Variant report

Variant	nsv8100
Chromosome Location	chr7:62030693-62695413
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1344)
CpG islands
(count:1892)
Chromatin interactive
region (count:11)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:62039929-62040292	K562	blood:	n/a	n/a
2	ATF1	chr7:62546931-62547029	K562	blood:	n/a	n/a
3	ATF1	chr7:62330338-62330635	K562	blood:	n/a	n/a
4	ATF1	chr7:62071176-62071544	K562	blood:	n/a	n/a
5	BACH1	chr7:62435606-62435658	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:62601389-62601434	K562	blood:	n/a	n/a
7	BACH1	chr7:62031748-62032429	K562	blood:	n/a	n/a
8	BATF	chr7:62031446-62031758	GM12878	blood:	n/a	n/a
9	BATF	chr7:62188677-62188824	GM12878	blood:	n/a	n/a
10	BATF	chr7:62032839-62033167	GM12878	blood:	n/a	n/a
11	BATF	chr7:62565070-62565257	GM12878	blood:	n/a	chr7:62565199-62565210
12	BATF	chr7:62031502-62031772	GM12878	blood:	n/a	n/a
13	BATF	chr7:62400667-62400824	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:62032887-62033140	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:62031479-62031795	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:62032885-62033176	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:62188685-62188838	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:62031464-62031707	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:62031491-62031663	HepG2	liver:	n/a	n/a
20	BHLHE40	chr7:62188666-62188877	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:62211584-62211597	K562	blood:	n/a	n/a
22	BHLHE40	chr7:62032928-62033195	HepG2	liver:	n/a	n/a
23	BHLHE40	chr7:62468805-62468905	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:62031747-62032429	K562	blood:	n/a	n/a
25	BHLHE40	chr7:62476052-62476283	K562	blood:	n/a	n/a
26	BHLHE40	chr7:62092973-62093345	K562	blood:	n/a	n/a
27	BHLHE40	chr7:62248579-62248799	HepG2	liver:	n/a	n/a
28	BRCA1	chr7:62112613-62112988	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr7:62031748-62032474	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr7:62403774-62404151	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr7:62081040-62081416	GM12878	blood:	n/a	n/a
32	CEBPB	chr7:62668869-62669111	MCF-7	breast:	n/a	n/a
33	CEBPB	chr7:62603841-62603852	K562	blood:	n/a	n/a
34	CEBPB	chr7:62398267-62398576	A549	lung:	n/a	chr7:62398413-62398424
35	CEBPB	chr7:62597727-62598013	HepG2	liver:	n/a	chr7:62597864-62597875
36	CEBPB	chr7:62253811-62254011	K562	blood:	n/a	n/a
37	CEBPB	chr7:62571990-62572132	K562	blood:	n/a	chr7:62572079-62572090
38	CEBPB	chr7:62571888-62572134	MCF-7	breast:	n/a	chr7:62572079-62572090
39	CEBPB	chr7:62137014-62137228	A549	lung:	n/a	chr7:62137149-62137160
40	CEBPB	chr7:62603856-62604105	K562	blood:	n/a	n/a
41	CEBPB	chr7:62668778-62669023	MCF-7	breast:	n/a	n/a
42	CEBPB	chr7:62398244-62398589	IMR90	lung:	n/a	chr7:62398413-62398424
43	CEBPB	chr7:62597721-62598026	K562	blood:	n/a	chr7:62597864-62597875
44	CEBPB	chr7:62398403-62398420	K562	blood:	n/a	n/a
45	CEBPB	chr7:62603875-62604040	A549	lung:	n/a	n/a
46	CEBPB	chr7:62597783-62598034	A549	lung:	n/a	chr7:62597864-62597875
47	CEBPB	chr7:62398241-62398594	HepG2	liver:	n/a	chr7:62398413-62398424
48	CEBPB	chr7:62403775-62404151	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:62507136-62507365	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:62572008-62572212	HepG2	liver:	n/a	chr7:62572079-62572090

