Variant report

Variant	nsv549227
Chromosome Location	chr1:220845610-220885612
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:857)
CpG islands
(count:1038)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:220863484-220863890	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:220864705-220864894	HepG2	liver:	n/a	n/a
3	ATF2	chr1:220875258-220875664	GM12878	blood:	n/a	n/a
4	ATF3	chr1:220863316-220863888	A549	lung:	n/a	chr1:220863653-220863662
5	BACH1	chr1:220864044-220864382	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:220863472-220863672	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr1:220884819-220885052	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:220884868-220885024	GM12878	blood:	n/a	n/a
9	BCL3	chr1:220863293-220863686	A549	lung:	n/a	chr1:220863652-220863661 chr1:220863671-220863680
10	BHLHE40	chr1:220876744-220876841	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:220863217-220864249	HepG2	liver:	n/a	chr1:220863625-220863641
12	BHLHE40	chr1:220882302-220882596	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:220875525-220875538	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:220884795-220885093	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:220863447-220863804	GM12878	blood:	n/a	chr1:220863625-220863641
16	BRCA1	chr1:220864717-220864858	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:220876135-220876268	HepG2	liver:	n/a	chr1:220876189-220876200
18	CEBPB	chr1:220872122-220872478	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:220865922-220866215	IMR90	lung:	n/a	chr1:220866072-220866083
20	CEBPB	chr1:220872040-220872578	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:220866062-220866087	K562	blood:	n/a	chr1:220866072-220866083
22	CEBPB	chr1:220864641-220865064	HepG2	liver:	n/a	chr1:220864865-220864876
23	CEBPB	chr1:220863441-220863686	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr1:220865908-220866218	HepG2	liver:	n/a	chr1:220866072-220866083
25	CEBPB	chr1:220864715-220865033	HepG2	liver:	n/a	chr1:220864865-220864876
26	CEBPB	chr1:220864740-220864944	HepG2	liver:	n/a	chr1:220864865-220864876
27	CEBPB	chr1:220872148-220872355	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:220872105-220872485	HepG2	liver:	n/a	n/a
29	CEBPD	chr1:220863420-220863972	HepG2	liver:	n/a	n/a
30	CEBPD	chr1:220863458-220863789	HepG2	liver:	n/a	n/a
31	CHD1	chr1:220863617-220864025	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr1:220876660-220876903	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr1:220869021-220869075	HepG2	liver:	n/a	n/a
34	CHD2	chr1:220861198-220861511	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr1:220861141-220861534	K562	blood:	n/a	n/a
36	CHD2	chr1:220861262-220861445	HepG2	liver:	n/a	n/a
37	CHD2	chr1:220863476-220863869	HepG2	liver:	n/a	n/a
38	CHD2	chr1:220884627-220884629	HepG2	liver:	n/a	n/a
39	CHD2	chr1:220863379-220863761	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr1:220863447-220863899	A549	lung:	n/a	n/a
41	CTBP2	chr1:220863399-220864305	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr1:220864032-220864094	GM19238	blood:	n/a	n/a
43	CTCF	chr1:220853500-220853650	HL-60	blood:	n/a	chr1:220853587-220853605 chr1:220853589-220853610
44	CTCF	chr1:220853500-220853650	HRE	kidney:	n/a	chr1:220853587-220853605 chr1:220853589-220853610
45	CTCF	chr1:220863540-220863690	HRPEpiC	eye:	n/a	chr1:220863623-220863636 chr1:220863625-220863635 chr1:220863572-220863582 chr1:220863621-220863637
46	CTCF	chr1:220863462-220863760	MCF-7	breast:	n/a	chr1:220863623-220863636 chr1:220863625-220863635 chr1:220863572-220863582 chr1:220863621-220863637
47	CTCF	chr1:220853500-220853650	GM12801	blood:	n/a	chr1:220853587-220853605 chr1:220853589-220853610
48	CTCF	chr1:220863500-220863650	HBMEC	blood vessel:	n/a	chr1:220863623-220863636 chr1:220863625-220863635 chr1:220863572-220863582 chr1:220863621-220863637
49	CTCF	chr1:220863560-220863710	HAc	cerebellar:	n/a	chr1:220863623-220863636 chr1:220863625-220863635 chr1:220863572-220863582 chr1:220863621-220863637
50	CTCF	chr1:220863500-220863650	HCFaa	heart:	n/a	chr1:220863623-220863636 chr1:220863625-220863635 chr1:220863572-220863582 chr1:220863621-220863637

