Variant report

Variant	esv2763396
Chromosome Location	chr4:148516769-148535636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 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	chr4:148528625-148528960	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:148535176-148535480	K562	blood:	n/a	n/a
3	CEBPB	chr4:148520416-148520654	IMR90	lung:	n/a	chr4:148520502-148520513
4	CEBPB	chr4:148520339-148521322	Hela-S3	cervix:	n/a	chr4:148520502-148520513
5	CEBPB	chr4:148520978-148521318	IMR90	lung:	n/a	n/a
6	CEBPB	chr4:148528661-148529047	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:148523938-148524128	A549	lung:	n/a	chr4:148523961-148523972
8	CEBPB	chr4:148520458-148520659	HepG2	liver:	n/a	chr4:148520502-148520513
9	CEBPB	chr4:148518055-148518564	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:148518220-148518584	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:148523921-148524122	HepG2	liver:	n/a	chr4:148523961-148523972
12	CEBPB	chr4:148523859-148524097	IMR90	lung:	n/a	chr4:148523961-148523972
13	CEBPB	chr4:148520387-148520612	K562	blood:	n/a	chr4:148520502-148520513
14	CHD2	chr4:148518054-148518477	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr4:148517520-148517670	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr4:148517600-148517750	HCFaa	heart:	n/a	n/a
17	CTCF	chr4:148517600-148517750	HA-sp	spinal cord:	n/a	n/a
18	CTCF	chr4:148517620-148517770	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr4:148517591-148517773	GM12878	blood:	n/a	n/a
20	CTCF	chr4:148517494-148517927	HCT-116	colon:	n/a	n/a
21	CTCF	chr4:148517586-148517750	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr4:148517604-148517757	LNCaP	prostate:	n/a	n/a
23	CTCF	chr4:148517630-148517705	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr4:148517660-148517810	HFF	foreskin:	n/a	n/a
25	CTCF	chr4:148517580-148517730	RPTEC	kidney:	n/a	n/a
26	CTCF	chr4:148517760-148517910	NHLF	lung:	n/a	n/a
27	CTCF	chr4:148517580-148517730	GM12865	blood:	n/a	n/a
28	CTCF	chr4:148517660-148517810	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr4:148517580-148517730	NHLF	lung:	n/a	n/a
30	CTCF	chr4:148517567-148517891	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:148517540-148517690	GM12869	blood:	n/a	n/a
32	CTCF	chr4:148517600-148517750	AG04449	skin:	n/a	n/a
33	CTCF	chr4:148517580-148517730	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr4:148517520-148517670	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr4:148517524-148517774	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:148517640-148517790	Caco-2	colon:	n/a	n/a
37	CTCF	chr4:148517600-148517750	HCT-116	colon:	n/a	n/a
38	CTCF	chr4:148517540-148517901	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:148517560-148517710	HAc	cerebellar:	n/a	n/a
40	CTCF	chr4:148517520-148517670	BJ	skin:	n/a	n/a
41	CTCF	chr4:148517600-148517750	HMEC	breast:	n/a	n/a
42	CTCF	chr4:148517600-148517750	HMF	breast:	n/a	n/a
43	CTCF	chr4:148517436-148518118	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr4:148517580-148517730	AG09319	gingival:	n/a	n/a
45	CTCF	chr4:148517600-148517750	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:148517580-148517730	GM12864	blood:	n/a	n/a
47	CTCF	chr4:148517580-148517730	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr4:148517605-148517736	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:148517620-148517770	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:148517600-148517750	GM06990	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148535164-148535214	NHBE	bronchial:	n/a
2	chr4:148535164-148535214	GM12892	blood:	n/a
3	chr4:148535164-148535214	NT2-D1	testis:	n/a
4	chr4:148535164-148535214	A549	lung:	n/a
5	chr4:148535164-148535214	H1-hESC	embryonic stem cell:	embryo
6	chr4:148535164-148535214	GM06990	blood:	n/a
7	chr4:148535164-148535214	SKMC	muscle:	n/a
8	chr4:148535164-148535214	NHDF-neo	bronchial:	n/a
9	chr4:148535164-148535214	HEK293	kidney:	embryo
10	chr4:148535164-148535214	GM19239	blood:	n/a
11	chr4:148535164-148535214	AG04450	lung:	fetal
12	chr4:148535164-148535214	BJ	skin:	n/a
13	chr4:148535164-148535214	IMR90	lung:	fetal
14	chr4:148535164-148535214	ProgFib	skin:	n/a
15	chr4:148535164-148535214	U87	brain:	n/a
16	chr4:148535164-148535214	HAEpiC	amniotic membrane:	n/a
17	chr4:148535164-148535214	AoSMC	blood vessel:	n/a
18	chr4:148535164-148535214	T-47D	breast:	n/a
19	chr4:148535164-148535214	GM12878	blood:	n/a
20	chr4:148535164-148535214	NH-A	brain:	n/a
21	chr4:148535164-148535214	PANC-1	pancreas:	n/a
22	chr4:148535164-148535214	NB4	blood:	n/a
23	chr4:148535164-148535214	HRCEpiC	kidney:	n/a
24	chr4:148535164-148535214	Caco-2	colon:	n/a
25	chr4:148535164-148535214	HCM	heart:	n/a
26	chr4:148535164-148535214	AG04449	skin:	fetal
27	chr4:148535164-148535214	HUVEC	blood vessel:	n/a
28	chr4:148535164-148535214	ovcar-3	ovarian:	n/a
29	chr4:148535164-148535214	AG09319	gingival:	n/a
30	chr4:148535164-148535214	GM12891	blood:	n/a
31	chr4:148535164-148535214	SK-N-SH_RA	brain:	n/a
32	chr4:148535164-148535214	HCPEpiC	choroid plexus:	n/a
33	chr4:148535164-148535214	AG09309	skin:	n/a
34	chr4:148535164-148535214	HCT-116	colon:	n/a
35	chr4:148535164-148535214	HL-60	blood:	n/a
