Variant report

Variant	nsv548406
Chromosome Location	chr1:186742947-186803226
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	BATF	chr1:186788292-186788555	GM12878	blood:	n/a	chr1:186788453-186788464
2	BCLAF1	chr1:186768847-186769250	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:186798456-186798522	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:186788387-186788587	GM12878	blood:	n/a	n/a
5	BRCA1	chr1:186797977-186799227	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:186745370-186745611	Hela-S3	cervix:	n/a	chr1:186745440-186745453 chr1:186745506-186745517
7	CEBPB	chr1:186776349-186776656	Hela-S3	cervix:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
8	CEBPB	chr1:186754711-186755028	A549	lung:	n/a	chr1:186754819-186754830
9	CEBPB	chr1:186765717-186765923	A549	lung:	n/a	chr1:186765780-186765791
10	CEBPB	chr1:186745330-186745679	IMR90	lung:	n/a	chr1:186745440-186745453 chr1:186745506-186745517
11	CEBPB	chr1:186776331-186776675	K562	blood:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
12	CEBPB	chr1:186798377-186798567	A549	lung:	n/a	n/a
13	CEBPB	chr1:186782415-186782623	A549	lung:	n/a	chr1:186782535-186782548 chr1:186782534-186782551
14	CEBPB	chr1:186799005-186799500	Hela-S3	cervix:	n/a	chr1:186799322-186799333 chr1:186799323-186799334 chr1:186799312-186799323 chr1:186799311-186799324 chr1:186799311-186799322 chr1:186799311-186799324
15	CEBPB	chr1:186776363-186776647	MCF-7	breast:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
16	CEBPB	chr1:186799217-186799445	HepG2	liver:	n/a	chr1:186799322-186799333 chr1:186799323-186799334 chr1:186799312-186799323 chr1:186799311-186799324 chr1:186799311-186799322 chr1:186799311-186799324
17	CEBPB	chr1:186759337-186759535	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:186745335-186745658	HepG2	liver:	n/a	chr1:186745440-186745453 chr1:186745506-186745517
19	CEBPB	chr1:186745332-186745662	A549	lung:	n/a	chr1:186745440-186745453 chr1:186745506-186745517
20	CEBPB	chr1:186754676-186754999	Hela-S3	cervix:	n/a	chr1:186754819-186754830
21	CEBPB	chr1:186776307-186776685	IMR90	lung:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
22	CEBPB	chr1:186775674-186775911	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:186752034-186752308	IMR90	lung:	n/a	chr1:186752154-186752171
24	CEBPB	chr1:186776318-186776679	A549	lung:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
25	CEBPB	chr1:186787642-186787888	HepG2	liver:	n/a	chr1:186787755-186787766 chr1:186787754-186787767 chr1:186787754-186787767 chr1:186787754-186787767 chr1:186787754-186787765
26	CEBPB	chr1:186754811-186754912	H1-hESC	embryonic stem cell:	n/a	chr1:186754819-186754830
27	CEBPB	chr1:186765636-186765936	HepG2	liver:	n/a	chr1:186765780-186765791
28	CEBPB	chr1:186746131-186746430	IMR90	lung:	n/a	chr1:186746373-186746386 chr1:186746217-186746228
29	CEBPB	chr1:186776229-186776747	A549	lung:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
30	CEBPB	chr1:186776294-186776660	A549	lung:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
31	CEBPB	chr1:186771613-186771859	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:186776336-186776647	H1-hESC	embryonic stem cell:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
33	CEBPB	chr1:186781636-186782722	IMR90	lung:	n/a	chr1:186782535-186782548 chr1:186782534-186782551
34	CEBPB	chr1:186776328-186776680	HepG2	liver:	n/a	chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776493-186776502 chr1:186776492-186776503
35	CEBPB	chr1:186746197-186746457	A549	lung:	n/a	chr1:186746373-186746386 chr1:186746217-186746228
36	CEBPB	chr1:186771617-186771840	A549	lung:	n/a	n/a
37	CEBPB	chr1:186754681-186755007	HepG2	liver:	n/a	chr1:186754819-186754830
38	CEBPB	chr1:186754659-186755012	A549	lung:	n/a	chr1:186754819-186754830
39	CEBPB	chr1:186799102-186799459	A549	lung:	n/a	chr1:186799322-186799333 chr1:186799323-186799334 chr1:186799312-186799323 chr1:186799311-186799324 chr1:186799311-186799322 chr1:186799311-186799324
40	CEBPB	chr1:186797996-186798665	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:186787626-186787906	A549	lung:	n/a	chr1:186787755-186787766 chr1:186787754-186787767 chr1:186787754-186787767 chr1:186787754-186787767 chr1:186787754-186787765
