Variant report

Variant	nsv830108
Chromosome Location	chr4:148114652-148311104
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:148299886-148300372	HCT-116	colon:	n/a	n/a
2	ATF3	chr4:148292792-148293328	HCT-116	colon:	n/a	n/a
3	ATF3	chr4:148300036-148300218	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr4:148299925-148300250	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:148213946-148213985	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr4:148261839-148262240	GM12878	blood:	n/a	n/a
7	BATF	chr4:148261867-148262233	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:148119641-148119804	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr4:148261742-148262052	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:148119611-148119868	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr4:148261694-148262154	GM12878	blood:	n/a	n/a
12	CBX3	chr4:148292767-148293367	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:148186332-148186711	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:148292726-148293362	HCT-116	colon:	n/a	n/a
15	CBX3	chr4:148186333-148186658	HCT-116	colon:	n/a	n/a
16	CBX3	chr4:148282716-148283448	HCT-116	colon:	n/a	n/a
17	CBX3	chr4:148261189-148262132	HCT-116	colon:	n/a	n/a
18	CBX3	chr4:148299905-148300454	HCT-116	colon:	n/a	n/a
19	CEBPB	chr4:148292859-148293121	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:148148552-148148747	HepG2	liver:	n/a	chr4:148148573-148148584
21	CEBPB	chr4:148282728-148283535	HCT-116	colon:	n/a	chr4:148283324-148283332
22	CEBPB	chr4:148150470-148150491	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:148289330-148289548	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:148299891-148300350	MCF-7	breast:	n/a	chr4:148300259-148300272 chr4:148300256-148300273 chr4:148300259-148300270 chr4:148300261-148300272 chr4:148300261-148300272 chr4:148300296-148300304 chr4:148300259-148300272 chr4:148300259-148300272
25	CEBPB	chr4:148287305-148287678	A549	lung:	n/a	chr4:148287541-148287552
26	CEBPB	chr4:148272222-148272948	Hela-S3	cervix:	n/a	chr4:148272450-148272461
27	CEBPB	chr4:148160406-148160651	A549	lung:	n/a	chr4:148160521-148160533 chr4:148160532-148160543
28	CEBPB	chr4:148261346-148261634	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:148287392-148287710	K562	blood:	n/a	chr4:148287541-148287552
30	CEBPB	chr4:148206444-148206641	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:148124302-148124520	Hela-S3	cervix:	n/a	chr4:148124413-148124424 chr4:148124378-148124389
32	CEBPB	chr4:148160321-148160621	IMR90	lung:	n/a	chr4:148160521-148160533 chr4:148160532-148160543
33	CEBPB	chr4:148287371-148287736	HepG2	liver:	n/a	chr4:148287541-148287552
34	CEBPB	chr4:148299749-148300525	HCT-116	colon:	n/a	chr4:148300259-148300272 chr4:148300256-148300273 chr4:148300259-148300270 chr4:148300261-148300272 chr4:148300261-148300272 chr4:148300296-148300304 chr4:148300259-148300272 chr4:148300259-148300272
35	CEBPB	chr4:148160228-148160622	H1-hESC	embryonic stem cell:	n/a	chr4:148160521-148160533 chr4:148160532-148160543
36	CEBPB	chr4:148272310-148272570	HepG2	liver:	n/a	chr4:148272450-148272461
37	CEBPB	chr4:148299724-148300616	HCT-116	colon:	n/a	chr4:148300259-148300272 chr4:148300256-148300273 chr4:148300259-148300270 chr4:148300261-148300272 chr4:148300261-148300272 chr4:148300296-148300304 chr4:148300259-148300272 chr4:148300259-148300272
38	CEBPB	chr4:148272323-148272603	K562	blood:	n/a	chr4:148272450-148272461
39	CEBPB	chr4:148299915-148300360	Hela-S3	cervix:	n/a	chr4:148300259-148300272 chr4:148300256-148300273 chr4:148300259-148300270 chr4:148300261-148300272 chr4:148300261-148300272 chr4:148300296-148300304 chr4:148300259-148300272 chr4:148300259-148300272
40	CEBPB	chr4:148208741-148208953	Hela-S3	cervix:	n/a	chr4:148208811-148208822
41	CEBPB	chr4:148281452-148281873	IMR90	lung:	n/a	n/a
42	CEBPB	chr4:148117825-148118026	HepG2	liver:	n/a	chr4:148117899-148117910
43	CEBPB	chr4:148282883-148283387	IMR90	lung:	n/a	chr4:148283324-148283332
44	CEBPB	chr4:148300016-148300407	HepG2	liver:	n/a	chr4:148300259-148300272 chr4:148300256-148300273 chr4:148300259-148300270 chr4:148300261-148300272 chr4:148300261-148300272 chr4:148300296-148300304 chr4:148300259-148300272 chr4:148300259-148300272
