Variant report

Variant	nsv608317
Chromosome Location	chr7:118958980-119133195
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	BACH1	chr7:119122299-119123000	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr7:119122424-119122604	GM12878	blood:	n/a	n/a
3	CEBPB	chr7:119078390-119078544	K562	blood:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
4	CEBPB	chr7:119112731-119113061	K562	blood:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
5	CEBPB	chr7:118997442-118997653	A549	lung:	n/a	n/a
6	CEBPB	chr7:119024371-119024597	K562	blood:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
7	CEBPB	chr7:119024379-119024647	IMR90	lung:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
8	CEBPB	chr7:119005301-119005424	A549	lung:	n/a	n/a
9	CEBPB	chr7:119112634-119113091	HepG2	liver:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
10	CEBPB	chr7:119024356-119024693	HepG2	liver:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
11	CEBPB	chr7:119112723-119113013	A549	lung:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
12	CEBPB	chr7:119112798-119112948	HepG2	liver:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
13	CEBPB	chr7:118997471-118997594	K562	blood:	n/a	n/a
14	CEBPB	chr7:119043095-119043321	HepG2	liver:	n/a	chr7:119043190-119043203 chr7:119043190-119043201 chr7:119043192-119043203 chr7:119043190-119043203
15	CEBPB	chr7:119112736-119113039	H1-hESC	embryonic stem cell:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
16	CEBPB	chr7:118981917-118982143	HepG2	liver:	n/a	chr7:118981977-118981988 chr7:118982054-118982065
17	CEBPB	chr7:119112687-119113157	MCF-7	breast:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
18	CEBPB	chr7:119055965-119055997	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:119112600-119113033	HCT-116	colon:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
20	CEBPB	chr7:118974488-118974690	HepG2	liver:	n/a	chr7:118974654-118974665
21	CEBPB	chr7:119078338-119078628	A549	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
22	CEBPB	chr7:119112667-119113038	MCF-7	breast:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
23	CEBPB	chr7:119024394-119024680	A549	lung:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
24	CEBPB	chr7:119043069-119043327	IMR90	lung:	n/a	chr7:119043190-119043203 chr7:119043190-119043201 chr7:119043192-119043203 chr7:119043190-119043203
25	CEBPB	chr7:118990943-118991254	HepG2	liver:	n/a	chr7:118991067-118991078
26	CEBPB	chr7:119112604-119113132	HCT-116	colon:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
27	CEBPB	chr7:119078392-119078635	IMR90	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
28	CEBPB	chr7:119078319-119078656	HepG2	liver:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
29	CEBPB	chr7:119112728-119113065	IMR90	lung:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
30	CHD1	chr7:119083449-119083466	GM12878	blood:	n/a	n/a
31	CTCF	chr7:119122380-119122530	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr7:118960480-118960630	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr7:119122400-119122550	RPTEC	kidney:	n/a	n/a
34	CTCF	chr7:119069048-119069085	GM13977	blood:	n/a	n/a
35	CTCF	chr7:119122220-119122370	WI-38	lung:	n/a	n/a
36	CTCF	chr7:118960440-118960590	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr7:118960400-118960550	HCT-116	colon:	n/a	n/a
38	CTCF	chr7:118960477-118960631	Gliobla	brain:	n/a	n/a
39	CTCF	chr7:119122129-119122669	A549	lung:	n/a	n/a
40	CTCF	chr7:119122420-119122570	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr7:119122109-119122209	Gliobla	brain:	n/a	n/a
42	CTCF	chr7:119122299-119122550	K562	blood:	n/a	n/a
43	CTCF	chr7:119122380-119122530	GM12871	blood:	n/a	n/a
44	CTCF	chr7:118960420-118960570	HMEC	breast:	n/a	n/a
45	CTCF	chr7:119122348-119122540	GM12891	blood:	n/a	n/a
46	CTCF	chr7:119122380-119122530	AG04450	lung:	n/a	n/a
47	CTCF	chr7:119122340-119122490	HRE	kidney:	n/a	n/a
48	CTCF	chr7:119122298-119122617	K562	blood:	n/a	n/a
49	CTCF	chr7:119122419-119122540	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr7:119122335-119122565	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119121235-119121285	IMR90	lung:	fetal
2	chr7:119121235-119121285	ECC-1	luminal epithelium:	n/a
3	chr7:119121235-119121285	CMK	blood:	n/a
4	chr7:119121235-119121285	GM19239	blood:	n/a
5	chr7:119121235-119121285	HRCEpiC	kidney:	n/a
6	chr7:119121235-119121285	HCPEpiC	choroid plexus:	n/a
7	chr7:119121235-119121285	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:119121235-119121285	HEEpiC	esophagus:	n/a
9	chr7:119121235-119121285	HRPEpiC	eye:	n/a
10	chr7:119121235-119121285	Hepatocyte	liver:	n/a
11	chr7:119121235-119121285	BE2_C	brain:	n/a
12	chr7:119121235-119121285	HL-60	blood:	n/a
13	chr7:119121235-119121285	Caco-2	colon:	n/a
14	chr7:119121235-119121285	ProgFib	skin:	n/a
15	chr7:119121235-119121285	GM12892	blood:	n/a
16	chr7:119121235-119121285	NT2-D1	testis:	n/a
17	chr7:119121235-119121285	Hela-S3	cervix:	n/a
18	chr7:119121235-119121285	K562	blood:	n/a
19	chr7:119121235-119121285	AoSMC	blood vessel:	n/a
20	chr7:119121235-119121285	LNCaP	prostate:	n/a
21	chr7:119121235-119121285	A549	lung:	n/a
22	chr7:119121235-119121285	AG10803	skin:	n/a
