Variant report

Variant	nsv879008
Chromosome Location	chr4:48473439-48496804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:325)
CpG islands
(count:1954)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48477763-48478047	K562	blood:	n/a	n/a
2	ARID3A	chr4:48483723-48484037	K562	blood:	n/a	n/a
3	ARID3A	chr4:48487020-48487153	K562	blood:	n/a	n/a
4	ARID3A	chr4:48484962-48485247	K562	blood:	n/a	n/a
5	ATF1	chr4:48483638-48483988	K562	blood:	n/a	n/a
6	BACH1	chr4:48493250-48493536	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:48485381-48485382	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:48486855-48487010	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:48485777-48486288	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr4:48477903-48478176	K562	blood:	n/a	n/a
11	BHLHE40	chr4:48485470-48485714	K562	blood:	n/a	chr4:48485560-48485576
12	BHLHE40	chr4:48483691-48483965	K562	blood:	n/a	n/a
13	BHLHE40	chr4:48486934-48487121	K562	blood:	n/a	n/a
14	CBX3	chr4:48485746-48486116	K562	blood:	n/a	n/a
15	CBX3	chr4:48483613-48484010	K562	blood:	n/a	n/a
16	CCNT2	chr4:48483694-48483987	K562	blood:	n/a	n/a
17	CCNT2	chr4:48477848-48478194	K562	blood:	n/a	n/a
18	CCNT2	chr4:48486352-48486939	K562	blood:	n/a	n/a
19	CCNT2	chr4:48492468-48492539	K562	blood:	n/a	n/a
20	CCNT2	chr4:48485129-48486088	K562	blood:	n/a	n/a
21	CEBPB	chr4:48495733-48496564	HepG2	liver:	n/a	chr4:48495877-48495888 chr4:48495898-48495909 chr4:48495875-48495888 chr4:48495875-48495886 chr4:48496412-48496425
22	CEBPB	chr4:48496266-48496538	A549	lung:	n/a	chr4:48496412-48496425
23	CEBPB	chr4:48495753-48496031	A549	lung:	n/a	chr4:48495877-48495888 chr4:48495898-48495909 chr4:48495875-48495888 chr4:48495875-48495886
24	CEBPB	chr4:48496352-48496429	Hela-S3	cervix:	n/a	chr4:48496412-48496425
25	CEBPB	chr4:48495830-48496030	Hela-S3	cervix:	n/a	chr4:48495877-48495888 chr4:48495898-48495909 chr4:48495875-48495888 chr4:48495875-48495886
26	CEBPB	chr4:48490836-48490940	K562	blood:	n/a	n/a
27	CEBPB	chr4:48495754-48496057	IMR90	lung:	n/a	chr4:48495877-48495888 chr4:48495898-48495909 chr4:48495875-48495888 chr4:48495875-48495886
28	CEBPB	chr4:48483480-48483916	K562	blood:	n/a	chr4:48483581-48483594 chr4:48483583-48483594
29	CEBPB	chr4:48496302-48496532	IMR90	lung:	n/a	chr4:48496412-48496425
30	CEBPB	chr4:48490809-48491079	HepG2	liver:	n/a	chr4:48490992-48491003
31	CEBPD	chr4:48483548-48484092	K562	blood:	n/a	n/a
32	CEBPD	chr4:48483530-48484088	K562	blood:	n/a	n/a
33	CHD2	chr4:48483568-48483726	K562	blood:	n/a	n/a
34	CHD2	chr4:48493281-48493570	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:48478980-48479020	K562	blood:	n/a	n/a
36	CHD2	chr4:48485558-48485586	K562	blood:	n/a	n/a
37	CHD2	chr4:48486715-48486814	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr4:48485358-48485716	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr4:48485290-48485607	A549	lung:	n/a	n/a
40	CTBP2	chr4:48491559-48494045	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr4:48485327-48486322	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr4:48486260-48486283	GM20000	blood:	n/a	n/a
43	CTCF	chr4:48486020-48486170	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr4:48479123-48479139	K562	blood:	n/a	n/a
45	CTCF	chr4:48477520-48477670	HFF	foreskin:	n/a	n/a
46	CTCF	chr4:48478960-48479110	K562	blood:	n/a	n/a
47	CTCF	chr4:48485940-48486090	AG04449	skin:	n/a	n/a
48	CTCF	chr4:48485933-48485975	NHEK	skin:	n/a	n/a
49	CTCF	chr4:48485900-48486050	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr4:48485869-48486030	A549	lung:	n/a	n/a

