Variant report

Variant	nsv546451
Chromosome Location	chr1:69894849-69975660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:69945717-69946058	K562	blood:	n/a	n/a
2	ARID3A	chr1:69948367-69948539	K562	blood:	n/a	n/a
3	ATF1	chr1:69963671-69963852	K562	blood:	n/a	n/a
4	BACH1	chr1:69970443-69970467	K562	blood:	n/a	n/a
5	BHLHE40	chr1:69968997-69969058	K562	blood:	n/a	n/a
6	BHLHE40	chr1:69962622-69962939	K562	blood:	n/a	n/a
7	BHLHE40	chr1:69970556-69970821	K562	blood:	n/a	n/a
8	CBX3	chr1:69924940-69925265	K562	blood:	n/a	n/a
9	CBX3	chr1:69970528-69970826	K562	blood:	n/a	n/a
10	CCNT2	chr1:69963491-69963904	K562	blood:	n/a	chr1:69963787-69963807
11	CEBPB	chr1:69926548-69926741	HepG2	liver:	n/a	chr1:69926648-69926659
12	CEBPB	chr1:69957135-69957448	HepG2	liver:	n/a	chr1:69957279-69957290
13	CEBPB	chr1:69898171-69898387	K562	blood:	n/a	chr1:69898277-69898288 chr1:69898275-69898288 chr1:69898275-69898288
14	CEBPB	chr1:69958595-69958788	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:69969562-69969863	K562	blood:	n/a	n/a
16	CEBPB	chr1:69898839-69899159	IMR90	lung:	n/a	chr1:69899008-69899017 chr1:69899006-69899017
17	CEBPB	chr1:69896937-69896996	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:69957101-69957458	IMR90	lung:	n/a	chr1:69957279-69957290
19	CEBPB	chr1:69957190-69957403	A549	lung:	n/a	chr1:69957279-69957290
20	CEBPB	chr1:69957107-69957470	K562	blood:	n/a	chr1:69957279-69957290
21	CEBPB	chr1:69907945-69908096	K562	blood:	n/a	n/a
22	CEBPD	chr1:69963481-69963942	K562	blood:	n/a	n/a
23	CTCF	chr1:69925040-69925190	AG09319	gingival:	n/a	n/a
24	CTCF	chr1:69925111-69925142	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr1:69929772-69929800	GM10266	blood:	n/a	n/a
26	CTCF	chr1:69925000-69925150	SAEC	small airway:	n/a	n/a
27	CTCF	chr1:69916980-69917130	GM12871	blood:	n/a	n/a
28	CTCF	chr1:69925000-69925150	HMEC	breast:	n/a	n/a
29	CTCF	chr1:69925040-69925190	HEK293	kidney:	n/a	n/a
30	CTCF	chr1:69924952-69925345	K562	blood:	n/a	n/a
31	CTCF	chr1:69925068-69925145	LNCaP	prostate:	n/a	n/a
32	CTCF	chr1:69924980-69925130	AG10803	skin:	n/a	n/a
33	CTCF	chr1:69924957-69925224	GM12878	blood:	n/a	n/a
34	CTCF	chr1:69925020-69925170	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr1:69961285-69961286	GM13976	blood:	n/a	n/a
36	CTCF	chr1:69925100-69925250	K562	blood:	n/a	n/a
37	CTCF	chr1:69963032-69963115	K562	blood:	n/a	n/a
38	CTCF	chr1:69961213-69961284	GM13976	blood:	n/a	n/a
39	CTCF	chr1:69925021-69925225	K562	blood:	n/a	n/a
40	CTCF	chr1:69905092-69905244	K562	blood:	n/a	n/a
41	CTCF	chr1:69924927-69925174	K562	blood:	n/a	n/a
42	CTCF	chr1:69925061-69925113	ProgFib	skin:	n/a	n/a
43	CTCF	chr1:69924980-69925130	WERI-Rb-1	eye:	n/a	n/a
44	CUX1	chr1:69964363-69964367	K562	blood:	n/a	n/a
45	CUX1	chr1:69937397-69937424	K562	blood:	n/a	n/a
46	CUX1	chr1:69963466-69963767	K562	blood:	n/a	chr1:69963654-69963665
47	CUX1	chr1:69973291-69973388	K562	blood:	n/a	n/a
48	CUX1	chr1:69964767-69965250	K562	blood:	n/a	n/a
49	E2F4	chr1:69943275-69943724	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr1:69935872-69935898	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:69916760-69916810	Caco-2	colon:	n/a
2	chr1:69916760-69916810	SAEC	small airway:	n/a
3	chr1:69916760-69916810	BE2_C	brain:	n/a
4	chr1:69916760-69916810	NHBE	bronchial:	n/a
5	chr1:69916760-69916810	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:69916760-69916810	ovcar-3	ovarian:	n/a
7	chr1:69916760-69916810	HCPEpiC	choroid plexus:	n/a
8	chr1:69916760-69916810	U87	brain:	n/a
9	chr1:69916760-69916810	NB4	blood:	n/a
10	chr1:69916760-69916810	GM12891	blood:	n/a
11	chr1:69916760-69916810	AG09319	gingival:	n/a
12	chr1:69916760-69916810	ECC-1	luminal epithelium:	n/a
13	chr1:69916760-69916810	MCF-7	breast:	n/a
14	chr1:69916760-69916810	MCF10A-Er-Src	breast:	n/a
15	chr1:69916760-69916810	HAEpiC	amniotic membrane:	n/a
16	chr1:69916760-69916810	AG04450	lung:	fetal
17	chr1:69916760-69916810	BJ	skin:	n/a
18	chr1:69916760-69916810	Hepatocyte	liver:	n/a
19	chr1:69916760-69916810	SKMC	muscle:	n/a
20	chr1:69916760-69916810	NT2-D1	testis:	n/a
21	chr1:69916760-69916810	PANC-1	pancreas:	n/a
22	chr1:69916760-69916810	ProgFib	skin:	n/a
23	chr1:69916760-69916810	HRCEpiC	kidney:	n/a
24	chr1:69916760-69916810	SK-N-SH	brain:	n/a
25	chr1:69916760-69916810	NH-A	brain:	n/a
26	chr1:69916760-69916810	AG10803	skin:	n/a
27	chr1:69916760-69916810	HCT-116	colon:	n/a
28	chr1:69916760-69916810	HRPEpiC	eye:	n/a
29	chr1:69916760-69916810	SK-N-SH_RA	brain:	n/a
30	chr1:69916760-69916810	HEK293	kidney:	embryo
31	chr1:69916760-69916810	K562	blood:	n/a
32	chr1:69916760-69916810	CMK	blood:	n/a
33	chr1:69916760-69916810	Hela-S3	cervix:	n/a
34	chr1:69916760-69916810	HMEC	breast:	n/a
35	chr1:69916760-69916810	HL-60	blood:	n/a
36	chr1:69916760-69916810	HepG2	liver:	n/a
37	chr1:69916760-69916810	AG04449	skin:	fetal
38	chr1:69916760-69916810	RPTEC	kidney:	n/a
39	chr1:69916760-69916810	SK-N-MC	brain:	n/a
40	chr1:69916760-69916810	HCF	heart:	n/a
41	chr1:69916760-69916810	GM06990	blood:	n/a
42	chr1:69916760-69916810	AG09309	skin:	n/a
43	chr1:69916760-69916810	AoSMC	blood vessel:	n/a
44	chr1:69916760-69916810	HRE	kidney:	n/a
45	chr1:69916760-69916810	HIPEpiC	eye:	n/a
46	chr1:69916760-69916810	HNPCEpiC	eye:	n/a
47	chr1:69916760-69916810	GM12878	blood:	n/a
48	chr1:69916760-69916810	HCM	heart:	n/a
49	chr1:69916760-69916810	LNCaP	prostate:	n/a
50	chr1:69916760-69916810	H1-hESC	embryonic stem cell:	embryo

