Variant report

Variant	nsv1013937
Chromosome Location	chr1:242749727-242854431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:358)
CpG islands
(count:122)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:242749196-242749772	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr1:242765415-242765554	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:242848092-242848258	K562	blood:	n/a	n/a
4	BACH1	chr1:242802067-242802078	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr1:242843399-242843681	GM12878	blood:	n/a	n/a
6	BCL3	chr1:242843343-242843676	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:242749358-242749729	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr1:242798548-242798608	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:242774541-242774804	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:242766628-242766982	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:242815630-242815862	A549	lung:	n/a	n/a
12	CEBPB	chr1:242766634-242766975	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:242798128-242798506	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:242791286-242791544	HepG2	liver:	n/a	chr1:242791427-242791436 chr1:242791479-242791490 chr1:242791479-242791492 chr1:242791425-242791436 chr1:242791480-242791491 chr1:242791479-242791492 chr1:242791479-242791490
15	CEBPB	chr1:242774529-242774815	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:242749263-242749763	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:242774611-242774728	A549	lung:	n/a	n/a
18	CEBPB	chr1:242815292-242815888	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:242766651-242766980	A549	lung:	n/a	n/a
20	CEBPB	chr1:242766610-242766982	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr1:242749188-242749790	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr1:242815188-242815370	MCF-7	breast:	n/a	n/a
23	CTCF	chr1:242853908-242854007	HepG2	liver:	n/a	n/a
24	CTCF	chr1:242815160-242815310	HEK293	kidney:	n/a	n/a
25	CTCF	chr1:242815180-242815330	GM12873	blood:	n/a	n/a
26	CTCF	chr1:242815185-242815379	GM12891	blood:	n/a	n/a
27	CTCF	chr1:242804340-242804490	HMEC	breast:	n/a	chr1:242804410-242804428 chr1:242804405-242804426
28	CTCF	chr1:242815198-242815359	A549	lung:	n/a	n/a
29	CTCF	chr1:242853880-242854030	HMEC	breast:	n/a	n/a
30	CTCF	chr1:242815180-242815330	GM12875	blood:	n/a	n/a
31	CTCF	chr1:242815020-242815170	GM12871	blood:	n/a	n/a
32	CTCF	chr1:242815220-242815370	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr1:242815220-242815370	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:242815200-242815350	GM12871	blood:	n/a	n/a
35	CTCF	chr1:242815160-242815310	GM12870	blood:	n/a	n/a
36	CTCF	chr1:242815180-242815330	GM12865	blood:	n/a	n/a
37	CTCF	chr1:242815240-242815390	GM12801	blood:	n/a	n/a
38	CTCF	chr1:242815179-242815410	GM12892	blood:	n/a	n/a
39	CTCF	chr1:242815160-242815310	GM12873	blood:	n/a	n/a
40	CTCF	chr1:242853840-242853990	HMEC	breast:	n/a	n/a
41	CTCF	chr1:242853860-242854010	HEK293	kidney:	n/a	n/a
42	CTCF	chr1:242815242-242815333	GM10248	blood:	n/a	n/a
43	CTCF	chr1:242804360-242804510	HMEC	breast:	n/a	chr1:242804410-242804428 chr1:242804405-242804426
44	CTCF	chr1:242815240-242815390	GM12871	blood:	n/a	n/a
45	CTCF	chr1:242825170-242825217	LNCaP	prostate:	n/a	n/a
46	CTCF	chr1:242815236-242815344	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr1:242853922-242853995	K562	blood:	n/a	n/a
48	CTCF	chr1:242815190-242815396	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr1:242815220-242815370	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr1:242815200-242815350	RPTEC	kidney:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242767942-242767992	HMEC	breast:	n/a
2	chr1:242767942-242767992	HCF	heart:	n/a
3	chr1:242767727-242767777	HIPEpiC	eye:	n/a
4	chr1:242767942-242767992	NB4	blood:	n/a
5	chr1:242767727-242767777	A549	lung:	n/a
6	chr1:242767727-242767777	H1-hESC	embryonic stem cell:	embryo
7	chr1:242767727-242767777	HRCEpiC	kidney:	n/a
8	chr1:242767727-242767777	AG09309	skin:	n/a
9	chr1:242767942-242767992	HUVEC	blood vessel:	n/a
10	chr1:242767942-242767992	MCF10A-Er-Src	breast:	n/a
11	chr1:242767727-242767777	Hepatocyte	liver:	n/a
12	chr1:242767727-242767777	AG10803	skin:	n/a
13	chr1:242767942-242767992	SK-N-MC	brain:	n/a
14	chr1:242767727-242767777	NB4	blood:	n/a
15	chr1:242767942-242767992	Caco-2	colon:	n/a
16	chr1:242767727-242767777	LNCaP	prostate:	n/a
17	chr1:242767727-242767777	HCM	heart:	n/a
18	chr1:242767942-242767992	AG10803	skin:	n/a
19	chr1:242767727-242767777	ProgFib	skin:	n/a
20	chr1:242767727-242767777	MCF-7	breast:	n/a
21	chr1:242767942-242767992	PANC-1	pancreas:	n/a
22	chr1:242767942-242767992	BJ	skin:	n/a
23	chr1:242767727-242767777	PANC-1	pancreas:	n/a
24	chr1:242767942-242767992	SAEC	small airway:	n/a
25	chr1:242767727-242767777	GM12892	blood:	n/a
26	chr1:242767727-242767777	ovcar-3	ovarian:	n/a
27	chr1:242767942-242767992	AG04450	lung:	fetal
28	chr1:242767727-242767777	SK-N-MC	brain:	n/a
29	chr1:242767942-242767992	HL-60	blood:	n/a
30	chr1:242767942-242767992	ECC-1	luminal epithelium:	n/a
31	chr1:242767942-242767992	AG04449	skin:	fetal
32	chr1:242767727-242767777	NHBE	bronchial:	n/a
33	chr1:242767942-242767992	SK-N-SH_RA	brain:	n/a
34	chr1:242767942-242767992	GM12892	blood:	n/a
35	chr1:242767727-242767777	CMK	blood:	n/a
36	chr1:242767727-242767777	GM12891	blood:	n/a
37	chr1:242767942-242767992	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:242767942-242767992	SKMC	muscle:	n/a
39	chr1:242767727-242767777	GM19239	blood:	n/a
40	chr1:242767942-242767992	U87	brain:	n/a
41	chr1:242767727-242767777	Hela-S3	cervix:	n/a
42	chr1:242767942-242767992	NHDF-neo	bronchial:	n/a
43	chr1:242767727-242767777	PFSK-1	brain:	n/a
44	chr1:242767942-242767992	AG09309	skin:	n/a
45	chr1:242767727-242767777	AG04449	skin:	fetal
46	chr1:242767942-242767992	HCM	heart:	n/a
47	chr1:242767727-242767777	RPTEC	kidney:	n/a
48	chr1:242767727-242767777	ECC-1	luminal epithelium:	n/a
49	chr1:242767942-242767992	GM06990	blood:	n/a
50	chr1:242767727-242767777	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SDCCAG8-4	chr1:242834442-242834878	NONHSAT010573

