Variant report

Variant	nsv482826
Chromosome Location	chr7:78548319-78717605
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	chr7:78707803-78707913	HepG2	liver:	n/a	n/a
2	BACH1	chr7:78681414-78681594	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr7:78638128-78638397	GM12878	blood:	n/a	n/a
4	CCNT2	chr7:78609549-78609738	K562	blood:	n/a	n/a
5	CEBPB	chr7:78567264-78567467	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:78660536-78660843	HepG2	liver:	n/a	chr7:78660683-78660694
7	CEBPB	chr7:78675401-78675634	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr7:78589925-78590195	IMR90	lung:	n/a	n/a
9	CEBPB	chr7:78675382-78675700	IMR90	lung:	n/a	n/a
10	CEBPB	chr7:78685304-78685681	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr7:78701651-78701829	HepG2	liver:	n/a	chr7:78701714-78701725 chr7:78701691-78701703
12	CEBPB	chr7:78618177-78618380	HepG2	liver:	n/a	chr7:78618297-78618308 chr7:78618297-78618310
13	CEBPB	chr7:78548257-78548436	HepG2	liver:	n/a	chr7:78548317-78548328
14	CEBPB	chr7:78709067-78709249	HepG2	liver:	n/a	chr7:78709184-78709195 chr7:78709159-78709170 chr7:78709160-78709171
15	CEBPB	chr7:78578296-78578499	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:78675426-78675675	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:78589941-78590090	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:78588733-78589309	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:78584287-78584532	IMR90	lung:	n/a	chr7:78584423-78584434
20	CEBPB	chr7:78660521-78660831	IMR90	lung:	n/a	chr7:78660683-78660694
21	CEBPB	chr7:78548261-78548411	K562	blood:	n/a	chr7:78548317-78548328
22	CEBPB	chr7:78584324-78584524	HepG2	liver:	n/a	chr7:78584423-78584434
23	CEBPB	chr7:78568824-78569487	IMR90	lung:	n/a	chr7:78569427-78569439
24	CEBPB	chr7:78593679-78593926	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:78693550-78693854	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:78584282-78584538	A549	lung:	n/a	chr7:78584423-78584434
27	CHD1	chr7:78553897-78554370	IMR90	lung:	n/a	n/a
28	CTCF	chr7:78692740-78692890	WI-38	lung:	n/a	chr7:78692808-78692817
29	CTCF	chr7:78692720-78692870	HMF	breast:	n/a	chr7:78692808-78692817
30	CTCF	chr7:78654494-78654567	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr7:78554080-78554230	AoAF	blood vessel:	n/a	chr7:78554110-78554128 chr7:78554105-78554126 chr7:78554111-78554127
32	CTCF	chr7:78692662-78692935	IMR90	lung:	n/a	chr7:78692808-78692817
33	CTCF	chr7:78692420-78692570	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr7:78554020-78554183	SK-N-SH_RA	brain:	n/a	chr7:78554110-78554128 chr7:78554105-78554126 chr7:78554111-78554127
35	CTCF	chr7:78692780-78692930	MCF-7	breast:	n/a	chr7:78692808-78692817
36	CTCF	chr7:78692680-78692830	HVMF	connective:	n/a	chr7:78692808-78692817
37	CTCF	chr7:78705460-78705610	GM06990	blood:	n/a	n/a
38	CTCF	chr7:78614949-78615129	K562	blood:	n/a	chr7:78615007-78615023 chr7:78615001-78615022
39	CTCF	chr7:78637940-78638090	AG09309	skin:	n/a	n/a
40	CTCF	chr7:78692680-78692830	HRPEpiC	eye:	n/a	chr7:78692808-78692817
41	CTCF	chr7:78692720-78692870	HPF	lung:	n/a	chr7:78692808-78692817
42	CTCF	chr7:78554060-78554210	AG09309	skin:	n/a	chr7:78554110-78554128 chr7:78554105-78554126 chr7:78554111-78554127
43	CTCF	chr7:78692800-78692950	AG09319	gingival:	n/a	chr7:78692808-78692817
44	CTCF	chr7:78554040-78554190	HCFaa	heart:	n/a	chr7:78554110-78554128 chr7:78554105-78554126 chr7:78554111-78554127
45	CTCF	chr7:78692660-78692810	HEK293	kidney:	n/a	n/a
46	CTCF	chr7:78554020-78554170	AG10803	skin:	n/a	chr7:78554110-78554128 chr7:78554105-78554126 chr7:78554111-78554127
47	CTCF	chr7:78553958-78554306	HCT-116	colon:	n/a	chr7:78554110-78554128 chr7:78554105-78554126 chr7:78554111-78554127
48	CTCF	chr7:78553980-78554130	Caco-2	colon:	n/a	chr7:78554110-78554128 chr7:78554105-78554126 chr7:78554111-78554127
49	CTCF	chr7:78692760-78692910	SK-N-SH_RA	brain:	n/a	chr7:78692808-78692817
50	CTCF	chr7:78554029-78554149	HepG2	liver:	n/a	chr7:78554110-78554128 chr7:78554105-78554126 chr7:78554111-78554127

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:78588037-78588087	HIPEpiC	eye:	n/a
2	chr7:78588037-78588087	HIPEpiC	eye:	n/a
3	chr7:78659337-78659387	MCF-7	breast:	n/a
4	chr7:78588037-78588087	SKMC	muscle:	n/a
5	chr7:78659337-78659387	HCM	heart:	n/a
6	chr7:78588037-78588087	AG09319	gingival:	n/a
7	chr7:78600265-78600315	NH-A	brain:	n/a
8	chr7:78569240-78569290	AG04450	lung:	fetal
9	chr7:78588037-78588087	LNCaP	prostate:	n/a
10	chr7:78659337-78659387	Hepatocyte	liver:	n/a
11	chr7:78588037-78588087	HRPEpiC	eye:	n/a
12	chr7:78569240-78569290	BJ	skin:	n/a
13	chr7:78588037-78588087	AG04450	lung:	fetal
14	chr7:78588037-78588087	ECC-1	luminal epithelium:	n/a
15	chr7:78588037-78588087	GM12878	blood:	n/a
16	chr7:78659337-78659387	A549	lung:	n/a
17	chr7:78588037-78588087	SAEC	small airway:	n/a
18	chr7:78600265-78600315	AG09309	skin:	n/a
19	chr7:78600265-78600315	AG04450	lung:	fetal
20	chr7:78588037-78588087	AG04449	skin:	fetal
21	chr7:78588037-78588087	ovcar-3	ovarian:	n/a
22	chr7:78600265-78600315	GM12891	blood:	n/a
23	chr7:78659337-78659387	LNCaP	prostate:	n/a
24	chr7:78569240-78569290	IMR90	lung:	fetal
25	chr7:78659337-78659387	PANC-1	pancreas:	n/a
26	chr7:78569240-78569290	PFSK-1	brain:	n/a
27	chr7:78600265-78600315	ProgFib	skin:	n/a
28	chr7:78600265-78600315	HCF	heart:	n/a
