Variant report

Variant	esv3453087
Chromosome Location	chr1:155186728-155191926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:155188710-155188996	K562	blood:	n/a	n/a
2	ATF3	chr1:155188686-155188991	GM12878	blood:	n/a	chr1:155188822-155188831 chr1:155188842-155188851
3	ATF3	chr1:155189353-155189656	H1-hESC	embryonic stem cell:	n/a	chr1:155189481-155189490
4	ATF3	chr1:155189276-155189599	K562	blood:	n/a	chr1:155189481-155189490
5	ATF3	chr1:155188647-155189041	H1-hESC	embryonic stem cell:	n/a	chr1:155188822-155188831 chr1:155188842-155188851
6	ATF3	chr1:155189316-155189697	GM12878	blood:	n/a	chr1:155189481-155189490
7	ATF3	chr1:155188661-155188974	H1-hESC	embryonic stem cell:	n/a	chr1:155188822-155188831 chr1:155188842-155188851
8	ATF3	chr1:155188700-155189110	HepG2	liver:	n/a	chr1:155188822-155188831 chr1:155188842-155188851
9	ATF3	chr1:155188657-155188922	HepG2	liver:	n/a	chr1:155188822-155188831 chr1:155188842-155188851
10	ATF3	chr1:155188638-155189090	GM12878	blood:	n/a	chr1:155188822-155188831 chr1:155188842-155188851
11	ATF3	chr1:155189186-155189737	H1-hESC	embryonic stem cell:	n/a	chr1:155189481-155189490
12	ATF3	chr1:155189415-155189608	GM12878	blood:	n/a	chr1:155189481-155189490
13	ATF3	chr1:155188671-155188931	K562	blood:	n/a	chr1:155188822-155188831 chr1:155188842-155188851
14	BHLHE40	chr1:155189313-155189626	K562	blood:	n/a	n/a
15	BHLHE40	chr1:155188705-155188957	K562	blood:	n/a	chr1:155188816-155188837
16	CBX3	chr1:155188581-155189108	K562	blood:	n/a	n/a
17	CEBPB	chr1:155188739-155189534	IMR90	lung:	n/a	chr1:155189137-155189148
18	CEBPB	chr1:155188676-155190182	Hela-S3	cervix:	n/a	chr1:155189137-155189148
19	CEBPB	chr1:155189997-155190081	A549	lung:	n/a	n/a
20	CEBPB	chr1:155188822-155189250	HepG2	liver:	n/a	chr1:155189137-155189148
21	CEBPB	chr1:155188711-155189263	ECC-1	luminal epithelium:	n/a	chr1:155189137-155189148
22	CEBPB	chr1:155188701-155189193	H1-hESC	embryonic stem cell:	n/a	chr1:155189137-155189148
23	CEBPB	chr1:155190034-155190118	K562	blood:	n/a	n/a
24	CEBPB	chr1:155188777-155189230	A549	lung:	n/a	chr1:155189137-155189148
25	CEBPB	chr1:155188725-155189757	K562	blood:	n/a	chr1:155189137-155189148
26	CHD2	chr1:155188825-155188857	K562	blood:	n/a	n/a
27	CHD2	chr1:155187724-155187831	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr1:155189354-155189684	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr1:155187680-155187830	Hela-S3	cervix:	n/a	n/a
30	CUX1	chr1:155189238-155189361	GM12878	blood:	n/a	n/a
31	EGR1	chr1:155188645-155189141	HCT-116	colon:	n/a	chr1:155188852-155188861
32	EGR1	chr1:155188761-155189058	ECC-1	luminal epithelium:	n/a	chr1:155188852-155188861
33	EGR1	chr1:155189290-155189764	ECC-1	luminal epithelium:	n/a	n/a
34	EGR1	chr1:155188662-155189856	HCT-116	colon:	n/a	chr1:155188852-155188861
35	ELF1	chr1:155188561-155189155	MCF-7	breast:	n/a	chr1:155188848-155188861
36	ELF1	chr1:155188624-155189219	SK-N-SH	brain:	n/a	chr1:155188848-155188861
37	ELF1	chr1:155188652-155189041	K562	blood:	n/a	chr1:155188848-155188861
38	ELF1	chr1:155189375-155189869	K562	blood:	n/a	n/a
39	ELF1	chr1:155188696-155189030	HepG2	liver:	n/a	chr1:155188848-155188861
40	ELF1	chr1:155188639-155189213	HCT-116	colon:	n/a	chr1:155188848-155188861
41	ELF1	chr1:155188642-155189060	A549	lung:	n/a	chr1:155188848-155188861
42	ELF1	chr1:155188740-155189038	SK-N-SH	brain:	n/a	chr1:155188848-155188861
43	ELF1	chr1:155188595-155189839	HCT-116	colon:	n/a	chr1:155188848-155188861
44	ELF1	chr1:155188682-155189113	GM12878	blood:	n/a	chr1:155188848-155188861
45	ELF1	chr1:155188634-155188971	A549	lung:	n/a	chr1:155188848-155188861
46	ELF1	chr1:155188693-155189087	MCF-7	breast:	n/a	chr1:155188848-155188861
47	ELF1	chr1:155188669-155188986	HepG2	liver:	n/a	chr1:155188848-155188861
48	ELK1	chr1:155188711-155189677	Hela-S3	cervix:	n/a	n/a
49	ELK1	chr1:155187539-155187797	Hela-S3	cervix:	n/a	n/a
50	ELK1	chr1:155188788-155189081	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155188904-155188954	SK-N-SH	brain:	n/a
