Variant report

Variant	esv1812234
Chromosome Location	chr10:118977123-119004095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:917)
Chromatin interactive
region (count:34)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:118978297-118978588	K562	blood:	n/a	n/a
2	ATF3	chr10:118980727-118981131	A549	lung:	n/a	n/a
3	BACH1	chr10:119001150-119001313	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr10:118980652-118981113	A549	lung:	n/a	n/a
5	BHLHE40	chr10:118980732-118981151	A549	lung:	n/a	n/a
6	BHLHE40	chr10:118978241-118978751	K562	blood:	n/a	n/a
7	CBX3	chr10:118996934-118997271	K562	blood:	n/a	n/a
8	CCNT2	chr10:119001126-119001665	K562	blood:	n/a	n/a
9	CEBPB	chr10:118991846-118991909	HepG2	liver:	n/a	chr10:118991865-118991876
10	CEBPB	chr10:118986424-118986773	K562	blood:	n/a	n/a
11	CEBPB	chr10:118986419-118986738	A549	lung:	n/a	n/a
12	CEBPB	chr10:118986382-118986704	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr10:118978203-118978486	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr10:119000506-119000541	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr10:118999944-119000859	H1-hESC	embryonic stem cell:	n/a	chr10:119000574-119000587
16	CREB1	chr10:118980892-118981186	A549	lung:	n/a	n/a
17	CREB1	chr10:119000198-119000806	H1-hESC	embryonic stem cell:	n/a	chr10:119000574-119000587
18	CTBP2	chr10:118999810-119000801	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr10:118977500-118977650	GM12870	blood:	n/a	n/a
20	CTCF	chr10:118986500-118986650	NHLF	lung:	n/a	n/a
21	CTCF	chr10:118986443-118986680	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr10:118986460-118986610	HCT-116	colon:	n/a	n/a
23	CTCF	chr10:118986446-118986682	GM10266	blood:	n/a	n/a
24	CTCF	chr10:118986520-118986670	K562	blood:	n/a	n/a
25	CTCF	chr10:118986460-118986610	GM12878	blood:	n/a	n/a
26	CTCF	chr10:118986425-118986658	MCF-7	breast:	n/a	n/a
27	CTCF	chr10:118986500-118986650	GM12864	blood:	n/a	n/a
28	CTCF	chr10:118986431-118986678	HepG2	liver:	n/a	n/a
29	CTCF	chr10:118986520-118986670	HMF	breast:	n/a	n/a
30	CTCF	chr10:118986480-118986630	AG09309	skin:	n/a	n/a
31	CTCF	chr10:118986460-118986610	HAc	cerebellar:	n/a	n/a
32	CTCF	chr10:118986460-118986610	GM12874	blood:	n/a	n/a
33	CTCF	chr10:118986460-118986610	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr10:118986480-118986630	GM12867	blood:	n/a	n/a
35	CTCF	chr10:118986520-118986670	SAEC	small airway:	n/a	n/a
36	CTCF	chr10:118986425-118986673	GM12878	blood:	n/a	n/a
37	CTCF	chr10:118986418-118986675	GM19238	blood:	n/a	n/a
38	CTCF	chr10:118986227-118986797	MCF-7	breast:	n/a	n/a
39	CTCF	chr10:118986520-118986670	A549	lung:	n/a	n/a
40	CTCF	chr10:118986340-118986659	ECC-1	luminal epithelium:	n/a	n/a
41	CTCF	chr10:118986414-118986669	GM12892	blood:	n/a	n/a
42	CTCF	chr10:118986429-118986652	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr10:118986440-118986590	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr10:118986440-118986590	GM12873	blood:	n/a	n/a
45	CTCF	chr10:118986272-118986726	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr10:118986480-118986630	HepG2	liver:	n/a	n/a
47	CTCF	chr10:118986440-118986590	HRE	kidney:	n/a	n/a
48	CTCF	chr10:118986460-118986610	GM12864	blood:	n/a	n/a
49	CTCF	chr10:118986469-118986668	LNCaP	prostate:	n/a	n/a
50	CTCF	chr10:118986440-118986590	GM12801	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:119001590-119001640	BE2_C	brain:	n/a
2	chr10:119003687-119003737	AG09309	skin:	n/a
3	chr10:119001590-119001640	BE2_C	brain:	n/a
4	chr10:119003687-119003737	AG09309	skin:	n/a
5	chr10:119001529-119001579	ovcar-3	ovarian:	n/a
6	chr10:119001427-119001477	HUVEC	blood vessel:	n/a
7	chr10:119000236-119000286	HNPCEpiC	eye:	n/a
8	chr10:119000236-119000286	LNCaP	prostate:	n/a
9	chr10:118980094-118980144	SKMC	muscle:	n/a
10	chr10:119000991-119001041	MCF10A-Er-Src	breast:	n/a
11	chr10:119001250-119001300	GM12891	blood:	n/a
12	chr10:118980094-118980144	H1-hESC	embryonic stem cell:	embryo
13	chr10:118997146-118997196	HIPEpiC	eye:	n/a
14	chr10:119001427-119001477	HCT-116	colon:	n/a
15	chr10:118980094-118980144	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:119001529-119001579	HCT-116	colon:	n/a
17	chr10:119001529-119001579	HEK293	kidney:	embryo
18	chr10:119001427-119001477	AG09309	skin:	n/a
19	chr10:119000215-119000265	LNCaP	prostate:	n/a
20	chr10:119001066-119001116	NHDF-neo	bronchial:	n/a
