Variant report

Variant	nsv887699
Chromosome Location	chr7:13868601-13899446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:272)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:13889765-13890070	K562	blood:	n/a	n/a
2	ATF1	chr7:13889729-13890161	K562	blood:	n/a	n/a
3	ATF3	chr7:13889705-13890029	K562	blood:	n/a	n/a
4	BACH1	chr7:13873923-13874075	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:13889847-13890003	H1-hESC	embryonic stem cell:	n/a	chr7:13889889-13889903
6	BHLHE40	chr7:13889782-13890158	K562	blood:	n/a	n/a
7	CBX3	chr7:13889637-13890195	K562	blood:	n/a	n/a
8	CBX3	chr7:13889571-13890520	HCT-116	colon:	n/a	n/a
9	CBX3	chr7:13889630-13890509	HCT-116	colon:	n/a	n/a
10	CBX3	chr7:13889755-13890146	K562	blood:	n/a	n/a
11	CCNT2	chr7:13889753-13890143	K562	blood:	n/a	n/a
12	CEBPB	chr7:13869718-13870004	HepG2	liver:	n/a	chr7:13869838-13869849
13	CEBPB	chr7:13886140-13886336	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:13869641-13870504	IMR90	lung:	n/a	chr7:13869838-13869849
15	CEBPB	chr7:13880963-13881277	IMR90	lung:	n/a	chr7:13881124-13881135
16	CEBPB	chr7:13869719-13869926	K562	blood:	n/a	chr7:13869838-13869849
17	CEBPB	chr7:13891431-13891773	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:13889742-13890398	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:13871986-13872328	K562	blood:	n/a	chr7:13872154-13872167 chr7:13872154-13872167 chr7:13872156-13872167
20	CEBPB	chr7:13880970-13881205	A549	lung:	n/a	chr7:13881124-13881135
21	CEBPB	chr7:13886155-13886335	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:13889794-13890080	K562	blood:	n/a	n/a
23	CEBPB	chr7:13873289-13873292	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:13886123-13886339	K562	blood:	n/a	n/a
25	CEBPB	chr7:13880948-13881315	HepG2	liver:	n/a	chr7:13881124-13881135
26	CEBPB	chr7:13886050-13886429	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:13871988-13872319	IMR90	lung:	n/a	chr7:13872154-13872167 chr7:13872154-13872167 chr7:13872156-13872167
28	CEBPB	chr7:13881008-13881269	K562	blood:	n/a	chr7:13881124-13881135
29	CEBPB	chr7:13880992-13881274	H1-hESC	embryonic stem cell:	n/a	chr7:13881124-13881135
30	CEBPB	chr7:13869741-13869988	A549	lung:	n/a	chr7:13869838-13869849
31	CEBPB	chr7:13886138-13886375	A549	lung:	n/a	n/a
32	CHD2	chr7:13873933-13874094	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr7:13873279-13873288	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:13888927-13888929	K562	blood:	n/a	n/a
35	CTCF	chr7:13889820-13890234	K562	blood:	n/a	chr7:13889868-13889886 chr7:13889863-13889884
36	CTCF	chr7:13877865-13877940	Lung_OC	lung:	n/a	n/a
37	CTCF	chr7:13888618-13888716	Lung_OC	lung:	n/a	n/a
38	CUX1	chr7:13889755-13890437	K562	blood:	n/a	n/a
39	E2F4	chr7:13889537-13890256	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr7:13869676-13869961	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F6	chr7:13889705-13890054	K562	blood:	n/a	n/a
42	E2F6	chr7:13889772-13889971	K562	blood:	n/a	n/a
43	EBF1	chr7:13889866-13890003	GM12878	blood:	n/a	n/a
44	EP300	chr7:13889531-13890634	SK-N-SH	brain:	n/a	chr7:13890097-13890111 chr7:13889891-13889900 chr7:13890098-13890107
45	EP300	chr7:13891983-13892298	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr7:13889660-13890436	SK-N-SH_RA	brain:	n/a	chr7:13890097-13890111 chr7:13889891-13889900 chr7:13890098-13890107
47	EP300	chr7:13889724-13890156	K562	blood:	n/a	chr7:13890097-13890111 chr7:13889891-13889900 chr7:13890098-13890107
48	EP300	chr7:13875024-13875496	H1-hESC	embryonic stem cell:	n/a	n/a
49	EP300	chr7:13889443-13890571	SK-N-SH	brain:	n/a	chr7:13890097-13890111 chr7:13889891-13889900 chr7:13890098-13890107
50	EP300	chr7:13873411-13875315	SK-N-SH	brain:	n/a	chr7:13874312-13874326 chr7:13873837-13873851