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48486316-48486366	MCF10A-Er-Src	breast:	n/a
2	chr4:48484997-48485047	HepG2	liver:	n/a
3	chr4:48486316-48486366	MCF10A-Er-Src	breast:	n/a
4	chr4:48484997-48485047	HepG2	liver:	n/a
5	chr4:48485233-48485283	NHBE	bronchial:	n/a
6	chr4:48493846-48493896	MCF-7	breast:	n/a
7	chr4:48485306-48485356	NHBE	bronchial:	n/a
8	chr4:48491968-48492018	GM12892	blood:	n/a
9	chr4:48485293-48485343	HEK293	kidney:	embryo
10	chr4:48491941-48491991	PANC-1	pancreas:	n/a
11	chr4:48486785-48486835	HEK293	kidney:	embryo
12	chr4:48492848-48492898	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:48493350-48493400	HEK293	kidney:	embryo
14	chr4:48486154-48486204	K562	blood:	n/a
15	chr4:48486316-48486366	U87	brain:	n/a
16	chr4:48485293-48485343	HCM	heart:	n/a
17	chr4:48493846-48493896	SAEC	small airway:	n/a
18	chr4:48496404-48496454	AG10803	skin:	n/a
19	chr4:48485306-48485356	HRE	kidney:	n/a
20	chr4:48485328-48485378	HNPCEpiC	eye:	n/a
21	chr4:48492848-48492898	PFSK-1	brain:	n/a
22	chr4:48486785-48486835	HCT-116	colon:	n/a
23	chr4:48493846-48493896	HCM	heart:	n/a
24	chr4:48485090-48485140	RPTEC	kidney:	n/a
25	chr4:48489221-48489271	HNPCEpiC	eye:	n/a
26	chr4:48485289-48485339	GM12892	blood:	n/a
27	chr4:48485301-48485351	SAEC	small airway:	n/a
28	chr4:48491941-48491991	HRE	kidney:	n/a
29	chr4:48493420-48493470	NHDF-neo	bronchial:	n/a
30	chr4:48486472-48486522	NB4	blood:	n/a
31	chr4:48485293-48485343	HUVEC	blood vessel:	n/a
32	chr4:48484997-48485047	HRCEpiC	kidney:	n/a
33	chr4:48492122-48492172	PrEC	prostate:	n/a
34	chr4:48483244-48483294	GM12891	blood:	n/a
35	chr4:48484997-48485047	Hela-S3	cervix:	n/a
36	chr4:48492845-48492895	HNPCEpiC	eye:	n/a
37	chr4:48486154-48486204	A549	lung:	n/a
38	chr4:48483244-48483294	HCF	heart:	n/a
39	chr4:48489221-48489271	NH-A	brain:	n/a
40	chr4:48492118-48492168	ovcar-3	ovarian:	n/a
41	chr4:48493420-48493470	HAEpiC	amniotic membrane:	n/a
42	chr4:48492196-48492246	Caco-2	colon:	n/a
43	chr4:48496404-48496454	IMR90	lung:	fetal
44	chr4:48492122-48492172	MCF-7	breast:	n/a
45	chr4:48496404-48496454	CMK	blood:	n/a
46	chr4:48492304-48492354	NHDF-neo	bronchial:	n/a
47	chr4:48486154-48486204	HRCEpiC	kidney:	n/a
48	chr4:48491968-48492018	IMR90	lung:	fetal
49	chr4:48492344-48492394	SAEC	small airway:	n/a
50	chr4:48493846-48493896	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:48474711..48478093-chr4:48481760..48484353,3	K562	blood:
2	chr4:48478067..48481410-chr4:48493413..48496125,3	K562	blood:
3	chr4:48489612..48492154-chr4:48493154..48495602,2	K562	blood:
4	chr4:48478067..48481410-chr4:48493413..48496125,3	K562	blood:
5	chr4:48341909..48343469-chr4:48483589..48486077,2	K562	blood:
6	chr4:48473818..48475564-chr4:48478853..48480558,2	K562	blood:
7	chr4:48485954..48488857-chr4:48528912..48531083,2	K562	blood:
8	chr4:48474711..48478093-chr4:48481760..48484353,3	K562	blood:
9	chr4:48341467..48343836-chr4:48476769..48479508,2	K562	blood:
10	chr4:48492886..48494734-chr4:48535449..48537970,2	K562	blood:
11	chr4:48473818..48475564-chr4:48478853..48480558,2	K562	blood:
12	chr4:48478979..48481680-chr4:48482843..48484535,2	K562	blood:
13	chr4:48478979..48481680-chr4:48482843..48484535,2	K562	blood:
14	chr4:48489612..48492154-chr4:48493154..48495602,2	K562	blood:
15	chr4:48477174..48479386-chr4:48484669..48486658,3	K562	blood:
16	chr4:48484114..48487251-chr4:48504187..48509460,5	K562	blood:
17	chr4:48470613..48473605-chr4:48483199..48486711,3	K562	blood:

No data

Variant related genes	Relation type
SLC10A4	TF binding region
ZAR1	TF binding region
SLC10A4	CpG island
ZAR1	CpG island
ENSG00000109171	chromatin interactions
ENSG00000075539	chromatin interactions
ENSG00000145248	chromatin interactions

Extended variants
information (count: 795 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs745761	chr4:48473439-48473440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147793580	chr4:48473448-48473449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs141142089	chr4:48473464-48473465	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113855024	chr4:48473480-48473481	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75647634	chr4:48473481-48473482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117137444	chr4:48473491-48473492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs79982135	chr4:48473570-48473571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184237618	chr4:48473571-48473572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs4998005	chr4:48473592-48473593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs187534071	chr4:48473633-48473634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34766627	chr4:48473659-48473660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138206464	chr4:48473753-48473754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529118431	chr4:48473779-48473780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546996594	chr4:48473849-48473850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565490848	chr4:48473877-48473878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141766049	chr4:48473953-48473954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557557482	chr4:48473965-48473966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573904562	chr4:48473981-48473982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538465211	chr4:48474182-48474183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542321525	chr4:48474237-48474238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542483767	chr4:48474244-48474245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192785791	chr4:48474254-48474255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184620649	chr4:48474313-48474314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536109144	chr4:48474322-48474323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187096350	chr4:48474324-48474325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572341793	chr4:48474326-48474327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546311911	chr4:48474359-48474360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564401027	chr4:48474384-48474385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115545905	chr4:48474433-48474434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543228339	chr4:48474464-48474465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191905099	chr4:48474498-48474499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138616890	chr4:48474517-48474518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547369870	chr4:48474709-48474710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184377863	chr4:48474777-48474778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149292512	chr4:48474821-48474822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551331528	chr4:48474851-48474852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569669410	chr4:48474865-48474866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189111523	chr4:48474980-48474981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79967036	chr4:48475012-48475013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568668657	chr4:48475021-48475022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536197294	chr4:48475025-48475026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554155167	chr4:48475100-48475101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572429903	chr4:48475133-48475134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528596201	chr4:48475146-48475147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539468510	chr4:48475162-48475163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs55986500	chr4:48475165-48475166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs541219779	chr4:48475257-48475258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140060094	chr4:48475398-48475399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374030708	chr4:48475458-48475459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561594092	chr4:48475487-48475488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	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
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	22522925	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48470000-48474400	Weak transcription	Osteobl	bone
2	chr4:48471600-48473600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:48471600-48473600	Enhancers	Brain Germinal Matrix	brain
4	chr4:48473000-48482000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:48473000-48483600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:48473600-48479400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr4:48475200-48475600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:48475200-48475600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:48475200-48475600	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr4:48475400-48475600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:48477600-48478600	Enhancers	K562	blood
12	chr4:48478000-48478200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr4:48478200-48479400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr4:48478400-48479200	Weak transcription	Osteobl	bone
15	chr4:48478600-48479000	Weak transcription	K562	blood
16	chr4:48479000-48479400	Enhancers	K562	blood
17	chr4:48479200-48480200	Enhancers	Osteobl	bone
18	chr4:48479400-48479800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr4:48479400-48479800	Flanking Active TSS	K562	blood
20	chr4:48479400-48480000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr4:48479400-48481000	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr4:48479800-48480000	Enhancers	K562	blood
23	chr4:48479800-48484200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:48480000-48483400	Weak transcription	K562	blood
25	chr4:48480000-48484000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr4:48482000-48482200	Enhancers	Brain Germinal Matrix	brain
27	chr4:48483400-48484600	Enhancers	K562	blood
28	chr4:48483600-48484400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:48483800-48484000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:48484000-48484800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr4:48484200-48484600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
32	chr4:48484200-48484600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:48484200-48484800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:48484400-48484600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr4:48484400-48484600	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
36	chr4:48484400-48484800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:48484400-48484800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
38	chr4:48484400-48484800	Enhancers	A549	lung
39	chr4:48484600-48484800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
40	chr4:48484600-48484800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
41	chr4:48484600-48485000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
42	chr4:48484600-48485000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
43	chr4:48484600-48485000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
44	chr4:48484600-48485000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
45	chr4:48484600-48485000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:48484600-48485200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
47	chr4:48484600-48485200	Flanking Active TSS	K562	blood
48	chr4:48484600-48486600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr4:48484600-48486600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
50	chr4:48484800-48485000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell

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