Variant report

Variant	nsv871888
Chromosome Location	chr1:103349419-103379918
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	chr1:103363004-103363495	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr1:103363066-103363488	A549	lung:	n/a	n/a
3	CHD2	chr1:103363173-103363438	Hela-S3	cervix:	n/a	n/a
4	E2F4	chr1:103379321-103379492	MCF10A-Er-Src	breast:	n/a	n/a
5	EBF1	chr1:103354364-103354554	GM12878	blood:	n/a	chr1:103354472-103354483
6	EP300	chr1:103357417-103358172	SK-N-SH_RA	brain:	n/a	n/a
7	EP300	chr1:103363076-103363463	Hela-S3	cervix:	n/a	n/a
8	EP300	chr1:103361815-103362435	SK-N-SH	brain:	n/a	n/a
9	EP300	chr1:103357391-103358384	SK-N-SH	brain:	n/a	n/a
10	EP300	chr1:103363020-103363602	SK-N-SH	brain:	n/a	n/a
11	EP300	chr1:103363065-103363695	SK-N-SH	brain:	n/a	n/a
12	EP300	chr1:103357430-103358192	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr1:103363099-103363337	SK-N-SH_RA	brain:	n/a	n/a
14	FOS	chr1:103363119-103363644	HUVEC	blood vessel:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
15	FOS	chr1:103363109-103363464	MCF10A-Er-Src	breast:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
16	FOS	chr1:103363063-103363464	MCF10A-Er-Src	breast:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
17	FOS	chr1:103363053-103363472	Hela-S3	cervix:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
18	FOS	chr1:103357578-103358133	MCF10A-Er-Src	breast:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
19	FOS	chr1:103357659-103358082	MCF10A-Er-Src	breast:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
20	FOS	chr1:103357663-103358117	MCF10A-Er-Src	breast:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
21	FOS	chr1:103357677-103358543	HUVEC	blood vessel:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
22	FOS	chr1:103357453-103358283	MCF10A-Er-Src	breast:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357847 chr1:103357836-103357848 chr1:103357838-103357847 chr1:103357872-103357883
23	FOS	chr1:103363102-103363463	MCF10A-Er-Src	breast:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
24	FOS	chr1:103363093-103363464	MCF10A-Er-Src	breast:	n/a	chr1:103363274-103363281 chr1:103363272-103363283
25	FOSL1	chr1:103357702-103358130	HCT-116	colon:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357848 chr1:103357838-103357847
26	FOSL2	chr1:103357661-103358080	SK-N-SH	brain:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357848 chr1:103357838-103357847
27	FOSL2	chr1:103363041-103363377	MCF-7	breast:	n/a	chr1:103363274-103363281
28	FOSL2	chr1:103363068-103363361	A549	lung:	n/a	chr1:103363274-103363281
29	FOSL2	chr1:103363015-103363564	SK-N-SH	brain:	n/a	chr1:103363274-103363281 chr1:103363020-103363030 chr1:103363020-103363030
30	FOSL2	chr1:103362977-103363541	A549	lung:	n/a	chr1:103363274-103363281 chr1:103363020-103363030 chr1:103363020-103363030
31	FOSL2	chr1:103363083-103363499	MCF-7	breast:	n/a	chr1:103363274-103363281
32	FOSL2	chr1:103357458-103358309	SK-N-SH	brain:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357848 chr1:103357838-103357847
33	FOSL2	chr1:103363047-103363548	SK-N-SH	brain:	n/a	chr1:103363274-103363281
34	FOSL2	chr1:103367578-103368066	SK-N-SH	brain:	n/a	chr1:103367815-103367822 chr1:103367793-103367805 chr1:103367795-103367803
35	FOSL2	chr1:103357546-103358078	A549	lung:	n/a	chr1:103357837-103357847 chr1:103357719-103357731 chr1:103357836-103357848 chr1:103357838-103357847
36	FOXA1	chr1:103363086-103363340	T-47D	breast:	n/a	chr1:103363173-103363188
37	FOXA1	chr1:103363011-103363275	T-47D	breast:	n/a	chr1:103363173-103363188
38	GATA3	chr1:103364349-103364467	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr1:103363054-103363394	T-47D	breast:	n/a	chr1:103363272-103363281
40	GATA3	chr1:103357364-103358328	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr1:103361718-103362531	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr1:103362955-103363655	SK-N-SH	brain:	n/a	chr1:103363272-103363281
43	GATA3	chr1:103353083-103353242	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr1:103362860-103363584	A549	lung:	n/a	chr1:103363272-103363281
45	GATA3	chr1:103362858-103363706	SK-N-SH	brain:	n/a	chr1:103363272-103363281
46	GATA3	chr1:103354159-103354359	SH-SY5Y	brain:	n/a	chr1:103354338-103354348 chr1:103354192-103354203
47	GATA3	chr1:103362857-103363401	MCF-7	breast:	n/a	chr1:103363272-103363281
48	GATA3	chr1:103362327-103362447	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr1:103363056-103363366	A549	lung:	n/a	chr1:103363272-103363281
50	GATA3	chr1:103361730-103362463	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:103373284..103376255-chr1:103376543..103379257,2	K562	blood:
2	chr1:103373284..103376255-chr1:103376543..103379257,2	K562	blood:

Variant related genes	Relation type
COL11A1	TF binding region

Extended variants
information (count: 1234 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55702802	chr1:103349419-103349420	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116801205	chr1:103349477-103349478	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563429992	chr1:103349506-103349507	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191111422	chr1:103349516-103349517	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530637547	chr1:103349575-103349576	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555018529	chr1:103349627-103349628	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114475042	chr1:103349650-103349651	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528072121	chr1:103349693-103349694	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182153738	chr1:103349709-103349710	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144017196	chr1:103349714-103349715	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12025494	chr1:103349738-103349739	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs556647499	chr1:103349762-103349763	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567375774	chr1:103349816-103349817	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536305007	chr1:103349818-103349819	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73000267	chr1:103349862-103349863	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs554821798	chr1:103349924-103349925	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs573237172	chr1:103349965-103349966	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs534525018	chr1:103350002-103350003	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs566503633	chr1:103350059-103350060	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs534046414	chr1:103350067-103350068	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs74517108	chr1:103350112-103350113	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2169608	chr1:103350118-103350119	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs187168126	chr1:103350125-103350126	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs570754812	chr1:103350156-103350157	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs563014318	chr1:103350161-103350162	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575486275	chr1:103350177-103350178	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146854028	chr1:103350178-103350179	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558191868	chr1:103350188-103350189	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs578170808	chr1:103350199-103350200	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371351445	chr1:103350207-103350208	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11588336	chr1:103350243-103350244	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191670254	chr1:103350257-103350258	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1241184	chr1:103350264-103350265	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs183812946	chr1:103350281-103350282	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575033104	chr1:103350301-103350302	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557086995	chr1:103350320-103350321	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188708374	chr1:103350337-103350338	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148551212	chr1:103350349-103350350	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192840391	chr1:103350403-103350404	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185783058	chr1:103350406-103350407	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1241185	chr1:103350409-103350410	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548341952	chr1:103350428-103350429	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2169609	chr1:103350437-103350438	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs190305876	chr1:103350482-103350483	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559239913	chr1:103350500-103350501	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180989713	chr1:103350526-103350527	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183742353	chr1:103350533-103350534	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565792303	chr1:103350536-103350537	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556677254	chr1:103350549-103350550	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142915473	chr1:103350552-103350553	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	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
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
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103334000-103349800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:103335400-103350000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:103338400-103369400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:103338800-103357200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:103339200-103349800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:103340800-103350000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:103341400-103349800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr1:103341600-103352000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:103342400-103349800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:103343400-103352000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:103343400-103355800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:103343400-103356200	Weak transcription	Fetal Heart	heart
13	chr1:103343400-103366000	Weak transcription	Fetal Brain Female	brain
14	chr1:103344400-103349800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr1:103345600-103350600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:103345600-103385600	Weak transcription	HSMMtube	muscle
17	chr1:103345800-103357200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:103346000-103350200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr1:103346200-103357400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:103346200-103357400	Weak transcription	NH-A	brain
21	chr1:103347000-103350800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:103348000-103352000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:103348000-103352200	Weak transcription	HMEC	breast
24	chr1:103348200-103352200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:103348200-103352200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:103348200-103357400	Weak transcription	HSMM	muscle
27	chr1:103348200-103357400	Weak transcription	Osteobl	bone
28	chr1:103348800-103349600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:103349000-103352200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:103349400-103350400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr1:103349600-103349800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr1:103349600-103350200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr1:103349600-103350200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:103349600-103350200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr1:103349600-103350200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:103349600-103350400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:103349800-103350000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:103349800-103350200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:103349800-103350400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:103349800-103350400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr1:103349800-103350400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:103349800-103350600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr1:103349800-103356000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr1:103350000-103350200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr1:103350000-103350200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr1:103350000-103350200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr1:103350000-103350400	Enhancers	Fetal Muscle Trunk	muscle
48	chr1:103350000-103369400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:103350200-103350400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr1:103350200-103350400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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