Variant report

Variant	esv3376697
Chromosome Location	chr18:7565777-7568525
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:507)
CpG islands
(count:732)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7567159-7567359	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7567223-7567257	K562	blood:	n/a	n/a
3	ATF3	chr18:7567156-7567368	K562	blood:	n/a	chr18:7567347-7567356 chr18:7567273-7567283
4	BACH1	chr18:7566548-7566660	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr18:7566904-7567617	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr18:7566784-7567400	HepG2	liver:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
7	BHLHE40	chr18:7566522-7567366	K562	blood:	n/a	chr18:7567340-7567356 chr18:7566691-7566707 chr18:7567117-7567133
8	BHLHE40	chr18:7567045-7567395	GM12878	blood:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
9	BRCA1	chr18:7566113-7566632	Hela-S3	cervix:	n/a	n/a
10	CCNT2	chr18:7566537-7567551	K562	blood:	n/a	n/a
11	CHD1	chr18:7568086-7568380	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chr18:7566627-7566933	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr18:7565958-7569508	IMR90	lung:	n/a	chr18:7567084-7567094
14	CHD1	chr18:7567168-7567252	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr18:7568188-7568727	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr18:7567294-7567335	HepG2	liver:	n/a	n/a
17	CHD2	chr18:7566988-7567580	Hela-S3	cervix:	n/a	chr18:7567084-7567094
18	CHD2	chr18:7566856-7567052	HepG2	liver:	n/a	n/a
19	CHD2	chr18:7566721-7566935	K562	blood:	n/a	n/a
20	CREB1	chr18:7566544-7566952	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr18:7567001-7567445	K562	blood:	n/a	n/a
22	CREB1	chr18:7567120-7567445	A549	lung:	n/a	n/a
23	CREB1	chr18:7566663-7567589	A549	lung:	n/a	n/a
24	CREB1	chr18:7566645-7567541	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr18:7567887-7568154	A549	lung:	n/a	n/a
26	CREB1	chr18:7567063-7567481	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr18:7566858-7567601	HepG2	liver:	n/a	n/a
28	CTBP2	chr18:7566540-7567821	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTBP2	chr18:7568128-7568834	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr18:7567200-7567350	HMEC	breast:	n/a	n/a
31	CTCF	chr18:7568480-7568630	WI-38	lung:	n/a	n/a
32	CTCF	chr18:7566700-7566850	SK-N-SH_RA	brain:	n/a	chr18:7566742-7566758
33	CTCF	chr18:7567079-7567472	A549	lung:	n/a	n/a
34	CTCF	chr18:7567140-7567290	HPF	lung:	n/a	n/a
35	CTCF	chr18:7568520-7568670	SAEC	small airway:	n/a	n/a
36	CTCF	chr18:7567220-7567370	AG10803	skin:	n/a	n/a
37	CTCF	chr18:7566700-7566850	HCPEpiC	choroid plexus:	n/a	chr18:7566742-7566758
38	CTCF	chr18:7568200-7568350	AG04449	skin:	n/a	n/a
39	CTCF	chr18:7567180-7567330	AG04450	lung:	n/a	n/a
40	CTCF	chr18:7567220-7567370	NHEK	skin:	n/a	n/a
41	CTCF	chr18:7568184-7568447	HepG2	liver:	n/a	n/a
42	CTCF	chr18:7567200-7567350	HEK293	kidney:	n/a	n/a
43	CTCF	chr18:7568480-7568630	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr18:7567099-7567407	Fibrobl	skin:	n/a	n/a
45	CTCF	chr18:7566736-7566973	Fibrobl	skin:	n/a	chr18:7566742-7566758
46	CTCF	chr18:7566680-7566830	HPAF	blood vessel:	n/a	chr18:7566742-7566758
47	CTCF	chr18:7568200-7568350	HMEC	breast:	n/a	n/a
48	CTCF	chr18:7567180-7567330	AG09319	gingival:	n/a	n/a
49	CTCF	chr18:7567159-7567379	Lung_OC	lung:	n/a	n/a
50	CTCF	chr18:7566633-7566806	HepG2	liver:	n/a	chr18:7566742-7566758

