Variant report

Variant	nsv871365
Chromosome Location	chr1:103476179-103548497
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	ARID3A	chr1:103502292-103502351	K562	blood:	n/a	n/a
2	CEBPB	chr1:103522115-103522329	IMR90	lung:	n/a	chr1:103522213-103522224
3	CEBPB	chr1:103519790-103519887	H1-hESC	embryonic stem cell:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
4	CEBPB	chr1:103519664-103520007	IMR90	lung:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
5	CEBPB	chr1:103519671-103520003	HepG2	liver:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
6	CEBPB	chr1:103519688-103519996	A549	lung:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
7	CEBPB	chr1:103519692-103519989	ECC-1	luminal epithelium:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
8	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
9	CEBPB	chr1:103522064-103522370	HepG2	liver:	n/a	chr1:103522213-103522224
10	CTCF	chr1:103489061-103489081	Fibrobl	skin:	n/a	n/a
11	CTCF	chr1:103529460-103529610	AoAF	blood vessel:	n/a	n/a
12	EP300	chr1:103495066-103495343	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr1:103482033-103482177	K562	blood:	n/a	chr1:103482034-103482043
14	EP300	chr1:103497514-103497813	SK-N-SH_RA	brain:	n/a	chr1:103497580-103497588 chr1:103497645-103497652
15	FAM48A	chr1:103481060-103481095	GM12878	blood:	n/a	n/a
16	FOXA2	chr1:103516523-103517022	A549	lung:	n/a	n/a
17	FOXA2	chr1:103534858-103535060	HepG2	liver:	n/a	n/a
18	GATA3	chr1:103495167-103495348	SH-SY5Y	brain:	n/a	n/a
19	GATA3	chr1:103544852-103545023	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr1:103483910-103484121	SH-SY5Y	brain:	n/a	chr1:103483910-103483926 chr1:103484011-103484019 chr1:103484008-103484021 chr1:103483984-103483991 chr1:103483911-103483921 chr1:103484010-103484019 chr1:103483957-103483973 chr1:103483959-103483971 chr1:103484012-103484019
21	GATA3	chr1:103500817-103500879	SH-SY5Y	brain:	n/a	n/a
22	JUND	chr1:103498509-103498704	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAFF	chr1:103500871-103501071	HepG2	liver:	n/a	chr1:103500984-103501002
24	MAFF	chr1:103500931-103500933	K562	blood:	n/a	n/a
25	MAFF	chr1:103522922-103522973	HepG2	liver:	n/a	n/a
26	MAFK	chr1:103488469-103488807	HepG2	liver:	n/a	chr1:103488748-103488768
27	MAFK	chr1:103522892-103523008	HepG2	liver:	n/a	n/a
28	MAFK	chr1:103535685-103535852	HepG2	liver:	n/a	n/a
29	MAFK	chr1:103500869-103501153	HepG2	liver:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
30	MAFK	chr1:103500873-103501086	HepG2	liver:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
31	MAFK	chr1:103488526-103488726	IMR90	lung:	n/a	n/a
32	MAFK	chr1:103522877-103522988	H1-hESC	embryonic stem cell:	n/a	n/a
33	MAFK	chr1:103500893-103501127	IMR90	lung:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
34	MAX	chr1:103498532-103498732	NB4	blood:	n/a	n/a
35	MAZ	chr1:103510189-103510210	Hela-S3	cervix:	n/a	n/a
36	MAZ	chr1:103477655-103477827	HepG2	liver:	n/a	n/a
37	MXI1	chr1:103476805-103476816	K562	blood:	n/a	n/a
38	MYC	chr1:103547817-103547903	MCF10A-Er-Src	breast:	n/a	n/a
39	NFYA	chr1:103491625-103491853	GM12878	blood:	n/a	n/a
40	NR3C1	chr1:103522056-103522268	ECC-1	luminal epithelium:	n/a	n/a
41	NR3C1	chr1:103522013-103522303	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr1:103532049-103532182	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr1:103489703-103489763	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr1:103498773-103498930	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr1:103523589-103523618	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr1:103522059-103522288	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr1:103529462-103529605	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr1:103547888-103548088	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr1:103497360-103497385	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr1:103522661-103522778	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:103471408..103474127-chr1:103476869..103478860,2	MCF-7	breast:

Variant related genes	Relation type
COL11A1	TF binding region
ENSG00000060718	chromatin interactions

Extended variants
information (count: 3087 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3087 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2622839	chr1:103476179-103476180	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554933565	chr1:103476194-103476195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549911386	chr1:103476213-103476214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566890912	chr1:103476249-103476250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78136637	chr1:103476275-103476276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535465148	chr1:103476279-103476280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377574971	chr1:103476295-103476296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12078741	chr1:103476296-103476297	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs558733449	chr1:103476297-103476298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190136385	chr1:103476313-103476314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182410644	chr1:103476323-103476324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188744064	chr1:103476334-103476335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191493182	chr1:103476369-103476370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2485317	chr1:103476370-103476371	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556172412	chr1:103476381-103476382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188728084	chr1:103476382-103476383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201348591	chr1:103476394-103476395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12043105	chr1:103476439-103476440	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs36031902	chr1:103476492-103476493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560312959	chr1:103476498-103476499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527348935	chr1:103476503-103476504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546429752	chr1:103476537-103476538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564624493	chr1:103476541-103476542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537569100	chr1:103476543-103476544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368275524	chr1:103476554-103476555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550491209	chr1:103476592-103476593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568637643	chr1:103476597-103476598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529310080	chr1:103476623-103476624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115127893	chr1:103476673-103476674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2786120	chr1:103476677-103476678	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs539499362	chr1:103476742-103476743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542679732	chr1:103476757-103476758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570351189	chr1:103476778-103476779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12135980	chr1:103476848-103476849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2622840	chr1:103476879-103476880	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs574618929	chr1:103476950-103476951	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143784993	chr1:103476954-103476955	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553762652	chr1:103477013-103477014	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572175828	chr1:103477053-103477054	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545968469	chr1:103477152-103477153	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs3861742	chr1:103477167-103477168	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs531960142	chr1:103477178-103477179	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2786121	chr1:103477226-103477227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs545360414	chr1:103477238-103477239	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35157468	chr1:103477254-103477255	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs397863562	chr1:103477260-103477261	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146891633	chr1:103477310-103477311	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10458505	chr1:103477398-103477399	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs547387447	chr1:103477403-103477404	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565780852	chr1:103477433-103477434	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	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:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103369600-103498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:103386200-103482000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:103415800-103485200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:103425000-103478000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:103446800-103497800	Weak transcription	HSMM	muscle
6	chr1:103449200-103545200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:103453400-103490000	Weak transcription	NH-A	brain
8	chr1:103460200-103516400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:103468400-103478600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr1:103469800-103486600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr1:103471400-103476600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:103471400-103486600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:103474400-103476800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:103474800-103483600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:103475000-103476200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:103475800-103516600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:103476200-103486800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:103476600-103477600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:103476800-103477000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:103477000-103478200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:103477600-103484800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:103478200-103479800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:103478600-103479400	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:103479400-103487000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr1:103479800-103480600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:103480200-103480400	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr1:103480600-103483200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:103483000-103484000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:103483200-103485200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:103484000-103484600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:103484600-103484800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:103484800-103486600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:103485200-103486800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:103485200-103487000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr1:103486600-103487600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:103486600-103489200	Strong transcription	Cortex derived primary cultured neurospheres	brain
37	chr1:103486600-103491800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:103486800-103489600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:103486800-103491200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:103487000-103491600	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr1:103487000-103492200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:103487600-103493600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:103488000-103490800	Weak transcription	Brain Germinal Matrix	brain
44	chr1:103489200-103516400	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr1:103489600-103506000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:103490000-103491600	Strong transcription	NH-A	brain
47	chr1:103490800-103491200	Enhancers	Brain Germinal Matrix	brain
48	chr1:103491200-103491600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:103491200-103492400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:103491400-103492000	Enhancers	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links