Variant report

Variant	nsv945406
Chromosome Location	chr1:241992115-241996420
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	chr1:241992816-241992894	HepG2	liver:	n/a	n/a
2	BHLHE40	chr1:241995475-241995775	K562	blood:	n/a	n/a
3	CEBPB	chr1:241991845-241992225	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:241991946-241992181	K562	blood:	n/a	n/a
5	CEBPB	chr1:241992665-241993111	A549	lung:	n/a	n/a
6	CUX1	chr1:241992162-241992517	K562	blood:	n/a	n/a
7	E2F4	chr1:241992009-241992190	MCF10A-Er-Src	breast:	n/a	n/a
8	EBF1	chr1:241994595-241994902	GM12878	blood:	n/a	chr1:241994754-241994765
9	EP300	chr1:241995885-241995887	GM12878	blood:	n/a	n/a
10	FOS	chr1:241991968-241992277	MCF10A-Er-Src	breast:	n/a	chr1:241992156-241992163 chr1:241992155-241992163 chr1:241992155-241992163
11	FOS	chr1:241991919-241992312	MCF10A-Er-Src	breast:	n/a	chr1:241992156-241992163 chr1:241992155-241992163 chr1:241992155-241992163
12	FOS	chr1:241991932-241992286	MCF10A-Er-Src	breast:	n/a	chr1:241992156-241992163 chr1:241992155-241992163 chr1:241992155-241992163
13	FOS	chr1:241992011-241992260	MCF10A-Er-Src	breast:	n/a	chr1:241992156-241992163 chr1:241992155-241992163 chr1:241992155-241992163
14	FOXA1	chr1:241992676-241993048	HepG2	liver:	n/a	chr1:241992806-241992821
15	FOXA1	chr1:241992716-241992965	T-47D	breast:	n/a	chr1:241992806-241992821
16	FOXA1	chr1:241992561-241993122	HepG2	liver:	n/a	chr1:241992806-241992821
17	FOXA2	chr1:241992530-241993118	HepG2	liver:	n/a	n/a
18	FOXA2	chr1:241992656-241993204	A549	lung:	n/a	n/a
19	GATA2	chr1:241992101-241992434	SH-SY5Y	brain:	n/a	n/a
20	IRF1	chr1:241994030-241994055	K562	blood:	n/a	n/a
21	JUND	chr1:241991970-241992272	K562	blood:	n/a	chr1:241992156-241992163 chr1:241992155-241992163 chr1:241992155-241992163
22	KAP1	chr1:241991992-241992350	U2OS	brain:	n/a	n/a
23	MAFK	chr1:241992082-241992150	HepG2	liver:	n/a	n/a
24	MAFK	chr1:241991950-241992273	IMR90	lung:	n/a	chr1:241992153-241992163
25	MAFK	chr1:241992039-241992290	K562	blood:	n/a	chr1:241992153-241992163
26	MAFK	chr1:241991940-241992212	Hela-S3	cervix:	n/a	chr1:241992153-241992163
27	MAZ	chr1:241991869-241992290	IMR90	lung:	n/a	chr1:241992154-241992163
28	MYC	chr1:241992082-241992197	MCF10A-Er-Src	breast:	n/a	chr1:241992154-241992163
29	MYC	chr1:241992057-241992157	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr1:241995383-241995403	Gliobla	brain:	n/a	n/a
31	POLR2A	chr1:241991913-241992515	H1-neurons	neurons:	n/a	n/a
32	POLR2A	chr1:241991879-241992487	H1-neurons	neurons:	n/a	n/a
33	POLR2A	chr1:241994009-241994036	Gliobla	brain:	n/a	n/a
34	POLR2A	chr1:241994040-241994137	Gliobla	brain:	n/a	n/a
35	RCOR1	chr1:241991944-241992341	K562	blood:	n/a	n/a
36	RCOR1	chr1:241995490-241995493	K562	blood:	n/a	n/a
37	REST	chr1:241991703-241992510	H1-neurons	neurons:	n/a	n/a
38	REST	chr1:241991839-241992533	H1-neurons	neurons:	n/a	n/a
39	RFX5	chr1:241993612-241993784	K562	blood:	n/a	n/a
40	SP1	chr1:241992660-241993089	A549	lung:	n/a	n/a
41	STAT3	chr1:241991906-241992229	MCF10A-Er-Src	breast:	n/a	chr1:241992068-241992079
42	STAT3	chr1:241991904-241992257	MCF10A-Er-Src	breast:	n/a	chr1:241992068-241992079
43	STAT3	chr1:241991997-241992234	MCF10A-Er-Src	breast:	n/a	chr1:241992068-241992079
44	STAT3	chr1:241991949-241992230	MCF10A-Er-Src	breast:	n/a	chr1:241992068-241992079
45	TCF7L2	chr1:241991978-241992467	Hela-S3	cervix:	n/a	n/a
46	UBTF	chr1:241994053-241994070	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:241992272-241992322	HEEpiC	esophagus:	n/a
2	chr1:241992272-241992322	GM12891	blood:	n/a
3	chr1:241992272-241992322	PrEC	prostate:	n/a
4	chr1:241992272-241992322	NB4	blood:	n/a
5	chr1:241992272-241992322	IMR90	lung:	fetal
6	chr1:241992272-241992322	AG10803	skin:	n/a
7	chr1:241992272-241992322	HRCEpiC	kidney:	n/a
8	chr1:241992272-241992322	HL-60	blood:	n/a
9	chr1:241992272-241992322	MCF10A-Er-Src	breast:	n/a
10	chr1:241992272-241992322	ovcar-3	ovarian:	n/a
11	chr1:241992272-241992322	Jurkat	blood:	n/a
12	chr1:241992272-241992322	SAEC	small airway:	n/a
13	chr1:241992272-241992322	HCPEpiC	choroid plexus:	n/a
14	chr1:241992272-241992322	PANC-1	pancreas:	n/a
15	chr1:241992272-241992322	AG04449	skin:	fetal
16	chr1:241992272-241992322	K562	blood:	n/a
17	chr1:241992272-241992322	Caco-2	colon:	n/a
18	chr1:241992272-241992322	BJ	skin:	n/a
19	chr1:241992272-241992322	NH-A	brain:	n/a
20	chr1:241992272-241992322	HIPEpiC	eye:	n/a
21	chr1:241992272-241992322	T-47D	breast:	n/a
22	chr1:241992272-241992322	GM06990	blood:	n/a
23	chr1:241992272-241992322	HUVEC	blood vessel:	n/a
24	chr1:241992272-241992322	MCF-7	breast:	n/a
25	chr1:241992272-241992322	Hela-S3	cervix:	n/a
26	chr1:241992272-241992322	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:241992272-241992322	HEK293	kidney:	embryo
