Variant report

Variant	nsv5821
Chromosome Location	chr7:84159713-84204468
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	ATF3	chr7:84165356-84165961	A549	lung:	n/a	n/a
2	ATF3	chr7:84165333-84165902	A549	lung:	n/a	n/a
3	BCL11A	chr7:84177692-84177958	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr7:84165165-84166072	A549	lung:	n/a	n/a
5	BCL3	chr7:84165334-84165953	A549	lung:	n/a	n/a
6	CEBPB	chr7:84159932-84160096	K562	blood:	n/a	chr7:84159971-84159984
7	CEBPB	chr7:84178114-84178352	K562	blood:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
8	CEBPB	chr7:84159810-84160131	IMR90	lung:	n/a	chr7:84159971-84159984
9	CEBPB	chr7:84178757-84179118	ECC-1	luminal epithelium:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
10	CEBPB	chr7:84178770-84179209	A549	lung:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
11	CEBPB	chr7:84178751-84179115	K562	blood:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
12	CEBPB	chr7:84178758-84179104	HepG2	liver:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
13	CEBPB	chr7:84178769-84179117	A549	lung:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
14	CEBPB	chr7:84178069-84178389	IMR90	lung:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
15	CEBPB	chr7:84159787-84160156	Hela-S3	cervix:	n/a	chr7:84159971-84159984
16	CEBPB	chr7:84177668-84178447	ECC-1	luminal epithelium:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
17	CEBPB	chr7:84178130-84178390	HepG2	liver:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
18	CEBPB	chr7:84159800-84160116	A549	lung:	n/a	chr7:84159971-84159984
19	CEBPB	chr7:84178071-84178396	Hela-S3	cervix:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
20	CEBPB	chr7:84178760-84179074	H1-hESC	embryonic stem cell:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
21	CEBPB	chr7:84177667-84178429	ECC-1	luminal epithelium:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
22	CEBPB	chr7:84161478-84161912	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:84178732-84179117	ECC-1	luminal epithelium:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
24	CEBPB	chr7:84178753-84179115	Hela-S3	cervix:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
25	CEBPB	chr7:84165419-84166142	A549	lung:	n/a	n/a
26	CEBPB	chr7:84178742-84179124	IMR90	lung:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
27	CEBPB	chr7:84178056-84178365	A549	lung:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
28	CEBPB	chr7:84165297-84166222	MCF-7	breast:	n/a	n/a
29	CEBPB	chr7:84165421-84166199	A549	lung:	n/a	n/a
30	CEBPB	chr7:84165263-84166264	A549	lung:	n/a	n/a
31	CEBPB	chr7:84178229-84178319	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr7:84161541-84161800	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr7:84177738-84177801	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:84171140-84171290	BE2_C	brain:	n/a	n/a
35	CTCF	chr7:84171160-84171310	GM12872	blood:	n/a	n/a
36	CTCF	chr7:84171160-84171310	GM06990	blood:	n/a	n/a
37	CTCF	chr7:84171180-84171330	GM12878	blood:	n/a	n/a
38	CTCF	chr7:84171180-84171330	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr7:84171200-84171350	HCT-116	colon:	n/a	n/a
40	CTCF	chr7:84171120-84171270	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr7:84171120-84171270	AG04450	lung:	n/a	n/a
42	CTCF	chr7:84178380-84178530	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr7:84171180-84171330	HRE	kidney:	n/a	n/a
44	CTCF	chr7:84171100-84171250	GM12865	blood:	n/a	n/a
45	CTCF	chr7:84164950-84165002	Fibrobl	skin:	n/a	n/a
46	CTCF	chr7:84171140-84171290	GM12869	blood:	n/a	n/a
47	CTCF	chr7:84171100-84171250	A549	lung:	n/a	n/a
48	CTCF	chr7:84178400-84178550	AG04450	lung:	n/a	n/a
49	CTCF	chr7:84171120-84171270	HAc	cerebellar:	n/a	n/a
50	CTCF	chr7:84170960-84171110	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84161420-84161470	PrEC	prostate:	n/a
2	chr7:84161222-84161272	AoSMC	blood vessel:	n/a
3	chr7:84177905-84177955	AG09319	gingival:	n/a
4	chr7:84177905-84177955	A549	lung:	n/a
5	chr7:84161222-84161272	HIPEpiC	eye:	n/a
6	chr7:84161420-84161470	HIPEpiC	eye:	n/a
7	chr7:84161222-84161272	HEEpiC	esophagus:	n/a
8	chr7:84161222-84161272	AG09319	gingival:	n/a
9	chr7:84177905-84177955	HNPCEpiC	eye:	n/a
10	chr7:84177905-84177955	SKMC	muscle:	n/a
11	chr7:84161420-84161470	HCM	heart:	n/a
12	chr7:84161420-84161470	HRE	kidney:	n/a
13	chr7:84161222-84161272	Caco-2	colon:	n/a
14	chr7:84161222-84161272	ovcar-3	ovarian:	n/a
15	chr7:84161222-84161272	AG04449	skin:	fetal
16	chr7:84161222-84161272	HCPEpiC	choroid plexus:	n/a
17	chr7:84161420-84161470	HUVEC	blood vessel:	n/a
18	chr7:84161222-84161272	PrEC	prostate:	n/a
19	chr7:84177905-84177955	HL-60	blood:	n/a
20	chr7:84161222-84161272	NT2-D1	testis:	n/a
21	chr7:84177905-84177955	MCF10A-Er-Src	breast:	n/a
22	chr7:84161420-84161470	MCF-7	breast:	n/a
23	chr7:84161222-84161272	HCF	heart:	n/a
24	chr7:84161420-84161470	HRPEpiC	eye:	n/a
25	chr7:84177905-84177955	AG09309	skin:	n/a
26	chr7:84161420-84161470	AG09309	skin:	n/a
27	chr7:84161222-84161272	SK-N-SH_RA	brain:	n/a
28	chr7:84161222-84161272	NH-A	brain:	n/a
29	chr7:84177905-84177955	HEEpiC	esophagus:	n/a
30	chr7:84161420-84161470	CMK	blood:	n/a
31	chr7:84161420-84161470	HEEpiC	esophagus:	n/a
