Variant report

Variant	nsv889109
Chromosome Location	chr7:119068130-119177670
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	CCNT2	chr7:119174992-119175057	K562	blood:	n/a	n/a
4	CEBPB	chr7:119152429-119152660	HepG2	liver:	n/a	chr7:119152514-119152525
5	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
6	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
7	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
8	CEBPB	chr7:119139694-119139733	K562	blood:	n/a	chr7:119139713-119139722
9	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
10	CEBPB	chr7:119078338-119078628	A549	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
11	CEBPB	chr7:119078319-119078656	HepG2	liver:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
12	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
13	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
14	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
15	CEBPB	chr7:119158599-119158739	HepG2	liver:	n/a	chr7:119158656-119158667
16	CEBPB	chr7:119078392-119078635	IMR90	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
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	chr7:119112731-119113061	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
19	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
20	CEBPB	chr7:119078390-119078544	K562	blood:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
21	CHD1	chr7:119083449-119083466	GM12878	blood:	n/a	n/a
22	CTCF	chr7:119122340-119122490	HRE	kidney:	n/a	n/a
23	CTCF	chr7:119122170-119122608	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:119122392-119122532	NHEK	skin:	n/a	n/a
25	CTCF	chr7:119122400-119122550	GM12870	blood:	n/a	n/a
26	CTCF	chr7:119122400-119122550	HMF	breast:	n/a	n/a
27	CTCF	chr7:119141241-119141291	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:119122379-119122568	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr7:119069048-119069085	GM13977	blood:	n/a	n/a
30	CTCF	chr7:119168511-119168565	GM13976	blood:	n/a	n/a
31	CTCF	chr7:119122374-119122574	LNCaP	prostate:	n/a	n/a
32	CTCF	chr7:119122400-119122550	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr7:119122420-119122570	GM12869	blood:	n/a	n/a
34	CTCF	chr7:119122360-119122510	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr7:119122360-119122510	K562	blood:	n/a	n/a
36	CTCF	chr7:119122197-119122650	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr7:119122420-119122570	A549	lung:	n/a	n/a
38	CTCF	chr7:119122420-119122570	GM12875	blood:	n/a	n/a
39	CTCF	chr7:119122350-119122525	GM19238	blood:	n/a	n/a
40	CTCF	chr7:119122440-119122590	HEK293	kidney:	n/a	n/a
41	CTCF	chr7:119122420-119122570	HCM	heart:	n/a	n/a
42	CTCF	chr7:119122388-119122569	HepG2	liver:	n/a	n/a
43	CTCF	chr7:119122340-119122552	ProgFib	skin:	n/a	n/a
44	CTCF	chr7:119122100-119122250	GM12871	blood:	n/a	n/a
45	CTCF	chr7:119122320-119122470	GM12875	blood:	n/a	n/a
46	CTCF	chr7:119122220-119122370	WI-38	lung:	n/a	n/a
47	CTCF	chr7:119122239-119122670	K562	blood:	n/a	n/a
48	CTCF	chr7:119122364-119122549	A549	lung:	n/a	n/a
49	CTCF	chr7:119122380-119122530	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:119122321-119122544	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119121235-119121285	NHBE	bronchial:	n/a
2	chr7:119175916-119175966	K562	blood:	n/a
3	chr7:119175916-119175966	AoSMC	blood vessel:	n/a
4	chr7:119121235-119121285	PANC-1	pancreas:	n/a
5	chr7:119175916-119175966	HUVEC	blood vessel:	n/a
6	chr7:119121235-119121285	NHDF-neo	bronchial:	n/a
7	chr7:119121235-119121285	HEK293	kidney:	embryo
8	chr7:119121235-119121285	Hela-S3	cervix:	n/a
9	chr7:119175916-119175966	NT2-D1	testis:	n/a
10	chr7:119175916-119175966	HMEC	breast:	n/a
11	chr7:119121235-119121285	HEEpiC	esophagus:	n/a
12	chr7:119175916-119175966	U87	brain:	n/a
13	chr7:119175916-119175966	GM12892	blood:	n/a
14	chr7:119175916-119175966	RPTEC	kidney:	n/a
15	chr7:119175916-119175966	MCF-7	breast:	n/a
16	chr7:119121235-119121285	BE2_C	brain:	n/a
17	chr7:119175916-119175966	HRCEpiC	kidney:	n/a
18	chr7:119121235-119121285	CMK	blood:	n/a
19	chr7:119175916-119175966	NH-A	brain:	n/a
20	chr7:119121235-119121285	GM12878	blood:	n/a
21	chr7:119175916-119175966	Hela-S3	cervix:	n/a
22	chr7:119175916-119175966	BE2_C	brain:	n/a
23	chr7:119121235-119121285	HepG2	liver:	n/a
24	chr7:119121235-119121285	SK-N-SH	brain:	n/a
25	chr7:119175916-119175966	SK-N-SH	brain:	n/a
26	chr7:119121235-119121285	RPTEC	kidney:	n/a
27	chr7:119175916-119175966	HRPEpiC	eye:	n/a
28	chr7:119175916-119175966	H1-hESC	embryonic stem cell:	embryo
29	chr7:119175916-119175966	HCPEpiC	choroid plexus:	n/a
30	chr7:119175916-119175966	ProgFib	skin:	n/a
31	chr7:119175916-119175966	HCT-116	colon:	n/a
32	chr7:119121235-119121285	SKMC	muscle:	n/a
33	chr7:119175916-119175966	GM06990	blood:	n/a
34	chr7:119121235-119121285	HRCEpiC	kidney:	n/a
35	chr7:119121235-119121285	HRE	kidney:	n/a
36	chr7:119175916-119175966	IMR90	lung:	fetal
37	chr7:119175916-119175966	HCF	heart:	n/a
38	chr7:119175916-119175966	HNPCEpiC	eye:	n/a
39	chr7:119121235-119121285	K562	blood:	n/a
40	chr7:119175916-119175966	Jurkat	blood:	n/a
41	chr7:119121235-119121285	ovcar-3	ovarian:	n/a
42	chr7:119175916-119175966	LNCaP	prostate:	n/a
43	chr7:119175916-119175966	PrEC	prostate:	n/a
44	chr7:119121235-119121285	U87	brain:	n/a
45	chr7:119175916-119175966	HEEpiC	esophagus:	n/a
46	chr7:119175916-119175966	SK-N-MC	brain:	n/a
47	chr7:119121235-119121285	HNPCEpiC	eye:	n/a
48	chr7:119121235-119121285	Jurkat	blood:	n/a
49	chr7:119121235-119121285	HRPEpiC	eye:	n/a
50	chr7:119175916-119175966	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
2	chr7:119171216..119174031-chr7:119180101..119182290,2	K562	blood:
3	chr6:81998528..81999232-chr7:119153061..119154054,2	MCF-7	breast:
4	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
5	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
6	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
7	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
8	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
9	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
10	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
11	chr7:119090628..119092465-chr7:119234986..119236766,2	K562	blood:
12	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
13	chr7:119174664..119177243-chr7:119179086..119181541,2	K562	blood:
14	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
15	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:
16	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
17	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
18	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
19	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:
20	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
21	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
22	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:

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

Extended variants
information (count: 459 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571113749	chr7:119089672-119089673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs377381372	chr7:119089683-119089684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533487715	chr7:119089692-119089693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574356491	chr7:119089700-119089701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148398526	chr7:119089720-119089721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570282837	chr7:119089727-119089728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537904740	chr7:119089732-119089733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554713096	chr7:119089734-119089735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11973668	chr7:119089749-119089750	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs376328913	chr7:119089784-119089785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190206655	chr7:119089812-119089813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370255841	chr7:119089851-119089852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373467490	chr7:119089864-119089865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553528759	chr7:119089865-119089866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559445694	chr7:119089908-119089909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182827057	chr7:119089923-119089924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142532201	chr7:119089958-119089959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555913696	chr7:119089963-119089964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150955910	chr7:119089966-119089967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557232637	chr7:119089987-119089988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561635739	chr7:119112436-119112437	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs527594623	chr7:119112445-119112446	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs139321573	chr7:119112456-119112457	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs570626315	chr7:119112524-119112525	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs184199177	chr7:119112547-119112548	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs144134676	chr7:119112566-119112567	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs28433446	chr7:119112584-119112585	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs113700143	chr7:119112601-119112602	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555832314	chr7:119112684-119112685	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs572750170	chr7:119112718-119112719	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs188517848	chr7:119112725-119112726	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs139244599	chr7:119112731-119112732	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs539033792	chr7:119112733-119112734	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs114321934	chr7:119112745-119112746	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs1385376	chr7:119112784-119112785	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs149995922	chr7:119112865-119112866	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs372428381	chr7:119112876-119112877	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs555770575	chr7:119112974-119112975	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs113508097	chr7:119112989-119112990	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs112874748	chr7:119113003-119113004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192942183	chr7:119113010-119113011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564008156	chr7:119113058-119113059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374229996	chr7:119113069-119113070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570949720	chr7:119113095-119113096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575705689	chr7:119113107-119113108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377274073	chr7:119113111-119113112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185434619	chr7:119113119-119113120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190355447	chr7:119113123-119113124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs192339449	chr7:119117698-119117699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532857600	chr7:119117725-119117726	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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	22037309	CNVD
Cancer	20164919	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119089600-119090000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:119112400-119112600	Active TSS	Liver	Liver
3	chr7:119112400-119112600	Enhancers	Fetal Intestine Large	intestine
4	chr7:119112400-119112800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:119112600-119112800	Flanking Active TSS	Liver	Liver
6	chr7:119112600-119112800	Enhancers	Pancreas	Pancrea
7	chr7:119112600-119113000	Flanking Active TSS	Fetal Intestine Large	intestine
8	chr7:119112600-119113000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr7:119112800-119113000	Enhancers	Liver	Liver
10	chr7:119113000-119113200	Enhancers	Fetal Intestine Large	intestine
11	chr7:119117600-119118000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr7:119118000-119122200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:119120800-119121200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:119122000-119122400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:119122000-119122400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:119122000-119123000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:119122000-119123600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:119122200-119122400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:119122200-119122800	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr7:119122200-119123000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr7:119122200-119123000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr7:119122200-119123000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr7:119122200-119123000	Enhancers	Liver	Liver
24	chr7:119122200-119123200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:119123000-119123400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr7:119133400-119134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:119134400-119135400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:119135400-119135800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:119154400-119155600	Enhancers	Liver	Liver
30	chr7:119173400-119175200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr7:119174600-119174800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr7:119174800-119175400	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr7:119174800-119175800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:119175200-119175600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr7:119175400-119176000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:119175600-119176000	Enhancers	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links