28	chr1:241992272-241992322	GM19239	blood:	n/a
29	chr1:241992272-241992322	HMEC	breast:	n/a
30	chr1:241992272-241992322	GM12892	blood:	n/a
31	chr1:241992272-241992322	RPTEC	kidney:	n/a
32	chr1:241992272-241992322	HCT-116	colon:	n/a
33	chr1:241992272-241992322	Hepatocyte	liver:	n/a
34	chr1:241992272-241992322	SK-N-SH_RA	brain:	n/a
35	chr1:241992272-241992322	NT2-D1	testis:	n/a
36	chr1:241992272-241992322	HCF	heart:	n/a
37	chr1:241992272-241992322	PFSK-1	brain:	n/a
38	chr1:241992272-241992322	HAEpiC	amniotic membrane:	n/a
39	chr1:241992272-241992322	AoSMC	blood vessel:	n/a
40	chr1:241992272-241992322	HRE	kidney:	n/a
41	chr1:241992272-241992322	NHDF-neo	bronchial:	n/a
42	chr1:241992272-241992322	A549	lung:	n/a
43	chr1:241992272-241992322	H1-hESC	embryonic stem cell:	embryo
44	chr1:241992272-241992322	CMK	blood:	n/a
45	chr1:241992272-241992322	U87	brain:	n/a
46	chr1:241992272-241992322	AG04450	lung:	fetal
47	chr1:241992272-241992322	HCM	heart:	n/a
48	chr1:241992272-241992322	SKMC	muscle:	n/a
49	chr1:241992272-241992322	ProgFib	skin:	n/a
50	chr1:241992272-241992322	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:241802310..241805173-chr1:241993132..241995327,2	K562	blood:
2	chr1:241994931..241996990-chr1:242009652..242011355,2	K562	blood:
3	chr1:241988238..241990297-chr1:241995533..241997207,2	K562	blood:
4	chr1:241785761..241788632-chr1:241996400..241998922,2	MCF-7	breast:
5	chr1:241992525..241994073-chr1:242002310..242004336,2	K562	blood:

Variant related genes	Relation type
ENSG00000229022	TF binding region
ENSG00000229022	CpG island
ENSG00000054277	chromatin interactions
ENSG00000174371	chromatin interactions

Extended variants
information (count: 158 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:158 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192387374	chr1:241992148-241992149	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs185085452	chr1:241992177-241992178	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs558633724	chr1:241992193-241992194	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs11811179	chr1:241992310-241992311	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs186794240	chr1:241992315-241992316	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs148248990	chr1:241992351-241992352	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs530448111	chr1:241992369-241992370	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs540828560	chr1:241992441-241992442	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560706872	chr1:241992493-241992494	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs7524386	chr1:241992538-241992539	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs1635523	chr1:241992577-241992578	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs192775364	chr1:241992580-241992581	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs12047688	chr1:241992642-241992643	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs7540780	chr1:241992692-241992693	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs201738964	chr1:241992716-241992717	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368952621	chr1:241992717-241992718	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs71174859	chr1:241992743-241992744	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs376195706	chr1:241992744-241992745	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369379651	chr1:241992746-241992747	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs372057978	chr1:241992747-241992748	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536191732	chr1:241992761-241992762	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs184694311	chr1:241992786-241992787	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs142831542	chr1:241992787-241992788	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs189701222	chr1:241992844-241992845	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs559026565	chr1:241992861-241992862	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs12037438	chr1:241992902-241992903	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs530235251	chr1:241992919-241992920	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs76950741	chr1:241992925-241992926	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs554714582	chr1:241992929-241992930	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs145278922	chr1:241992938-241992939	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs192745347	chr1:241992940-241992941	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs560619128	chr1:241992971-241992972	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs532773088	chr1:241993114-241993115	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567070888	chr1:241993175-241993176	