Variant report

Variant	esv1849256
Chromosome Location	chr1:242948712-243152920
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	chr1:243088083-243088303	K562	blood:	n/a	n/a
2	ATF1	chr1:243148543-243148578	K562	blood:	n/a	n/a
3	ATF2	chr1:242976778-242977056	GM12878	blood:	n/a	n/a
4	BACH1	chr1:242996994-242996997	K562	blood:	n/a	n/a
5	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
6	BCL11A	chr1:242976721-242977165	GM12878	blood:	n/a	chr1:242976959-242976968
7	BCL11A	chr1:242976760-242977140	GM12878	blood:	n/a	chr1:242976959-242976968
8	BHLHE40	chr1:242976782-242977230	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
10	BHLHE40	chr1:243031757-243031938	GM12878	blood:	n/a	n/a
11	BRCA1	chr1:242954012-242954043	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr1:242997383-242997489	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr1:243130209-243130606	K562	blood:	n/a	n/a
14	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
15	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
16	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
17	CCNT2	chr1:243129321-243129526	K562	blood:	n/a	n/a
18	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
19	CEBPB	chr1:242998985-242999533	A549	lung:	n/a	n/a
20	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
21	CEBPB	chr1:243148513-243148717	K562	blood:	n/a	n/a
22	CEBPB	chr1:243118303-243118616	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
23	CEBPB	chr1:243118344-243118540	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
24	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
25	CEBPB	chr1:243118288-243118578	Hela-S3	cervix:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
26	CEBPB	chr1:242955789-242955931	A549	lung:	n/a	n/a
27	CEBPB	chr1:243118268-243118571	HepG2	liver:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
28	CEBPB	chr1:243118300-243118585	A549	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
29	CEBPB	chr1:243118280-243118602	IMR90	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
30	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
31	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
32	CEBPB	chr1:242998320-242998357	HepG2	liver:	n/a	chr1:242998327-242998338
33	CEBPB	chr1:243118255-243118634	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
34	CEBPB	chr1:243088005-243088218	K562	blood:	n/a	n/a
35	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
36	CHD1	chr1:242976654-242977278	GM12878	blood:	n/a	n/a
37	CHD2	chr1:243087993-243088116	K562	blood:	n/a	n/a
38	CHD2	chr1:243005456-243005619	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr1:242976690-242977268	GM12878	blood:	n/a	n/a
40	CHD2	chr1:243080927-243080928	K562	blood:	n/a	n/a
41	CHD2	chr1:242991732-242991777	HepG2	liver:	n/a	n/a
42	CTCF	chr1:243100100-243100250	GM12871	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
43	CTCF	chr1:243100100-243100250	HMEC	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
44	CTCF	chr1:243100115-243100384	K562	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
45	CTCF	chr1:242991630-242991817	GM12878	blood:	n/a	chr1:242991719-242991740
46	CTCF	chr1:243098510-243098600	HepG2	liver:	n/a	chr1:243098556-243098577 chr1:243098554-243098572
47	CTCF	chr1:243099640-243099729	GM10248	blood:	n/a	n/a
48	CTCF	chr1:242991700-242991850	BE2_C	brain:	n/a	chr1:242991719-242991740
49	CTCF	chr1:242956780-242956930	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:243018120-243018158	GM10248	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243054071-243054121	Caco-2	colon:	n/a
2	chr1:243138527-243138577	SAEC	small airway:	n/a
3	chr1:243054071-243054121	HAEpiC	amniotic membrane:	n/a
4	chr1:243057080-243057130	AG04450	lung:	fetal
5	chr1:243054071-243054121	HRE	kidney:	n/a
6	chr1:243054071-243054121	PFSK-1	brain:	n/a
7	chr1:243053865-243053915	PANC-1	pancreas:	n/a
8	chr1:243053425-243053475	NH-A	brain:	n/a
9	chr1:243053865-243053915	A549	lung:	n/a
10	chr1:243138527-243138577	HRE	kidney:	n/a
11	chr1:243050875-243050925	SK-N-MC	brain:	n/a
12	chr1:243054071-243054121	Hepatocyte	liver:	n/a
13	chr1:243050875-243050925	ovcar-3	ovarian:	n/a
14	chr1:243053673-243053723	Hela-S3	cervix:	n/a
15	chr1:243053425-243053475	Caco-2	colon:	n/a
16	chr1:243053865-243053915	GM06990	blood:	n/a
17	chr1:243053673-243053723	AG04449	skin:	fetal
18	chr1:243053934-243053984	PANC-1	pancreas:	n/a
19	chr1:243057080-243057130	PFSK-1	brain:	n/a
20	chr1:243053425-243053475	PANC-1	pancreas:	n/a
21	chr1:243054071-243054121	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:243053934-243053984	HEEpiC	esophagus:	n/a
23	chr1:243057080-243057130	HEK293	kidney:	embryo
24	chr1:243138527-243138577	Hela-S3	cervix:	n/a
25	chr1:243053934-243053984	BJ	skin:	n/a
26	chr1:243138527-243138577	HCPEpiC	choroid plexus:	n/a
27	chr1:243053865-243053915	K562	blood:	n/a
28	chr1:243053425-243053475	Hepatocyte	liver:	n/a
29	chr1:243053934-243053984	ECC-1	luminal epithelium:	n/a
30	chr1:243050875-243050925	NH-A	brain:	n/a
31	chr1:243054071-243054121	HCF	heart:	n/a
32	chr1:243057080-243057130	HRE	kidney:	n/a
33	chr1:243138527-243138577	SK-N-SH_RA	brain:	n/a