21	chr10:119001529-119001579	RPTEC	kidney:	n/a
22	chr10:119000927-119000977	ProgFib	skin:	n/a
23	chr10:119001427-119001477	HAEpiC	amniotic membrane:	n/a
24	chr10:119001529-119001579	HAEpiC	amniotic membrane:	n/a
25	chr10:119001427-119001477	MCF10A-Er-Src	breast:	n/a
26	chr10:119001590-119001640	GM12878	blood:	n/a
27	chr10:119001250-119001300	SK-N-MC	brain:	n/a
28	chr10:119001427-119001477	NB4	blood:	n/a
29	chr10:118980094-118980144	BJ	skin:	n/a
30	chr10:119000215-119000265	SK-N-MC	brain:	n/a
31	chr10:119000927-119000977	AG09319	gingival:	n/a
32	chr10:118997146-118997196	U87	brain:	n/a
33	chr10:119001590-119001640	ovcar-3	ovarian:	n/a
34	chr10:119003687-119003737	PFSK-1	brain:	n/a
35	chr10:119000927-119000977	HCPEpiC	choroid plexus:	n/a
36	chr10:119000236-119000286	Caco-2	colon:	n/a
37	chr10:118980094-118980144	HRPEpiC	eye:	n/a
38	chr10:118997146-118997196	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:118997146-118997196	LNCaP	prostate:	n/a
40	chr10:119001250-119001300	A549	lung:	n/a
41	chr10:118997146-118997196	NB4	blood:	n/a
42	chr10:119000991-119001041	SK-N-SH	brain:	n/a
43	chr10:119000991-119001041	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:119001529-119001579	HL-60	blood:	n/a
45	chr10:119001250-119001300	RPTEC	kidney:	n/a
46	chr10:119000215-119000265	NHDF-neo	bronchial:	n/a
47	chr10:118997146-118997196	AG04450	lung:	fetal
48	chr10:119001427-119001477	Caco-2	colon:	n/a
49	chr10:119000236-119000286	NH-A	brain:	n/a
50	chr10:118980094-118980144	HAEpiC	amniotic membrane:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:119001180..119002700-chr17:41464210..41468296,3	K562	blood:
2	chr10:118981865..118984447-chr10:118987245..118988846,2	K562	blood:
3	chr10:119001180..119002700-chr3:73158602..73160591,2	K562	blood:
4	chr10:119001200..119002700-chr11:62609117..62610696,2	K562	blood:
5	chr10:118981865..118984447-chr10:118987245..118988846,2	K562	blood:
6	chr10:118986135..118987184-chr10:119077937..119079062,4	MCF-7	breast:
7	chr10:118991944..118994819-chr10:118998275..118999824,2	MCF-7	breast:
8	chr10:118986124..118987057-chr10:119078134..119080313,8	MCF-7	breast:
9	chr10:118986106..118987073-chr10:119079163..119080252,5	MCF-7	breast:
10	chr10:118991944..118994819-chr10:118998275..118999824,2	MCF-7	breast:
11	chr10:118975358..118977652-chr10:119078316..119080186,2	MCF-7	breast:
12	chr10:118975868..118977282-chr10:119208595..119209916,7	K562	blood:
13	chr10:119001180..119002700-chr17:41466350..41468296,2	K562	blood:
14	chr10:118973979..118977978-chr10:119077721..119080771,4	MCF-7	breast:
15	chr10:118975183..118978653-chr10:118979198..118982710,3	MCF-7	breast:
16	chr10:118975183..118978653-chr10:118979198..118982710,3	MCF-7	breast:
17	chr10:118983149..118985231-chr10:118987345..118990233,2	MCF-7	breast:
18	chr10:118991795..118993402-chr10:118997326..118999628,2	MCF-7	breast:
19	chr10:118991863..118993895-chr10:118994626..118997606,2	K562	blood:
20	chr10:118975810..118976793-chr10:118986044..118987013,2	MCF-7	breast:
21	chr10:118999700..119002680-chr17:41380895..41383406,2	K562	blood:
22	chr10:118976223..118977870-chr10:118979893..118982882,2	K562	blood:
23	chr10:119001180..119002700-chr3:73158543..73161387,2	MCF-7	breast:
24	chr10:118991795..118993402-chr10:118997326..118999628,2	MCF-7	breast:
25	chr10:118984170..118986549-chr10:118992208..118994790,2	K562	blood:
26	chr10:118984170..118986549-chr10:118992208..118994790,2	K562	blood:
27	chr10:118975767..118976754-chr10:118986014..118987065,3	K562	blood:
28	chr10:118975266..118977159-chr10:119077947..119080264,23	MCF-7	breast:
29	chr10:118991863..118993895-chr10:118994626..118997606,2	K562	blood:
30	chr10:118983149..118985231-chr10:118987345..118990233,2	MCF-7	breast:
31	chr10:119001180..119001700-chr11:62609120..62609716,2	Hela-S3	cervix:
32	chr10:118976223..118977870-chr10:118979893..118982882,2	K562	blood:
33	chr10:118975747..118977593-chr10:119078147..119080329,46	MCF-7	breast:
34	chr10:118986459..118987203-chr10:119079340..119080149,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDZD8-1	chr10:118999111-118999692	ENSG00000225936.1
2	lnc-PDZD8-1	chr10:119001172-119001294	ENSG00000225936.1
3	lnc-PDZD8-1	chr10:118998545-118999684	NONHSAT016512
4	lnc-PDZD8-1	chr10:118999832-119000515	NONHSAT016512
5	lnc-PDZD8-1	chr10:119001396-119001434	ENSG00000225936.1

No data

Variant related genes	Relation type