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs150830862	chr1:241993195-241993196	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564977336	chr1:241993228-241993229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs9428902	chr1:241993283-241993284	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs184168760	chr1:241993299-241993300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs552633195	chr1:241993329-241993330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs139229602	chr1:241993343-241993344	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs374546683	chr1:241993357-241993358	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs115096498	chr1:241993447-241993448	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs546512868	chr1:241993453-241993454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs188964368	chr1:241993494-241993495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538814647	chr1:241993526-241993527	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs570409906	chr1:241993558-241993559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529326430	chr1:241993565-241993566	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs569333254	chr1:241993588-241993589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs150012680	chr1:241993602-241993603	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs115089715	chr1:241993607-241993608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Cancer	20164919	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
Glioblastoma	18772890	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Brain overgrowth syndrome	24179207	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241989000-241992400	Enhancers	Fetal Brain Male	brain
2	chr1:241989600-241992600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr1:241990800-241992400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:241991200-241992200	Weak transcription	Aorta	Aorta
5	chr1:241991600-241992400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr1:241991600-241992600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:241991800-241992400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:241991800-241992400	Enhancers	NHLF	lung
9	chr1:241991800-241992800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:241992000-241992200	Flanking Active TSS	HSMMtube	muscle
11	chr1:241992000-241992200	Flanking Active TSS	K562	blood
12	chr1:241992000-241992400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:241992000-241992400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:241992000-241992400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:241992000-241992400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:241992000-241992400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr1:241992000-241992400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:241992000-241992400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:241992000-241992400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:241992000-241992400	Enhancers	Brain Germinal Matrix	brain
21	chr1:241992000-241992400	Flanking Active TSS	Fetal Heart	heart
22	chr1:241992000-241992400	Enhancers	Left Ventricle	heart
23	chr1:241992000-241992400	Enhancers	Lung	lung
24	chr1:241992000-241992400	Enhancers	Ovary	ovary
25	chr1:241992000-241992400	Enhancers	Rectal Smooth Muscle	rectum
26	chr1:241992000-241992400	Enhancers	Right Ventricle	heart
27	chr1:241992000-241992400	Flanking Active TSS	A549	lung
28	chr1:241992000-241992400	Enhancers	HSMM	muscle
29	chr1:241992000-241992400	Enhancers	NH-A	brain
30	chr1:241992000-241992400	Enhancers	NHDF-Ad	bronchial
31	chr1:241992000-241992400	Enhancers	NHEK	skin
32	chr1:241992000-241992400	Enhancers	Osteobl	bone
33	chr1:241992200-241992400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:241992200-241992400	Enhancers	Aorta	Aorta
35	chr1:241992200-241992400	Enhancers	HSMMtube	muscle
36	chr1:241992200-241992400	Enhancers	K562	blood
37	chr1:241992400-241992600	Enhancers	A549	lung
38	chr1:241992400-241992600	Flanking Active TSS	K562	blood
39	chr1:241992400-241993000	Enhancers	Fetal Heart	heart
40	chr1:241992400-241994000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:241992400-242000800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:241992600-241992800	Enhancers	K562	blood
43	chr1:241992600-241993000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr1:241992600-241995800	Weak transcription	A549	lung
45	chr1:241992800-241995400	Weak transcription	K562	blood
46	chr1:241994000-241994200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:241995400-241997000	Enhancers	K562	blood
48	chr1:241995600-241995800	Enhancers	NHLF	lung
49	chr1:241995800-241996800	Enhancers	A549	lung

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