Variant report

Variant	nsv1021455
Chromosome Location	chr7:26061848-26113797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:26085056-26085433	HepG2	liver:	n/a	n/a
2	ATF1	chr7:26079822-26079973	K562	blood:	n/a	n/a
3	BCLAF1	chr7:26101253-26101643	GM12878	blood:	n/a	n/a
4	BHLHE40	chr7:26101343-26101531	K562	blood:	n/a	n/a
5	BHLHE40	chr7:26101304-26101622	GM12878	blood:	n/a	n/a
6	CBX3	chr7:26092227-26093181	HCT-116	colon:	n/a	n/a
7	CEBPB	chr7:26069633-26069874	Hela-S3	cervix:	n/a	chr7:26069749-26069766
8	CEBPB	chr7:26069589-26069932	IMR90	lung:	n/a	chr7:26069749-26069766
9	CEBPB	chr7:26075034-26075200	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:26069612-26069889	K562	blood:	n/a	chr7:26069749-26069766
11	CEBPB	chr7:26069646-26069817	HepG2	liver:	n/a	chr7:26069749-26069766
12	CEBPB	chr7:26073835-26074025	HepG2	liver:	n/a	chr7:26073872-26073883
13	CEBPB	chr7:26062559-26062893	H1-hESC	embryonic stem cell:	n/a	chr7:26062876-26062889
14	CEBPB	chr7:26113403-26113603	HepG2	liver:	n/a	chr7:26113507-26113518
15	CEBPB	chr7:26061917-26062232	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:26074943-26075230	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:26069585-26069890	A549	lung:	n/a	chr7:26069749-26069766
18	CEBPB	chr7:26073896-26073908	K562	blood:	n/a	n/a
19	CEBPB	chr7:26113425-26113625	H1-hESC	embryonic stem cell:	n/a	chr7:26113507-26113518
20	CEBPB	chr7:26069563-26069832	MCF-7	breast:	n/a	chr7:26069749-26069766
21	CEBPB	chr7:26062034-26062128	K562	blood:	n/a	n/a
22	CEBPB	chr7:26069575-26069932	HepG2	liver:	n/a	chr7:26069749-26069766
23	CHD1	chr7:26101346-26101348	GM12878	blood:	n/a	n/a
24	CTCF	chr7:26100940-26101090	RPTEC	kidney:	n/a	n/a
25	CTCF	chr7:26104520-26104670	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:26101292-26101600	ECC-1	luminal epithelium:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
27	CTCF	chr7:26101355-26101632	A549	lung:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
28	CTCF	chr7:26101378-26101624	SK-N-SH_RA	brain:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
29	CTCF	chr7:26101400-26101550	GM12866	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
30	CTCF	chr7:26101440-26101590	HPAF	blood vessel:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
31	CTCF	chr7:26101680-26101830	GM12871	blood:	n/a	n/a
32	CTCF	chr7:26101420-26101570	GM06990	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
33	CTCF	chr7:26101400-26101550	NHDF-neo	bronchial:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
34	CTCF	chr7:26083800-26083950	GM12864	blood:	n/a	n/a
35	CTCF	chr7:26101325-26101587	A549	lung:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
36	CTCF	chr7:26101440-26101590	HRPEpiC	eye:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
37	CTCF	chr7:26101735-26101813	LNCaP	prostate:	n/a	n/a
38	CTCF	chr7:26101400-26101550	GM12869	blood:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
39	CTCF	chr7:26101440-26101590	BE2_C	brain:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
40	CTCF	chr7:26105405-26105459	GM12878	blood:	n/a	n/a
41	CTCF	chr7:26101400-26101550	HRE	kidney:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
42	CTCF	chr7:26101296-26101616	A549	lung:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
43	CTCF	chr7:26101400-26101550	HCPEpiC	choroid plexus:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
44	CTCF	chr7:26100800-26100950	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:26101420-26101570	HPF	lung:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
46	CTCF	chr7:26101400-26101550	HFF	foreskin:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
47	CTCF	chr7:26101420-26101570	AG09319	gingival:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
48	CTCF	chr7:26100760-26100910	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr7:26101271-26101678	H1-hESC	embryonic stem cell:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494
50	CTCF	chr7:26101380-26101530	Hela-S3	cervix:	n/a	chr7:26101474-26101495 chr7:26101481-26101494 chr7:26101479-26101497 chr7:26101485-26101494

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:26112215-26112265	GM12878	blood:	n/a
2	chr7:26112215-26112265	CMK	blood:	n/a
3	chr7:26112215-26112265	MCF10A-Er-Src	breast:	n/a
4	chr7:26112215-26112265	NT2-D1	testis:	n/a
5	chr7:26112215-26112265	Hepatocyte	liver:	n/a
