Variant report

Variant	nsv4396
Chromosome Location	chr4:78935347-78980705
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:970)
CpG islands
(count:1531)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:970 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:78980572-78981241	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:78941939-78942247	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:78979826-78980124	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:78935920-78936964	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:78979156-78979372	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:78977230-78978408	HepG2	liver:	n/a	chr4:78978120-78978135
7	ATF2	chr4:78977710-78978164	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:78977256-78978284	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:78978591-78979398	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:78980442-78981005	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:78977265-78978275	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:78979644-78980227	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr4:78977739-78978072	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:78977275-78978783	HepG2	liver:	n/a	chr4:78978542-78978558
15	BHLHE40	chr4:78980496-78981017	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:78975979-78976016	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:78979191-78979342	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:78977900-78978198	K562	blood:	n/a	n/a
19	BHLHE40	chr4:78980693-78980991	K562	blood:	n/a	n/a
20	BHLHE40	chr4:78941856-78942239	HepG2	liver:	n/a	n/a
21	BHLHE40	chr4:78977726-78978176	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:78936046-78936572	HepG2	liver:	n/a	n/a
23	BHLHE40	chr4:78980592-78981024	GM12878	blood:	n/a	n/a
24	BRCA1	chr4:78979195-78979196	HepG2	liver:	n/a	n/a
25	CCNT2	chr4:78980171-78980315	K562	blood:	n/a	n/a
26	CEBPB	chr4:78979019-78979415	HepG2	liver:	n/a	chr4:78979218-78979229
27	CEBPB	chr4:78979110-78979441	ECC-1	luminal epithelium:	n/a	chr4:78979218-78979229
28	CEBPB	chr4:78977703-78978087	A549	lung:	n/a	n/a
29	CEBPB	chr4:78978937-78979434	Hela-S3	cervix:	n/a	chr4:78979218-78979229
30	CEBPB	chr4:78977212-78978108	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:78978981-78979350	HepG2	liver:	n/a	chr4:78979218-78979229
32	CEBPB	chr4:78978981-78979463	ECC-1	luminal epithelium:	n/a	chr4:78979218-78979229
33	CEBPB	chr4:78978976-78979389	MCF-7	breast:	n/a	chr4:78979218-78979229
34	CEBPB	chr4:78979066-78979469	MCF-7	breast:	n/a	chr4:78979218-78979229
35	CEBPB	chr4:78953984-78954137	A549	lung:	n/a	n/a
36	CEBPB	chr4:78979046-78979401	IMR90	lung:	n/a	chr4:78979218-78979229
37	CEBPB	chr4:78941862-78942060	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:78979051-78979397	H1-hESC	embryonic stem cell:	n/a	chr4:78979218-78979229
39	CEBPB	chr4:78978354-78978381	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:78979037-78979413	A549	lung:	n/a	chr4:78979218-78979229
41	CEBPB	chr4:78979831-78980147	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:78941810-78942188	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:78979027-78979416	HepG2	liver:	n/a	chr4:78979218-78979229
44	CEBPB	chr4:78977208-78978436	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:78979082-78979301	HepG2	liver:	n/a	chr4:78979218-78979229
46	CEBPB	chr4:78978988-78979534	A549	lung:	n/a	chr4:78979218-78979229
47	CEBPB	chr4:78979101-78979372	K562	blood:	n/a	chr4:78979218-78979229
48	CEBPB	chr4:78936121-78936432	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:78977806-78978188	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr4:78941829-78942159	HepG2	liver:	n/a	n/a

