Variant report

Variant	esv3371034
Chromosome Location	chr4:1398152-1402550
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	BACH1	chr4:1400460-1400505	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:1400954-1401084	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr4:1399593-1399806	K562	blood:	n/a	n/a
4	CTCF	chr4:1399840-1399990	WERI-Rb-1	eye:	n/a	n/a
5	CTCF	chr4:1402380-1402530	HBMEC	blood vessel:	n/a	chr4:1402397-1402410
6	CTCF	chr4:1402320-1402487	Medullo	brain:	n/a	chr4:1402397-1402410
7	CTCF	chr4:1402297-1402465	A549	lung:	n/a	chr4:1402397-1402410
8	CTCF	chr4:1402293-1402433	SK-N-SH_RA	brain:	n/a	chr4:1402397-1402410
9	CTCF	chr4:1402240-1402390	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr4:1402330-1402482	LNCaP	prostate:	n/a	chr4:1402397-1402410
11	CTCF	chr4:1402260-1402410	HRE	kidney:	n/a	chr4:1402397-1402410
12	CTCF	chr4:1402320-1402478	K562	blood:	n/a	chr4:1402397-1402410
13	CTCF	chr4:1402174-1402650	K562	blood:	n/a	chr4:1402397-1402410
14	CTCF	chr4:1402179-1402584	H1-hESC	embryonic stem cell:	n/a	chr4:1402397-1402410
15	CTCF	chr4:1402300-1402450	HRPEpiC	eye:	n/a	chr4:1402397-1402410
16	CTCF	chr4:1402320-1402470	BE2_C	brain:	n/a	chr4:1402397-1402410
17	CTCF	chr4:1402300-1402450	HMEC	breast:	n/a	chr4:1402397-1402410
18	CTCF	chr4:1402333-1402458	HepG2	liver:	n/a	chr4:1402397-1402410
19	CTCF	chr4:1402240-1402390	GM12874	blood:	n/a	n/a
20	CTCF	chr4:1402180-1402410	SK-N-SH_RA	brain:	n/a	chr4:1402397-1402410
21	CTCF	chr4:1402387-1402441	MCF-7	breast:	n/a	chr4:1402397-1402410
22	CTCF	chr4:1399840-1399990	AG04449	skin:	n/a	n/a
23	CTCF	chr4:1402294-1402485	LNCaP	prostate:	n/a	chr4:1402397-1402410
24	CTCF	chr4:1402333-1402437	SK-N-SH_RA	brain:	n/a	chr4:1402397-1402410
25	CTCF	chr4:1402386-1402449	MCF-7	breast:	n/a	chr4:1402397-1402410
26	CTCF	chr4:1399854-1399974	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:1402320-1402470	K562	blood:	n/a	chr4:1402397-1402410
28	CTCF	chr4:1402360-1402510	HRE	kidney:	n/a	chr4:1402397-1402410
29	CTCF	chr4:1399840-1399990	HEK293	kidney:	n/a	n/a
30	CTCF	chr4:1401200-1401350	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr4:1402320-1402470	HepG2	liver:	n/a	chr4:1402397-1402410
32	CTCF	chr4:1402304-1402517	HepG2	liver:	n/a	chr4:1402397-1402410
33	CTCF	chr4:1402360-1402510	HRPEpiC	eye:	n/a	chr4:1402397-1402410
34	CTCF	chr4:1402253-1402475	K562	blood:	n/a	chr4:1402397-1402410
35	CTCF	chr4:1402400-1402550	K562	blood:	n/a	n/a
36	CTCF	chr4:1402200-1402350	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr4:1402340-1402490	GM12873	blood:	n/a	chr4:1402397-1402410
38	CTCF	chr4:1402220-1402370	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr4:1402460-1402610	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr4:1402340-1402490	WERI-Rb-1	eye:	n/a	chr4:1402397-1402410
41	CTCF	chr4:1399900-1400050	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr4:1402374-1402426	GM10266	blood:	n/a	chr4:1402397-1402410
43	CTCF	chr4:1402300-1402450	HEK293	kidney:	n/a	chr4:1402397-1402410
44	CTCF	chr4:1402340-1402490	A549	lung:	n/a	chr4:1402397-1402410
45	CTCF	chr4:1399902-1400002	NHEK	skin:	n/a	n/a
46	CTCF	chr4:1402280-1402430	BE2_C	brain:	n/a	chr4:1402397-1402410
47	CTCF	chr4:1402346-1402474	NHEK	skin:	n/a	chr4:1402397-1402410
48	CTCF	chr4:1402303-1402540	K562	blood:	n/a	chr4:1402397-1402410
49	CTCF	chr4:1402320-1402470	WERI-Rb-1	eye:	n/a	chr4:1402397-1402410
50	CTCF	chr4:1402340-1402490	HFF-Myc	foreskin:	n/a	chr4:1402397-1402410

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1399938-1399988	MCF10A-Er-Src	breast:	n/a
2	chr4:1399938-1399988	HEK293	kidney:	embryo
3	chr4:1398139-1398189	SK-N-SH_RA	brain:	n/a
4	chr4:1401409-1401459	AG09309	skin:	n/a
5	chr4:1399235-1399285	T-47D	breast:	n/a
6	chr4:1401409-1401459	Hela-S3	cervix:	n/a
7	chr4:1401854-1401904	AG09319	gingival:	n/a
8	chr4:1402343-1402393	AoSMC	blood vessel:	n/a
9	chr4:1402198-1402248	HEEpiC	esophagus:	n/a
10	chr4:1398798-1398848	AG04450	lung:	fetal
11	chr4:1402343-1402393	ovcar-3	ovarian:	n/a
12	chr4:1399516-1399566	HCPEpiC	choroid plexus:	n/a
13	chr4:1398599-1398649	MCF-7	breast:	n/a
14	chr4:1401409-1401459	HCM	heart:	n/a
15	chr4:1402198-1402248	HL-60	blood:	n/a
16	chr4:1400869-1400919	GM12892	blood:	n/a
17	chr4:1398383-1398433	MCF10A-Er-Src	breast:	n/a
18	chr4:1399938-1399988	AG09309	skin:	n/a
19	chr4:1400189-1400239	A549	lung:	n/a
20	chr4:1402434-1402484	NT2-D1	testis:	n/a
21	chr4:1401409-1401459	BE2_C	brain:	n/a
22	chr4:1398383-1398433	T-47D	breast:	n/a
23	chr4:1399938-1399988	ECC-1	luminal epithelium:	n/a
24	chr4:1399516-1399566	HCF	heart:	n/a
25	chr4:1398139-1398189	ECC-1	luminal epithelium:	n/a
26	chr4:1402343-1402393	HAEpiC	amniotic membrane:	n/a
27	chr4:1398798-1398848	HRPEpiC	eye:	n/a
28	chr4:1401409-1401459	AG10803	skin:	n/a
