Variant report

Variant	nsv830910
Chromosome Location	chr7:15011028-15212309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:969)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:969 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:15055726-15056046	HepG2	liver:	n/a	n/a
2	BACH1	chr7:15051037-15051612	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:15136729-15136926	K562	blood:	n/a	n/a
4	BACH1	chr7:15052301-15052317	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:15035586-15035785	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:15055872-15056060	K562	blood:	n/a	n/a
7	BHLHE40	chr7:15055727-15055963	GM12878	blood:	n/a	n/a
8	CEBPB	chr7:15170197-15170614	Hela-S3	cervix:	n/a	chr7:15170345-15170358
9	CEBPB	chr7:15056178-15057050	HCT-116	colon:	n/a	chr7:15056927-15056938
10	CEBPB	chr7:15170275-15170771	IMR90	lung:	n/a	chr7:15170345-15170358
11	CEBPB	chr7:15107141-15107395	HepG2	liver:	n/a	chr7:15107268-15107279
12	CEBPB	chr7:15107146-15107394	A549	lung:	n/a	chr7:15107268-15107279
13	CEBPB	chr7:15170279-15170520	A549	lung:	n/a	chr7:15170345-15170358
14	CEBPB	chr7:15170168-15170617	A549	lung:	n/a	chr7:15170345-15170358 chr7:15170176-15170187
15	CEBPB	chr7:15107126-15107433	IMR90	lung:	n/a	chr7:15107268-15107279
16	CEBPB	chr7:15077096-15077349	HepG2	liver:	n/a	chr7:15077196-15077207
17	CEBPB	chr7:15126038-15126244	HepG2	liver:	n/a	chr7:15126178-15126189
18	CEBPB	chr7:15080351-15081311	Hela-S3	cervix:	n/a	chr7:15081129-15081142
19	CEBPB	chr7:15107136-15107410	Hela-S3	cervix:	n/a	chr7:15107268-15107279
20	CEBPB	chr7:15185415-15185701	HepG2	liver:	n/a	chr7:15185503-15185515
21	CEBPB	chr7:15126040-15126347	Hela-S3	cervix:	n/a	chr7:15126178-15126189
22	CEBPB	chr7:15040679-15040860	HepG2	liver:	n/a	chr7:15040775-15040786 chr7:15040775-15040788
23	CEBPB	chr7:15126055-15126326	IMR90	lung:	n/a	chr7:15126178-15126189
24	CTCF	chr7:15055820-15055970	HMF	breast:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
25	CTCF	chr7:15046920-15047070	HMF	breast:	n/a	n/a
26	CTCF	chr7:15055097-15056226	SK-N-SH	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
27	CTCF	chr7:15055821-15055958	Lung_OC	lung:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
28	CTCF	chr7:15055780-15055930	BE2_C	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
29	CTCF	chr7:15056740-15056890	AG10803	skin:	n/a	n/a
30	CTCF	chr7:15047320-15047470	GM12870	blood:	n/a	n/a
31	CTCF	chr7:15047220-15047370	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr7:15047305-15047314	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:15047196-15047421	NHEK	skin:	n/a	n/a
34	CTCF	chr7:15047220-15047370	HRE	kidney:	n/a	n/a
35	CTCF	chr7:15047233-15047375	GM19239	blood:	n/a	n/a
36	CTCF	chr7:15055540-15055690	GM12865	blood:	n/a	n/a
37	CTCF	chr7:15055737-15056033	T-47D	breast:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
38	CTCF	chr7:15055820-15055970	HPAF	blood vessel:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
39	CTCF	chr7:15047240-15047390	HPF	lung:	n/a	n/a
40	CTCF	chr7:15208286-15208448	LNCaP	prostate:	n/a	chr7:15208354-15208362
41	CTCF	chr7:15047260-15047410	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr7:15208260-15208410	HCFaa	heart:	n/a	chr7:15208354-15208362
43	CTCF	chr7:15055840-15055990	AG09319	gingival:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
44	CTCF	chr7:15055680-15055950	NHDF-neo	bronchial:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
45	CTCF	chr7:15047240-15047390	GM12872	blood:	n/a	n/a
46	CTCF	chr7:15208300-15208450	BJ	skin:	n/a	chr7:15208354-15208362
47	CTCF	chr7:15028940-15029090	BE2_C	brain:	n/a	n/a
48	CTCF	chr7:15055900-15056050	WI-38	lung:	n/a	n/a
49	CTCF	chr7:15208321-15208408	Kidney_OC	kidney:	n/a	chr7:15208354-15208362
50	CTCF	chr7:15208260-15208410	RPTEC	kidney:	n/a	chr7:15208354-15208362

