Variant report

Variant	nsv546850
Chromosome Location	chr1:94479468-94485277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:94480375-94480974	K562	blood:	n/a	n/a
2	ATF1	chr1:94484900-94485186	K562	blood:	n/a	n/a
3	ATF3	chr1:94480451-94481047	K562	blood:	n/a	chr1:94480831-94480844
4	BHLHE40	chr1:94480403-94481020	K562	blood:	n/a	n/a
5	CCNT2	chr1:94480621-94480980	K562	blood:	n/a	n/a
6	CEBPB	chr1:94480798-94480855	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:94480617-94481004	K562	blood:	n/a	n/a
8	CEBPB	chr1:94480674-94481019	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:94480675-94481016	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:94480557-94481142	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:94480751-94480965	K562	blood:	n/a	n/a
12	CEBPB	chr1:94480617-94481031	K562	blood:	n/a	n/a
13	CTCF	chr1:94482000-94482150	GM12874	blood:	n/a	n/a
14	E2F4	chr1:94480802-94480895	MCF10A-Er-Src	breast:	n/a	n/a
15	EP300	chr1:94480659-94480945	Hela-S3	cervix:	n/a	chr1:94480847-94480854
16	EP300	chr1:94480415-94481299	K562	blood:	n/a	chr1:94480847-94480854
17	FOS	chr1:94483173-94483333	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr1:94483028-94483292	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr1:94480747-94480890	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr1:94483027-94483348	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr1:94480775-94480927	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr1:94480858-94480922	MCF10A-Er-Src	breast:	n/a	n/a
23	HCFC1	chr1:94480606-94480978	K562	blood:	n/a	n/a
24	HEY1	chr1:94480204-94480640	K562	blood:	n/a	n/a
25	JUN	chr1:94480404-94481071	K562	blood:	n/a	n/a
26	JUN	chr1:94480267-94481683	K562	blood:	n/a	n/a
27	JUND	chr1:94480385-94481426	K562	blood:	n/a	n/a
28	JUND	chr1:94483057-94483335	K562	blood:	n/a	n/a
29	JUND	chr1:94485085-94485244	K562	blood:	n/a	n/a
30	KAP1	chr1:94480567-94480880	U2OS	brain:	n/a	n/a
31	MAFK	chr1:94480470-94480971	K562	blood:	n/a	chr1:94480864-94480874
32	MAX	chr1:94480652-94480962	Hela-S3	cervix:	n/a	chr1:94480833-94480842
33	MAX	chr1:94483620-94483649	NB4	blood:	n/a	n/a
34	MAX	chr1:94480435-94481273	K562	blood:	n/a	chr1:94480833-94480842
35	MAX	chr1:94483068-94483297	K562	blood:	n/a	n/a
36	MAZ	chr1:94484970-94485293	K562	blood:	n/a	n/a
37	MAZ	chr1:94480408-94481254	K562	blood:	n/a	chr1:94480833-94480842
38	MYC	chr1:94480553-94481031	K562	blood:	n/a	chr1:94480833-94480842
39	MYC	chr1:94480574-94480994	K562	blood:	n/a	chr1:94480833-94480842
40	MYC	chr1:94480310-94481202	K562	blood:	n/a	chr1:94480833-94480842
41	PML	chr1:94480258-94480635	K562	blood:	n/a	n/a
42	POLR2A	chr1:94480722-94481092	HCT-116	colon:	n/a	n/a
43	POLR2A	chr1:94480948-94480958	K562	blood:	n/a	n/a
44	RCOR1	chr1:94485052-94485358	K562	blood:	n/a	n/a
45	RCOR1	chr1:94479906-94481335	K562	blood:	n/a	n/a
46	STAT3	chr1:94483986-94484056	MCF10A-Er-Src	breast:	n/a	n/a
47	TBL1XR1	chr1:94480624-94481045	K562	blood:	n/a	n/a
48	TBL1XR1	chr1:94480296-94480300	K562	blood:	n/a	n/a
49	TEAD4	chr1:94480617-94481058	K562	blood:	n/a	n/a
50	ZMIZ1	chr1:94480225-94481114	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94483746-94483796	HMEC	breast:	n/a
2	chr1:94483746-94483796	HCT-116	colon:	n/a
3	chr1:94483746-94483796	HRPEpiC	eye:	n/a
4	chr1:94483746-94483796	U87	brain:	n/a
5	chr1:94483746-94483796	HRE	kidney:	n/a
6	chr1:94483746-94483796	ProgFib	skin:	n/a
7	chr1:94483746-94483796	BE2_C	brain:	n/a
8	chr1:94483746-94483796	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:94483746-94483796	NH-A	brain:	n/a
10	chr1:94483746-94483796	SAEC	small airway:	n/a
11	chr1:94483746-94483796	T-47D	breast:	n/a
12	chr1:94483746-94483796	NHDF-neo	bronchial:	n/a
13	chr1:94483746-94483796	HUVEC	blood vessel:	n/a
14	chr1:94483746-94483796	ECC-1	luminal epithelium:	n/a
15	chr1:94483746-94483796	NHBE	bronchial:	n/a
16	chr1:94483746-94483796	Jurkat	blood:	n/a
17	chr1:94483746-94483796	H1-hESC	embryonic stem cell:	embryo
18	chr1:94483746-94483796	Caco-2	colon:	n/a
19	chr1:94483746-94483796	A549	lung:	n/a
20	chr1:94483746-94483796	GM06990	blood:	n/a
21	chr1:94483746-94483796	RPTEC	kidney:	n/a
22	chr1:94483746-94483796	K562	blood:	n/a
23	chr1:94483746-94483796	SK-N-SH	brain:	n/a
24	chr1:94483746-94483796	AG09319	gingival:	n/a
25	chr1:94483746-94483796	SKMC	muscle:	n/a
26	chr1:94483746-94483796	HL-60	blood:	n/a
27	chr1:94483746-94483796	AG04449	skin:	fetal
28	chr1:94483746-94483796	GM12892	blood:	n/a
29	chr1:94483746-94483796	SK-N-SH_RA	brain:	n/a
30	chr1:94483746-94483796	HRCEpiC	kidney:	n/a
31	chr1:94483746-94483796	AG10803	skin:	n/a
32	chr1:94483746-94483796	PANC-1	pancreas:	n/a
33	chr1:94483746-94483796	HCM	heart:	n/a
