Variant report

Variant	nsv1010798
Chromosome Location	chr1:223498145-223538989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:915)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:223538550-223538750	K562	blood:	n/a	n/a
2	ATF1	chr1:223503476-223503539	K562	blood:	n/a	n/a
3	ATF1	chr1:223510838-223510864	K562	blood:	n/a	n/a
4	BACH1	chr1:223537905-223538237	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:223532394-223532440	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:223537063-223537589	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr1:223536627-223536677	K562	blood:	n/a	n/a
8	BHLHE40	chr1:223517140-223517264	K562	blood:	n/a	n/a
9	BHLHE40	chr1:223538485-223538731	K562	blood:	n/a	n/a
10	CBX3	chr1:223537298-223537571	K562	blood:	n/a	n/a
11	CCNT2	chr1:223537418-223538160	K562	blood:	n/a	n/a
12	CEBPB	chr1:223538560-223538655	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:223505131-223505665	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:223505112-223505272	HepG2	liver:	n/a	n/a
15	CHD2	chr1:223537326-223537511	GM12878	blood:	n/a	n/a
16	CHD2	chr1:223538089-223538289	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr1:223537333-223537528	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr1:223536406-223536658	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr1:223516650-223516654	GM12878	blood:	n/a	n/a
20	CREB1	chr1:223537234-223537736	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr1:223537176-223537594	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr1:223537772-223538667	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr1:223536947-223537533	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:223537405-223537613	K562	blood:	n/a	n/a
25	CTCF	chr1:223519185-223519406	MCF-7	breast:	n/a	chr1:223519277-223519295
26	CTCF	chr1:223537440-223537590	GM12871	blood:	n/a	n/a
27	CTCF	chr1:223532240-223532390	NHEK	skin:	n/a	n/a
28	CTCF	chr1:223532174-223532491	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:223537457-223537496	NHEK	skin:	n/a	n/a
30	CTCF	chr1:223506891-223507095	K562	blood:	n/a	n/a
31	CTCF	chr1:223532260-223532410	HEK293	kidney:	n/a	n/a
32	CTCF	chr1:223532240-223532390	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr1:223519200-223519350	HRPEpiC	eye:	n/a	chr1:223519277-223519295
34	CTCF	chr1:223532220-223532370	NHEK	skin:	n/a	n/a
35	CTCF	chr1:223532316-223532401	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:223519210-223519352	K562	blood:	n/a	chr1:223519277-223519295
37	CTCF	chr1:223519013-223519538	MCF-7	breast:	n/a	chr1:223519277-223519295
38	CTCF	chr1:223502700-223502850	AG09309	skin:	n/a	n/a
39	CTCF	chr1:223519208-223519409	H1-hESC	embryonic stem cell:	n/a	chr1:223519277-223519295
40	CTCF	chr1:223532320-223532470	RPTEC	kidney:	n/a	n/a
41	CTCF	chr1:223532240-223532390	HRE	kidney:	n/a	n/a
42	CTCF	chr1:223519225-223519366	NHEK	skin:	n/a	chr1:223519277-223519295
43	CTCF	chr1:223519260-223519410	GM12865	blood:	n/a	chr1:223519277-223519295
44	CTCF	chr1:223532200-223532350	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr1:223510860-223511010	HEK293	kidney:	n/a	n/a
46	CTCF	chr1:223537426-223537531	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr1:223529200-223529350	SAEC	small airway:	n/a	chr1:223529304-223529312
48	CTCF	chr1:223519200-223519350	A549	lung:	n/a	chr1:223519277-223519295
49	CTCF	chr1:223519300-223519450	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr1:223532335-223532384	A549	lung:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223537363-223537413	SKMC	muscle:	n/a
2	chr1:223534046-223534096	HRE	kidney:	n/a
3	chr1:223538957-223539007	NHDF-neo	bronchial:	n/a
4	chr1:223538957-223539007	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:223526402-223526452	GM19239	blood:	n/a
6	chr1:223537435-223537485	GM06990	blood:	n/a
7	chr1:223537363-223537413	HL-60	blood:	n/a
8	chr1:223537199-223537249	GM12878	blood:	n/a
9	chr1:223537199-223537249	PFSK-1	brain:	n/a
10	chr1:223536296-223536346	IMR90	lung:	fetal
11	chr1:223538623-223538673	HUVEC	blood vessel:	n/a
12	chr1:223538957-223539007	HEK293	kidney:	embryo
13	chr1:223538379-223538429	ECC-1	luminal epithelium:	n/a
14	chr1:223526402-223526452	HCPEpiC	choroid plexus:	n/a
15	chr1:223538601-223538651	HMEC	breast:	n/a
16	chr1:223538359-223538409	AG10803	skin:	n/a
