Variant report

Variant	nsv1026024
Chromosome Location	chr7:70301346-70594292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:828)
CpG islands
(count:977)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:828 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:70473461-70473667	K562	blood:	n/a	n/a
2	ATF2	chr7:70359196-70359849	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
4	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:70321901-70322317	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:70578379-70578450	K562	blood:	n/a	n/a
9	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:70384908-70384986	K562	blood:	n/a	n/a
11	BCL11A	chr7:70359245-70359587	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr7:70470205-70470386	K562	blood:	n/a	n/a
13	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
14	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
15	BHLHE40	chr7:70498977-70499038	K562	blood:	n/a	n/a
16	BHLHE40	chr7:70482560-70482896	K562	blood:	n/a	n/a
17	CBX3	chr7:70515518-70515757	K562	blood:	n/a	n/a
18	CBX3	chr7:70538895-70539134	K562	blood:	n/a	n/a
19	CBX3	chr7:70482488-70483015	K562	blood:	n/a	n/a
20	CCNT2	chr7:70543176-70543345	K562	blood:	n/a	n/a
21	CEBPB	chr7:70528604-70528901	A549	lung:	n/a	chr7:70528754-70528765
22	CEBPB	chr7:70518557-70518568	K562	blood:	n/a	n/a
23	CEBPB	chr7:70473715-70474044	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:70473682-70474054	K562	blood:	n/a	n/a
25	CEBPB	chr7:70520536-70520878	MCF-7	breast:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
26	CEBPB	chr7:70314283-70314959	H1-hESC	embryonic stem cell:	n/a	chr7:70314674-70314686
27	CEBPB	chr7:70571075-70571241	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:70426400-70426506	A549	lung:	n/a	n/a
29	CEBPB	chr7:70473685-70474059	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:70473695-70474052	A549	lung:	n/a	n/a
32	CEBPB	chr7:70528607-70528917	IMR90	lung:	n/a	chr7:70528754-70528765
33	CEBPB	chr7:70477784-70478010	H1-hESC	embryonic stem cell:	n/a	chr7:70477953-70477964
34	CEBPB	chr7:70426416-70426613	K562	blood:	n/a	n/a
35	CEBPB	chr7:70528739-70528775	H1-hESC	embryonic stem cell:	n/a	chr7:70528754-70528765
36	CEBPB	chr7:70359237-70359569	H1-hESC	embryonic stem cell:	n/a	chr7:70359363-70359375
37	CEBPB	chr7:70477839-70478111	IMR90	lung:	n/a	chr7:70477953-70477964
38	CEBPB	chr7:70536265-70536412	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:70349310-70349766	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:70520490-70520869	K562	blood:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
41	CEBPB	chr7:70477829-70478104	K562	blood:	n/a	chr7:70477953-70477964
42	CEBPB	chr7:70477923-70478050	HepG2	liver:	n/a	chr7:70477953-70477964
43	CEBPB	chr7:70518584-70518708	A549	lung:	n/a	n/a
44	CEBPB	chr7:70520499-70520875	HepG2	liver:	n/a	chr7:70520680-70520691 chr7:70520691-70520702
45	CEBPB	chr7:70443503-70443748	HepG2	liver:	n/a	chr7:70443649-70443660 chr7:70443597-70443608
46	CEBPB	chr7:70536360-70536397	K562	blood:	n/a	n/a
47	CEBPB	chr7:70582974-70583308	HepG2	liver:	n/a	chr7:70583233-70583242 chr7:70583231-70583242 chr7:70583012-70583025
48	CEBPB	chr7:70491206-70491381	K562	blood:	n/a	chr7:70491297-70491308
49	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
50	CEBPB	chr7:70518473-70518696	HepG2	liver:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70561125-70561175	SK-N-SH	brain:	n/a
2	chr7:70561125-70561175	SK-N-SH	brain:	n/a
3	chr7:70543490-70543540	SK-N-MC	brain:	n/a
4	chr7:70543605-70543655	CMK	blood:	n/a
5	chr7:70311532-70311582	T-47D	breast:	n/a
6	chr7:70311435-70311485	SK-N-MC	brain:	n/a
7	chr7:70543800-70543850	HepG2	liver:	n/a
8	chr7:70543079-70543129	Caco-2	colon:	n/a
9	chr7:70543079-70543129	HL-60	blood:	n/a
10	chr7:70482891-70482941	HepG2	liver:	n/a
11	chr7:70482771-70482821	GM06990	blood:	n/a
12	chr7:70482891-70482941	CMK	blood:	n/a
13	chr7:70311435-70311485	SAEC	small airway:	n/a
14	chr7:70561125-70561175	HNPCEpiC	eye:	n/a
15	chr7:70311435-70311485	Jurkat	blood:	n/a
16	chr7:70577170-70577220	AG09319	gingival:	n/a
17	chr7:70311532-70311582	AG09319	gingival:	n/a
18	chr7:70482771-70482821	Hepatocyte	liver:	n/a
19	chr7:70543800-70543850	SK-N-SH_RA	brain:	n/a
20	chr7:70311435-70311485	CMK	blood:	n/a
21	chr7:70543800-70543850	Hepatocyte	liver:	n/a
22	chr7:70482891-70482941	AG09309	skin:	n/a
23	chr7:70592898-70592948	HRCEpiC	kidney:	n/a
24	chr7:70543800-70543850	NHDF-neo	bronchial:	n/a
25	chr7:70311435-70311485	HRCEpiC	kidney:	n/a
26	chr7:70543605-70543655	U87	brain:	n/a
27	chr7:70311532-70311582	SK-N-SH_RA	brain:	n/a
28	chr7:70482891-70482941	BE2_C	brain:	n/a
29	chr7:70311321-70311371	RPTEC	kidney:	n/a
30	chr7:70592898-70592948	U87	brain:	n/a
31	chr7:70311435-70311485	AG04449	skin:	fetal
32	chr7:70592898-70592948	BJ	skin:	n/a
33	chr7:70482891-70482941	NHBE	bronchial:	n/a
34	chr7:70543320-70543370	PrEC	prostate:	n/a
35	chr7:70311532-70311582	GM12891	blood:	n/a
36	chr7:70543605-70543655	HNPCEpiC	eye:	n/a
37	chr7:70543800-70543850	NHBE	bronchial:	n/a
38	chr7:70543320-70543370	GM12891	blood:	n/a
39	chr7:70359655-70359705	Caco-2	colon:	n/a
