Variant report

Variant	nsv1028221
Chromosome Location	chr7:121818974-121899162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:121859375-121859662	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:121857139-121857576	HepG2	liver:	n/a	n/a
3	BRCA1	chr7:121878353-121878599	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr7:121865049-121865361	IMR90	lung:	n/a	n/a
5	CEBPB	chr7:121857184-121857556	HepG2	liver:	n/a	chr7:121857346-121857357
6	CEBPB	chr7:121897595-121897817	HepG2	liver:	n/a	chr7:121897726-121897737
7	CEBPB	chr7:121857154-121857575	HepG2	liver:	n/a	chr7:121857346-121857357
8	CEBPB	chr7:121857242-121857575	MCF-7	breast:	n/a	chr7:121857346-121857357
9	CEBPB	chr7:121865062-121865220	A549	lung:	n/a	n/a
10	CEBPB	chr7:121878401-121879106	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:121837334-121837410	A549	lung:	n/a	chr7:121837363-121837374
12	CEBPB	chr7:121865021-121865376	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:121896413-121896572	K562	blood:	n/a	n/a
14	CEBPB	chr7:121835135-121835314	HepG2	liver:	n/a	chr7:121835232-121835241
15	CEBPB	chr7:121857173-121857477	HepG2	liver:	n/a	chr7:121857346-121857357
16	CEBPB	chr7:121865125-121865328	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:121837207-121837469	HepG2	liver:	n/a	chr7:121837363-121837374
18	CEBPB	chr7:121838832-121839712	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr7:121857247-121857462	HepG2	liver:	n/a	chr7:121857346-121857357
20	CEBPB	chr7:121865066-121865289	K562	blood:	n/a	n/a
21	CEBPB	chr7:121857128-121857582	MCF-7	breast:	n/a	chr7:121857346-121857357
22	CEBPB	chr7:121857212-121857507	A549	lung:	n/a	chr7:121857346-121857357
23	CEBPB	chr7:121857162-121857556	Hela-S3	cervix:	n/a	chr7:121857346-121857357
24	CHD2	chr7:121878882-121879118	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr7:121859420-121859570	WI-38	lung:	n/a	chr7:121859504-121859525
26	CTCF	chr7:121859340-121859490	HMEC	breast:	n/a	n/a
27	CTCF	chr7:121859380-121859530	Hela-S3	cervix:	n/a	chr7:121859504-121859525
28	CTCF	chr7:121859400-121859550	HEK293	kidney:	n/a	chr7:121859504-121859525
29	CTCF	chr7:121859420-121859570	GM12875	blood:	n/a	chr7:121859504-121859525
30	CTCF	chr7:121859460-121859610	AG10803	skin:	n/a	chr7:121859504-121859525
31	CTCF	chr7:121859420-121859570	GM12865	blood:	n/a	chr7:121859504-121859525
32	CTCF	chr7:121859416-121859571	GM13976	blood:	n/a	chr7:121859504-121859525
33	CTCF	chr7:121859360-121859510	NHLF	lung:	n/a	n/a
34	CTCF	chr7:121859370-121859666	HUVEC	blood vessel:	n/a	chr7:121859504-121859525
35	CTCF	chr7:121859379-121859626	HepG2	liver:	n/a	chr7:121859504-121859525
36	CTCF	chr7:121859440-121859590	AG09309	skin:	n/a	chr7:121859504-121859525
37	CTCF	chr7:121859405-121859656	GM13977	blood:	n/a	chr7:121859504-121859525
38	CTCF	chr7:121859358-121859591	SK-N-SH_RA	brain:	n/a	chr7:121859504-121859525
39	CTCF	chr7:121859362-121859707	Medullo	brain:	n/a	chr7:121859504-121859525
40	CTCF	chr7:121859440-121859590	K562	blood:	n/a	chr7:121859504-121859525
41	CTCF	chr7:121839060-121839210	HepG2	liver:	n/a	n/a
42	CTCF	chr7:121859420-121859570	SK-N-SH_RA	brain:	n/a	chr7:121859504-121859525
43	CTCF	chr7:121859440-121859590	MCF-7	breast:	n/a	chr7:121859504-121859525
44	CTCF	chr7:121859420-121859570	BE2_C	brain:	n/a	chr7:121859504-121859525
45	CTCF	chr7:121859440-121859590	BJ	skin:	n/a	chr7:121859504-121859525
46	CTCF	chr7:121843684-121843686	GM10266	blood:	n/a	n/a
47	CTCF	chr7:121859480-121859630	HRE	kidney:	n/a	chr7:121859504-121859525
48	CTCF	chr7:121859440-121859590	HRE	kidney:	n/a	chr7:121859504-121859525
49	CTCF	chr7:121859400-121859550	AG04449	skin:	n/a	chr7:121859504-121859525
50	CTCF	chr7:121859420-121859570	HCPEpiC	choroid plexus:	n/a	chr7:121859504-121859525