17	chr1:223538601-223538651	BJ	skin:	n/a
18	chr1:223534046-223534096	ECC-1	luminal epithelium:	n/a
19	chr1:223536296-223536346	PANC-1	pancreas:	n/a
20	chr1:223537435-223537485	HRPEpiC	eye:	n/a
21	chr1:223538627-223538677	BJ	skin:	n/a
22	chr1:223538623-223538673	SAEC	small airway:	n/a
23	chr1:223538957-223539007	AG10803	skin:	n/a
24	chr1:223538623-223538673	ovcar-3	ovarian:	n/a
25	chr1:223538174-223538224	AG04449	skin:	fetal
26	chr1:223537435-223537485	PFSK-1	brain:	n/a
27	chr1:223534046-223534096	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:223536296-223536346	HCT-116	colon:	n/a
29	chr1:223537363-223537413	HRPEpiC	eye:	n/a
30	chr1:223538601-223538651	AG04449	skin:	fetal
31	chr1:223536296-223536346	HAEpiC	amniotic membrane:	n/a
32	chr1:223534046-223534096	HCM	heart:	n/a
33	chr1:223537199-223537249	HEK293	kidney:	embryo
34	chr1:223526402-223526452	PANC-1	pancreas:	n/a
35	chr1:223534046-223534096	PFSK-1	brain:	n/a
36	chr1:223538627-223538677	SKMC	muscle:	n/a
37	chr1:223538601-223538651	HUVEC	blood vessel:	n/a
38	chr1:223537363-223537413	HepG2	liver:	n/a
39	chr1:223537363-223537413	NHDF-neo	bronchial:	n/a
40	chr1:223537199-223537249	AG09319	gingival:	n/a
41	chr1:223537363-223537413	AG10803	skin:	n/a
42	chr1:223537199-223537249	BJ	skin:	n/a
43	chr1:223534046-223534096	PrEC	prostate:	n/a
44	chr1:223537435-223537485	BJ	skin:	n/a
45	chr1:223537199-223537249	HRCEpiC	kidney:	n/a
46	chr1:223538359-223538409	Hepatocyte	liver:	n/a
47	chr1:223538601-223538651	SK-N-SH	brain:	n/a
48	chr1:223537435-223537485	HCF	heart:	n/a
49	chr1:223538957-223539007	NT2-D1	testis:	n/a
50	chr1:223538174-223538224	PrEC	prostate:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:223527067..223530000-chr1:223534908..223536771,2	K562	blood:
2	chr1:223519202..223521587-chr1:223525632..223530010,3	MCF-7	breast:
3	chr1:223348150..223348802-chr1:223518891..223519605,2	MCF-7	breast:
4	chr1:223497612..223499362-chr1:223501611..223504069,2	MCF-7	breast:
5	chr1:223536301..223536801-chr22:50639192..50639860,2	HCT-116	colon:
6	chr1:223514593..223516719-chr1:223519953..223521559,2	K562	blood:
7	chr1:223348177..223349036-chr1:223518828..223519736,4	MCF-7	breast:
8	chr1:223534957..223537393-chr1:223566287..223567830,2	MCF-7	breast:
9	chr1:223496498..223499043-chr1:223513776..223516102,2	K562	blood:
10	chr1:223497129..223500114-chr1:223509294..223511393,2	K562	blood:
11	chr1:223380921..223383120-chr1:223521452..223523645,2	K562	blood:
12	chr1:223536038..223539069-chr1:223546089..223550790,4	MCF-7	breast:
13	chr1:223504054..223506980-chr1:223508583..223510799,2	K562	blood:
14	chr1:223497612..223499362-chr1:223501611..223504069,2	MCF-7	breast:
15	chr1:223530700..223533144-chr1:223535218..223537707,3	MCF-7	breast:
16	chr1:223505491..223507807-chr1:223513867..223516012,2	K562	blood:
17	chr1:223528933..223533041-chr1:223533611..223537910,6	MCF-7	breast:
18	chr1:223471938..223473458-chr1:223497150..223499757,2	K562	blood:
19	chr1:223316125..223316646-chr1:223531902..223532782,2	MCF-7	breast:
20	chr1:223496498..223499043-chr1:223513776..223516102,2	K562	blood:
21	chr1:223518091..223519665-chr1:223535911..223537575,2	MCF-7	breast:
22	chr1:223497129..223500114-chr1:223509294..223511393,2	K562	blood:
23	chr1:223508432..223510410-chr1:223512972..223514710,2	K562	blood:
24	chr1:223505491..223507807-chr1:223513867..223516012,2	K562	blood:
25	chr1:223510081..223513953-chr1:223514794..223517151,3	K562	blood:
26	chr1:223523045..223525039-chr1:223526417..223529119,2	K562	blood:
27	chr1:223519202..223521587-chr1:223525632..223530010,3	MCF-7	breast:
28	chr1:223503941..223506228-chr1:223511294..223513326,2	MCF-7	breast:
29	chr1:223503941..223506228-chr1:223511294..223513326,2	MCF-7	breast:
30	chr1:223314972..223318417-chr1:223500837..223503788,3	MCF-7	breast:
31	chr1:223514593..223516719-chr1:223519953..223521559,2	K562	blood:
32	chr1:223523045..223525039-chr1:223526417..223529119,2	K562	blood:
33	chr1:223510081..223513953-chr1:223514794..223517151,3	K562	blood:
34	chr1:223528181..223530000-chr1:223535151..223536771,2	K562	blood:
35	chr1:223502794..223505270-chr1:223535922..223537884,2	MCF-7	breast:
36	chr1:223531318..223534020-chr1:223565340..223568095,2	MCF-7	breast:
37	chr1:223504054..223506980-chr1:223508583..223510799,2	K562	blood:
38	chr1:223386672..223389352-chr1:223528747..223530917,2	MCF-7	breast:
39	chr1:223526043..223528249-chr1:223565401..223568259,2	K562	blood:
40	chr1:223508432..223510410-chr1:223512972..223514710,2	K562	blood:
41	chr1:223533339..223535356-chr1:223536427..223538674,2	MCF-7	breast:
42	chr1:223305860..223308306-chr1:223535536..223539484,5	MCF-7	breast:

No data

Variant related genes	Relation type
SUSD4	TF binding region
SUSD4	CpG island
ENSG00000143502	chromatin interactions
ENSG00000178395	chromatin interactions
ENSG00000236846	chromatin interactions
ENSG00000073169	chromatin interactions
ENSG00000251789	chromatin interactions
ENSG00000187554	chromatin interactions

Extended variants
information (count: 1379 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1379 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs825113	chr1:223498145-223498146	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146623728	chr1:223498222-223498223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77901468	chr1:223498252-223498253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
4	rs75616958	chr1:223498270-223498271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141429271	chr1:223498281-223498282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539230113	chr1:223498293-223498294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532795788	chr1:223498348-223498349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189934914	chr1:223498383-223498384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555784836	chr1:223498411-223498412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575708051	chr1:223498425-223498426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566339679	chr1:223498451-223498452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551260999	chr1:223498452-223498453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538379666	chr1:223498469-223498470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142482151	chr1:223498470-223498471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557898451	chr1:223498503-223498504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181980699	chr1:223498508-223498509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538412197	chr1:223498603-223498604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556912060	chr1:223498652-223498653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10495206	chr1:223498661-223498662	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs538660140	chr1:223498677-223498678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34909949	chr1:223498682-223498683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572341806	chr1:223498706-223498707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186364215	chr1:223498742-223498743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112970847	chr1:223498748-223498749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572886100	chr1:223498775-223498776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533698135	chr1:223498805-223498806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189202400	chr1:223498968-223498969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574316754	chr1:223498995-223498996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573524963	chr1:223499036-223499037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543041502	chr1:223499128-223499129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111677551	chr1:223499144-223499145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140565881	chr1:223499160-223499161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562898378	chr1:223499176-223499177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533302656	chr1:223499185-223499186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150107152	chr1:223499238-223499239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531825487	chr1:223499320-223499321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180879059	chr1:223499326-223499327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185773264	chr1:223499328-223499329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567334820	chr1:223499414-223499415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1856932	chr1:223499434-223499435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs116013909	