Variant report

Variant	nsv967466
Chromosome Location	chr7:96630712-96634026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:916)
Chromatin interactive
region (count:1)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:96631241-96631977	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr7:96630782-96630918	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTBP2	chr7:96631025-96633671	H1-hESC	embryonic stem cell:	n/a	n/a
4	HDAC2	chr7:96631266-96631546	H1-hESC	embryonic stem cell:	n/a	n/a
5	HDAC2	chr7:96631100-96631625	H1-hESC	embryonic stem cell:	n/a	n/a
6	JUND	chr7:96631387-96631504	H1-hESC	embryonic stem cell:	n/a	n/a
7	MAX	chr7:96631198-96631392	H1-hESC	embryonic stem cell:	n/a	n/a
8	MXI1	chr7:96633643-96636712	SK-N-SH	brain:	n/a	n/a
9	POLR2A	chr7:96629453-96654775	H1-neurons	neurons:	n/a	n/a
10	POLR2A	chr7:96631757-96631810	MCF-7	breast:	n/a	n/a
11	POLR2A	chr7:96631969-96631986	MCF-7	breast:	n/a	n/a
12	POLR2A	chr7:96632983-96633941	K562	blood:	n/a	n/a
13	POLR2A	chr7:96633203-96633224	HepG2	liver:	n/a	n/a
14	POLR2A	chr7:96628026-96649797	H1-neurons	neurons:	n/a	n/a
15	POLR2A	chr7:96632722-96632737	HepG2	liver:	n/a	n/a
16	POLR2A	chr7:96634023-96634075	MCF10A-Er-Src	breast:	n/a	n/a
17	REST	chr7:96633990-96635799	H1-neurons	neurons:	n/a	chr7:96635204-96635222 chr7:96634677-96634690
18	REST	chr7:96624507-96656402	H1-neurons	neurons:	n/a	chr7:96626900-96626913 chr7:96628274-96628287 chr7:96653242-96653252 chr7:96638441-96638449 chr7:96644780-96644790 chr7:96627625-96627635 chr7:96628223-96628236 chr7:96655951-96655958 chr7:96625513-96625526 chr7:96635204-96635222 chr7:96634677-96634690 chr7:96628302-96628315 chr7:96652071-96652084 chr7:96650634-96650647 chr7:96628298-96628318 chr7:96628298-96628318
19	REST	chr7:96630994-96633107	H1-neurons	neurons:	n/a	n/a
20	RFX5	chr7:96633626-96636275	SK-N-SH	brain:	n/a	n/a
21	SP1	chr7:96631119-96631646	H1-hESC	embryonic stem cell:	n/a	chr7:96631400-96631414
22	SP1	chr7:96630931-96631732	H1-hESC	embryonic stem cell:	n/a	chr7:96631400-96631414
23	SUZ12	chr7:96630535-96633649	H1-hESC	embryonic stem cell:	n/a	n/a
24	SUZ12	chr7:96631319-96633614	NT2-D1	testis:	n/a	n/a
25	TAF1	chr7:96632204-96632950	H1-neurons	neurons:	n/a	n/a
26	TAF1	chr7:96633311-96633766	H1-neurons	neurons:	n/a	n/a
27	TAF1	chr7:96631262-96632899	H1-neurons	neurons:	n/a	n/a
28	TAF1	chr7:96632906-96633296	H1-neurons	neurons:	n/a	n/a
29	TBP	chr7:96631161-96631718	H1-hESC	embryonic stem cell:	n/a	n/a
30	TCF12	chr7:96630968-96631222	H1-hESC	embryonic stem cell:	n/a	chr7:96631078-96631087
31	TCF12	chr7:96631293-96631561	H1-hESC	embryonic stem cell:	n/a	n/a
32	TCF12	chr7:96633045-96633215	H1-hESC	embryonic stem cell:	n/a	n/a
33	TCF12	chr7:96631037-96631620	H1-hESC	embryonic stem cell:	n/a	chr7:96631078-96631087
34	ZNF143	chr7:96631084-96631742	H1-hESC	embryonic stem cell:	n/a	chr7:96631486-96631496 chr7:96631487-96631497

