Variant report

Variant	nsv437559
Chromosome Location	chr7:97361784-97383320
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:366)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:97362075-97362381	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:97362622-97363312	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr7:97371177-97371373	K562	blood:	n/a	n/a
4	CEBPB	chr7:97383227-97383406	HepG2	liver:	n/a	n/a
5	CEBPB	chr7:97380882-97381312	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr7:97380928-97381253	ECC-1	luminal epithelium:	n/a	n/a
7	CHD2	chr7:97362241-97362510	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr7:97361122-97363337	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr7:97362097-97362172	Fibrobl	skin:	n/a	n/a
10	E2F4	chr7:97381138-97381376	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr7:97364849-97365233	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F6	chr7:97360888-97361840	H1-hESC	embryonic stem cell:	n/a	chr7:97361420-97361430 chr7:97361529-97361539
13	E2F6	chr7:97361951-97363055	H1-hESC	embryonic stem cell:	n/a	n/a
14	E2F6	chr7:97362026-97363014	H1-hESC	embryonic stem cell:	n/a	n/a
15	EP300	chr7:97366118-97366135	GM12878	blood:	n/a	n/a
16	FOXA1	chr7:97381566-97381784	HepG2	liver:	n/a	n/a
17	GATA3	chr7:97383056-97383175	SH-SY5Y	brain:	n/a	n/a
18	GTF2F1	chr7:97362361-97362584	H1-hESC	embryonic stem cell:	n/a	n/a
19	IRF1	chr7:97378431-97378504	K562	blood:	n/a	n/a
20	JUN	chr7:97364572-97364624	HepG2	liver:	n/a	chr7:97364574-97364587 chr7:97364578-97364587
21	JUND	chr7:97362152-97362202	H1-hESC	embryonic stem cell:	n/a	n/a
22	JUND	chr7:97364451-97364744	HepG2	liver:	n/a	chr7:97364578-97364587
23	KAP1	chr7:97365428-97365628	K562	blood:	n/a	n/a
24	MAFF	chr7:97377910-97378091	K562	blood:	n/a	n/a
25	MAFF	chr7:97377825-97378141	HepG2	liver:	n/a	n/a
26	MAFK	chr7:97367943-97368110	HepG2	liver:	n/a	chr7:97368040-97368051 chr7:97368041-97368052 chr7:97368039-97368053 chr7:97368041-97368052 chr7:97368036-97368052
27	MAFK	chr7:97377854-97378102	HepG2	liver:	n/a	n/a
28	MAFK	chr7:97377846-97378171	IMR90	lung:	n/a	n/a
29	MAFK	chr7:97377955-97378049	Hela-S3	cervix:	n/a	n/a
30	MAFK	chr7:97377916-97378082	K562	blood:	n/a	n/a
31	MAFK	chr7:97377812-97378158	HepG2	liver:	n/a	n/a
32	MAX	chr7:97362378-97362966	ECC-1	luminal epithelium:	n/a	n/a
33	MAX	chr7:97361897-97363062	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAX	chr7:97362352-97362855	H1-hESC	embryonic stem cell:	n/a	n/a
35	MAX	chr7:97362258-97362965	ECC-1	luminal epithelium:	n/a	n/a
36	MAX	chr7:97361949-97363399	H1-hESC	embryonic stem cell:	n/a	n/a
37	MXI1	chr7:97362425-97362678	H1-hESC	embryonic stem cell:	n/a	n/a
38	MYC	chr7:97362031-97362143	MCF-7	breast:	n/a	n/a
39	MYC	chr7:97372451-97372521	MCF10A-Er-Src	breast:	n/a	n/a
40	MYC	chr7:97362136-97362147	MCF-7	breast:	n/a	n/a
41	MYC	chr7:97362149-97362170	MCF-7	breast:	n/a	n/a
42	NFIC	chr7:97380724-97381406	ECC-1	luminal epithelium:	n/a	n/a
43	NFIC	chr7:97380819-97381328	ECC-1	luminal epithelium:	n/a	n/a
44	NRF1	chr7:97369775-97369877	HepG2	liver:	n/a	n/a
45	POLR2A	chr7:97360893-97361833	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr7:97382565-97382577	GM12878	blood:	n/a	n/a
47	POLR2A	chr7:97360738-97363977	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr7:97370013-97370439	H1-neurons	neurons:	n/a	n/a
49	POLR2A	chr7:97362390-97362495	MCF-7	breast:	n/a	n/a
50	POLR2A	chr7:97360795-97364005	H1-neurons	neurons:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97362308-97362358	AoSMC	blood vessel:	n/a
2	chr7:97362705-97362755	GM12878	blood:	n/a
3	chr7:97361759-97361809	HRE	kidney:	n/a
4	chr7:97362705-97362755	HAEpiC	amniotic membrane:	n/a
5	chr7:97366840-97366890	HCPEpiC	choroid plexus:	n/a
6	chr7:97361759-97361809	PrEC	prostate:	n/a
7	chr7:97363080-97363130	HEK293	kidney:	embryo
8	chr7:97363080-97363130	HMEC	breast:	n/a
9	chr7:97363080-97363130	NHBE	bronchial:	n/a
10	chr7:97366840-97366890	IMR90	lung:	fetal
11	chr7:97366840-97366890	AG09319	gingival:	n/a
12	chr7:97362705-97362755	SK-N-SH	brain:	n/a
13	chr7:97362308-97362358	HCF	heart:	n/a
14	chr7:97361759-97361809	AG04449	skin:	fetal
15	chr7:97362308-97362358	AG04450	lung:	fetal
16	chr7:97362523-97362573	Caco-2	colon:	n/a
17	chr7:97362523-97362573	NHDF-neo	bronchial:	n/a
18	chr7:97362523-97362573	H1-hESC	embryonic stem cell:	embryo
19	chr7:97362308-97362358	SK-N-SH_RA	brain:	n/a
20	chr7:97362308-97362358	A549	lung:	n/a
21	chr7:97363080-97363130	HCPEpiC	choroid plexus:	n/a
22	chr7:97362523-97362573	AoSMC	blood vessel:	n/a
23	chr7:97361759-97361809	MCF10A-Er-Src	breast:	n/a
24	chr7:97362705-97362755	HUVEC	blood vessel:	n/a
25	chr7:97362523-97362573	HCM	heart:	n/a
26	chr7:97366840-97366890	T-47D	breast:	n/a
27	chr7:97362308-97362358	BJ	skin:	n/a
28	chr7:97361759-97361809	GM12891	blood:	n/a
29	chr7:97362523-97362573	GM12878	blood:	n/a
30	chr7:97366840-97366890	NT2-D1	testis:	n/a
