Variant report

Variant	nsv947385
Chromosome Location	chr1:222716788-222720718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:240)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:240 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr1:222720226-222720703	A549	lung:	n/a	n/a
2	ATF3	chr1:222720127-222720838	A549	lung:	n/a	n/a
3	BCL3	chr1:222720210-222721099	A549	lung:	n/a	n/a
4	BCL3	chr1:222720221-222720707	A549	lung:	n/a	n/a
5	BHLHE40	chr1:222717162-222717347	K562	blood:	n/a	n/a
6	BRCA1	chr1:222717329-222717332	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:222720355-222720608	K562	blood:	n/a	n/a
8	CEBPB	chr1:222720277-222720687	IMR90	lung:	n/a	n/a
9	CEBPB	chr1:222720211-222720734	MCF-7	breast:	n/a	n/a
10	CEBPB	chr1:222720098-222720837	A549	lung:	n/a	chr1:222720767-222720778
11	CEBPB	chr1:222720235-222720664	A549	lung:	n/a	n/a
12	CEBPB	chr1:222720282-222720653	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:222720266-222720725	MCF-7	breast:	n/a	n/a
14	CEBPB	chr1:222720272-222720685	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:222720280-222720682	A549	lung:	n/a	n/a
16	CHD2	chr1:222717403-222717404	HepG2	liver:	n/a	n/a
17	CHD2	chr1:222720371-222720694	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr1:222717279-222717284	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr1:222720474-222720795	A549	lung:	n/a	n/a
20	CTCF	chr1:222720560-222720710	HMEC	breast:	n/a	chr1:222720650-222720663
21	CTCF	chr1:222720563-222720624	Gliobla	brain:	n/a	n/a
22	CTCF	chr1:222720620-222720770	RPTEC	kidney:	n/a	chr1:222720650-222720663
23	CTCF	chr1:222720520-222720670	AG10803	skin:	n/a	chr1:222720650-222720663
24	CTCF	chr1:222720500-222720650	HepG2	liver:	n/a	n/a
25	CTCF	chr1:222720460-222720610	AG10803	skin:	n/a	n/a
26	CTCF	chr1:222717238-222717441	HepG2	liver:	n/a	n/a
27	CTCF	chr1:222720460-222720610	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr1:222720500-222720650	AG09319	gingival:	n/a	n/a
29	CTCF	chr1:222720460-222720610	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:222717240-222717390	A549	lung:	n/a	n/a
31	CTCF	chr1:222717273-222717389	A549	lung:	n/a	n/a
32	CTCF	chr1:222717256-222717408	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr1:222720660-222720810	HCM	heart:	n/a	n/a
34	CTCF	chr1:222720640-222720790	SK-N-SH_RA	brain:	n/a	chr1:222720650-222720663
35	CTCF	chr1:222720520-222720670	HAc	cerebellar:	n/a	chr1:222720650-222720663
36	CTCF	chr1:222720540-222720690	AG04449	skin:	n/a	chr1:222720650-222720663
37	CTCF	chr1:222720500-222720650	HEK293	kidney:	n/a	n/a
38	CTCF	chr1:222720440-222720590	HVMF	connective:	n/a	n/a
39	CTCF	chr1:222717085-222717499	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:222720560-222720710	AG09319	gingival:	n/a	chr1:222720650-222720663
41	CTCF	chr1:222717300-222717450	HCT-116	colon:	n/a	n/a
42	CTCF	chr1:222717300-222717376	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:222720300-222720450	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr1:222720560-222720710	HRPEpiC	eye:	n/a	chr1:222720650-222720663