42	CEBPB	chr1:186787602-186787910	IMR90	lung:	n/a	chr1:186787755-186787766 chr1:186787754-186787767 chr1:186787754-186787767 chr1:186787754-186787767 chr1:186787754-186787765
43	CEBPB	chr1:186746202-186746409	HepG2	liver:	n/a	chr1:186746373-186746386 chr1:186746217-186746228
44	CTCF	chr1:186763600-186763750	K562	blood:	n/a	n/a
45	CTCF	chr1:186775740-186775890	Caco-2	colon:	n/a	n/a
46	CTCF	chr1:186775571-186775962	A549	lung:	n/a	n/a
47	CTCF	chr1:186798417-186798431	GM13977	blood:	n/a	n/a
48	CTCF	chr1:186772380-186772670	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr1:186775772-186775862	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr1:186798060-186798210	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:186799481-186799531	AoSMC	blood vessel:	n/a
2	chr1:186799481-186799531	AoSMC	blood vessel:	n/a
3	chr1:186798107-186798157	HEK293	kidney:	embryo
4	chr1:186799481-186799531	ECC-1	luminal epithelium:	n/a
5	chr1:186799481-186799531	NB4	blood:	n/a
6	chr1:186798107-186798157	BJ	skin:	n/a
7	chr1:186798107-186798157	MCF10A-Er-Src	breast:	n/a
8	chr1:186799481-186799531	U87	brain:	n/a
9	chr1:186799481-186799531	IMR90	lung:	fetal
10	chr1:186798107-186798157	LNCaP	prostate:	n/a
11	chr1:186798107-186798157	HRCEpiC	kidney:	n/a
12	chr1:186798107-186798157	GM12878	blood:	n/a
13	chr1:186798107-186798157	T-47D	breast:	n/a
14	chr1:186799481-186799531	HCF	heart:	n/a
15	chr1:186798107-186798157	Caco-2	colon:	n/a
16	chr1:186798107-186798157	HNPCEpiC	eye:	n/a
17	chr1:186798107-186798157	SK-N-SH_RA	brain:	n/a
18	chr1:186798107-186798157	HCT-116	colon:	n/a
19	chr1:186798107-186798157	HAEpiC	amniotic membrane:	n/a
20	chr1:186798107-186798157	PrEC	prostate:	n/a
21	chr1:186798107-186798157	NB4	blood:	n/a
22	chr1:186798107-186798157	NHBE	bronchial:	n/a
23	chr1:186798107-186798157	MCF-7	breast:	n/a
24	chr1:186799481-186799531	BJ	skin:	n/a
25	chr1:186798107-186798157	GM12892	blood:	n/a
26	chr1:186799481-186799531	RPTEC	kidney:	n/a
27	chr1:186799481-186799531	GM06990	blood:	n/a
28	chr1:186798107-186798157	ovcar-3	ovarian:	n/a
29	chr1:186798107-186798157	AG04449	skin:	fetal
30	chr1:186799481-186799531	K562	blood:	n/a
31	chr1:186798107-186798157	AG10803	skin:	n/a
32	chr1:186798107-186798157	SK-N-SH	brain:	n/a
33	chr1:186799481-186799531	HCPEpiC	choroid plexus:	n/a
34	chr1:186799481-186799531	A549	lung:	n/a
35	chr1:186798107-186798157	GM12891	blood:	n/a
36	chr1:186799481-186799531	Caco-2	colon:	n/a
37	chr1:186798107-186798157	SAEC	small airway:	n/a
38	chr1:186799481-186799531	AG04449	skin:	fetal
39	chr1:186799481-186799531	AG10803	skin:	n/a
40	chr1:186799481-186799531	HepG2	liver:	n/a
41	chr1:186799481-186799531	NHBE	bronchial:	n/a
42	chr1:186798107-186798157	HCPEpiC	choroid plexus:	n/a
43	chr1:186799481-186799531	HEK293	kidney:	embryo
44	chr1:186798107-186798157	NT2-D1	testis:	n/a
45	chr1:186798107-186798157	HCF	heart:	n/a
46	chr1:186799481-186799531	SK-N-SH	brain:	n/a
47	chr1:186799481-186799531	AG09319	gingival:	n/a
48	chr1:186798107-186798157	NHDF-neo	bronchial:	n/a
49	chr1:186798107-186798157	ECC-1	luminal epithelium:	n/a
50	chr1:186798107-186798157	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:186790146..186792440-chr1:186793837..186796185,2	MCF-7	breast:
2	chr1:186451484..186452471-chr1:186775451..186776233,2	MCF-7	breast:
3	chr1:186727470..186729684-chr1:186748131..186750420,2	MCF-7	breast:
4	chr1:186679169..186680841-chr1:186782963..186785926,2	K562	blood:
5	chr1:186719442..186721469-chr1:186796069..186797645,2	MCF-7	breast:
6	chr1:186793156..186795805-chr1:186804858..186807640,2	K562	blood:
7	chr1:186782948..186785138-chr1:186786790..186788311,2	K562	blood:
8	chr1:186798323..186798999-chr2:128284697..128285443,2	Hela-S3	cervix:
9	chr1:186762087..186763977-chr1:186766711..186768575,2	MCF-7	breast:
10	chr1:186691511..186692410-chr1:186775381..186776252,3	MCF-7	breast:
11	chr1:186574767..186576085-chr1:186775295..186776491,7	MCF-7	breast:
12	chr1:186648920..186649846-chr1:186775558..186776313,3	MCF-7	breast:
13	chr1:186779659..186780568-chr15:84582418..84583402,2	MCF-7	breast:
14	chr1:186733738..186735467-chr1:186745495..186747169,2	MCF-7	breast:
15	chr1:186782948..186785138-chr1:186786790..186788311,2	K562	blood:
16	chr1:186790146..186792440-chr1:186793837..186796185,2	MCF-7	breast:
17	chr1:186762087..186763977-chr1:186766711..186768575,2	MCF-7	breast:
18	chr1:186451520..186452510-chr1:186775360..186775901,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA2G4A-8	chr1:186764950-186765131	NONHSAT008452
2	lnc-PLA2G4A-8	chr1:186771510-186771612	NONHSAT008452
3	lnc-PLA2G4A-8	chr1:186771887-186772219	NONHSAT008452
4	lnc-PLA2G4A-8	chr1:186744292-186744419	NONHSAT008452

Variant related genes	Relation type
PLA2G4A	TF binding region
PLA2G4A	CpG island
ENSG00000073756	chromatin interactions
ENSG00000273129	chromatin interactions

Extended variants
information (count: 2014 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10489401	chr1:186742947-186742948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553624605	chr1:186742950-186742951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569171645	chr1:186742956-186742957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374250364	chr1:186743085-186743086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141019443	chr1:186743088-186743089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567049866	chr1:186743146-186743147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534167565	chr1:186743160-186743161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143447752	chr1:186743190-186743191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188318883	chr1:186743193-186743194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199880539	chr1:186743196-186743197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs57376790	chr1:186743204-186743205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200691751	chr1:186743205-186743206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370471863	chr1:186743206-186743207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115894300	chr1:186743264-186743265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544589289	chr1:186743337-186743338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556581813	chr1:186743345-186743346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180736573	chr1:186743350-186743351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376278482	chr1:186743356-186743357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542144141	chr1:186743430-186743431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560229592	chr1:186743476-186743477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187303270	chr1:186743479-186743480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545684210	chr1:186743491-186743492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564182885	chr1:186743499-186743500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531325262	chr1:186743547-186743548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563984488	chr1:186743583-186743584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575667729	chr1:186743584-186743585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567693042	chr1:186743624-186743625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79449199	chr1:186743674-186743675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs386369003	chr1:186743676-186743677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371695236	chr1:186743681-186743682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs59576911	chr1:186743682-186743683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528901288	chr1:186743709-186743710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114394867	chr1:186743710-186743711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34369697	chr1:186743726-186743727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs74530748	chr1:186743750-186743751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs66507208	chr1:186743752-186743753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75191853	chr1:186743763-186743764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs55986211	chr1:186743765-186743766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10911921	chr1:186743766-186743767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567059446	chr1:186743772-186743773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200534012	