Variant report

Variant	esv3374659
Chromosome Location	chr18:9333577-9336325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:672)
CpG islands
(count:671)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr18:9334168-9334514	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr18:9334126-9334510	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr18:9334566-9335175	GM12878	blood:	n/a	chr18:9335047-9335060 chr18:9334843-9334856
4	BHLHE40	chr18:9334201-9334409	K562	blood:	n/a	n/a
5	BHLHE40	chr18:9333999-9335081	GM12878	blood:	n/a	chr18:9334845-9334861 chr18:9334159-9334168 chr18:9334463-9334479
6	BRCA1	chr18:9334632-9334696	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr18:9333836-9334866	K562	blood:	n/a	n/a
8	CCNT2	chr18:9334346-9335407	K562	blood:	n/a	n/a
9	CCNT2	chr18:9333900-9333980	K562	blood:	n/a	n/a
10	CEBPB	chr18:9336222-9336534	K562	blood:	n/a	chr18:9336477-9336488
11	CEBPB	chr18:9336214-9336458	K562	blood:	n/a	n/a
12	CEBPD	chr18:9334322-9335046	HepG2	liver:	n/a	n/a
13	CHD1	chr18:9334769-9335746	GM12878	blood:	n/a	chr18:9334809-9334819
14	CHD1	chr18:9334870-9335308	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr18:9333764-9334297	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr18:9333658-9335948	IMR90	lung:	n/a	chr18:9334809-9334819
17	CHD2	chr18:9334326-9334464	HepG2	liver:	n/a	n/a
18	CHD2	chr18:9334265-9334500	K562	blood:	n/a	n/a
19	CHD2	chr18:9334627-9335239	GM12878	blood:	n/a	chr18:9334809-9334819
20	CHD2	chr18:9334880-9335026	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr18:9334012-9334664	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr18:9334313-9335145	Hela-S3	cervix:	n/a	chr18:9334809-9334819
23	CREB1	chr18:9334304-9334857	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr18:9333825-9334074	A549	lung:	n/a	n/a
25	CREB1	chr18:9333681-9334907	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr18:9334353-9335002	GM12878	blood:	n/a	n/a
27	CREB1	chr18:9334255-9334949	A549	lung:	n/a	n/a
28	CTCF	chr18:9334573-9334804	NHEK	skin:	n/a	n/a
29	CTCF	chr18:9334576-9334799	GM10266	blood:	n/a	n/a
30	CTCF	chr18:9334820-9334823	MCF-7	breast:	n/a	n/a
31	CTCF	chr18:9333840-9333990	AG09319	gingival:	n/a	n/a
32	CTCF	chr18:9335140-9335290	Caco-2	colon:	n/a	n/a
33	CTCF	chr18:9334640-9334790	GM12865	blood:	n/a	n/a
34	CTCF	chr18:9334606-9334747	MCF-7	breast:	n/a	n/a
35	CTCF	chr18:9334585-9334760	A549	lung:	n/a	n/a
36	CTCF	chr18:9334600-9334750	GM06990	blood:	n/a	n/a
37	CTCF	chr18:9335300-9335450	GM12865	blood:	n/a	n/a
38	CTCF	chr18:9335160-9335310	GM12875	blood:	n/a	n/a
39	CTCF	chr18:9334600-9334750	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr18:9335160-9335310	GM12870	blood:	n/a	n/a
41	CTCF	chr18:9335180-9335330	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr18:9334640-9334790	HPF	lung:	n/a	n/a
43	CTCF	chr18:9334620-9334770	BJ	skin:	n/a	n/a
44	CTCF	chr18:9334566-9334842	Fibrobl	skin:	n/a	n/a
45	CTCF	chr18:9334600-9334750	GM12874	blood:	n/a	n/a
46	CTCF	chr18:9334894-9334935	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr18:9335160-9335310	HMEC	breast:	n/a	n/a
48	CTCF	chr18:9335140-9335290	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr18:9333859-9334034	MCF-7	breast:	n/a	n/a