34	chr1:94483746-94483796	BJ	skin:	n/a
35	chr1:94483746-94483796	ovcar-3	ovarian:	n/a
36	chr1:94483746-94483796	HIPEpiC	eye:	n/a
37	chr1:94483746-94483796	Hela-S3	cervix:	n/a
38	chr1:94483746-94483796	GM12891	blood:	n/a
39	chr1:94483746-94483796	GM12878	blood:	n/a
40	chr1:94483746-94483796	HEK293	kidney:	embryo
41	chr1:94483746-94483796	PFSK-1	brain:	n/a
42	chr1:94483746-94483796	CMK	blood:	n/a
43	chr1:94483746-94483796	LNCaP	prostate:	n/a
44	chr1:94483746-94483796	MCF10A-Er-Src	breast:	n/a
45	chr1:94483746-94483796	HepG2	liver:	n/a
46	chr1:94483746-94483796	AoSMC	blood vessel:	n/a
47	chr1:94483746-94483796	IMR90	lung:	fetal
48	chr1:94483746-94483796	HNPCEpiC	eye:	n/a
49	chr1:94483746-94483796	GM19239	blood:	n/a
50	chr1:94483746-94483796	NT2-D1	testis:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:94474811..94477803-chr1:94479025..94480714,3	K562	blood:
2	chr1:94475934..94477619-chr1:94484327..94486550,2	K562	blood:
3	chr1:94478608..94480498-chr1:94484594..94486437,2	MCF-7	breast:
4	chr1:94474260..94476324-chr1:94481823..94483711,2	K562	blood:
5	chr1:94467932..94470358-chr1:94480661..94482981,2	K562	blood:
6	chr1:94471999..94474175-chr1:94483788..94486677,2	MCF-7	breast:
7	chr1:94372270..94376088-chr1:94480112..94484516,4	K562	blood:
8	chr1:94478608..94480498-chr1:94484594..94486437,2	MCF-7	breast:

No data

Variant related genes	Relation type
ABCA4	TF binding region
ABCA4	CpG island
ENSG00000198691	chromatin interactions
ENSG00000023909	chromatin interactions

Extended variants
information (count: 322 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12049183	chr1:94479468-94479469	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs61782239	chr1:94479483-94479484	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs373349053	chr1:94479500-94479501	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561023177	chr1:94479507-94479508	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs79929849	chr1:94479538-94479539	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376590641	chr1:94479575-94479576	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs191443064	chr1:94479579-94479580	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565044063	chr1:94479592-94479593	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs143779350	chr1:94479613-94479614	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs547498233	chr1:94479621-94479622	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565706043	chr1:94479692-94479693	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs12083701	chr1:94479725-94479726	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556537567	chr1:94479738-94479739	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549689061	chr1:94479749-94479750	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs386633543	chr1:94479751-94479752	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200072777	chr1:94479752-94479753	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs113594015	chr1:94479755-94479756	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs74636246	chr1:94479759-94479760	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs370813149	chr1:94479760-94479761	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs67492609	chr1:94479761-94479762	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538783098	chr1:94479767-94479768	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs553828934	chr1:94479807-94479808	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563360844	chr1:94479837-94479838	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs72958420	chr1:94479877-94479878	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs111535415	chr1:94479880-94479881	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576876234	chr1:94479903-94479904	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs143222183	chr1:94479920-94479921	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184754951	chr1:94479922-94479923	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs375415519	chr1:94479928-94479929	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs376691218	chr1:94479929-94479930	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373940998	chr1:94479930-94479931	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372109426	chr1:94479931-94479932	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs559631345	chr1:94479932-94479933	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561288527	chr1:94479962-94479963	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs375217676	chr1:94479993-94479994	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189526468	chr1:94480015-94480016	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs565109791	chr1:94480017-94480018	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs532321621	chr1:94480018-94480019	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs547559687	chr1:94480025-94480026	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs2275033	chr1:94480037-94480038	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