23	chr7:119121235-119121285	HCT-116	colon:	n/a
24	chr7:119121235-119121285	PrEC	prostate:	n/a
25	chr7:119121235-119121285	HCM	heart:	n/a
26	chr7:119121235-119121285	RPTEC	kidney:	n/a
27	chr7:119121235-119121285	HIPEpiC	eye:	n/a
28	chr7:119121235-119121285	HNPCEpiC	eye:	n/a
29	chr7:119121235-119121285	SK-N-SH	brain:	n/a
30	chr7:119121235-119121285	HEK293	kidney:	embryo
31	chr7:119121235-119121285	NH-A	brain:	n/a
32	chr7:119121235-119121285	SK-N-SH_RA	brain:	n/a
33	chr7:119121235-119121285	T-47D	breast:	n/a
34	chr7:119121235-119121285	NHBE	bronchial:	n/a
35	chr7:119121235-119121285	HCF	heart:	n/a
36	chr7:119121235-119121285	NHDF-neo	bronchial:	n/a
37	chr7:119121235-119121285	NB4	blood:	n/a
38	chr7:119121235-119121285	AG04450	lung:	fetal
39	chr7:119121235-119121285	GM12891	blood:	n/a
40	chr7:119121235-119121285	AG04449	skin:	fetal
41	chr7:119121235-119121285	MCF10A-Er-Src	breast:	n/a
42	chr7:119121235-119121285	ovcar-3	ovarian:	n/a
43	chr7:119121235-119121285	BJ	skin:	n/a
44	chr7:119121235-119121285	H1-hESC	embryonic stem cell:	embryo
45	chr7:119121235-119121285	HRE	kidney:	n/a
46	chr7:119121235-119121285	HMEC	breast:	n/a
47	chr7:119121235-119121285	SK-N-MC	brain:	n/a
48	chr7:119121235-119121285	HepG2	liver:	n/a
49	chr7:119121235-119121285	MCF-7	breast:	n/a
50	chr7:119121235-119121285	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
2	chr7:119057102..119059266-chr7:119065046..119067833,2	K562	blood:
3	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:
4	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
5	chr2:32036680..32037459-chr7:119025565..119026383,2	MCF-7	breast:
6	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
7	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:
8	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
9	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
10	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
11	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
12	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
13	chr7:119057102..119059266-chr7:119065046..119067833,2	K562	blood:
14	chr7:119055228..119059267-chr7:119060829..119064124,3	K562	blood:
15	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
16	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
17	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
18	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
19	chr7:119055228..119059267-chr7:119060829..119064124,3	K562	blood:
20	chr7:119090628..119092465-chr7:119234986..119236766,2	K562	blood:
21	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
22	chr7:118997927..118999902-chr7:119000028..119001713,2	K562	blood:
23	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
24	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
25	chr7:118997927..118999902-chr7:119000028..119001713,2	K562	blood:

Variant related genes	Relation type
ENSG00000263692	TF binding region
ENSG00000263692	CpG island

Extended variants
information (count: 700 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199964686	chr7:118965064-118965065	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs376402585	chr7:118965072-118965073	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs181871282	chr7:118965106-118965107	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs186426957	chr7:118965287-118965288	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545794985	chr7:118965292-118965293	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs147432237	chr7:118965347-118965348	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs576143409	chr7:118965365-118965366	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs140686922	chr7:118965366-118965367	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs201247182	chr7:118970615-118970616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201858999	chr7:118970617-118970618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs77217402	chr7:118970627-118970628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530223963	chr7:118970659-118970660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184277941	chr7:118970664-118970665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140110559	chr7:118970667-118970668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574740490	chr7:118970675-118970676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548935544	chr7:118970683-118970684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35509297	chr7:118970707-118970708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540763803	chr7:118970740-118970741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143833551	chr7:118970750-118970751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190343112	chr7:118970765-118970766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546010420	chr7:118970767-118970768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193093614	chr7:118970800-118970801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531918057	chr7:118970806-118970807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537715363	chr7:118970817-118970818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79011342	chr7:118970847-118970848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567292983	