Variant report

Variant	esv1824383
Chromosome Location	chr1:174764839-174801748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:568)
CpG islands
(count:183)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174781657-174782212	HepG2	liver:	n/a	n/a
2	ATF1	chr1:174769981-174770160	K562	blood:	n/a	n/a
3	ATF1	chr1:174784312-174784545	K562	blood:	n/a	n/a
4	ATF1	chr1:174768688-174769078	K562	blood:	n/a	n/a
5	ATF2	chr1:174784425-174785216	GM12878	blood:	n/a	n/a
6	ATF2	chr1:174787293-174787853	GM12878	blood:	n/a	n/a
7	ATF2	chr1:174768485-174769398	GM12878	blood:	n/a	n/a
8	ATF2	chr1:174784116-174785183	GM12878	blood:	n/a	n/a
9	ATF2	chr1:174768311-174769484	GM12878	blood:	n/a	n/a
10	ATF2	chr1:174768580-174769355	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr1:174768663-174769294	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr1:174784258-174784445	K562	blood:	n/a	n/a
13	BATF	chr1:174784888-174785146	GM12878	blood:	n/a	chr1:174785020-174785029
14	BATF	chr1:174784177-174784536	GM12878	blood:	n/a	chr1:174784373-174784384 chr1:174784370-174784380
15	BATF	chr1:174779065-174779350	GM12878	blood:	n/a	n/a
16	BATF	chr1:174784538-174784849	GM12878	blood:	n/a	n/a
17	BATF	chr1:174787405-174787726	GM12878	blood:	n/a	n/a
18	BATF	chr1:174768674-174769257	GM12878	blood:	n/a	n/a
19	BATF	chr1:174778991-174779324	GM12878	blood:	n/a	n/a
20	BATF	chr1:174787335-174787763	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:174784263-174785084	GM12878	blood:	n/a	chr1:174784718-174784727
22	BCL11A	chr1:174784199-174784485	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:174784573-174784806	GM12878	blood:	n/a	chr1:174784718-174784727
24	BCL11A	chr1:174768669-174769271	GM12878	blood:	n/a	chr1:174769257-174769266
25	BCL3	chr1:174784538-174784967	GM12878	blood:	n/a	chr1:174784718-174784727
26	BCLAF1	chr1:174784450-174784986	GM12878	blood:	n/a	chr1:174784718-174784727
27	BCLAF1	chr1:174768460-174769315	GM12878	blood:	n/a	chr1:174769257-174769266 chr1:174769263-174769272
28	BCLAF1	chr1:174768356-174769647	GM12878	blood:	n/a	chr1:174769257-174769266 chr1:174769263-174769272
29	BHLHE40	chr1:174784248-174784424	K562	blood:	n/a	n/a
30	BHLHE40	chr1:174784377-174784923	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:174768941-174769116	K562	blood:	n/a	n/a
32	BHLHE40	chr1:174768617-174769344	GM12878	blood:	n/a	n/a
33	BRCA1	chr1:174768581-174768679	GM12878	blood:	n/a	n/a
34	BRCA1	chr1:174792885-174792920	HepG2	liver:	n/a	n/a
35	CBX3	chr1:174783974-174784695	HCT-116	colon:	n/a	n/a
36	CBX3	chr1:174783976-174784598	HCT-116	colon:	n/a	n/a
37	CEBPB	chr1:174784001-174784717	HCT-116	colon:	n/a	n/a
38	CEBPB	chr1:174787360-174787707	K562	blood:	n/a	chr1:174787536-174787547
39	CEBPB	chr1:174768245-174768597	A549	lung:	n/a	chr1:174768414-174768427
40	CEBPB	chr1:174768356-174769457	GM12878	blood:	n/a	chr1:174768414-174768427
41	CEBPB	chr1:174796899-174797136	HepG2	liver:	n/a	chr1:174797066-174797077 chr1:174797043-174797054 chr1:174797043-174797056 chr1:174797044-174797055
42	CEBPB	chr1:174792805-174792942	A549	lung:	n/a	n/a
43	CEBPB	chr1:174787283-174787890	GM12878	blood:	n/a	chr1:174787536-174787547
44	CEBPB	chr1:174787413-174787673	Hela-S3	cervix:	n/a	chr1:174787536-174787547
45	CEBPB	chr1:174797016-174797075	K562	blood:	n/a	chr1:174797043-174797054 chr1:174797043-174797056 chr1:174797044-174797055
46	CEBPB	chr1:174787364-174787721	HepG2	liver:	n/a	chr1:174787536-174787547
47	CEBPB	chr1:174777402-174777669	HepG2	liver:	n/a	chr1:174777542-174777553
48	CEBPB	chr1:174768253-174769171	IMR90	lung:	n/a	chr1:174768414-174768427
49	CEBPB	chr1:174768512-174769088	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr1:174787365-174787713	H1-hESC	embryonic stem cell:	n/a	chr1:174787536-174787547

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174769548-174769598	HUVEC	blood vessel:	n/a
2	chr1:174787829-174787879	HCPEpiC	choroid plexus:	n/a
3	chr1:174787829-174787879	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:174769548-174769598	HCF	heart:	n/a
5	chr1:174787829-174787879	HRCEpiC	kidney:	n/a
6	chr1:174769548-174769598	AG10803	skin:	n/a
7	chr1:174769548-174769598	NH-A	brain:	n/a