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:220864321-220864371	AG09309	skin:	n/a
2	chr1:220864321-220864371	AG09309	skin:	n/a
3	chr1:220864279-220864329	HIPEpiC	eye:	n/a
4	chr1:220863382-220863432	HRCEpiC	kidney:	n/a
5	chr1:220863263-220863313	HRE	kidney:	n/a
6	chr1:220864248-220864298	NHBE	bronchial:	n/a
7	chr1:220863382-220863432	NHDF-neo	bronchial:	n/a
8	chr1:220863407-220863457	ECC-1	luminal epithelium:	n/a
9	chr1:220863263-220863313	NB4	blood:	n/a
10	chr1:220871403-220871453	SKMC	muscle:	n/a
11	chr1:220863407-220863457	HNPCEpiC	eye:	n/a
12	chr1:220871403-220871453	Jurkat	blood:	n/a
13	chr1:220864119-220864169	MCF10A-Er-Src	breast:	n/a
14	chr1:220863407-220863457	AoSMC	blood vessel:	n/a
15	chr1:220864321-220864371	NH-A	brain:	n/a
16	chr1:220871403-220871453	HCF	heart:	n/a
17	chr1:220876396-220876446	Hepatocyte	liver:	n/a
18	chr1:220863407-220863457	HEEpiC	esophagus:	n/a
19	chr1:220864248-220864298	GM06990	blood:	n/a
20	chr1:220863766-220863816	PrEC	prostate:	n/a
21	chr1:220863766-220863816	Caco-2	colon:	n/a
22	chr1:220863796-220863846	AoSMC	blood vessel:	n/a
23	chr1:220864279-220864329	HCF	heart:	n/a
24	chr1:220864248-220864298	HMEC	breast:	n/a
25	chr1:220863347-220863397	HRCEpiC	kidney:	n/a
26	chr1:220860831-220860881	MCF10A-Er-Src	breast:	n/a
27	chr1:220863347-220863397	T-47D	breast:	n/a
28	chr1:220860831-220860881	ovcar-3	ovarian:	n/a
29	chr1:220860831-220860881	U87	brain:	n/a
30	chr1:220876396-220876446	HRCEpiC	kidney:	n/a
31	chr1:220860831-220860881	PrEC	prostate:	n/a
32	chr1:220863263-220863313	NHDF-neo	bronchial:	n/a
33	chr1:220864279-220864329	HRPEpiC	eye:	n/a
34	chr1:220864119-220864169	AG10803	skin:	n/a
35	chr1:220863382-220863432	ECC-1	luminal epithelium:	n/a
36	chr1:220864248-220864298	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:220863796-220863846	H1-hESC	embryonic stem cell:	embryo
38	chr1:220864321-220864371	H1-hESC	embryonic stem cell:	embryo
39	chr1:220863796-220863846	BE2_C	brain:	n/a
40	chr1:220863572-220863622	AG04449	skin:	fetal
41	chr1:220863513-220863563	GM12878	blood:	n/a
42	chr1:220863462-220863512	HEEpiC	esophagus:	n/a
43	chr1:220863462-220863512	HRE	kidney:	n/a
44	chr1:220860831-220860881	NHBE	bronchial:	n/a
45	chr1:220863796-220863846	T-47D	breast:	n/a
46	chr1:220860831-220860881	HRPEpiC	eye:	n/a
47	chr1:220863347-220863397	HepG2	liver:	n/a
48	chr1:220863766-220863816	ProgFib	skin:	n/a
49	chr1:220864279-220864329	A549	lung:	n/a
50	chr1:220864279-220864329	GM12891	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:220856870..220860235-chr1:220863184..220865949,3	MCF-7	breast:
2	chr1:9850230..9850981-chr1:220848009..220848904,2	MCF-7	breast:
3	chr1:220862639..220865186-chr1:220879178..220882320,3	K562	blood:
4	chr1:220853771..220855747-chr1:220856132..220859014,2	MCF-7	breast:
5	chr1:220869909..220871487-chr1:220872006..220873594,2	K562	blood:
6	chr1:220862132..220866220-chr1:220920879..220923309,4	MCF-7	breast:
7	chr1:220852892..220854538-chr1:220905833..220907061,7	MCF-7	breast:
8	chr1:220853123..220854093-chr1:220949753..220950686,4	K562	blood:
9	chr1:220848519..220851962-chr1:220854951..220857000,3	K562	blood:
10	chr1:220444386..220446640-chr1:220883296..220885894,2	K562	blood:
11	chr1:220799540..220802603-chr1:220876987..220879444,3	K562	blood:
12	chr1:220869909..220871487-chr1:220872006..220873594,2	K562	blood:
13	chr1:220843694..220846448-chr1:220920771..220922652,2	K562	blood:
14	chr1:220863249..220864128-chr1:220950068..220950638,2	K562	blood:
15	chr1:220853076..220854091-chr1:220906545..220907064,3	K562	blood:
16	chr1:220454527..220455068-chr1:220853160..220854109,2	MCF-7	breast:
17	chr1:220853771..220855747-chr1:220856132..220859014,2	MCF-7	breast:
18	chr1:220848519..220851962-chr1:220854951..220857000,3	K562	blood:
19	chr1:220863523..220864334-chr9:138304273..138305038,2	MCF-7	breast:

No data

Variant related genes	Relation type
C1orf115	TF binding region
C1orf115	CpG island
ENSG00000233012	chromatin interactions
ENSG00000118873	chromatin interactions
ENSG00000117791	chromatin interactions
ENSG00000162817	chromatin interactions

Extended variants