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:96633530-96633580	PFSK-1	brain:	n/a
2	chr7:96633530-96633580	PFSK-1	brain:	n/a
3	chr7:96631902-96631952	AG04449	skin:	fetal
4	chr7:96632460-96632510	RPTEC	kidney:	n/a
5	chr7:96633311-96633361	K562	blood:	n/a
6	chr7:96632841-96632891	LNCaP	prostate:	n/a
7	chr7:96633530-96633580	AoSMC	blood vessel:	n/a
8	chr7:96632777-96632827	HEK293	kidney:	embryo
9	chr7:96631089-96631139	AG04450	lung:	fetal
10	chr7:96632635-96632685	PrEC	prostate:	n/a
11	chr7:96633726-96633776	ProgFib	skin:	n/a
12	chr7:96632841-96632891	NH-A	brain:	n/a
13	chr7:96632460-96632510	T-47D	breast:	n/a
14	chr7:96632841-96632891	HCT-116	colon:	n/a
15	chr7:96633530-96633580	PANC-1	pancreas:	n/a
16	chr7:96633060-96633110	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:96633530-96633580	HCM	heart:	n/a
18	chr7:96631089-96631139	MCF-7	breast:	n/a
19	chr7:96633311-96633361	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:96633311-96633361	HRPEpiC	eye:	n/a
21	chr7:96633530-96633580	NT2-D1	testis:	n/a
22	chr7:96631902-96631952	AG09309	skin:	n/a
23	chr7:96631680-96631730	PANC-1	pancreas:	n/a
24	chr7:96632294-96632344	NT2-D1	testis:	n/a
25	chr7:96632460-96632510	NB4	blood:	n/a
26	chr7:96632294-96632344	HCT-116	colon:	n/a
27	chr7:96633631-96633681	HCPEpiC	choroid plexus:	n/a
28	chr7:96631680-96631730	HCM	heart:	n/a
29	chr7:96631089-96631139	T-47D	breast:	n/a
30	chr7:96633631-96633681	HCF	heart:	n/a
31	chr7:96633060-96633110	IMR90	lung:	fetal
32	chr7:96632841-96632891	Hepatocyte	liver:	n/a
33	chr7:96633530-96633580	IMR90	lung:	fetal
34	chr7:96631580-96631630	AG09309	skin:	n/a
35	chr7:96632294-96632344	MCF10A-Er-Src	breast:	n/a
36	chr7:96633311-96633361	ECC-1	luminal epithelium:	n/a
37	chr7:96633726-96633776	HRE	kidney:	n/a
38	chr7:96632635-96632685	SKMC	muscle:	n/a
39	chr7:96631384-96631434	GM06990	blood:	n/a
40	chr7:96631680-96631730	GM06990	blood:	n/a
41	chr7:96633060-96633110	GM12878	blood:	n/a
42	chr7:96631089-96631139	Hela-S3	cervix:	n/a
43	chr7:96631384-96631434	GM12878	blood:	n/a
44	chr7:96632294-96632344	SK-N-SH_RA	brain:	n/a
45	chr7:96631680-96631730	A549	lung:	n/a
46	chr7:96632460-96632510	U87	brain:	n/a
47	chr7:96631580-96631630	U87	brain:	n/a
48	chr7:96631089-96631139	HepG2	liver:	n/a
49	chr7:96633726-96633776	MCF10A-Er-Src	breast:	n/a
50	chr7:96631384-96631434	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:96624402..96628038-chr7:96629326..96632472,4	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLX5-2	chr7:96632821-96633610	ENSG00000231764.4
2	lnc-DLX6-1	chr7:96633915-96634172	NONHSAT122136
3	lnc-DLX5-2	chr7:96632821-96633610	ENSG00000231764.2

No data

Variant related genes	Relation type
DLX6	TF binding region
DLX6-AS1	TF binding region
DLX6	CpG island
DLX6-AS1	CpG island

