Variant report

Variant	nsv1018550
Chromosome Location	chr7:27844038-27925645
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:404)
CpG islands
(count:366)
Chromatin interactive
region (count:27)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:27908158-27908332	K562	blood:	n/a	n/a
2	ATF1	chr7:27865035-27865180	K562	blood:	n/a	n/a
3	BACH1	chr7:27848293-27848514	K562	blood:	n/a	n/a
4	BCL3	chr7:27875838-27876545	A549	lung:	n/a	n/a
5	BHLHE40	chr7:27907673-27907936	HepG2	liver:	n/a	n/a
6	BHLHE40	chr7:27888854-27888870	K562	blood:	n/a	n/a
7	BHLHE40	chr7:27907621-27908006	K562	blood:	n/a	n/a
8	BHLHE40	chr7:27892980-27893130	K562	blood:	n/a	n/a
9	CEBPB	chr7:27907831-27907860	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:27843774-27844052	HepG2	liver:	n/a	chr7:27843931-27843942
11	CEBPB	chr7:27907709-27907967	K562	blood:	n/a	n/a
12	CEBPB	chr7:27907671-27907946	K562	blood:	n/a	n/a
13	CEBPB	chr7:27863114-27863192	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:27851519-27851657	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:27907672-27907974	IMR90	lung:	n/a	n/a
16	CHD2	chr7:27913717-27914168	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr7:27882683-27882687	HepG2	liver:	n/a	n/a
18	CREB1	chr7:27903585-27903919	K562	blood:	n/a	n/a
19	CTCF	chr7:27881840-27881990	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr7:27890300-27890450	A549	lung:	n/a	n/a
21	CTCF	chr7:27881820-27881970	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr7:27916640-27916790	K562	blood:	n/a	chr7:27916713-27916726
23	CTCF	chr7:27874340-27874490	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr7:27881820-27881970	AG10803	skin:	n/a	n/a
25	CTCF	chr7:27890260-27890410	K562	blood:	n/a	n/a
26	CTCF	chr7:27916649-27916763	K562	blood:	n/a	chr7:27916713-27916726
27	CTCF	chr7:27845800-27845844	GM20000	blood:	n/a	n/a
28	CTCF	chr7:27922720-27922870	BE2_C	brain:	n/a	chr7:27922860-27922869
29	CTCF	chr7:27881800-27881950	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr7:27885207-27885291	GM12891	blood:	n/a	n/a
31	CTCF	chr7:27866673-27866698	Fibrobl	skin:	n/a	n/a
32	CTCF	chr7:27881800-27881950	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr7:27881816-27882001	Medullo	brain:	n/a	n/a
34	CTCF	chr7:27866840-27866990	GM12868	blood:	n/a	n/a
35	CTCF	chr7:27881840-27881990	HFF	foreskin:	n/a	n/a
36	CTCF	chr7:27881779-27882087	K562	blood:	n/a	n/a
37	CTCF	chr7:27876300-27876450	HCFaa	heart:	n/a	n/a
38	CTCF	chr7:27881820-27881970	K562	blood:	n/a	n/a
39	CTCF	chr7:27888837-27888856	K562	blood:	n/a	n/a
40	CTCF	chr7:27885226-27885285	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:27888827-27888905	MCF-7	breast:	n/a	chr7:27888872-27888885
42	CTCF	chr7:27876240-27876390	A549	lung:	n/a	n/a
43	CTCF	chr7:27881780-27881930	AG09309	skin:	n/a	n/a
44	CTCF	chr7:27881820-27881970	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr7:27876200-27876350	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr7:27890160-27890310	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr7:27922906-27922959	Lung_OC	lung:	n/a	n/a
48	CTCF	chr7:27881820-27881970	HepG2	liver:	n/a	n/a