information (count: 1601 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1601 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3849288	chr1:220845610-220845611	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554956877	chr1:220845612-220845613	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574762765	chr1:220845617-220845618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540552652	chr1:220845662-220845663	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189992345	chr1:220845737-220845738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs28620658	chr1:220845784-220845785	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs28534842	chr1:220845785-220845786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534751598	chr1:220845809-220845810	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs182607290	chr1:220845818-220845819	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187071942	chr1:220845828-220845829	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562802274	chr1:220845918-220845919	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375861735	chr1:220845978-220845979	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542219342	chr1:220845991-220845992	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs3897868	chr1:220846039-220846040	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs138155159	chr1:220846054-220846055	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs3897869	chr1:220846080-220846081	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs149549690	chr1:220846111-220846112	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532934858	chr1:220846127-220846128	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146058608	chr1:220846141-220846142	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569615649	chr1:220846183-220846184	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2069044	chr1:220846200-220846201	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs12034209	chr1:220846269-220846270	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs11118590	chr1:220846275-220846276	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs534218891	chr1:220846279-220846280	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs543320675	chr1:220846294-220846295	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553998272	chr1:220846351-220846352	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs566452965	chr1:220846421-220846422	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs577476639	chr1:220846423-220846424	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528002792	chr1:220846431-220846432	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs138902139	chr1:220846497-220846498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556741877	chr1:220846511-220846512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192945520	chr1:220846547-220846548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs767374	chr1:220846703-220846704	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs562051063	chr1:220846770-220846771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527731524	chr1:220846780-220846781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76887488	chr1:220846789-220846790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564183762	chr1:220846794-220846795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61830218	chr1:220846839-220846840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183258613	chr1:220846850-220846851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79099803	chr1:220846851-220846852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563526517	chr1:220846913-220846914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528940122	chr1:220846929-220846930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548716186	chr1:220846956-220846957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146372831	chr1:220846968-220846969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79228934	chr1:220846976-220846977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112556072	chr1:220847004-220847005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551374386	chr1:220847008-220847009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571031584	chr1:220847020-220847021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139663266	chr1:220847037-220847038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142983052	chr1:220847041-220847042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Breast cancer	17603634	CNVD