8	chr1:174779911-174779961	SK-N-SH	brain:	n/a
9	chr1:174779911-174779961	HIPEpiC	eye:	n/a
10	chr1:174779911-174779961	HCT-116	colon:	n/a
11	chr1:174787829-174787879	ovcar-3	ovarian:	n/a
12	chr1:174769548-174769598	GM19239	blood:	n/a
13	chr1:174787829-174787879	SK-N-SH_RA	brain:	n/a
14	chr1:174779911-174779961	Hepatocyte	liver:	n/a
15	chr1:174779911-174779961	HCF	heart:	n/a
16	chr1:174769548-174769598	IMR90	lung:	fetal
17	chr1:174787829-174787879	LNCaP	prostate:	n/a
18	chr1:174769548-174769598	HEEpiC	esophagus:	n/a
19	chr1:174787829-174787879	HAEpiC	amniotic membrane:	n/a
20	chr1:174787829-174787879	HEK293	kidney:	embryo
21	chr1:174787829-174787879	HCM	heart:	n/a
22	chr1:174769548-174769598	A549	lung:	n/a
23	chr1:174779911-174779961	SK-N-SH_RA	brain:	n/a
24	chr1:174769548-174769598	PANC-1	pancreas:	n/a
25	chr1:174779911-174779961	IMR90	lung:	fetal
26	chr1:174779911-174779961	BE2_C	brain:	n/a
27	chr1:174769548-174769598	T-47D	breast:	n/a
28	chr1:174779911-174779961	HCM	heart:	n/a
29	chr1:174779911-174779961	PrEC	prostate:	n/a
30	chr1:174779911-174779961	GM12891	blood:	n/a
31	chr1:174787829-174787879	NT2-D1	testis:	n/a
32	chr1:174769548-174769598	NHBE	bronchial:	n/a
33	chr1:174779911-174779961	U87	brain:	n/a
34	chr1:174769548-174769598	ProgFib	skin:	n/a
35	chr1:174769548-174769598	K562	blood:	n/a
36	chr1:174787829-174787879	HIPEpiC	eye:	n/a
37	chr1:174779911-174779961	HEK293	kidney:	embryo
38	chr1:174769548-174769598	HCT-116	colon:	n/a
39	chr1:174769548-174769598	Hela-S3	cervix:	n/a
40	chr1:174769548-174769598	MCF10A-Er-Src	breast:	n/a
41	chr1:174769548-174769598	U87	brain:	n/a
42	chr1:174787829-174787879	HEEpiC	esophagus:	n/a
43	chr1:174779911-174779961	LNCaP	prostate:	n/a
44	chr1:174787829-174787879	AG04450	lung:	fetal
45	chr1:174779911-174779961	HL-60	blood:	n/a
46	chr1:174787829-174787879	MCF-7	breast:	n/a
47	chr1:174779911-174779961	Jurkat	blood:	n/a
48	chr1:174769548-174769598	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:174779911-174779961	ECC-1	luminal epithelium:	n/a
50	chr1:174779911-174779961	SK-N-MC	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:174729839..174732288-chr1:174778725..174780565,2	K562	blood:
2	chr1:174775809..174777668-chr1:174781118..174782806,2	K562	blood:
3	chr1:174768282..174770482-chr1:174964486..174966155,2	MCF-7	breast:
4	chr1:174779274..174782139-chr1:174966617..174968862,2	MCF-7	breast:
5	chr1:174769617..174771382-chr1:174773976..174776245,2	K562	blood:
6	chr1:174787877..174789729-chr1:174792923..174795229,2	K562	blood:
7	chr1:174787877..174789729-chr1:174792923..174795229,2	K562	blood:
8	chr1:174790148..174791754-chr1:174795715..174797239,2	K562	blood:
9	chr1:174772425..174774399-chr1:174777517..174779217,2	MCF-7	breast:
10	chr1:174798481..174800550-chr1:174807771..174810609,2	MCF-7	breast:
11	chr1:174780388..174782499-chr1:174789949..174791564,2	MCF-7	breast:
12	chr1:174787124..174790078-chr1:174796659..174798420,2	K562	blood:
13	chr1:174765067..174766755-chr1:174768476..174771205,2	MCF-7	breast:
14	chr1:174790254..174793205-chr1:174795715..174797901,2	K562	blood:
15	chr1:174760005..174762413-chr1:174764252..174765776,2	K562	blood:
16	chr1:174772425..174774399-chr1:174777517..174779217,2	MCF-7	breast:
17	chr1:174780388..174782499-chr1:174789949..174791564,2	MCF-7	breast:
18	chr1:174769617..174771382-chr1:174773976..174776245,2	K562	blood:
19	chr1:174787266..174788950-chr1:174846455..174848064,2	K562	blood:
20	chr1:174766907..174768674-chr1:174967181..174969614,2	K562	blood:
21	chr1:174793359..174795191-chr1:174840553..174843195,2	MCF-7	breast:
22	chr1:174763378..174766267-chr1:174992763..174994276,2	MCF-7	breast:
23	chr1:174787124..174790078-chr1:174796659..174798420,2	K562	blood:
24	chr1:174775809..174777668-chr1:174781118..174782806,2	K562	blood:
25	chr1:174790254..174793205-chr1:174795715..174797901,2	K562	blood:
26	chr1:174780849..174783447-chr1:174946547..174949179,2	K562	blood:
27	chr1:174132422..174134111-chr1:174800626..174802567,2	K562	blood:
28	chr1:174761076..174764017-chr1:174764212..174765845,2	MCF-7	breast:
29	chr1:174790148..174791754-chr1:174795715..174797239,2	K562	blood:
30	chr1:174784763..174785588-chr2:221356052..221356647,2	MCF-7	breast:

No data

Variant related genes	Relation type
RABGAP1L	TF binding region
RABGAP1L	CpG island
ENSG00000152061	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000252552	chromatin interactions

Extended variants
information (count: 1214 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1214 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1126207	chr1:174764839-174764840	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375617390	chr1:174764870-174764871	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs568977228	chr1:174764872-174764873	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs367858500	chr1:174764891-174764892	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs538071099	chr1:174765024-174765025	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs551567058	chr1:174765082-174765083	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs571444759	chr1:174765152-174765153	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs138386588	chr1:174765162-174765163	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142964396	chr1:174765166-174765167	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs79127598	chr1:174765247-174765248	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs536566698	chr1:174765256-174765257	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs146138836	chr1:174765263-174765264	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs531137768	chr1:174765273-174765274	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs576539460	chr1:174765316-174765317	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs545618333	chr1:174765344-174765345	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs564015949	chr1:174765367-174765368	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577814977	chr1:174765428-174765429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs1793320	chr1:174765446-174765447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs185108677	chr1:174765453-174765454	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs77298890	chr1:174765482-174765483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542533720	chr1:174765497-174765498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs76607799	chr1:174765514-174765515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554499559	chr1:174765584-174765585	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531393487	chr1:174765606-174765607	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190789541	chr1:174765630-174765631	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs374111614	chr1:174765723-174765724	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571363254	chr1:174765743-174765744	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527793247	chr1:174765773-174765774	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547354535	chr1:174765774-174765775	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs78869093	chr1:174765823-174765824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs368730381	chr1:174765844-174765845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536679713	chr1:174765859-174765860	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556565705	chr1:174765913-174765914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs570368792	chr1:174765918-174765919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538855102	chr1:174765947-174765948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112716795	chr1:174766002-174766003	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78583223	chr1:174766014-174766015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553936234	chr1:174766017-174766018	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368230430	chr1:174766101-174766102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553433549	chr1:174766131-174766132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs11339856	chr1:174766145-174766146	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs397981992	chr1:174766156-174766157	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566822891	chr1:174766193-174766194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562634092	chr1:174766212-174766213	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538839470	chr1:174766217-174766218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544838722	chr1:174766237-174766238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1754366	chr1:174766252-174766253	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs61828087	chr1:174766269-174766270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs376812711	chr1:174766341-174766342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs527753337	chr1:174766385-174766386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
