Variant report

Variant	nsv873415
Chromosome Location	chr1:246455842-246502153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:518)
CpG islands
(count:122)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246472537-246472962	K562	blood:	n/a	n/a
2	ARID3A	chr1:246476713-246476913	K562	blood:	n/a	n/a
3	ARID3A	chr1:246495436-246495765	K562	blood:	n/a	n/a
4	ARID3A	chr1:246468839-246469426	K562	blood:	n/a	n/a
5	ARID3A	chr1:246469874-246470465	K562	blood:	n/a	n/a
6	ATF1	chr1:246495450-246495686	K562	blood:	n/a	n/a
7	ATF1	chr1:246469981-246470295	K562	blood:	n/a	n/a
8	ATF1	chr1:246501515-246501774	K562	blood:	n/a	n/a
9	ATF2	chr1:246492949-246493723	GM12878	blood:	n/a	n/a
10	ATF2	chr1:246501723-246502313	GM12878	blood:	n/a	n/a
11	ATF2	chr1:246493100-246493631	GM12878	blood:	n/a	n/a
12	BACH1	chr1:246469926-246470676	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:246469042-246469374	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:246469627-246470581	K562	blood:	n/a	n/a
15	BACH1	chr1:246469053-246469366	K562	blood:	n/a	n/a
16	BATF	chr1:246493105-246493597	GM12878	blood:	n/a	chr1:246493346-246493357
17	BATF	chr1:246493051-246493632	GM12878	blood:	n/a	chr1:246493346-246493357
18	BATF	chr1:246501825-246502142	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:246493003-246493636	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
20	BCL11A	chr1:246493088-246493638	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
21	BCL3	chr1:246474759-246475054	GM12878	blood:	n/a	n/a
22	BCL3	chr1:246493055-246493585	GM12878	blood:	n/a	chr1:246493349-246493358
23	BCL3	chr1:246500317-246500521	GM12878	blood:	n/a	n/a
24	BCLAF1	chr1:246493053-246493656	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
25	BCLAF1	chr1:246493000-246493668	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
26	BHLHE40	chr1:246469899-246470287	K562	blood:	n/a	n/a
27	BHLHE40	chr1:246501857-246502115	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:246493081-246493626	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:246495569-246495766	K562	blood:	n/a	n/a
30	BHLHE40	chr1:246501485-246501808	K562	blood:	n/a	n/a
31	CBX3	chr1:246469114-246469749	K562	blood:	n/a	chr1:246469383-246469394
32	CBX3	chr1:246469834-246470418	K562	blood:	n/a	n/a
33	CCNT2	chr1:246470003-246470249	K562	blood:	n/a	n/a
34	CCNT2	chr1:246495455-246495669	K562	blood:	n/a	n/a
35	CCNT2	chr1:246472666-246473033	K562	blood:	n/a	n/a
36	CEBPB	chr1:246487962-246488318	A549	lung:	n/a	n/a
37	CEBPB	chr1:246488024-246488342	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:246490440-246490704	MCF-7	breast:	n/a	n/a
39	CEBPB	chr1:246487659-246487768	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr1:246483696-246483900	HepG2	liver:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
41	CEBPB	chr1:246464902-246465231	K562	blood:	n/a	chr1:246465056-246465067
42	CEBPB	chr1:246501582-246501763	K562	blood:	n/a	n/a
43	CEBPB	chr1:246488028-246488279	MCF-7	breast:	n/a	n/a
44	CEBPB	chr1:246464871-246465238	A549	lung:	n/a	chr1:246465056-246465067
45	CEBPB	chr1:246495527-246495684	K562	blood:	n/a	n/a
46	CEBPB	chr1:246474391-246474534	K562	blood:	n/a	n/a
47	CEBPB	chr1:246464896-246465226	HepG2	liver:	n/a	chr1:246465056-246465067
48	CEBPB	chr1:246483583-246483947	IMR90	lung:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
49	CEBPB	chr1:246464897-246465244	IMR90	lung:	n/a	chr1:246465056-246465067
50	CEBPB	chr1:246483728-246483819	H1-hESC	embryonic stem cell:	n/a	chr1:246483758-246483769 chr1:246483760-246483769

