-60	blood:	n/a
9	chr4:147557859-147557909	ECC-1	luminal epithelium:	n/a
10	chr4:147560282-147560332	HRPEpiC	eye:	n/a
11	chr4:147559423-147559473	HIPEpiC	eye:	n/a
12	chr4:147557859-147557909	PFSK-1	brain:	n/a
13	chr4:147558239-147558289	HCT-116	colon:	n/a
14	chr4:147560282-147560332	HMEC	breast:	n/a
15	chr4:147561775-147561825	HMEC	breast:	n/a
16	chr4:147561775-147561825	ovcar-3	ovarian:	n/a
17	chr4:147561339-147561389	HUVEC	blood vessel:	n/a
18	chr4:147558435-147558485	Hela-S3	cervix:	n/a
19	chr4:147560770-147560820	HEK293	kidney:	embryo
20	chr4:147560286-147560336	HepG2	liver:	n/a
21	chr4:147559648-147559698	NT2-D1	testis:	n/a
22	chr4:147560282-147560332	ovcar-3	ovarian:	n/a
23	chr4:147561203-147561253	HCPEpiC	choroid plexus:	n/a
24	chr4:147559579-147559629	SK-N-SH	brain:	n/a
25	chr4:147561775-147561825	T-47D	breast:	n/a
26	chr4:147557859-147557909	BE2_C	brain:	n/a
27	chr4:147558544-147558594	AG04450	lung:	fetal
28	chr4:147558544-147558594	HUVEC	blood vessel:	n/a
29	chr4:147558239-147558289	NHDF-neo	bronchial:	n/a
30	chr4:147559579-147559629	HCF	heart:	n/a
31	chr4:147561900-147561950	SK-N-MC	brain:	n/a
32	chr4:147559648-147559698	RPTEC	kidney:	n/a
33	chr4:147559648-147559698	PFSK-1	brain:	n/a
34	chr4:147560286-147560336	ProgFib	skin:	n/a
35	chr4:147560282-147560332	A549	lung:	n/a
36	chr4:147560286-147560336	AG04449	skin:	fetal
37	chr4:147558544-147558594	T-47D	breast:	n/a
38	chr4:147560770-147560820	HCM	heart:	n/a
39	chr4:147558544-147558594	HCF	heart:	n/a
40	chr4:147559579-147559629	ECC-1	luminal epithelium:	n/a
41	chr4:147560286-147560336	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:147557774-147557824	ECC-1	luminal epithelium:	n/a
43	chr4:147558544-147558594	CMK	blood:	n/a
44	chr4:147560770-147560820	Caco-2	colon:	n/a
45	chr4:147561900-147561950	HL-60	blood:	n/a
46	chr4:147561339-147561389	PANC-1	pancreas:	n/a
47	chr4:147561203-147561253	PFSK-1	brain:	n/a
48	chr4:147562073-147562123	HNPCEpiC	eye:	n/a
49	chr4:147557859-147557909	IMR90	lung:	fetal
50	chr4:147560286-147560336	BJ	skin:	n/a

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	POU4F2	hsa-miR-23a-3p	chr4:147562409-147562430
2	POU4F2	hsa-miR-23a-3p	chr4:147562120-147562140
3	POU4F2	hsa-miR-214-3p	chr4:147562574-147562580
4	POU4F2	hsa-miR-214-3p	chr4:147562560-147562581
5	POU4F2	hsa-miR-23a-3p	chr4:147562049-147562069
6	POU4F2	hsa-miR-23a-3p	chr4:147562062-147562069

Variant related genes	Relation type
POU4F2	TF binding region
ENSG00000264323	TF binding region
POU4F2	CpG island
ENSG00000264323	CpG island

