Variant report

Variant	nsv1008210
Chromosome Location	chr1:72099161-72374197
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	chr1:72246439-72246725	GM12878	blood:	n/a	chr1:72246586-72246597 chr1:72246587-72246597
2	BATF	chr1:72246451-72246721	GM12878	blood:	n/a	chr1:72246586-72246597 chr1:72246587-72246597
3	BHLHE40	chr1:72205203-72205242	GM12878	blood:	n/a	n/a
4	CEBPB	chr1:72132874-72133198	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
5	CEBPB	chr1:72294559-72294726	HepG2	liver:	n/a	chr1:72294674-72294685
6	CEBPB	chr1:72132850-72133320	Hela-S3	cervix:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
7	CEBPB	chr1:72353101-72353423	IMR90	lung:	n/a	chr1:72353242-72353253
8	CEBPB	chr1:72290112-72290442	HepG2	liver:	n/a	chr1:72290286-72290297
9	CEBPB	chr1:72120017-72120305	HepG2	liver:	n/a	chr1:72120144-72120155
10	CEBPB	chr1:72322163-72322385	HepG2	liver:	n/a	chr1:72322284-72322295
11	CEBPB	chr1:72290198-72290381	H1-hESC	embryonic stem cell:	n/a	chr1:72290286-72290297
12	CEBPB	chr1:72353137-72353285	K562	blood:	n/a	chr1:72353242-72353253
13	CEBPB	chr1:72290161-72290431	A549	lung:	n/a	chr1:72290286-72290297
14	CEBPB	chr1:72132278-72133317	IMR90	lung:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
15	CEBPB	chr1:72240165-72240391	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:72230419-72230782	HepG2	liver:	n/a	chr1:72230589-72230600
17	CEBPB	chr1:72290106-72290476	IMR90	lung:	n/a	chr1:72290286-72290297
18	CEBPB	chr1:72214678-72215002	IMR90	lung:	n/a	chr1:72214832-72214845
19	CEBPB	chr1:72230467-72230667	H1-hESC	embryonic stem cell:	n/a	chr1:72230589-72230600
20	CEBPB	chr1:72230432-72230774	A549	lung:	n/a	chr1:72230589-72230600
21	CEBPB	chr1:72161508-72161870	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:72132885-72133214	HepG2	liver:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
23	CEBPB	chr1:72290139-72290394	K562	blood:	n/a	chr1:72290286-72290297
24	CEBPB	chr1:72122476-72122921	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:72103843-72104179	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:72230408-72230785	IMR90	lung:	n/a	chr1:72230589-72230600
27	CEBPB	chr1:72132835-72133315	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
28	CEBPB	chr1:72230483-72230683	Hela-S3	cervix:	n/a	chr1:72230589-72230600
29	CEBPB	chr1:72326736-72327069	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:72353163-72353392	HepG2	liver:	n/a	chr1:72353242-72353253
31	CEBPB	chr1:72274296-72274496	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:72128205-72128324	HepG2	liver:	n/a	chr1:72128261-72128272
33	CEBPB	chr1:72326678-72327071	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:72138249-72138465	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:72353187-72353408	A549	lung:	n/a	chr1:72353242-72353253
36	CTCF	chr1:72261898-72261907	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:72187380-72187530	GM12869	blood:	n/a	n/a
38	CTCF	chr1:72277700-72277850	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr1:72277680-72277830	HepG2	liver:	n/a	n/a
40	CTCF	chr1:72261840-72261990	HMEC	breast:	n/a	n/a
41	CTCF	chr1:72174840-72174893	GM13976	blood:	n/a	n/a
42	CTCF	chr1:72171840-72171990	AG04450	lung:	n/a	n/a
43	CTCF	chr1:72261820-72261970	GM12867	blood:	n/a	n/a
44	CTCF	chr1:72261820-72261970	GM06990	blood:	n/a	n/a
45	CTCF	chr1:72171820-72171970	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr1:72261820-72261970	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr1:72187320-72187470	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:72172120-72172270	AG04450	lung:	n/a	n/a
49	CTCF	chr1:72171760-72171910	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr1:72261860-72262010	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72354156-72354206	HRCEpiC	kidney:	n/a
2	chr1:72354156-72354206	NB4	blood:	n/a
3	chr1:72354156-72354206	AG09309	skin:	n/a
4	chr1:72354156-72354206	NHDF-neo	bronchial:	n/a
5	chr1:72354156-72354206	HCT-116	colon:	n/a
6	chr1:72354156-72354206	HCF	heart:	n/a
7	chr1:72354156-72354206	RPTEC	kidney:	n/a
8	chr1:72354156-72354206	GM12878	blood:	n/a
9	chr1:72302970-72303020	SK-N-SH_RA	brain:	n/a
10	chr1:72302970-72303020	HCF	heart:	n/a
11	chr1:72302970-72303020	PANC-1	pancreas:	n/a
12	chr1:72190606-72190656	AG09319	gingival:	n/a
13	chr1:72354156-72354206	ECC-1	luminal epithelium:	n/a
14	chr1:72302970-72303020	ProgFib	skin:	n/a
15	chr1:72354156-72354206	HepG2	liver:	n/a
16	chr1:72302970-72303020	AG04449	skin:	fetal
17	chr1:72190606-72190656	HEK293	kidney:	embryo
18	chr1:72190606-72190656	AG09309	skin:	n/a
19	chr1:72190606-72190656	H1-hESC	embryonic stem cell:	embryo
20	chr1:72302970-72303020	HEEpiC	esophagus:	n/a
21	chr1:72190606-72190656	RPTEC	kidney:	n/a
22	chr1:72190606-72190656	PFSK-1	brain:	n/a
23	chr1:72190606-72190656	AG10803	skin:	n/a
24	chr1:72190606-72190656	CMK	blood:	n/a
25	chr1:72354156-72354206	T-47D	breast:	n/a
26	chr1:72190606-72190656	NB4	blood:	n/a
27	chr1:72354156-72354206	K562	blood:	n/a
28	chr1:72302970-72303020	HCM	heart:	n/a