34	chr1:243054071-243054121	U87	brain:	n/a
35	chr1:243053934-243053984	Hepatocyte	liver:	n/a
36	chr1:243053425-243053475	GM12878	blood:	n/a
37	chr1:243053673-243053723	HRE	kidney:	n/a
38	chr1:243053425-243053475	SK-N-SH_RA	brain:	n/a
39	chr1:243053865-243053915	GM19239	blood:	n/a
40	chr1:243053673-243053723	HRCEpiC	kidney:	n/a
41	chr1:243053865-243053915	BE2_C	brain:	n/a
42	chr1:243057080-243057130	GM12891	blood:	n/a
43	chr1:243057080-243057130	HNPCEpiC	eye:	n/a
44	chr1:243053934-243053984	T-47D	breast:	n/a
45	chr1:243139525-243139575	NH-A	brain:	n/a
46	chr1:243053865-243053915	HL-60	blood:	n/a
47	chr1:243050875-243050925	MCF-7	breast:	n/a
48	chr1:243050875-243050925	T-47D	breast:	n/a
49	chr1:243053425-243053475	HL-60	blood:	n/a
50	chr1:243053934-243053984	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
2	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
3	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
4	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
5	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
6	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
7	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
8	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
9	chr1:242617838..242618342-chr1:242955947..242956813,2	MCF-7	breast:
10	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
11	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
12	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
13	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
14	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
15	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
16	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
17	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
18	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-
2	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
3	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-
4	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
5	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778

Variant related genes	Relation type
ENSG00000230199	TF binding region
ENSG00000270818	TF binding region
ENSG00000264972	TF binding region
ENSG00000230199	CpG island
ENSG00000270818	CpG island
ENSG00000264972	CpG island

Extended variants
information (count: 2800 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2800 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146573629	chr1:242948762-242948763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142096762	chr1:242948795-242948796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546671746	chr1:242948798-242948799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2151552	chr1:242948893-242948894	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs568580959	chr1:242948923-242948924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534470004	chr1:242948934-242948935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2067299	chr1:242948965-242948966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs397810840	chr1:242948966-242948967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2151551	chr1:242948987-242948988	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs570799923	chr1:242949002-242949003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539889148	chr1:242949005-242949006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553036388	chr1:242949007-242949008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569139700	chr1:242949031-242949032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141372898	chr1:242949050-242949051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377285223	chr1:242949062-242949063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535954360	chr1:242949075-242949076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12082179	chr1:242949091-242949092	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs180997774	chr1:242949127-242949128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145096401	chr1:242949131-242949132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560217197	chr1:242949168-242949169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563406062	chr1:242949200-242949201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2809883	chr1:242949207-242949208	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs562156233	chr1:242949213-242949214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531261504	chr1:242949272-242949273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111517559	chr1:242949317-242949318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139033844	chr1:242949339-242949340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527905405	chr1:242949413-242949414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140616162	chr1:242949500-242949501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571098489	chr1:242949555-242949556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545409991	chr1:242949571-242949572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150475181	chr1:242949621-242949622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185014207	