Variant report

Variant	nsv830467
Chromosome Location	chr5:120344662-120507868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:448)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:120480659-120480718	K562	blood:	n/a	n/a
2	BHLHE40	chr5:120355613-120355776	K562	blood:	n/a	n/a
3	CEBPB	chr5:120490481-120490746	A549	lung:	n/a	chr5:120490627-120490638
4	CEBPB	chr5:120489377-120489704	K562	blood:	n/a	chr5:120489508-120489519
5	CEBPB	chr5:120388712-120389167	MCF-7	breast:	n/a	n/a
6	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
7	CEBPB	chr5:120344890-120345090	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:120500288-120500607	K562	blood:	n/a	n/a
9	CEBPB	chr5:120362859-120363138	HepG2	liver:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
10	CEBPB	chr5:120386100-120386431	HepG2	liver:	n/a	chr5:120386256-120386267
11	CEBPB	chr5:120386141-120386392	A549	lung:	n/a	chr5:120386256-120386267
12	CEBPB	chr5:120497794-120498111	K562	blood:	n/a	chr5:120497966-120497977
13	CEBPB	chr5:120500293-120500606	K562	blood:	n/a	n/a
14	CEBPB	chr5:120344818-120345134	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:120362867-120363103	K562	blood:	n/a	chr5:120362980-120362991
16	CEBPB	chr5:120489367-120489679	A549	lung:	n/a	chr5:120489508-120489519
17	CEBPB	chr5:120362854-120363100	A549	lung:	n/a	chr5:120362980-120362991
18	CEBPB	chr5:120344767-120345102	A549	lung:	n/a	n/a
19	CEBPB	chr5:120489382-120489687	HepG2	liver:	n/a	chr5:120489508-120489519
20	CEBPB	chr5:120497839-120498066	HepG2	liver:	n/a	chr5:120497966-120497977
21	CEBPB	chr5:120407480-120407657	HepG2	liver:	n/a	chr5:120407589-120407602
22	CEBPB	chr5:120489328-120489659	H1-hESC	embryonic stem cell:	n/a	chr5:120489508-120489519
23	CEBPB	chr5:120465336-120465526	K562	blood:	n/a	chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447 chr5:120465434-120465445 chr5:120465434-120465447 chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447
24	CEBPB	chr5:120362833-120363079	IMR90	lung:	n/a	chr5:120362980-120362991
25	CEBPB	chr5:120497807-120498101	IMR90	lung:	n/a	chr5:120497966-120497977
26	CEBPB	chr5:120497904-120498020	A549	lung:	n/a	chr5:120497966-120497977
27	CEBPB	chr5:120388756-120389126	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:120362842-120363162	H1-hESC	embryonic stem cell:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
29	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
30	CEBPD	chr5:120480488-120480808	K562	blood:	n/a	n/a
31	CEBPD	chr5:120480469-120480757	K562	blood:	n/a	n/a
32	CHD2	chr5:120469053-120469156	K562	blood:	n/a	n/a
33	CTCF	chr5:120386313-120386365	Lung_OC	lung:	n/a	n/a
34	CTCF	chr5:120423660-120423810	GM12873	blood:	n/a	n/a
35	CTCF	chr5:120360220-120360370	BE2_C	brain:	n/a	n/a
36	CTCF	chr5:120389160-120389310	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:120480651-120480821	LNCaP	prostate:	n/a	n/a
38	CTCF	chr5:120489960-120490110	HMF	breast:	n/a	chr5:120490086-120490107
39	CTCF	chr5:120480636-120480780	Gliobla	brain:	n/a	n/a
40	CTCF	chr5:120443661-120443763	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr5:120480440-120480590	HCM	heart:	n/a	n/a
42	CTCF	chr5:120480660-120480810	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr5:120398360-120398510	HVMF	connective:	n/a	n/a
44	CTCF	chr5:120480653-120480819	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr5:120396480-120396630	GM12875	blood:	n/a	n/a
46	CTCF	chr5:120480660-120480810	HMF	breast:	n/a	n/a
47	CTCF	chr5:120345376-120345438	GM20000	blood:	n/a	n/a
48	CTCF	chr5:120480620-120480770	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr5:120423520-120423670	GM12868	blood:	n/a	n/a