29	chr4:1400869-1400919	PrEC	prostate:	n/a
30	chr4:1400189-1400239	Hepatocyte	liver:	n/a
31	chr4:1401854-1401904	CMK	blood:	n/a
32	chr4:1399516-1399566	CMK	blood:	n/a
33	chr4:1401409-1401459	HCPEpiC	choroid plexus:	n/a
34	chr4:1401854-1401904	LNCaP	prostate:	n/a
35	chr4:1401409-1401459	HUVEC	blood vessel:	n/a
36	chr4:1398139-1398189	AG09319	gingival:	n/a
37	chr4:1402434-1402484	HRE	kidney:	n/a
38	chr4:1399135-1399185	PrEC	prostate:	n/a
39	chr4:1399938-1399988	HCPEpiC	choroid plexus:	n/a
40	chr4:1398798-1398848	H1-hESC	embryonic stem cell:	embryo
41	chr4:1398599-1398649	HRE	kidney:	n/a
42	chr4:1399135-1399185	ECC-1	luminal epithelium:	n/a
43	chr4:1399235-1399285	SK-N-SH	brain:	n/a
44	chr4:1399516-1399566	HRCEpiC	kidney:	n/a
45	chr4:1398599-1398649	AG04449	skin:	fetal
46	chr4:1401409-1401459	Hepatocyte	liver:	n/a
47	chr4:1401729-1401779	SKMC	muscle:	n/a
48	chr4:1402343-1402393	AG10803	skin:	n/a
49	chr4:1399135-1399185	Caco-2	colon:	n/a
50	chr4:1401409-1401459	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:1391809..1396481-chr4:1400263..1404304,5	K562	blood:
2	chr4:1397408..1399062-chr4:1402095..1403760,2	K562	blood:
3	chr4:1398123..1401195-chr4:1402046..1405937,3	K562	blood:
4	chr4:1397408..1399062-chr4:1402095..1403760,2	K562	blood:
5	chr4:1395958..1398402-chr4:1416178..1419090,2	K562	blood:
6	chr4:1400709..1403410-chr4:1544391..1546329,2	K562	blood:
7	chr4:1393172..1395524-chr4:1397007..1399469,2	K562	blood:

Variant related genes	Relation type
NKX1-1	TF binding region
NKX1-1	CpG island
ENSG00000235608	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542431890	chr4:1398174-1398175	ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs11248002	chr4:1398235-1398236	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs527763958	chr4:1398332-1398333	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546235438	chr4:1398341-1398342	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564477847	chr4:1398356-1398357	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531511971	chr4:1398364-1398365	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367918254	chr4:1398415-1398416	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550011003	chr4:1398503-1398504	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568256990	chr4:1398522-1398523	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373044815	chr4:1398566-1398567	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192128887	chr4:1398589-1398590	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372208022	chr4:1398597-1398598	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183206193	chr4:1398703-1398704	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565475520	chr4:1398722-1398723	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376437706	chr4:1398770-1398771	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539109128	chr4:1398780-1398781	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551110205	chr4:1398813-1398814	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187533226	chr4:1398832-1398833	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376169664	chr4:1398836-1398837	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538163433	chr4:1398850-1398851	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556854760	chr4:1398888-1398889	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575206501	chr4:1398893-1398894	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11731672	chr4:1398897-1398898	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs554391400	chr4:1398905-1398906	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572594203	chr4:1398906-1398907	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374512947	chr4:1398980-1398981	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546232535	chr4:1398992-1398993	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192833730	chr4:1399002-1399003	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372519320	chr4:1399051-1399052	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576425686	chr4:1399081-1399082	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543451878	chr4:1399094-1399095	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375762856	chr4:1399138-1399139	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73797207	chr4:1399205-1399206	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538136561	chr4:1399206-1399207	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs369948703	chr4:1399208-1399209	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571935861	chr4:1399214-1399215	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184838390	chr4:1399227-1399228	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189348441	chr4:1399263-1399264	