chr1:186743775-186743776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375897093	chr1:186743778-186743779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs146763429	chr1:186743783-186743784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574900270	chr1:186743795-186743796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12145089	chr1:186743830-186743831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12145091	chr1:186743840-186743841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564599496	chr1:186743845-186743846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558907149	chr1:186743885-186743886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10911922	chr1:186743903-186743904	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs79760908	chr1:186743917-186743918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	19197363	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186741400-186745200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:186743400-186745400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:186743400-186745600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:186743600-186744400	Enhancers	Rectal Smooth Muscle	rectum
5	chr1:186743800-186744200	Enhancers	Colon Smooth Muscle	Colon
6	chr1:186743800-186744200	Enhancers	Fetal Stomach	stomach
7	chr1:186743800-186745400	Enhancers	Fetal Lung	lung
8	chr1:186744600-186745400	Enhancers	Dnd41	blood
9	chr1:186744800-186745400	Enhancers	Primary hematopoietic stem cells	blood
10	chr1:186744800-186745400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr1:186745000-186745400	Enhancers	HMEC	breast
12	chr1:186745000-186745600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:186745200-186745400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:186745200-186745600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:186745200-186745600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:186745200-186745600	Enhancers	NHEK	skin
17	chr1:186745400-186748600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:186745400-186751000	Weak transcription	Fetal Lung	lung
19	chr1:186745600-186748400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:186745600-186751000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:186745600-186751000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:186745600-186751000	Weak transcription	NHEK	skin
23	chr1:186745800-186746400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:186746400-186751000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:186748400-186749800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:186748600-186749400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:186748800-186749800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:186750600-186752000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:186750800-186751200	Enhancers	Adipose Nuclei	Adipose
30	chr1:186751000-186751200	Enhancers	Fetal Lung	lung
31	chr1:186751000-186751400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:186751000-186752200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr1:186751000-186752200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:186751000-186752400	Enhancers	Colon Smooth Muscle	Colon
35	chr1:186751000-186752800	Enhancers	NHEK	skin
36	chr1:186751200-186752000	Weak transcription	Fetal Lung	lung
37	chr1:186752000-186752400	Enhancers	NH-A	brain
38	chr1:186752000-186752600	Enhancers	Fetal Lung	lung
39	chr1:186752000-186752600	Enhancers	HMEC	breast
40	chr1:186752400-186762000	Weak transcription	NH-A	brain
41	chr1:186753600-186754600	Enhancers	HUVEC	blood vessel
42	chr1:186754600-186755000	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr1:186761800-186763200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:186762000-186762200	Enhancers	NH-A	brain
45	chr1:186762000-186762400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:186762000-186762400	Enhancers	HMEC	breast
47	chr1:186762000-186762400	Enhancers	Osteobl	bone
48	chr1:186762000-186763000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:186762200-186762600	Flanking Active TSS	NH-A	brain
50	chr1:186762200-186762800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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