Variant report

Variant	nsv1004772
Chromosome Location	chr4:78906866-78976561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:655)
CpG islands
(count:244)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:78941939-78942247	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:78915566-78916000	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:78935920-78936964	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:78917243-78917648	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:78912050-78912450	HepG2	liver:	n/a	n/a
6	BATF	chr4:78929622-78929894	GM12878	blood:	n/a	n/a
7	BATF	chr4:78929661-78929894	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:78929628-78929950	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:78929619-78929887	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:78941856-78942239	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:78975979-78976016	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:78929601-78929908	HepG2	liver:	n/a	n/a
13	BHLHE40	chr4:78936046-78936572	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:78933098-78933293	A549	lung:	n/a	chr4:78933175-78933186
15	CEBPB	chr4:78933076-78933274	K562	blood:	n/a	chr4:78933175-78933186
16	CEBPB	chr4:78941810-78942188	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:78915279-78915563	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:78933064-78933304	HepG2	liver:	n/a	chr4:78933175-78933186
19	CEBPB	chr4:78953984-78954137	A549	lung:	n/a	n/a
20	CEBPB	chr4:78933084-78933234	H1-hESC	embryonic stem cell:	n/a	chr4:78933175-78933186
21	CEBPB	chr4:78911597-78912340	HepG2	liver:	n/a	chr4:78911733-78911744
22	CEBPB	chr4:78936121-78936432	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:78911631-78911883	A549	lung:	n/a	chr4:78911733-78911744
24	CEBPB	chr4:78941829-78942159	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:78915380-78915511	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:78941862-78942060	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:78933107-78933302	IMR90	lung:	n/a	chr4:78933175-78933186
28	CEBPD	chr4:78929584-78930105	K562	blood:	n/a	n/a
29	CHD2	chr4:78950689-78950709	K562	blood:	n/a	n/a
30	CTCF	chr4:78915654-78915914	T-47D	breast:	n/a	n/a
31	CTCF	chr4:78915672-78915947	HepG2	liver:	n/a	n/a
32	CTCF	chr4:78915680-78915830	HPF	lung:	n/a	n/a
33	CTCF	chr4:78953536-78953958	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:78915680-78915830	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr4:78915653-78915910	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:78915680-78915830	Caco-2	colon:	n/a	n/a
37	CTCF	chr4:78915691-78915920	NHEK	skin:	n/a	n/a
38	CTCF	chr4:78915320-78915470	HCT-116	colon:	n/a	n/a
39	CTCF	chr4:78915440-78915590	AG10803	skin:	n/a	n/a
40	CTCF	chr4:78915660-78915810	GM12866	blood:	n/a	n/a
41	CTCF	chr4:78915539-78915984	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr4:78915720-78915870	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr4:78915420-78915570	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr4:78915620-78915770	HCM	heart:	n/a	n/a
45	CTCF	chr4:78915644-78915943	Gliobla	brain:	n/a	n/a
46	CTCF	chr4:78914925-78916235	A549	lung:	n/a	n/a
47	CTCF	chr4:78915720-78915870	BJ	skin:	n/a	n/a
48	CTCF	chr4:78915598-78915943	K562	blood:	n/a	n/a
49	CTCF	chr4:78943920-78944070	HMF	breast:	n/a	n/a
50	CTCF	chr4:78915700-78915850	BE2_C	brain:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78916381-78916431	AoSMC	blood vessel:	n/a
2	chr4:78916381-78916431	HCT-116	colon:	n/a
3	chr4:78916381-78916431	HNPCEpiC	eye:	n/a
4	chr4:78976261-78976311	NH-A	brain:	n/a
5	chr4:78916381-78916431	PFSK-1	brain:	n/a
6	chr4:78976261-78976311	IMR90	lung:	fetal
7	chr4:78976261-78976311	AG04449	skin:	fetal
8	chr4:78928450-78928500	SKMC	muscle:	n/a
9	chr4:78941960-78942010	K562	blood:	n/a
10	chr4:78941960-78942010	Hepatocyte	liver:	n/a
11	chr4:78976261-78976311	HCM	heart:	n/a
12	chr4:78976261-78976311	AG09309	skin:	n/a
13	chr4:78976261-78976311	MCF-7	breast:	n/a
14	chr4:78928450-78928500	NT2-D1	testis:	n/a
15	chr4:78916381-78916431	Jurkat	blood:	n/a
16	chr4:78916381-78916431	U87	brain:	n/a
17	chr4:78916381-78916431	T-47D	breast:	n/a
18	chr4:78976261-78976311	Jurkat	blood:	n/a
19	chr4:78928450-78928500	GM12891	blood:	n/a
20	chr4:78941960-78942010	ovcar-3	ovarian:	n/a
21	chr4:78976261-78976311	GM12878	blood:	n/a
22	chr4:78976261-78976311	U87	brain:	n/a
23	chr4:78916381-78916431	MCF10A-Er-Src	breast:	n/a
24	chr4:78928450-78928500	HEK293	kidney:	embryo
25	chr4:78941960-78942010	HMEC	breast:	n/a
26	chr4:78941960-78942010	HCM	heart:	n/a
27	chr4:78916381-78916431	NT2-D1	testis:	n/a
28	chr4:78941960-78942010	BE2_C	brain:	n/a
29	chr4:78928450-78928500	HNPCEpiC	eye:	n/a
30	chr4:78976261-78976311	K562	blood:	n/a
31	chr4:78976261-78976311	HL-60	blood:	n/a
32	chr4:78916381-78916431	HRPEpiC	eye:	n/a
33	chr4:78976261-78976311	HMEC	breast:	n/a
34	chr4:78916381-78916431	RPTEC	kidney:	n/a
35	chr4:78941960-78942010	SKMC	muscle:	n/a
36	chr4:78928450-78928500	SK-N-MC	brain:	n/a
37	chr4:78916381-78916431	ECC-1	luminal epithelium:	n/a
38	chr4:78916381-78916431	ProgFib	skin:	n/a
39	chr4:78928450-78928500	SK-N-SH	brain:	n/a
40	chr4:78941960-78942010	A549	lung:	n/a
41	chr4:78928450-78928500	HCT-116	colon:	n/a
42	chr4:78916381-78916431	SK-N-MC	brain:	n/a
43	chr4:78941960-78942010	AG04449	skin:	fetal
44	chr4:78941960-78942010	GM12891	blood:	n/a
45	chr4:78928450-78928500	AG09319	gingival:	n/a
46	chr4:78928450-78928500	GM19239	blood:	n/a
47	chr4:78976261-78976311	Hepatocyte	liver:	n/a
48	chr4:78928450-78928500	HEEpiC	esophagus:	n/a
49	chr4:78941960-78942010	SAEC	small airway:	n/a
50	chr4:78976261-78976311	H1-hESC	embryonic stem cell:	embryo