ENSG00000225936	TF binding region
SLC18A2	TF binding region
ENSG00000225936	CpG island
SLC18A2	CpG island
ENSG00000236383	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000165650	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000223247	chromatin interactions

Extended variants
information (count: 893 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2619105	chr10:118977123-118977124	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116722391	chr10:118977135-118977136	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548810989	chr10:118977181-118977182	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537340945	chr10:118977209-118977210	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs550559466	chr10:118977287-118977288	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184892802	chr10:118977301-118977302	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539417663	chr10:118977302-118977303	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs190142936	chr10:118977304-118977305	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183137640	chr10:118977334-118977335	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535700563	chr10:118977394-118977395	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs74159047	chr10:118977423-118977424	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs575889855	chr10:118977480-118977481	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs370109536	chr10:118977527-118977528	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12571226	chr10:118977576-118977577	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs564723758	chr10:118977580-118977581	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546367788	chr10:118977603-118977604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374904437	chr10:118977606-118977607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565152884	chr10:118977614-118977615	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576936718	chr10:118977615-118977616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545799503	chr10:118977638-118977639	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191741666	chr10:118977649-118977650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114910802	chr10:118977669-118977670	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548124534	chr10:118977671-118977672	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561927190	chr10:118977679-118977680	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs149576386	chr10:118977720-118977721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs61872361	chr10:118977744-118977745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs184034948	chr10:118977749-118977750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35423801	chr10:118977782-118977783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550481094	chr10:118977851-118977852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs187854568	chr10:118977878-118977879	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147275748	chr10:118977916-118977917	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191604426	chr10:118977951-118977952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs149065450	chr10:118978009-118978010	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145558315	chr10:118978010-118978011	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs397702173	chr10:118978011-118978012	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs566901102	chr10:118978155-118978156	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs535937615	chr10:118978168-118978169	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs555539732	chr10:118978186-118978187	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs539858614	chr10:118978200-118978201	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182296469	chr10:118978209-118978210	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs11815373	chr10:118978213-118978214	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs558522086	chr10:118978230-118978231	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs578244543	chr10:118978299-118978300	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs139631351	chr10:118978352-118978353	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs186627009	chr10:118978388-118978389	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs191828844	