Variant report

Variant	nsv967427
Chromosome Location	chr7:13139839-13155007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:123)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:123 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:13143806-13144072	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:13143855-13144055	K562	blood:	n/a	n/a
3	ATF1	chr7:13143829-13144112	K562	blood:	n/a	n/a
4	CBX3	chr7:13149470-13149761	K562	blood:	n/a	n/a
5	CEBPB	chr7:13154797-13155156	K562	blood:	n/a	n/a
6	CEBPB	chr7:13154823-13155166	K562	blood:	n/a	n/a
7	CEBPB	chr7:13147885-13147964	K562	blood:	n/a	chr7:13147889-13147897
8	CEBPB	chr7:13147374-13147981	A549	lung:	n/a	chr7:13147889-13147897
9	CEBPB	chr7:13147632-13147985	HepG2	liver:	n/a	chr7:13147889-13147897
10	CEBPB	chr7:13144926-13145120	HepG2	liver:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
11	CEBPB	chr7:13154819-13155176	MCF-7	breast:	n/a	n/a
12	CEBPB	chr7:13147629-13147716	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:13144858-13145220	HepG2	liver:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
14	CEBPB	chr7:13143804-13144134	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:13154568-13155190	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr7:13154829-13155112	K562	blood:	n/a	n/a
17	CEBPB	chr7:13154952-13155171	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:13144953-13145094	K562	blood:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
19	CEBPB	chr7:13154840-13155180	A549	lung:	n/a	n/a
20	CEBPB	chr7:13154798-13155176	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:13144878-13145220	K562	blood:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
22	CEBPB	chr7:13154809-13155057	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:13143857-13144090	K562	blood:	n/a	n/a
24	CTCF	chr7:13150764-13150825	GM13977	blood:	n/a	n/a
25	CTCF	chr7:13154900-13155050	HVMF	connective:	n/a	n/a
26	CTCF	chr7:13155000-13155150	NHEK	skin:	n/a	n/a
27	CTCF	chr7:13146180-13146330	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr7:13147780-13147930	GM12872	blood:	n/a	n/a
29	CTCF	chr7:13154940-13155090	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr7:13151014-13151099	GM20000	blood:	n/a	n/a
31	CTCF	chr7:13149040-13149190	HepG2	liver:	n/a	n/a
32	CTCF	chr7:13154920-13155070	HAc	cerebellar:	n/a	n/a
33	CTCF	chr7:13146260-13146410	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr7:13155000-13155150	K562	blood:	n/a	n/a
35	CTCF	chr7:13150600-13150750	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr7:13154954-13155279	MCF-7	breast:	n/a	chr7:13155137-13155155 chr7:13155132-13155153
37	CTCF	chr7:13154942-13155243	K562	blood:	n/a	chr7:13155137-13155155 chr7:13155132-13155153
38	CTCF	chr7:13150673-13150758	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:13154740-13154890	HCM	heart:	n/a	n/a
40	CUX1	chr7:13143789-13143865	K562	blood:	n/a	n/a
41	ELF1	chr7:13149674-13149984	GM12878	blood:	n/a	n/a
42	EP300	chr7:13154815-13155206	K562	blood:	n/a	chr7:13154940-13154950
43	EP300	chr7:13154737-13155158	Hela-S3	cervix:	n/a	chr7:13154940-13154950
44	EP300	chr7:13143823-13144120	HepG2	liver:	n/a	chr7:13143990-13143999
45	EP300	chr7:13143847-13144090	K562	blood:	n/a	chr7:13143990-13143999
46	EP300	chr7:13143797-13144121	HepG2	liver:	n/a	chr7:13143990-13143999
47	FOS	chr7:13150979-13151128	MCF10A-Er-Src	breast:	n/a	chr7:13151102-13151113
48	FOS	chr7:13150981-13151374	HUVEC	blood vessel:	n/a	chr7:13151102-13151113
49	FOS	chr7:13151043-13151123	MCF10A-Er-Src	breast:	n/a	chr7:13151102-13151113
50	FOXA1	chr7:13144864-13145231	HepG2	liver:	n/a	chr7:13144981-13144993 chr7:13145172-13145184