No data

Variant related genes	Relation type
ENSG00000270859	TF binding region
ENSG00000270859	CpG island

Extended variants
information (count: 3618 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3618 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78056378	chr1:242749754-242749755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575689394	chr1:242749774-242749775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541914858	chr1:242749813-242749814	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs12117394	chr1:242749856-242749857	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs527903781	chr1:242749877-242749878	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs150592979	chr1:242749907-242749908	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs564748661	chr1:242749908-242749909	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs72766845	chr1:242749919-242749920	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191046156	chr1:242749931-242749932	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs2096433	chr1:242749969-242749970	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs535924756	chr1:242749972-242749973	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs180887126	chr1:242749977-242749978	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs568100054	chr1:242749993-242749994	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs529363724	chr1:242749999-242750000	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs116626765	chr1:242750001-242750002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547456476	chr1:242750002-242750003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533966014	chr1:242750027-242750028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565936308	chr1:242750069-242750070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553728326	chr1:242750085-242750086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539982769	chr1:242750097-242750098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539354446	chr1:242750114-242750115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185768944	chr1:242750172-242750173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559285364	chr1:242750173-242750174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541528340	chr1:242750187-242750188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191072242	chr1:242750205-242750206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572076554	chr1:242750207-242750208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373810139	chr1:242750212-242750213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564711458	chr1:242750228-242750229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533626608	chr1:242750230-242750231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376976994	chr1:242750238-242750239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550517014	chr1:242750245-242750246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182834425	chr1:242750246-242750247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529270427	chr1:242750335-242750336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35985369	chr1:242750347-242750348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75187015	chr1:242750348-242750349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs398053986	chr1:242750362-242750363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs57688975	chr1:242750363-242750364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139599966	chr1:242750366-242750367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369282202	chr1:242750374-242750375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370455864	chr1:242750377-242750378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187256176	chr1:242750392-242750393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149983969	chr1:242750406-242750407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1938330	chr1:242750423-242750424	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs539323526	chr1:242750431-242750432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570371205	chr1:242750452-242750453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537319242	chr1:242750456-242750457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190558826	chr1:242750457-242750458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556058222	chr1:242750472-242750473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183163600	chr1:242750479-242750480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535411032	chr1:242750483-242750484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242748400-242750000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr1:242748400-242750200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr1:242748600-242750000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr1:242748800-242749800	Enhancers	Brain Germinal Matrix	brain
5	chr1:242748800-242750200	Enhancers	H9 Cell Line	embryonic stem cell
6	chr1:242748800-242750200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:242748800-242750200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:242748800-242750600	Enhancers	H1 Cell Line	embryonic stem cell
9	chr1:242749000-242750600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:242749000-242750800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:242749200-242749800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:242749200-242750200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr1:242749200-242750600	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr1:242749400-242749800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr1:242749600-242750200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:242749600-242750200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr1:242749600-242750200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr1:242749800-242750000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr1:242750200-242753000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr1:242750600-242751000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:242755600-242756200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:242756800-242757000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:242757000-242757200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:242757200-242757400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:242757400-242762000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:242761800-242766400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:242765200-242765400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr1:242765200-242765400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:242765200-242765400	Enhancers	HMEC	breast
30	chr1:242765400-242766400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:242765400-242766400	Weak transcription	HMEC	breast
32	chr1:242765600-242765800	Enhancers	HSMMtube	muscle
33	chr1:242765600-242767200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:242766400-242766600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr1:242766400-242767200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr1:242766400-242770000	Enhancers	HMEC	breast
37	chr1:242766400-242770400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:242766600-242767000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:242766600-242767200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr1:242766600-242767200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr1:242766600-242767200	Enhancers	A549	lung
42	chr1:242766600-242767600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:242766800-242767400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr1:242767200-242767400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:242767200-242768000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr1:242767400-242768200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:242767600-242768000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:242768200-242768800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:242768800-242771600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:242770000-242770800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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