Variant report

Variant	nsv428503
Chromosome Location	chr7:70295677-70463201
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	ARID3A	chr7:70295432-70295731	HepG2	liver:	n/a	n/a
2	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
5	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70359196-70359849	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	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:70384908-70384986	K562	blood:	n/a	n/a
10	BCL11A	chr7:70359245-70359587	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
12	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
13	BHLHE40	chr7:70295491-70295711	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:70409678-70409872	HepG2	liver:	n/a	chr7:70409738-70409749
16	CEBPB	chr7:70299422-70299775	IMR90	lung:	n/a	chr7:70299603-70299614
17	CEBPB	chr7:70314283-70314959	H1-hESC	embryonic stem cell:	n/a	chr7:70314674-70314686
18	CEBPB	chr7:70359237-70359569	H1-hESC	embryonic stem cell:	n/a	chr7:70359363-70359375
19	CEBPB	chr7:70349310-70349766	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:70299521-70299730	H1-hESC	embryonic stem cell:	n/a	chr7:70299603-70299614
21	CEBPB	chr7:70443503-70443748	HepG2	liver:	n/a	chr7:70443649-70443660 chr7:70443597-70443608
22	CEBPB	chr7:70426416-70426613	K562	blood:	n/a	n/a
23	CEBPB	chr7:70295428-70295714	HepG2	liver:	n/a	chr7:70295552-70295563
24	CEBPB	chr7:70299453-70299778	A549	lung:	n/a	chr7:70299603-70299614
25	CEBPB	chr7:70299455-70299763	K562	blood:	n/a	chr7:70299603-70299614
26	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
27	CEBPB	chr7:70299440-70299798	HepG2	liver:	n/a	chr7:70299603-70299614
28	CEBPB	chr7:70295315-70295710	HepG2	liver:	n/a	chr7:70295552-70295563
29	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
30	CEBPB	chr7:70426400-70426506	A549	lung:	n/a	n/a
31	CEBPB	chr7:70388372-70388507	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPD	chr7:70437477-70438272	K562	blood:	n/a	n/a
33	CEBPD	chr7:70437707-70438104	K562	blood:	n/a	n/a
34	CHD1	chr7:70359526-70359680	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr7:70323263-70323459	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr7:70439933-70440263	K562	blood:	n/a	n/a
37	CHD2	chr7:70314201-70315062	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr7:70390387-70390729	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr7:70359101-70359582	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chr7:70349262-70350113	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr7:70359107-70360262	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr7:70322040-70322190	AG04449	skin:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
43	CTCF	chr7:70321960-70322217	A549	lung:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
44	CTCF	chr7:70321560-70321710	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr7:70322040-70322190	GM12873	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
46	CTCF	chr7:70321640-70321790	NHEK	skin:	n/a	n/a
47	CTCF	chr7:70321360-70321510	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr7:70322040-70322190	GM12867	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
49	CTCF	chr7:70321932-70322235	GM12878	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108
50	CTCF	chr7:70321893-70322482	K562	blood:	n/a	chr7:70322093-70322106 chr7:70322092-70322113 chr7:70322091-70322107 chr7:70322095-70322105 chr7:70322093-70322106 chr7:70322093-70322102 chr7:70322090-70322108