32	chr7:84177905-84177955	HRCEpiC	kidney:	n/a
33	chr7:84161222-84161272	U87	brain:	n/a
34	chr7:84161420-84161470	SK-N-SH_RA	brain:	n/a
35	chr7:84161222-84161272	HMEC	breast:	n/a
36	chr7:84161420-84161470	GM12891	blood:	n/a
37	chr7:84177905-84177955	HepG2	liver:	n/a
38	chr7:84161222-84161272	HNPCEpiC	eye:	n/a
39	chr7:84177905-84177955	PFSK-1	brain:	n/a
40	chr7:84161222-84161272	HCM	heart:	n/a
41	chr7:84161222-84161272	HEK293	kidney:	embryo
42	chr7:84161420-84161470	NB4	blood:	n/a
43	chr7:84161420-84161470	AG04449	skin:	fetal
44	chr7:84177905-84177955	RPTEC	kidney:	n/a
45	chr7:84161420-84161470	AG09319	gingival:	n/a
46	chr7:84161420-84161470	BJ	skin:	n/a
47	chr7:84161420-84161470	Hela-S3	cervix:	n/a
48	chr7:84177905-84177955	GM06990	blood:	n/a
49	chr7:84161420-84161470	SAEC	small airway:	n/a
50	chr7:84161222-84161272	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:84165149..84166023-chr7:84582151..84583096,5	MCF-7	breast:
2	chr7:84165204..84166004-chr7:84499385..84500020,2	MCF-7	breast:
3	chr7:83904428..83905120-chr7:84165177..84165677,2	MCF-7	breast:
4	chr7:84165149..84165684-chr7:84582450..84583007,2	MCF-7	breast:
5	chr7:84165144..84166088-chr7:84499191..84500054,5	MCF-7	breast:
6	chr1:149857245..149858849-chr7:84173495..84175226,2	MCF-7	breast:
7	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
8	chr7:84172414..84174090-chr7:84421942..84424878,2	K562	blood:
9	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
10	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
11	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
12	chr7:84165588..84166207-chr7:84499370..84499987,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-2	chr7:84200295-84200423	XLOC_006159
2	lnc-GRM3-2	chr7:84178521-84178569	NONHSAT121790
3	lnc-GRM3-2	chr7:84178463-84178569	NR_110080
4	lnc-GRM3-2	chr7:84161792-84161923	NR_110080
5	lnc-GRM3-2	chr7:84178463-84178569	XLOC_006159
6	lnc-GRM3-2	chr7:84200295-84200423	NR_110080
7	lnc-GRM3-2	chr7:84178522-84178569	XLOC_006159
8	lnc-GRM3-2	chr7:84200294-84200423	NONHSAT121790
9	lnc-GRM3-2	chr7:84200295-84204159	XLOC_006159
10	lnc-GRM3-2	chr7:84161792-84161923	XLOC_006159

Variant related genes	Relation type
ENSG00000235139	TF binding region
RPL7P30	TF binding region
ENSG00000235139	CpG island
RPL7P30	CpG island
ENSG00000184260	chromatin interactions
ENSG00000184678	chromatin interactions
ARFIP1	miRNA target sites
ARFGEF1	miRNA target sites

Extended variants
information (count: 1175 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555801375	chr7:84159717-84159718	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs541013264	chr7:84159734-84159735	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs530638368	chr7:84159755-84159756	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs3047979	chr7:84159768-84159769	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs377402046	chr7:84159769-84159770	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs370751229	chr7:84159770-84159771	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs59598117	chr7:84159796-84159797	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs56093223	chr7:84159799-84159800	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs4434564	chr7:84159887-84159888	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs541596817	chr7:84159907-84159908	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs115052731	chr7:84159945-84159946	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs572231875	chr7:84159950-84159951	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs185525539	chr7:84159954-84159955	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs189409324	chr7:84160025-84160026	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs181416910	chr7:84160048-84160049	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs543942431	chr7:84160078-84160079	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs543384452	chr7:84160170-84160171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114668586	chr7:84160227-84160228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs151319786	chr7:84160228-84160229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547974038	chr7:84160265-84160266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566407679	chr7:84160284-84160285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139427030	chr7:84160302-84160303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552192857	chr7:84160377-84160378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570365717	chr7:84160456-84160457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144196412	chr7:84160505-84160506	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs371401003	chr7:84160588-84160589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567782778	chr7:84160591-84160592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185996998	chr7:84160607-84160608	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs140387561	chr7:84160609-84160610	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs190015975	chr7:84160660-84160661	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs572351657	chr7:84160663-84160664	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs545769922	chr7:84160706-84160707	