Variant report

Variant	nsv888163
Chromosome Location	chr7:61817936-62012221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2641)
CpG islands
(count:976)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2641 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:62003077-62003278	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:61906420-61906785	K562	blood:	n/a	n/a
3	ARID3A	chr7:61995014-61995043	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:61968776-61971670	HepG2	liver:	n/a	n/a
5	ATF1	chr7:61972545-61973623	K562	blood:	n/a	n/a
6	ATF1	chr7:62007999-62008153	K562	blood:	n/a	n/a
7	ATF1	chr7:61985965-61986420	K562	blood:	n/a	n/a
8	ATF1	chr7:61968773-61971689	K562	blood:	n/a	n/a
9	ATF1	chr7:62008700-62008898	K562	blood:	n/a	n/a
10	ATF1	chr7:61990607-61990893	K562	blood:	n/a	n/a
11	ATF1	chr7:61982793-61983165	K562	blood:	n/a	n/a
12	ATF1	chr7:62004903-62005165	K562	blood:	n/a	n/a
13	ATF1	chr7:61995014-61995028	K562	blood:	n/a	n/a
14	ATF1	chr7:61974872-61975409	K562	blood:	n/a	n/a
15	ATF1	chr7:61906413-61906787	K562	blood:	n/a	n/a
16	ATF1	chr7:61967171-61968455	K562	blood:	n/a	n/a
17	ATF1	chr7:61980513-61980520	K562	blood:	n/a	n/a
18	ATF2	chr7:61968742-61969785	GM12878	blood:	n/a	n/a
19	ATF3	chr7:61969166-61969576	GM12878	blood:	n/a	n/a
20	ATF3	chr7:61968751-61969722	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr7:61968853-61969701	GM12878	blood:	n/a	n/a
22	ATF3	chr7:61968873-61969699	HepG2	liver:	n/a	n/a
23	ATF3	chr7:61968885-61969100	GM12878	blood:	n/a	n/a
24	ATF3	chr7:61970921-61971315	GM12878	blood:	n/a	n/a
25	ATF3	chr7:61974958-61975207	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr7:61968750-61969626	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:61970815-61972697	K562	blood:	n/a	n/a
28	BACH1	chr7:61974873-61976628	K562	blood:	n/a	n/a
29	BATF	chr7:61994851-61995393	GM12878	blood:	n/a	n/a
30	BATF	chr7:61833066-61833342	GM12878	blood:	n/a	n/a
31	BATF	chr7:61988959-61989761	GM12878	blood:	n/a	n/a
32	BATF	chr7:61993825-61994127	GM12878	blood:	n/a	n/a
33	BATF	chr7:62009661-62009940	GM12878	blood:	n/a	n/a
34	BATF	chr7:61818826-61819180	GM12878	blood:	n/a	n/a
35	BATF	chr7:61984439-61984996	GM12878	blood:	n/a	n/a
36	BATF	chr7:61817481-61818430	GM12878	blood:	n/a	n/a
37	BATF	chr7:61985948-61986390	GM12878	blood:	n/a	n/a
38	BATF	chr7:61981447-61982325	GM12878	blood:	n/a	n/a
39	BATF	chr7:61991905-61992094	GM12878	blood:	n/a	n/a
40	BATF	chr7:61818500-61818732	GM12878	blood:	n/a	n/a
41	BATF	chr7:61823412-61823570	GM12878	blood:	n/a	n/a
42	BATF	chr7:61832749-61832982	GM12878	blood:	n/a	n/a
43	BATF	chr7:61975296-61977251	GM12878	blood:	n/a	n/a
44	BATF	chr7:61994851-61995246	GM12878	blood:	n/a	n/a
45	BATF	chr7:62004355-62004614	GM12878	blood:	n/a	n/a
46	BATF	chr7:62009727-62009918	GM12878	blood:	n/a	n/a
47	BATF	chr7:61990451-61991067	GM12878	blood:	n/a	n/a
48	BATF	chr7:61986008-61986393	GM12878	blood:	n/a	n/a
49	BATF	chr7:62002963-62003344	GM12878	blood:	n/a	n/a
50	BATF	chr7:61832086-61832275	GM12878	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:61821762-61821812	NB4	blood:	n/a
2	chr7:61968988-61969038	PrEC	prostate:	n/a
3	chr7:61822021-61822071	Hela-S3	cervix:	n/a
4	chr7:61818348-61818398	HRPEpiC	eye:	n/a
5	chr7:61969337-61969387	MCF-7	breast:	n/a
6	chr7:61969520-61969570	U87	brain:	n/a
7	chr7:61969078-61969128	HCT-116	colon:	n/a
8	chr7:61818740-61818790	LNCaP	prostate:	n/a
9	chr7:61821762-61821812	HAEpiC	amniotic membrane:	n/a
10	chr7:61968148-61968198	GM19239	blood:	n/a
11	chr7:61821762-61821812	HNPCEpiC	eye:	n/a
12	chr7:61818348-61818398	AG09309	skin:	n/a
13	chr7:61820842-61820892	GM12891	blood:	n/a
14	chr7:61969570-61969620	MCF10A-Er-Src	breast:	n/a
15	chr7:61974919-61974969	SKMC	muscle:	n/a
16	chr7:61822021-61822071	HIPEpiC	eye:	n/a
17	chr7:61820842-61820892	HRCEpiC	kidney:	n/a
18	chr7:61818348-61818398	A549	lung:	n/a
19	chr7:61818740-61818790	HepG2	liver:	n/a
20	chr7:61969337-61969387	SKMC	muscle:	n/a
21	chr7:61969337-61969387	Jurkat	blood:	n/a
22	chr7:61853231-61853281	GM12892	blood:	n/a
23	chr7:61969485-61969535	Caco-2	colon:	n/a
24	chr7:61969485-61969535	PANC-1	pancreas:	n/a
25	chr7:61822021-61822071	Hepatocyte	liver:	n/a