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:69935852..69938420-chr1:69942565..69946682,4	K562	blood:
2	chr1:69905842..69908777-chr1:69909714..69912512,3	K562	blood:
3	chr1:69937099..69938936-chr1:70016278..70017863,2	K562	blood:
4	chr1:69958198..69960123-chr1:69960268..69963066,3	K562	blood:
5	chr1:69935852..69938420-chr1:69942565..69946682,4	K562	blood:
6	chr1:69923912..69926155-chr1:69945256..69947864,2	K562	blood:
7	chr1:69905907..69908777-chr1:69910942..69912719,3	K562	blood:
8	chr1:69949360..69952101-chr1:69962614..69964917,2	K562	blood:
9	chr1:69934461..69936977-chr1:70003421..70005202,2	K562	blood:
10	chr1:69969499..69972053-chr1:69974366..69976832,2	K562	blood:
11	chr1:69905842..69908777-chr1:69909714..69912512,3	K562	blood:
12	chr1:69939983..69942231-chr1:69948105..69950639,2	K562	blood:
13	chr1:69961073..69963506-chr1:69987765..69990141,2	K562	blood:
14	chr1:69949360..69952101-chr1:69962614..69964917,2	K562	blood:
15	chr1:69905907..69908777-chr1:69910942..69912719,3	K562	blood:
16	chr1:69935852..69938331-chr1:69943499..69946682,3	K562	blood:
17	chr1:69935852..69938331-chr1:69943499..69946682,3	K562	blood:
18	chr1:69969499..69972053-chr1:69974366..69976832,2	K562	blood:
19	chr1:69939983..69942231-chr1:69948105..69950639,2	K562	blood:
20	chr1:69923912..69926155-chr1:69945256..69947864,2	K562	blood:
21	chr1:69958198..69960123-chr1:69960268..69963066,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC7-3	chr1:69898938-69898988	XLOC_000243
2	lnc-LRRC7-3	chr1:69900686-69901092	XLOC_000243
3	lnc-LRRC7-3	chr1:69900685-69901092	NONHSAT003835
4	lnc-LRRC7-3	chr1:69898834-69898988	NONHSAT003835

