Variant report

Variant	esv1825834
Chromosome Location	chr4:69344666-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1228)
CpG islands
(count:734)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1228 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
8	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
9	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
10	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
12	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
13	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
14	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
15	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
18	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
19	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
20	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
24	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
28	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
29	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
30	CEBPB	chr4:69574389-69574642	A549	lung:	n/a	chr4:69574511-69574522
31	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
33	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
34	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
36	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
37	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
38	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
39	CEBPB	chr4:69574361-69574618	HepG2	liver:	n/a	chr4:69574511-69574522
40	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
41	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
42	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
43	CEBPB	chr4:69580237-69580432	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
45	CHD1	chr4:69583916-69583936	GM12878	blood:	n/a	n/a
46	CTCF	chr4:69364240-69364390	HEEpiC	esophagus:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
47	CTCF	chr4:69434916-69435037	K562	blood:	n/a	n/a
48	CTCF	chr4:69537037-69537264	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:69364240-69364390	HMF	breast:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
50	CTCF	chr4:69443419-69443589	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69435601-69435651	SK-N-SH_RA	brain:	n/a
2	chr4:69435601-69435651	NHBE	bronchial:	n/a
3	chr4:69435601-69435651	SK-N-SH_RA	brain:	n/a
4	chr4:69435601-69435651	NHBE	bronchial:	n/a
5	chr4:69536319-69536369	HepG2	liver:	n/a
6	chr4:69537806-69537856	HEK293	kidney:	embryo
7	chr4:69435250-69435300	HepG2	liver:	n/a
8	chr4:69435601-69435651	HIPEpiC	eye:	n/a
9	chr4:69537806-69537856	K562	blood:	n/a
10	chr4:69537826-69537876	ProgFib	skin:	n/a
11	chr4:69537806-69537856	PANC-1	pancreas:	n/a
12	chr4:69522639-69522689	HAEpiC	amniotic membrane:	n/a
13	chr4:69514031-69514081	NT2-D1	testis:	n/a
14	chr4:69522639-69522689	HEEpiC	esophagus:	n/a
15	chr4:69434475-69434525	GM06990	blood:	n/a
16	chr4:69514031-69514081	HCM	heart:	n/a
17	chr4:69522639-69522689	ovcar-3	ovarian:	n/a
18	chr4:69537806-69537856	HUVEC	blood vessel:	n/a
19	chr4:69381368-69381418	HCM	heart:	n/a
20	chr4:69537826-69537876	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:69355121-69355171	SK-N-SH_RA	brain:	n/a
22	chr4:69537806-69537856	RPTEC	kidney:	n/a
23	chr4:69522639-69522689	IMR90	lung:	fetal
24	chr4:69522639-69522689	NH-A	brain:	n/a
25	chr4:69514031-69514081	HRCEpiC	kidney:	n/a
26	chr4:69435593-69435643	NB4	blood:	n/a
27	chr4:69435601-69435651	HCF	heart:	n/a
28	chr4:69355121-69355171	LNCaP	prostate:	n/a
29	chr4:69434475-69434525	CMK	blood:	n/a
30	chr4:69522639-69522689	SK-N-MC	brain:	n/a
31	chr4:69536319-69536369	HCF	heart:	n/a
32	chr4:69537806-69537856	AG10803	skin:	n/a
33	chr4:69537589-69537639	HUVEC	blood vessel:	n/a
34	chr4:69536319-69536369	NHDF-neo	bronchial:	n/a
35	chr4:69435601-69435651	HRCEpiC	kidney:	n/a
36	chr4:69435601-69435651	Hepatocyte	liver:	n/a
37	chr4:69435601-69435651	HepG2	liver:	n/a
38	chr4:69355121-69355171	HCM	heart:	n/a
39	chr4:69536319-69536369	HUVEC	blood vessel:	n/a
40	chr4:69435593-69435643	Hela-S3	cervix:	n/a
41	chr4:69537589-69537639	NHBE	bronchial:	n/a
42	chr4:69537826-69537876	AG10803	skin:	n/a
43	chr4:69536319-69536369	GM12878	blood:	n/a
44	chr4:69537826-69537876	H1-hESC	embryonic stem cell:	embryo
45	chr4:69536319-69536369	NT2-D1	testis:	n/a
46	chr4:69435250-69435300	NHBE	bronchial:	n/a
47	chr4:69522639-69522689	SAEC	small airway:	n/a
48	chr4:69514031-69514081	RPTEC	kidney:	n/a
49	chr4:69381368-69381418	LNCaP	prostate:	n/a
50	chr4:69537806-69537856	SK-N-MC	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
2	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
3	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
4	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
5	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
6	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
7	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
8	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
9	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
2	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
3	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
4	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
5	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
6	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
UGT2B29P	TF binding region
ENSG00000248635	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island
ENSG00000248635	CpG island
ENSG00000083896	chromatin interactions
ENSG00000249985	chromatin interactions
ENSG00000272626	chromatin interactions

