Variant report

Variant	nsv1023477
Chromosome Location	chr7:3185993-3224102
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:604)
CpG islands
(count:735)
Chromatin interactive
region (count:22)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3203948-3204296	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3186430-3186815	K562	blood:	n/a	n/a
3	ARID3A	chr7:3221006-3221355	HepG2	liver:	n/a	n/a
4	BACH1	chr7:3186456-3186829	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:3186439-3186846	K562	blood:	n/a	n/a
6	BATF	chr7:3192746-3193040	GM12878	blood:	n/a	chr7:3192912-3192923
7	BCL11A	chr7:3192760-3193070	GM12878	blood:	n/a	chr7:3192915-3192924 chr7:3192916-3192925
8	BCL11A	chr7:3192749-3193044	GM12878	blood:	n/a	chr7:3192915-3192924 chr7:3192916-3192925
9	BCL3	chr7:3221093-3221491	GM12878	blood:	n/a	n/a
10	BCL3	chr7:3220998-3221446	GM12878	blood:	n/a	n/a
11	BCLAF1	chr7:3194415-3194858	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:3186430-3186949	K562	blood:	n/a	n/a
13	BHLHE40	chr7:3216612-3216813	K562	blood:	n/a	n/a
14	BRCA1	chr7:3191484-3191701	GM12878	blood:	n/a	n/a
15	CCNT2	chr7:3186464-3186878	K562	blood:	n/a	chr7:3186464-3186473
16	CEBPB	chr7:3215918-3216112	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:3186370-3186914	A549	lung:	n/a	n/a
18	CEBPB	chr7:3220965-3221379	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:3186997-3187012	K562	blood:	n/a	n/a
20	CEBPB	chr7:3221076-3221267	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:3186407-3186786	K562	blood:	n/a	n/a
22	CHD2	chr7:3188625-3188930	K562	blood:	n/a	n/a
23	CHD2	chr7:3191548-3191696	GM12878	blood:	n/a	n/a
24	CHD2	chr7:3191510-3191704	K562	blood:	n/a	n/a
25	CHD2	chr7:3221032-3221442	HepG2	liver:	n/a	n/a
26	CTCF	chr7:3194495-3194801	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:3194692-3194732	GM12892	blood:	n/a	n/a
28	CTCF	chr7:3202040-3202190	HCM	heart:	n/a	n/a
29	CTCF	chr7:3202060-3202210	GM12866	blood:	n/a	n/a
30	CTCF	chr7:3194600-3194750	NHEK	skin:	n/a	n/a
31	CTCF	chr7:3201860-3202010	GM06990	blood:	n/a	n/a
32	CTCF	chr7:3202042-3202172	GM12892	blood:	n/a	n/a
33	CTCF	chr7:3201980-3202130	BE2_C	brain:	n/a	chr7:3202038-3202045
34	CTCF	chr7:3194200-3194350	AG10803	skin:	n/a	n/a
35	CTCF	chr7:3194680-3194830	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr7:3202020-3202170	Hela-S3	cervix:	n/a	chr7:3202038-3202045
37	CTCF	chr7:3194552-3194562	LNCaP	prostate:	n/a	n/a
38	CTCF	chr7:3202020-3202170	AG04450	lung:	n/a	chr7:3202038-3202045
39	CTCF	chr7:3194530-3194946	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:3201980-3202130	GM06990	blood:	n/a	chr7:3202038-3202045
41	CTCF	chr7:3202020-3202170	HBMEC	blood vessel:	n/a	chr7:3202038-3202045
42	CTCF	chr7:3194089-3195197	SK-N-SH	brain:	n/a	n/a
43	CTCF	chr7:3194520-3194670	WI-38	lung:	n/a	n/a
44	CTCF	chr7:3200710-3200745	GM13976	blood:	n/a	n/a
45	CTCF	chr7:3194605-3194836	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:3194620-3194770	GM12866	blood:	n/a	n/a
47	CTCF	chr7:3194550-3194836	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr7:3194620-3194770	RPTEC	kidney:	n/a	n/a
49	CTCF	chr7:3194620-3194770	BJ	skin:	n/a	n/a
50	CTCF	chr7:3202040-3202190	GM12875	blood:	n/a	n/a