50	CTCF	chr18:9334566-9334775	Hela-S3	cervix:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:9334049-9334099	Caco-2	colon:	n/a
2	chr18:9335432-9335482	T-47D	breast:	n/a
3	chr18:9335102-9335152	ProgFib	skin:	n/a
4	chr18:9334792-9334842	HAEpiC	amniotic membrane:	n/a
5	chr18:9335347-9335397	LNCaP	prostate:	n/a
6	chr18:9334488-9334538	BE2_C	brain:	n/a
7	chr18:9334699-9334749	SK-N-MC	brain:	n/a
8	chr18:9334049-9334099	MCF10A-Er-Src	breast:	n/a
9	chr18:9335432-9335482	HCM	heart:	n/a
10	chr18:9335347-9335397	AG04450	lung:	fetal
11	chr18:9334497-9334547	HCPEpiC	choroid plexus:	n/a
12	chr18:9333974-9334024	SK-N-SH	brain:	n/a
13	chr18:9335432-9335482	NH-A	brain:	n/a
14	chr18:9334497-9334547	SK-N-MC	brain:	n/a
15	chr18:9335432-9335482	Caco-2	colon:	n/a
16	chr18:9335102-9335152	HIPEpiC	eye:	n/a
17	chr18:9335102-9335152	MCF10A-Er-Src	breast:	n/a
18	chr18:9334699-9334749	MCF-7	breast:	n/a
19	chr18:9334693-9334743	GM12891	blood:	n/a
20	chr18:9334792-9334842	PrEC	prostate:	n/a
21	chr18:9333974-9334024	SKMC	muscle:	n/a
22	chr18:9334792-9334842	AG09319	gingival:	n/a
23	chr18:9334497-9334547	T-47D	breast:	n/a
24	chr18:9334049-9334099	HEEpiC	esophagus:	n/a
25	chr18:9335347-9335397	K562	blood:	n/a
26	chr18:9334639-9334689	SK-N-SH_RA	brain:	n/a
27	chr18:9334049-9334099	Hela-S3	cervix:	n/a
28	chr18:9334699-9334749	IMR90	lung:	fetal
29	chr18:9335102-9335152	NB4	blood:	n/a
30	chr18:9334693-9334743	HRPEpiC	eye:	n/a
31	chr18:9334488-9334538	HRPEpiC	eye:	n/a
32	chr18:9333974-9334024	MCF-7	breast:	n/a
33	chr18:9334699-9334749	HRCEpiC	kidney:	n/a
34	chr18:9334699-9334749	HPAEpiC	pulmonary alveolar:	n/a
35	chr18:9334639-9334689	MCF-7	breast:	n/a
36	chr18:9334497-9334547	PANC-1	pancreas:	n/a
37	chr18:9333974-9334024	HCM	heart:	n/a
38	chr18:9333974-9334024	SK-N-MC	brain:	n/a
39	chr18:9335102-9335152	AoSMC	blood vessel:	n/a
40	chr18:9334488-9334538	ProgFib	skin:	n/a
41	chr18:9334639-9334689	HL-60	blood:	n/a
42	chr18:9334049-9334099	NHBE	bronchial:	n/a
43	chr18:9334049-9334099	HMEC	breast:	n/a
44	chr18:9335347-9335397	AG04449	skin:	fetal
45	chr18:9334497-9334547	BJ	skin:	n/a
46	chr18:9335102-9335152	HepG2	liver:	n/a
47	chr18:9334639-9334689	AG09319	gingival:	n/a
48	chr18:9334497-9334547	AG04450	lung:	fetal
49	chr18:9334693-9334743	Caco-2	colon:	n/a
50	chr18:9334792-9334842	ProgFib	skin:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:9334537..9336244-chr18:9518482..9520647,3	K562	blood:
2	chr18:8704001..8705732-chr18:9332474..9334627,2	K562	blood:
3	chr18:9334415..9335137-chr5:179159528..179160063,2	HCT-116	colon:
4	chr18:9137078..9139236-chr18:9332503..9334760,2	K562	blood:
5	chr18:8608384..8610361-chr18:9333343..9335226,2	K562	blood:
6	chr18:9321590..9324393-chr18:9335176..9336771,2	K562	blood:
7	chr18:9333428..9336571-chr18:9474335..9476989,6	MCF-7	breast:
8	chr18:9334546..9336965-chr18:9474025..9476757,3	K562	blood:
9	chr18:9331992..9337338-chr18:9472584..9477624,6	MCF-7	breast:
10	chr18:9334524..9335342-chr3:31573805..31574542,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP4R1-2	chr18:9334135-9334439	ENSG00000264964.1
2	lnc-PPP4R1-2	chr18:9334135-9334332	XLOC_012754
3	lnc-PPP4R1-2	chr18:9334135-9334313	XLOC_012754
4	lnc-PPP4R1-2	chr18:9334135-9334462	XLOC_012754