Extended variants
information (count: 278 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569309860	chr4:147557368-147557369	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs572723190	chr4:147557425-147557426	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs529075228	chr4:147557469-147557470	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs111942673	chr4:147557479-147557480	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs181961526	chr4:147557493-147557494	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs537551050	chr4:147557494-147557495	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs374211623	chr4:147557525-147557526	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs185008160	chr4:147557560-147557561	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs189874014	chr4:147557590-147557591	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs557600412	chr4:147557643-147557644	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs533578227	chr4:147557665-147557666	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs554022716	chr4:147557685-147557686	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs376259988	chr4:147557697-147557698	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs574017868	chr4:147557706-147557707	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs182984086	chr4:147557731-147557732	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs556490163	chr4:147557747-147557748	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs546548263	chr4:147557777-147557778	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
18	rs576435807	chr4:147557785-147557786	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
19	rs545168074	chr4:147557803-147557804	Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
20	rs564754620	chr4:147557851-147557852	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs150355022	chr4:147557866-147557867	Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
22	rs116274489	chr4:147557867-147557868	Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
23	rs543837092	chr4:147557880-147557881	Bivalent Enhancer	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
24	rs370917088	chr4:147557911-147557912	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs188272488	chr4:147557913-147557914	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs191413927	chr4:147557944-147557945	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs183763420	chr4:147557946-147557947	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs563315566	chr4:147557948-147557949	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs11450165	chr4:147557949-147557950	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs146446290	chr4:147557983-147557984	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs568956639	chr4:147557995-147557996	Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs531576492	chr4:147558007-147558008	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs551176184	chr4:147558017-147558018	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs571040128	chr4:147558069-147558070	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs6537428	chr4:147558072-147558073	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs140944046	chr4:147558090-147558091	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
37	rs567580431	chr4:147558094-147558095	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
38	rs144600994	chr4:147558098-147558099	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
39	rs536548503	chr4:147558128-147558129	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
40	rs556862489	chr4:147558132-147558133	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
41	rs188493620	chr4:147558158-147558159	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs566577813	chr4:147558181-147558182	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs545617917	chr4:147558199-147558200	Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs1910595	chr4:147558237-147558238	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs76832102	chr4:147558243-147558244	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs115134269	chr4:147558244-147558245	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs561275046	chr4:147558280-147558281	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
48	rs536706150	chr4:147558284-147558285	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
49	rs529137398	chr4:147558294-147558295	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs542550609	chr4:147558332-147558333	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
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
Breast cancer	16272173	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147557800-147558200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
2	chr4:147558000-147558200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
3	chr4:147558000-147558200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:147558000-147558200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
5	chr4:147558000-147558200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:147558000-147558200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr4:147558000-147558200	Bivalent Enhancer	HSMMtube	muscle
8	chr4:147558000-147558400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:147558000-147558400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:147558000-147558600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:147558000-147558800	Bivalent Enhancer	Esophagus	oesophagus
12	chr4:147558000-147558800	Bivalent Enhancer	Placenta	Placenta
13	chr4:147558000-147559000	Bivalent Enhancer	Fetal Heart	heart
14	chr4:147558000-147559200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr4:147558000-147559400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:147558000-147562000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
17	chr4:147558000-147562000	Enhancers	Pancreas	Pancrea
18	chr4:147558200-147558400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
19	chr4:147558200-147558400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:147558200-147558400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
21	chr4:147558200-147558400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:147558200-147558400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:147558200-147558400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:147558200-147558400	Bivalent Enhancer	Small Intestine	intestine
25	chr4:147558200-147558400	Bivalent Enhancer	Stomach Mucosa	stomach
26	chr4:147558200-147558400	Bivalent/Poised TSS	HSMMtube	muscle
27	chr4:147558200-147558400	Bivalent Enhancer	Osteobl	bone
28	chr4:147558200-147558600	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
29	chr4:147558200-147558600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr4:147558200-147558600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:147558200-147558600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:147558200-147558600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
33	chr4:147558200-147558600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
34	chr4:147558200-147558600	Enhancers	Gastric	stomach
35	chr4:147558200-147558600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
36	chr4:147558200-147558600	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
37	chr4:147558200-147558800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
38	chr4:147558200-147559000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr4:147558200-147559000	Enhancers	Right Ventricle	heart
40	chr4:147558200-147559200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:147558200-147559200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:147558200-147559200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:147558200-147560600	Bivalent/Poised TSS	NH-A	brain
44	chr4:147558200-147561200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
45	chr4:147558200-147561800	Bivalent Enhancer	Lung	lung
46	chr4:147558200-147562200	Bivalent Enhancer	Fetal Brain Male	brain
47	chr4:147558400-147558600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
48	chr4:147558400-147558600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
49	chr4:147558400-147558600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
50	chr4:147558400-147558600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell

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