29	chr1:72302970-72303020	GM06990	blood:	n/a
30	chr1:72302970-72303020	U87	brain:	n/a
31	chr1:72354156-72354206	HMEC	breast:	n/a
32	chr1:72302970-72303020	HRCEpiC	kidney:	n/a
33	chr1:72302970-72303020	K562	blood:	n/a
34	chr1:72302970-72303020	ECC-1	luminal epithelium:	n/a
35	chr1:72302970-72303020	PrEC	prostate:	n/a
36	chr1:72190606-72190656	GM19239	blood:	n/a
37	chr1:72354156-72354206	HRE	kidney:	n/a
38	chr1:72302970-72303020	NHBE	bronchial:	n/a
39	chr1:72190606-72190656	GM12891	blood:	n/a
40	chr1:72190606-72190656	BE2_C	brain:	n/a
41	chr1:72354156-72354206	LNCaP	prostate:	n/a
42	chr1:72302970-72303020	HIPEpiC	eye:	n/a
43	chr1:72302970-72303020	HCT-116	colon:	n/a
44	chr1:72302970-72303020	BE2_C	brain:	n/a
45	chr1:72190606-72190656	HNPCEpiC	eye:	n/a
46	chr1:72302970-72303020	GM12878	blood:	n/a
47	chr1:72190606-72190656	NHDF-neo	bronchial:	n/a
48	chr1:72302970-72303020	GM12892	blood:	n/a
49	chr1:72190606-72190656	ProgFib	skin:	n/a
50	chr1:72302970-72303020	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
2	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
3	chr1:72142368..72144115-chr1:72151008..72153823,2	K562	blood:
4	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
5	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
6	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:
7	chr1:72142368..72144115-chr1:72151008..72153823,2	K562	blood:
8	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
9	chr1:71915989..71918426-chr1:72103464..72106010,2	K562	blood:
10	chr1:72129396..72131726-chr1:72132350..72134861,2	K562	blood:
11	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:
12	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
13	chr1:72129396..72131726-chr1:72132350..72134861,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRANB2-1	chr1:72263758-72263953	ENSG00000228853.1
2	lnc-ZRANB2-1	chr1:72259915-72260219	ENSG00000228853.1
3	lnc-ZRANB2-1	chr1:72302663-72302695	ENSG00000228853.1

Variant related genes	Relation type
NEGR1-IT1	TF binding region
NEGR1	TF binding region
ENSG00000271618	TF binding region
NEGR1-IT1	CpG island
NEGR1	CpG island
ENSG00000271618	CpG island

Extended variants
information (count: 7598 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:7598 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141669816	chr1:72099207-72099208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536429835	chr1:72099230-72099231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574686529	chr1:72099234-72099235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17091540	chr1:72099244-72099245	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554770619	chr1:72099290-72099291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185628343	chr1:72099388-72099389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576473379	chr1:72099420-72099421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545481993	chr1:72099421-72099422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559418196	chr1:72099478-72099479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368714551	chr1:72099517-72099518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572511410	chr1:72099531-72099532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117996835	chr1:72099534-72099535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188263510	chr1:72099554-72099555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145432223	chr1:72099559-72099560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576124816	chr1:72099605-72099606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572298247	chr1:72099658-72099659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550535418	chr1:72099667-72099668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563657807	chr1:72099678-72099679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs180806475	chr1:72099763-72099764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151100306	chr1:72099767-72099768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141042264	chr1:72099813-72099814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534933701	chr1:72099940-72099941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528233952	chr1:72099953-72099954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558007511	chr1:72099958-72099959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34309797	chr1:72099988-72099989	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs183689640	chr1:72104006-72104007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565865007	chr1:72104030-72104031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs145248934	chr1:72104072-72104073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563428211	chr1:72104085-72104086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571660727	chr1:72104093-72104094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188009195	chr1:72104110-72104111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554274299	chr1:72104137-72104138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573845125	