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15055459-15055509	Hepatocyte	liver:	n/a
2	chr7:15055459-15055509	HCF	heart:	n/a
3	chr7:15055459-15055509	MCF-7	breast:	n/a
4	chr7:15055459-15055509	GM06990	blood:	n/a
5	chr7:15055459-15055509	GM12878	blood:	n/a
6	chr7:15055459-15055509	IMR90	lung:	fetal
7	chr7:15055459-15055509	HRPEpiC	eye:	n/a
8	chr7:15055459-15055509	NHDF-neo	bronchial:	n/a
9	chr7:15055459-15055509	T-47D	breast:	n/a
10	chr7:15055459-15055509	HUVEC	blood vessel:	n/a
11	chr7:15055459-15055509	ovcar-3	ovarian:	n/a
12	chr7:15055459-15055509	NHBE	bronchial:	n/a
13	chr7:15055459-15055509	Jurkat	blood:	n/a
14	chr7:15055459-15055509	NB4	blood:	n/a
15	chr7:15055459-15055509	SAEC	small airway:	n/a
16	chr7:15055459-15055509	BJ	skin:	n/a
17	chr7:15055459-15055509	PFSK-1	brain:	n/a
18	chr7:15055459-15055509	SK-N-SH_RA	brain:	n/a
19	chr7:15055459-15055509	LNCaP	prostate:	n/a
20	chr7:15055459-15055509	A549	lung:	n/a
21	chr7:15055459-15055509	AG09319	gingival:	n/a
22	chr7:15055459-15055509	PrEC	prostate:	n/a
23	chr7:15055459-15055509	SK-N-MC	brain:	n/a
24	chr7:15055459-15055509	AG04449	skin:	fetal
25	chr7:15055459-15055509	HCM	heart:	n/a
26	chr7:15055459-15055509	HMEC	breast:	n/a
27	chr7:15055459-15055509	RPTEC	kidney:	n/a
28	chr7:15055459-15055509	PANC-1	pancreas:	n/a
29	chr7:15055459-15055509	AG10803	skin:	n/a
30	chr7:15055459-15055509	ECC-1	luminal epithelium:	n/a
31	chr7:15055459-15055509	HNPCEpiC	eye:	n/a
32	chr7:15055459-15055509	MCF10A-Er-Src	breast:	n/a
33	chr7:15055459-15055509	SK-N-SH	brain:	n/a
34	chr7:15055459-15055509	HCT-116	colon:	n/a
35	chr7:15055459-15055509	GM19239	blood:	n/a
36	chr7:15055459-15055509	HAEpiC	amniotic membrane:	n/a
37	chr7:15055459-15055509	HIPEpiC	eye:	n/a
38	chr7:15055459-15055509	HCPEpiC	choroid plexus:	n/a
39	chr7:15055459-15055509	Caco-2	colon:	n/a
40	chr7:15055459-15055509	CMK	blood:	n/a
41	chr7:15055459-15055509	AoSMC	blood vessel:	n/a
42	chr7:15055459-15055509	HRCEpiC	kidney:	n/a
43	chr7:15055459-15055509	U87	brain:	n/a
44	chr7:15055459-15055509	GM12891	blood:	n/a
45	chr7:15055459-15055509	SKMC	muscle:	n/a
46	chr7:15055459-15055509	ProgFib	skin:	n/a
47	chr7:15055459-15055509	NT2-D1	testis:	n/a
48	chr7:15055459-15055509	H1-hESC	embryonic stem cell:	embryo
49	chr7:15055459-15055509	K562	blood:	n/a
50	chr7:15055459-15055509	BE2_C	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:15002300..15004911-chr7:15009747..15012507,2	MCF-7	breast:
2	chr7:15181881..15184605-chr7:15186174..15189124,2	K562	blood:
3	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
4	chr7:14756304..14757028-chr7:15055834..15056611,2	MCF-7	breast:
5	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
6	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:
7	chr7:14737644..14738448-chr7:15055761..15056392,2	MCF-7	breast:
8	chr7:14995312..14997683-chr7:15009030..15011950,2	K562	blood:
9	chr7:14757467..14758291-chr7:15055705..15056411,2	MCF-7	breast:
10	chr7:15003480..15005257-chr7:15044429..15047091,2	K562	blood:
11	chr7:15148394..15150106-chr7:15160727..15163235,2	K562	blood:
12	chr7:14757081..14758001-chr7:15054605..15056087,5	MCF-7	breast:
13	chr7:13317591..13319993-chr7:15056107..15057980,2	K562	blood:
14	chr7:15033798..15035958-chr7:15043965..15046706,2	K562	blood:
15	chr6:10529800..10530510-chr7:15146578..15147089,2	MCF-7	breast:
16	chr7:15181881..15184605-chr7:15186174..15189124,2	K562	blood:
17	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:
18	chr7:15033798..15035958-chr7:15043965..15046706,2	K562	blood:
19	chr7:15148394..15150106-chr7:15160727..15163235,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-4	chr7:15105832-15106137	XLOC_005990
2	lnc-AC006035.2-8	chr7:15193488-15193542	NONHSAT119275
3	lnc-AC006035.2-4	chr7:15107930-15108276	XLOC_005990
4	lnc-AC006035.2-8	chr7:15192805-15192944	NONHSAT119275
5	lnc-AC006035.2-8	chr7:15191535-15191712	NONHSAT119275
6	lnc-AC006035.2-9	chr7:15074455-15074801	NONHSAT119273
7	lnc-DGKB-1	chr7:15025003-15025699	NONHSAT119271
8	lnc-AC006035.2-9	chr7:15072357-15072662	NONHSAT119273