26	chr7:61969078-61969128	AG04450	lung:	fetal
27	chr7:61820842-61820892	PrEC	prostate:	n/a
28	chr7:61969520-61969570	HCT-116	colon:	n/a
29	chr7:61969078-61969128	NT2-D1	testis:	n/a
30	chr7:61821180-61821230	MCF-7	breast:	n/a
31	chr7:61968148-61968198	Hela-S3	cervix:	n/a
32	chr7:61821180-61821230	U87	brain:	n/a
33	chr7:61853231-61853281	CMK	blood:	n/a
34	chr7:61969520-61969570	HCM	heart:	n/a
35	chr7:61818740-61818790	NH-A	brain:	n/a
36	chr7:61821762-61821812	NHDF-neo	bronchial:	n/a
37	chr7:61974919-61974969	HRPEpiC	eye:	n/a
38	chr7:61821762-61821812	SKMC	muscle:	n/a
39	chr7:61971401-61971451	AG10803	skin:	n/a
40	chr7:61968988-61969038	IMR90	lung:	fetal
41	chr7:61822021-61822071	GM12878	blood:	n/a
42	chr7:61974919-61974969	IMR90	lung:	fetal
43	chr7:61969337-61969387	H1-hESC	embryonic stem cell:	embryo
44	chr7:61821180-61821230	RPTEC	kidney:	n/a
45	chr7:61821180-61821230	AG04450	lung:	fetal
46	chr7:61968148-61968198	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:61974919-61974969	A549	lung:	n/a
48	chr7:61969570-61969620	HRE	kidney:	n/a
49	chr7:61821180-61821230	H1-hESC	embryonic stem cell:	embryo
50	chr7:61968148-61968198	SKMC	muscle:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:61967856..61970847-chr8:58714316..58715816,2	K562	blood:
2	chr10:42526395..42527915-chr7:61967791..61969507,5	MCF-7	breast:
3	chr4:8654425..8657330-chr7:61967859..61969474,2	MCF-7	breast:
4	chr20:46692208..46692789-chr7:61968943..61969520,2	MCF-7	breast:
5	chr10:42527395..42527915-chr7:61970565..61971091,3	MCF-7	breast:
6	chr10:42525601..42527915-chr7:61967079..61969278,2	K562	blood:
7	chr1:191006072..191007919-chr7:61967833..61970042,2	MCF-7	breast:
8	chr10:42527395..42527923-chr7:61968860..61969524,4	MCF-7	breast:
9	chr10:42527395..42527914-chr7:61968778..61969295,2	MCF-7	breast:
10	chr10:42527415..42527915-chr7:61968777..61969450,2	MCF-7	breast:
11	chr4:91025999..91028875-chr7:61969348..61970976,2	MCF-7	breast:
12	chr10:42526394..42527915-chr7:61967791..61969362,3	MCF-7	breast:
13	chr20:52370017..52370874-chr7:61969357..61969967,2	MCF-7	breast:
14	chr20:55824160..55824726-chr7:61968550..61969274,2	MCF-7	breast:
15	chr1:121483889..121484797-chr7:61974740..61975240,2	MCF-7	breast:
16	chr16:1429819..1431603-chr7:61967775..61969442,2	MCF-7	breast:
17	chr7:61967856..61971070-chr8:58714316..58715816,4	K562	blood:
18	chr2:230809935..230810929-chr7:61969025..61969969,2	MCF-7	breast:
19	chr17:59939771..59941744-chr7:61968022..61970059,2	MCF-7	breast:
20	chr14:102551841..102553604-chr7:61969473..61971085,2	MCF-7	breast:
21	chr17:73511595..73513321-chr7:61968020..61970850,2	MCF-7	breast:
22	chr11:63950861..63953375-chr7:61969464..61971091,2	K562	blood:
23	chr18:33251821..33252438-chr7:61968851..61969524,2	K562	blood:
24	chr14:29714914..29715705-chr7:61970951..61971586,2	MCF-7	breast:
25	chr3:64043547..64044153-chr7:61969362..61969878,2	MCF-7	breast:
26	chr7:61969210..61969976-chr8:53657642..53658150,2	MCF-7	breast:
27	chr17:59328333..59331074-chr7:61967802..61970795,2	MCF-7	breast:
28	chr7:61967943..61970858-chr7:75931774..75934475,2	MCF-7	breast:
29	chr18:18518513..18519030-chr7:61979393..61979915,2	MCF-7	breast:
30	chr10:42527395..42527915-chr7:61968790..61969454,6	MCF-7	breast:
31	chr19:14627777..14629340-chr7:61968008..61969542,2	MCF-7	breast:
32	chr1:149221735..149223983-chr7:61969300..61970873,2	K562	blood:
33	chr20:49942718..49943230-chr7:61968963..61969517,2	MCF-7	breast:
34	chr13:53432415..53433397-chr7:61969357..61970027,2	MCF-7	breast:
35	chr10:42525601..42527915-chr7:61967079..61969468,3	K562	blood:
36	chr20:3786959..3788753-chr7:61967828..61969450,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006455.1-12	chr7:61968944-61969128	NONHSAT120885
2	lnc-AC006455.1-12	chr7:61971118-61971191	NONHSAT120885
3	lnc-AC006455.1-12	chr7:61969203-61969572	NONHSAT120885
4	lnc-AC006455.1-12	chr7:61970441-61970493	NONHSAT120885

No data

Variant related genes	Relation type
ENSG00000233918	TF binding region
ENSG00000233918	CpG island
ENSG00000182173	chromatin interactions
ENSG00000132002	chromatin interactions
ENSG00000099797	chromatin interactions
ENSG00000106211	chromatin interactions
ENSG00000177303	chromatin interactions