No data

Variant related genes	Relation type
ENSG00000229639	TF binding region
ENSG00000229639	CpG island

Extended variants
information (count: 2060 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2060 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371183095	chr1:69895454-69895455	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs535314342	chr1:69895462-69895463	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs193163082	chr1:69895483-69895484	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs542943653	chr1:69895520-69895521	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs562728531	chr1:69895527-69895528	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531622620	chr1:69895548-69895549	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs556727063	chr1:69895553-69895554	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs199769370	chr1:69895577-69895578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200693768	chr1:69895578-69895579	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs397715630	chr1:69895580-69895581	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs113855707	chr1:69895581-69895582	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs368213832	chr1:69895582-69895583	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs184981113	chr1:69895597-69895598	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs571397164	chr1:69895648-69895649	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs527428459	chr1:69895667-69895668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs190220555	chr1:69895670-69895671	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs140380057	chr1:69895701-69895702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs369346077	chr1:69895794-69895795	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs535799383	chr1:69895800-69895801	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs550236734	chr1:69896318-69896319	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs398074030	chr1:69896329-69896330	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs397715287	chr1:69896330-69896331	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs117981508	chr1:69896351-69896352	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs186607797	chr1:69896383-69896384	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs549413975	chr1:69896388-69896389	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs189391933	chr1:69896406-69896407	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs539000264	chr1:69896458-69896459	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs552804148	chr1:69896496-69896497	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs566167844	chr1:69896524-69896525	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs115024163	chr1:69896943-69896944	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs74086378	chr1:69896968-69896969	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs183386307	chr1:69896969-69896970	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs529769257	chr1:69897004-69897005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549450900	chr1:69897006-69897007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76657735	chr1:69897012-69897013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186148518	chr1:69897024-69897025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373978226	chr1:69897058-69897059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189771765	chr1:69897089-69897090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34853469	chr1:69897102-69897103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542477130	chr1:69897127-69897128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535329775	chr1:69897147-69897148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148175581	chr1:69897155-69897156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182071451	chr1:69897209-69897210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576029784	chr1:69897230-69897231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188270321	chr1:69897237-69897238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192795560	chr1:69897260-69897261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141979683	chr1:69897333-69897334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539779500	chr1:69897366-69897367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561268003	chr1:69897617-69897618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554378452	chr1:69897619-69897620	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69897000-69897400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:69897600-69898000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:69898200-69899400	Enhancers	NHEK	skin
4	chr1:69898600-69899400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:69899000-69899400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:69899000-69899400	Enhancers	HMEC	breast
7	chr1:69899400-69906800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:69901200-69901400	Enhancers	K562	blood
9	chr1:69901400-69901800	Flanking Active TSS	K562	blood
10	chr1:69901800-69902400	Enhancers	K562	blood
11	chr1:69904000-69904400	Enhancers	Fetal Kidney	kidney
12	chr1:69906800-69907400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:69907400-69907800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:69915800-69917400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr1:69916000-69916600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:69916400-69916600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:69916400-69916800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr1:69916800-69917400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr1:69917200-69917400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr1:69921400-69921800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:69921400-69921800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:69925200-69925600	Enhancers	Pancreas	Pancrea
23	chr1:69928200-69928600	Enhancers	Fetal Heart	heart
24	chr1:69928600-69933000	Weak transcription	Fetal Heart	heart
25	chr1:69929200-69929600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:69935600-69936800	Enhancers	HMEC	breast
27	chr1:69935800-69937000	Enhancers	NHEK	skin
28	chr1:69936000-69936800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:69936200-69936600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:69936400-69936800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:69936600-69940200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:69936800-69940000	Weak transcription	HMEC	breast
33	chr1:69936800-69940200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:69936800-69940200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:69937000-69940200	Weak transcription	NHEK	skin
36	chr1:69940000-69941600	Enhancers	HMEC	breast
37	chr1:69940200-69941600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:69940200-69941600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:69940200-69941600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:69940200-69941600	Enhancers	NHEK	skin
41	chr1:69941400-69941800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:69941600-69942600	Weak transcription	NHEK	skin
43	chr1:69942600-69942800	Enhancers	NHEK	skin
44	chr1:69942600-69943000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:69943000-69945400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:69944800-69946000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:69945200-69945800	Enhancers	K562	blood
48	chr1:69945400-69945800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:69945800-69948400	Weak transcription	K562	blood
50	chr1:69948400-69949800	Enhancers	K562	blood

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