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:78945694..78947405-chr4:78955374..78957277,2	K562	blood:
2	chr4:78964181..78966409-chr4:78967968..78969521,2	K562	blood:
3	chr4:78944137..78946353-chr4:78952391..78954056,2	K562	blood:
4	chr4:78936253..78937804-chr4:78949496..78951569,2	K562	blood:
5	chr4:78925853..78927440-chr4:78976402..78978682,2	MCF-7	breast:
6	chr4:78959979..78963172-chr4:78976662..78978901,3	MCF-7	breast:
7	chr4:78944137..78946353-chr4:78952391..78954056,2	K562	blood:
8	chr4:78913096..78915245-chr4:78935885..78937796,2	K562	blood:
9	chr4:78975304..78979082-chr4:79472141..79474367,3	MCF-7	breast:
10	chr4:78953783..78955341-chr4:78989296..78991201,2	K562	blood:
11	chr4:78925853..78927440-chr4:78976402..78978682,2	MCF-7	breast:
12	chr4:78945694..78947405-chr4:78955374..78957277,2	K562	blood:
13	chr4:78909839..78911739-chr4:78914254..78917095,2	MCF-7	breast:
14	chr4:78929618..78932382-chr4:78935391..78936931,2	K562	blood:
15	chr4:78936253..78937804-chr4:78949496..78951569,2	K562	blood:
16	chr4:78913096..78915245-chr4:78935885..78937796,2	K562	blood:
17	chr4:78915311..78916190-chr4:79437915..79438836,3	K562	blood:
18	chr4:78915334..78916174-chr4:79437913..79438840,4	MCF-7	breast:
19	chr4:78964181..78966409-chr4:78967968..78969521,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL1-2	chr4:78924297-78924593	NONHSAT097062
2	lnc-CNOT6L-3	chr4:78960128-78960462	expReg_chr4_3663_-

No data

Variant related genes	Relation type
FRAS1	TF binding region
HNRNPA1P56	TF binding region
ENSG00000248128	TF binding region
ENSG00000249072	TF binding region
FRAS1	CpG island
HNRNPA1P56	CpG island
ENSG00000248128	CpG island
ENSG00000249072	CpG island
ENSG00000248640	chromatin interactions
ENSG00000249072	chromatin interactions
ENSG00000138759	chromatin interactions
ENSG00000138772	chromatin interactions