ENSG00000168439	chromatin interactions
ENSG00000136492	chromatin interactions
ENSG00000080824	chromatin interactions

Extended variants
information (count: 16892 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:16892 , 50 per page) page: 1 2 3 4 5 6 7 ... 338

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9329162	chr7:61817936-61817937	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs529651341	chr7:61817951-61817952	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs533355597	chr7:61817954-61817955	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs551629786	chr7:61817965-61817966	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs570086676	chr7:61817973-61817974	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs9769410	chr7:61817986-61817987	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs9691886	chr7:61818004-61818005	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs536858554	chr7:61818011-61818012	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs555110354	chr7:61818012-61818013	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs7797526	chr7:61818018-61818019	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs9770479	chr7:61818019-61818020	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs9770693	chr7:61818021-61818022	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs78121106	chr7:61818022-61818023	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs534635047	chr7:61818041-61818042	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs370894714	chr7:61818043-61818044	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs374357301	chr7:61818044-61818045	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs553222810	chr7:61818047-61818048	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs377477007	chr7:61818052-61818053	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs577612502	chr7:61818056-61818057	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs113105263	chr7:61818062-61818063	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs371223565	chr7:61818084-61818085	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs544940343	chr7:61818087-61818088	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7776575	chr7:61818090-61818091	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs10903308	chr7:61818096-61818097	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs9770013	chr7:61818097-61818098	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs10903309	chr7:61818101-61818102	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs56774288	chr7:61818103-61818104	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs373223575	chr7:61818105-61818106	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs61560939	chr7:61818106-61818107	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs4088463	chr7:61818111-61818112	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs544050405	chr7:61818113-61818114	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs562298206	chr7:61818123-61818124	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs28405985	chr7:61818125-61818126	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529497491	chr7:61818126-61818127	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs9286058	chr7:61818147-61818148	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs111430930	chr7:61818151-61818152	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs7797658	chr7:61818160-61818161	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs533176748	chr7:61818162-61818163	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs551713226	chr7:61818164-61818165	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs570068929	chr7:61818178-61818179	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530939435	chr7:61818184-61818185	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs549048686	chr7:61818186-61818187	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs57628241	chr7:61818187-61818188	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs9770701	chr7:61818193-61818194	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs534506447	chr7:61818206-61818207	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs4102197	chr7:61818236-61818237	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs552992819	chr7:61818242-61818243	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs11249873	chr7:61818243-61818244	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs11767069	chr7:61818252-61818253	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs11771146	chr7:61818268-61818269	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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