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
Acute lymphoblastic leukemia	17443227	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
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
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	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
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Pancreatic cancer	17952125	CNVD
Autism	21865298	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220829400-220847200	Weak transcription	Right Ventricle	heart
2	chr1:220829600-220845800	Weak transcription	Fetal Heart	heart
3	chr1:220831400-220845800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:220845800-220846200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:220845800-220848000	Enhancers	Fetal Heart	heart
6	chr1:220846000-220846200	Bivalent Enhancer	Small Intestine	intestine
7	chr1:220847400-220847600	Enhancers	Right Ventricle	heart
8	chr1:220847600-220847800	Enhancers	Duodenum Mucosa	Duodenum
9	chr1:220848000-220853600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr1:220850600-220851200	Enhancers	Fetal Brain Male	brain
11	chr1:220851200-220852000	Weak transcription	Fetal Brain Male	brain
12	chr1:220852000-220852200	Enhancers	Fetal Brain Male	brain
13	chr1:220853600-220853800	Enhancers	Primary T cells fromperipheralblood	blood
14	chr1:220853600-220853800	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr1:220853600-220854000	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr1:220853600-220854000	Enhancers	Rectal Smooth Muscle	rectum
17	chr1:220853600-220854400	Enhancers	Duodenum Mucosa	Duodenum
18	chr1:220853600-220854400	Enhancers	Hela-S3	cervix
19	chr1:220853600-220854600	Enhancers	Liver	Liver
20	chr1:220853600-220854600	Enhancers	Pancreas	Pancrea
21	chr1:220853600-220854800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:220853600-220854800	Enhancers	Adipose Nuclei	Adipose
23	chr1:220853600-220854800	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr1:220853600-220854800	Enhancers	Stomach Mucosa	stomach
25	chr1:220853600-220854800	Enhancers	HepG2	liver
26	chr1:220854200-220854600	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr1:220854400-220854600	Enhancers	Esophagus	oesophagus
28	chr1:220854400-220854600	Flanking Active TSS	NHDF-Ad	bronchial
29	chr1:220854400-220854800	Enhancers	Ovary	ovary
30	chr1:220854400-220854800	Flanking Active TSS	Hela-S3	cervix
31	chr1:220854400-220854800	Enhancers	HUVEC	blood vessel
32	chr1:220854400-220854800	Enhancers	NHLF	lung
33	chr1:220854400-220855200	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr1:220854600-220854800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:220854600-220854800	Flanking Active TSS	Liver	Liver
36	chr1:220854600-220855000	Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr1:220854600-220855200	Active TSS	NHDF-Ad	bronchial
38	chr1:220854600-220863200	Weak transcription	Esophagus	oesophagus
39	chr1:220854800-220855000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:220854800-220855000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:220854800-220855000	Flanking Active TSS	HepG2	liver
42	chr1:220854800-220855200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:220854800-220855200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:220854800-220855200	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr1:220854800-220855200	Active TSS	Liver	Liver
46	chr1:220854800-220855200	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr1:220854800-220855200	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr1:220854800-220855200	Active TSS	Right Atrium	heart
49	chr1:220854800-220855200	Active TSS	Stomach Mucosa	stomach
50	chr1:220854800-220855200	Active TSS	Hela-S3	cervix

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