6	chr7:26112215-26112265	IMR90	lung:	fetal
7	chr7:26112215-26112265	Hela-S3	cervix:	n/a
8	chr7:26112215-26112265	SKMC	muscle:	n/a
9	chr7:26112215-26112265	Caco-2	colon:	n/a
10	chr7:26112215-26112265	AG09309	skin:	n/a
11	chr7:26112215-26112265	AG09319	gingival:	n/a
12	chr7:26112215-26112265	NH-A	brain:	n/a
13	chr7:26112215-26112265	ProgFib	skin:	n/a
14	chr7:26112215-26112265	HCPEpiC	choroid plexus:	n/a
15	chr7:26112215-26112265	ECC-1	luminal epithelium:	n/a
16	chr7:26112215-26112265	BJ	skin:	n/a
17	chr7:26112215-26112265	AG10803	skin:	n/a
18	chr7:26112215-26112265	NHBE	bronchial:	n/a
19	chr7:26112215-26112265	K562	blood:	n/a
20	chr7:26112215-26112265	HEEpiC	esophagus:	n/a
21	chr7:26112215-26112265	GM19239	blood:	n/a
22	chr7:26112215-26112265	HNPCEpiC	eye:	n/a
23	chr7:26112215-26112265	GM06990	blood:	n/a
24	chr7:26112215-26112265	HCT-116	colon:	n/a
25	chr7:26112215-26112265	AG04450	lung:	fetal
26	chr7:26112215-26112265	HEK293	kidney:	embryo
27	chr7:26112215-26112265	HRPEpiC	eye:	n/a
28	chr7:26112215-26112265	HCF	heart:	n/a
29	chr7:26112215-26112265	HAEpiC	amniotic membrane:	n/a
30	chr7:26112215-26112265	AoSMC	blood vessel:	n/a
31	chr7:26112215-26112265	LNCaP	prostate:	n/a
32	chr7:26112215-26112265	AG04449	skin:	fetal
33	chr7:26112215-26112265	GM12891	blood:	n/a
34	chr7:26112215-26112265	MCF-7	breast:	n/a
35	chr7:26112215-26112265	A549	lung:	n/a
36	chr7:26112215-26112265	SK-N-MC	brain:	n/a
37	chr7:26112215-26112265	ovcar-3	ovarian:	n/a
38	chr7:26112215-26112265	HL-60	blood:	n/a
39	chr7:26112215-26112265	GM12892	blood:	n/a
40	chr7:26112215-26112265	HMEC	breast:	n/a
41	chr7:26112215-26112265	SK-N-SH	brain:	n/a
42	chr7:26112215-26112265	SK-N-SH_RA	brain:	n/a
43	chr7:26112215-26112265	PANC-1	pancreas:	n/a
44	chr7:26112215-26112265	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:26112215-26112265	Jurkat	blood:	n/a
46	chr7:26112215-26112265	HIPEpiC	eye:	n/a
47	chr7:26112215-26112265	H1-hESC	embryonic stem cell:	embryo
48	chr7:26112215-26112265	HepG2	liver:	n/a
49	chr7:26112215-26112265	HUVEC	blood vessel:	n/a
50	chr7:26112215-26112265	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:26107192..26109459-chr7:26238936..26241371,3	MCF-7	breast:
2	chr7:26100956..26102621-chr7:26104473..26107390,2	K562	blood:
3	chr7:25989483..25991459-chr7:26105625..26107540,2	K562	blood:
4	chr7:25935063..25935626-chr7:26100854..26101524,2	K562	blood:
5	chr7:25990207..25991830-chr7:26094178..26097069,2	MCF-7	breast:
6	chr6:8102268..8102945-chr7:26101163..26101679,2	HCT-116	colon:
7	chr7:26035423..26036364-chr7:26100860..26101483,2	MCF-7	breast:
8	chr7:25934813..25935616-chr7:26101041..26101955,3	MCF-7	breast:
9	chr7:26102797..26105180-chr7:26108229..26111038,2	K562	blood:
10	chr7:26109451..26111180-chr7:26113272..26116179,2	MCF-7	breast:
11	chr7:26109451..26111180-chr7:26113272..26116179,2	MCF-7	breast:
12	chr7:26111175..26113730-chr7:26115998..26118801,2	MCF-7	breast:
13	chr7:25990709..25992651-chr7:26072086..26075062,2	MCF-7	breast:
14	chr7:26100956..26102621-chr7:26104473..26107390,2	K562	blood:
15	chr7:26044346..26047065-chr7:26096452..26098804,2	MCF-7	breast:
16	chr7:26102797..26105180-chr7:26108229..26111038,2	K562	blood:
17	chr7:25989811..25992726-chr7:26096097..26097704,2	MCF-7	breast:
18	chr7:26035382..26036550-chr7:26101032..26101905,6	MCF-7	breast:
19	chr7:26112064..26114800-chr7:26118641..26120981,2	K562	blood:
20	chr7:26110644..26115952-chr7:26225900..26230055,7	K562	blood:
21	chr7:26108042..26110669-chr7:26111318..26113129,2	K562	blood:
22	chr7:26096714..26102069-chr7:26240159..26243560,6	MCF-7	breast:
23	chr7:26111985..26114950-chr7:26225900..26229450,4	K562	blood:
24	chr7:26108042..26110669-chr7:26111318..26113129,2	K562	blood:
25	chr7:26093464..26095409-chr7:26225078..26227432,2	K562	blood:
26	chr7:25990246..25992488-chr7:26100564..26102799,3	MCF-7	breast:
27	chr7:26108059..26110541-chr7:26114751..26116494,2	K562	blood:
28	chr7:26076616..26078985-chr7:26226158..26229090,2	K562	blood:
29	chr7:26112324..26114738-chr7:26221263..26223725,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPA2B1-3	chr7:26097832-26098434	NONHSAT119611
2	lnc-HNRNPA2B1-2	chr7:26109126-26109421	XLOC_006385
3	lnc-HNRNPA2B1-3	chr7:26101163-26101262	XLOC_006384
4	lnc-HNRNPA2B1-3	chr7:26097439-26098434	XLOC_006384
5	lnc-HNRNPA2B1-2	chr7:26109126-26109421	XLOC_006385