chr7:118970868-118970869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185846556	chr7:118970880-118970881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146871357	chr7:118970884-118970885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566593324	chr7:118970899-118970900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140460955	chr7:118970900-118970901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555360643	chr7:118970901-118970902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538703578	chr7:118970970-118970971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73207712	chr7:118970971-118970972	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557651685	chr7:118981601-118981602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6967617	chr7:118981618-118981619	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543349596	chr7:118981619-118981620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563742819	chr7:118981637-118981638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529314866	chr7:118981649-118981650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141050176	chr7:118981650-118981651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559909792	chr7:118981684-118981685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528563195	chr7:118981691-118981692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551987646	chr7:118981714-118981715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192872868	chr7:118981732-118981733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150883945	chr7:118981753-118981754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531286760	chr7:118981758-118981759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550997917	chr7:118981765-118981766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184934621	chr7:118981790-118981791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188778468	chr7:118981799-118981800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554906985	chr7:118981844-118981845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569810720	chr7:118981864-118981865	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118965000-118965200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:118965200-118965400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:118970600-118971000	Enhancers	Brain Substantia Nigra	brain
4	chr7:118981600-118984200	Enhancers	Liver	Liver
5	chr7:118990400-118990800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:118991400-118991600	Enhancers	Liver	Liver
7	chr7:118991400-118991600	ZNF genes & repeats	Esophagus	oesophagus
8	chr7:118992200-118992400	Enhancers	Liver	Liver
9	chr7:118996800-118997200	Active TSS	Gastric	stomach
10	chr7:119034600-119034800	Active TSS	Liver	Liver
11	chr7:119034800-119035400	Flanking Active TSS	Liver	Liver
12	chr7:119035400-119035600	Active TSS	Liver	Liver
13	chr7:119035600-119037200	Weak transcription	Liver	Liver
14	chr7:119037200-119037600	Enhancers	Liver	Liver
15	chr7:119037200-119037600	Enhancers	GM12878-XiMat	blood
16	chr7:119044000-119046800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:119044800-119045000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:119048200-119048800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:119048200-119049400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr7:119061600-119062200	Enhancers	Liver	Liver
21	chr7:119089600-119090000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:119112400-119112600	Active TSS	Liver	Liver
23	chr7:119112400-119112600	Enhancers	Fetal Intestine Large	intestine
24	chr7:119112400-119112800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr7:119112600-119112800	Flanking Active TSS	Liver	Liver
26	chr7:119112600-119112800	Enhancers	Pancreas	Pancrea
27	chr7:119112600-119113000	Flanking Active TSS	Fetal Intestine Large	intestine
28	chr7:119112600-119113000	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr7:119112800-119113000	Enhancers	Liver	Liver
30	chr7:119113000-119113200	Enhancers	Fetal Intestine Large	intestine
31	chr7:119117600-119118000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:119118000-119122200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr7:119120800-119121200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:119122000-119122400	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr7:119122000-119122400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:119122000-119123000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr7:119122000-119123600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr7:119122200-119122400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr7:119122200-119122800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr7:119122200-119123000	Enhancers	H9 Cell Line	embryonic stem cell
41	chr7:119122200-119123000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr7:119122200-119123000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:119122200-119123000	Enhancers	Liver	Liver
44	chr7:119122200-119123200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr7:119123000-119123400	Weak transcription	H9 Cell Line	embryonic stem cell

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