Extended variants
information (count: 1497 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1497 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370073727	chr4:78910879-78910880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs142249906	chr4:78910933-78910934	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs532633530	chr4:78910966-78910967	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs17450655	chr4:78911023-78911024	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs562872913	chr4:78911084-78911085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565577210	chr4:78911088-78911089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551444564	chr4:78911102-78911103	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs531716930	chr4:78911108-78911109	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs35589310	chr4:78911125-78911126	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571534994	chr4:78911203-78911204	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs146258236	chr4:78911241-78911242	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs182333374	chr4:78911296-78911297	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs6533372	chr4:78911389-78911390	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527791935	chr4:78911451-78911452	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs78668700	chr4:78911454-78911455	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368129367	chr4:78911464-78911465	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs538861672	chr4:78911541-78911542	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs558873646	chr4:78911565-78911566	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs567866846	chr4:78911568-78911569	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536950007	chr4:78911590-78911591	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs553046379	chr4:78911627-78911628	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs537847749	chr4:78911707-78911708	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs114826086	chr4:78911713-78911714	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs574436137	chr4:78911745-78911746	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs186993192	chr4:78911777-78911778	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs537067748	chr4:78911855-78911856	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs553920381	chr4:78911891-78911892	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs138818762	chr4:78911906-78911907	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572862543	chr4:78911942-78911943	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs75109014	chr4:78912007-78912008	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs538767944	chr4:78912168-78912169	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs577789980	chr4:78912172-78912173	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs113354270	chr4:78912184-78912185	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs141235699	chr4:78912200-78912201	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs576665706	chr4:78912241-78912242	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs542166141	chr4:78912244-78912245	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs561953395	chr4:78912259-78912260	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558709998	chr4:78912262-78912263	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs150350265	chr4:78912281-78912282	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs375780068	chr4:78912288-78912289	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs547887009	chr4:78912307-78912308	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs544089024	chr4:78912326-78912327	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564602305	chr4:78912384-78912385	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs191946165	chr4:78912442-78912443	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs3920099	chr4:78912445-78912446	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs183012248	chr4:78912535-78912536	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs537762979	chr4:78912587-78912588	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs548137857	chr4:78912595-78912596	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs374276336	chr4:78912597-78912598	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs567986096	chr4:78912606-78912607	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Breast cancer	21364760	CNVD
colon cancer	22000013	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78911000-78913800	Enhancers	Fetal Lung	lung
2	chr4:78911200-78911400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:78911200-78912200	Enhancers	Fetal Stomach	stomach
4	chr4:78911200-78912600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:78911200-78912600	Enhancers	Fetal Brain Male	brain
6	chr4:78911200-78912600	Enhancers	HepG2	liver
7	chr4:78911400-78912200	Enhancers	HUVEC	blood vessel
8	chr4:78911400-78912400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:78911400-78912400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:78911400-78915200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:78911600-78913200	Enhancers	Fetal Brain Female	brain
12	chr4:78911800-78912200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:78911800-78912400	Enhancers	Brain Germinal Matrix	brain
14	chr4:78911800-78913400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:78911800-78913400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr4:78912000-78912400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr4:78912000-78912400	Enhancers	NHDF-Ad	bronchial
18	chr4:78912000-78912800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:78912200-78912800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr4:78912200-78913000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:78912200-78914000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr4:78912400-78913000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:78912400-78913200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:78912400-78913400	Weak transcription	Brain Germinal Matrix	brain
25	chr4:78912400-78915000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr4:78912400-78915200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr4:78912400-78915200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:78912600-78913800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:78912600-78915000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:78912600-78915000	Weak transcription	HepG2	liver
31	chr4:78912800-78915200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr4:78913000-78915200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr4:78913000-78915200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr4:78913200-78913400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr4:78913200-78915200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:78913400-78914200	Enhancers	Brain Germinal Matrix	brain
37	chr4:78913400-78915200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr4:78913400-78915200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr4:78913400-78915400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr4:78913800-78915200	Weak transcription	Fetal Lung	lung
41	chr4:78913800-78915400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:78914000-78915200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr4:78915000-78915400	Enhancers	HepG2	liver
44	chr4:78915000-78916000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:78915000-78916000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr4:78915000-78916000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr4:78915200-78915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr4:78915200-78915400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr4:78915200-78915600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:78915200-78915800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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