Variant report

Variant	nsv522156
Chromosome Location	chr1:102309649-102421714
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:173)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:173 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:102331101-102331231	K562	blood:	n/a	n/a
2	BACH1	chr1:102311592-102311621	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr1:102346057-102346369	GM12878	blood:	n/a	n/a
4	BATF	chr1:102346026-102346355	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:102346126-102346353	GM12878	blood:	n/a	n/a
6	CEBPB	chr1:102350238-102350441	Hela-S3	cervix:	n/a	chr1:102350368-102350379
7	CEBPB	chr1:102350217-102350529	H1-hESC	embryonic stem cell:	n/a	chr1:102350368-102350379
8	CEBPB	chr1:102350191-102350554	HepG2	liver:	n/a	chr1:102350368-102350379
9	CEBPB	chr1:102339223-102339523	HepG2	liver:	n/a	chr1:102339379-102339390
10	CEBPB	chr1:102419871-102420030	K562	blood:	n/a	chr1:102419972-102419983
11	CEBPB	chr1:102371408-102371417	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:102365093-102365285	HepG2	liver:	n/a	chr1:102365175-102365186 chr1:102365175-102365186 chr1:102365173-102365184
13	CEBPB	chr1:102419807-102420140	IMR90	lung:	n/a	chr1:102419972-102419983
14	CEBPB	chr1:102339263-102339513	K562	blood:	n/a	chr1:102339379-102339390
15	CEBPB	chr1:102419814-102420160	HepG2	liver:	n/a	chr1:102419972-102419983
16	CEBPB	chr1:102419855-102420123	A549	lung:	n/a	chr1:102419972-102419983
17	CEBPB	chr1:102363806-102363953	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:102339294-102339480	H1-hESC	embryonic stem cell:	n/a	chr1:102339379-102339390
19	CEBPB	chr1:102383891-102384166	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:102350238-102350560	IMR90	lung:	n/a	chr1:102350368-102350379
21	CTCF	chr1:102312400-102312550	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr1:102411540-102411690	BE2_C	brain:	n/a	n/a
23	CTCF	chr1:102404014-102404116	GM12878	blood:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
24	CTCF	chr1:102312420-102312570	HRE	kidney:	n/a	n/a
25	CTCF	chr1:102312420-102312570	NHEK	skin:	n/a	n/a
26	CTCF	chr1:102404006-102404127	MCF-7	breast:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
27	CTCF	chr1:102404000-102404150	GM12873	blood:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
28	CTCF	chr1:102403980-102404130	GM12865	blood:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
29	CTCF	chr1:102411580-102411730	GM12866	blood:	n/a	n/a
30	CTCF	chr1:102411480-102411630	GM12874	blood:	n/a	n/a
31	CTCF	chr1:102312360-102312510	BE2_C	brain:	n/a	n/a
32	CTCF	chr1:102312480-102312630	RPTEC	kidney:	n/a	n/a
33	CTCF	chr1:102324136-102324269	Lung_OC	lung:	n/a	n/a
34	CTCF	chr1:102403900-102404050	GM12869	blood:	n/a	n/a
35	CTCF	chr1:102318800-102318950	BE2_C	brain:	n/a	n/a
36	CTCF	chr1:102411560-102411710	BE2_C	brain:	n/a	n/a
37	CTCF	chr1:102346980-102346997	GM20000	blood:	n/a	n/a
38	CTCF	chr1:102403990-102404152	LNCaP	prostate:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
39	CTCF	chr1:102312300-102312450	BE2_C	brain:	n/a	n/a
40	CTCF	chr1:102403941-102404201	GM12878	blood:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
41	CTCF	chr1:102404008-102404120	Pancreas_OC	pancreas:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
42	CTCF	chr1:102347078-102347165	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:102345816-102345888	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr1:102312420-102312570	RPTEC	kidney:	n/a	n/a
45	CTCF	chr1:102404000-102404150	HMEC	breast:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
46	CTCF	chr1:102411520-102411670	GM12872	blood:	n/a	n/a
47	CTCF	chr1:102411580-102411730	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:102350159-102350268	GM13976	blood:	n/a	n/a
49	CTCF	chr1:102404049-102404084	GM10266	blood:	n/a	n/a
50	CTCF	chr1:102365940-102366090	GM12872	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:102312610-102312660	ProgFib	skin:	n/a
2	chr1:102312610-102312660	NT2-D1	testis:	n/a
3	chr1:102312608-102312658	PrEC	prostate:	n/a
4	chr1:102312608-102312658	Hepatocyte	liver:	n/a
5	chr1:102312671-102312721	NT2-D1	testis:	n/a
6	chr1:102312610-102312660	GM12891	blood:	n/a
7	chr1:102312608-102312658	AoSMC	blood vessel:	n/a
8	chr1:102312608-102312658	PFSK-1	brain:	n/a
9	chr1:102312671-102312721	GM06990	blood:	n/a
10	chr1:102312608-102312658	NB4	blood:	n/a
11	chr1:102312610-102312660	NHBE	bronchial:	n/a
12	chr1:102312671-102312721	RPTEC	kidney:	n/a
13	chr1:102312608-102312658	HUVEC	blood vessel:	n/a
14	chr1:102312608-102312658	HEEpiC	esophagus:	n/a
15	chr1:102312608-102312658	ovcar-3	ovarian:	n/a
16	chr1:102312610-102312660	HRE	kidney:	n/a
17	chr1:102312608-102312658	HNPCEpiC	eye:	n/a
18	chr1:102312671-102312721	HL-60	blood:	n/a
19	chr1:102312671-102312721	HUVEC	blood vessel:	n/a
20	chr1:102312671-102312721	BJ	skin:	n/a
21	chr1:102312610-102312660	SK-N-SH	brain:	n/a
22	chr1:102312610-102312660	AG09319	gingival:	n/a
23	chr1:102312608-102312658	HIPEpiC	eye:	n/a
24	chr1:102312671-102312721	MCF10A-Er-Src	breast:	n/a
25	chr1:102312610-102312660	SK-N-MC	brain:	n/a
