Variant report

Variant	nsv522073
Chromosome Location	chr1:184986725-185013349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:121)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:121 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:184987028-184987082	K562	blood:	n/a	n/a
2	ATF1	chr1:184986573-184986850	K562	blood:	n/a	n/a
3	BHLHE40	chr1:185013258-185013285	K562	blood:	n/a	n/a
4	CBX3	chr1:184996382-184996777	K562	blood:	n/a	n/a
5	CBX3	chr1:184996320-184996775	K562	blood:	n/a	n/a
6	CEBPB	chr1:184986485-184986727	K562	blood:	n/a	chr1:184986640-184986651
7	CEBPB	chr1:185001889-185002091	Hela-S3	cervix:	n/a	chr1:185002069-185002080
8	CEBPB	chr1:185010103-185010393	K562	blood:	n/a	chr1:185010245-185010256
9	CEBPB	chr1:184986484-184986844	MCF-7	breast:	n/a	chr1:184986640-184986651
10	CEBPB	chr1:184986466-184986815	A549	lung:	n/a	chr1:184986640-184986651
11	CEBPB	chr1:185010099-185010331	HepG2	liver:	n/a	chr1:185010245-185010256
12	CEBPB	chr1:184986444-184986896	A549	lung:	n/a	chr1:184986640-184986651
13	CEBPB	chr1:184986436-184986851	IMR90	lung:	n/a	chr1:184986640-184986651
14	CEBPB	chr1:184986465-184986837	K562	blood:	n/a	chr1:184986640-184986651
15	CEBPB	chr1:184986525-184986782	ECC-1	luminal epithelium:	n/a	chr1:184986640-184986651
16	CEBPB	chr1:184986357-184986983	A549	lung:	n/a	chr1:184986640-184986651
17	CEBPB	chr1:184986149-184986856	Hela-S3	cervix:	n/a	chr1:184986640-184986651
18	CEBPB	chr1:184986426-184986894	MCF-7	breast:	n/a	chr1:184986640-184986651
19	CEBPB	chr1:184986193-184986945	HCT-116	colon:	n/a	chr1:184986640-184986651
20	CEBPB	chr1:184986482-184986824	K562	blood:	n/a	chr1:184986640-184986651
21	CEBPB	chr1:185001861-185002160	HepG2	liver:	n/a	chr1:185002069-185002080
22	CEBPB	chr1:184986138-184987104	HCT-116	colon:	n/a	chr1:184986640-184986651
23	CEBPB	chr1:184986562-184986815	HepG2	liver:	n/a	chr1:184986640-184986651
24	CTCF	chr1:185003060-185003210	Caco-2	colon:	n/a	n/a
25	CTCF	chr1:184995989-184996046	GM13976	blood:	n/a	n/a
26	CTCF	chr1:185003000-185003150	Caco-2	colon:	n/a	n/a
27	CTCF	chr1:184995774-184995865	Lung_OC	lung:	n/a	n/a
28	CTCF	chr1:185005020-185005170	GM12873	blood:	n/a	n/a
29	CTCF	chr1:185008291-185008497	K562	blood:	n/a	chr1:185008330-185008346 chr1:185008331-185008352
30	CTCF	chr1:184989020-184989170	AG09319	gingival:	n/a	n/a
31	CTCF	chr1:185000755-185000797	Fibrobl	skin:	n/a	n/a
32	CTCF	chr1:185008308-185008368	K562	blood:	n/a	chr1:185008330-185008346 chr1:185008331-185008352
33	CUX1	chr1:185003013-185003169	K562	blood:	n/a	n/a
34	CUX1	chr1:184988843-184988943	K562	blood:	n/a	n/a
35	E2F4	chr1:185002309-185002319	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr1:185004296-185004358	GM12878	blood:	n/a	chr1:185004342-185004353 chr1:185004342-185004355 chr1:185004343-185004353 chr1:185004344-185004353
37	EP300	chr1:184986436-184986803	Hela-S3	cervix:	n/a	n/a
38	EP300	chr1:185013248-185013323	K562	blood:	n/a	n/a
39	ESR1	chr1:184986606-184986912	ECC-1	luminal epithelium:	n/a	n/a
40	FAM48A	chr1:184999270-184999416	GM12878	blood:	n/a	n/a
41	FAM48A	chr1:185009431-185009631	GM12878	blood:	n/a	n/a
42	FOS	chr1:184986396-184986812	MCF10A-Er-Src	breast:	n/a	chr1:184986587-184986598
43	FOS	chr1:184986321-184986848	MCF10A-Er-Src	breast:	n/a	chr1:184986587-184986598
44	FOS	chr1:184986440-184986796	Hela-S3	cervix:	n/a	chr1:184986587-184986598
45	FOS	chr1:185000251-185000276	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr1:184986370-184986789	HUVEC	blood vessel:	n/a	chr1:184986587-184986598
47	FOS	chr1:184986392-184986875	MCF10A-Er-Src	breast:	n/a	chr1:184986587-184986598
48	FOS	chr1:184986401-184986812	MCF10A-Er-Src	breast:	n/a	chr1:184986587-184986598
49	FOS	chr1:185000219-185000235	MCF10A-Er-Src	breast:	n/a	n/a
50	FOSL1	chr1:184986137-184987159	HCT-116	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:185012220-185012270	U87	brain:	n/a
2	chr1:185012220-185012270	Jurkat	blood:	n/a
3	chr1:185012220-185012270	SK-N-MC	brain:	n/a
4	chr1:185012220-185012270	PFSK-1	brain:	n/a
5	chr1:185012220-185012270	HAEpiC	amniotic membrane:	n/a
6	chr1:185012220-185012270	A549	lung:	n/a
7	chr1:185012220-185012270	RPTEC	kidney:	n/a
8	chr1:185012220-185012270	HEK293	kidney:	embryo
