Variant report

Variant	esv3438516
Chromosome Location	chr17:37782451-37785299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:31)
CpG islands
(count:612)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:31 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:37782605-37782894	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr17:37782250-37782877	K562	blood:	n/a	n/a
3	CHD2	chr17:37782984-37782994	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr17:37782779-37783417	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr17:37782761-37782843	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr17:37783740-37783890	WERI-Rb-1	eye:	n/a	n/a
7	EGR1	chr17:37782438-37782918	K562	blood:	n/a	chr17:37782588-37782603 chr17:37782589-37782602 chr17:37782590-37782600 chr17:37782589-37782602
8	EGR1	chr17:37782443-37782877	K562	blood:	n/a	chr17:37782588-37782603 chr17:37782589-37782602 chr17:37782590-37782600 chr17:37782589-37782602
9	HDAC2	chr17:37782705-37783307	H1-hESC	embryonic stem cell:	n/a	n/a
10	MAX	chr17:37782370-37782901	K562	blood:	n/a	n/a
11	MAZ	chr17:37784716-37784755	K562	blood:	n/a	n/a
12	MXI1	chr17:37782742-37782810	H1-hESC	embryonic stem cell:	n/a	n/a
13	NFIC	chr17:37782715-37783282	ECC-1	luminal epithelium:	n/a	n/a
14	NFIC	chr17:37782649-37783234	ECC-1	luminal epithelium:	n/a	n/a
15	PBX3	chr17:37782663-37782827	GM12878	blood:	n/a	n/a
16	POLR2A	chr17:37782395-37782872	H1-neurons	neurons:	n/a	n/a
17	POLR2A	chr17:37782409-37782710	H1-neurons	neurons:	n/a	n/a
18	POLR2A	chr17:37784957-37785028	K562	blood:	n/a	n/a
19	POLR2A	chr17:37782930-37783411	SK-N-MC	brain:	n/a	n/a
20	RCOR1	chr17:37782708-37782741	K562	blood:	n/a	n/a
21	RFX5	chr17:37784372-37784528	HepG2	liver:	n/a	chr17:37784440-37784455
22	SIN3A	chr17:37784196-37784694	H1-hESC	embryonic stem cell:	n/a	chr17:37784388-37784397
23	SIN3A	chr17:37782665-37783544	H1-hESC	embryonic stem cell:	n/a	chr17:37783451-37783462
24	SIN3AK20	chr17:37782889-37783413	H1-hESC	embryonic stem cell:	n/a	n/a
25	USF2	chr17:37782889-37782899	H1-hESC	embryonic stem cell:	n/a	n/a
26	YY1	chr17:37782740-37783285	H1-hESC	embryonic stem cell:	n/a	chr17:37782927-37782938 chr17:37783151-37783160
27	ZBTB7A	chr17:37782860-37783976	ECC-1	luminal epithelium:	n/a	chr17:37783015-37783023 chr17:37783444-37783453 chr17:37783016-37783024
28	ZBTB7A	chr17:37783490-37783654	K562	blood:	n/a	n/a
29	ZBTB7A	chr17:37782934-37783617	ECC-1	luminal epithelium:	n/a	chr17:37783015-37783023 chr17:37783444-37783453 chr17:37783016-37783024
30	ZNF143	chr17:37782742-37783475	H1-hESC	embryonic stem cell:	n/a	n/a
31	ZNF263	chr17:37782469-37782768	HEK293-T-REx	kidney:	n/a	chr17:37782576-37782597

