Variant report

Variant	nsv533779
Chromosome Location	chr1:72124095-72241965
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:192)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:192 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:72205203-72205242	GM12878	blood:	n/a	n/a
2	CEBPB	chr1:72230467-72230667	H1-hESC	embryonic stem cell:	n/a	chr1:72230589-72230600
3	CEBPB	chr1:72138249-72138465	HepG2	liver:	n/a	n/a
4	CEBPB	chr1:72161508-72161870	IMR90	lung:	n/a	n/a
5	CEBPB	chr1:72240165-72240391	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:72230408-72230785	IMR90	lung:	n/a	chr1:72230589-72230600
7	CEBPB	chr1:72230432-72230774	A549	lung:	n/a	chr1:72230589-72230600
8	CEBPB	chr1:72230483-72230683	Hela-S3	cervix:	n/a	chr1:72230589-72230600
9	CEBPB	chr1:72128205-72128324	HepG2	liver:	n/a	chr1:72128261-72128272
10	CEBPB	chr1:72132874-72133198	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
11	CEBPB	chr1:72230419-72230782	HepG2	liver:	n/a	chr1:72230589-72230600
12	CEBPB	chr1:72132885-72133214	HepG2	liver:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
13	CEBPB	chr1:72132835-72133315	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
14	CEBPB	chr1:72132278-72133317	IMR90	lung:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
15	CEBPB	chr1:72132850-72133320	Hela-S3	cervix:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
16	CEBPB	chr1:72214678-72215002	IMR90	lung:	n/a	chr1:72214832-72214845
17	CTCF	chr1:72171840-72171990	AG04450	lung:	n/a	n/a
18	CTCF	chr1:72171820-72171970	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr1:72187380-72187530	GM12869	blood:	n/a	n/a
20	CTCF	chr1:72172100-72172250	BE2_C	brain:	n/a	n/a
21	CTCF	chr1:72187340-72187490	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr1:72187278-72187552	GM12878	blood:	n/a	n/a
23	CTCF	chr1:72187320-72187470	HMEC	breast:	n/a	n/a
24	CTCF	chr1:72187360-72187510	HRE	kidney:	n/a	n/a
25	CTCF	chr1:72195915-72195982	HUVEC	blood vessel:	n/a	chr1:72195921-72195939
26	CTCF	chr1:72187260-72187410	HMEC	breast:	n/a	n/a
27	CTCF	chr1:72187211-72187521	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:72172142-72172201	NHEK	skin:	n/a	n/a
29	CTCF	chr1:72187320-72187470	GM12874	blood:	n/a	n/a
30	CTCF	chr1:72172156-72172187	ProgFib	skin:	n/a	n/a
31	CTCF	chr1:72187280-72187430	RPTEC	kidney:	n/a	n/a
32	CTCF	chr1:72172060-72172210	HepG2	liver:	n/a	n/a
33	CTCF	chr1:72172140-72172290	AG09319	gingival:	n/a	n/a
34	CTCF	chr1:72219500-72219650	WI-38	lung:	n/a	n/a
35	CTCF	chr1:72187200-72187350	RPTEC	kidney:	n/a	n/a
36	CTCF	chr1:72187409-72187470	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr1:72187440-72187590	NB4	blood:	n/a	n/a
38	CTCF	chr1:72172020-72172170	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr1:72187380-72187530	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr1:72219856-72219911	Fibrobl	skin:	n/a	n/a
41	CTCF	chr1:72172143-72172220	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr1:72187340-72187490	NHEK	skin:	n/a	n/a
43	CTCF	chr1:72187340-72187490	HEK293	kidney:	n/a	n/a
44	CTCF	chr1:72172080-72172230	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr1:72171780-72171930	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr1:72172120-72172270	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr1:72187380-72187530	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:72187340-72187490	GM12873	blood:	n/a	n/a
49	CTCF	chr1:72187280-72187430	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr1:72171760-72171910	NHDF-neo	bronchial:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72190606-72190656	HUVEC	blood vessel:	n/a
2	chr1:72190606-72190656	CMK	blood:	n/a
3	chr1:72190606-72190656	MCF-7	breast:	n/a
4	chr1:72190606-72190656	U87	brain:	n/a
5	chr1:72190606-72190656	NHBE	bronchial:	n/a
6	chr1:72190606-72190656	HIPEpiC	eye:	n/a
7	chr1:72190606-72190656	T-47D	breast:	n/a
8	chr1:72190606-72190656	Hela-S3	cervix:	n/a
9	chr1:72190606-72190656	Jurkat	blood:	n/a
10	chr1:72190606-72190656	ECC-1	luminal epithelium:	n/a
11	chr1:72190606-72190656	NT2-D1	testis:	n/a
12	chr1:72190606-72190656	LNCaP	prostate:	n/a
13	chr1:72190606-72190656	HAEpiC	amniotic membrane:	n/a
14	chr1:72190606-72190656	AG09319	gingival:	n/a
15	chr1:72190606-72190656	SK-N-SH	brain:	n/a
16	chr1:72190606-72190656	AG09309	skin:	n/a
17	chr1:72190606-72190656	GM06990	blood:	n/a
18	chr1:72190606-72190656	IMR90	lung:	fetal
19	chr1:72190606-72190656	GM12891	blood:	n/a
20	chr1:72190606-72190656	BJ	skin:	n/a
21	chr1:72190606-72190656	AG04450	lung:	fetal
22	chr1:72190606-72190656	NH-A	brain:	n/a
23	chr1:72190606-72190656	A549	lung:	n/a
24	chr1:72190606-72190656	GM12878	blood:	n/a
25	chr1:72190606-72190656	AG04449	skin:	fetal
26	chr1:72190606-72190656	H1-hESC	embryonic stem cell:	embryo
27	chr1:72190606-72190656	SAEC	small airway:	n/a
28	chr1:72190606-72190656	HCT-116	colon:	n/a
29	chr1:72190606-72190656	HRCEpiC	kidney:	n/a
30	chr1:72190606-72190656	HEK293	kidney:	embryo
31	chr1:72190606-72190656	RPTEC	kidney:	n/a
32	chr1:72190606-72190656	K562	blood:	n/a
33	chr1:72190606-72190656	AG10803	skin:	n/a
34	chr1:72190606-72190656	HCPEpiC	choroid plexus:	n/a
35	chr1:72190606-72190656	MCF10A-Er-Src	breast:	n/a
36	chr1:72190606-72190656	AoSMC	blood vessel:	n/a
37	chr1:72190606-72190656	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:72190606-72190656	HL-60	blood:	n/a
39	chr1:72190606-72190656	PANC-1	pancreas:	n/a
40	chr1:72190606-72190656	BE2_C	brain:	n/a
41	chr1:72190606-72190656	SK-N-SH_RA	brain:	n/a
42	chr1:72190606-72190656	HCM	heart:	n/a
43	chr1:72190606-72190656	PFSK-1	brain:	n/a
44	chr1:72190606-72190656	HNPCEpiC	eye:	n/a
45	chr1:72190606-72190656	HRPEpiC	eye:	n/a
46	chr1:72190606-72190656	SK-N-MC	brain:	n/a
47	chr1:72190606-72190656	Caco-2	colon:	n/a
48	chr1:72190606-72190656	HRE	kidney:	n/a
49	chr1:72190606-72190656	HCF	heart:	n/a
50	chr1:72190606-72190656	HepG2	liver:	n/a

(count:12 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3228 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3228 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536316341	chr1:72124179-72124180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555842367	chr1:72124186-72124187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78350643	chr1:72124240-72124241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181312695	chr1:72124250-72124251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544392113	chr1:72124251-72124252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559562282	chr1:72124295-72124296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376260075	chr1:72124339-72124340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529931104	chr1:72124358-72124359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370723947	chr1:72124399-72124400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112690894	chr1:72124451-72124452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577902066	