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3208793-3208843	HRE	kidney:	n/a
2	chr7:3186766-3186816	Hepatocyte	liver:	n/a
3	chr7:3221150-3221200	MCF-7	breast:	n/a
4	chr7:3208793-3208843	HRE	kidney:	n/a
5	chr7:3186766-3186816	Hepatocyte	liver:	n/a
6	chr7:3221150-3221200	MCF-7	breast:	n/a
7	chr7:3215287-3215337	HEK293	kidney:	embryo
8	chr7:3215543-3215593	HMEC	breast:	n/a
9	chr7:3215543-3215593	AG09319	gingival:	n/a
10	chr7:3208793-3208843	GM12878	blood:	n/a
11	chr7:3221150-3221200	HepG2	liver:	n/a
12	chr7:3208793-3208843	CMK	blood:	n/a
13	chr7:3214400-3214450	Jurkat	blood:	n/a
14	chr7:3186766-3186816	RPTEC	kidney:	n/a
15	chr7:3221373-3221423	ProgFib	skin:	n/a
16	chr7:3214289-3214339	H1-hESC	embryonic stem cell:	embryo
17	chr7:3214289-3214339	SAEC	small airway:	n/a
18	chr7:3214400-3214450	AG04450	lung:	fetal
19	chr7:3214400-3214450	HRE	kidney:	n/a
20	chr7:3214400-3214450	AG04449	skin:	fetal
21	chr7:3214289-3214339	HRE	kidney:	n/a
22	chr7:3214289-3214339	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:3186788-3186838	IMR90	lung:	fetal
24	chr7:3221228-3221278	PrEC	prostate:	n/a
25	chr7:3221373-3221423	AG09309	skin:	n/a
26	chr7:3207719-3207769	HRE	kidney:	n/a
27	chr7:3208493-3208543	A549	lung:	n/a
28	chr7:3221228-3221278	AG09309	skin:	n/a
29	chr7:3208793-3208843	K562	blood:	n/a
30	chr7:3221373-3221423	HCM	heart:	n/a
31	chr7:3207719-3207769	GM12878	blood:	n/a
32	chr7:3186788-3186838	AG09319	gingival:	n/a
33	chr7:3221150-3221200	GM12892	blood:	n/a
34	chr7:3186766-3186816	AG10803	skin:	n/a
35	chr7:3221228-3221278	AoSMC	blood vessel:	n/a
36	chr7:3214289-3214339	CMK	blood:	n/a
37	chr7:3186766-3186816	CMK	blood:	n/a
38	chr7:3221150-3221200	H1-hESC	embryonic stem cell:	embryo
39	chr7:3214289-3214339	A549	lung:	n/a
40	chr7:3186788-3186838	PFSK-1	brain:	n/a
41	chr7:3208793-3208843	HEK293	kidney:	embryo
42	chr7:3208793-3208843	HUVEC	blood vessel:	n/a
43	chr7:3221150-3221200	HNPCEpiC	eye:	n/a
44	chr7:3208493-3208543	GM12891	blood:	n/a
45	chr7:3186766-3186816	Hela-S3	cervix:	n/a
46	chr7:3214400-3214450	AoSMC	blood vessel:	n/a
47	chr7:3221373-3221423	HCT-116	colon:	n/a
48	chr7:3215287-3215337	HRPEpiC	eye:	n/a
49	chr7:3221228-3221278	ProgFib	skin:	n/a
50	chr7:3221373-3221423	GM06990	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:2913057..2915172-chr7:3198284..3201204,2	MCF-7	breast:
2	chr7:3205607..3207977-chr7:3220687..3223407,2	K562	blood:
3	chr7:3201417..3202351-chr7:3240242..3240878,3	MCF-7	breast:
4	chr7:3194510..3195232-chr7:3340158..3340723,2	MCF-7	breast:
5	chr7:2914055..2915867-chr7:3204506..3206043,2	MCF-7	breast:
6	chr7:3210617..3212945-chr7:3214732..3216839,2	K562	blood:
7	chr7:3198032..3200716-chr7:3210631..3213455,2	MCF-7	breast:
8	chr7:2710484..2711053-chr7:3194317..3194955,2	K562	blood:
9	chr7:3105046..3105933-chr7:3194248..3194999,3	K562	blood:
10	chr7:3184853..3186673-chr7:3189363..3191376,2	K562	blood:
11	chr7:3205607..3207977-chr7:3220687..3223407,2	K562	blood:
12	chr7:2925307..2926930-chr7:3193219..3196331,3	MCF-7	breast:
13	chr7:3105018..3105890-chr7:3193882..3195188,3	MCF-7	breast:
14	chr7:3210553..3212945-chr7:3214110..3216839,3	K562	blood:
15	chr7:3104949..3105997-chr7:3194351..3195035,3	MCF-7	breast:
16	chr7:3210592..3212478-chr7:3220599..3222530,2	K562	blood:
17	chr7:2926262..2927534-chr7:3194238..3195613,6	MCF-7	breast:
18	chr7:3210592..3212478-chr7:3220599..3222530,2	K562	blood:
19	chr7:3184853..3186673-chr7:3189363..3191376,2	K562	blood:
20	chr7:3210617..3212945-chr7:3214732..3216839,2	K562	blood:
21	chr7:3194262..3194922-chr7:3439333..3439841,2	MCF-7	breast:
22	chr7:2904357..2905298-chr7:3194209..3195076,4	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD11-4	chr7:3202784-3203088	NONHSAT118845
2	lnc-AC091801.1.1-1	chr7:3214230-3214287	XLOC_006339
3	lnc-AC091801.1.1-1	chr7:3186629-3186905	NONHSAT118844
4	lnc-CARD11-4	chr7:3204353-3204414	NONHSAT118845
5	lnc-AC091801.1.1-1	chr7:3197771-3197975	XLOC_006339
6	lnc-AC091801.1.1-1	chr7:3186629-3186905	XLOC_006339
7	lnc-AC091801.1.1-1	chr7:3205664-3205764	NONHSAT118844
8	lnc-AC091801.1.1-1	chr7:3197771-3197888	XLOC_006339
9	lnc-AC091801.1.1-1	chr7:3214230-3214287	NONHSAT118844
10	lnc-CARD11-4	chr7:3204171-3204221	NONHSAT118845
11	lnc-AC091801.1.1-1	chr7:3205664-3205764	XLOC_006339