2	chr1:155188904-155188954	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:155188904-155188954	AG04449	skin:	fetal
4	chr1:155189053-155189103	Caco-2	colon:	n/a
5	chr1:155189053-155189103	SKMC	muscle:	n/a
6	chr1:155189053-155189103	HRPEpiC	eye:	n/a
7	chr1:155188904-155188954	HAEpiC	amniotic membrane:	n/a
8	chr1:155189053-155189103	HEEpiC	esophagus:	n/a
9	chr1:155189053-155189103	LNCaP	prostate:	n/a
10	chr1:155189053-155189103	MCF-7	breast:	n/a
11	chr1:155188904-155188954	BJ	skin:	n/a
12	chr1:155188904-155188954	ECC-1	luminal epithelium:	n/a
13	chr1:155189053-155189103	PANC-1	pancreas:	n/a
14	chr1:155189053-155189103	ECC-1	luminal epithelium:	n/a
15	chr1:155189053-155189103	GM12878	blood:	n/a
16	chr1:155189053-155189103	AG10803	skin:	n/a
17	chr1:155188904-155188954	HUVEC	blood vessel:	n/a
18	chr1:155188904-155188954	HEK293	kidney:	embryo
19	chr1:155188904-155188954	H1-hESC	embryonic stem cell:	embryo
20	chr1:155189053-155189103	NHDF-neo	bronchial:	n/a
21	chr1:155188904-155188954	HCT-116	colon:	n/a
22	chr1:155189053-155189103	U87	brain:	n/a
23	chr1:155188904-155188954	AG09309	skin:	n/a
24	chr1:155188904-155188954	AG10803	skin:	n/a
25	chr1:155188904-155188954	HL-60	blood:	n/a
26	chr1:155188904-155188954	SKMC	muscle:	n/a
27	chr1:155189053-155189103	HMEC	breast:	n/a
28	chr1:155188904-155188954	K562	blood:	n/a
29	chr1:155189053-155189103	MCF10A-Er-Src	breast:	n/a
30	chr1:155188904-155188954	HEEpiC	esophagus:	n/a
31	chr1:155188904-155188954	Hepatocyte	liver:	n/a
32	chr1:155189053-155189103	Hepatocyte	liver:	n/a
33	chr1:155188904-155188954	NB4	blood:	n/a
34	chr1:155189053-155189103	ovcar-3	ovarian:	n/a
35	chr1:155189053-155189103	CMK	blood:	n/a
36	chr1:155188904-155188954	HCPEpiC	choroid plexus:	n/a
37	chr1:155188904-155188954	ProgFib	skin:	n/a
38	chr1:155188904-155188954	GM06990	blood:	n/a
39	chr1:155189053-155189103	NT2-D1	testis:	n/a
40	chr1:155188904-155188954	CMK	blood:	n/a
41	chr1:155189053-155189103	HL-60	blood:	n/a
42	chr1:155189053-155189103	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:155188904-155188954	IMR90	lung:	fetal
44	chr1:155189053-155189103	GM06990	blood:	n/a
45	chr1:155189053-155189103	SAEC	small airway:	n/a
46	chr1:155188904-155188954	A549	lung:	n/a
47	chr1:155188904-155188954	AoSMC	blood vessel:	n/a
48	chr1:155189053-155189103	AoSMC	blood vessel:	n/a
49	chr1:155189053-155189103	SK-N-SH	brain:	n/a
50	chr1:155189053-155189103	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:155155866..155157645-chr1:155191595..155193213,2	MCF-7	breast:
2	chr1:155189654..155191436-chr1:155193964..155195496,2	K562	blood:
3	chr1:155187157..155191331-chr1:155209670..155212928,5	MCF-7	breast:
4	chr1:155186661..155189522-chr1:155194169..155197986,6	K562	blood:
5	chr1:155187302..155192095-chr1:155195846..155198767,7	MCF-7	breast:
6	chr1:155187581..155189617-chr1:155195998..155199387,4	MCF-7	breast:
7	chr1:155170199..155172108-chr1:155187853..155191276,3	MCF-7	breast:
8	chr1:155190873..155193241-chr1:155231143..155233279,2	MCF-7	breast:
9	chr1:155174605..155182734-chr1:155187211..155200915,43	MCF-7	breast:
10	chr1:155143901..155153030-chr1:155191166..155199183,23	MCF-7	breast:
11	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
12	chr1:155169679..155172666-chr1:155186873..155189391,3	MCF-7	breast:
13	chr1:155188805..155190957-chr1:155195706..155197646,3	K562	blood:
14	chr1:155191881..155194028-chr1:155195597..155197149,2	MCF-7	breast:
15	chr1:155175739..155181576-chr1:155185947..155190429,10	K562	blood:
16	chr1:155162028..155164533-chr1:155190701..155192344,2	MCF-7	breast:
17	chr1:155186477..155191173-chr1:155191711..155194571,4	MCF-7	breast:
18	chr1:155175944..155179285-chr1:155187472..155192193,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000236263	TF binding region
GBAP1	TF binding region
ENSG00000236263	CpG island
GBAP1	CpG island
ENSG00000163462	chromatin interactions
ENSG00000231064	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000185499	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000271748	chromatin interactions

Extended variants
