Variant report

Variant	nsv870762
Chromosome Location	chr1:72300968-72376262
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	CEBPB	chr1:72353187-72353408	A549	lung:	n/a	chr1:72353242-72353253
2	CEBPB	chr1:72326736-72327069	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:72326678-72327071	IMR90	lung:	n/a	n/a
4	CEBPB	chr1:72353163-72353392	HepG2	liver:	n/a	chr1:72353242-72353253
5	CEBPB	chr1:72322163-72322385	HepG2	liver:	n/a	chr1:72322284-72322295
6	CEBPB	chr1:72353137-72353285	K562	blood:	n/a	chr1:72353242-72353253
7	CEBPB	chr1:72353101-72353423	IMR90	lung:	n/a	chr1:72353242-72353253
8	CTCF	chr1:72328657-72328672	LNCaP	prostate:	n/a	n/a
9	CTCF	chr1:72329920-72330070	HFF-Myc	foreskin:	n/a	n/a
10	CUX1	chr1:72360285-72360377	K562	blood:	n/a	n/a
11	CUX1	chr1:72301117-72301463	GM12878	blood:	n/a	chr1:72301247-72301256
12	E2F4	chr1:72336257-72336706	MCF10A-Er-Src	breast:	n/a	chr1:72336449-72336458
13	E2F4	chr1:72366239-72366462	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr1:72368266-72368426	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr1:72326618-72327027	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr1:72301190-72301452	GM12878	blood:	n/a	n/a
17	ELK1	chr1:72366268-72366339	GM12878	blood:	n/a	n/a
18	EP300	chr1:72326830-72327040	Hela-S3	cervix:	n/a	n/a
19	EP300	chr1:72305240-72306317	SK-N-SH	brain:	n/a	n/a
20	EP300	chr1:72308696-72309029	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr1:72334841-72335572	SK-N-SH	brain:	n/a	chr1:72335056-72335070 chr1:72335446-72335460
22	EP300	chr1:72305569-72305989	SK-N-SH_RA	brain:	n/a	n/a
23	FAM48A	chr1:72350621-72350821	GM12878	blood:	n/a	n/a
24	FOS	chr1:72327480-72327549	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:72326671-72327130	HUVEC	blood vessel:	n/a	chr1:72326887-72326898 chr1:72326901-72326912
26	FOS	chr1:72326683-72327128	MCF10A-Er-Src	breast:	n/a	chr1:72326887-72326898 chr1:72326901-72326912
27	FOS	chr1:72321968-72322318	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:72323779-72323781	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:72336106-72336520	MCF10A-Er-Src	breast:	n/a	chr1:72336273-72336285 chr1:72336274-72336284 chr1:72336275-72336283 chr1:72336274-72336284
30	FOS	chr1:72351024-72351182	MCF10A-Er-Src	breast:	n/a	chr1:72351075-72351086
31	FOS	chr1:72306291-72306531	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:72326697-72327108	MCF10A-Er-Src	breast:	n/a	chr1:72326887-72326898 chr1:72326901-72326912
33	FOS	chr1:72306290-72306490	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:72336109-72336553	MCF10A-Er-Src	breast:	n/a	chr1:72336273-72336285 chr1:72336274-72336284 chr1:72336275-72336283 chr1:72336274-72336284
35	FOS	chr1:72323649-72323660	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:72326585-72327185	MCF10A-Er-Src	breast:	n/a	chr1:72326887-72326898 chr1:72326901-72326912
37	FOS	chr1:72316806-72316943	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:72326650-72327161	MCF10A-Er-Src	breast:	n/a	chr1:72326887-72326898 chr1:72326901-72326912
39	FOS	chr1:72336078-72336543	MCF10A-Er-Src	breast:	n/a	chr1:72336273-72336285 chr1:72336274-72336284 chr1:72336275-72336283 chr1:72336274-72336284
40	FOS	chr1:72336115-72336540	MCF10A-Er-Src	breast:	n/a	chr1:72336273-72336285 chr1:72336274-72336284 chr1:72336275-72336283 chr1:72336274-72336284
41	FOS	chr1:72305054-72305248	MCF10A-Er-Src	breast:	n/a	n/a
42	FOXA2	chr1:72354053-72354634	A549	lung:	n/a	n/a
43	FOXA2	chr1:72354001-72354604	A549	lung:	n/a	n/a
44	FOXP2	chr1:72374733-72375081	SK-N-MC	brain:	n/a	n/a
45	FOXP2	chr1:72322191-72322433	SK-N-MC	brain:	n/a	n/a
46	GATA1	chr1:72347311-72348087	PBDE	blood:	n/a	chr1:72347614-72347627 chr1:72347943-72347952
47	GATA1	chr1:72300360-72301357	PBDE	blood:	n/a	chr1:72301272-72301282 chr1:72300426-72300436
48	GATA1	chr1:72332263-72332756	PBDE	blood:	n/a	chr1:72332522-72332529 chr1:72332517-72332533 chr1:72332520-72332530 chr1:72332522-72332529 chr1:72332522-72332529
49	GATA2	chr1:72335098-72335475	SH-SY5Y	brain:	n/a	chr1:72335230-72335246 chr1:72335235-72335242
50	GATA2	chr1:72308711-72309266	SH-SY5Y	brain:	n/a	chr1:72309006-72309014

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72302970-72303020	ECC-1	luminal epithelium:	n/a
2	chr1:72302970-72303020	BJ	skin:	n/a
3	chr1:72354156-72354206	HCPEpiC	choroid plexus:	n/a
4	chr1:72354156-72354206	GM12878	blood:	n/a
5	chr1:72302970-72303020	AG10803	skin:	n/a
6	chr1:72302970-72303020	A549	lung:	n/a
7	chr1:72354156-72354206	GM06990	blood:	n/a
8	chr1:72302970-72303020	MCF-7	breast:	n/a
9	chr1:72302970-72303020	CMK	blood:	n/a
10	chr1:72354156-72354206	GM19239	blood:	n/a
11	chr1:72354156-72354206	Caco-2	colon:	n/a
12	chr1:72302970-72303020	ovcar-3	ovarian:	n/a
13	chr1:72302970-72303020	GM12892	blood:	n/a
14	chr1:72354156-72354206	K562	blood:	n/a
15	chr1:72354156-72354206	LNCaP	prostate:	n/a
16	chr1:72354156-72354206	NB4	blood:	n/a
17	chr1:72302970-72303020	HL-60	blood:	n/a