26	chr1:102312608-102312658	PANC-1	pancreas:	n/a
27	chr1:102312610-102312660	PFSK-1	brain:	n/a
28	chr1:102312671-102312721	SAEC	small airway:	n/a
29	chr1:102312610-102312660	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:102312610-102312660	Hela-S3	cervix:	n/a
31	chr1:102312610-102312660	BJ	skin:	n/a
32	chr1:102312610-102312660	ECC-1	luminal epithelium:	n/a
33	chr1:102312608-102312658	GM12878	blood:	n/a
34	chr1:102312608-102312658	A549	lung:	n/a
35	chr1:102312608-102312658	AG04450	lung:	fetal
36	chr1:102312608-102312658	SAEC	small airway:	n/a
37	chr1:102312671-102312721	ProgFib	skin:	n/a
38	chr1:102312608-102312658	GM12891	blood:	n/a
39	chr1:102312671-102312721	SK-N-MC	brain:	n/a
40	chr1:102312610-102312660	AG04449	skin:	fetal
41	chr1:102312671-102312721	U87	brain:	n/a
42	chr1:102312610-102312660	HAEpiC	amniotic membrane:	n/a
43	chr1:102312610-102312660	NB4	blood:	n/a
44	chr1:102312608-102312658	HL-60	blood:	n/a
45	chr1:102312608-102312658	RPTEC	kidney:	n/a
46	chr1:102312608-102312658	GM19239	blood:	n/a
47	chr1:102312671-102312721	HNPCEpiC	eye:	n/a
48	chr1:102312671-102312721	GM12891	blood:	n/a
49	chr1:102312608-102312658	Caco-2	colon:	n/a
50	chr1:102312671-102312721	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:102310233..102312368-chr1:102385841..102387762,2	MCF-7	breast:
2	chr1:102310233..102312368-chr1:102385841..102387762,2	MCF-7	breast:
3	chr1:102308106..102310001-chr1:102313421..102315280,2	K562	blood:
4	chr1:102308106..102310001-chr1:102313421..102315280,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-S1PR1-13	chr1:102358613-102360299	NONHSAT004867
2	lnc-S1PR1-13	chr1:102358661-102359603	NONHSAT004869
3	lnc-S1PR1-13	chr1:102337567-102337661	NONHSAT004867
4	lnc-S1PR1-12	chr1:102348072-102348450	NONHSAT004868

No data

Variant related genes	Relation type
RNU6-352P	TF binding region
OLFM3	TF binding region
ENSG00000271277	TF binding region
DNAJA1P5	TF binding region
RNU6-352P	CpG island
OLFM3	CpG island
ENSG00000271277	CpG island
DNAJA1P5	CpG island

Extended variants
information (count: 2199 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71483853	chr1:102309649-102309650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4908194	chr1:102309650-102309651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186522651	chr1:102309707-102309708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115046344	chr1:102309717-102309718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543670251	chr1:102309727-102309728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562138056	chr1:102309729-102309730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150512374	chr1:102309762-102309763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140366571	chr1:102309829-102309830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142766342	chr1:102309866-102309867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533403907	chr1:102309887-102309888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551771124	chr1:102309937-102309938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191907747	chr1:102310082-102310083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559127062	chr1:102310151-102310152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548218638	chr1:102310168-102310169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183003744	chr1:102310170-102310171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549179448	chr1:102310277-102310278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2185618	chr1:102310279-102310280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535181934	chr1:102310284-102310285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147294790	chr1:102310300-102310301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140962404	chr1:102310310-102310311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75347076	chr1:102310372-102310373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150967211	chr1:102310373-102310374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111838227	chr1:102310408-102310409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74107951	chr1:102310431-102310432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs11164310	chr1:102310443-102310444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs543609304	chr1:102310519-102310520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191421438	chr1:102310645-102310646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573928380	chr1:102310671-102310672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182401571	chr1:102310681-102310682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187438760	chr1:102310703-102310704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4908195	chr1:102310706-102310707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs558864307	chr1:102310720-102310721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1445223	chr1:102310723-102310724	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs11580820	chr1:102310737-102310738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528224473	