Variant report

Variant	nsv1009628
Chromosome Location	chr4:69670507-69713817
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	ARID3A	chr4:69680934-69681903	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69683102-69684193	HepG2	liver:	n/a	chr4:69683103-69683119
3	BHLHE40	chr4:69681403-69681779	HepG2	liver:	n/a	n/a
4	CBX3	chr4:69710563-69710928	K562	blood:	n/a	n/a
5	CEBPB	chr4:69685477-69685793	HepG2	liver:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
6	CEBPB	chr4:69678841-69679067	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:69681686-69681867	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:69681485-69681922	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:69685586-69685776	H1-hESC	embryonic stem cell:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
10	CEBPB	chr4:69684063-69684187	K562	blood:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
11	CEBPB	chr4:69683737-69684291	HepG2	liver:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
12	CEBPB	chr4:69684002-69684205	A549	lung:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
13	CEBPB	chr4:69685492-69685778	IMR90	lung:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
14	CEBPB	chr4:69712445-69712703	HepG2	liver:	n/a	chr4:69712549-69712560
15	CEBPB	chr4:69685580-69685738	A549	lung:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
16	CEBPB	chr4:69685485-69685717	K562	blood:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
17	CEBPB	chr4:69684015-69684280	IMR90	lung:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
18	CEBPD	chr4:69681639-69681887	HepG2	liver:	n/a	n/a
19	CTCF	chr4:69678039-69678143	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr4:69681974-69682009	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr4:69674820-69674970	GM12873	blood:	n/a	n/a
22	CTCF	chr4:69683829-69683943	Lung_OC	lung:	n/a	n/a
23	CTCF	chr4:69713220-69713370	GM12872	blood:	n/a	n/a
24	CTCF	chr4:69675017-69675085	Lung_OC	lung:	n/a	n/a
25	CTCF	chr4:69692957-69692997	Kidney_OC	kidney:	n/a	n/a
26	EP300	chr4:69681482-69681788	HepG2	liver:	n/a	chr4:69681630-69681640
27	EP300	chr4:69681295-69681781	A549	lung:	n/a	chr4:69681630-69681640
28	EP300	chr4:69683627-69684145	HepG2	liver:	n/a	chr4:69683716-69683730 chr4:69683632-69683642
29	EP300	chr4:69681124-69681935	A549	lung:	n/a	chr4:69681630-69681640
30	EP300	chr4:69705426-69705448	K562	blood:	n/a	n/a
31	EP300	chr4:69681227-69681937	HepG2	liver:	n/a	chr4:69681630-69681640
32	EP300	chr4:69683119-69683383	HepG2	liver:	n/a	n/a
33	EP300	chr4:69683110-69683464	HepG2	liver:	n/a	chr4:69683437-69683451
34	EP300	chr4:69681270-69682024	HepG2	liver:	n/a	chr4:69681630-69681640
35	EP300	chr4:69683551-69684101	HepG2	liver:	n/a	chr4:69683716-69683730 chr4:69683632-69683642
36	FOSL2	chr4:69681428-69682033	HepG2	liver:	n/a	n/a
37	FOSL2	chr4:69683663-69683966	HepG2	liver:	n/a	n/a
38	FOSL2	chr4:69687855-69688221	HepG2	liver:	n/a	n/a
39	FOSL2	chr4:69693621-69693993	A549	lung:	n/a	n/a
40	FOSL2	chr4:69682047-69682360	HepG2	liver:	n/a	n/a
41	FOSL2	chr4:69683671-69684057	HepG2	liver:	n/a	chr4:69683978-69683990
42	FOSL2	chr4:69681366-69682455	HepG2	liver:	n/a	n/a
43	FOSL2	chr4:69687920-69688219	HepG2	liver:	n/a	n/a
44	FOXA1	chr4:69681274-69681920	HepG2	liver:	n/a	chr4:69681561-69681576
45	FOXA1	chr4:69682696-69684401	HepG2	liver:	n/a	n/a
46	FOXA1	chr4:69681268-69681979	HepG2	liver:	n/a	chr4:69681561-69681576
47	FOXA1	chr4:69683674-69684035	HepG2	liver:	n/a	n/a
48	FOXA1	chr4:69683614-69684060	HepG2	liver:	n/a	n/a
49	FOXA1	chr4:69683088-69683422	HepG2	liver:	n/a	n/a
50	FOXA1	chr4:69683068-69684396	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69681824-69681874	PANC-1	pancreas:	n/a
2	chr4:69681824-69681874	HEEpiC	esophagus:	n/a
3	chr4:69681824-69681874	PrEC	prostate:	n/a
4	chr4:69681824-69681874	HEK293	kidney:	embryo
5	chr4:69681824-69681874	HCM	heart:	n/a
6	chr4:69681824-69681874	A549	lung:	n/a
7	chr4:69681824-69681874	Hela-S3	cervix:	n/a
8	chr4:69681824-69681874	GM19239	blood:	n/a
9	chr4:69681824-69681874	AG10803	skin:	n/a
10	chr4:69681824-69681874	CMK	blood:	n/a
11	chr4:69681824-69681874	HMEC	breast:	n/a
12	chr4:69681824-69681874	Jurkat	blood:	n/a
13	chr4:69681824-69681874	Caco-2	colon:	n/a
14	chr4:69681824-69681874	GM12891	blood:	n/a
15	chr4:69681824-69681874	ECC-1	luminal epithelium:	n/a
16	chr4:69681824-69681874	U87	brain:	n/a
17	chr4:69681824-69681874	AG09319	gingival:	n/a
18	chr4:69681824-69681874	Hepatocyte	liver:	n/a
19	chr4:69681824-69681874	HRE	kidney:	n/a
20	chr4:69681824-69681874	NH-A	brain:	n/a
21	chr4:69681824-69681874	IMR90	lung:	fetal
22	chr4:69681824-69681874	HCF	heart:	n/a