(count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:62528241-62528291	GM19239	blood:	n/a
2	chr7:62528241-62528291	GM19239	blood:	n/a
3	chr7:62574200-62574250	Jurkat	blood:	n/a
4	chr7:62574200-62574250	HEEpiC	esophagus:	n/a
5	chr7:62576406-62576456	GM12892	blood:	n/a
6	chr7:62531318-62531368	HL-60	blood:	n/a
7	chr7:62528852-62528902	H1-hESC	embryonic stem cell:	embryo
8	chr7:62514477-62514527	HUVEC	blood vessel:	n/a
9	chr7:62577907-62577957	HAEpiC	amniotic membrane:	n/a
10	chr7:62514673-62514723	GM12891	blood:	n/a
11	chr7:62555691-62555741	Hela-S3	cervix:	n/a
12	chr7:62191825-62191875	AG04449	skin:	fetal
13	chr7:62514926-62514976	RPTEC	kidney:	n/a
14	chr7:62514572-62514622	IMR90	lung:	fetal
15	chr7:62153290-62153340	NH-A	brain:	n/a
16	chr7:62528691-62528741	SKMC	muscle:	n/a
17	chr7:62555691-62555741	HRPEpiC	eye:	n/a
18	chr7:62528691-62528741	AG09309	skin:	n/a
19	chr7:62198343-62198393	GM12892	blood:	n/a
20	chr7:62541571-62541621	A549	lung:	n/a
21	chr7:62693631-62693681	PANC-1	pancreas:	n/a
22	chr7:62577907-62577957	AG04449	skin:	fetal
23	chr7:62541571-62541621	BJ	skin:	n/a
24	chr7:62153290-62153340	H1-hESC	embryonic stem cell:	embryo
25	chr7:62531318-62531368	Caco-2	colon:	n/a
26	chr7:62541571-62541621	HEK293	kidney:	embryo
27	chr7:62575098-62575148	GM12892	blood:	n/a
28	chr7:62555691-62555741	NH-A	brain:	n/a
29	chr7:62693610-62693660	NH-A	brain:	n/a
30	chr7:62555691-62555741	SK-N-SH_RA	brain:	n/a
31	chr7:62560487-62560537	HEEpiC	esophagus:	n/a
32	chr7:62555691-62555741	NHBE	bronchial:	n/a
33	chr7:62490514-62490564	U87	brain:	n/a
34	chr7:62198343-62198393	HUVEC	blood vessel:	n/a
35	chr7:62562718-62562768	HEEpiC	esophagus:	n/a
36	chr7:62574479-62574529	BJ	skin:	n/a
37	chr7:62576406-62576456	HMEC	breast:	n/a
38	chr7:62560487-62560537	BJ	skin:	n/a
39	chr7:62528852-62528902	Jurkat	blood:	n/a
40	chr7:62514673-62514723	NH-A	brain:	n/a
41	chr7:62517839-62517889	PANC-1	pancreas:	n/a
42	chr7:62198343-62198393	SKMC	muscle:	n/a
43	chr7:62541571-62541621	HRCEpiC	kidney:	n/a
44	chr7:62528852-62528902	SKMC	muscle:	n/a
45	chr7:62577907-62577957	NT2-D1	testis:	n/a
46	chr7:62576406-62576456	NHDF-neo	bronchial:	n/a
47	chr7:62528610-62528660	GM12891	blood:	n/a
48	chr7:62490514-62490564	AG04450	lung:	fetal
49	chr7:62510825-62510875	HEEpiC	esophagus:	n/a
50	chr7:62541571-62541621	MCF-7	breast:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:62475749..62476533-chr7:100925981..100926817,2	MCF-7	breast:
2	chr7:61552820..61553340-chr7:62284727..62285248,3	MCF-7	breast:
3	chr17:41398894..41400557-chr7:62191292..62192792,2	K562	blood:
4	chr7:62093615..62095373-chr7:62122563..62125212,2	K562	blood:
5	chr17:41380312..41382165-chr7:62191292..62192792,2	K562	blood:
6	chr5:178209012..178209534-chr7:62475815..62476717,2	MCF-7	breast:
7	chr17:41380367..41382313-chr7:62191292..62192792,2	MCF-7	breast:
8	chr17:41399589..41402142-chr7:62189772..62191292,2	K562	blood:
9	chr7:62093615..62095373-chr7:62122563..62125212,2	K562	blood:
10	chr17:22017005..22017989-chr7:62476147..62476710,2	MCF-7	breast:
11	chr7:62284727..62285228-chr9:30620902..30621883,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006455.1-11	chr7:62517831-62517952	NONHSAT120889
2	lnc-AC006455.1-11	chr7:62520310-62520462	NONHSAT120889
3	lnc-ZNF680-44	chr7:62547448-62548639	NONHSAT120891
4	lnc-ZNF680-11	chr7:62452942-62453054	XLOC_006462
5	lnc-ZNF680-10	chr7:62514734-62514809	XLOC_006463
6	lnc-ZNF680-10	chr7:62505205-62505547	XLOC_006463
7	lnc-ZNF680-11	chr7:62441009-62441326	XLOC_006462
8	lnc-AC006455.1-8	chr7:62669597-62669710	NONHSAT120895
9	lnc-AC006455.1-8	chr7:62672054-62672200	NONHSAT120895

No data

Variant related genes	Relation type
ENSG00000234312	TF binding region
ENSG00000199231	TF binding region
ENSG00000231523	TF binding region
ZNF90P3	TF binding region
ENSG00000265865	TF binding region
ENSG00000227148	TF binding region
PHKG1P1	TF binding region
ENSG00000237572	TF binding region
RNU6-417P	TF binding region
ENSG00000233454	TF binding region
ENSG00000234312	CpG island
ENSG00000199231	CpG island
ENSG00000231523	CpG island
ZNF90P3	CpG island
ENSG00000265865	CpG island
ENSG00000227148	CpG island
PHKG1P1	CpG island
ENSG00000237572	CpG island
RNU6-417P	CpG island
ENSG00000233454	CpG island
ENSG00000236383	chromatin interactions