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13141735-13141785	HUVEC	blood vessel:	n/a
2	chr7:13141735-13141785	GM19239	blood:	n/a
3	chr7:13141735-13141785	HNPCEpiC	eye:	n/a
4	chr7:13141735-13141785	NHDF-neo	bronchial:	n/a
5	chr7:13141735-13141785	K562	blood:	n/a
6	chr7:13141735-13141785	HRE	kidney:	n/a
7	chr7:13141735-13141785	HCPEpiC	choroid plexus:	n/a
8	chr7:13141735-13141785	HCF	heart:	n/a
9	chr7:13141735-13141785	IMR90	lung:	fetal
10	chr7:13141735-13141785	SK-N-MC	brain:	n/a
11	chr7:13141735-13141785	HMEC	breast:	n/a
12	chr7:13141735-13141785	SK-N-SH	brain:	n/a
13	chr7:13141735-13141785	AG10803	skin:	n/a
14	chr7:13141735-13141785	ECC-1	luminal epithelium:	n/a
15	chr7:13141735-13141785	H1-hESC	embryonic stem cell:	embryo
16	chr7:13141735-13141785	T-47D	breast:	n/a
17	chr7:13141735-13141785	AG04450	lung:	fetal
18	chr7:13141735-13141785	SK-N-SH_RA	brain:	n/a
19	chr7:13141735-13141785	NT2-D1	testis:	n/a
20	chr7:13141735-13141785	SAEC	small airway:	n/a
21	chr7:13141735-13141785	U87	brain:	n/a
22	chr7:13141735-13141785	NHBE	bronchial:	n/a
23	chr7:13141735-13141785	HCT-116	colon:	n/a
24	chr7:13141735-13141785	BJ	skin:	n/a
25	chr7:13141735-13141785	HEK293	kidney:	embryo
26	chr7:13141735-13141785	PrEC	prostate:	n/a
27	chr7:13141735-13141785	GM12878	blood:	n/a
28	chr7:13141735-13141785	HIPEpiC	eye:	n/a
29	chr7:13141735-13141785	GM12891	blood:	n/a
30	chr7:13141735-13141785	AG09309	skin:	n/a
31	chr7:13141735-13141785	Hela-S3	cervix:	n/a
32	chr7:13141735-13141785	AG09319	gingival:	n/a
33	chr7:13141735-13141785	HL-60	blood:	n/a
34	chr7:13141735-13141785	RPTEC	kidney:	n/a
35	chr7:13141735-13141785	AoSMC	blood vessel:	n/a
36	chr7:13141735-13141785	ProgFib	skin:	n/a
37	chr7:13141735-13141785	ovcar-3	ovarian:	n/a
38	chr7:13141735-13141785	AG04449	skin:	fetal
39	chr7:13141735-13141785	LNCaP	prostate:	n/a
40	chr7:13141735-13141785	HRPEpiC	eye:	n/a
41	chr7:13141735-13141785	HCM	heart:	n/a
42	chr7:13141735-13141785	MCF-7	breast:	n/a
43	chr7:13141735-13141785	BE2_C	brain:	n/a
44	chr7:13141735-13141785	HEEpiC	esophagus:	n/a
45	chr7:13141735-13141785	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:13141735-13141785	GM06990	blood:	n/a
47	chr7:13141735-13141785	NH-A	brain:	n/a
48	chr7:13141735-13141785	Caco-2	colon:	n/a
49	chr7:13141735-13141785	HepG2	liver:	n/a
50	chr7:13141735-13141785	PANC-1	pancreas:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:13146440..13148600-chr7:13150373..13152655,2	K562	blood:
2	chr7:12980961..12983258-chr7:13154370..13156023,2	MCF-7	breast:
3	chr7:13146440..13148600-chr7:13150373..13152655,2	K562	blood:
4	chr7:12726065..12729797-chr7:13154020..13158072,4	MCF-7	breast:
5	chr7:12726190..12728016-chr7:13138204..13140895,2	K562	blood:
6	chr7:13146450..13148956-chr7:13151839..13153573,2	MCF-7	breast:
7	chr7:13145074..13147493-chr7:13153724..13155360,2	MCF-7	breast:
8	chr7:12726542..12728897-chr7:13150585..13153553,2	MCF-7	breast:
9	chr7:13146450..13148956-chr7:13151839..13153573,2	MCF-7	breast:
10	chr7:12726572..12727399-chr7:13154701..13155615,3	MCF-7	breast:
11	chr7:13145074..13147493-chr7:13153724..13155360,2	MCF-7	breast:
12	chr6:155003966..155004703-chr7:13139161..13140000,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL4A-1	chr7:13141097-13141208	XLOC_005988