9	chr1:185012220-185012270	NH-A	brain:	n/a
10	chr1:185012220-185012270	HMEC	breast:	n/a
11	chr1:185012220-185012270	HEEpiC	esophagus:	n/a
12	chr1:185012220-185012270	HNPCEpiC	eye:	n/a
13	chr1:185012220-185012270	LNCaP	prostate:	n/a
14	chr1:185012220-185012270	IMR90	lung:	fetal
15	chr1:185012220-185012270	SKMC	muscle:	n/a
16	chr1:185012220-185012270	MCF10A-Er-Src	breast:	n/a
17	chr1:185012220-185012270	GM12878	blood:	n/a
18	chr1:185012220-185012270	NB4	blood:	n/a
19	chr1:185012220-185012270	GM12891	blood:	n/a
20	chr1:185012220-185012270	K562	blood:	n/a
21	chr1:185012220-185012270	SK-N-SH_RA	brain:	n/a
22	chr1:185012220-185012270	BJ	skin:	n/a
23	chr1:185012220-185012270	AoSMC	blood vessel:	n/a
24	chr1:185012220-185012270	T-47D	breast:	n/a
25	chr1:185012220-185012270	HRPEpiC	eye:	n/a
26	chr1:185012220-185012270	GM06990	blood:	n/a
27	chr1:185012220-185012270	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:185012220-185012270	BE2_C	brain:	n/a
29	chr1:185012220-185012270	PrEC	prostate:	n/a
30	chr1:185012220-185012270	SAEC	small airway:	n/a
31	chr1:185012220-185012270	AG10803	skin:	n/a
32	chr1:185012220-185012270	HRE	kidney:	n/a
33	chr1:185012220-185012270	GM19239	blood:	n/a
34	chr1:185012220-185012270	HCF	heart:	n/a
35	chr1:185012220-185012270	HepG2	liver:	n/a
36	chr1:185012220-185012270	HL-60	blood:	n/a
37	chr1:185012220-185012270	ProgFib	skin:	n/a
38	chr1:185012220-185012270	SK-N-SH	brain:	n/a
39	chr1:185012220-185012270	ECC-1	luminal epithelium:	n/a
40	chr1:185012220-185012270	MCF-7	breast:	n/a
41	chr1:185012220-185012270	CMK	blood:	n/a
42	chr1:185012220-185012270	AG09319	gingival:	n/a
43	chr1:185012220-185012270	PANC-1	pancreas:	n/a
44	chr1:185012220-185012270	NHDF-neo	bronchial:	n/a
45	chr1:185012220-185012270	ovcar-3	ovarian:	n/a
46	chr1:185012220-185012270	Hela-S3	cervix:	n/a
47	chr1:185012220-185012270	AG04450	lung:	fetal
48	chr1:185012220-185012270	Hepatocyte	liver:	n/a
49	chr1:185012220-185012270	HCPEpiC	choroid plexus:	n/a
50	chr1:185012220-185012270	AG09309	skin:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:185002898..185006050-chr1:185012086..185014669,3	MCF-7	breast:
2	chr1:185010099..185012707-chr1:185046027..185047994,2	K562	blood:
3	chr1:184987937..184990442-chr1:185124992..185126944,2	MCF-7	breast:
4	chr1:184983211..184985118-chr1:185007746..185010406,2	K562	blood:
5	chr1:184939347..184942263-chr1:185006471..185008277,2	K562	blood:
6	chr1:185012738..185016714-chr1:185123889..185127545,9	K562	blood:
7	chr1:185000396..185004587-chr1:185007338..185010464,3	K562	blood:
8	chr1:184986624..184988154-chr1:185012581..185015445,2	K562	blood:
9	chr1:184978593..184980252-chr1:184987075..184988788,2	MCF-7	breast:
10	chr1:184996571..184998477-chr1:185000710..185002993,2	K562	blood:
11	chr1:184985716..184988331-chr1:184988994..184992281,3	K562	blood:
12	chr1:185010943..185013509-chr1:185124566..185127368,2	MCF-7	breast:
13	chr1:185010844..185012522-chr1:185016130..185018992,2	MCF-7	breast:
14	chr1:184977262..184980396-chr1:184986788..184988626,3	K562	blood:
15	chr1:184984889..184988154-chr1:185012581..185015445,4	K562	blood:
16	chr1:184948681..184951312-chr1:184986477..184988243,2	K562	blood:
17	chr1:185009803..185012714-chr1:185013040..185014804,2	MCF-7	breast:
18	chr1:184996571..184998477-chr1:185000710..185002993,2	K562	blood:
19	chr1:185006708..185009603-chr1:185013387..185015554,2	MCF-7	breast:
20	chr1:185012738..185017820-chr1:185123187..185127311,9	K562	blood:
21	chr1:184985716..184988331-chr1:184988994..184992281,3	K562	blood:
22	chr1:185002306..185004011-chr1:185022303..185025099,2	MCF-7	breast:
23	chr1:184941138..184943515-chr1:185012025..185014366,2	K562	blood:
24	chr1:184999264..185001806-chr1:185002551..185005032,2	K562	blood:
25	chr1:185010303..185011857-chr1:185026196..185028630,2	K562	blood:
26	chr1:184999264..185001806-chr1:185002551..185005032,2	K562	blood:
27	chr1:185000396..185004587-chr1:185007338..185010464,3	K562	blood:

No data

Variant related genes	Relation type
RNF2	TF binding region
RNA5SP72	TF binding region
RNF2	CpG island
RNA5SP72	CpG island
ENSG00000201312	chromatin interactions
ENSG00000121481	chromatin interactions