chr1:72104141-72104142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530745170	chr1:72104185-72104186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542862017	chr1:72104202-72104203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556448585	chr1:72104221-72104222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551950341	chr1:72104233-72104234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148732277	chr1:72104238-72104239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564190768	chr1:72104241-72104242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576397372	chr1:72104243-72104244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545372140	chr1:72104280-72104281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534875878	chr1:72104313-72104314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112402443	chr1:72104316-72104317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564706143	chr1:72104320-72104321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572043924	chr1:72104357-72104358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540735653	chr1:72104368-72104369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571771269	chr1:72104381-72104382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561061610	chr1:72104384-72104385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1041676	chr1:72104447-72104448	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546571701	chr1:72104463-72104464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Epilepsy	20502679	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD

Chromatin state (count:803 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72099200-72099600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:72099200-72100000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:72104000-72104400	Enhancers	NHDF-Ad	bronchial
4	chr1:72104000-72104600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:72104000-72104600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr1:72104000-72105600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:72104000-72105800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:72104200-72104400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:72104200-72104600	Enhancers	HSMM	muscle
10	chr1:72104200-72104800	Enhancers	Osteobl	bone
11	chr1:72104400-72105400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:72104600-72105800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:72104600-72105800	Weak transcription	HSMM	muscle
14	chr1:72104800-72105200	Enhancers	Thymus	Thymus
15	chr1:72105200-72107200	Weak transcription	Thymus	Thymus
16	chr1:72105400-72106200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr1:72105400-72106800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:72105600-72106200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:72105600-72106200	Enhancers	Adipose Nuclei	Adipose
20	chr1:72105600-72106400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:72105600-72106400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:72105600-72107200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:72105800-72106200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:72105800-72106400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:72105800-72106600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:72106000-72106200	Enhancers	HSMM	muscle
27	chr1:72106200-72107800	Weak transcription	Adipose Nuclei	Adipose
28	chr1:72106200-72108400	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr1:72106400-72106800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:72106400-72108200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:72106400-72109000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:72106600-72107000	Enhancers	Brain Substantia Nigra	brain
33	chr1:72106800-72107000	Enhancers	Right Atrium	heart
34	chr1:72107200-72107800	Enhancers	Thymus	Thymus
35	chr1:72107200-72108800	Enhancers	Fetal Thymus	thymus
36	chr1:72107400-72107600	Enhancers	Left Ventricle	heart
37	chr1:72107600-72107800	Enhancers	Right Atrium	heart
38	chr1:72107800-72108200	Enhancers	Adipose Nuclei	Adipose
39	chr1:72107800-72109000	Enhancers	Colon Smooth Muscle	Colon
40	chr1:72108400-72111800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr1:72109000-72109800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:72109000-72114000	Weak transcription	Colon Smooth Muscle	Colon
43	chr1:72111800-72112400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr1:72113200-72113400	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr1:72113200-72113600	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr1:72113200-72115200	Enhancers	Fetal Stomach	stomach
47	chr1:72113400-72113800	Enhancers	Rectal Smooth Muscle	rectum
48	chr1:72113800-72114000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr1:72114000-72114200	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr1:72114000-72114400	Enhancers	Rectal Smooth Muscle	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links