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37784694-37784744	NT2-D1	testis:	n/a
2	chr17:37784694-37784744	SK-N-SH_RA	brain:	n/a
3	chr17:37784694-37784744	NT2-D1	testis:	n/a
4	chr17:37784694-37784744	SK-N-SH_RA	brain:	n/a
5	chr17:37784895-37784945	Hepatocyte	liver:	n/a
6	chr17:37782685-37782735	HIPEpiC	eye:	n/a
7	chr17:37783488-37783538	ECC-1	luminal epithelium:	n/a
8	chr17:37784024-37784074	SK-N-SH	brain:	n/a
9	chr17:37784694-37784744	PANC-1	pancreas:	n/a
10	chr17:37784895-37784945	SK-N-MC	brain:	n/a
11	chr17:37784024-37784074	MCF-7	breast:	n/a
12	chr17:37783879-37783929	HNPCEpiC	eye:	n/a
13	chr17:37783879-37783929	NHDF-neo	bronchial:	n/a
14	chr17:37784024-37784074	AG04450	lung:	fetal
15	chr17:37784024-37784074	NHBE	bronchial:	n/a
16	chr17:37784699-37784749	GM12878	blood:	n/a
17	chr17:37783011-37783061	SAEC	small airway:	n/a
18	chr17:37784694-37784744	NB4	blood:	n/a
19	chr17:37784694-37784744	BE2_C	brain:	n/a
20	chr17:37783011-37783061	NHBE	bronchial:	n/a
21	chr17:37783488-37783538	GM12892	blood:	n/a
22	chr17:37782685-37782735	AoSMC	blood vessel:	n/a
23	chr17:37783011-37783061	A549	lung:	n/a
24	chr17:37784895-37784945	HRE	kidney:	n/a
25	chr17:37783488-37783538	AG09309	skin:	n/a
26	chr17:37784694-37784744	IMR90	lung:	fetal
27	chr17:37784699-37784749	HCF	heart:	n/a
28	chr17:37782685-37782735	T-47D	breast:	n/a
29	chr17:37782685-37782735	GM12892	blood:	n/a
30	chr17:37784699-37784749	AG04449	skin:	fetal
31	chr17:37783879-37783929	HUVEC	blood vessel:	n/a
32	chr17:37783689-37783739	NHDF-neo	bronchial:	n/a
33	chr17:37784711-37784761	ECC-1	luminal epithelium:	n/a
34	chr17:37784699-37784749	NHBE	bronchial:	n/a
35	chr17:37784024-37784074	H1-hESC	embryonic stem cell:	embryo
36	chr17:37784694-37784744	RPTEC	kidney:	n/a
37	chr17:37783689-37783739	Caco-2	colon:	n/a
38	chr17:37783689-37783739	NB4	blood:	n/a
39	chr17:37784895-37784945	HRCEpiC	kidney:	n/a
40	chr17:37784711-37784761	HRPEpiC	eye:	n/a
41	chr17:37782685-37782735	AG09309	skin:	n/a
42	chr17:37783689-37783739	HCM	heart:	n/a
43	chr17:37783011-37783061	HRE	kidney:	n/a
44	chr17:37783879-37783929	Caco-2	colon:	n/a
45	chr17:37784694-37784744	HRCEpiC	kidney:	n/a
46	chr17:37783879-37783929	HCF	heart:	n/a
47	chr17:37784895-37784945	GM06990	blood:	n/a
48	chr17:37784711-37784761	SAEC	small airway:	n/a
49	chr17:37784024-37784074	HCF	heart:	n/a
50	chr17:37783488-37783538	MCF10A-Er-Src	breast:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:37782428..37784390-chr17:37785390..37788111,2	K562	blood:
2	chr17:37777756..37783081-chr17:37819129..37825010,9	K562	blood:
3	chr17:37782244..37782963-chr17:37790351..37790853,2	K562	blood:
4	chr17:37780595..37782911-chr17:37786267..37787886,2	MCF-7	breast:
5	chr17:37682088..37684502-chr17:37782691..37785037,2	MCF-7	breast:
6	chr17:37784126..37786007-chr17:37898999..37901042,2	K562	blood:
7	chr17:37781012..37783798-chr17:37885303..37888164,4	K562	blood:

No data

Variant related genes	Relation type
PPP1R1B	TF binding region
PPP1R1B	CpG island
ENSG00000141738	chromatin interactions
ENSG00000141741	chromatin interactions
ENSG00000141744	chromatin interactions
ENSG00000173991	chromatin interactions
ENSG00000167258	chromatin interactions
ENSG00000131771	chromatin interactions