chr1:102310749-102310750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111762741	chr1:102310785-102310786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567518794	chr1:102310822-102310823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540305222	chr1:102310898-102310899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200099884	chr1:102310944-102310945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146553878	chr1:102311001-102311002	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs565106341	chr1:102311111-102311112	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs547163839	chr1:102311145-102311146	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs371091131	chr1:102311237-102311238	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs565796482	chr1:102311245-102311246	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs191979412	chr1:102311263-102311264	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs557751802	chr1:102311318-102311319	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs569811521	chr1:102311337-102311338	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs537338419	chr1:102311358-102311359	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs555738567	chr1:102311426-102311427	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72987940	chr1:102311480-102311481	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:102268400-102311200	Weak transcription	Fetal Intestine Large	intestine
2	chr1:102294400-102311200	Weak transcription	Fetal Intestine Small	intestine
3	chr1:102307000-102310200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr1:102307600-102312400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:102307800-102310200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:102308200-102309800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr1:102308200-102310000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr1:102308400-102310000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr1:102308800-102310200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr1:102309000-102310000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr1:102309000-102312400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:102309200-102310000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:102309200-102312400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr1:102309400-102309800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:102309400-102310000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:102309600-102311800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:102309600-102311800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr1:102309800-102310000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:102309800-102312200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr1:102310000-102311000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:102310000-102312200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr1:102310000-102312200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr1:102310000-102312200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:102310000-102312400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:102310000-102312400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:102310200-102311200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr1:102310200-102312200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr1:102310200-102312200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:102311000-102313000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr1:102311200-102311400	Flanking Active TSS	Fetal Intestine Small	intestine
31	chr1:102311200-102312200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr1:102311200-102313400	Active TSS	Fetal Intestine Large	intestine
33	chr1:102311400-102313400	Active TSS	Fetal Intestine Small	intestine
34	chr1:102311800-102312200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:102311800-102312200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr1:102312200-102312400	Active TSS	H1 Cell Line	embryonic stem cell
37	chr1:102312200-102312400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr1:102312200-102312400	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr1:102312200-102312400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr1:102312200-102312400	Enhancers	Brain Germinal Matrix	brain
41	chr1:102312200-102312400	Enhancers	Fetal Brain Female	brain
42	chr1:102312200-102312800	Active TSS	H9 Cell Line	embryonic stem cell
43	chr1:102312200-102312800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr1:102312200-102312800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr1:102312200-102312800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:102312200-102312800	Active TSS	Fetal Kidney	kidney
47	chr1:102312200-102313000	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr1:102312200-102313000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr1:102312200-102313000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr1:102312400-102312600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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