50	CTCF	chr5:120367460-120367610	NHDF-neo	bronchial:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120400115-120400165	GM12891	blood:	n/a
2	chr5:120400115-120400165	HEEpiC	esophagus:	n/a
3	chr5:120444080-120444130	GM19239	blood:	n/a
4	chr5:120400115-120400165	HAEpiC	amniotic membrane:	n/a
5	chr5:120444080-120444130	SK-N-SH	brain:	n/a
6	chr5:120400115-120400165	AG10803	skin:	n/a
7	chr5:120444080-120444130	HRCEpiC	kidney:	n/a
8	chr5:120400115-120400165	HNPCEpiC	eye:	n/a
9	chr5:120400115-120400165	A549	lung:	n/a
10	chr5:120400115-120400165	HCPEpiC	choroid plexus:	n/a
11	chr5:120400115-120400165	AG04449	skin:	fetal
12	chr5:120444080-120444130	NT2-D1	testis:	n/a
13	chr5:120400115-120400165	MCF-7	breast:	n/a
14	chr5:120444080-120444130	HL-60	blood:	n/a
15	chr5:120444080-120444130	PANC-1	pancreas:	n/a
16	chr5:120444080-120444130	MCF-7	breast:	n/a
17	chr5:120400115-120400165	Hepatocyte	liver:	n/a
18	chr5:120444080-120444130	RPTEC	kidney:	n/a
19	chr5:120400115-120400165	RPTEC	kidney:	n/a
20	chr5:120444080-120444130	AG10803	skin:	n/a
21	chr5:120444080-120444130	HCM	heart:	n/a
22	chr5:120444080-120444130	HNPCEpiC	eye:	n/a
23	chr5:120444080-120444130	Caco-2	colon:	n/a
24	chr5:120400115-120400165	HCM	heart:	n/a
25	chr5:120400115-120400165	AG09309	skin:	n/a
26	chr5:120400115-120400165	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:120400115-120400165	H1-hESC	embryonic stem cell:	embryo
28	chr5:120444080-120444130	AG04449	skin:	fetal
29	chr5:120400115-120400165	LNCaP	prostate:	n/a
30	chr5:120400115-120400165	HCF	heart:	n/a
31	chr5:120444080-120444130	BJ	skin:	n/a
32	chr5:120400115-120400165	HL-60	blood:	n/a
33	chr5:120444080-120444130	H1-hESC	embryonic stem cell:	embryo
34	chr5:120400115-120400165	ProgFib	skin:	n/a
35	chr5:120444080-120444130	AoSMC	blood vessel:	n/a
36	chr5:120400115-120400165	GM12878	blood:	n/a
37	chr5:120444080-120444130	PFSK-1	brain:	n/a
38	chr5:120444080-120444130	HMEC	breast:	n/a
39	chr5:120444080-120444130	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:120444080-120444130	Jurkat	blood:	n/a
41	chr5:120444080-120444130	NHBE	bronchial:	n/a
42	chr5:120444080-120444130	ovcar-3	ovarian:	n/a
43	chr5:120444080-120444130	NB4	blood:	n/a
44	chr5:120400115-120400165	SAEC	small airway:	n/a
45	chr5:120444080-120444130	ECC-1	luminal epithelium:	n/a
46	chr5:120444080-120444130	PrEC	prostate:	n/a
47	chr5:120400115-120400165	HRCEpiC	kidney:	n/a
48	chr5:120444080-120444130	HRPEpiC	eye:	n/a
49	chr5:120444080-120444130	CMK	blood:	n/a
50	chr5:120400115-120400165	NHBE	bronchial:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
2	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
3	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
4	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
5	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
6	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
7	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
8	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
9	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
10	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
11	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
12	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
13	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
14	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
15	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
16	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
17	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
2	lnc-PRR16-2	chr5:120375785-120376277	NONHSAT103450
3	lnc-PRR16-2	chr5:120376385-120376432	NONHSAT103450
4	lnc-PRR16-2	chr5:120379384-120379727	NONHSAT103450
5	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451