chr1:242949626-242949627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570086318	chr1:242949645-242949646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190214795	chr1:242949692-242949693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187581893	chr1:242949712-242949713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555615424	chr1:242949735-242949736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12747838	chr1:242949740-242949741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565452069	chr1:242949748-242949749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568225570	chr1:242949769-242949770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533793364	chr1:242949811-242949812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554028976	chr1:242949816-242949817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576689339	chr1:242949825-242949826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376483234	chr1:242949831-242949832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181176637	chr1:242949859-242949860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575664385	chr1:242949863-242949864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541500412	chr1:242949866-242949867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376385498	chr1:242949901-242949902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577701291	chr1:242949905-242949906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201199543	chr1:242949906-242949907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs58821996	chr1:242949920-242949921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242945800-242955000	Enhancers	Primary B cells from peripheral blood	blood
2	chr1:242947200-242948800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:242947600-242948800	Enhancers	HSMM	muscle
4	chr1:242948000-242951800	Enhancers	Primary B cells from cord blood	blood
5	chr1:242948200-242948800	Enhancers	Brain Substantia Nigra	brain
6	chr1:242948200-242950800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:242948400-242948800	Enhancers	Brain Hippocampus Middle	brain
8	chr1:242948400-242950600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:242948400-242951800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:242948600-242950600	Weak transcription	HSMMtube	muscle
11	chr1:242948800-242950800	Weak transcription	HSMM	muscle
12	chr1:242948800-242951800	Weak transcription	GM12878-XiMat	blood
13	chr1:242950600-242950800	ZNF genes & repeats	HSMMtube	muscle
14	chr1:242950600-242951000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:242950600-242951200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:242950600-242951400	Enhancers	Placenta Amnion	Placenta Amnion
17	chr1:242950800-242951000	Enhancers	HSMM	muscle
18	chr1:242950800-242951200	Weak transcription	HSMMtube	muscle
19	chr1:242950800-242952000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:242950800-242952200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr1:242951000-242952200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr1:242951000-242952800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:242951200-242951400	Enhancers	HSMMtube	muscle
24	chr1:242951200-242951800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr1:242951400-242951600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:242951400-242951800	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr1:242951800-242952200	Enhancers	Primary hematopoietic stem cells	blood
28	chr1:242951800-242952200	Enhancers	Placenta Amnion	Placenta Amnion
29	chr1:242951800-242952600	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr1:242951800-242953000	Enhancers	GM12878-XiMat	blood
31	chr1:242952600-242953800	Enhancers	Primary B cells from cord blood	blood
32	chr1:242952800-242953000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:242953000-242953400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:242953400-242954000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:242953600-242954000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:242953600-242954400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:242953800-242955800	Weak transcription	Primary B cells from cord blood	blood
38	chr1:242954800-242955200	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr1:242955200-242955400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
40	chr1:242955800-242956000	ZNF genes & repeats	Primary B cells from cord blood	blood
41	chr1:242963600-242964000	Enhancers	GM12878-XiMat	blood
42	chr1:242974000-242975000	Enhancers	HMEC	breast
43	chr1:242974600-242975200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:242976400-242976600	Enhancers	GM12878-XiMat	blood
45	chr1:242976400-242977000	Enhancers	Primary B cells from cord blood	blood
46	chr1:242976400-242977200	Enhancers	Primary B cells from peripheral blood	blood
47	chr1:242976600-242977200	Flanking Active TSS	GM12878-XiMat	blood
48	chr1:242977200-242977400	Enhancers	GM12878-XiMat	blood
49	chr1:242987200-242988800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:242987200-242991000	Enhancers	HMEC	breast

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