Extended variants
information (count: 6491 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6491 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs137885953	chr4:69344730-69344731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2603180	chr4:69344733-69344734	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs188590272	chr4:69344775-69344776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537487366	chr4:69344798-69344799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557440870	chr4:69344868-69344869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570965144	chr4:69344877-69344878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2603179	chr4:69344883-69344884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs553114334	chr4:69344884-69344885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200365633	chr4:69344888-69344889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571454045	chr4:69344947-69344948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572989903	chr4:69344995-69344996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148248418	chr4:69344997-69344998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192955523	chr4:69345010-69345011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549147282	chr4:69345012-69345013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374324908	chr4:69345027-69345028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184691763	chr4:69345042-69345043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189480050	chr4:69345067-69345068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141231776	chr4:69345069-69345070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1377870	chr4:69345132-69345133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs1377869	chr4:69345142-69345143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs3100650	chr4:69345156-69345157	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs571338661	chr4:69345179-69345180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554211020	chr4:69345196-69345197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140009857	chr4:69345334-69345335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562370213	chr4:69345342-69345343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530883843	chr4:69345435-69345436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1377868	chr4:69345436-69345437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570889586	chr4:69345437-69345438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539910131	chr4:69345503-69345504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374886111	chr4:69345550-69345551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566657919	chr4:69345560-69345561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35890966	chr4:69345580-69345581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs2603178	chr4:69345598-69345599	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35258587	chr4:69345659-69345660	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs539874414	chr4:69345743-69345744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567748088	chr4:69345746-69345747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191123246	chr4:69345749-69345750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370088837	chr4:69345755-69345756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577251934	chr4:69345790-69345791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540313757	chr4:69345846-69345847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560034911	chr4:69345866-69345867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs984808	chr4:69345909-69345910	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs61287671	chr4:69345933-69345934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372334762	chr4:69345935-69345936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199637571	chr4:69345936-69345937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183631937	chr4:69346005-69346006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs202056292	chr4:69346030-69346031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189434693	chr4:69346044-69346045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531211885	chr4:69346081-69346082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551332820	chr4:69346127-69346128	Weak transcription Enhancers	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	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
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69326200-69348800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:69333200-69349400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:69339600-69355000	Weak transcription	Esophagus	oesophagus
4	chr4:69345600-69346000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:69345600-69346000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:69345600-69346200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:69345600-69346400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:69348800-69349000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:69350400-69358000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:69355000-69355400	ZNF genes & repeats	Esophagus	oesophagus
11	chr4:69355200-69355400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:69355200-69355400	ZNF genes & repeats	Pancreas	Pancrea
13	chr4:69355200-69355800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:69355400-69362000	Weak transcription	Esophagus	oesophagus
15	chr4:69357600-69358400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:69359400-69360800	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr4:69359800-69360600	Enhancers	Duodenum Mucosa	Duodenum
18	chr4:69359800-69360800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr4:69360000-69360400	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr4:69360000-69360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:69360000-69360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr4:69360200-69360600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:69360200-69360600	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr4:69360200-69360600	Enhancers	GM12878-XiMat	blood
25	chr4:69360200-69360800	Enhancers	Primary B cells from peripheral blood	blood
26	chr4:69360200-69360800	Enhancers	Primary hematopoietic stem cells	blood
27	chr4:69360200-69360800	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr4:69360400-69360800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:69360400-69360800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr4:69360400-69360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr4:69360400-69361000	Enhancers	Primary T cells from cord blood	blood
32	chr4:69360800-69364400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr4:69361800-69362000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:69363600-69364000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr4:69363600-69364000	Enhancers	Fetal Kidney	kidney
36	chr4:69363600-69364200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr4:69363600-69365000	Enhancers	A549	lung
38	chr4:69363600-69365600	Enhancers	HepG2	liver
39	chr4:69364000-69364400	Enhancers	Fetal Intestine Large	intestine
40	chr4:69364000-69364600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr4:69364000-69365200	Enhancers	Liver	Liver
42	chr4:69364200-69364600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:69364400-69364600	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr4:69364400-69364800	Enhancers	Primary hematopoietic stem cells	blood
45	chr4:69364400-69364800	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr4:69364400-69365000	Active TSS	Fetal Intestine Large	intestine
47	chr4:69364400-69365000	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr4:69364600-69364800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr4:69364800-69365000	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr4:69365000-69365400	Enhancers	Rectal Mucosa Donor 29	rectum

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