information (count: 178 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:178 , 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	rs28445596	chr1:155186729-155186730	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs1057941	chr1:155186742-155186743	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs534945574	chr1:155186858-155186859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs576110621	chr1:155187123-155187124	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs1135668	chr1:155187144-155187145	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs543492157	chr1:155187159-155187160	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs562109299	chr1:155187191-155187192	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs529224941	chr1:155187197-155187198	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs548079483	chr1:155187246-155187247	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs560059210	chr1:155187273-155187274	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs189023460	chr1:155187274-155187275	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs551989029	chr1:155187286-155187287	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs576819611	chr1:155187347-155187348	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs545472020	chr1:155187371-155187372	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs150329785	chr1:155187391-155187392	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs562636829	chr1:155187395-155187396	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs138010627	chr1:155187409-155187410	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs376060298	chr1:155187537-155187538	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs568059848	chr1:155187572-155187573	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs535074369	chr1:155187608-155187609	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs554053793	chr1:155187659-155187660	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs59692280	chr1:155187668-155187669	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539284747	chr1:155187693-155187694	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs557522717	chr1:155187700-155187701	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs576176716	chr1:155187725-155187726	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs543902046	chr1:155187729-155187730	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs185115702	chr1:155187761-155187762	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs149513274	chr1:155187786-155187787	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs574001024	chr1:155187828-155187829	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs371567185	chr1:155187904-155187905	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs374514520	chr1:155187908-155187909	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs533656290	chr1:155187936-155187937	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs545662566	chr1:155187943-155187944	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs143182104	chr1:155187996-155187997	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs530965155	chr1:155188023-155188024	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs138784147	chr1:155188130-155188131	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs199800595	chr1:155188229-155188230	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs200883877	chr1:155188248-155188249	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs187070337	chr1:155188251-155188252	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs191564448	chr1:155188253-155188254	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs561829143	chr1:155188295-155188296	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs527591421	chr1:155188332-155188333	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs569524824	chr1:155188338-155188339	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs536811869	chr1:155188368-155188369	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs377388148	