(count:1531 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78979746-78979796	NHDF-neo	bronchial:	n/a
2	chr4:78941960-78942010	HIPEpiC	eye:	n/a
3	chr4:78980101-78980151	NB4	blood:	n/a
4	chr4:78976261-78976311	NB4	blood:	n/a
5	chr4:78978772-78978822	GM12892	blood:	n/a
6	chr4:78978133-78978183	GM12878	blood:	n/a
7	chr4:78979746-78979796	NHDF-neo	bronchial:	n/a
8	chr4:78941960-78942010	HIPEpiC	eye:	n/a
9	chr4:78980101-78980151	NB4	blood:	n/a
10	chr4:78976261-78976311	NB4	blood:	n/a
11	chr4:78978772-78978822	GM12892	blood:	n/a
12	chr4:78978133-78978183	GM12878	blood:	n/a
13	chr4:78979559-78979609	HRPEpiC	eye:	n/a
14	chr4:78979894-78979944	HepG2	liver:	n/a
15	chr4:78980193-78980243	CMK	blood:	n/a
16	chr4:78980101-78980151	SK-N-SH	brain:	n/a
17	chr4:78978133-78978183	SK-N-MC	brain:	n/a
18	chr4:78978722-78978772	MCF10A-Er-Src	breast:	n/a
19	chr4:78980382-78980432	HCF	heart:	n/a
20	chr4:78978537-78978587	ovcar-3	ovarian:	n/a
21	chr4:78977223-78977273	GM19239	blood:	n/a
22	chr4:78980533-78980583	HAEpiC	amniotic membrane:	n/a
23	chr4:78978722-78978772	PrEC	prostate:	n/a
24	chr4:78980193-78980243	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:78980533-78980583	Caco-2	colon:	n/a
26	chr4:78978705-78978755	GM12891	blood:	n/a
27	chr4:78978848-78978898	HL-60	blood:	n/a
28	chr4:78977690-78977740	HMEC	breast:	n/a
29	chr4:78979559-78979609	HEK293	kidney:	embryo
30	chr4:78979207-78979257	HAEpiC	amniotic membrane:	n/a
31	chr4:78977322-78977372	SAEC	small airway:	n/a
32	chr4:78977690-78977740	HL-60	blood:	n/a
33	chr4:78977223-78977273	HIPEpiC	eye:	n/a
34	chr4:78977420-78977470	Caco-2	colon:	n/a
35	chr4:78980533-78980583	AG09309	skin:	n/a
36	chr4:78979559-78979609	PFSK-1	brain:	n/a
37	chr4:78979807-78979857	HUVEC	blood vessel:	n/a
38	chr4:78978133-78978183	SK-N-SH	brain:	n/a
39	chr4:78979894-78979944	AG04450	lung:	fetal
40	chr4:78978722-78978772	NHBE	bronchial:	n/a
41	chr4:78978772-78978822	BJ	skin:	n/a
42	chr4:78978697-78978747	SK-N-MC	brain:	n/a
43	chr4:78978565-78978615	ECC-1	luminal epithelium:	n/a
44	chr4:78978697-78978747	NHDF-neo	bronchial:	n/a
45	chr4:78979559-78979609	GM12891	blood:	n/a
46	chr4:78941960-78942010	PrEC	prostate:	n/a
47	chr4:78980533-78980583	NHDF-neo	bronchial:	n/a
48	chr4:78979559-78979609	K562	blood:	n/a
49	chr4:78978708-78978758	SAEC	small airway:	n/a
50	chr4:78976261-78976311	AG04449	skin:	fetal

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:78945694..78947405-chr4:78955374..78957277,2	K562	blood:
2	chr4:78978883..78980863-chr4:79393127..79395107,2	MCF-7	breast:
3	chr4:78977205..78980008-chr4:79470660..79474757,5	MCF-7	breast:
4	chr4:78929618..78932382-chr4:78935391..78936931,2	K562	blood:
5	chr4:78964181..78966409-chr4:78967968..78969521,2	K562	blood:
6	chr4:78944137..78946353-chr4:78952391..78954056,2	K562	blood:
7	chr4:78936253..78937804-chr4:78949496..78951569,2	K562	blood:
8	chr4:78944137..78946353-chr4:78952391..78954056,2	K562	blood:
9	chr4:78980165..78981369-chr4:79437966..79439156,9	MCF-7	breast:
10	chr4:78975304..78979082-chr4:79472141..79474367,3	MCF-7	breast:
11	chr4:78936253..78937804-chr4:78949496..78951569,2	K562	blood:
12	chr4:78739575..78742806-chr4:78977392..78979889,3	MCF-7	breast:
13	chr4:78945694..78947405-chr4:78955374..78957277,2	K562	blood:
14	chr4:78964181..78966409-chr4:78967968..78969521,2	K562	blood:
15	chr4:78980443..78981479-chr4:79437986..79438999,5	MCF-7	breast:
16	chr4:78959979..78963172-chr4:78976662..78978901,3	MCF-7	breast:
17	chr4:78953783..78955341-chr4:78989296..78991201,2	K562	blood:
18	chr4:78925853..78927440-chr4:78976402..78978682,2	MCF-7	breast:
19	chr4:78913096..78915245-chr4:78935885..78937796,2	K562	blood:
20	chr4:78980297..78981139-chr4:79092342..79093264,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNOT6L-3	chr4:78960128-78960462	expReg_chr4_3663_-

No data

Variant related genes	Relation type
FRAS1	TF binding region
FRAS1	CpG island
ENSG00000138772	chromatin interactions
ENSG00000138767	chromatin interactions
ENSG00000138759	chromatin interactions
ENSG00000249072	chromatin interactions