23	chr4:69681824-69681874	HCT-116	colon:	n/a
24	chr4:69681824-69681874	AG09309	skin:	n/a
25	chr4:69681824-69681874	ProgFib	skin:	n/a
26	chr4:69681824-69681874	GM06990	blood:	n/a
27	chr4:69681824-69681874	H1-hESC	embryonic stem cell:	embryo
28	chr4:69681824-69681874	NHDF-neo	bronchial:	n/a
29	chr4:69681824-69681874	SK-N-SH_RA	brain:	n/a
30	chr4:69681824-69681874	HepG2	liver:	n/a
31	chr4:69681824-69681874	SK-N-MC	brain:	n/a
32	chr4:69681824-69681874	GM12878	blood:	n/a
33	chr4:69681824-69681874	NB4	blood:	n/a
34	chr4:69681824-69681874	HNPCEpiC	eye:	n/a
35	chr4:69681824-69681874	HRPEpiC	eye:	n/a
36	chr4:69681824-69681874	HRCEpiC	kidney:	n/a
37	chr4:69681824-69681874	HL-60	blood:	n/a
38	chr4:69681824-69681874	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:69681824-69681874	HCPEpiC	choroid plexus:	n/a
40	chr4:69681824-69681874	HUVEC	blood vessel:	n/a
41	chr4:69681824-69681874	MCF-7	breast:	n/a
42	chr4:69681824-69681874	HAEpiC	amniotic membrane:	n/a
43	chr4:69681824-69681874	HIPEpiC	eye:	n/a
44	chr4:69681824-69681874	BJ	skin:	n/a
45	chr4:69681824-69681874	ovcar-3	ovarian:	n/a
46	chr4:69681824-69681874	SAEC	small airway:	n/a
47	chr4:69681824-69681874	T-47D	breast:	n/a
48	chr4:69681824-69681874	SKMC	muscle:	n/a
49	chr4:69681824-69681874	AG04449	skin:	fetal
50	chr4:69681824-69681874	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B10-1	chr4:69679713-69680445	NONHSAT096742

Variant related genes	Relation type
ENSG00000251236	TF binding region
UGT2B10	TF binding region
ENSG00000251424	TF binding region
ENSG00000251236	CpG island
UGT2B10	CpG island
ENSG00000251424	CpG island

Extended variants
information (count: 1800 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1800 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs294761	chr4:69670507-69670508	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112765281	chr4:69670531-69670532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369394749	chr4:69670562-69670563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532486402	chr4:69670589-69670590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552465787	chr4:69670610-69670611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75770051	chr4:69670638-69670639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113822051	chr4:69670664-69670665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111782234	chr4:69670673-69670674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534564606	chr4:69670682-69670683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371394408	chr4:69670688-69670689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568193893	chr4:69670728-69670729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190299921	chr4:69670744-69670745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556373554	chr4:69670746-69670747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111756936	chr4:69670757-69670758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201754348	chr4:69670812-69670813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183244628	chr4:69670867-69670868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576195420	chr4:69670875-69670876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182657761	chr4:69670876-69670877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545313214	chr4:69670878-69670879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188004118	chr4:69670879-69670880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11737527	chr4:69670886-69670887	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572356274	chr4:69670899-69670900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541454088	chr4:69670933-69670934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561124487	chr4:69670936-69670937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530247906	chr4:69670982-69670983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143479474	chr4:69670995-69670996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543920333	chr4:69671045-69671046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs294762	chr4:69671064-69671065	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs532317571	chr4:69671105-69671106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552504220	chr4:69671106-69671107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565926413	chr4:69671107-69671108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116118995	chr4:69671130-69671131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114827170	chr4:69671145-69671146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567947212	chr4:69671153-69671154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201635922	