No data

Variant related genes	Relation type
ENSG00000229618	TF binding region
ENSG00000229618	CpG island
ENSG00000122644	chromatin interactions

Extended variants
information (count: 754 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185571864	chr7:13139840-13139841	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs66473460	chr7:13139876-13139877	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs567033319	chr7:13139892-13139893	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201751419	chr7:13139914-13139915	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147975347	chr7:13139933-13139934	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs141647963	chr7:13139959-13139960	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs150526890	chr7:13139960-13139961	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs555370247	chr7:13139977-13139978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs6971600	chr7:13139983-13139984	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs375362844	chr7:13139987-13139988	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs370342663	chr7:13139992-13139993	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs112635908	chr7:13140008-13140009	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs368281466	chr7:13140058-13140059	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577420561	chr7:13140130-13140131	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs4421265	chr7:13140150-13140151	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs556758672	chr7:13140174-13140175	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111988119	chr7:13140189-13140190	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs190034812	chr7:13140198-13140199	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183051091	chr7:13140221-13140222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142779947	chr7:13140228-13140229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538053686	chr7:13140258-13140259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs6954638	chr7:13140268-13140269	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs554850769	chr7:13140300-13140301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563691023	chr7:13140325-13140326	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs569295860	chr7:13140327-13140328	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532871422	chr7:13140346-13140347	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs147406994	chr7:13140362-13140363	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs563545143	chr7:13140385-13140386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs529063173	chr7:13140394-13140395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185779087	chr7:13140405-13140406	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs368967457	chr7:13140504-13140505	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565858338	chr7:13140513-13140514	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534868902	chr7:13140531-13140532	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs79357877	chr7:13140571-13140572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs570851578	chr7:13140577-13140578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs539987674	chr7:13140586-13140587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139704068	chr7:13140587-13140588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs576607792	chr7:13140591-13140592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs145294587	chr7:13140630-13140631	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555898905	chr7:13140675-13140676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572408129	chr7:13140712-13140713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs12671645	chr7:13140765-13140766	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs563778560	chr7:13140818-13140819	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192342138	chr7:13140827-13140828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543532699	chr7:13140832-13140833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563255665	chr7:13140871-13140872	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs183711110	chr7:13140889-13140890	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528955105	chr7:13140893-13140894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187596828	chr7:13140898-13140899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192274422	chr7:13140910-13140911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13134600-13143600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:13136200-13143400	Weak transcription	HepG2	liver
3	chr7:13138200-13143400	Weak transcription	Liver	Liver
4	chr7:13139200-13146600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:13139200-13147200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:13139800-13140200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:13142400-13147600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:13143400-13143600	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr7:13143400-13144200	Enhancers	Liver	Liver
10	chr7:13143400-13144400	Enhancers	Stomach Mucosa	stomach
11	chr7:13143400-13144600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr7:13143400-13144600	Enhancers	HepG2	liver
13	chr7:13143400-13145600	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr7:13143600-13144400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:13143600-13144400	Enhancers	K562	blood
16	chr7:13143600-13144400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr7:13144000-13144400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr7:13144200-13149000	Weak transcription	Liver	Liver
19	chr7:13144400-13145200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr7:13144600-13148800	Weak transcription	HepG2	liver
21	chr7:13146600-13147800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:13147200-13147600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:13147600-13147800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr7:13147600-13147800	Enhancers	Esophagus	oesophagus
25	chr7:13147800-13148800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:13147800-13149200	Weak transcription	Esophagus	oesophagus
27	chr7:13148800-13149200	Enhancers	HepG2	liver
28	chr7:13148800-13149400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:13148800-13150000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:13149000-13149200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:13149000-13149400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:13149000-13149400	Enhancers	Liver	Liver
33	chr7:13149000-13150000	Enhancers	Gastric	stomach
34	chr7:13149200-13149800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:13149200-13150000	ZNF genes & repeats	Esophagus	oesophagus
36	chr7:13149200-13150200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:13149200-13154600	Weak transcription	HepG2	liver
38	chr7:13149800-13150000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:13150000-13150800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:13150000-13154400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:13153400-13154000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:13154000-13154400	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr7:13154400-13155000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:13154400-13155200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr7:13154400-13155400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:13154400-13155400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr7:13154400-13155400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:13154400-13155400	Enhancers	Placenta	Placenta
49	chr7:13154400-13155400	Enhancers	HMEC	breast
50	chr7:13154400-13155400	Enhancers	K562	blood

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