chr1:72124457-72124458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111669754	chr1:72124504-72124505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565895473	chr1:72124530-72124531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1610385	chr1:72124722-72124723	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548514649	chr1:72124746-72124747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549419374	chr1:72124750-72124751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116740145	chr1:72124755-72124756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531891940	chr1:72124787-72124788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552143778	chr1:72124804-72124805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551577068	chr1:72124819-72124820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373245648	chr1:72124945-72124946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571497995	chr1:72124975-72124976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186273793	chr1:72124987-72124988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547395002	chr1:72125020-72125021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567204938	chr1:72125021-72125022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190427426	chr1:72125062-72125063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532791080	chr1:72125085-72125086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555780764	chr1:72125086-72125087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140976876	chr1:72125118-72125119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2152219	chr1:72125154-72125155	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs377016823	chr1:72125160-72125161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143430173	chr1:72125211-72125212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374235606	chr1:72125292-72125293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs578126890	chr1:72125346-72125347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565899162	chr1:72125403-72125404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370104665	chr1:72125409-72125410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143855758	chr1:72125437-72125438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12563509	chr1:72125448-72125449	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs574318871	chr1:72125475-72125476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142103112	chr1:72125543-72125544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562895951	chr1:72125614-72125615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531822522	chr1:72125650-72125651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551919098	chr1:72125657-72125658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181695906	chr1:72125714-72125715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186816402	chr1:72125726-72125727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547628114	chr1:72125766-72125767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375150235	chr1:72125848-72125849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567438108	chr1:72125942-72125943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539562778	chr1:72126006-72126007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536596270	chr1:72126019-72126020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72122400-72126000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:72122600-72124400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:72122600-72126200	Enhancers	NHDF-Ad	bronchial
4	chr1:72123200-72124800	Enhancers	Colon Smooth Muscle	Colon
5	chr1:72123200-72125000	Enhancers	Adipose Nuclei	Adipose
6	chr1:72123400-72124200	Enhancers	Stomach Smooth Muscle	stomach
7	chr1:72123600-72124800	Weak transcription	Fetal Stomach	stomach
8	chr1:72123800-72126200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:72124000-72125000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:72124000-72130400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr1:72124400-72125800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:72124800-72125200	Enhancers	Fetal Stomach	stomach
13	chr1:72125000-72125200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:72125200-72125600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:72125600-72126200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:72125800-72126200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:72125800-72126400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:72126200-72129600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:72126200-72130600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:72126400-72130400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:72129600-72129800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:72129800-72130200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:72130200-72130800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:72130400-72131200	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr1:72130400-72132200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:72130600-72132600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:72130800-72132000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:72131200-72133000	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr1:72131800-72134200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:72132000-72132400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr1:72132000-72134200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:72132000-72134400	Enhancers	Osteobl	bone
33	chr1:72132200-72132400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:72132200-72132800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr1:72132200-72133200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr1:72132200-72134200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:72132400-72132600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:72132600-72133000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:72132600-72133200	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr1:72132600-72133400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:72132800-72133200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:72132800-72133200	Enhancers	NHDF-Ad	bronchial
43	chr1:72132800-72133400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr1:72132800-72133400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:72132800-72133800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr1:72132800-72134200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:72132800-72134200	Enhancers	Adipose Nuclei	Adipose
48	chr1:72133000-72133400	Enhancers	Colon Smooth Muscle	Colon
49	chr1:72133000-72133800	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr1:72133000-72134200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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