6	lnc-HNRNPA2B1-9	chr7:26078832-26078858	l_3383_chr7:26064190-26136923_testes
7	lnc-HNRNPA2B1-9	chr7:26064191-26064959	l_3383_chr7:26064190-26136923_testes
8	lnc-HNRNPA2B1-9	chr7:26075647-26075946	l_3383_chr7:26064190-26136923_testes
9	lnc-HNRNPA2B1-9	chr7:26067688-26067844	l_3383_chr7:26064190-26136923_testes
10	lnc-HNRNPA2B1-2	chr7:26112307-26112316	XLOC_006385

Variant related genes	Relation type
ENSG00000266430	TF binding region
ENSG00000266430	CpG island
ENSG00000265818	chromatin interactions
ENSG00000199085	chromatin interactions
ENSG00000124802	chromatin interactions
ENSG00000050344	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000122565	chromatin interactions
LRRFIP1	miRNA target sites
EP300	miRNA target sites
ZNF700	miRNA target sites
ZEB1	miRNA target sites

Extended variants
information (count: 1316 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180951769	chr7:26061849-26061850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs117029591	chr7:26061851-26061852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551068673	chr7:26061918-26061919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570666606	chr7:26061963-26061964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533718063	chr7:26061988-26061989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533191574	chr7:26061990-26061991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546473052	chr7:26061993-26061994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566783974	chr7:26061998-26061999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144337528	chr7:26062015-26062016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567705274	chr7:26062044-26062045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148384802	chr7:26062047-26062048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185180646	chr7:26062057-26062058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537550510	chr7:26062059-26062060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142232532	chr7:26062071-26062072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577656839	chr7:26062072-26062073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146384062	chr7:26062077-26062078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139538088	chr7:26062091-26062092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573518013	chr7:26062105-26062106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189393638	chr7:26062108-26062109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181388588	chr7:26062109-26062110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375912784	chr7:26062161-26062162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558494926	chr7:26062188-26062189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575462966	chr7:26062221-26062222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544605784	chr7:26062261-26062262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564647468	chr7:26062262-26062263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186545907	chr7:26062279-26062280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6968009	chr7:26062280-26062281	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs80220370	chr7:26062327-26062328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574474982	chr7:26062370-26062371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77199187	chr7:26062397-26062398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370972659	chr7:26062398-26062399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548817240	chr7:26062412-26062413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116829653	chr7:26062520-26062521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537488741	chr7:26062541-26062542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560145659	chr7:26062566-26062567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75102925	chr7:26062577-26062578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571348894	chr7:26062642-26062643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533637379	chr7:26062676-26062677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372078953	chr7:26062699-26062700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376936313	chr7:26062760-26062761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573331346	chr7:26062776-26062777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536161905	