No data

Variant related genes	Relation type
ENSG00000251135	TF binding region
ENSG00000248853	TF binding region
ENSG00000251135	CpG island
ENSG00000248853	CpG island

Extended variants
information (count: 3587 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3587 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547713353	chr5:120344690-120344691	Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566122236	chr5:120344743-120344744	Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539828303	chr5:120344763-120344764	Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368763826	chr5:120344781-120344782	Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138430372	chr5:120344793-120344794	Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570107871	chr5:120344885-120344886	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537264459	chr5:120344908-120344909	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555886875	chr5:120344910-120344911	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573997416	chr5:120344921-120344922	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541371686	chr5:120344943-120344944	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533173944	chr5:120344980-120344981	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551393298	chr5:120344981-120344982	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571739582	chr5:120345015-120345016	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149620117	chr5:120345052-120345053	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564046224	chr5:120345108-120345109	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531400874	chr5:120345117-120345118	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs17147214	chr5:120345122-120345123	Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs143323253	chr5:120345184-120345185	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183648201	chr5:120345214-120345215	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4895294	chr5:120345218-120345219	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188696488	chr5:120345239-120345240	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192878928	chr5:120345300-120345301	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185060972	chr5:120345315-120345316	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17147215	chr5:120345330-120345331	Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537999969	chr5:120345503-120345504	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148379151	chr5:120345531-120345532	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17147216	chr5:120345544-120345545	Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs2406285	chr5:120345568-120345569	Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs553770231	chr5:120345571-120345572	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567560188	chr5:120345595-120345596	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376317272	chr5:120345600-120345601	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571942394	chr5:120345720-120345721	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534870433	chr5:120345723-120345724	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553276702	chr5:120345742-120345743	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577885478	chr5:120345787-120345788	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142199719	chr5:120345810-120345811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557691031	chr5:120345855-120345856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575947331	chr5:120345907-120345908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543547110	chr5:120345912-120345913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187887535	chr5:120345913-120345914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371898549	chr5:120345935-120345936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56930945	chr5:120345946-120345947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs67475995	chr5:120345954-120345955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13157482	chr5:120345959-120345960	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs78204360	chr5:120345972-120345973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191424853	chr5:120346003-120346004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533214282	chr5:120346004-120346005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551486452	chr5:120346014-120346015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35182561	chr5:120346021-120346022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77345560	chr5:120346064-120346065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120343600-120345600	Strong transcription	Dnd41	blood
2	chr5:120343800-120345800	Bivalent Enhancer	Fetal Heart	heart
3	chr5:120344400-120344800	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr5:120345600-120347000	Weak transcription	Dnd41	blood
5	chr5:120347000-120347400	Enhancers	Dnd41	blood
6	chr5:120347400-120348600	Weak transcription	Dnd41	blood
7	chr5:120348600-120348800	Enhancers	Dnd41	blood
8	chr5:120348800-120349000	Genic enhancers	Dnd41	blood
9	chr5:120349000-120350200	Weak transcription	Dnd41	blood
10	chr5:120350200-120351800	Enhancers	Dnd41	blood
11	chr5:120351800-120352200	Active TSS	Dnd41	blood
12	chr5:120352200-120352600	Flanking Active TSS	Dnd41	blood
13	chr5:120352600-120353000	Enhancers	Dnd41	blood
14	chr5:120353000-120355800	Flanking Active TSS	Dnd41	blood
15	chr5:120353400-120353600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:120353600-120354600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr5:120354600-120355000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr5:120354600-120355000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr5:120355800-120357600	Enhancers	Dnd41	blood
20	chr5:120356200-120357600	Bivalent Enhancer	Fetal Lung	lung
21	chr5:120356800-120357600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:120357600-120358000	Flanking Bivalent TSS/Enh	Fetal Lung	lung
23	chr5:120357600-120358000	Enhancers	Pancreas	Pancrea
24	chr5:120357600-120358000	Flanking Active TSS	Dnd41	blood
25	chr5:120357800-120358000	Enhancers	Fetal Stomach	stomach
26	chr5:120358000-120358200	Bivalent Enhancer	Fetal Lung	lung
27	chr5:120358000-120358200	Enhancers	Dnd41	blood
28	chr5:120358200-120358800	Genic enhancers	Dnd41	blood
29	chr5:120358600-120358800	Enhancers	Fetal Stomach	stomach
30	chr5:120358800-120360400	Enhancers	Dnd41	blood
31	chr5:120360400-120361600	Flanking Active TSS	Dnd41	blood
32	chr5:120361600-120368400	Enhancers	Dnd41	blood
33	chr5:120364000-120364200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr5:120365200-120367000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr5:120365600-120367000	Enhancers	NHDF-Ad	bronchial
36	chr5:120365800-120366000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:120366000-120366800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:120366800-120367000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:120366800-120367200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr5:120366800-120367600	Enhancers	Fetal Heart	heart
41	chr5:120366800-120367600	Enhancers	Fetal Muscle Leg	muscle
42	chr5:120366800-120367800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr5:120367000-120367200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr5:120367000-120367200	Flanking Active TSS	NHDF-Ad	bronchial
45	chr5:120367000-120367600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:120367000-120367600	Enhancers	Adipose Nuclei	Adipose
47	chr5:120367000-120367800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr5:120367000-120367800	Bivalent Enhancer	Fetal Lung	lung
49	chr5:120367200-120367400	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr5:120367200-120367400	Active TSS	NHDF-Ad	bronchial

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