Variant report

Variant	nsv945313
Chromosome Location	chr1:224048561-224060636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:165)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:165 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:224060633-224061180	K562	blood:	n/a	n/a
2	ATF1	chr1:224058318-224058581	K562	blood:	n/a	n/a
3	CBX3	chr1:224060624-224061253	K562	blood:	n/a	n/a
4	CBX3	chr1:224058172-224059252	K562	blood:	n/a	n/a
5	CBX3	chr1:224059380-224059843	K562	blood:	n/a	n/a
6	CCNT2	chr1:224058409-224058609	K562	blood:	n/a	n/a
7	CEBPB	chr1:224058951-224059102	K562	blood:	n/a	chr1:224059023-224059034
8	CEBPB	chr1:224058918-224059142	HepG2	liver:	n/a	chr1:224059023-224059034
9	CEBPD	chr1:224058237-224058827	K562	blood:	n/a	n/a
10	CEBPD	chr1:224060022-224060350	K562	blood:	n/a	n/a
11	CEBPD	chr1:224058241-224058840	K562	blood:	n/a	n/a
12	CHD2	chr1:224058447-224058685	K562	blood:	n/a	n/a
13	CTCF	chr1:224052502-224052538	ProgFib	skin:	n/a	n/a
14	E2F4	chr1:224049637-224049837	MCF10A-Er-Src	breast:	n/a	n/a
15	EGR1	chr1:224060606-224060873	K562	blood:	n/a	chr1:224060729-224060739 chr1:224060727-224060740 chr1:224060723-224060745 chr1:224060728-224060739 chr1:224060728-224060739 chr1:224060727-224060740 chr1:224060727-224060741 chr1:224060729-224060739
16	EGR1	chr1:224060611-224060994	K562	blood:	n/a	chr1:224060729-224060739 chr1:224060727-224060740 chr1:224060723-224060745 chr1:224060728-224060739 chr1:224060728-224060739 chr1:224060727-224060740 chr1:224060727-224060741 chr1:224060729-224060739
17	EGR1	chr1:224058382-224058729	K562	blood:	n/a	n/a
18	ELF1	chr1:224058903-224059238	K562	blood:	n/a	n/a
19	EP300	chr1:224058289-224058660	K562	blood:	n/a	n/a
20	ETS1	chr1:224058253-224058628	K562	blood:	n/a	n/a
21	ETS1	chr1:224058361-224058578	K562	blood:	n/a	n/a
22	GABPA	chr1:224058211-224058704	K562	blood:	n/a	n/a
23	GABPA	chr1:224058253-224058736	K562	blood:	n/a	n/a
24	GATA1	chr1:224057574-224059072	PBDE	blood:	n/a	n/a
25	GATA1	chr1:224058143-224059356	K562	blood:	n/a	n/a
26	GATA1	chr1:224058298-224058725	PBDEFetal	blood:	n/a	n/a
27	GATA2	chr1:224058281-224058725	K562	blood:	n/a	n/a
28	GATA2	chr1:224058151-224058722	K562	blood:	n/a	n/a
29	GATA2	chr1:224058289-224058697	K562	blood:	n/a	n/a
30	GATA2	chr1:224059997-224060310	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr1:224050240-224050680	MCF-7	breast:	n/a	n/a
32	GATA3	chr1:224050170-224050642	MCF-7	breast:	n/a	n/a
33	GATA3	chr1:224050426-224050651	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr1:224051442-224051789	MCF-7	breast:	n/a	n/a
35	HDAC2	chr1:224058294-224058605	K562	blood:	n/a	n/a
36	HEY1	chr1:224052103-224052487	K562	blood:	n/a	n/a
37	HEY1	chr1:224050739-224051065	K562	blood:	n/a	n/a
38	HEY1	chr1:224050740-224050969	HepG2	liver:	n/a	n/a
39	HEY1	chr1:224052191-224052482	K562	blood:	n/a	n/a
40	HEY1	chr1:224050790-224050961	K562	blood:	n/a	n/a
41	IRF1	chr1:224058388-224058577	K562	blood:	n/a	n/a
42	JUND	chr1:224058463-224058534	K562	blood:	n/a	n/a
43	KAP1	chr1:224060075-224061163	HEK293	kidney:	n/a	n/a
44	MAFF	chr1:224049677-224049952	HepG2	liver:	n/a	chr1:224049810-224049828
45	MAFF	chr1:224049654-224049951	K562	blood:	n/a	chr1:224049810-224049828
46	MAFK	chr1:224049643-224049963	HepG2	liver:	n/a	chr1:224049811-224049826
47	MAFK	chr1:224049714-224049932	K562	blood:	n/a	chr1:224049811-224049826
48	MAFK	chr1:224049640-224049975	HepG2	liver:	n/a	chr1:224049811-224049826
49	MAFK	chr1:224049650-224049958	IMR90	lung:	n/a	chr1:224049811-224049826
50	MAX	chr1:224058494-224058650	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224051868-224051918	Jurkat	blood:	n/a
2	chr1:224052083-224052133	AG09309	skin:	n/a
3	chr1:224052083-224052133	HEK293	kidney:	embryo
4	chr1:224051868-224051918	U87	brain:	n/a
5	chr1:224051868-224051918	MCF10A-Er-Src	breast:	n/a
6	chr1:224052083-224052133	GM12891	blood:	n/a
7	chr1:224051868-224051918	HNPCEpiC	eye:	n/a
8	chr1:224052083-224052133	PFSK-1	brain:	n/a
9	chr1:224052083-224052133	HIPEpiC	eye:	n/a
10	chr1:224052083-224052133	AG09319	gingival:	n/a
11	chr1:224052083-224052133	LNCaP	prostate:	n/a
12	chr1:224052083-224052133	K562	blood:	n/a
13	chr1:224051868-224051918	HCT-116	colon:	n/a
14	chr1:224051868-224051918	ovcar-3	ovarian:	n/a
15	chr1:224052083-224052133	ProgFib	skin:	n/a
16	chr1:224051868-224051918	SK-N-MC	brain:	n/a
17	chr1:224052083-224052133	GM06990	blood:	n/a
18	chr1:224051868-224051918	H1-hESC	embryonic stem cell:	embryo
19	chr1:224051868-224051918	IMR90	lung:	fetal
20	chr1:224051868-224051918	NB4	blood:	n/a
21	chr1:224052083-224052133	HRE	kidney:	n/a
22	chr1:224051868-224051918	CMK	blood:	n/a
23	chr1:224052083-224052133	HMEC	breast:	n/a
24	chr1:224052083-224052133	HepG2	liver:	n/a
25	chr1:224052083-224052133	SKMC	muscle:	n/a
26	chr1:224051868-224051918	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:224052083-224052133	HNPCEpiC	eye:	n/a
28	chr1:224052083-224052133	PrEC	prostate:	n/a
29	chr1:224051868-224051918	AoSMC	blood vessel:	n/a