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
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174747000-174768400	Weak transcription	Primary B cells from cord blood	blood
2	chr1:174758200-174768400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:174758800-174768000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:174758800-174768200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr1:174759400-174768000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr1:174759400-174768400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:174759400-174768400	Weak transcription	Osteobl	bone
8	chr1:174760000-174768400	Weak transcription	HSMMtube	muscle
9	chr1:174761000-174768200	Weak transcription	GM12878-XiMat	blood
10	chr1:174761200-174768000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr1:174761400-174766600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr1:174761400-174768200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:174761400-174768200	Weak transcription	HSMM	muscle
14	chr1:174761400-174768400	Weak transcription	Right Atrium	heart
15	chr1:174761800-174768200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:174762000-174766400	Weak transcription	K562	blood
17	chr1:174762000-174768400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:174762800-174768400	Weak transcription	Right Ventricle	heart
19	chr1:174763600-174765200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:174764000-174765000	Enhancers	Fetal Intestine Large	intestine
21	chr1:174764000-174765200	Enhancers	Fetal Intestine Small	intestine
22	chr1:174764000-174765400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:174764000-174765400	Enhancers	NHEK	skin
24	chr1:174764200-174765000	Enhancers	Duodenum Mucosa	Duodenum
25	chr1:174764200-174765200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:174764200-174765200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:174764200-174765200	Enhancers	HMEC	breast
28	chr1:174764600-174765000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:174764600-174765400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:174764800-174766400	Weak transcription	Small Intestine	intestine
31	chr1:174764800-174768200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr1:174765000-174765800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:174765000-174768200	Weak transcription	Fetal Intestine Large	intestine
34	chr1:174765000-174768400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr1:174765000-174768800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr1:174765200-174765400	Flanking Active TSS	NH-A	brain
37	chr1:174765200-174768200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr1:174765200-174768400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:174765200-174768400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:174765200-174768400	Weak transcription	Fetal Intestine Small	intestine
41	chr1:174765200-174768400	Weak transcription	HMEC	breast
42	chr1:174765400-174765600	Enhancers	NH-A	brain
43	chr1:174765400-174765800	Enhancers	A549	lung
44	chr1:174765400-174768000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:174765400-174768000	Weak transcription	NHEK	skin
46	chr1:174765400-174768400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:174765600-174765800	Bivalent Enhancer	NH-A	brain
48	chr1:174765800-174767000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:174765800-174768400	Weak transcription	A549	lung
50	chr1:174766400-174766800	Enhancers	K562	blood

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