No data

Variant related genes	Relation type
DGKB	TF binding region
ENSG00000225816	TF binding region
ENSG00000227489	TF binding region
DGKB	CpG island
ENSG00000225816	CpG island
ENSG00000227489	CpG island
ENSG00000111846	chromatin interactions

Extended variants
information (count: 5570 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:5570 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10236031	chr7:15011043-15011044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189670331	chr7:15011048-15011049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545713491	chr7:15011069-15011070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565519839	chr7:15011072-15011073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531119366	chr7:15011074-15011075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550824234	chr7:15011152-15011153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558894339	chr7:15011170-15011171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572392351	chr7:15011172-15011173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs151252078	chr7:15011197-15011198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34245953	chr7:15011230-15011231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576042590	chr7:15011270-15011271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535325238	chr7:15011273-15011274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538597608	chr7:15011303-15011304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552035216	chr7:15011306-15011307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115654344	chr7:15011317-15011318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528591490	chr7:15011319-15011320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs17168565	chr7:15011374-15011375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35652785	chr7:15011387-15011388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs386409570	chr7:15011388-15011389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74951904	chr7:15011403-15011404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71004349	chr7:15011404-15011405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76525191	chr7:15011428-15011429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554381787	chr7:15011430-15011431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555444041	chr7:15011476-15011477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574432037	chr7:15011479-15011480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533772250	chr7:15011502-15011503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10268757	chr7:15011508-15011509	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576897746	chr7:15011518-15011519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545750578	chr7:15011530-15011531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543576984	chr7:15011531-15011532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140585100	chr7:15011544-15011545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544758680	chr7:15011552-15011553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182224467	chr7:15011581-15011582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4997211	chr7:15011673-15011674	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560331028	chr7:15011723-15011724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377261130	chr7:15011768-15011769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560157931	chr7:15011780-15011781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532347427	chr7:15011816-15011817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2214617	chr7:15011835-15011836	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs569097079	chr7:15011862-15011863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537652558	chr7:15011916-15011917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145717670	chr7:15011921-15011922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568158280	chr7:15011927-15011928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73290614	chr7:15011934-15011935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534222952	chr7:15011986-15011987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2097846	chr7:15011988-15011989	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs570489767	chr7:15012003-15012004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368126095	chr7:15012066-15012067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539412735	chr7:15012082-15012083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562435252	chr7:15012151-15012152	Weak transcription	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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15010800-15011600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr7:15010800-15013600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr7:15011000-15011400	Enhancers	HUVEC	blood vessel
4	chr7:15011400-15017600	Weak transcription	HUVEC	blood vessel
5	chr7:15011600-15011800	Enhancers	Adipose Nuclei	Adipose
6	chr7:15011600-15013600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:15013600-15014000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:15013600-15014000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr7:15013600-15014000	Enhancers	Liver	Liver
10	chr7:15013600-15014200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:15016400-15017200	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr7:15017600-15019800	Enhancers	HUVEC	blood vessel
13	chr7:15039000-15040600	Enhancers	Liver	Liver
14	chr7:15039600-15040000	Enhancers	HepG2	liver
15	chr7:15047000-15048200	Enhancers	Liver	Liver
16	chr7:15047400-15047600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:15047600-15055000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:15049400-15049600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:15049600-15055000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:15050600-15051000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:15050600-15051600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:15050800-15051200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:15050800-15051200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr7:15050800-15051800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr7:15050800-15052000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr7:15051000-15051400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr7:15051000-15051800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:15051200-15051600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:15051200-15051600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr7:15051200-15052800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:15051200-15054800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr7:15051400-15051600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:15051600-15052200	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr7:15051600-15052200	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr7:15051600-15054400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr7:15051600-15054800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr7:15051600-15054800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr7:15051600-15055000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr7:15051800-15052200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:15051800-15055000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr7:15051800-15055000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:15052000-15052200	Enhancers	Right Ventricle	heart
43	chr7:15052000-15055000	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr7:15052200-15052400	Enhancers	Left Ventricle	heart
45	chr7:15052200-15054200	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr7:15052200-15055000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr7:15052200-15055200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:15052200-15055200	Weak transcription	Right Ventricle	heart
49	chr7:15052800-15055000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:15054000-15054200	Enhancers	Psoas Muscle	Psoas

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