30	chr1:224051868-224051918	HCF	heart:	n/a
31	chr1:224051868-224051918	NH-A	brain:	n/a
32	chr1:224052083-224052133	AG04450	lung:	fetal
33	chr1:224051868-224051918	ProgFib	skin:	n/a
34	chr1:224052083-224052133	GM12892	blood:	n/a
35	chr1:224052083-224052133	AG10803	skin:	n/a
36	chr1:224051868-224051918	GM12891	blood:	n/a
37	chr1:224051868-224051918	GM12878	blood:	n/a
38	chr1:224051868-224051918	PFSK-1	brain:	n/a
39	chr1:224051868-224051918	HRCEpiC	kidney:	n/a
40	chr1:224052083-224052133	NB4	blood:	n/a
41	chr1:224052083-224052133	HAEpiC	amniotic membrane:	n/a
42	chr1:224051868-224051918	AG04450	lung:	fetal
43	chr1:224052083-224052133	Hepatocyte	liver:	n/a
44	chr1:224051868-224051918	AG04449	skin:	fetal
45	chr1:224051868-224051918	T-47D	breast:	n/a
46	chr1:224052083-224052133	BE2_C	brain:	n/a
47	chr1:224052083-224052133	HCM	heart:	n/a
48	chr1:224052083-224052133	ECC-1	luminal epithelium:	n/a
49	chr1:224052083-224052133	GM12878	blood:	n/a
50	chr1:224051868-224051918	SAEC	small airway:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:224048345..224051041-chr1:224057644..224060087,2	K562	blood:
2	chr1:224032494..224036254-chr1:224057433..224064259,8	K562	blood:
3	chr1:224032237..224035602-chr1:224046110..224051630,7	MCF-7	breast:
4	chr1:224043695..224046031-chr1:224047315..224049831,3	K562	blood:
5	chr1:224042155..224044743-chr1:224047523..224049219,2	MCF-7	breast:
6	chr1:224048345..224051041-chr1:224057644..224060087,2	K562	blood:
7	chr1:224031941..224034592-chr1:224054767..224056750,2	K562	blood:
8	chr1:224030773..224035996-chr1:224045738..224052159,10	MCF-7	breast:
9	chr1:224033607..224035143-chr1:224060636..224062476,2	MCF-7	breast:

No data

Variant related genes	Relation type
ACTBP11	TF binding region
PHBP11	TF binding region
ACTBP11	CpG island
PHBP11	CpG island
ENSG00000227621	chromatin interactions
ENSG00000143514	chromatin interactions

Extended variants
information (count: 487 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187030327	chr1:224048575-224048576	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs558979761	chr1:224048627-224048628	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs544719051	chr1:224048635-224048636	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs191567220	chr1:224048639-224048640	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs10915891	chr1:224048645-224048646	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs72749588	chr1:224048665-224048666	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs561586036	chr1:224048670-224048671	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs371372640	chr1:224048690-224048691	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs543965693	chr1:224048718-224048719	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs182938966	chr1:224048757-224048758	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs140485213	chr1:224048765-224048766	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532785321	chr1:224048849-224048850	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs73114501	chr1:224048867-224048868	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs10915892	chr1:224048910-224048911	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs372923547	chr1:224048923-224048924	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145062178	chr1:224048936-224048937	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs548613655	chr1:224048990-224048991	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs567508202	chr1:224049070-224049071	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148691280	chr1:224049074-224049075	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs556290462	chr1:224049124-224049125	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs543471038	chr1:224049155-224049156	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs369917129	chr1:224049189-224049190	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532083089	chr1:224049190-224049191	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs34545372	chr1:224049206-224049207	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs367688005	chr1:224049208-224049209	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs571338385	chr1:224049230-224049231	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs188313837	chr1:224049294-224049295	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs142145785	chr1:224049332-224049333	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs557432088	chr1:224049347-224049348	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375827578	chr1:224049353-224049354	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs6604730	chr1:224049363-224049364	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs147822053	chr1:224049409-224049410	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549307647	chr1:224049425-224049426	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs543740420	chr1:224049454-224049455	