chr10:118978389-118978390	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs572708168	chr10:118978397-118978398	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs541910707	chr10:118978430-118978431	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs561597924	chr10:118978460-118978461	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs530745941	chr10:118978509-118978510	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neuroticism	17667963	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118975400-118977200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr10:118975600-118977600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr10:118975800-118977200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
4	chr10:118975800-118977200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
5	chr10:118975800-118977200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr10:118975800-118977200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr10:118975800-118977200	Enhancers	Spleen	Spleen
8	chr10:118976000-118977200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr10:118976000-118977200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr10:118976000-118977200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr10:118976000-118977200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
12	chr10:118976000-118977200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr10:118976000-118977200	Flanking Active TSS	HMEC	breast
14	chr10:118976000-118977200	Bivalent/Poised TSS	Osteobl	bone
15	chr10:118976000-118977400	Bivalent Enhancer	Fetal Brain Male	brain
16	chr10:118976000-118977600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
17	chr10:118976200-118977200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:118976200-118977200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr10:118976200-118977200	Flanking Active TSS	Pancreas	Pancrea
20	chr10:118976400-118977200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr10:118976400-118977200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
22	chr10:118976400-118977200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:118976400-118977200	Flanking Active TSS	Primary hematopoietic stem cells	blood
24	chr10:118976400-118977200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr10:118976400-118977200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr10:118976400-118977200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
27	chr10:118976400-118977200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
28	chr10:118976400-118977200	Flanking Active TSS	Ovary	ovary
29	chr10:118976400-118977200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
30	chr10:118976400-118977200	Flanking Bivalent TSS/Enh	HepG2	liver
31	chr10:118976400-118977200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
32	chr10:118976400-118977400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
33	chr10:118976400-118977400	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
34	chr10:118976600-118977200	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:118976600-118977200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr10:118976600-118977200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
37	chr10:118976600-118977200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr10:118976600-118977200	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
39	chr10:118976600-118977600	Flanking Active TSS	Esophagus	oesophagus
40	chr10:118976800-118977200	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr10:118976800-118977200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr10:118976800-118977200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
43	chr10:118976800-118977200	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
44	chr10:118976800-118977200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
45	chr10:118976800-118977200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
46	chr10:118976800-118977200	Bivalent Enhancer	Fetal Heart	heart
47	chr10:118976800-118977200	Enhancers	Gastric	stomach
48	chr10:118976800-118977200	Active TSS	HSMM	muscle
49	chr10:118976800-118977600	Bivalent/Poised TSS	Primary T cells from cord blood	blood
50	chr10:118977000-118977200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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