Extended variants
information (count: 95 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573774017	chr7:96630774-96630775	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs576317653	chr7:96630814-96630815	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536200772	chr7:96630826-96630827	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs537129915	chr7:96630838-96630839	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs553236930	chr7:96630861-96630862	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs368454715	chr7:96630892-96630893	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs73404521	chr7:96630904-96630905	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs545039727	chr7:96630945-96630946	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs564845137	chr7:96630998-96630999	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs112946366	chr7:96631024-96631025	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs77569000	chr7:96631031-96631032	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs150628729	chr7:96631046-96631047	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs529485617	chr7:96631076-96631077	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs549263539	chr7:96631077-96631078	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs369440676	chr7:96631115-96631116	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs559628221	chr7:96631155-96631156	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs528733713	chr7:96631188-96631189	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551391293	chr7:96631205-96631206	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs571292373	chr7:96631220-96631221	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs2240295	chr7:96631235-96631236	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
21	rs551052871	chr7:96631299-96631300	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs555219559	chr7:96631300-96631301	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs567608649	chr7:96631310-96631311	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs536457719	chr7:96631319-96631320	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs552860012	chr7:96631331-96631332	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs377309478	chr7:96631435-96631436	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs573574641	chr7:96631495-96631496	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs540632335	chr7:96631526-96631527	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs370674302	chr7:96631534-96631535	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs538911242	chr7:96631538-96631539	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs73708837	chr7:96631539-96631540	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs575299675	chr7:96631558-96631559	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs544023665	chr7:96631565-96631566	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs140081825	chr7:96631657-96631658	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs574408760	chr7:96631690-96631691	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs74570108	chr7:96631703-96631704	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs559500400	chr7:96631774-96631775	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs560857025	chr7:96631797-96631798	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs545287583	chr7:96631890-96631891	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs564985076	chr7:96631975-96631976	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs143788731	chr7:96632015-96632016	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs550661923	chr7:96632049-96632050	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577889774	chr7:96632066-96632067	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs545311727	chr7:96632098-96632099	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs78006708	chr7:96632151-96632152	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs540291626	chr7:96632168-96632169	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs530111316	chr7:96632291-96632292	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs34246189	chr7:96632301-96632302	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs372694910	chr7:96632313-96632314	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs546842246	chr7:96632371-96632372	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
abnormal development	18461090	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96625000-96644000	Bivalent/Poised TSS	Fetal Brain Female	brain
2	chr7:96625200-96631800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:96626000-96633800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:96626200-96633200	Weak transcription	Pancreas	Pancrea
5	chr7:96627400-96634800	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr7:96627800-96631000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr7:96628000-96631000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
8	chr7:96628000-96643200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
9	chr7:96628400-96634000	Weak transcription	HepG2	liver
10	chr7:96629800-96631000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
11	chr7:96629800-96631600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr7:96630000-96631000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr7:96630000-96631600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:96630000-96632000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
15	chr7:96630000-96632800	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
16	chr7:96630200-96632000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:96630400-96630800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
18	chr7:96630400-96631200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
19	chr7:96630400-96631600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
20	chr7:96630600-96631400	Bivalent Enhancer	Placenta	Placenta
21	chr7:96630600-96631800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:96630600-96632200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:96630600-96632600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:96630800-96631000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
25	chr7:96631000-96631200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
26	chr7:96631000-96631200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
27	chr7:96631000-96631200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
28	chr7:96631000-96631200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
29	chr7:96631000-96632000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
30	chr7:96631000-96632000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
31	chr7:96631200-96631400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
32	chr7:96631200-96631400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
33	chr7:96631200-96631400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
34	chr7:96631200-96631600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr7:96631200-96634200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
36	chr7:96631400-96631600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
37	chr7:96631400-96631800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
38	chr7:96631400-96632000	Flanking Bivalent TSS/Enh	Placenta	Placenta
39	chr7:96631400-96632400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
40	chr7:96631600-96631800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:96631600-96631800	Bivalent Enhancer	Colon Smooth Muscle	Colon
42	chr7:96631600-96632000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
43	chr7:96631600-96632000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
44	chr7:96631600-96632000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
45	chr7:96631600-96632000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
46	chr7:96631600-96632200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:96631600-96633200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr7:96631600-96633800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
49	chr7:96631800-96632000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:96631800-96632000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell

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