40	chr7:70482891-70482941	PrEC	prostate:	n/a
41	chr7:70543800-70543850	A549	lung:	n/a
42	chr7:70543490-70543540	HRE	kidney:	n/a
43	chr7:70592898-70592948	PANC-1	pancreas:	n/a
44	chr7:70543800-70543850	T-47D	breast:	n/a
45	chr7:70561125-70561175	PrEC	prostate:	n/a
46	chr7:70311435-70311485	GM19239	blood:	n/a
47	chr7:70482771-70482821	AG09309	skin:	n/a
48	chr7:70311321-70311371	PANC-1	pancreas:	n/a
49	chr7:70417419-70417469	AoSMC	blood vessel:	n/a
50	chr7:70359655-70359705	RPTEC	kidney:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
2	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
3	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
4	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
5	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
6	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
7	chr7:70574285..70576318-chr7:70581134..70583277,2	K562	blood:
8	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
9	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
10	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
11	chr7:70472764..70475068-chr7:70478258..70480877,2	K562	blood:
12	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
13	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
14	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
15	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
16	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
17	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
18	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
19	chr7:70574285..70576318-chr7:70581134..70583277,2	K562	blood:
20	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
21	chr7:70472764..70475068-chr7:70478258..70480877,2	K562	blood:
22	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
23	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
24	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
25	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
26	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AUTS2-3	chr7:70302724-70302999	NONHSAT121342

No data

Variant related genes	Relation type
WBSCR17	TF binding region
ENSG00000236978	TF binding region
WBSCR17	CpG island
ENSG00000236978	CpG island

Extended variants
information (count: 8276 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:8276 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12698946	chr7:70301346-70301347	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149991347	chr7:70301501-70301502	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs190443200	chr7:70301530-70301531	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs182770261	chr7:70301535-70301536	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs568436462	chr7:70301553-70301554	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs576266958	chr7:70301558-70301559	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs145183915	chr7:70301595-70301596	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs148914329	chr7:70301606-70301607	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs536792085	chr7:70301643-70301644	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs558514935	chr7:70301665-70301666	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs35343508	chr7:70301666-70301667	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs13232813	chr7:70301667-70301668	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs553273425	chr7:70301688-70301689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187570779	chr7:70301714-70301715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542027923	chr7:70301716-70301717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142688670	chr7:70301717-70301718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147615962	chr7:70301741-70301742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564611309	chr7:70301774-70301775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191808773	chr7:70301796-70301797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs28658473	chr7:70301802-70301803	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182898235	chr7:70301862-70301863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529108779	chr7:70301864-70301865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529573038	chr7:70301872-70301873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550757517	chr7:70301882-70301883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187558516	chr7:70301888-70301889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561513163	chr7:70301893-70301894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533582385	chr7:70301901-70301902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142129071	chr7:70301904-70301905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547668495	chr7:70301945-70301946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570545821	chr7:70301987-70301988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79113089	chr7:70301994-70301995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs28499173	chr7:70301997-70301998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376802228	