18	chr1:72354156-72354206	AoSMC	blood vessel:	n/a
19	chr1:72354156-72354206	HAEpiC	amniotic membrane:	n/a
20	chr1:72354156-72354206	Hepatocyte	liver:	n/a
21	chr1:72354156-72354206	MCF10A-Er-Src	breast:	n/a
22	chr1:72302970-72303020	SK-N-SH_RA	brain:	n/a
23	chr1:72354156-72354206	NHBE	bronchial:	n/a
24	chr1:72354156-72354206	HepG2	liver:	n/a
25	chr1:72354156-72354206	PrEC	prostate:	n/a
26	chr1:72354156-72354206	AG09319	gingival:	n/a
27	chr1:72302970-72303020	HMEC	breast:	n/a
28	chr1:72302970-72303020	NH-A	brain:	n/a
29	chr1:72302970-72303020	PrEC	prostate:	n/a
30	chr1:72354156-72354206	SK-N-MC	brain:	n/a
31	chr1:72354156-72354206	A549	lung:	n/a
32	chr1:72302970-72303020	GM06990	blood:	n/a
33	chr1:72302970-72303020	HRPEpiC	eye:	n/a
34	chr1:72302970-72303020	BE2_C	brain:	n/a
35	chr1:72354156-72354206	T-47D	breast:	n/a
36	chr1:72302970-72303020	GM12891	blood:	n/a
37	chr1:72302970-72303020	HCPEpiC	choroid plexus:	n/a
38	chr1:72302970-72303020	HNPCEpiC	eye:	n/a
39	chr1:72354156-72354206	GM12892	blood:	n/a
40	chr1:72354156-72354206	IMR90	lung:	fetal
41	chr1:72302970-72303020	GM12878	blood:	n/a
42	chr1:72354156-72354206	BE2_C	brain:	n/a
43	chr1:72302970-72303020	PANC-1	pancreas:	n/a
44	chr1:72302970-72303020	HUVEC	blood vessel:	n/a
45	chr1:72354156-72354206	HNPCEpiC	eye:	n/a
46	chr1:72302970-72303020	Caco-2	colon:	n/a
47	chr1:72302970-72303020	NHDF-neo	bronchial:	n/a
48	chr1:72302970-72303020	K562	blood:	n/a
49	chr1:72302970-72303020	HEEpiC	esophagus:	n/a
50	chr1:72354156-72354206	RPTEC	kidney:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRANB2-1	chr1:72302663-72302695	ENSG00000228853.1

Variant related genes	Relation type
NEGR1-IT1	TF binding region
NEGR1-IT1	CpG island

Extended variants
information (count: 2111 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:2111 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs522451	chr1:72300968-72300969	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372714624	chr1:72300993-72300994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377050633	chr1:72301064-72301065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183998346	chr1:72301095-72301096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541087311	chr1:72301097-72301098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538920369	chr1:72301127-72301128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561397922	chr1:72301146-72301147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142368773	chr1:72301154-72301155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572989664	chr1:72301169-72301170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569909706	chr1:72301177-72301178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532436329	chr1:72301214-72301215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552532812	chr1:72301220-72301221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539353253	chr1:72301242-72301243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs36034907	chr1:72301252-72301253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150818798	chr1:72301268-72301269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189693884	chr1:72301339-72301340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192934816	chr1:72301389-72301390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112734747	chr1:72301451-72301452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74089012	chr1:72301453-72301454	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs185171933	chr1:72301498-72301499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536750366	chr1:72301522-72301523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561676560	chr1:72301537-72301538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556715380	chr1:72301584-72301585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147144618	chr1:72301604-72301605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576270590	chr1:72301612-72301613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530936073	chr1:72301636-72301637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558797120	chr1:72301660-72301661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563002649	chr1:72301679-72301680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs61765275	chr1:72301728-72301729	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs145622827	chr1:72301740-72301741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561128618	chr1:72301742-72301743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190496228	chr1:72301758-72301759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543590647	chr1:72301771-72301772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147747230	chr1:72301832-72301833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116657682	chr1:72301840-72301841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76194924	chr1:72301841-72301842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113758431	