Variant report

Variant	esv1808964
Chromosome Location	chr4:69434902-69569777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:707)
CpG islands
(count:549)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
7	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
8	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
9	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
10	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
13	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
14	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
15	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
16	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
17	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
18	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
19	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
20	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
22	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
23	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
26	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
27	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
28	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
30	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
31	CTCF	chr4:69434832-69435088	GM19238	blood:	n/a	n/a
32	CTCF	chr4:69537020-69537170	HEK293	kidney:	n/a	n/a
33	CTCF	chr4:69443441-69443533	ProgFib	skin:	n/a	n/a
34	CTCF	chr4:69434845-69435046	GM19239	blood:	n/a	n/a
35	CTCF	chr4:69434820-69434970	K562	blood:	n/a	n/a
36	CTCF	chr4:69537345-69537422	GM10248	blood:	n/a	n/a
37	CTCF	chr4:69537000-69537150	GM12873	blood:	n/a	n/a
38	CTCF	chr4:69435086-69435087	NHEK	skin:	n/a	n/a
39	CTCF	chr4:69511582-69511727	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr4:69443417-69443543	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr4:69538960-69539110	GM12869	blood:	n/a	n/a
42	CTCF	chr4:69523077-69523274	GM10266	blood:	n/a	n/a
43	CTCF	chr4:69443461-69443509	A549	lung:	n/a	n/a
44	CTCF	chr4:69434856-69435015	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr4:69538990-69539148	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr4:69443320-69443470	RPTEC	kidney:	n/a	n/a
47	CTCF	chr4:69534349-69534466	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:69443620-69443770	GM12865	blood:	n/a	n/a
49	CTCF	chr4:69539120-69539270	GM12864	blood:	n/a	n/a
50	CTCF	chr4:69538954-69539224	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69537806-69537856	HL-60	blood:	n/a
2	chr4:69537806-69537856	AG04449	skin:	fetal
3	chr4:69514031-69514081	GM12892	blood:	n/a
4	chr4:69435593-69435643	ovcar-3	ovarian:	n/a
5	chr4:69522639-69522689	BJ	skin:	n/a
6	chr4:69514031-69514081	NHDF-neo	bronchial:	n/a
7	chr4:69537806-69537856	A549	lung:	n/a
8	chr4:69522639-69522689	PANC-1	pancreas:	n/a
9	chr4:69536319-69536369	PANC-1	pancreas:	n/a
10	chr4:69435593-69435643	HRE	kidney:	n/a
11	chr4:69536319-69536369	GM06990	blood:	n/a
12	chr4:69537806-69537856	U87	brain:	n/a
13	chr4:69537806-69537856	AoSMC	blood vessel:	n/a
14	chr4:69537589-69537639	HL-60	blood:	n/a
15	chr4:69435250-69435300	BJ	skin:	n/a
16	chr4:69435601-69435651	MCF10A-Er-Src	breast:	n/a
17	chr4:69514031-69514081	HIPEpiC	eye:	n/a
18	chr4:69537826-69537876	ECC-1	luminal epithelium:	n/a
19	chr4:69435593-69435643	SK-N-MC	brain:	n/a
20	chr4:69435593-69435643	Jurkat	blood:	n/a
21	chr4:69514031-69514081	HAEpiC	amniotic membrane:	n/a
22	chr4:69536319-69536369	HNPCEpiC	eye:	n/a
23	chr4:69435601-69435651	HNPCEpiC	eye:	n/a
24	chr4:69536319-69536369	PrEC	prostate:	n/a
25	chr4:69537826-69537876	ProgFib	skin:	n/a
26	chr4:69522639-69522689	HRPEpiC	eye:	n/a
27	chr4:69514031-69514081	AG09309	skin:	n/a
28	chr4:69514031-69514081	HCPEpiC	choroid plexus:	n/a
29	chr4:69435250-69435300	Jurkat	blood:	n/a
30	chr4:69435593-69435643	GM12892	blood:	n/a
31	chr4:69522639-69522689	MCF10A-Er-Src	breast:	n/a
32	chr4:69537806-69537856	K562	blood:	n/a
33	chr4:69522639-69522689	HIPEpiC	eye:	n/a
34	chr4:69536319-69536369	NHDF-neo	bronchial:	n/a
35	chr4:69536319-69536369	ovcar-3	ovarian:	n/a
36	chr4:69537589-69537639	HAEpiC	amniotic membrane:	n/a
37	chr4:69435250-69435300	GM12892	blood:	n/a
38	chr4:69435593-69435643	HCM	heart:	n/a
39	chr4:69435593-69435643	GM12891	blood:	n/a
40	chr4:69536319-69536369	Caco-2	colon:	n/a
41	chr4:69435601-69435651	LNCaP	prostate:	n/a
42	chr4:69536319-69536369	Hela-S3	cervix:	n/a
43	chr4:69522639-69522689	HCT-116	colon:	n/a
44	chr4:69537806-69537856	SK-N-SH_RA	brain:	n/a
45	chr4:69435601-69435651	BJ	skin:	n/a
46	chr4:69537806-69537856	HAEpiC	amniotic membrane:	n/a
47	chr4:69435250-69435300	HCPEpiC	choroid plexus:	n/a
48	chr4:69537806-69537856	SAEC	small airway:	n/a
49	chr4:69537826-69537876	SK-N-SH_RA	brain:	n/a
50	chr4:69537806-69537856	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
2	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
2	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
3	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
4	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737