No data

Variant related genes	Relation type
TWSG1	TF binding region
ENSG00000264964	TF binding region
TWSG1	CpG island
ENSG00000264964	CpG island
ENSG00000161021	chromatin interactions
ENSG00000273335	chromatin interactions
ENSG00000163527	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000206418	chromatin interactions
ENSG00000168502	chromatin interactions
ENSG00000273352	chromatin interactions
ENSG00000101745	chromatin interactions

Extended variants
information (count: 89 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530688045	chr18:9333641-9333642	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs541038315	chr18:9333651-9333652	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs182891776	chr18:9333687-9333688	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs550884282	chr18:9333698-9333699	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs371639466	chr18:9333772-9333773	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs528264730	chr18:9333795-9333796	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs187236812	chr18:9333804-9333805	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs568441137	chr18:9333806-9333807	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs5823048	chr18:9333829-9333830	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs535879874	chr18:9333849-9333850	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs557359626	chr18:9333872-9333873	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs191684357	chr18:9333885-9333886	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs569595796	chr18:9333911-9333912	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs570720454	chr18:9333915-9333916	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs540094395	chr18:9333928-9333929	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs7242593	chr18:9333937-9333938	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs139060983	chr18:9333987-9333988	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs540447698	chr18:9334005-9334006	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs553065438	chr18:9334065-9334066	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs2165909	chr18:9334071-9334072	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs143994679	chr18:9334094-9334095	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs566564674	chr18:9334190-9334191	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
23	rs375071833	chr18:9334205-9334206	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs78991469	chr18:9334216-9334217	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
25	rs145079924	chr18:9334222-9334223	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
26	rs374683071	chr18:9334223-9334224	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
27	rs184661117	chr18:9334295-9334296	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
28	rs72939957	chr18:9334336-9334337	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs368293649	chr18:9334364-9334365	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
30	rs12955762	chr18:9334379-9334380	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
31	rs546464704	chr18:9334392-9334393	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
32	rs572173455	chr18:9334425-9334426	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs529381062	chr18:9334441-9334442	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
34	rs551000897	chr18:9334454-9334455	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
35	rs574892877	chr18:9334469-9334470	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs546868843	chr18:9334479-9334480	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs569311267	chr18:9334541-9334542	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs539836740	chr18:9334563-9334564	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs558514008	chr18:9334639-9334640	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs567035425	chr18:9334643-9334644	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs55759113	chr18:9334654-9334655	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs534419451	chr18:9334667-9334668	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs28372752	chr18:9334685-9334686	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs574477515	chr18:9334733-9334734	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs541484067	chr18:9334784-9334785	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs556629113	chr18:9334806-9334807	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs574942223	chr18:9334843-9334844	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs537405979	chr18:9334941-9334942	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs545373746	chr18:9334948-9334949	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs564440546	chr18:9334951-9334952	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
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
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9320200-9333800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr18:9321800-9333600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr18:9321800-9333600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr18:9324600-9334000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr18:9329600-9333600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr18:9330600-9333600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr18:9333400-9333600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr18:9333400-9333600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr18:9333400-9333600	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr18:9333400-9333600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr18:9333400-9333600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr18:9333400-9333600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr18:9333400-9333600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr18:9333400-9333600	Enhancers	Fetal Muscle Leg	muscle
15	chr18:9333400-9333600	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr18:9333400-9333600	Enhancers	Stomach Smooth Muscle	stomach
17	chr18:9333400-9333800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr18:9333400-9333800	Enhancers	Aorta	Aorta
19	chr18:9333400-9333800	Enhancers	Spleen	Spleen
20	chr18:9333400-9334000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr18:9333400-9334200	ZNF genes & repeats	Fetal Thymus	thymus
22	chr18:9333400-9334400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr18:9333400-9334400	Flanking Active TSS	Placenta	Placenta
24	chr18:9333400-9336400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr18:9333600-9333800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr18:9333600-9333800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr18:9333600-9333800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr18:9333600-9333800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
29	chr18:9333600-9333800	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
30	chr18:9333600-9333800	Enhancers	Primary B cells from cord blood	blood
31	chr18:9333600-9333800	Enhancers	Primary B cells from peripheral blood	blood
32	chr18:9333600-9333800	Enhancers	Primary hematopoietic stem cells	blood
33	chr18:9333600-9333800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr18:9333600-9333800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr18:9333600-9333800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr18:9333600-9333800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr18:9333600-9333800	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr18:9333600-9333800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr18:9333600-9333800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr18:9333600-9333800	Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr18:9333600-9333800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr18:9333600-9333800	Enhancers	Adipose Nuclei	Adipose
43	chr18:9333600-9333800	Enhancers	Liver	Liver
44	chr18:9333600-9333800	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr18:9333600-9333800	Active TSS	Colonic Mucosa	Colon
46	chr18:9333600-9333800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr18:9333600-9333800	Enhancers	Fetal Brain Male	brain
48	chr18:9333600-9333800	Enhancers	Fetal Heart	heart
49	chr18:9333600-9333800	Bivalent/Poised TSS	Fetal Intestine Large	intestine
50	chr18:9333600-9333800	Enhancers	Fetal Stomach	stomach

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