chr1:72301851-72301852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528387321	chr1:72301879-72301880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144815371	chr1:72301897-72301898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568010769	chr1:72301978-72301979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181879736	chr1:72302003-72302004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117390137	chr1:72302004-72302005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs202142653	chr1:72302090-72302091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4650124	chr1:72302120-72302121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112774660	chr1:72302121-72302122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4649951	chr1:72302137-72302138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558734253	chr1:72302139-72302140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4649952	chr1:72302159-72302160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374055765	chr1:72302163-72302164	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71699403	chr1:72302164-72302165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
abnormal development	18461090	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
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72293200-72301800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:72294800-72302200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr1:72294800-72302400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr1:72294800-72302600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr1:72295200-72302600	Weak transcription	Brain Anterior Caudate	brain
6	chr1:72295600-72301800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr1:72295600-72302400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:72298400-72302800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:72299400-72301000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr1:72299600-72304600	Enhancers	Fetal Heart	heart
11	chr1:72300000-72301000	Enhancers	Brain Cingulate Gyrus	brain
12	chr1:72300000-72301000	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr1:72300000-72301000	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr1:72300200-72301000	Enhancers	Colon Smooth Muscle	Colon
15	chr1:72300200-72301000	Enhancers	Fetal Intestine Small	intestine
16	chr1:72300400-72301200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr1:72300400-72301400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:72300600-72301000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:72300600-72301000	Enhancers	Primary B cells from peripheral blood	blood
20	chr1:72300600-72301000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:72300600-72301400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr1:72300600-72301800	Enhancers	Primary B cells from cord blood	blood
23	chr1:72300800-72301200	Enhancers	Brain Substantia Nigra	brain
24	chr1:72301000-72302400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr1:72301400-72302400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:72301600-72303800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:72301800-72303200	Enhancers	H1 Cell Line	embryonic stem cell
28	chr1:72301800-72303400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr1:72301800-72303800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr1:72302200-72303600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr1:72302400-72302800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr1:72302400-72302800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr1:72302400-72302800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:72302400-72303400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr1:72302600-72302800	Enhancers	Brain Anterior Caudate	brain
36	chr1:72302600-72303600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:72302800-72303000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:72302800-72303000	Enhancers	Brain Cingulate Gyrus	brain
39	chr1:72302800-72303600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr1:72306000-72306600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:72307600-72308800	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr1:72308800-72309200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr1:72310000-72310600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:72310200-72310600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:72310200-72310600	Enhancers	Ovary	ovary
46	chr1:72310400-72311000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:72310600-72313000	Weak transcription	Ovary	ovary
48	chr1:72315800-72316400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:72316000-72317800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:72316400-72316800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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