Variant report

Variant	esv2763805
Chromosome Location	chr4:69244434-69344612
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	ATF2	chr4:69271320-69273979	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:69274062-69274402	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:69275508-69277104	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:69272567-69273233	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:69269806-69270384	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:69271370-69272360	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:69273374-69273928	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:69274713-69275097	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:69269850-69270608	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
11	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr4:69275877-69276040	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr4:69273602-69273847	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr4:69250331-69250703	K562	blood:	n/a	n/a
15	BHLHE40	chr4:69249117-69249120	K562	blood:	n/a	n/a
16	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:69272255-69272927	H1-hESC	embryonic stem cell:	n/a	n/a
18	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
19	CEBPB	chr4:69279178-69279415	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:69277211-69277380	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:69245383-69245660	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr4:69300055-69300288	A549	lung:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
23	CEBPB	chr4:69300033-69300365	HepG2	liver:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
24	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
25	CEBPB	chr4:69279112-69279415	K562	blood:	n/a	n/a
26	CEBPB	chr4:69271428-69272246	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
28	CEBPB	chr4:69278558-69278870	K562	blood:	n/a	n/a
29	CEBPB	chr4:69248884-69249141	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:69271962-69272301	K562	blood:	n/a	n/a
31	CEBPB	chr4:69310875-69311174	IMR90	lung:	n/a	chr4:69310996-69311009 chr4:69310996-69311009 chr4:69310996-69311007
32	CEBPB	chr4:69266996-69267452	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:69279166-69279328	K562	blood:	n/a	n/a
34	CEBPB	chr4:69278653-69278888	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:69312976-69313282	MCF-7	breast:	n/a	n/a
36	CEBPB	chr4:69273497-69273975	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
38	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
39	CEBPB	chr4:69300028-69300381	IMR90	lung:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
40	CEBPB	chr4:69300021-69300356	K562	blood:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
41	CEBPB	chr4:69308568-69308582	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:69279172-69279414	K562	blood:	n/a	n/a
43	CEBPB	chr4:69300096-69300253	H1-hESC	embryonic stem cell:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
44	CHD1	chr4:69271883-69275842	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr4:69270706-69270858	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr4:69275782-69276810	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr4:69269923-69270798	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:69271475-69273932	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr4:69248964-69248966	K562	blood:	n/a	n/a
50	CREB1	chr4:69272138-69272676	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69313197-69313247	HRPEpiC	eye:	n/a
2	chr4:69312514-69312564	HUVEC	blood vessel:	n/a
3	chr4:69340916-69340966	PFSK-1	brain:	n/a
4	chr4:69312104-69312154	AG09309	skin:	n/a
5	chr4:69340916-69340966	HCM	heart:	n/a
6	chr4:69312514-69312564	A549	lung:	n/a
7	chr4:69312514-69312564	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:69312104-69312154	AG04449	skin:	fetal
9	chr4:69313197-69313247	AoSMC	blood vessel:	n/a
10	chr4:69340916-69340966	HRPEpiC	eye:	n/a
11	chr4:69312104-69312154	AG04450	lung:	fetal
12	chr4:69340916-69340966	HEEpiC	esophagus:	n/a
13	chr4:69312514-69312564	PANC-1	pancreas:	n/a
14	chr4:69312104-69312154	Jurkat	blood:	n/a
15	chr4:69340916-69340966	SK-N-SH_RA	brain:	n/a
16	chr4:69312104-69312154	HMEC	breast:	n/a
17	chr4:69340916-69340966	GM12878	blood:	n/a
18	chr4:69340916-69340966	HCF	heart:	n/a
19	chr4:69340916-69340966	BE2_C	brain:	n/a
20	chr4:69312514-69312564	T-47D	breast:	n/a
21	chr4:69312104-69312154	BJ	skin:	n/a
22	chr4:69312514-69312564	RPTEC	kidney:	n/a
23	chr4:69313197-69313247	HEEpiC	esophagus:	n/a
24	chr4:69312104-69312154	HCF	heart:	n/a
25	chr4:69312104-69312154	GM12891	blood:	n/a
26	chr4:69313197-69313247	HUVEC	blood vessel:	n/a
27	chr4:69313197-69313247	MCF-7	breast:	n/a
28	chr4:69340916-69340966	Caco-2	colon:	n/a
29	chr4:69312514-69312564	AoSMC	blood vessel:	n/a
30	chr4:69313197-69313247	HL-60	blood:	n/a
31	chr4:69313197-69313247	HIPEpiC	eye:	n/a
32	chr4:69313197-69313247	SK-N-SH_RA	brain:	n/a
33	chr4:69312104-69312154	HCM	heart:	n/a
34	chr4:69312514-69312564	HRE	kidney:	n/a
35	chr4:69340916-69340966	H1-hESC	embryonic stem cell:	embryo
36	chr4:69340916-69340966	AG09309	skin:	n/a
37	chr4:69313197-69313247	BE2_C	brain:	n/a
38	chr4:69312104-69312154	SKMC	muscle:	n/a
39	chr4:69340916-69340966	AG10803	skin:	n/a
40	chr4:69312514-69312564	AG09309	skin:	n/a
41	chr4:69313197-69313247	ProgFib	skin:	n/a
42	chr4:69312104-69312154	HEK293	kidney:	embryo
43	chr4:69340916-69340966	HAEpiC	amniotic membrane:	n/a
44	chr4:69340916-69340966	HCPEpiC	choroid plexus:	n/a
45	chr4:69312104-69312154	MCF10A-Er-Src	breast:	n/a
46	chr4:69340916-69340966	Hela-S3	cervix:	n/a
47	chr4:69312514-69312564	NHBE	bronchial:	n/a
48	chr4:69312514-69312564	IMR90	lung:	fetal
49	chr4:69313197-69313247	HAEpiC	amniotic membrane:	n/a
50	chr4:69313197-69313247	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
2	chr4:69177090..69179857-chr4:69251602..69253290,2	MCF-7	breast:
3	chr4:69214168..69215842-chr4:69249504..69252039,2	MCF-7	breast:
4	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
5	chr4:69213603..69215709-chr4:69245624..69247287,2	K562	blood:
6	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
7	chr4:69261479..69263949-chr4:69265088..69267687,3	K562	blood:
8	chr4:69261479..69263949-chr4:69265088..69267687,3	K562	blood:
9	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
10	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
11	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
12	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
13	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
14	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
15	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
16	chr4:69243264..69245251-chr4:69248916..69251183,2	K562	blood:
17	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
18	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
19	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
20	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
21	chr4:69243264..69245251-chr4:69248916..69251183,2	K562	blood:
22	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:

Variant related genes	Relation type
TMPRSS11E	TF binding region
TMPRSS11E	CpG island
ENSG00000087128	chromatin interactions
ENSG00000083896	chromatin interactions

Extended variants
information (count: 3856 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3856 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34032921	chr4:69244435-69244436	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531397214	chr4:69244480-69244481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139113116	chr4:69244489-69244490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565020811	chr4:69244490-69244491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149876420	chr4:69244495-69244496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547250619	chr4:69244499-69244500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561196443	chr4:69244507-69244508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2056802	chr4:69244510-69244511	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs549311356	chr4:69244518-69244519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34527218	chr4:69244539-69244540	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs559616805	chr4:69244564-69244565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548628400	chr4:69244600-69244601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537889154	chr4:69244613-69244614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200236767	chr4:69244685-69244686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557824924	chr4:69244691-69244692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201213839	chr4:69244696-69244697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571434673	chr4:69244697-69244698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369098754	chr4:69244700-69244701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372677249	chr4:69244701-69244702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368435998	chr4:69244711-69244712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112161491	chr4:69244732-69244733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533719658	chr4:69244766-69244767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144477728	chr4:69244798-69244799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147855405	chr4:69244923-69244924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34223548	chr4:69244969-69244970	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188775232	chr4:69244992-69244993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142634850	chr4:69245033-69245034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs151060304	chr4:69245088-69245089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564958196	chr4:69245106-69245107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527398815	chr4:69245107-69245108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62316052	chr4:69245140-69245141	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs560523087	chr4:69245175-69245176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529549310	chr4:69245211-69245212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181582761	chr4:69245231-69245232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569578593	chr4:69245234-69245235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571508920	chr4:69245246-69245247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35964416	chr4:69245271-69245272	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs551393394	chr4:69245297-69245298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571370186	chr4:69245318-69245319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534034573	chr4:69245388-69245389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547532264	chr4:69245399-69245400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75990365	chr4:69245433-69245434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113076762	chr4:69245454-69245455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140526876	chr4:69245482-69245483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556164065	chr4:69245485-69245486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4860932	chr4:69245493-69245494	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs138494537	chr4:69245509-69245510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4860933	chr4:69245515-69245516	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs572122934	chr4:69245517-69245518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541137173	chr4:69245527-69245528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	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
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69232200-69255600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:69240000-69245000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:69241800-69249000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:69242200-69245000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:69242200-69245000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr4:69242200-69245600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:69242200-69255400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr4:69242400-69244600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:69242400-69245200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:69242400-69246800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr4:69242400-69247000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr4:69243000-69245400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:69243200-69245200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr4:69244200-69244600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:69244200-69244600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr4:69244200-69244600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr4:69244200-69245000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:69244400-69245200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:69244400-69245400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:69244600-69245000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr4:69244600-69245600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:69245000-69245600	Enhancers	H9 Cell Line	embryonic stem cell
23	chr4:69245000-69245600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:69245000-69245600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:69245000-69245600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:69245000-69245800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:69245000-69245800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:69245200-69245600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:69245200-69245800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:69245400-69245800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:69245600-69246800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr4:69245600-69246800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:69245600-69250600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr4:69245600-69252800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr4:69245800-69254200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:69246800-69247000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr4:69246800-69248000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:69247000-69247200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr4:69247000-69247600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr4:69247200-69247400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr4:69248000-69248800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:69248600-69249400	Enhancers	Fetal Intestine Large	intestine
43	chr4:69248800-69249000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:69248800-69249200	Enhancers	HepG2	liver
45	chr4:69249000-69249200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:69249400-69254600	Weak transcription	Fetal Intestine Large	intestine
47	chr4:69250600-69250800	Enhancers	Esophagus	oesophagus
48	chr4:69250600-69251400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr4:69251400-69252800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr4:69252800-69253000	Enhancers	H1 Cell Line	embryonic stem cell

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