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246466280-246466330	MCF10A-Er-Src	breast:	n/a
2	chr1:246457244-246457294	BE2_C	brain:	n/a
3	chr1:246466280-246466330	IMR90	lung:	fetal
4	chr1:246466280-246466330	HCPEpiC	choroid plexus:	n/a
5	chr1:246466280-246466330	NHDF-neo	bronchial:	n/a
6	chr1:246457244-246457294	NH-A	brain:	n/a
7	chr1:246466280-246466330	NH-A	brain:	n/a
8	chr1:246466280-246466330	GM19239	blood:	n/a
9	chr1:246457244-246457294	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:246466280-246466330	ovcar-3	ovarian:	n/a
11	chr1:246457244-246457294	ovcar-3	ovarian:	n/a
12	chr1:246466280-246466330	HRCEpiC	kidney:	n/a
13	chr1:246466280-246466330	AG04449	skin:	fetal
14	chr1:246466280-246466330	SAEC	small airway:	n/a
15	chr1:246466280-246466330	MCF-7	breast:	n/a
16	chr1:246457244-246457294	PANC-1	pancreas:	n/a
17	chr1:246457244-246457294	K562	blood:	n/a
18	chr1:246466280-246466330	AG09309	skin:	n/a
19	chr1:246466280-246466330	CMK	blood:	n/a
20	chr1:246466280-246466330	Jurkat	blood:	n/a
21	chr1:246457244-246457294	GM19239	blood:	n/a
22	chr1:246457244-246457294	AG10803	skin:	n/a
23	chr1:246466280-246466330	NB4	blood:	n/a
24	chr1:246457244-246457294	GM12891	blood:	n/a
25	chr1:246457244-246457294	Hepatocyte	liver:	n/a
26	chr1:246457244-246457294	HAEpiC	amniotic membrane:	n/a
27	chr1:246457244-246457294	BJ	skin:	n/a
28	chr1:246466280-246466330	Hela-S3	cervix:	n/a
29	chr1:246457244-246457294	SAEC	small airway:	n/a
30	chr1:246466280-246466330	HepG2	liver:	n/a
31	chr1:246466280-246466330	BJ	skin:	n/a
32	chr1:246466280-246466330	GM12891	blood:	n/a
33	chr1:246466280-246466330	GM06990	blood:	n/a
34	chr1:246466280-246466330	SKMC	muscle:	n/a
35	chr1:246466280-246466330	H1-hESC	embryonic stem cell:	embryo
36	chr1:246466280-246466330	SK-N-MC	brain:	n/a
37	chr1:246466280-246466330	HNPCEpiC	eye:	n/a
38	chr1:246457244-246457294	HEK293	kidney:	embryo
39	chr1:246466280-246466330	NT2-D1	testis:	n/a
40	chr1:246466280-246466330	HPAEpiC	pulmonary alveolar:	n/a
41	chr1:246466280-246466330	Hepatocyte	liver:	n/a
42	chr1:246457244-246457294	Hela-S3	cervix:	n/a
43	chr1:246457244-246457294	PFSK-1	brain:	n/a
44	chr1:246457244-246457294	SKMC	muscle:	n/a
45	chr1:246457244-246457294	CMK	blood:	n/a
46	chr1:246457244-246457294	MCF10A-Er-Src	breast:	n/a
47	chr1:246457244-246457294	H1-hESC	embryonic stem cell:	embryo
48	chr1:246466280-246466330	A549	lung:	n/a
49	chr1:246466280-246466330	RPTEC	kidney:	n/a
50	chr1:246457244-246457294	HRCEpiC	kidney:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246452108..246454615-chr1:246458116..246460010,2	K562	blood:
2	chr1:246451778..246454398-chr1:246470226..246471898,2	K562	blood:
3	chr1:246464800..246467604-chr1:246470299..246472286,2	MCF-7	breast:
4	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
5	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
6	chr1:246480625..246484494-chr1:246484509..246487913,3	K562	blood:
7	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
8	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
9	chr1:246151420..246154131-chr1:246468233..246469966,2	K562	blood:
10	chr1:246464800..246467604-chr1:246470299..246472286,2	MCF-7	breast:
11	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
12	chr1:246478448..246480701-chr1:246489976..246492079,2	MCF-7	breast:
13	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
14	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
15	chr1:246477291..246479573-chr1:246484385..246486637,2	K562	blood:
16	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
17	chr1:246478448..246480701-chr1:246489976..246492079,2	MCF-7	breast:
18	chr1:246470110..246471825-chr1:246585890..246587442,2	K562	blood:
19	chr1:246482654..246484211-chr1:246484942..246487391,2	MCF-7	breast:
20	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
21	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
22	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFB2M-2	chr1:246484965-246485170	ENSG00000230184.1
2	lnc-TFB2M-2	chr1:246485586-246485740	ENSG00000230184.1