ENSG00000116668	chromatin interactions
ENSG00000121486	chromatin interactions

Extended variants
information (count: 509 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12040650	chr1:184986725-184986726	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143387455	chr1:184986776-184986777	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs115075413	chr1:184986780-184986781	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531702744	chr1:184986833-184986834	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs75049039	chr1:184986834-184986835	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs568362198	chr1:184986863-184986864	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs72739678	chr1:184986971-184986972	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554132596	chr1:184987011-184987012	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs189444866	chr1:184987035-184987036	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs76511622	chr1:184987036-184987037	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs148365773	chr1:184987067-184987068	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576749707	chr1:184987125-184987126	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs141522143	chr1:184987130-184987131	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555466606	chr1:184987137-184987138	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs573541735	chr1:184987179-184987180	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541037451	chr1:184987252-184987253	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531940606	chr1:184987269-184987270	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559358687	chr1:184987285-184987286	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs533061388	chr1:184987311-184987312	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544766747	chr1:184987353-184987354	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542743683	chr1:184987364-184987365	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181384773	chr1:184987450-184987451	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370752858	chr1:184987451-184987452	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563135675	chr1:184987453-184987454	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376166532	chr1:184987510-184987511	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185230248	chr1:184987520-184987521	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs12118854	chr1:184987546-184987547	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs549843709	chr1:184987582-184987583	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547291308	chr1:184987633-184987634	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568553882	chr1:184987642-184987643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190037948	chr1:184987648-184987649	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs183341769	chr1:184987669-184987670	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145766360	chr1:184987676-184987677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12118881	chr1:184987679-184987680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540126174	chr1:184987689-184987690	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs6694692	chr1:184987690-184987691	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554449335	chr1:184987696-184987697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs57293663	chr1:184987713-184987714	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs397959240	chr1:184987735-184987736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187008267	chr1:184987742-184987743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141619998	chr1:184987769-184987770	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373552782	chr1:184987771-184987772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192304088	chr1:184987785-184987786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs59129408	chr1:184987830-184987831	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146191039	chr1:184987885-184987886	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12038087	chr1:184987891-184987892	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139034557	chr1:184987913-184987914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558972483	chr1:184987915-184987916	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183317674	chr1:184987958-184987959	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs577262122	chr1:184987975-184987976	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Bladder cancer	19088036	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