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs13247631	chr7:84160718-84160719	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs576360669	chr7:84160791-84160792	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs529071066	chr7:84160800-84160801	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs376856805	chr7:84160951-84160952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561345168	chr7:84160969-84160970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35279156	chr7:84161012-84161013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370587224	chr7:84161030-84161031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201863545	chr7:84161089-84161090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543809125	chr7:84161096-84161097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542845671	chr7:84161130-84161131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562177176	chr7:84161133-84161134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs59724256	chr7:84161145-84161146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs397940330	chr7:84161151-84161152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566462803	chr7:84161196-84161197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528824702	chr7:84161209-84161210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181587231	chr7:84161296-84161297	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs61105784	chr7:84161323-84161324	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs548923232	chr7:84161361-84161362	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Neurodevelopmental disorder	22521361	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
Williams-beuren syndrome	16826523	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
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84157400-84160800	Enhancers	Hela-S3	cervix
2	chr7:84157600-84162400	Enhancers	Fetal Intestine Small	intestine
3	chr7:84158000-84160000	Enhancers	NHEK	skin
4	chr7:84158000-84160800	Enhancers	NHDF-Ad	bronchial
5	chr7:84158200-84161000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:84158400-84160000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:84158400-84162600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:84158600-84160000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr7:84158600-84160600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr7:84158600-84161200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:84159200-84160200	Enhancers	Rectal Smooth Muscle	rectum
12	chr7:84159200-84161000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:84159200-84161000	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr7:84159400-84161200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr7:84159400-84161400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr7:84159400-84161400	Enhancers	A549	lung
17	chr7:84159400-84165000	Weak transcription	Colon Smooth Muscle	Colon
18	chr7:84159600-84161400	Weak transcription	Fetal Intestine Large	intestine
19	chr7:84160000-84161200	Weak transcription	NHEK	skin
20	chr7:84160000-84165400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:84160200-84160600	Weak transcription	Rectal Smooth Muscle	rectum
22	chr7:84160600-84160800	Enhancers	Rectal Smooth Muscle	rectum
23	chr7:84160600-84162200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr7:84160800-84161200	Weak transcription	NHDF-Ad	bronchial
25	chr7:84160800-84165200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr7:84160800-84165200	Weak transcription	Hela-S3	cervix
27	chr7:84161000-84162800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr7:84161000-84163000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr7:84161000-84163200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:84161200-84161800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr7:84161200-84161800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr7:84161200-84162000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr7:84161200-84162000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr7:84161200-84162200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr7:84161200-84162800	Enhancers	NHDF-Ad	bronchial
36	chr7:84161400-84161600	Enhancers	NHEK	skin
37	chr7:84161400-84161800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:84161400-84161800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr7:84161400-84161800	Enhancers	Fetal Intestine Large	intestine
40	chr7:84161400-84162200	Flanking Active TSS	A549	lung
41	chr7:84161800-84163000	Active TSS	Fetal Kidney	kidney
42	chr7:84161800-84164800	Weak transcription	Fetal Intestine Large	intestine
43	chr7:84161800-84165400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr7:84161800-84165400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr7:84162000-84164800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr7:84162000-84164800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:84162200-84162400	Enhancers	A549	lung
48	chr7:84162200-84162800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:84162400-84164200	Weak transcription	A549	lung
50	chr7:84162400-84164600	Weak transcription	Fetal Intestine Small	intestine

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