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13889871-13889921	HNPCEpiC	eye:	n/a
2	chr7:13889871-13889921	HCF	heart:	n/a
3	chr7:13889871-13889921	Hela-S3	cervix:	n/a
4	chr7:13889871-13889921	MCF10A-Er-Src	breast:	n/a
5	chr7:13889871-13889921	HCT-116	colon:	n/a
6	chr7:13889871-13889921	SK-N-SH_RA	brain:	n/a
7	chr7:13889871-13889921	LNCaP	prostate:	n/a
8	chr7:13889871-13889921	GM12891	blood:	n/a
9	chr7:13889871-13889921	IMR90	lung:	fetal
10	chr7:13889871-13889921	HUVEC	blood vessel:	n/a
11	chr7:13889871-13889921	PANC-1	pancreas:	n/a
12	chr7:13889871-13889921	AG04449	skin:	fetal
13	chr7:13889871-13889921	AG09319	gingival:	n/a
14	chr7:13889871-13889921	HRPEpiC	eye:	n/a
15	chr7:13889871-13889921	NHBE	bronchial:	n/a
16	chr7:13889871-13889921	T-47D	breast:	n/a
17	chr7:13889871-13889921	A549	lung:	n/a
18	chr7:13889871-13889921	AG10803	skin:	n/a
19	chr7:13889871-13889921	ovcar-3	ovarian:	n/a
20	chr7:13889871-13889921	HIPEpiC	eye:	n/a
21	chr7:13889871-13889921	PFSK-1	brain:	n/a
22	chr7:13889871-13889921	GM19239	blood:	n/a
23	chr7:13889871-13889921	GM12892	blood:	n/a
24	chr7:13889871-13889921	SAEC	small airway:	n/a
25	chr7:13889871-13889921	NH-A	brain:	n/a
26	chr7:13889871-13889921	ECC-1	luminal epithelium:	n/a
27	chr7:13889871-13889921	BJ	skin:	n/a
28	chr7:13889871-13889921	Caco-2	colon:	n/a
29	chr7:13889871-13889921	SK-N-MC	brain:	n/a
30	chr7:13889871-13889921	MCF-7	breast:	n/a
31	chr7:13889871-13889921	HMEC	breast:	n/a
32	chr7:13889871-13889921	AoSMC	blood vessel:	n/a
33	chr7:13889871-13889921	HEK293	kidney:	embryo
34	chr7:13889871-13889921	HAEpiC	amniotic membrane:	n/a
35	chr7:13889871-13889921	U87	brain:	n/a
36	chr7:13889871-13889921	SKMC	muscle:	n/a
37	chr7:13889871-13889921	HL-60	blood:	n/a
38	chr7:13889871-13889921	SK-N-SH	brain:	n/a
39	chr7:13889871-13889921	K562	blood:	n/a
40	chr7:13889871-13889921	HRE	kidney:	n/a
41	chr7:13889871-13889921	H1-hESC	embryonic stem cell:	embryo
42	chr7:13889871-13889921	HRCEpiC	kidney:	n/a
43	chr7:13889871-13889921	HEEpiC	esophagus:	n/a
44	chr7:13889871-13889921	CMK	blood:	n/a
45	chr7:13889871-13889921	GM06990	blood:	n/a
46	chr7:13889871-13889921	HepG2	liver:	n/a
47	chr7:13889871-13889921	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:13889871-13889921	Jurkat	blood:	n/a
49	chr7:13889871-13889921	HCPEpiC	choroid plexus:	n/a
50	chr7:13889871-13889921	ProgFib	skin:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:
2	chr7:13894294..13896373-chr7:13930641..13933578,2	K562	blood:
3	chr7:13869026..13872125-chr7:13876719..13879737,3	K562	blood:
4	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
5	chr7:13882109..13884330-chr7:14031307..14033942,2	K562	blood:
6	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
7	chr7:13888923..13892464-chr7:13896702..13899775,3	K562	blood:
8	chr7:13869026..13872125-chr7:13876719..13879737,3	K562	blood:
9	chr7:13888536..13892464-chr7:13896702..13899784,3	K562	blood:
10	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETV1-1	chr7:13898560-13898650	XLOC_006359
2	lnc-ETV1-1	chr7:13893980-13894247	XLOC_006359

No data

Variant related genes	Relation type
ENSG00000224330	TF binding region
ENSG00000224330	CpG island
ENSG00000224330	chromatin interactions