Extended variants
information (count: 96 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:96 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551401816	chr17:37782473-37782474	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs145201208	chr17:37782498-37782499	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs185067293	chr17:37782526-37782527	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs376655579	chr17:37782583-37782584	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs111571178	chr17:37782601-37782602	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs565388216	chr17:37782609-37782610	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs191046388	chr17:37782610-37782611	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs532746416	chr17:37782611-37782612	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs181944246	chr17:37782613-37782614	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs541189910	chr17:37782615-37782616	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs138090539	chr17:37782638-37782639	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs3029545	chr17:37782658-37782659	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs71147367	chr17:37782660-37782661	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs181637774	chr17:37782685-37782686	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs548594430	chr17:37782686-37782687	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs560922454	chr17:37782693-37782694	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs149529378	chr17:37782731-37782732	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs114627644	chr17:37782743-37782744	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs547468196	chr17:37782744-37782745	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs115415353	chr17:37782759-37782760	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs538845865	chr17:37782821-37782822	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs116088419	chr17:37782870-37782871	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs566008726	chr17:37782930-37782931	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs193359	chr17:37782931-37782932	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs536536971	chr17:37782987-37782988	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs555044670	chr17:37783063-37783064	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs576383906	chr17:37783067-37783068	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs77632651	chr17:37783193-37783194	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs186334474	chr17:37783194-37783195	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs189378616	chr17:37783220-37783221	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs34445181	chr17:37783226-37783227	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs79160742	chr17:37783265-37783266	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs34056202	chr17:37783318-37783319	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs574825515	chr17:37783416-37783417	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs542106523	chr17:37783451-37783452	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs182030476	chr17:37783480-37783481	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs531338932	chr17:37783503-37783504	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs368239379	chr17:37783534-37783535	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs77771105	chr17:37783535-37783536	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs532223906	chr17:37783607-37783608	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs547648169	chr17:37783662-37783663	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs367543178	chr17:37783717-37783718	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs565872755	chr17:37783760-37783761	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs536597649	chr17:37783785-37783786	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs3751903	chr17:37783787-37783788	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs377677978	chr17:37783798-37783799	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs569813281	chr17:37783811-37783812	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs537471807	chr17:37783821-37783822	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs558648345	chr17:37783832-37783833	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs188108397	chr17:37783907-37783908	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37775200-37782600	Weak transcription	Lung	lung
2	chr17:37775200-37782800	Weak transcription	Right Atrium	heart
3	chr17:37775400-37782800	Weak transcription	Right Ventricle	heart
4	chr17:37778400-37782600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr17:37778800-37790600	Weak transcription	K562	blood
6	chr17:37779600-37782600	Weak transcription	Fetal Heart	heart
7	chr17:37780200-37783000	Weak transcription	Ovary	ovary
8	chr17:37780800-37783200	Enhancers	Esophagus	oesophagus
9	chr17:37781000-37782600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr17:37781200-37782600	Weak transcription	Fetal Brain Male	brain
11	chr17:37781200-37782600	Bivalent Enhancer	Fetal Stomach	stomach
12	chr17:37781200-37783000	Bivalent Enhancer	Stomach Mucosa	stomach
13	chr17:37781400-37782600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr17:37781400-37782600	Bivalent Enhancer	Fetal Intestine Small	intestine
15	chr17:37781400-37782600	Enhancers	Pancreas	Pancrea
16	chr17:37781400-37782600	Enhancers	HMEC	breast
17	chr17:37781400-37782800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr17:37781400-37783000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr17:37781600-37782600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
20	chr17:37781600-37782600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr17:37781600-37782600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr17:37781600-37782800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr17:37781600-37782800	Bivalent Enhancer	NHEK	skin
24	chr17:37781600-37783000	Bivalent Enhancer	Fetal Muscle Leg	muscle
25	chr17:37781800-37782600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
26	chr17:37781800-37782600	Bivalent Enhancer	Brain Hippocampus Middle	brain
27	chr17:37781800-37783000	Bivalent Enhancer	Fetal Thymus	thymus
28	chr17:37781800-37783000	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
29	chr17:37782000-37782800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
30	chr17:37782000-37782800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
31	chr17:37782000-37783000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr17:37782200-37782600	Bivalent Enhancer	Fetal Intestine Large	intestine
33	chr17:37782200-37782800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
34	chr17:37782200-37783000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
35	chr17:37782200-37783000	Bivalent Enhancer	HepG2	liver
36	chr17:37782400-37782600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr17:37782400-37782600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
38	chr17:37782400-37782600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr17:37782400-37782600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr17:37782400-37782600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr17:37782400-37782600	Bivalent Enhancer	Adipose Nuclei	Adipose
42	chr17:37782400-37782600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
43	chr17:37782400-37782600	Bivalent/Poised TSS	Colonic Mucosa	Colon
44	chr17:37782400-37782800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr17:37782400-37782800	Bivalent Enhancer	Primary T cells from cord blood	blood
46	chr17:37782400-37782800	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr17:37782400-37783000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr17:37782400-37783000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
49	chr17:37782400-37783000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
50	chr17:37782400-37783000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood

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