45	CEBPB	chr4:148282949-148283420	A549	lung:	n/a	chr4:148283324-148283332
46	CEBPB	chr4:148287333-148287749	ECC-1	luminal epithelium:	n/a	chr4:148287541-148287552
47	CEBPB	chr4:148210339-148210586	HepG2	liver:	n/a	chr4:148210456-148210467
48	CEBPB	chr4:148118909-148119097	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr4:148272284-148273134	IMR90	lung:	n/a	chr4:148272450-148272461
50	CEBPB	chr4:148300036-148300280	A549	lung:	n/a	chr4:148300259-148300272 chr4:148300256-148300273 chr4:148300259-148300270 chr4:148300261-148300272 chr4:148300261-148300272 chr4:148300259-148300272 chr4:148300259-148300272

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148291437-148291487	HMEC	breast:	n/a
2	chr4:148291437-148291487	HMEC	breast:	n/a
3	chr4:148279079-148279129	NB4	blood:	n/a
4	chr4:148260510-148260560	BJ	skin:	n/a
5	chr4:148254941-148254991	HepG2	liver:	n/a
6	chr4:148254941-148254991	U87	brain:	n/a
7	chr4:148116386-148116436	PrEC	prostate:	n/a
8	chr4:148283066-148283116	PANC-1	pancreas:	n/a
9	chr4:148260510-148260560	NH-A	brain:	n/a
10	chr4:148233162-148233212	BJ	skin:	n/a
11	chr4:148279079-148279129	Jurkat	blood:	n/a
12	chr4:148260510-148260560	HRE	kidney:	n/a
13	chr4:148116386-148116436	SK-N-MC	brain:	n/a
14	chr4:148233162-148233212	AG04449	skin:	fetal
15	chr4:148119477-148119527	AoSMC	blood vessel:	n/a
16	chr4:148291437-148291487	AG04449	skin:	fetal
17	chr4:148283066-148283116	ProgFib	skin:	n/a
18	chr4:148283066-148283116	HepG2	liver:	n/a
19	chr4:148116386-148116436	AG04449	skin:	fetal
20	chr4:148260510-148260560	BE2_C	brain:	n/a
21	chr4:148260510-148260560	NHBE	bronchial:	n/a
22	chr4:148260510-148260560	Caco-2	colon:	n/a
23	chr4:148254941-148254991	HCF	heart:	n/a
24	chr4:148116386-148116436	HCPEpiC	choroid plexus:	n/a
25	chr4:148116386-148116436	GM12892	blood:	n/a
26	chr4:148260510-148260560	AG09319	gingival:	n/a
27	chr4:148260510-148260560	NB4	blood:	n/a
28	chr4:148233162-148233212	LNCaP	prostate:	n/a
29	chr4:148291437-148291487	HRCEpiC	kidney:	n/a
30	chr4:148260510-148260560	SK-N-MC	brain:	n/a
31	chr4:148254941-148254991	GM19239	blood:	n/a
32	chr4:148116386-148116436	HEK293	kidney:	embryo
33	chr4:148283066-148283116	HCM	heart:	n/a
34	chr4:148291437-148291487	AoSMC	blood vessel:	n/a
35	chr4:148254941-148254991	Jurkat	blood:	n/a
36	chr4:148254941-148254991	HEEpiC	esophagus:	n/a
37	chr4:148116386-148116436	AG10803	skin:	n/a
38	chr4:148116386-148116436	HRCEpiC	kidney:	n/a
39	chr4:148119477-148119527	CMK	blood:	n/a
40	chr4:148260510-148260560	CMK	blood:	n/a
41	chr4:148254941-148254991	HCM	heart:	n/a
42	chr4:148233162-148233212	SAEC	small airway:	n/a
43	chr4:148233162-148233212	AG09319	gingival:	n/a
44	chr4:148254941-148254991	PrEC	prostate:	n/a
45	chr4:148116386-148116436	HEEpiC	esophagus:	n/a
46	chr4:148116386-148116436	HCT-116	colon:	n/a
47	chr4:148283066-148283116	AG04449	skin:	fetal
48	chr4:148260510-148260560	H1-hESC	embryonic stem cell:	embryo
49	chr4:148254941-148254991	MCF10A-Er-Src	breast:	n/a
50	chr4:148279079-148279129	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:148201722..148203853-chr4:148204436..148207128,2	K562	blood:
2	chr4:148078475..148079202-chr4:148299618..148300406,2	MCF-7	breast:
3	chr4:148282434..148285155-chr4:148286485..148289056,2	K562	blood:
4	chr4:148229582..148231427-chr4:148235135..148238116,2	K562	blood:
5	chr4:148272436..148274239-chr4:148281813..148283538,2	MCF-7	breast:
6	chr4:148081823..148082362-chr4:148299859..148300742,2	MCF-7	breast:
7	chr12:54519933..54522634-chr4:148134863..148137147,2	MCF-7	breast:
8	chr4:148134867..148136847-chr4:148142304..148144965,2	MCF-7	breast:
9	chr4:148160683..148161374-chr5:115362795..115363673,2	MCF-7	breast:
10	chr4:148157546..148159164-chr4:148159658..148162438,2	K562	blood:
11	chr4:148229582..148231427-chr4:148235135..148238116,2	K562	blood:
12	chr4:148134867..148136847-chr4:148142304..148144965,2	MCF-7	breast:
13	chr4:148201722..148203853-chr4:148204436..148207128,2	K562	blood:
14	chr4:148167189..148168690-chr8:125868444..125870063,3	MCF-7	breast:
15	chr4:148167022..148169732-chr4:149288503..149290776,2	K562	blood:
16	chr4:148157546..148159164-chr4:148159658..148162438,2	K562	blood:
17	chr4:148282434..148285155-chr4:148286485..148289056,2	K562	blood:
18	chr4:148272436..148274239-chr4:148281813..148283538,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548g-3p	chr4:148265795-148265816	MIMAT0005912
hsa-miR-548g-5p	chr4:148265833-148265855	MIMAT0022722

Variant related genes	Relation type
MIR548G	TF binding region
MIR548G	CpG island
ENSG00000151623	chromatin interactions
ENSG00000255080	chromatin interactions

Extended variants
information (count: 5244 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:5244 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529933419	chr4:148114660-148114661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs62342963	chr4:148114807-148114808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs183359377	chr4:148114837-148114838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563141969	chr4:148114871-148114872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532119340	chr4:148114899-148114900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532826552	chr4:148114904-148114905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374826599	chr4:148114975-148114976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565339780	chr4:148115037-148115038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369108559	chr4:148115164-148115165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537498955	chr4:148115193-148115194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112692307	chr4:148115195-148115196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528063077	chr4:148115199-148115200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35951613	chr4:148115215-148115216	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs75119158	chr4:148115345-148115346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537321118	chr4:148115403-148115404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186524444	chr4:148115568-148115569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571047081	chr4:148115571-148115572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539946926	chr4:148115574-148115575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553454686	chr4:148115575-148115576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369324562	chr4:148115628-148115629	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs149633901	chr4:148115630-148115631	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs555456078	chr4:148115784-148115785	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs144347130	chr4:148115875-148115876	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs543307179	chr4:148115888-148115889	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs139193965	chr4:148115893-148115894	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs541845202	chr4:148115926-148115927	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs576583748	chr4:148115955-148115956	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs545516767	chr4:148115968-148115969	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs143204269	chr4:148115988-148115989	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs539978332	chr4:148115993-148115994	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs548196033	chr4:148116007-148116008	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs147493533	chr4:148116097-148116098	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs531277336	chr4:148116176-148116177	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs564645973	chr4:148116199-148116200	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs551254975	chr4:148116247-148116248	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556749468	chr4:148116248-148116249	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs571056902	chr4:148116273-148116274	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs77764826	chr4:148116300-148116301	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs532062556	chr4:148116304-148116305	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs547129978	chr4:148116346-148116347	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs369418137	chr4:148116347-148116348	