chr7:70302037-70302038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559957468	chr7:70302039-70302040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568363076	chr7:70302081-70302082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543025875	chr7:70302111-70302112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28610179	chr7:70302112-70302113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs374197986	chr7:70302139-70302140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539642424	chr7:70302142-70302143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532719803	chr7:70302144-70302145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557937290	chr7:70302168-70302169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573322230	chr7:70302172-70302173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540212690	chr7:70302192-70302193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145890460	chr7:70302255-70302256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573983401	chr7:70302351-70302352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544463141	chr7:70302366-70302367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563198349	chr7:70302375-70302376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533334533	chr7:70302377-70302378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549135688	chr7:70302401-70302402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551963456	chr7:70302438-70302439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Wilms tumour	21544195	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
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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70295400-70301800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:70301200-70312200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:70301200-70314200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:70301400-70302000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr7:70301800-70302000	Enhancers	H9 Cell Line	embryonic stem cell
6	chr7:70303000-70303600	Enhancers	Esophagus	oesophagus
7	chr7:70303200-70303800	Enhancers	HepG2	liver
8	chr7:70310400-70310600	Active TSS	HSMM	muscle
9	chr7:70310600-70310800	Flanking Active TSS	HSMM	muscle
10	chr7:70314200-70315000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:70314200-70315000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:70315000-70321600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr7:70316000-70316800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr7:70316800-70321600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr7:70319400-70320000	Enhancers	Fetal Stomach	stomach
16	chr7:70319800-70320400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr7:70320200-70320400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:70320400-70320600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:70320400-70321200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr7:70320600-70321600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:70320600-70321800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:70321200-70323600	Enhancers	H9 Cell Line	embryonic stem cell
23	chr7:70321400-70322000	Enhancers	Fetal Muscle Trunk	muscle
24	chr7:70321400-70322200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr7:70321400-70322800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:70321400-70325000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:70321600-70322000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:70321600-70322000	Enhancers	Placenta	Placenta
29	chr7:70321600-70322000	Bivalent Enhancer	Fetal Stomach	stomach
30	chr7:70321600-70322400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr7:70321600-70323400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:70321600-70323400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr7:70321600-70323600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:70321800-70322800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:70322000-70322200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:70322000-70322800	Enhancers	Fetal Stomach	stomach
37	chr7:70322200-70322800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr7:70322200-70322800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr7:70322200-70323400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr7:70322400-70322800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr7:70322400-70322800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:70322800-70323000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:70322800-70323400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:70322800-70323400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:70322800-70323600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr7:70322800-70323600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:70323000-70323400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr7:70323400-70323800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:70323400-70323800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr7:70323400-70324200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links