31	chr7:97362308-97362358	HRCEpiC	kidney:	n/a
32	chr7:97362523-97362573	LNCaP	prostate:	n/a
33	chr7:97366840-97366890	HEEpiC	esophagus:	n/a
34	chr7:97363080-97363130	PFSK-1	brain:	n/a
35	chr7:97366840-97366890	HUVEC	blood vessel:	n/a
36	chr7:97362705-97362755	BE2_C	brain:	n/a
37	chr7:97366840-97366890	GM12891	blood:	n/a
38	chr7:97362705-97362755	NB4	blood:	n/a
39	chr7:97363080-97363130	AG04449	skin:	fetal
40	chr7:97362523-97362573	NH-A	brain:	n/a
41	chr7:97362523-97362573	PrEC	prostate:	n/a
42	chr7:97363080-97363130	GM12892	blood:	n/a
43	chr7:97362523-97362573	AG04450	lung:	fetal
44	chr7:97366840-97366890	BE2_C	brain:	n/a
45	chr7:97366840-97366890	PFSK-1	brain:	n/a
46	chr7:97363080-97363130	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:97362705-97362755	SKMC	muscle:	n/a
48	chr7:97362705-97362755	AG09309	skin:	n/a
49	chr7:97361759-97361809	HCM	heart:	n/a
50	chr7:97362705-97362755	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:97367330..97369358-chr7:97372378..97374711,2	K562	blood:
2	chr7:97372375..97375018-chr7:97378274..97380975,3	K562	blood:
3	chr7:97367998..97369892-chr7:97372461..97374150,2	MCF-7	breast:
4	chr7:97367330..97369358-chr7:97372378..97374711,2	K562	blood:
5	chr7:97372375..97375018-chr7:97378274..97380975,3	K562	blood:
6	chr7:97383052..97385272-chr7:97499637..97501845,2	K562	blood:
7	chr7:97367998..97369892-chr7:97372461..97374150,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TAC1	hsa-miR-320a	chr7:97369242-97369263
2	TAC1	hsa-miR-130a-3p	chr7:97369284-97369306

Variant related genes	Relation type
TAC1	TF binding region
TAC1	CpG island
ENSG00000070669	chromatin interactions

Extended variants
information (count: 138 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:138 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2072100	chr7:97361784-97361785	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs6971011	chr7:97361844-97361845	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs188969055	chr7:97361848-97361849	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs6971427	chr7:97361868-97361869	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs369815201	chr7:97361881-97361882	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569523099	chr7:97361898-97361899	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs373923390	chr7:97361902-97361903	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs530629112	chr7:97361910-97361911	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs201382322	chr7:97361936-97361937	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs149261667	chr7:97361951-97361952	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs376650997	chr7:97361954-97361955	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs143780517	chr7:97361960-97361961	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs534052563	chr7:97362035-97362036	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs200332107	chr7:97362052-97362053	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs202015230	chr7:97362056-97362057	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs545784830	chr7:97362090-97362091	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs34707813	chr7:97362092-97362093	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs562688887	chr7:97362097-97362098	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs576265370	chr7:97362114-97362115	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs541693148	chr7:97362161-97362162	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs113581170	chr7:97362264-97362265	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs527454548	chr7:97362284-97362285	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs2072099	chr7:97362335-97362336	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs564129425	chr7:97362350-97362351	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs532997366	chr7:97362383-97362384	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs530947761	chr7:97362421-97362422	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs549744627	chr7:97362425-97362426	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs569476563	chr7:97362435-97362436	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs369190197	chr7:97362436-97362437	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs569732702	chr7:97362622-97362623	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs141117557	chr7:97362630-97362631	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535425812	chr7:97362652-97362653	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs568322293	chr7:97362657-97362658	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs534088886	chr7:97362668-97362669	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs62499561	chr7:97362714-97362715	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs576923960	chr7:97362785-97362786	