No data

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3-IT1	TF binding region
SMYD3	CpG island
SMYD3-IT1	CpG island
ENSG00000185420	chromatin interactions
ENSG00000230184	chromatin interactions

Extended variants
information (count: 1702 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1702 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10924677	chr1:246455842-246455843	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs56158544	chr1:246455847-246455848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550551324	chr1:246455905-246455906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187482623	chr1:246455932-246455933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536180149	chr1:246455994-246455995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192342931	chr1:246456003-246456004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182515411	chr1:246456018-246456019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139370356	chr1:246456026-246456027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536932741	chr1:246456056-246456057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558082759	chr1:246456090-246456091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575292075	chr1:246456106-246456107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6657911	chr1:246456165-246456166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537935940	chr1:246456199-246456200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145505985	chr1:246456204-246456205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557307199	chr1:246456223-246456224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs386641711	chr1:246456243-246456244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12409083	chr1:246456244-246456245	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs73142858	chr1:246456257-246456258	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs140441523	chr1:246456305-246456306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs58487495	chr1:246456327-246456328	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs144303234	chr1:246456344-246456345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75840202	chr1:246456391-246456392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73142860	chr1:246456416-246456417	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188311238	chr1:246456428-246456429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548580617	chr1:246456471-246456472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145475662	chr1:246456498-246456499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546347541	chr1:246456555-246456556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1770029	chr1:246456556-246456557	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs192200203	chr1:246456590-246456591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538543322	chr1:246456591-246456592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551796475	chr1:246456595-246456596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148818929	chr1:246456637-246456638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537571137	chr1:246456667-246456668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143609702	chr1:246456669-246456670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568030466	chr1:246456729-246456730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564481567	chr1:246456758-246456759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375165230	chr1:246456759-246456760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532076095	chr1:246456806-246456807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151002079	chr1:246456875-246456876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140830429	chr1:246456889-246456890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545709496	chr1:246456909-246456910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144822878	chr1:246456919-246456920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575613806	chr1:246456920-246456921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544244535	chr1:246456934-246456935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561440807	chr1:246456939-246456940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530091795	chr1:246456985-246456986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112378939	chr1:246456987-246456988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138669676	chr1:246457024-246457025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559906633	chr1:246457030-246457031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12087985	chr1:246457068-246457069	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

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
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
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246423400-246509000	Weak transcription	Aorta	Aorta
2	chr1:246435400-246460200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:246441800-246506600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:246442600-246460400	Weak transcription	Osteobl	bone
5	chr1:246443200-246469000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:246444800-246456400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:246447600-246459000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:246447600-246482400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:246447600-246502800	Weak transcription	Left Ventricle	heart
10	chr1:246452000-246458800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:246452000-246465200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:246454200-246456000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:246454600-246456000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:246454800-246456000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr1:246454800-246456000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr1:246454800-246458600	Weak transcription	Brain Germinal Matrix	brain
17	chr1:246455000-246463600	Weak transcription	Fetal Kidney	kidney
18	chr1:246455000-246493000	Weak transcription	Primary B cells from cord blood	blood
19	chr1:246455800-246456600	Enhancers	HUVEC	blood vessel
20	chr1:246456000-246456200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:246456000-246456600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:246456000-246456600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:246456000-246456800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:246456000-246457200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr1:246456000-246457400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:246456200-246457000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:246456200-246457200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:246456400-246457000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr1:246456400-246457200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:246456600-246458400	Weak transcription	HUVEC	blood vessel
31	chr1:246456800-246466000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:246457000-246458400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:246457200-246457600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:246457200-246470000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr1:246457800-246458000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr1:246458000-246459000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr1:246458400-246460000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:246458400-246461200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:246458400-246461600	Enhancers	HUVEC	blood vessel
40	chr1:246458600-246459200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr1:246458600-246461400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:246458800-246461400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:246459000-246460800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr1:246459000-246460800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:246459000-246461400	Enhancers	NHEK	skin
46	chr1:246459200-246459600	Enhancers	Fetal Lung	lung
47	chr1:246459200-246459600	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr1:246459200-246459800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr1:246459200-246459800	Enhancers	HSMMtube	muscle
50	chr1:246459200-246460000	Enhancers	Primary monocytes fromperipheralblood	blood

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