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
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island

Extended variants
information (count: 3702 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3702 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6857249	chr4:69434902-69434903	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs371769763	chr4:69434914-69434915	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs192017922	chr4:69434960-69434961	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs144638778	chr4:69434961-69434962	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs543365205	chr4:69435011-69435012	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs116181509	chr4:69435162-69435163	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs568945430	chr4:69435169-69435170	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs114790205	chr4:69435177-69435178	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs116610581	chr4:69435217-69435218	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs6858064	chr4:69435245-69435246	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs547216823	chr4:69435251-69435252	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs147867060	chr4:69435325-69435326	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs182540451	chr4:69435352-69435353	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs202224072	chr4:69435532-69435533	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs185228346	chr4:69435533-69435534	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs549671336	chr4:69435591-69435592	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569501516	chr4:69435788-69435789	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs538672351	chr4:69435813-69435814	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs141867461	chr4:69435882-69435883	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs572430815	chr4:69435887-69435888	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs114781747	chr4:69435907-69435908	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs115340336	chr4:69435908-69435909	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs74333491	chr4:69435938-69435939	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs565834142	chr4:69435939-69435940	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs190036017	chr4:69435964-69435965	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs574300891	chr4:69435975-69435976	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs151115619	chr4:69436004-69436005	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs112425340	chr4:69436145-69436146	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs72846068	chr4:69436186-69436187	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539655683	chr4:69436197-69436198	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs76011384	chr4:69436223-69436224	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs182657909	chr4:69436228-69436229	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs6817882	chr4:69436235-69436236	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs545419253	chr4:69436274-69436275	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs565212810	chr4:69436380-69436381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187223181	chr4:69436406-69436407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543666786	chr4:69436410-69436411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191648218	chr4:69436506-69436507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563543794	chr4:69436518-69436519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529840359	chr4:69436560-69436561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183533697	chr4:69436561-69436562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368260826	chr4:69436634-69436635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs137951550	chr4:69436635-69436636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529489687	chr4:69436636-69436637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542842829	chr4:69436639-69436640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188787158	chr4:69436652-69436653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561855932	chr4:69436693-69436694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115923225	chr4:69436730-69436731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554714997	chr4:69436756-69436757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534415671	chr4:69436804-69436805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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	17122850	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:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69429200-69439800	Weak transcription	Right Atrium	heart
2	chr4:69434000-69435000	Weak transcription	Liver	Liver
3	chr4:69434200-69439200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr4:69434600-69435200	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr4:69435000-69436200	Enhancers	Liver	Liver
6	chr4:69435200-69435800	Enhancers	Small Intestine	intestine
7	chr4:69435200-69436000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:69435200-69438000	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr4:69435400-69435800	Enhancers	Primary B cells from peripheral blood	blood
10	chr4:69435600-69436200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:69435800-69436800	Weak transcription	Primary B cells from peripheral blood	blood
12	chr4:69436000-69441800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr4:69436200-69446600	Weak transcription	Liver	Liver
14	chr4:69436800-69439000	Enhancers	Primary B cells from peripheral blood	blood
15	chr4:69438000-69438400	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr4:69438400-69439800	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr4:69439000-69441000	Weak transcription	Primary B cells from peripheral blood	blood
18	chr4:69439200-69439400	Enhancers	Duodenum Mucosa	Duodenum
19	chr4:69439400-69448200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:69439600-69440000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr4:69441000-69443000	Enhancers	Primary B cells from peripheral blood	blood
22	chr4:69441800-69442000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:69446600-69448000	Enhancers	Liver	Liver
24	chr4:69447400-69448000	Enhancers	NHEK	skin
25	chr4:69447600-69448200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:69447600-69448200	Enhancers	HepG2	liver
27	chr4:69448000-69448200	Flanking Active TSS	Liver	Liver
28	chr4:69448200-69448600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr4:69448200-69448600	Enhancers	Liver	Liver
30	chr4:69455400-69455600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr4:69455400-69456200	Enhancers	Fetal Heart	heart
32	chr4:69455400-69457400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:69455400-69457800	Enhancers	NHEK	skin
34	chr4:69455600-69455800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:69455600-69456600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr4:69455600-69457800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:69455600-69458000	Enhancers	HMEC	breast
38	chr4:69456000-69457000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr4:69456200-69456400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:69456200-69457200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr4:69456400-69458600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:69456600-69457000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:69456600-69457200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:69457000-69457400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:69457000-69457600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:69458600-69459000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:69458600-69459600	Enhancers	Liver	Liver
48	chr4:69459600-69459800	Flanking Active TSS	Liver	Liver
49	chr4:69459800-69460000	Enhancers	Liver	Liver
50	chr4:69460000-69460200	Flanking Active TSS	Liver	Liver

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