29	chr7:78659337-78659387	HRPEpiC	eye:	n/a
30	chr7:78600265-78600315	MCF-7	breast:	n/a
31	chr7:78569240-78569290	MCF10A-Er-Src	breast:	n/a
32	chr7:78588037-78588087	GM19239	blood:	n/a
33	chr7:78600265-78600315	AoSMC	blood vessel:	n/a
34	chr7:78588037-78588087	T-47D	breast:	n/a
35	chr7:78659337-78659387	PrEC	prostate:	n/a
36	chr7:78659337-78659387	HEEpiC	esophagus:	n/a
37	chr7:78600265-78600315	BE2_C	brain:	n/a
38	chr7:78600265-78600315	RPTEC	kidney:	n/a
39	chr7:78569240-78569290	LNCaP	prostate:	n/a
40	chr7:78659337-78659387	NHBE	bronchial:	n/a
41	chr7:78588037-78588087	HNPCEpiC	eye:	n/a
42	chr7:78600265-78600315	HAEpiC	amniotic membrane:	n/a
43	chr7:78588037-78588087	Caco-2	colon:	n/a
44	chr7:78659337-78659387	MCF10A-Er-Src	breast:	n/a
45	chr7:78600265-78600315	NT2-D1	testis:	n/a
46	chr7:78588037-78588087	K562	blood:	n/a
47	chr7:78600265-78600315	T-47D	breast:	n/a
48	chr7:78588037-78588087	NHDF-neo	bronchial:	n/a
49	chr7:78659337-78659387	CMK	blood:	n/a
50	chr7:78569240-78569290	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:78563822..78566270-chr7:78567927..78570810,2	K562	blood:
2	chr7:78216506..78217329-chr7:78553705..78554263,2	MCF-7	breast:
3	chr7:78557178..78560112-chr7:78561287..78563221,2	K562	blood:
4	chr7:78216823..78217508-chr7:78553648..78554465,2	MCF-7	breast:
5	chr7:78596854..78599110-chr7:78602576..78605115,2	K562	blood:
6	chr7:78680321..78683272-chr7:78686502..78688648,2	MCF-7	breast:
7	chr7:78680321..78683272-chr7:78686502..78688648,2	MCF-7	breast:
8	chr7:78557178..78560112-chr7:78561287..78563221,2	K562	blood:
9	chr7:78654781..78656773-chr7:78658469..78660779,2	K562	blood:
10	chr7:78656805..78659401-chr7:78662080..78664588,2	K562	blood:
11	chr7:78656805..78659401-chr7:78662080..78664588,2	K562	blood:
12	chr3:197128255..197129082-chr7:78592863..78593810,2	MCF-7	breast:
13	chr7:78677390..78680466-chr7:78680728..78684116,3	K562	blood:
14	chr7:78596854..78599110-chr7:78602576..78605115,2	K562	blood:
15	chr7:78677390..78680466-chr7:78680728..78684116,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHTF2-3	chr7:78640243-78640387	ENSG00000226978.1
2	lnc-PHTF2-2	chr7:78569166-78569200	ENSG00000251276.1
3	lnc-PHTF2-2	chr7:78569775-78570211	ENSG00000251276.1
4	lnc-PHTF2-3	chr7:78638304-78638440	ENSG00000226978.1
5	lnc-PHTF2-3	chr7:78641400-78641593	ENSG00000226978.1
6	lnc-TMEM60-2	chr7:78629521-78629614	ENSG00000235751.3

Variant related genes	Relation type
MAGI2-AS1	TF binding region
RNU6-337P	TF binding region
MAGI2-IT1	TF binding region
MAGI2-AS2	TF binding region
MAGI2-AS1	CpG island
RNU6-337P	CpG island
MAGI2-IT1	CpG island
MAGI2-AS2	CpG island
ENSG00000212545	chromatin interactions
ENSG00000251276	chromatin interactions

Extended variants
information (count: 3612 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3612 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567337672	chr7:78560638-78560639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554137650	chr7:78560683-78560684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556446870	chr7:78560687-78560688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576424327	chr7:78560727-78560728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544986458	chr7:78560744-78560745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567511426	chr7:78560801-78560802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141324191	chr7:78560803-78560804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572033776	chr7:78560819-78560820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540764349	chr7:78560871-78560872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs60040960	chr7:78560905-78560906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561049654	chr7:78560910-78560911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530187005	chr7:78560937-78560938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536966529	chr7:78560946-78560947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556551323	chr7:78560988-78560989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563605483	chr7:78561068-78561069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186177294	chr7:78561075-78561076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373452584	chr7:78561080-78561081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11772807	chr7:78561085-78561086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552865091	chr7:78561114-78561115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs55975127	chr7:78561126-78561127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561412364	chr7:78561129-78561130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138564009	chr7:78561132-78561133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528528976	chr7:78561163-78561164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545187629	chr7:78561174-78561175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189891020	chr7:78561180-78561181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568541832	chr7:78561223-78561224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs57247343	chr7:78561228-78561229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536420774	chr7:78561271-78561272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558279117	chr7:78561276-78561277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62467730	