chr1:223499452-223499453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571746438	chr1:223499456-223499457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539361413	chr1:223499463-223499464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191612597	chr1:223499490-223499491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566095192	chr1:223499527-223499528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370130985	chr1:223499543-223499544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565044295	chr1:223499567-223499568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374610944	chr1:223499650-223499651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182961903	chr1:223499774-223499775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554662247	chr1:223499785-223499786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:803 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223495200-223498400	Enhancers	Fetal Thymus	thymus
2	chr1:223495600-223498400	Enhancers	Primary T cells from cord blood	blood
3	chr1:223495600-223498400	Enhancers	Thymus	Thymus
4	chr1:223495800-223498200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr1:223496000-223498200	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr1:223496000-223498600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:223496200-223498200	Enhancers	Primary T cells fromperipheralblood	blood
8	chr1:223496200-223498200	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr1:223496400-223498200	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr1:223496400-223498200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:223496400-223498400	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr1:223497200-223504200	Weak transcription	Right Atrium	heart
13	chr1:223497200-223512600	Weak transcription	Pancreas	Pancrea
14	chr1:223497400-223510400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:223497600-223498400	Enhancers	Dnd41	blood
16	chr1:223497600-223504400	Weak transcription	Fetal Heart	heart
17	chr1:223497800-223498200	Enhancers	Primary hematopoietic stem cells	blood
18	chr1:223498200-223504600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr1:223498400-223504200	Weak transcription	Thymus	Thymus
20	chr1:223500800-223501400	Enhancers	Esophagus	oesophagus
21	chr1:223500800-223502200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:223500800-223502400	Enhancers	NHEK	skin
23	chr1:223500800-223502800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:223501000-223502400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:223501200-223502200	Enhancers	HMEC	breast
26	chr1:223501400-223501800	Weak transcription	Esophagus	oesophagus
27	chr1:223501400-223506400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr1:223501800-223503000	Enhancers	Esophagus	oesophagus
29	chr1:223502000-223502200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:223502200-223504000	Weak transcription	HMEC	breast
31	chr1:223502200-223505000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:223502400-223504400	Weak transcription	NHEK	skin
33	chr1:223502400-223504800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:223502800-223503000	Enhancers	Aorta	Aorta
35	chr1:223502800-223504600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:223503000-223503600	Enhancers	Fetal Kidney	kidney
37	chr1:223503000-223504000	Weak transcription	Aorta	Aorta
38	chr1:223503000-223505600	Enhancers	Ovary	ovary
39	chr1:223503000-223506000	Weak transcription	Esophagus	oesophagus
40	chr1:223503600-223504000	Weak transcription	Fetal Kidney	kidney
41	chr1:223503800-223505800	Enhancers	Fetal Lung	lung
42	chr1:223504000-223504200	Enhancers	Fetal Kidney	kidney
43	chr1:223504000-223504400	Enhancers	Brain Anterior Caudate	brain
44	chr1:223504000-223504400	Enhancers	Brain Cingulate Gyrus	brain
45	chr1:223504000-223505400	Enhancers	Aorta	Aorta
46	chr1:223504000-223506000	Enhancers	HMEC	breast
47	chr1:223504200-223504400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:223504200-223505000	Enhancers	Thymus	Thymus
49	chr1:223504200-223505200	Weak transcription	Fetal Kidney	kidney
50	chr1:223504200-223505600	Enhancers	Primary T cells from cord blood	blood

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