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565596434	chr1:224049464-224049465	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550235349	chr1:224049513-224049514	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs368245046	chr1:224049517-224049518	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529263325	chr1:224049564-224049565	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs532752315	chr1:224049566-224049567	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs17500138	chr1:224049586-224049587	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559846108	chr1:224049587-224049588	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs193280618	chr1:224049594-224049595	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs559368895	chr1:224049595-224049596	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs73116403	chr1:224049618-224049619	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs74228620	chr1:224049656-224049657	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs369069838	chr1:224049742-224049743	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs372819039	chr1:224049757-224049758	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs72749591	chr1:224049802-224049803	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs571248648	chr1:224049912-224049913	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs376036963	chr1:224049978-224049979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224044800-224051800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:224046000-224048600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:224047000-224048600	Enhancers	NHEK	skin
4	chr1:224047200-224048600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:224047200-224048600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:224047400-224048600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:224048400-224048600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:224048400-224048600	Enhancers	HMEC	breast
9	chr1:224048400-224052000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:224050200-224050400	Enhancers	Fetal Lung	lung
11	chr1:224051600-224051800	Bivalent Enhancer	HepG2	liver
12	chr1:224051800-224052400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:224052000-224052400	ZNF genes & repeats	Spleen	Spleen
14	chr1:224052000-224052600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:224052400-224052800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:224052600-224057800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:224052800-224058200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:224057600-224058200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:224057800-224058600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:224057800-224059400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:224057800-224059400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr1:224057800-224060600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:224057800-224062000	Enhancers	K562	blood
24	chr1:224058000-224058600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr1:224058000-224059400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr1:224058000-224059400	Enhancers	Placenta	Placenta
27	chr1:224058200-224058400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr1:224058200-224058600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr1:224058200-224058600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:224058200-224058600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:224058200-224058600	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr1:224058200-224058600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr1:224058200-224058800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
34	chr1:224058200-224059200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr1:224058200-224059200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:224058200-224059200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:224058400-224058600	Enhancers	Pancreas	Pancrea
38	chr1:224058400-224058800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:224058400-224058800	Enhancers	Dnd41	blood
40	chr1:224058400-224059000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr1:224058400-224059000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr1:224058400-224059000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr1:224058400-224059200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr1:224058400-224059200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr1:224058400-224059200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:224058400-224059400	Bivalent/Poised TSS	HepG2	liver
47	chr1:224058600-224058800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:224058600-224058800	Enhancers	Placenta Amnion	Placenta Amnion
49	chr1:224058600-224059000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:224058600-224059000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links