chr7:78561282-78561283	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs114992927	chr7:78561314-78561315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72358342	chr7:78561315-78561316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74480048	chr7:78561316-78561317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62467731	chr7:78561334-78561335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569899484	chr7:78561341-78561342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534171206	chr7:78561372-78561373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376553773	chr7:78561373-78561374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377643383	chr7:78561378-78561379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558857697	chr7:78561441-78561442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549046269	chr7:78561465-78561466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200772592	chr7:78561470-78561471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117720002	chr7:78561491-78561492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71555011	chr7:78561554-78561555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1642886	chr7:78561616-78561617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6952707	chr7:78561619-78561620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs574210439	chr7:78561625-78561626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181527908	chr7:78561640-78561641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs117696165	chr7:78561652-78561653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10237976	chr7:78561659-78561660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs2193712	chr7:78561663-78561664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Williams-beuren syndrome	16826523	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78560600-78560800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:78560800-78561000	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr7:78561000-78569000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:78569000-78569800	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr7:78569000-78570600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:78569800-78572000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr7:78572000-78572200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:78578000-78578800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:78582200-78584000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:78582200-78584000	Enhancers	NHDF-Ad	bronchial
11	chr7:78582400-78583200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:78582600-78583200	Enhancers	NHLF	lung
13	chr7:78582600-78584000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:78582800-78583200	Enhancers	Osteobl	bone
15	chr7:78583000-78583400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:78583200-78588200	Weak transcription	Osteobl	bone
17	chr7:78584000-78588200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr7:78588200-78588400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:78588200-78589200	Enhancers	Osteobl	bone
20	chr7:78588400-78588800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:78588800-78589600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:78588800-78589600	Enhancers	NHDF-Ad	bronchial
23	chr7:78596200-78596600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:78596400-78596800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr7:78596600-78599200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:78596800-78599400	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr7:78597200-78597400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr7:78597600-78599200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:78598000-78598400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr7:78598000-78598600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr7:78598200-78598600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:78598200-78598800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr7:78598200-78598800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:78598400-78598800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr7:78598600-78600000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr7:78598600-78603000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr7:78598800-78599000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr7:78598800-78599800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr7:78599000-78600200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr7:78599200-78599400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:78599200-78600600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:78599200-78600800	Enhancers	NHDF-Ad	bronchial
43	chr7:78599400-78599800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:78599400-78600400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr7:78599400-78600800	Enhancers	Osteobl	bone
46	chr7:78599800-78600200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:78599800-78600400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr7:78599800-78601200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr7:78600000-78600400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:78600000-78600400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links