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:121878634-121878684	NT2-D1	testis:	n/a
2	chr7:121878634-121878684	NT2-D1	testis:	n/a
3	chr7:121840731-121840781	HNPCEpiC	eye:	n/a
4	chr7:121840731-121840781	Caco-2	colon:	n/a
5	chr7:121840731-121840781	AG10803	skin:	n/a
6	chr7:121840731-121840781	SK-N-MC	brain:	n/a
7	chr7:121895636-121895686	AG04450	lung:	fetal
8	chr7:121895636-121895686	HCT-116	colon:	n/a
9	chr7:121895636-121895686	NHDF-neo	bronchial:	n/a
10	chr7:121878634-121878684	GM12878	blood:	n/a
11	chr7:121895636-121895686	Hepatocyte	liver:	n/a
12	chr7:121878634-121878684	NHDF-neo	bronchial:	n/a
13	chr7:121840731-121840781	HL-60	blood:	n/a
14	chr7:121878634-121878684	SKMC	muscle:	n/a
15	chr7:121895636-121895686	MCF-7	breast:	n/a
16	chr7:121840731-121840781	H1-hESC	embryonic stem cell:	embryo
17	chr7:121895636-121895686	A549	lung:	n/a
18	chr7:121878634-121878684	AoSMC	blood vessel:	n/a
19	chr7:121878634-121878684	MCF10A-Er-Src	breast:	n/a
20	chr7:121895636-121895686	AG10803	skin:	n/a
21	chr7:121895636-121895686	HRCEpiC	kidney:	n/a
22	chr7:121895636-121895686	HL-60	blood:	n/a
23	chr7:121878634-121878684	PrEC	prostate:	n/a
24	chr7:121840731-121840781	GM12892	blood:	n/a
25	chr7:121878634-121878684	MCF-7	breast:	n/a
26	chr7:121840731-121840781	NH-A	brain:	n/a
27	chr7:121878634-121878684	NB4	blood:	n/a
28	chr7:121895636-121895686	GM12892	blood:	n/a
29	chr7:121878634-121878684	GM19239	blood:	n/a
30	chr7:121878634-121878684	GM12892	blood:	n/a
31	chr7:121878634-121878684	U87	brain:	n/a
32	chr7:121840731-121840781	CMK	blood:	n/a
33	chr7:121878634-121878684	AG10803	skin:	n/a
34	chr7:121878634-121878684	RPTEC	kidney:	n/a
35	chr7:121895636-121895686	GM12878	blood:	n/a
36	chr7:121840731-121840781	PFSK-1	brain:	n/a
37	chr7:121878634-121878684	HCT-116	colon:	n/a
38	chr7:121878634-121878684	HAEpiC	amniotic membrane:	n/a
39	chr7:121895636-121895686	T-47D	breast:	n/a
40	chr7:121895636-121895686	K562	blood:	n/a
41	chr7:121840731-121840781	PANC-1	pancreas:	n/a
42	chr7:121895636-121895686	BE2_C	brain:	n/a
43	chr7:121895636-121895686	U87	brain:	n/a
44	chr7:121878634-121878684	PANC-1	pancreas:	n/a
45	chr7:121840731-121840781	HRPEpiC	eye:	n/a
46	chr7:121840731-121840781	GM12878	blood:	n/a
47	chr7:121895636-121895686	ovcar-3	ovarian:	n/a
48	chr7:121878634-121878684	AG04449	skin:	fetal
49	chr7:121840731-121840781	AoSMC	blood vessel:	n/a
50	chr7:121840731-121840781	GM19239	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:121858437..121859375-chr7:122168762..122169335,2	MCF-7	breast:
2	chr7:121859190..121860364-chr7:122168361..122169672,5	MCF-7	breast:
3	chr7:121889359..121891616-chr7:121898116..121900388,2	K562	blood:
4	chr7:121889359..121891616-chr7:121898116..121900388,2	K562	blood:
5	chr7:121856928..121858928-chr7:122169140..122170961,2	MCF-7	breast:
6	chr7:121859583..121860476-chr7:122165216..122166173,2	MCF-7	breast:
7	chr7:121859014..121859979-chr7:122172471..122173393,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRZ1-10	chr7:121874585-121874957	NONHSAT123024
2	lnc-PTPRZ1-1	chr7:121856401-121856516	XLOC_006220
3	lnc-PTPRZ1-9	chr7:121841308-121841524	NONHSAT123022
4	lnc-PTPRZ1-9	chr7:121837856-121838124	NONHSAT123022
5	lnc-PTPRZ1-1	chr7:121857023-121857082	XLOC_006220
6	lnc-PTPRZ1-11	chr7:121897939-121898595	NONHSAT123025
7	lnc-PTPRZ1-1	chr7:121858196-121858491	XLOC_006220

