Variant report

Variant	nsv549522
Chromosome Location	chr1:245979357-246005798
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	BATF	chr1:245992604-245992863	GM12878	blood:	n/a	n/a
2	BCL3	chr1:245986431-245986771	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:245986428-245986758	HepG2	liver:	n/a	n/a
4	BHLHE40	chr1:245986393-245986667	A549	lung:	n/a	n/a
5	CEBPB	chr1:246005252-246005546	A549	lung:	n/a	chr1:246005396-246005407
6	CEBPB	chr1:245986202-245986790	HCT-116	colon:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
7	CEBPB	chr1:245986344-245986737	A549	lung:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
8	CEBPB	chr1:245986442-245986595	K562	blood:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
9	CEBPB	chr1:246005278-246005544	IMR90	lung:	n/a	chr1:246005396-246005407
10	CEBPB	chr1:245986261-245986788	ECC-1	luminal epithelium:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
11	CEBPB	chr1:245986224-245986759	HCT-116	colon:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
12	CEBPB	chr1:245986358-245986775	MCF-7	breast:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
13	CEBPB	chr1:245986958-245987061	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:246005255-246005575	HepG2	liver:	n/a	chr1:246005396-246005407
15	CEBPB	chr1:245986262-245987157	IMR90	lung:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986855-245986867 chr1:245986540-245986551 chr1:245986857-245986868 chr1:245986538-245986551
16	CEBPB	chr1:245986260-245986954	A549	lung:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986855-245986867 chr1:245986540-245986551 chr1:245986857-245986868 chr1:245986538-245986551
17	CEBPB	chr1:245986189-245986747	Hela-S3	cervix:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
18	CEBPB	chr1:245986352-245986792	A549	lung:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
19	CEBPB	chr1:245986465-245986593	HepG2	liver:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
20	CEBPB	chr1:245986352-245986718	HepG2	liver:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
21	CEBPB	chr1:245986317-245986701	ECC-1	luminal epithelium:	n/a	chr1:245986540-245986551 chr1:245986538-245986549 chr1:245986540-245986551 chr1:245986538-245986551
22	CEBPZ	chr1:246003835-246003916	HepG2	liver:	n/a	n/a
23	CHD2	chr1:245986326-245986722	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr1:245988540-245988690	RPTEC	kidney:	n/a	chr1:245988600-245988621
25	CTCF	chr1:245988540-245988690	AG10803	skin:	n/a	chr1:245988600-245988621
26	CTCF	chr1:245988520-245988670	BJ	skin:	n/a	chr1:245988600-245988621
27	CTCF	chr1:245986240-245986390	AG09319	gingival:	n/a	n/a
28	CTCF	chr1:245988540-245988690	HRPEpiC	eye:	n/a	chr1:245988600-245988621
29	CTCF	chr1:245986280-245986430	AG10803	skin:	n/a	n/a
30	CTCF	chr1:245988520-245988670	Hela-S3	cervix:	n/a	chr1:245988600-245988621
31	CTCF	chr1:245988570-245988623	A549	lung:	n/a	chr1:245988600-245988621
32	CTCF	chr1:245988480-245988630	NHEK	skin:	n/a	chr1:245988600-245988621
33	CTCF	chr1:245988500-245988650	AG10803	skin:	n/a	chr1:245988600-245988621
34	CTCF	chr1:245988538-245988677	LNCaP	prostate:	n/a	chr1:245988600-245988621
35	CTCF	chr1:245988560-245988710	HBMEC	blood vessel:	n/a	chr1:245988600-245988621
36	CTCF	chr1:245988520-245988670	HPF	lung:	n/a	chr1:245988600-245988621
37	CTCF	chr1:245988600-245988750	HMEC	breast:	n/a	chr1:245988600-245988621
38	CTCF	chr1:245988500-245988650	HMF	breast:	n/a	chr1:245988600-245988621
39	CTCF	chr1:245988556-245988625	Hela-S3	cervix:	n/a	chr1:245988600-245988621
40	CTCF	chr1:245986280-245986430	BJ	skin:	n/a	n/a
41	CTCF	chr1:245988560-245988710	NHLF	lung:	n/a	chr1:245988600-245988621
42	CTCF	chr1:245988580-245988730	HMF	breast:	n/a	chr1:245988600-245988621
43	CTCF	chr1:245988600-245988750	AG09319	gingival:	n/a	chr1:245988600-245988621
44	CTCF	chr1:245986336-245986364	NHEK	skin:	n/a	n/a
45	CTCF	chr1:245988509-245988698	MCF-7	breast:	n/a	chr1:245988600-245988621
46	CTCF	chr1:245988540-245988690	HCM	heart:	n/a	chr1:245988600-245988621
47	CTCF	chr1:245988560-245988710	Caco-2	colon:	n/a	chr1:245988600-245988621
48	CTCF	chr1:245988560-245988710	HFF	foreskin:	n/a	chr1:245988600-245988621
49	CTCF	chr1:245988500-245988650	RPTEC	kidney:	n/a	chr1:245988600-245988621
50	CTCF	chr1:245988511-245988684	ProgFib	skin:	n/a	chr1:245988600-245988621