41	rs529750839	chr1:94480038-94480039	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201593377	chr1:94480060-94480061	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562309815	chr1:94480091-94480092	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371777196	chr1:94480096-94480097	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs61753030	chr1:94480098-94480099	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs62646875	chr1:94480100-94480101	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs1129480	chr1:94480108-94480109	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs61753029	chr1:94480146-94480147	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs569608594	chr1:94480150-94480151	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs202199507	chr1:94480153-94480154	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94471200-94480600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:94475400-94485600	Weak transcription	NH-A	brain
3	chr1:94476400-94480000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:94476600-94479600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr1:94476800-94480400	Enhancers	Fetal Intestine Large	intestine
6	chr1:94477000-94479800	Enhancers	Fetal Intestine Small	intestine
7	chr1:94477000-94481600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr1:94477200-94480400	Weak transcription	HMEC	breast
9	chr1:94477400-94479800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
10	chr1:94477400-94480000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr1:94477400-94480200	Enhancers	Brain Germinal Matrix	brain
12	chr1:94477800-94479800	Weak transcription	Spleen	Spleen
13	chr1:94478000-94479600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
14	chr1:94478000-94479800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
15	chr1:94478400-94479600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:94478400-94480000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
17	chr1:94478400-94480400	Weak transcription	Osteobl	bone
18	chr1:94478600-94480000	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr1:94478800-94479600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
20	chr1:94479000-94479600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr1:94479000-94479600	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr1:94479000-94480200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:94479000-94481600	Enhancers	K562	blood
24	chr1:94479200-94480200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:94479200-94484800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:94479400-94479600	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr1:94479400-94484800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:94479400-94484800	Weak transcription	Placenta	Placenta
29	chr1:94479400-94486000	Weak transcription	HSMM	muscle
30	chr1:94479600-94486200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr1:94479800-94480000	Enhancers	Spleen	Spleen
32	chr1:94479800-94489200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr1:94480000-94480200	Weak transcription	Spleen	Spleen
34	chr1:94480000-94480600	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr1:94480000-94480800	Enhancers	Fetal Muscle Leg	muscle
36	chr1:94480000-94484800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:94480200-94480600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:94480200-94481200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:94480200-94481400	Enhancers	NHDF-Ad	bronchial
40	chr1:94480400-94480800	Enhancers	HMEC	breast
41	chr1:94480400-94481000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr1:94480400-94481000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr1:94480400-94481200	Enhancers	Osteobl	bone
44	chr1:94480400-94481600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:94480400-94484800	Weak transcription	Fetal Intestine Large	intestine
46	chr1:94480600-94480800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:94480600-94481000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:94480600-94481000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:94480600-94481000	Enhancers	NHLF	lung
50	chr1:94480600-94482200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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