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs539478451	chr7:97362854-97362855	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs556506847	chr7:97362889-97362890	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs576323666	chr7:97362902-97362903	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs537118160	chr7:97362925-97362926	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs2189306	chr7:97362937-97362938	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs552916415	chr7:97362950-97362951	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs181650984	chr7:97362953-97362954	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs541216858	chr7:97362957-97362958	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs564214397	chr7:97362959-97362960	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs533035697	chr7:97362971-97362972	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs150265957	chr7:97362982-97362983	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs371142680	chr7:97362987-97362988	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs375904849	chr7:97362999-97363000	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs370538589	chr7:97363040-97363041	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97360600-97363200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr7:97360600-97363600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
3	chr7:97360600-97363600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
4	chr7:97360800-97361800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
5	chr7:97360800-97363200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
6	chr7:97360800-97363200	Bivalent Enhancer	Liver	Liver
7	chr7:97360800-97363400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
8	chr7:97360800-97363400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:97360800-97363400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:97360800-97363600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
11	chr7:97361000-97362000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:97361000-97362000	Bivalent Enhancer	Esophagus	oesophagus
13	chr7:97361000-97362000	Enhancers	Gastric	stomach
14	chr7:97361000-97362000	Bivalent Enhancer	Spleen	Spleen
15	chr7:97361000-97362200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:97361000-97362400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
17	chr7:97361000-97362400	Bivalent Enhancer	Fetal Stomach	stomach
18	chr7:97361000-97362600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:97361000-97362800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
20	chr7:97361000-97363000	Bivalent Enhancer	Lung	lung
21	chr7:97361000-97363200	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:97361000-97363200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:97361000-97363200	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
24	chr7:97361000-97363400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
25	chr7:97361000-97363400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
26	chr7:97361000-97363600	Bivalent Enhancer	Fetal Intestine Large	intestine
27	chr7:97361200-97361800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr7:97361200-97361800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
29	chr7:97361200-97361800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
30	chr7:97361200-97362200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
31	chr7:97361200-97362200	Bivalent/Poised TSS	Colonic Mucosa	Colon
32	chr7:97361200-97362200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
33	chr7:97361200-97362600	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:97361200-97362600	Bivalent Enhancer	Fetal Brain Male	brain
35	chr7:97361200-97362800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
36	chr7:97361200-97363400	Bivalent Enhancer	Left Ventricle	heart
37	chr7:97361200-97363600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
38	chr7:97361400-97362000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:97361400-97362200	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr7:97361400-97362200	Bivalent Enhancer	Psoas Muscle	Psoas
41	chr7:97361400-97362400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:97361400-97362400	Bivalent Enhancer	Brain Substantia Nigra	brain
43	chr7:97361400-97362600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:97361400-97362600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:97361400-97362600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
46	chr7:97361400-97362600	Bivalent Enhancer	Fetal Lung	lung
47	chr7:97361400-97363200	Bivalent Enhancer	Placenta	Placenta
48	chr7:97361600-97361800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:97361600-97361800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr7:97361600-97361800	Bivalent/Poised TSS	Fetal Brain Female	brain

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