chr7:26062866-26062867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191756769	chr7:26062880-26062881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576001913	chr7:26062896-26062897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183505351	chr7:26062899-26062900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553237038	chr7:26062965-26062966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564306270	chr7:26062994-26062995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs578059556	chr7:26062995-26062996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs61692361	chr7:26064193-26064194	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs538533475	chr7:26064232-26064233	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Breast cancer	18852474	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26060800-26063000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr7:26061200-26062400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:26061200-26063000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:26061400-26062200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr7:26061400-26062800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr7:26061400-26063000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:26061600-26063000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr7:26061800-26062200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:26061800-26063000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:26062200-26062400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:26062200-26062600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr7:26062400-26063000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:26062600-26062800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:26066000-26066400	Active TSS	H9 Cell Line	embryonic stem cell
15	chr7:26069800-26070200	Enhancers	HepG2	liver
16	chr7:26074000-26075600	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr7:26074200-26075400	Enhancers	Duodenum Mucosa	Duodenum
18	chr7:26074200-26075600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr7:26074400-26075400	Enhancers	Fetal Intestine Small	intestine
20	chr7:26074400-26075600	Enhancers	Fetal Intestine Large	intestine
21	chr7:26075600-26077800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr7:26077600-26077800	Enhancers	Primary T cells from cord blood	blood
23	chr7:26077600-26077800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:26077600-26078800	Enhancers	Fetal Thymus	thymus
25	chr7:26077800-26078000	Flanking Active TSS	Primary T cells from cord blood	blood
26	chr7:26077800-26078000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr7:26077800-26078000	Flanking Active TSS	Thymus	Thymus
28	chr7:26077800-26078000	Bivalent Enhancer	NHEK	skin
29	chr7:26077800-26078200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr7:26077800-26078200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr7:26077800-26078600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:26078000-26078200	Enhancers	Duodenum Smooth Muscle	Duodenum
33	chr7:26078000-26078400	Bivalent/Poised TSS	Sigmoid Colon	Sigmoid Colon
34	chr7:26078000-26078600	Enhancers	Fetal Heart	heart
35	chr7:26078000-26078600	Active TSS	Right Atrium	heart
36	chr7:26078000-26078800	Active TSS	Primary T cells from cord blood	blood
37	chr7:26078200-26078400	Enhancers	Pancreas	Pancrea
38	chr7:26078200-26078600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr7:26078200-26078600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr7:26078200-26078600	Enhancers	Aorta	Aorta
41	chr7:26078200-26078600	Enhancers	Fetal Lung	lung
42	chr7:26078400-26079800	Weak transcription	Pancreas	Pancrea
43	chr7:26078600-26078800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:26078600-26078800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
45	chr7:26079400-26079600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:26079800-26080000	Enhancers	Pancreas	Pancrea
47	chr7:26080000-26088200	Weak transcription	Pancreas	Pancrea
48	chr7:26081600-26086200	Weak transcription	Fetal Intestine Small	intestine
49	chr7:26083000-26083800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr7:26083400-26083600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood

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