chr1:155188403-155188404	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs547662657	chr1:155188406-155188407	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs574033545	chr1:155188501-155188502	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs3115531	chr1:155188508-155188509	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs541454242	chr1:155188562-155188563	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs553399443	chr1:155188575-155188576	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155179600-155188200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr1:155179600-155189000	Weak transcription	Stomach Mucosa	stomach
3	chr1:155179600-155189200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:155179600-155189200	Weak transcription	Colonic Mucosa	Colon
5	chr1:155179600-155189200	Weak transcription	Psoas Muscle	Psoas
6	chr1:155179600-155195400	Weak transcription	Aorta	Aorta
7	chr1:155179600-155195800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:155179600-155196200	Weak transcription	Pancreas	Pancrea
9	chr1:155179600-155196600	Weak transcription	Gastric	stomach
10	chr1:155179600-155196600	Weak transcription	Small Intestine	intestine
11	chr1:155179800-155188600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr1:155179800-155188600	Weak transcription	Brain Angular Gyrus	brain
13	chr1:155179800-155188800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:155179800-155188800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr1:155179800-155188800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr1:155179800-155189000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:155179800-155193800	Weak transcription	HSMMtube	muscle
18	chr1:155180000-155188600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:155180000-155188600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr1:155180000-155188600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr1:155180000-155188600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr1:155180000-155188800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:155180000-155188800	Weak transcription	Primary B cells from peripheral blood	blood
24	chr1:155180000-155189200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr1:155180000-155194000	Weak transcription	HUVEC	blood vessel
26	chr1:155180000-155195600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr1:155180200-155188200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:155180200-155188600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr1:155180200-155188600	Weak transcription	Fetal Kidney	kidney
30	chr1:155180200-155188600	Weak transcription	NHDF-Ad	bronchial
31	chr1:155180200-155188800	Weak transcription	NH-A	brain
32	chr1:155180200-155194000	Weak transcription	HSMM	muscle
33	chr1:155180600-155188600	Weak transcription	Hela-S3	cervix
34	chr1:155180600-155189000	Weak transcription	GM12878-XiMat	blood
35	chr1:155180600-155189600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr1:155180600-155195600	Weak transcription	HepG2	liver
37	chr1:155180800-155188600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:155180800-155188600	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr1:155180800-155188600	Weak transcription	K562	blood
40	chr1:155180800-155189000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:155181000-155189000	Weak transcription	Fetal Lung	lung
42	chr1:155182200-155187800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:155182200-155188600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr1:155182200-155188800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr1:155182200-155189200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:155182200-155195800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr1:155182200-155196400	Weak transcription	Esophagus	oesophagus
48	chr1:155182200-155196600	Weak transcription	Lung	lung
49	chr1:155182400-155188600	Weak transcription	Liver	Liver
50	chr1:155182400-155188800	Weak transcription	Ovary	ovary

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