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs566984706	chr4:148116386-148116387	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs373017020	chr4:148116387-148116388	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555775621	chr4:148116415-148116416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575510784	chr4:148116496-148116497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536951200	chr4:148116545-148116546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114166267	chr4:148116563-148116564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116410630	chr4:148116565-148116566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545629363	chr4:148116578-148116579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189784315	chr4:148116644-148116645	Enhancers Weak transcription Flanking Active TSS	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148105600-148115800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:148111800-148117800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:148114400-148115400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:148115200-148115600	Enhancers	Fetal Stomach	stomach
5	chr4:148115200-148115600	Enhancers	Right Atrium	heart
6	chr4:148115200-148115800	Enhancers	Fetal Heart	heart
7	chr4:148115200-148116200	Enhancers	Left Ventricle	heart
8	chr4:148115200-148117000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr4:148115200-148117000	Enhancers	HSMM	muscle
10	chr4:148115400-148115600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:148115400-148115600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr4:148115400-148115600	Enhancers	Ovary	ovary
13	chr4:148115400-148115600	Enhancers	Osteobl	bone
14	chr4:148115400-148116000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:148115400-148116200	Enhancers	Small Intestine	intestine
16	chr4:148115400-148116600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:148115400-148116600	Enhancers	HSMMtube	muscle
18	chr4:148115400-148116800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:148115400-148116800	Enhancers	NHDF-Ad	bronchial
20	chr4:148115400-148117000	Enhancers	NH-A	brain
21	chr4:148115600-148115800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:148115600-148116000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr4:148115600-148116000	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr4:148115600-148116000	Weak transcription	Fetal Stomach	stomach
25	chr4:148115600-148116000	Active TSS	Ovary	ovary
26	chr4:148115600-148116400	Flanking Active TSS	Osteobl	bone
27	chr4:148115800-148116000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:148115800-148116200	Active TSS	NHLF	lung
29	chr4:148115800-148116800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:148115800-148119400	Weak transcription	Fetal Heart	heart
31	chr4:148116000-148116200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:148116000-148116200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:148116000-148116200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:148116000-148116200	Enhancers	Fetal Stomach	stomach
35	chr4:148116000-148116600	Enhancers	Fetal Kidney	kidney
36	chr4:148116000-148116800	Enhancers	Ovary	ovary
37	chr4:148116200-148116600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr4:148116200-148116600	Enhancers	NHLF	lung
39	chr4:148116200-148119600	Weak transcription	Fetal Stomach	stomach
40	chr4:148116200-148120800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:148116400-148117000	Enhancers	Osteobl	bone
42	chr4:148116600-148116800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:148116600-148119000	Weak transcription	NHLF	lung
44	chr4:148116600-148119600	Weak transcription	HSMMtube	muscle
45	chr4:148116600-148119800	Weak transcription	Fetal Kidney	kidney
46	chr4:148116800-148117000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr4:148116800-148118800	Weak transcription	NHDF-Ad	bronchial
48	chr4:148116800-148119600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr4:148117000-148119000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr4:148117000-148119200	Weak transcription	HSMM	muscle

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