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7567799-7567849	SKMC	muscle:	n/a
2	chr18:7566656-7566706	NHDF-neo	bronchial:	n/a
3	chr18:7566558-7566608	HRCEpiC	kidney:	n/a
4	chr18:7567548-7567598	PANC-1	pancreas:	n/a
5	chr18:7566781-7566831	PrEC	prostate:	n/a
6	chr18:7568186-7568236	HEK293	kidney:	embryo
7	chr18:7568186-7568236	HCPEpiC	choroid plexus:	n/a
8	chr18:7566558-7566608	GM12891	blood:	n/a
9	chr18:7568186-7568236	NHBE	bronchial:	n/a
10	chr18:7568186-7568236	PANC-1	pancreas:	n/a
11	chr18:7567638-7567688	NHDF-neo	bronchial:	n/a
12	chr18:7567799-7567849	AG09309	skin:	n/a
13	chr18:7566656-7566706	AG04450	lung:	fetal
14	chr18:7567799-7567849	AG09319	gingival:	n/a
15	chr18:7568265-7568315	RPTEC	kidney:	n/a
16	chr18:7566258-7566308	ovcar-3	ovarian:	n/a
17	chr18:7566258-7566308	GM19239	blood:	n/a
18	chr18:7568159-7568209	GM12878	blood:	n/a
19	chr18:7566558-7566608	GM12892	blood:	n/a
20	chr18:7567638-7567688	Jurkat	blood:	n/a
21	chr18:7566558-7566608	ECC-1	luminal epithelium:	n/a
22	chr18:7567717-7567767	SK-N-SH_RA	brain:	n/a
23	chr18:7568186-7568236	SK-N-SH_RA	brain:	n/a
24	chr18:7566656-7566706	NB4	blood:	n/a
25	chr18:7566258-7566308	SKMC	muscle:	n/a
26	chr18:7568186-7568236	HAEpiC	amniotic membrane:	n/a
27	chr18:7566258-7566308	HCT-116	colon:	n/a
28	chr18:7566656-7566706	K562	blood:	n/a
29	chr18:7566656-7566706	LNCaP	prostate:	n/a
30	chr18:7568265-7568315	AG04449	skin:	fetal
31	chr18:7567426-7567476	AG09309	skin:	n/a
32	chr18:7567638-7567688	AG09309	skin:	n/a
33	chr18:7568265-7568315	SK-N-MC	brain:	n/a
34	chr18:7568159-7568209	HepG2	liver:	n/a
35	chr18:7567799-7567849	ECC-1	luminal epithelium:	n/a
36	chr18:7567799-7567849	H1-hESC	embryonic stem cell:	embryo
37	chr18:7566258-7566308	HRE	kidney:	n/a
38	chr18:7567638-7567688	AG09319	gingival:	n/a
39	chr18:7568265-7568315	HRPEpiC	eye:	n/a
40	chr18:7566656-7566706	SK-N-SH_RA	brain:	n/a
41	chr18:7567799-7567849	LNCaP	prostate:	n/a
42	chr18:7567638-7567688	HCF	heart:	n/a
43	chr18:7568186-7568236	HPAEpiC	pulmonary alveolar:	n/a
44	chr18:7566558-7566608	NT2-D1	testis:	n/a
45	chr18:7567717-7567767	HUVEC	blood vessel:	n/a
46	chr18:7566656-7566706	AG10803	skin:	n/a
47	chr18:7567548-7567598	HUVEC	blood vessel:	n/a
48	chr18:7567426-7567476	PrEC	prostate:	n/a
49	chr18:7568265-7568315	GM19239	blood:	n/a
50	chr18:7567548-7567598	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:7567923..7568423-chr20:61846958..61847561,2	MCF-7	breast:
2	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:

No data

Variant related genes	Relation type
PTPRM	TF binding region
PTPRM	CpG island
ENSG00000149658	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530215353	chr18:7565827-7565828	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs117379744	chr18:7565835-7565836	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs118187234	chr18:7565836-7565837	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs532600911	chr18:7565840-7565841	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs139435332	chr18:7565841-7565842	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs569395983	chr18:7565934-7565935	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs538291366	chr18:7565949-7565950	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs554547506	chr18:7566000-7566001	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs16952142	chr18:7566016-7566017	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs184006921	chr18:7566041-7566042	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs187622282	chr18:7566052-7566053	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs201854383	chr18:7566067-7566068	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs76069576	chr18:7566068-7566069	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs398079246	chr18:7566073-7566074	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs397858902	chr18:7566074-7566075	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs192602068	chr18:7566092-7566093	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545484178	chr18:7566095-7566096	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs555887171	chr18:7566116-7566117	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs368874789	chr18:7566136-7566137	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs370468538	chr18:7566147-7566148	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs145478470	chr18:7566153-7566154	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs184183130	chr18:7566159-7566160	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561543430	chr18:7566163-7566164	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs148816432	chr18:7566185-7566186	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs540570181	chr18:7566198-7566199	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs560692337	chr18:7566205-7566206	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs145147960	chr18:7566227-7566228	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs552703390	chr18:7566244-7566245	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs376324911	chr18:7566248-7566249	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs188978723	chr18:7566391-7566392	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs533909915	chr18:7566438-7566439	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs73941928	chr18:7566442-7566443	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370081736	chr18:7566465-7566466	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs117034170	chr18:7566466-7566467	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs548529031	chr18:7566479-7566480	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs567666953	chr18:7566486-7566487	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs192896098	chr18:7566539-7566540	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs147577781	chr18:7566584-7566585	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs534047461	chr18:7566625-7566626	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs556088351	chr18:7566657-7566658	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs547415281	chr18:7566675-7566676	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs184962336	chr18:7566687-7566688	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs374705501	chr18:7566699-7566700	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs555823854	chr18:7566712-7566713	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs575695618	chr18:7566783-7566784	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs535216951	chr18:7566844-7566845	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs555293549	chr18:7566865-7566866	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs571952797	chr18:7566897-7566898	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs540914892	chr18:7566946-7566947	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs560816797	chr18:7567057-7567058	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Breast cancer	17133270	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7558200-7566000	Weak transcription	Right Atrium	heart
2	chr18:7560200-7566200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr18:7560400-7566000	Weak transcription	Lung	lung
4	chr18:7560400-7566000	Weak transcription	Pancreas	Pancrea
5	chr18:7562200-7565800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr18:7562200-7566000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr18:7562400-7565800	Weak transcription	Brain Substantia Nigra	brain
8	chr18:7562400-7566000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr18:7564600-7566000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr18:7564600-7566000	Enhancers	Adipose Nuclei	Adipose
11	chr18:7564600-7566400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr18:7564800-7565800	Enhancers	Rectal Smooth Muscle	rectum
13	chr18:7564800-7566000	Enhancers	Brain Cingulate Gyrus	brain
14	chr18:7564800-7566000	Enhancers	Brain Hippocampus Middle	brain
15	chr18:7565000-7565800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr18:7565000-7565800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr18:7565000-7566000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr18:7565000-7566000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr18:7565000-7566000	Enhancers	Right Ventricle	heart
20	chr18:7565000-7566000	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr18:7565200-7565800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr18:7565200-7565800	Enhancers	NHDF-Ad	bronchial
23	chr18:7565200-7566000	Enhancers	Psoas Muscle	Psoas
24	chr18:7565200-7566000	Enhancers	Stomach Smooth Muscle	stomach
25	chr18:7565200-7566000	Weak transcription	Spleen	Spleen
26	chr18:7565400-7565800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
27	chr18:7565400-7565800	Weak transcription	Left Ventricle	heart
28	chr18:7565600-7565800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr18:7565600-7565800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr18:7565600-7566000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr18:7565600-7566000	Enhancers	Brain Anterior Caudate	brain
32	chr18:7565600-7566000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr18:7565600-7566000	Enhancers	Fetal Heart	heart
34	chr18:7565600-7566200	Flanking Active TSS	Colon Smooth Muscle	Colon
35	chr18:7565600-7566200	Bivalent Enhancer	Stomach Mucosa	stomach
36	chr18:7565600-7566400	Enhancers	Brain Angular Gyrus	brain
37	chr18:7565800-7566000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr18:7565800-7566000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr18:7565800-7566000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr18:7565800-7566000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr18:7565800-7566000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr18:7565800-7566000	Enhancers	Fetal Kidney	kidney
43	chr18:7565800-7566000	Enhancers	Fetal Lung	lung
44	chr18:7565800-7566000	Enhancers	Left Ventricle	heart
45	chr18:7565800-7566000	Enhancers	Hela-S3	cervix
46	chr18:7565800-7566000	Enhancers	Osteobl	bone
47	chr18:7565800-7566200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr18:7565800-7566200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
49	chr18:7565800-7566200	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
50	chr18:7565800-7566200	Enhancers	Fetal Brain Female	brain

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