chr4:69671185-69671186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536765505	chr4:69671196-69671197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538631960	chr4:69671203-69671204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550229648	chr4:69671226-69671227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs294763	chr4:69671235-69671236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs538805889	chr4:69671236-69671237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558873175	chr4:69671241-69671242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187022747	chr4:69671262-69671263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11737672	chr4:69671302-69671303	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs554984869	chr4:69671318-69671319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368098504	chr4:69671319-69671320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543956655	chr4:69671325-69671326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575892334	chr4:69671327-69671328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116540061	chr4:69671335-69671336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544521208	chr4:69671342-69671343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191859714	chr4:69671351-69671352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69669400-69673000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:69670400-69671000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr4:69670600-69671200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr4:69671000-69671200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:69671200-69673000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:69673000-69673600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:69673600-69674000	Enhancers	Liver	Liver
8	chr4:69676600-69678000	Enhancers	HepG2	liver
9	chr4:69678000-69678400	Weak transcription	HepG2	liver
10	chr4:69678400-69679200	Enhancers	HepG2	liver
11	chr4:69679200-69679600	Weak transcription	HepG2	liver
12	chr4:69679600-69681800	Enhancers	HepG2	liver
13	chr4:69680800-69681200	Enhancers	Liver	Liver
14	chr4:69681000-69682600	Enhancers	A549	lung
15	chr4:69681200-69681800	Weak transcription	Liver	Liver
16	chr4:69681400-69682000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr4:69681600-69684000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:69681800-69682200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:69681800-69682600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr4:69681800-69682600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:69681800-69683000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr4:69681800-69683000	Flanking Active TSS	HepG2	liver
23	chr4:69681800-69684600	Active TSS	Liver	Liver
24	chr4:69682000-69682200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr4:69682200-69682400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr4:69682200-69682800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:69682400-69682600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr4:69682400-69682800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr4:69682400-69682800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:69682600-69683200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr4:69682600-69683600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr4:69682600-69683600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr4:69682600-69683800	Weak transcription	A549	lung
34	chr4:69682800-69684200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:69683000-69683400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:69683000-69683600	Active TSS	HepG2	liver
37	chr4:69683200-69683600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr4:69683400-69684800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr4:69683600-69683800	Flanking Active TSS	HepG2	liver
40	chr4:69683600-69684200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:69683600-69684200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:69683800-69684000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:69683800-69684000	Enhancers	A549	lung
44	chr4:69683800-69684000	Active TSS	HepG2	liver
45	chr4:69684000-69684200	Flanking Active TSS	HepG2	liver
46	chr4:69684200-69684600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:69684200-69686000	Enhancers	HepG2	liver
48	chr4:69684600-69686000	Flanking Active TSS	Liver	Liver
49	chr4:69686000-69686600	Enhancers	Liver	Liver
50	chr4:69686000-69688000	Weak transcription	HepG2	liver

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