Extended variants
information (count: 27017 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:27017 , 50 per page) page: 1 2 3 4 5 6 7 ... 541

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551995354	chr7:62030702-62030703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114417068	chr7:62030717-62030718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191817882	chr7:62030718-62030719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56250314	chr7:62030719-62030720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556222770	chr7:62030752-62030753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575999845	chr7:62030757-62030758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545848371	chr7:62030772-62030773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116459316	chr7:62030778-62030779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555154811	chr7:62030793-62030794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112065067	chr7:62030794-62030795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116076290	chr7:62030825-62030826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547192472	chr7:62030834-62030835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147803580	chr7:62030843-62030844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183614882	chr7:62030879-62030880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577297219	chr7:62030881-62030882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114777109	chr7:62030943-62030944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs117249526	chr7:62030972-62030973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141205891	chr7:62030977-62030978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541722136	chr7:62030991-62030992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146939693	chr7:62030993-62030994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189265434	chr7:62031008-62031009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552221310	chr7:62031040-62031041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570430642	chr7:62031101-62031102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549932661	chr7:62031130-62031131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182259682	chr7:62031162-62031163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549800251	chr7:62031167-62031168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143071171	chr7:62031182-62031183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11971161	chr7:62031187-62031188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs202035552	chr7:62031188-62031189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199801902	chr7:62031196-62031197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536906115	chr7:62031200-62031201	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142264168	chr7:62031208-62031209	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140863617	chr7:62031211-62031212	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs151019259	chr7:62031215-62031216	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74815305	chr7:62031232-62031233	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112329645	chr7:62031248-62031249	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145203228	chr7:62031257-62031258	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554979697	chr7:62031260-62031261	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80342252	chr7:62031271-62031272	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567029510	chr7:62031273-62031274	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62476931	chr7:62031274-62031275	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113485860	chr7:62031280-62031281	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375710118	chr7:62031282-62031283	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62476932	chr7:62031290-62031291	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534111710	chr7:62031304-62031305	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368615188	chr7:62031308-62031309	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559143125	chr7:62031315-62031316	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577259734	chr7:62031325-62031326	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76205462	chr7:62031326-62031327	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs8188343	chr7:62031335-62031336	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
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
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
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	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
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	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
Glioblastoma	21080181	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Bipolar disorder	19214233	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Schizophrenia	23813976	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:62022000-62032000	Weak transcription	NH-A	brain
2	chr7:62031200-62047200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr7:62031400-62032000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:62031600-62032200	ZNF genes & repeats	HUVEC	blood vessel
5	chr7:62031600-62032400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:62031600-62047000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:62031800-62032200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
8	chr7:62031800-62032400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
9	chr7:62031800-62032600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
10	chr7:62031800-62032600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
11	chr7:62032000-62032200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
12	chr7:62032000-62032200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:62032000-62032200	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
14	chr7:62032000-62032200	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr7:62032000-62032200	ZNF genes & repeats	NH-A	brain
16	chr7:62034600-62036800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
17	chr7:62036400-62047800	ZNF genes & repeats	Liver	Liver
18	chr7:62038000-62041600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr7:62040000-62040200	Bivalent Enhancer	HSMM	muscle
20	chr7:62040000-62040200	ZNF genes & repeats	HSMMtube	muscle
21	chr7:62040000-62040200	ZNF genes & repeats	HUVEC	blood vessel
22	chr7:62040000-62040200	Active TSS	K562	blood
23	chr7:62040000-62040200	ZNF genes & repeats	NH-A	brain
24	chr7:62040000-62040200	Enhancers	NHLF	lung
25	chr7:62040000-62040200	Enhancers	Osteobl	bone
26	chr7:62040000-62040400	Active TSS	Aorta	Aorta
27	chr7:62040000-62040400	ZNF genes & repeats	HMEC	breast
28	chr7:62040000-62043000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
29	chr7:62045800-62047800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr7:62046000-62047000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
31	chr7:62048200-62049200	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr7:62049400-62050200	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr7:62049400-62053200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
34	chr7:62055600-62057600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:62056200-62057000	ZNF genes & repeats	Adipose Nuclei	Adipose
36	chr7:62061200-62062400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
37	chr7:62061600-62062800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:62069000-62073600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
39	chr7:62069600-62076000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
40	chr7:62069600-62076400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:62071600-62074400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr7:62075000-62075200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:62075000-62075400	ZNF genes & repeats	NH-A	brain
44	chr7:62075000-62076400	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr7:62075200-62075400	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:62075400-62076800	Weak transcription	NH-A	brain
47	chr7:62078400-62078800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:62080800-62084600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:62081000-62081400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:62081000-62083600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links