Extended variants
information (count: 1368 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1368 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2067634	chr7:13868601-13868602	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570807398	chr7:13868609-13868610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187401789	chr7:13868663-13868664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549972587	chr7:13868674-13868675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113159850	chr7:13868675-13868676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13226562	chr7:13868712-13868713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190379806	chr7:13868714-13868715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555137422	chr7:13868743-13868744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116158072	chr7:13868797-13868798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139286077	chr7:13868811-13868812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149593240	chr7:13868819-13868820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182880439	chr7:13868821-13868822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4560697	chr7:13868825-13868826	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557212455	chr7:13868842-13868843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573719884	chr7:13868844-13868845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6953236	chr7:13868899-13868900	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs6972874	chr7:13868913-13868914	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs144324317	chr7:13868932-13868933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140901760	chr7:13868935-13868936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188045899	chr7:13868955-13868956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533449372	chr7:13868977-13868978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550035323	chr7:13868983-13868984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550234897	chr7:13868986-13868987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570248412	chr7:13869011-13869012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529452612	chr7:13869022-13869023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549092512	chr7:13869023-13869024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144863388	chr7:13869046-13869047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534661428	chr7:13869064-13869065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192271929	chr7:13869067-13869068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571233361	chr7:13869068-13869069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147955227	chr7:13869072-13869073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556959650	chr7:13869074-13869075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7805583	chr7:13869106-13869107	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs542453968	chr7:13869109-13869110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566416692	chr7:13869130-13869131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184275216	chr7:13869227-13869228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538475818	chr7:13869231-13869232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187758806	chr7:13869270-13869271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538903067	chr7:13869286-13869287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557792823	chr7:13869293-13869294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564161945	chr7:13869386-13869387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533123897	chr7:13869399-13869400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116939103	chr7:13869418-13869419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1476661	chr7:13869433-13869434	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs140193931	chr7:13869461-13869462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549318762	chr7:13869487-13869488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142039531	chr7:13869505-13869506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528215872	chr7:13869512-13869513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551459433	chr7:13869522-13869523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571297425	chr7:13869524-13869525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	21298110	CNVD
Glioblastoma multiforme	22122801	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Prostate cancer	17079440	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13862000-13868800	Weak transcription	NHDF-Ad	bronchial
2	chr7:13862600-13871800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:13863000-13869000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:13867000-13869200	Weak transcription	Osteobl	bone
5	chr7:13867800-13870200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:13868000-13868800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:13868000-13870200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:13868400-13868800	Enhancers	Fetal Stomach	stomach
9	chr7:13868600-13871000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:13868800-13869200	Weak transcription	Fetal Stomach	stomach
11	chr7:13868800-13871000	Enhancers	NHDF-Ad	bronchial
12	chr7:13868800-13871400	Enhancers	Fetal Heart	heart
13	chr7:13868800-13873200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr7:13869000-13870400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:13869000-13870600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:13869200-13870600	Enhancers	Fetal Stomach	stomach
17	chr7:13869200-13870800	Enhancers	Osteobl	bone
18	chr7:13869400-13870200	Enhancers	HSMM	muscle
19	chr7:13869400-13870600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:13869400-13870600	Enhancers	HSMMtube	muscle
21	chr7:13869600-13870400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr7:13869600-13870400	Enhancers	Fetal Muscle Leg	muscle
23	chr7:13869600-13870600	Enhancers	Left Ventricle	heart
24	chr7:13869600-13871000	Enhancers	Fetal Lung	lung
25	chr7:13869800-13870400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:13869800-13870600	Enhancers	NHLF	lung
27	chr7:13869800-13871000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr7:13870000-13870400	Enhancers	Right Ventricle	heart
29	chr7:13870000-13870800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr7:13870200-13870400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:13870200-13870400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:13870200-13871000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr7:13870200-13871800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:13870200-13873800	Weak transcription	HSMM	muscle
35	chr7:13870400-13871800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr7:13870400-13873200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:13870400-13873800	Weak transcription	Fetal Muscle Leg	muscle
38	chr7:13870400-13874000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:13870600-13873600	Weak transcription	HSMMtube	muscle
40	chr7:13870800-13873400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr7:13870800-13873800	Weak transcription	Osteobl	bone
42	chr7:13871000-13871400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr7:13871000-13871800	Weak transcription	NHDF-Ad	bronchial
44	chr7:13871000-13873400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr7:13871000-13873600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr7:13871000-13873600	Weak transcription	Fetal Lung	lung
47	chr7:13871400-13871800	Weak transcription	Fetal Heart	heart
48	chr7:13871400-13872200	Enhancers	Muscle Satellite Cultured Cells	--
49	chr7:13871800-13872000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:13871800-13872000	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links