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70359655-70359705	HCT-116	colon:	n/a
2	chr7:70417419-70417469	MCF-7	breast:	n/a
3	chr7:70417419-70417469	H1-hESC	embryonic stem cell:	embryo
4	chr7:70311321-70311371	PANC-1	pancreas:	n/a
5	chr7:70322401-70322451	RPTEC	kidney:	n/a
6	chr7:70311321-70311371	HL-60	blood:	n/a
7	chr7:70417419-70417469	HL-60	blood:	n/a
8	chr7:70322401-70322451	Hela-S3	cervix:	n/a
9	chr7:70311321-70311371	MCF-7	breast:	n/a
10	chr7:70311435-70311485	ovcar-3	ovarian:	n/a
11	chr7:70322401-70322451	HCM	heart:	n/a
12	chr7:70359655-70359705	Hela-S3	cervix:	n/a
13	chr7:70311321-70311371	HCM	heart:	n/a
14	chr7:70417419-70417469	PANC-1	pancreas:	n/a
15	chr7:70311435-70311485	HL-60	blood:	n/a
16	chr7:70311321-70311371	HAEpiC	amniotic membrane:	n/a
17	chr7:70322401-70322451	HNPCEpiC	eye:	n/a
18	chr7:70359655-70359705	HCM	heart:	n/a
19	chr7:70311321-70311371	GM06990	blood:	n/a
20	chr7:70322401-70322451	ECC-1	luminal epithelium:	n/a
21	chr7:70322401-70322451	NHBE	bronchial:	n/a
22	chr7:70359655-70359705	A549	lung:	n/a
23	chr7:70417419-70417469	NT2-D1	testis:	n/a
24	chr7:70359655-70359705	NH-A	brain:	n/a
25	chr7:70311321-70311371	SAEC	small airway:	n/a
26	chr7:70311435-70311485	Jurkat	blood:	n/a
27	chr7:70311435-70311485	ProgFib	skin:	n/a
28	chr7:70322401-70322451	NHDF-neo	bronchial:	n/a
29	chr7:70311532-70311582	GM12892	blood:	n/a
30	chr7:70417419-70417469	GM19239	blood:	n/a
31	chr7:70417419-70417469	HAEpiC	amniotic membrane:	n/a
32	chr7:70322401-70322451	HRPEpiC	eye:	n/a
33	chr7:70311435-70311485	SK-N-SH	brain:	n/a
34	chr7:70311532-70311582	A549	lung:	n/a
35	chr7:70311532-70311582	GM12891	blood:	n/a
36	chr7:70359655-70359705	Jurkat	blood:	n/a
37	chr7:70311435-70311485	HUVEC	blood vessel:	n/a
38	chr7:70311435-70311485	PrEC	prostate:	n/a
39	chr7:70311321-70311371	HUVEC	blood vessel:	n/a
40	chr7:70417419-70417469	HMEC	breast:	n/a
41	chr7:70311532-70311582	HEEpiC	esophagus:	n/a
42	chr7:70359655-70359705	HUVEC	blood vessel:	n/a
43	chr7:70311435-70311485	HEEpiC	esophagus:	n/a
44	chr7:70417419-70417469	HUVEC	blood vessel:	n/a
45	chr7:70417419-70417469	HCM	heart:	n/a
46	chr7:70311532-70311582	PANC-1	pancreas:	n/a
47	chr7:70311321-70311371	NH-A	brain:	n/a
48	chr7:70359655-70359705	HRPEpiC	eye:	n/a
49	chr7:70417419-70417469	MCF10A-Er-Src	breast:	n/a
50	chr7:70417419-70417469	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
2	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
3	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
4	chr7:70462545..70464219-chr7:70469088..70471612,2	K562	blood:
5	chr7:70445361..70447643-chr7:70448432..70451410,2	K562	blood:
6	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
7	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
8	chr7:70419574..70421906-chr7:70424022..70425559,2	K562	blood:
9	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
10	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
11	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
12	chr7:70295507..70296249-chr7:71198004..71198896,2	MCF-7	breast:
13	chr7:70462461..70464194-chr7:70473424..70476009,2	K562	blood:
14	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
15	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
16	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
17	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
18	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
19	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
20	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
21	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:

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

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

Extended variants
information (count: 5450 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5450 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554201904	chr7:70295718-70295719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72173617	chr7:70295719-70295720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563587476	chr7:70295723-70295724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377620489	chr7:70295740-70295741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184367591	chr7:70295835-70295836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546044417	chr7:70295844-70295845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564572467	chr7:70295864-70295865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528613715	chr7:70295915-70295916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540600968	chr7:70295963-70295964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574264030	chr7:70295973-70295974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10950218	chr7:70295984-70295985	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs189492557	chr7:70296050-70296051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143510861	chr7:70296059-70296060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148015851	chr7:70296075-70296076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143511498	chr7:70296092-70296093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369539390	chr7:70296098-70296099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1105549	chr7:70296099-70296100	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs181890637	chr7:70296138-70296139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1105548	chr7:70296183-70296184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546521413	chr7:70296263-70296264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570509542	chr7:70296271-70296272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73172353	chr7:70296308-70296309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565301282	chr7:70296317-70296318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556853029	chr7:70296352-70296353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556997322	chr7:70296353-70296354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs59543989	chr7:70296356-70296357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs398005134	chr7:70296371-70296372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375959201	chr7:70296421-70296422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567926660	chr7:70296439-70296440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535448362	chr7:70296486-70296487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369732250	chr7:70296491-70296492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557267342	chr7:70296534-70296535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369891745	chr7:70296573-70296574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113614561	chr7:70296618-70296619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185489526	chr7:70296629-70296630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147150924	chr7:70296639-70296640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377498047	chr7:70296667-70296668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573285204	chr7:70296716-70296717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540412675	chr7:70296725-70296726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12698945	chr7:70296728-70296729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553319140	chr7:70296731-70296732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529203660	chr7:70296800-70296801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61052780	chr7:70296801-70296802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554416460	chr7:70296912-70296913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562806603	chr7:70296913-70296914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558004347	chr7:70296952-70296953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377735908	chr7:70296993-70296994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112402101	chr7:70297000-70297001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372414982	chr7:70297014-70297015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77751278	chr7:70297025-70297026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70294000-70296400	Enhancers	Liver	Liver
2	chr7:70294800-70298600	Weak transcription	NHEK	skin
3	chr7:70294800-70298600	Weak transcription	Osteobl	bone
4	chr7:70295000-70296600	Enhancers	HepG2	liver
5	chr7:70295000-70298400	Weak transcription	NH-A	brain
6	chr7:70295000-70298600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr7:70295200-70298600	Weak transcription	HSMM	muscle
8	chr7:70295400-70300200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr7:70295400-70301800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:70296000-70296400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:70298400-70298800	Enhancers	NH-A	brain
12	chr7:70298600-70298800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:70298600-70299000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr7:70298600-70299000	Enhancers	HSMM	muscle
15	chr7:70298600-70299000	Enhancers	NHEK	skin
16	chr7:70298600-70299000	Enhancers	Osteobl	bone
17	chr7:70298800-70299000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:70299000-70300000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:70299000-70300200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:70299200-70299600	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr7:70299400-70299600	Weak transcription	Liver	Liver
22	chr7:70299800-70300400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
23	chr7:70300200-70300800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:70300200-70301200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
25	chr7:70300800-70301000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:70300800-70301200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:70301200-70312200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:70301200-70314200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr7:70301400-70302000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr7:70301800-70302000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr7:70303000-70303600	Enhancers	Esophagus	oesophagus
32	chr7:70303200-70303800	Enhancers	HepG2	liver
33	chr7:70310400-70310600	Active TSS	HSMM	muscle
34	chr7:70310600-70310800	Flanking Active TSS	HSMM	muscle
35	chr7:70314200-70315000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr7:70314200-70315000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:70315000-70321600	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:70316000-70316800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
39	chr7:70316800-70321600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr7:70319400-70320000	Enhancers	Fetal Stomach	stomach
41	chr7:70319800-70320400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr7:70320200-70320400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr7:70320400-70320600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:70320400-70321200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr7:70320600-70321600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr7:70320600-70321800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:70321200-70323600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:70321400-70322000	Enhancers	Fetal Muscle Trunk	muscle
49	chr7:70321400-70322200	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr7:70321400-70322800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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