36	chr4:148535164-148535214	MCF10A-Er-Src	breast:	n/a
37	chr4:148535164-148535214	Hepatocyte	liver:	n/a
38	chr4:148535164-148535214	PFSK-1	brain:	n/a
39	chr4:148535164-148535214	HRE	kidney:	n/a
40	chr4:148535164-148535214	HRPEpiC	eye:	n/a
41	chr4:148535164-148535214	MCF-7	breast:	n/a
42	chr4:148535164-148535214	HEEpiC	esophagus:	n/a
43	chr4:148535164-148535214	BE2_C	brain:	n/a
44	chr4:148535164-148535214	SK-N-MC	brain:	n/a
45	chr4:148535164-148535214	HMEC	breast:	n/a
46	chr4:148535164-148535214	SK-N-SH	brain:	n/a
47	chr4:148535164-148535214	SAEC	small airway:	n/a
48	chr4:148535164-148535214	HCF	heart:	n/a
49	chr4:148535164-148535214	CMK	blood:	n/a
50	chr4:148535164-148535214	ECC-1	luminal epithelium:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:148518441..148521336-chr4:148523862..148526303,2	K562	blood:
2	chr4:148517290..148518095-chr4:148787896..148788545,2	MCF-7	breast:
3	chr4:148534491..148537230-chr4:148653257..148655916,2	MCF-7	breast:
4	chr4:148520581..148521262-chr4:148787695..148788489,2	MCF-7	breast:
5	chr16:78160853..78161510-chr4:148527480..148528015,2	MCF-7	breast:
6	chr4:148526097..148528506-chr4:148530218..148532114,2	K562	blood:
7	chr4:148512401..148515389-chr4:148519840..148522071,2	K562	blood:
8	chr4:148531636..148535570-chr4:148536355..148539737,5	K562	blood:
9	chr4:148515221..148517290-chr4:148603248..148605420,2	MCF-7	breast:
10	chr4:148526097..148528506-chr4:148530218..148532114,2	K562	blood:
11	chr4:148528379..148531648-chr4:148533404..148536404,5	MCF-7	breast:
12	chr4:148528379..148531648-chr4:148533404..148536404,5	MCF-7	breast:
13	chr4:148533282..148535358-chr4:148536772..148538526,4	MCF-7	breast:
14	chr4:148520672..148522853-chr4:148532687..148534632,2	K562	blood:
15	chr4:148515308..148517900-chr4:148536751..148539491,4	MCF-7	breast:
16	chr4:148533195..148535601-chr4:148603840..148606780,2	K562	blood:
17	chr4:148518441..148521336-chr4:148523862..148526303,2	K562	blood:
18	chr4:148518766..148521760-chr4:148537381..148538897,2	MCF-7	breast:
19	chr4:148517547..148518065-chr4:148788601..148789204,2	MCF-7	breast:
20	chr4:148511550..148513191-chr4:148525701..148528628,2	K562	blood:
21	chr4:148520672..148522853-chr4:148532687..148534632,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRMT10-1	chr4:148530703-148531112	XLOC_004115

No data

Variant related genes	Relation type
TMEM184C	TF binding region
TMEM184C	CpG island
ENSG00000164169	chromatin interactions
ENSG00000251298	chromatin interactions
ENSG00000164168	chromatin interactions

Extended variants
information (count: 682 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:682 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542798912	chr4:148516778-148516779	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs190852721	chr4:148516785-148516786	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs570214238	chr4:148516873-148516874	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs9998608	chr4:148516877-148516878	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs374995104	chr4:148516921-148516922	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs552575540	chr4:148516984-148516985	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs571118189	chr4:148516988-148516989	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs547032282	chr4:148516999-148517000	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs370902780	chr4:148517000-148517001	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs79320363	chr4:148517052-148517053	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs547121113	chr4:148517071-148517072	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs11737404	chr4:148517089-148517090	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs79254717	chr4:148517137-148517138	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs556359258	chr4:148517210-148517211	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs565186661	chr4:148517213-148517214	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs569886899	chr4:148517271-148517272	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs62342650	chr4:148517273-148517274	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs558823701	chr4:148517369-148517370	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs62342651	chr4:148517374-148517375	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs11729128	chr4:148517380-148517381	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs11737524	chr4:148517383-148517384	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs56742716	chr4:148517403-148517404	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs542737475	chr4:148517429-148517430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562697501	chr4:148517470-148517471	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs6849966	chr4:148517493-148517494	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs148901078	chr4:148517503-148517504	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs565567426	chr4:148517559-148517560	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs6849644	chr4:148517584-148517585	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs183222611	chr4:148517609-148517610	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs567284080	