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372462142	chr4:1399294-1399295	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569640135	chr4:1399329-1399330	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537094882	chr4:1399330-1399331	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548678735	chr4:1399359-1399360	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111710573	chr4:1399406-1399407	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113289381	chr4:1399448-1399449	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536127570	chr4:1399450-1399451	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554410066	chr4:1399461-1399462	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572631826	chr4:1399462-1399463	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113357746	chr4:1399474-1399475	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558280133	chr4:1399512-1399513	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576439662	chr4:1399529-1399530	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	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
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1395800-1399200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr4:1395800-1399400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr4:1396200-1400800	Enhancers	Pancreas	Pancrea
4	chr4:1396400-1398200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
5	chr4:1396800-1402600	Bivalent Enhancer	Fetal Brain Male	brain
6	chr4:1397000-1399600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
7	chr4:1397200-1399200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:1397200-1401000	Bivalent Enhancer	Brain Hippocampus Middle	brain
9	chr4:1397400-1399200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:1397600-1398200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
11	chr4:1397600-1398200	Bivalent Enhancer	Lung	lung
12	chr4:1397600-1399000	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr4:1397600-1401000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr4:1397600-1401200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:1397600-1402400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:1397800-1398200	Bivalent Enhancer	Fetal Brain Female	brain
17	chr4:1397800-1398400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
18	chr4:1397800-1398800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
19	chr4:1397800-1399200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
20	chr4:1397800-1399400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
21	chr4:1398000-1398200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
22	chr4:1398000-1398200	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
23	chr4:1398000-1398200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:1398000-1398200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:1398000-1398200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
26	chr4:1398000-1398200	Bivalent/Poised TSS	Right Ventricle	heart
27	chr4:1398000-1398200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
28	chr4:1398000-1398200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
29	chr4:1398000-1398400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:1398000-1398800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr4:1398000-1399400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
32	chr4:1398000-1400600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:1398000-1401600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
34	chr4:1398200-1398400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
35	chr4:1398200-1398600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr4:1398400-1398600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:1398400-1398600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
38	chr4:1398400-1398800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
39	chr4:1398400-1399200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:1398600-1398800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:1398600-1398800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:1398600-1398800	Bivalent Enhancer	Fetal Intestine Large	intestine
43	chr4:1398600-1398800	Enhancers	Gastric	stomach
44	chr4:1398600-1398800	Bivalent Enhancer	Lung	lung
45	chr4:1398600-1398800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
46	chr4:1398600-1399000	Bivalent Enhancer	Ovary	ovary
47	chr4:1398600-1399200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
48	chr4:1398600-1399200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
49	chr4:1398600-1402600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr4:1398800-1399000	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast

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