Chromatin state (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:61814800-61818800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:61815000-61818400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
3	chr7:61815000-61826200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr7:61817800-61819600	Weak transcription	Fetal Heart	heart
5	chr7:61818200-61819000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
6	chr7:61818200-61819200	ZNF genes & repeats	Adipose Nuclei	Adipose
7	chr7:61819000-61827800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr7:61819600-61819800	ZNF genes & repeats	Fetal Heart	heart
9	chr7:61819600-61822800	ZNF genes & repeats	Adipose Nuclei	Adipose
10	chr7:61819600-61825800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:61819800-61822200	Weak transcription	Fetal Heart	heart
12	chr7:61820000-61826200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
13	chr7:61820000-61826200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:61820200-61822600	ZNF genes & repeats	Fetal Stomach	stomach
15	chr7:61820200-61822600	ZNF genes & repeats	NHEK	skin
16	chr7:61820200-61826000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
17	chr7:61820400-61820600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
18	chr7:61820400-61820600	Bivalent Enhancer	Placenta	Placenta
19	chr7:61820400-61822000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr7:61820400-61822400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:61820400-61822400	ZNF genes & repeats	Right Ventricle	heart
22	chr7:61820400-61822600	ZNF genes & repeats	Fetal Muscle Leg	muscle
23	chr7:61820400-61822800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:61820400-61822800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:61820400-61822800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
26	chr7:61820400-61822800	ZNF genes & repeats	Lung	lung
27	chr7:61820400-61823000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
28	chr7:61820600-61821400	Flanking Bivalent TSS/Enh	Placenta	Placenta
29	chr7:61820600-61821800	ZNF genes & repeats	Fetal Intestine Large	intestine
30	chr7:61820600-61822000	ZNF genes & repeats	Colon Smooth Muscle	Colon
31	chr7:61820600-61822400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
32	chr7:61820600-61822800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
33	chr7:61821000-61822400	ZNF genes & repeats	Spleen	Spleen
34	chr7:61821200-61822400	ZNF genes & repeats	Colonic Mucosa	Colon
35	chr7:61821200-61822400	ZNF genes & repeats	A549	lung
36	chr7:61821200-61822600	ZNF genes & repeats	Pancreas	Pancrea
37	chr7:61821200-61822600	ZNF genes & repeats	Thymus	Thymus
38	chr7:61821200-61823000	ZNF genes & repeats	Liver	Liver
39	chr7:61821200-61824600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
40	chr7:61821200-61825800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr7:61821400-61822000	Bivalent Enhancer	Placenta	Placenta
42	chr7:61821400-61822200	ZNF genes & repeats	Fetal Intestine Small	intestine
43	chr7:61821400-61822400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:61821400-61822400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:61821400-61822600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:61821400-61823200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
47	chr7:61821400-61824200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
48	chr7:61821600-61821800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
49	chr7:61821600-61822000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
50	chr7:61821600-61822200	Bivalent/Poised TSS	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links