Trisomy 5 syndrome	21098271	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
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	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
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184984000-184987600	Enhancers	Fetal Intestine Large	intestine
2	chr1:184984600-184987400	Enhancers	K562	blood
3	chr1:184985000-184987200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:184985600-184987000	Enhancers	Hela-S3	cervix
5	chr1:184985600-184987400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:184985800-184987000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:184985800-184987000	Enhancers	Osteobl	bone
8	chr1:184985800-184987400	Enhancers	HMEC	breast
9	chr1:184985800-184987400	Enhancers	NHDF-Ad	bronchial
10	chr1:184985800-184987600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:184986000-184986800	Enhancers	NHLF	lung
12	chr1:184986000-184987000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:184986000-184987000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:184986000-184987000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:184986000-184987000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:184986000-184987000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr1:184986000-184987000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:184986000-184987000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:184986000-184987000	Enhancers	NHEK	skin
20	chr1:184986000-184987200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:184986000-184987200	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr1:184986200-184987000	Enhancers	NH-A	brain
23	chr1:184986200-184987400	Enhancers	HSMM	muscle
24	chr1:184986400-184986800	Enhancers	Placenta Amnion	Placenta Amnion
25	chr1:184986600-184987200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:184986600-184987200	Enhancers	A549	lung
27	chr1:184987000-184987600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:184987600-184988200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:184988200-184988400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:184988600-184989200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:184989600-184989800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:184996000-184997000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
33	chr1:184996400-184997000	ZNF genes & repeats	Aorta	Aorta
34	chr1:184996600-184997000	Weak transcription	Brain Angular Gyrus	brain
35	chr1:185007800-185008400	Enhancers	Fetal Lung	lung
36	chr1:185008000-185008400	Enhancers	Fetal Muscle Leg	muscle
37	chr1:185008000-185008400	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr1:185008400-185009600	Weak transcription	Fetal Muscle Leg	muscle
39	chr1:185008600-185010200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:185008800-185009400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:185009000-185010600	Enhancers	Primary hematopoietic stem cells	blood
42	chr1:185009000-185010600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:185009400-185010200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:185009400-185011000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr1:185009600-185010200	Enhancers	Fetal Muscle Leg	muscle
46	chr1:185010000-185010600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr1:185010200-185010400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:185010200-185014000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:185010200-185014000	Weak transcription	Fetal Muscle Leg	muscle
50	chr1:185010400-185010600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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