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:245986694-245986744	AoSMC	blood vessel:	n/a
2	chr1:245986694-245986744	HEEpiC	esophagus:	n/a
3	chr1:245986694-245986744	ovcar-3	ovarian:	n/a
4	chr1:245986694-245986744	SAEC	small airway:	n/a
5	chr1:245986694-245986744	NHBE	bronchial:	n/a
6	chr1:245986694-245986744	NB4	blood:	n/a
7	chr1:245986694-245986744	HRPEpiC	eye:	n/a
8	chr1:245986694-245986744	AG10803	skin:	n/a
9	chr1:245986694-245986744	HCF	heart:	n/a
10	chr1:245986694-245986744	HCT-116	colon:	n/a
11	chr1:245986694-245986744	HNPCEpiC	eye:	n/a
12	chr1:245986694-245986744	CMK	blood:	n/a
13	chr1:245986694-245986744	HMEC	breast:	n/a
14	chr1:245986694-245986744	NH-A	brain:	n/a
15	chr1:245986694-245986744	HepG2	liver:	n/a
16	chr1:245986694-245986744	HL-60	blood:	n/a
17	chr1:245986694-245986744	HIPEpiC	eye:	n/a
18	chr1:245986694-245986744	HEK293	kidney:	embryo
19	chr1:245986694-245986744	ECC-1	luminal epithelium:	n/a
20	chr1:245986694-245986744	NHDF-neo	bronchial:	n/a
21	chr1:245986694-245986744	HUVEC	blood vessel:	n/a
22	chr1:245986694-245986744	HCPEpiC	choroid plexus:	n/a
23	chr1:245986694-245986744	LNCaP	prostate:	n/a
24	chr1:245986694-245986744	SK-N-SH_RA	brain:	n/a
25	chr1:245986694-245986744	SK-N-MC	brain:	n/a
26	chr1:245986694-245986744	HRCEpiC	kidney:	n/a
27	chr1:245986694-245986744	RPTEC	kidney:	n/a
28	chr1:245986694-245986744	NT2-D1	testis:	n/a
29	chr1:245986694-245986744	ProgFib	skin:	n/a
30	chr1:245986694-245986744	H1-hESC	embryonic stem cell:	embryo
31	chr1:245986694-245986744	AG09319	gingival:	n/a
32	chr1:245986694-245986744	U87	brain:	n/a
33	chr1:245986694-245986744	Hela-S3	cervix:	n/a
34	chr1:245986694-245986744	AG09309	skin:	n/a
35	chr1:245986694-245986744	T-47D	breast:	n/a
36	chr1:245986694-245986744	K562	blood:	n/a
37	chr1:245986694-245986744	GM12878	blood:	n/a
38	chr1:245986694-245986744	SK-N-SH	brain:	n/a
39	chr1:245986694-245986744	GM19239	blood:	n/a
40	chr1:245986694-245986744	HAEpiC	amniotic membrane:	n/a
41	chr1:245986694-245986744	HCM	heart:	n/a
42	chr1:245986694-245986744	Jurkat	blood:	n/a
43	chr1:245986694-245986744	BE2_C	brain:	n/a
44	chr1:245986694-245986744	BJ	skin:	n/a
45	chr1:245986694-245986744	GM12891	blood:	n/a
46	chr1:245986694-245986744	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:245986694-245986744	AG04450	lung:	fetal
48	chr1:245986694-245986744	PFSK-1	brain:	n/a
49	chr1:245986694-245986744	HRE	kidney:	n/a
50	chr1:245986694-245986744	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:245992708..245995322-chr1:245995815..245998261,2	MCF-7	breast:
2	chr1:245988141..245989007-chr1:246166156..246166781,3	MCF-7	breast:
3	chr1:245999406..246001489-chr1:246004038..246006182,2	K562	blood:
4	chr1:245978284..245980210-chr1:245986167..245988754,2	K562	blood:
5	chr1:246004025..246006674-chr1:246026244..246028356,2	K562	blood:
6	chr1:246000797..246002890-chr1:246020641..246022922,2	K562	blood:
7	chr1:245990424..245993130-chr1:245997330..245999574,3	K562	blood:
8	chr1:246004939..246007582-chr1:246008449..246010264,2	K562	blood:
9	chr1:245988915..245992283-chr1:245996613..246000747,4	K562	blood:
10	chr1:245988107..245989157-chr1:246166116..246167095,4	MCF-7	breast:
11	chr1:245992708..245995322-chr1:245995815..245998261,2	MCF-7	breast:
12	chr1:245990424..245993130-chr1:245997330..245999574,3	K562	blood:
13	chr1:245988915..245992283-chr1:245996613..246000747,4	K562	blood:
14	chr1:246000997..246002904-chr1:246031374..246033364,2	K562	blood:
15	chr1:245978284..245980210-chr1:245986167..245988754,2	K562	blood:
16	chr1:245999406..246001489-chr1:246004038..246006182,2	K562	blood:

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3	CpG island
ENSG00000185420	chromatin interactions

Extended variants
information (count: 1256 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12031535	chr1:245979357-245979358	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114060930	chr1:245979459-245979460	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs76015774	chr1:245979477-245979478	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185358424	chr1:245979561-245979562	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs191242796	chr1:245979562-245979563	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs558722821	chr1:245979585-245979586	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs111738826	chr1:245979595-245979596	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs113150139	chr1:245979627-245979628	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs544117410	chr1:245979630-245979631	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs374086290	chr1:245979678-245979679	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs367914141	chr1:245979680-245979681	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs77025768	chr1:245979709-245979710	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs563400948	chr1:245979723-245979724	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs574071505	chr1:245979741-245979742	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs373803195	chr1:245979755-245979756	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs59589215	chr1:245979767-245979768	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs559980681	chr1:245979783-245979784	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532239893	chr1:245979805-245979806	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs368338394	chr1:245979819-245979820	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs143301747	chr1:245979820-245979821	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs59280511	chr1:245979841-245979842	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs371982145	chr1:245979858-245979859	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs565499859	chr1:245979859-245979860	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs531195046	chr1:245979892-245979893	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs551279333	chr1:245979894-245979895	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs568008080	chr1:245979909-245979910	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs185866121	chr1:245979940-245979941	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs12088137	chr1:245979967-245979968	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566808762	chr1:245979978-245979979	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs542663465	chr1:245979980-245979981	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs577789889	chr1:245979990-245979991	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs191211434	chr1:245979991-245979992	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs375057793	chr1:245979992-245979993	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs537676528	chr1:245979997-245979998	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs144405951	chr1:245980003-245980004	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs555140189	chr1:245980007-245980008	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs183328743	chr1:245980009-245980010	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs539800618	chr1:245980018-245980019	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs553733107	chr1:245980021-245980022	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs576835645	chr1:245980025-245980026	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs545898126	chr1:245980035-245980036	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs4294383	chr1:245980042-245980043	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs531125267	chr1:245980064-245980065	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544860950	chr1:245980069-245980070	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs563610461	chr1:245980082-245980083	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs373959235	chr1:245980083-245980084	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs561525937	chr1:245980088-245980089	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs546538698	chr1:245980089-245980090	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs187920226	chr1:245980092-245980093	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs199580577	chr1:245980097-245980098	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Multiple myeloma	16616336	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
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:245949200-245999600	Weak transcription	Gastric	stomach
2	chr1:245961800-245980000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:245968400-245985800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:245971200-245985800	Weak transcription	Osteobl	bone
5	chr1:245973200-245986400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:245974400-246020800	Weak transcription	Fetal Intestine Small	intestine
7	chr1:245975000-245979400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:245976200-245979400	Weak transcription	Placenta	Placenta
9	chr1:245979200-245987000	Weak transcription	K562	blood
10	chr1:245979400-245979800	Enhancers	Placenta	Placenta
11	chr1:245979600-245979800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr1:245979600-245979800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:245979800-245980000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr1:245979800-245980200	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr1:245979800-245980200	Active TSS	Placenta	Placenta
16	chr1:245979800-245980400	Active TSS	H9 Cell Line	embryonic stem cell
17	chr1:245979800-246000600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:245980000-245980600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:245980400-245980600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:245980600-245985800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:245984200-246005200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:245985400-246005600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:245985800-245986000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:245985800-245986000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:245985800-245986200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:245985800-245986200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr1:245985800-245986200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:245985800-245986200	Enhancers	NH-A	brain
29	chr1:245985800-245986200	Enhancers	NHDF-Ad	bronchial
30	chr1:245985800-245986200	Enhancers	Osteobl	bone
31	chr1:245985800-245986800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:245985800-245987000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:245985800-245987000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:245985800-245987000	Enhancers	HMEC	breast
35	chr1:245985800-245987000	Enhancers	HSMM	muscle
36	chr1:245985800-245987200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:245985800-245987400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:245985800-245987400	Enhancers	Placenta	Placenta
39	chr1:245985800-245987400	Enhancers	NHLF	lung
40	chr1:245986000-245986400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:245986000-245986400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:245986000-245986800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:245986000-245986800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:245986000-245986800	Enhancers	HSMMtube	muscle
45	chr1:245986000-245986800	Enhancers	NHEK	skin
46	chr1:245986000-245987000	Enhancers	A549	lung
47	chr1:245986000-245987200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:245986000-245987200	Enhancers	Hela-S3	cervix
49	chr1:245986000-245987400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:245986000-245987400	Enhancers	Placenta Amnion	Placenta Amnion

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