No data

Variant related genes	Relation type
ENSG00000217455	TF binding region
ENSG00000217455	CpG island
ENSG00000217455	chromatin interactions

Extended variants
information (count: 2115 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2115 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541319487	chr7:3185995-3185996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555268714	chr7:3185998-3185999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570816722	chr7:3186006-3186007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575054776	chr7:3186009-3186010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544017992	chr7:3186084-3186085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563898559	chr7:3186086-3186087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532240023	chr7:3186101-3186102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569602503	chr7:3186113-3186114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189069147	chr7:3186114-3186115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528092250	chr7:3186143-3186144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs74608790	chr7:3186151-3186152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568029391	chr7:3186191-3186192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550293388	chr7:3186193-3186194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73672268	chr7:3186247-3186248	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs376829195	chr7:3186258-3186259	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs148836877	chr7:3186268-3186269	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559015410	chr7:3186277-3186278	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs565910902	chr7:3186293-3186294	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs535034834	chr7:3186296-3186297	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs555038658	chr7:3186320-3186321	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs575162150	chr7:3186337-3186338	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs544172241	chr7:3186348-3186349	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs200000856	chr7:3186369-3186370	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs386709431	chr7:3186370-3186371	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs557577032	chr7:3186372-3186373	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs535655384	chr7:3186416-3186417	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs374247072	chr7:3186425-3186426	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs554315418	chr7:3186477-3186478	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs180937660	chr7:3186480-3186481	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs79478477	chr7:3186493-3186494	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs528039298	chr7:3186502-3186503	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs117123236	chr7:3186503-3186504	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs561394229	chr7:3186506-3186507	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs12534973	chr7:3186510-3186511	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs12531776	chr7:3186513-3186514	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs548454465	chr7:3186580-3186581	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs73037728	chr7:3186597-3186598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533176398	chr7:3186610-3186611	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs185460394	chr7:3186613-3186614	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs566150350	chr7:3186622-3186623	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs534836280	chr7:3186629-3186630	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
42	rs572452615	chr7:3186636-3186637	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
43	rs369295221	chr7:3186638-3186639	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
44	rs568505227	chr7:3186657-3186658	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
45	rs143441802	chr7:3186669-3186670	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
46	rs575631664	chr7:3186695-3186696	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
47	rs557689590	chr7:3186701-3186702	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
48	rs543143685	chr7:3186746-3186747	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
49	rs540037693	chr7:3186751-3186752	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
50	rs138159367	chr7:3186752-3186753	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3169800-3189400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:3178400-3204600	Weak transcription	Right Atrium	heart
3	chr7:3185200-3186000	Weak transcription	Brain Germinal Matrix	brain
4	chr7:3185600-3186200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:3185800-3187400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:3185800-3187800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr7:3186000-3186200	Enhancers	Brain Germinal Matrix	brain
8	chr7:3186000-3186200	Enhancers	A549	lung
9	chr7:3186000-3187000	Enhancers	K562	blood
10	chr7:3186000-3187200	Enhancers	Primary hematopoietic stem cells	blood
11	chr7:3186200-3187000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:3186200-3187000	Flanking Active TSS	A549	lung
13	chr7:3186200-3187600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr7:3186200-3192600	Weak transcription	Brain Germinal Matrix	brain
15	chr7:3186400-3186800	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr7:3186600-3187000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
17	chr7:3186600-3187000	Enhancers	NH-A	brain
18	chr7:3187000-3187800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:3187200-3189000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr7:3187400-3188800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:3187600-3188600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr7:3187800-3188800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:3187800-3189200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr7:3188600-3191600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr7:3188800-3189600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:3188800-3191000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:3189000-3190000	Enhancers	Fetal Thymus	thymus
28	chr7:3189000-3191400	Enhancers	Primary hematopoietic stem cells	blood
29	chr7:3189200-3190000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr7:3189200-3192200	Enhancers	Primary B cells from cord blood	blood
31	chr7:3189400-3190000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:3189600-3190000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr7:3189600-3190000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:3189600-3190200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr7:3189600-3192600	Enhancers	Primary B cells from peripheral blood	blood
36	chr7:3189800-3190400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr7:3190000-3194000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:3190200-3191600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:3191600-3193200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr7:3191600-3197200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:3192200-3197200	Weak transcription	Primary B cells from cord blood	blood
42	chr7:3192400-3193600	Enhancers	GM12878-XiMat	blood
43	chr7:3192600-3193200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:3192600-3193400	Enhancers	Brain Germinal Matrix	brain
45	chr7:3192600-3196800	Weak transcription	Primary B cells from peripheral blood	blood
46	chr7:3193200-3193600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr7:3193200-3193600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr7:3193200-3193800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr7:3193600-3194000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:3193600-3197000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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