chr4:148517633-148517634	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs529784993	chr4:148517702-148517703	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549904422	chr4:148517731-148517732	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs569827094	chr4:148517733-148517734	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs145506871	chr4:148517737-148517738	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs138005146	chr4:148517755-148517756	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs565949380	chr4:148517758-148517759	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539888405	chr4:148517797-148517798	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs6850429	chr4:148517852-148517853	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs553722802	chr4:148517913-148517914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140917724	chr4:148517942-148517943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552705218	chr4:148518043-148518044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74926454	chr4:148518048-148518049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201608787	chr4:148518050-148518051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35992219	chr4:148518051-148518052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199881776	chr4:148518052-148518053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377708377	chr4:148518129-148518130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545559025	chr4:148518130-148518131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144643128	chr4:148518132-148518133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572662467	chr4:148518137-148518138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536530728	chr4:148518153-148518154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148510200-148520800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:148512000-148517800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:148512400-148517800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:148512600-148518000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:148512600-148518000	Weak transcription	NHLF	lung
6	chr4:148512600-148518200	Weak transcription	Stomach Mucosa	stomach
7	chr4:148512800-148518000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:148516000-148518000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:148517600-148518600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:148517800-148518400	Enhancers	A549	lung
11	chr4:148517800-148518600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr4:148517800-148518600	Enhancers	NHEK	skin
13	chr4:148517800-148518800	Enhancers	HMEC	breast
14	chr4:148517800-148519000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:148518000-148518400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr4:148518000-148518600	Enhancers	HSMMtube	muscle
17	chr4:148518000-148518800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:148518000-148518800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr4:148518000-148518800	Enhancers	Pancreas	Pancrea
20	chr4:148518000-148518800	Enhancers	HSMM	muscle
21	chr4:148518000-148518800	Enhancers	HUVEC	blood vessel
22	chr4:148518000-148519000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr4:148518000-148519000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:148518000-148519000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr4:148518000-148519000	Enhancers	NHDF-Ad	bronchial
26	chr4:148518000-148519200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:148518000-148519200	Enhancers	NH-A	brain
28	chr4:148518000-148519200	Enhancers	NHLF	lung
29	chr4:148518000-148519200	Enhancers	Osteobl	bone
30	chr4:148518000-148519400	Enhancers	Hela-S3	cervix
31	chr4:148518000-148519800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr4:148518200-148518600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:148518200-148518600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:148518200-148518600	Enhancers	Stomach Mucosa	stomach
35	chr4:148518200-148518800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:148518200-148519000	Enhancers	Stomach Smooth Muscle	stomach
37	chr4:148518400-148518800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:148518400-148519200	Enhancers	Aorta	Aorta
39	chr4:148518400-148520800	Weak transcription	A549	lung
40	chr4:148518600-148519000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr4:148518600-148520600	Weak transcription	HSMMtube	muscle
42	chr4:148518600-148521000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr4:148518800-148520600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:148518800-148520800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:148518800-148520800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr4:148518800-148520800	Weak transcription	HMEC	breast
47	chr4:148518800-148520800	Weak transcription	HSMM	muscle
48	chr4:148519000-148519200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr4:148519000-148520600	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr4:148519000-148520800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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