No data

Variant related genes	Relation type
ENSG00000234418	TF binding region
ENSG00000213302	TF binding region
ENSG00000234418	CpG island
ENSG00000213302	CpG island

Extended variants
information (count: 1732 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1732 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144190118	chr7:121818993-121818994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542654612	chr7:121819046-121819047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117206750	chr7:121819057-121819058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189398417	chr7:121819145-121819146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544828870	chr7:121819154-121819155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564759581	chr7:121819197-121819198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150653295	chr7:121819212-121819213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77527929	chr7:121819373-121819374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377188273	chr7:121819451-121819452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182028309	chr7:121819457-121819458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568902327	chr7:121819499-121819500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73721108	chr7:121819532-121819533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs557663501	chr7:121819565-121819566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534402769	chr7:121819578-121819579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549370326	chr7:121819613-121819614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73226286	chr7:121819639-121819640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373217715	chr7:121819646-121819647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535143318	chr7:121819651-121819652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185976180	chr7:121819652-121819653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113451569	chr7:121819704-121819705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568301288	chr7:121819781-121819782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537670062	chr7:121819796-121819797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574632258	chr7:121819844-121819845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557685413	chr7:121819930-121819931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574428154	chr7:121819977-121819978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11761142	chr7:121819987-121819988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552934837	chr7:121820001-121820002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112379860	chr7:121820017-121820018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572823230	chr7:121820064-121820065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149787830	chr7:121820121-121820122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145815018	chr7:121820125-121820126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141722556	chr7:121820155-121820156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544047261	chr7:121820175-121820176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141169747	chr7:121820202-121820203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371203629	chr7:121820249-121820250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560837433	chr7:121820258-121820259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530007137	chr7:121820297-121820298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549081719	chr7:121820352-121820353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs284365	chr7:121820366-121820367	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs528513487	chr7:121820412-121820413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575150350	chr7:121820476-121820477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376172686	chr7:121820508-121820509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551884518	chr7:121820549-121820550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369056551	chr7:121820553-121820554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546052811	chr7:121820559-121820560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531119249	chr7:121820604-121820605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112642428	chr7:121820676-121820677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138405139	chr7:121820677-121820678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188993115	chr7:121820694-121820695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71172168	chr7:121820698-121820699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute monocytic leukemia	16498392	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121810200-121825800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:121822000-121822400	Enhancers	Left Ventricle	heart
3	chr7:121822000-121822800	ZNF genes & repeats	Aorta	Aorta
4	chr7:121829800-121830000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:121830600-121830800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:121832000-121838600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:121833800-121834000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:121833800-121834000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr7:121834000-121834600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr7:121834000-121838200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:121834600-121834800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr7:121834800-121839400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:121838000-121838200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr7:121838200-121838800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:121838200-121838800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr7:121838600-121839400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr7:121838800-121839000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr7:121838800-121839400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr7:121838800-121840000	Enhancers	Pancreas	Pancrea
20	chr7:121839000-121839400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr7:121839000-121840000	Enhancers	Liver	Liver
22	chr7:121839200-121839600	Enhancers	Fetal Heart	heart
23	chr7:121839400-121839600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr7:121839600-121841000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr7:121839600-121845800	Weak transcription	Fetal Heart	heart
26	chr7:121840800-121841000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr7:121840800-121841200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:121841000-121841200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:121841200-121841400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr7:121842800-121843000	ZNF genes & repeats	Left Ventricle	heart
31	chr7:121843000-121844400	Weak transcription	Left Ventricle	heart
32	chr7:121844400-121844600	ZNF genes & repeats	Left Ventricle	heart
33	chr7:121844600-121847000	Weak transcription	Left Ventricle	heart
34	chr7:121845200-121845400	Weak transcription	Brain Hippocampus Middle	brain
35	chr7:121845600-121847000	Weak transcription	Psoas Muscle	Psoas
36	chr7:121847000-121847400	ZNF genes & repeats	Psoas Muscle	Psoas
37	chr7:121847200-121847400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:121852800-121853200	Enhancers	HUVEC	blood vessel
39	chr7:121856800-121858000	Enhancers	Liver	Liver
40	chr7:121857200-121857800	Enhancers	HepG2	liver
41	chr7:121865000-121868800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:121865800-121867000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:121868200-121868600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:121868200-121869000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:121877400-121877600	Enhancers	Hela-S3	cervix
46	chr7:121877600-121878000	Flanking Active TSS	Hela-S3	cervix
47	chr7:121877800-121878600	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr7:121877800-121878800	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr7:121878000-121879000	Active TSS	Hela-S3	cervix
50	chr7:121878200-121878800	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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