45	CTCF	chr1:222720380-222720530	HPF	lung:	n/a	n/a
46	CTCF	chr1:222720500-222720650	SAEC	small airway:	n/a	n/a
47	CTCF	chr1:222720460-222720610	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr1:222717178-222717464	K562	blood:	n/a	n/a
49	CTCF	chr1:222717213-222717447	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:222717260-222717410	HBMEC	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:222717278-222717328	HepG2	liver:	n/a
2	chr1:222717104-222717154	U87	brain:	n/a
3	chr1:222717516-222717566	PFSK-1	brain:	n/a
4	chr1:222717104-222717154	NT2-D1	testis:	n/a
5	chr1:222717516-222717566	HIPEpiC	eye:	n/a
6	chr1:222717104-222717154	HMEC	breast:	n/a
7	chr1:222717278-222717328	PANC-1	pancreas:	n/a
8	chr1:222717516-222717566	SK-N-MC	brain:	n/a
9	chr1:222717516-222717566	HRE	kidney:	n/a
10	chr1:222717278-222717328	SKMC	muscle:	n/a
11	chr1:222717516-222717566	BE2_C	brain:	n/a
12	chr1:222717516-222717566	GM19239	blood:	n/a
13	chr1:222717278-222717328	HCF	heart:	n/a
14	chr1:222717516-222717566	RPTEC	kidney:	n/a
15	chr1:222717104-222717154	HIPEpiC	eye:	n/a
16	chr1:222717516-222717566	HEK293	kidney:	embryo
17	chr1:222717104-222717154	SKMC	muscle:	n/a
18	chr1:222717516-222717566	GM12892	blood:	n/a
19	chr1:222717516-222717566	HCF	heart:	n/a
20	chr1:222717104-222717154	CMK	blood:	n/a
21	chr1:222717104-222717154	PFSK-1	brain:	n/a
22	chr1:222717516-222717566	GM06990	blood:	n/a
23	chr1:222717104-222717154	Hepatocyte	liver:	n/a
24	chr1:222717516-222717566	ProgFib	skin:	n/a
25	chr1:222717278-222717328	BE2_C	brain:	n/a
26	chr1:222717104-222717154	Hela-S3	cervix:	n/a
27	chr1:222717278-222717328	Caco-2	colon:	n/a
28	chr1:222717104-222717154	HRE	kidney:	n/a
29	chr1:222717278-222717328	AG04449	skin:	fetal
30	chr1:222717104-222717154	HAEpiC	amniotic membrane:	n/a
31	chr1:222717516-222717566	MCF10A-Er-Src	breast:	n/a
32	chr1:222717278-222717328	HAEpiC	amniotic membrane:	n/a
33	chr1:222717104-222717154	HCM	heart:	n/a
34	chr1:222717516-222717566	NHBE	bronchial:	n/a
35	chr1:222717516-222717566	ovcar-3	ovarian:	n/a
36	chr1:222717278-222717328	AG10803	skin:	n/a
37	chr1:222717516-222717566	GM12878	blood:	n/a
38	chr1:222717278-222717328	K562	blood:	n/a
39	chr1:222717278-222717328	A549	lung:	n/a
40	chr1:222717516-222717566	AG09309	skin:	n/a
41	chr1:222717278-222717328	GM12892	blood:	n/a
42	chr1:222717516-222717566	K562	blood:	n/a
43	chr1:222717516-222717566	CMK	blood:	n/a
44	chr1:222717104-222717154	MCF10A-Er-Src	breast:	n/a
45	chr1:222717104-222717154	GM12892	blood:	n/a
46	chr1:222717278-222717328	HRE	kidney:	n/a
47	chr1:222717278-222717328	T-47D	breast:	n/a
48	chr1:222717516-222717566	SK-N-SH	brain:	n/a
49	chr1:222717516-222717566	HUVEC	blood vessel:	n/a
50	chr1:222717104-222717154	AoSMC	blood vessel:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:222720096..222721859-chr1:222816165..222817680,2	MCF-7	breast:
2	chr1:222716628..222718719-chr1:222762257..222764765,2	MCF-7	breast:
3	chr1:222718086..222720814-chr1:222790387..222793185,3	MCF-7	breast:
4	chr1:222716769..222717818-chr1:222807560..222808441,6	MCF-7	breast:

No data

Variant related genes	Relation type
HHIPL2	TF binding region
HHIPL2	CpG island
ENSG00000225265	chromatin interactions
ENSG00000143498	chromatin interactions
ENSG00000154305	chromatin interactions

Extended variants
information (count: 158 )
Associated
traits (count: 94 )

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	rs570123893	chr1:222716812-222716813	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs79034885	chr1:222716837-222716838	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs76380116	chr1:222716838-222716839	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528033996	chr1:222716874-222716875	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs367983202	chr1:222716915-222716916	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142197988	chr1:222716944-222716945	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs371714493	chr1:222716966-222716967	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs182148496	chr1:222716971-222716972	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs148477475	chr1:222716993-222716994	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs550780318	chr1:222717010-222717011	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs117940365	chr1:222717027-222717028	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs539949017	chr1:222717035-222717036	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs558235638	chr1:222717040-222717041	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150501722	chr1:222717066-222717067	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs374204425	chr1:222717070-222717071	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs139463892	chr1:222717071-222717072	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs534146315	chr1:222717083-222717084	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs147794680	chr1:222717104-222717105	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs574300642	chr1:222717118-222717119	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs145540643	chr1:222717126-222717127	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs149211314	chr1:222717131-222717132	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs3811466	chr1:222717132-222717133	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539287050	chr1:222717149-222717150	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs368391725	chr1:222717152-222717153	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs145663725	chr1:222717159-222717160	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs145415446	chr1:222717172-222717173	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs563140835	chr1:222717183-222717184	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs372652424	chr1:222717194-222717195	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs375872765	chr1:222717199-222717200	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs149523962	chr1:222717264-222717265	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs545498641	chr1:222717302-222717303	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs563813115	chr1:222717309-222717310	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs368972116	chr1:222717316-222717317	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs191876795	chr1:222717319-222717320	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs371367535	chr1:222717329-222717330	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs182677675	chr1:222717353-222717354	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs199780859	chr1:222717354-222717355	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs528220446	chr1:222717362-222717363	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs201993539	chr1:222717376-222717377	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs374728664	chr1:222717455-222717456	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369051817	chr1:222717473-222717474	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs373367712	chr1:222717490-222717491	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs561506558	chr1:222717508-222717509	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs529226554	chr1:222717516-222717517	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs376894621	chr1:222717517-222717518	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs550561377	chr1:222717567-222717568	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs541510300	chr1:222717578-222717579	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs372156859	chr1:222717582-222717583	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs569074325	chr1:222717587-222717588	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs539614477	chr1:222717663-222717664	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	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
Prostate cancer	18632612	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
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	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
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:222710200-222718600	Weak transcription	A549	lung
2	chr1:222712200-222717000	Weak transcription	K562	blood
3	chr1:222713400-222720000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:222713600-222720000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:222714400-222718400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:222714400-222719400	Weak transcription	Osteobl	bone
7	chr1:222714400-222719600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:222715000-222718400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:222717000-222717400	Enhancers	K562	blood
10	chr1:222717200-222717800	Active TSS	HepG2	liver
11	chr1:222717400-222719600	Weak transcription	K562	blood
12	chr1:222717800-222718200	Weak transcription	HepG2	liver
13	chr1:222718400-222718600	Enhancers	HepG2	liver
14	chr1:222718400-222718600	Enhancers	NHDF-Ad	bronchial
15	chr1:222718400-222719400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:222718400-222719800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:222718400-222721000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:222718600-222718800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:222718600-222718800	Enhancers	A549	lung
20	chr1:222718600-222718800	Enhancers	HSMM	muscle
21	chr1:222718600-222719200	Weak transcription	HepG2	liver
22	chr1:222718600-222719200	Weak transcription	NHDF-Ad	bronchial
23	chr1:222718600-222719800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr1:222718800-222719000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr1:222718800-222719200	Weak transcription	A549	lung
26	chr1:222718800-222719600	Weak transcription	HSMM	muscle
27	chr1:222718800-222719800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:222718800-222720200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:222718800-222722000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:222719000-222719600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr1:222719200-222719600	Enhancers	A549	lung
32	chr1:222719200-222719800	Enhancers	NHDF-Ad	bronchial
33	chr1:222719200-222720200	Enhancers	HepG2	liver
34	chr1:222719400-222719600	Enhancers	Hela-S3	cervix
35	chr1:222719400-222719600	Enhancers	Osteobl	bone
36	chr1:222719400-222720000	Enhancers	HSMMtube	muscle
37	chr1:222719400-222721400	Enhancers	HMEC	breast
38	chr1:222719400-222721600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:222719400-222721600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:222719600-222719800	Flanking Active TSS	Hela-S3	cervix
41	chr1:222719600-222719800	Enhancers	HSMM	muscle
42	chr1:222719600-222719800	Enhancers	K562	blood
43	chr1:222719600-222720000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:222719600-222720000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr1:222719600-222720400	Enhancers	Fetal Kidney	kidney
46	chr1:222719600-222720400	Flanking Active TSS	A549	lung
47	chr1:222719600-222720800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:222719600-222721000	Enhancers	NH-A	brain
49	chr1:222719600-222721000	Flanking Active TSS	Osteobl	bone
50	chr1:222719600-222721200	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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