Extended variants
information (count: 989 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539238650	chr4:78935348-78935349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374279988	chr4:78935356-78935357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549595965	chr4:78935421-78935422	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs569908934	chr4:78935423-78935424	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72654605	chr4:78935553-78935554	Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555646628	chr4:78935591-78935592	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2088994	chr4:78935658-78935659	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs534654525	chr4:78935671-78935672	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs571490727	chr4:78935730-78935731	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142653718	chr4:78935795-78935796	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs577849257	chr4:78935837-78935838	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201604000	chr4:78935884-78935885	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150241886	chr4:78935925-78935926	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537542880	chr4:78935944-78935945	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548024034	chr4:78935961-78935962	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2088995	chr4:78935963-78935964	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs574192067	chr4:78935977-78935978	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542910301	chr4:78936019-78936020	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559997382	chr4:78936023-78936024	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528463818	chr4:78936030-78936031	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs62310787	chr4:78936039-78936040	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs376848348	chr4:78936048-78936049	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2102191	chr4:78936074-78936075	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs530937789	chr4:78936100-78936101	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551071288	chr4:78936101-78936102	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372152531	chr4:78936118-78936119	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569713205	chr4:78936124-78936125	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371969023	chr4:78936167-78936168	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577029941	chr4:78936269-78936270	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs373492526	chr4:78936284-78936285	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188510461	chr4:78936394-78936395	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545332424	chr4:78936408-78936409	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535645339	chr4:78936466-78936467	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138907160	chr4:78936481-78936482	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566020004	chr4:78936510-78936511	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148954341	chr4:78936552-78936553	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181315514	chr4:78936594-78936595	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571286602	chr4:78936626-78936627	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537107967	chr4:78936651-78936652	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184268655	chr4:78936654-78936655	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563425444	chr4:78936721-78936722	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143732987	chr4:78936741-78936742	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539026087	chr4:78936766-78936767	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190137941	chr4:78936772-78936773	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553379504	chr4:78936810-78936811	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573232915	chr4:78936814-78936815	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138329499	chr4:78936815-78936816	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10000234	chr4:78936885-78936886	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530825235	chr4:78936890-78936891	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558676560	chr4:78936891-78936892	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
colon cancer	22000013	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD

Chromatin state (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78934800-78935400	Enhancers	HepG2	liver
2	chr4:78935400-78935600	Flanking Active TSS	HepG2	liver
3	chr4:78935600-78936000	Enhancers	HepG2	liver
4	chr4:78936000-78936600	Active TSS	HepG2	liver
5	chr4:78936600-78937200	Flanking Active TSS	HepG2	liver
6	chr4:78937200-78938000	Enhancers	HepG2	liver
7	chr4:78938000-78938800	Weak transcription	HepG2	liver
8	chr4:78938800-78940200	Enhancers	HepG2	liver
9	chr4:78938800-78940400	Enhancers	Fetal Lung	lung
10	chr4:78939000-78940800	Enhancers	Fetal Kidney	kidney
11	chr4:78939600-78939800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:78939600-78940000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:78940200-78941000	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr4:78940200-78941200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr4:78940200-78941600	Weak transcription	HepG2	liver
16	chr4:78940400-78941000	Weak transcription	Fetal Lung	lung
17	chr4:78940800-78943600	Weak transcription	Fetal Kidney	kidney
18	chr4:78941000-78941600	Enhancers	Fetal Lung	lung
19	chr4:78941600-78942600	Enhancers	HepG2	liver
20	chr4:78941600-78944800	Weak transcription	Fetal Lung	lung
21	chr4:78941800-78942400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr4:78941800-78942600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:78941800-78942600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:78941800-78943000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr4:78942000-78942400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:78942600-78943200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:78943200-78944400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:78943600-78944000	Enhancers	Fetal Kidney	kidney
29	chr4:78944200-78944400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:78944600-78945600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr4:78944800-78945000	Enhancers	Fetal Lung	lung
32	chr4:78944800-78946400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:78945200-78946400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:78945400-78946000	Enhancers	HUVEC	blood vessel
35	chr4:78945600-78946000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr4:78945600-78946000	Enhancers	NHDF-Ad	bronchial
37	chr4:78945600-78946200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:78951600-78951800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:78952200-78952600	Enhancers	Fetal Lung	lung
40	chr4:78952400-78953400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:78953200-78953600	Enhancers	Fetal Kidney	kidney
42	chr4:78953400-78954000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr4:78953400-78954000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr4:78953600-78953800	Enhancers	Placenta	Placenta
45	chr4:78953600-78954000	Enhancers	H9 Cell Line	embryonic stem cell
46	chr4:78958800-78960200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:78959400-78960000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:78960800-78963200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:78961400-78961600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:78961400-78962200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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