49	CTCF	chr7:27888832-27888917	MCF-7	breast:	n/a	chr7:27888872-27888885
50	CTCF	chr7:27873960-27874110	GM12874	blood:	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	chr7:27868767-27868817	IMR90	lung:	fetal
2	chr7:27882598-27882648	HRCEpiC	kidney:	n/a
3	chr7:27912112-27912162	NHBE	bronchial:	n/a
4	chr7:27912112-27912162	Hepatocyte	liver:	n/a
5	chr7:27908936-27908986	K562	blood:	n/a
6	chr7:27875760-27875810	BJ	skin:	n/a
7	chr7:27882598-27882648	U87	brain:	n/a
8	chr7:27875760-27875810	HCT-116	colon:	n/a
9	chr7:27912112-27912162	RPTEC	kidney:	n/a
10	chr7:27875760-27875810	GM06990	blood:	n/a
11	chr7:27875760-27875810	GM12878	blood:	n/a
12	chr7:27882598-27882648	H1-hESC	embryonic stem cell:	embryo
13	chr7:27896953-27897003	ECC-1	luminal epithelium:	n/a
14	chr7:27868767-27868817	SK-N-SH_RA	brain:	n/a
15	chr7:27896953-27897003	HMEC	breast:	n/a
16	chr7:27912112-27912162	PrEC	prostate:	n/a
17	chr7:27908936-27908986	HNPCEpiC	eye:	n/a
18	chr7:27882598-27882648	PANC-1	pancreas:	n/a
19	chr7:27912112-27912162	SK-N-SH_RA	brain:	n/a
20	chr7:27896953-27897003	HEK293	kidney:	embryo
21	chr7:27908936-27908986	AoSMC	blood vessel:	n/a
22	chr7:27868767-27868817	HL-60	blood:	n/a
23	chr7:27875760-27875810	PFSK-1	brain:	n/a
24	chr7:27875760-27875810	GM12892	blood:	n/a
25	chr7:27875760-27875810	HRE	kidney:	n/a
26	chr7:27896953-27897003	BE2_C	brain:	n/a
27	chr7:27868767-27868817	HEK293	kidney:	embryo
28	chr7:27908936-27908986	HIPEpiC	eye:	n/a
29	chr7:27912112-27912162	HIPEpiC	eye:	n/a
30	chr7:27882598-27882648	HMEC	breast:	n/a
31	chr7:27875760-27875810	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:27908936-27908986	U87	brain:	n/a
33	chr7:27896953-27897003	A549	lung:	n/a
34	chr7:27896953-27897003	AG04450	lung:	fetal
35	chr7:27868767-27868817	ovcar-3	ovarian:	n/a
36	chr7:27882598-27882648	AG10803	skin:	n/a
37	chr7:27882598-27882648	GM12878	blood:	n/a
38	chr7:27896953-27897003	NH-A	brain:	n/a
39	chr7:27912112-27912162	HNPCEpiC	eye:	n/a
40	chr7:27868767-27868817	ECC-1	luminal epithelium:	n/a
41	chr7:27868767-27868817	AG04450	lung:	fetal
42	chr7:27896953-27897003	GM06990	blood:	n/a
43	chr7:27882598-27882648	SK-N-SH	brain:	n/a
44	chr7:27896953-27897003	GM12891	blood:	n/a
45	chr7:27868767-27868817	GM19239	blood:	n/a
46	chr7:27882598-27882648	NB4	blood:	n/a
47	chr7:27896953-27897003	GM12878	blood:	n/a
48	chr7:27882598-27882648	HCF	heart:	n/a
49	chr7:27868767-27868817	HIPEpiC	eye:	n/a
50	chr7:27908936-27908986	Hela-S3	cervix:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:27874082..27877005-chr7:27878628..27880591,4	MCF-7	breast:
2	chr7:27910666..27913225-chr7:27921986..27924862,2	K562	blood:
3	chr7:27856504..27859420-chr7:27862843..27864597,2	K562	blood:
4	chr7:27701821..27704572-chr7:27873385..27875451,2	K562	blood:
5	chr7:27877025..27879466-chr7:27881187..27883994,3	K562	blood:
6	chr7:27701860..27704389-chr7:27881950..27883537,2	K562	blood:
7	chr7:27874082..27877005-chr7:27878628..27880591,4	MCF-7	breast:
8	chr7:27887045..27889162-chr7:27891561..27893671,2	MCF-7	breast:
9	chr7:27870030..27872206-chr7:27878302..27880164,2	MCF-7	breast:
10	chr7:27848154..27850966-chr7:27851903..27854305,3	MCF-7	breast:
11	chr7:27924120..27926440-chr7:27928203..27929824,2	K562	blood:
12	chr7:27877025..27879466-chr7:27881187..27883994,3	K562	blood:
13	chr7:27572850..27575032-chr7:27915614..27917476,2	K562	blood:
14	chr7:27832794..27834695-chr7:27850538..27852505,2	K562	blood:
15	chr7:27842369..27845574-chr7:27847275..27850626,3	K562	blood:
16	chr7:27646423..27648425-chr7:27891373..27893179,2	K562	blood:
17	chr7:27835817..27837849-chr7:27841961..27844840,2	K562	blood:
18	chr7:27877749..27879466-chr7:27881187..27883816,2	K562	blood:
19	chr7:27877749..27879466-chr7:27881187..27883816,2	K562	blood:
20	chr7:27910666..27913225-chr7:27921986..27924862,2	K562	blood:
21	chr7:27856504..27859420-chr7:27862843..27864597,2	K562	blood:
22	chr7:27861346..27863328-chr7:27865686..27868649,2	K562	blood:
23	chr7:27701552..27704256-chr7:27856861..27858548,2	K562	blood:
24	chr7:27887045..27889162-chr7:27891561..27893671,2	MCF-7	breast:
25	chr7:27842369..27845574-chr7:27847275..27850626,3	K562	blood:
26	chr7:27870030..27872206-chr7:27878302..27880164,2	MCF-7	breast:
27	chr7:27848154..27850966-chr7:27851903..27854305,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAX1BP1-2	chr7:27868247-27868402	NONHSAT119746
2	lnc-TAX1BP1-2	chr7:27880340-27880938	NONHSAT119746
3	lnc-TAX1BP1-3	chr7:27920106-27920397	NONHSAT119748
4	lnc-TAX1BP1-2	chr7:27867420-27867439	NONHSAT119746

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TAX1BP1	hsa-miR-130b-3p	chr7:27868737-27868761
2	TAX1BP1	hsa-miR-93-5p	chr7:27868544-27868569
3	JAZF1	hsa-miR-96-5p	chr7:27871477-27871499
4	JAZF1	hsa-miR-31-5p	chr7:27871777-27871770
5	JAZF1	hsa-miR-31-5p	chr7:27871807-27871827
6	JAZF1	hsa-miR-96-5p	chr7:27872401-27872395
7	JAZF1	hsa-miR-96-5p	chr7:27872395-27872416
8	TAX1BP1	hsa-miR-93-5p	chr7:27868565-27868587
9	JAZF1	hsa-miR-31-5p	chr7:27871771-27871792

Variant related genes	Relation type
TAX1BP1	TF binding region
JAZF1	TF binding region
RN7SL365P	TF binding region
TAX1BP1	CpG island
JAZF1	CpG island
RN7SL365P	CpG island
ENSG00000106052	chromatin interactions
ENSG00000106049	chromatin interactions

Extended variants
information (count: 3256 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3256 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6970578	chr7:27844038-27844039	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184686730	chr7:27844042-27844043	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs540308274	chr7:27844054-27844055	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs537506121	chr7:27844057-27844058	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs555946360	chr7:27844063-27844064	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs574263077	chr7:27844070-27844071	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs538501210	chr7:27844114-27844115	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs553683599	chr7:27844137-27844138	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189957695	chr7:27844191-27844192	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs546224173	chr7:27844263-27844264	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192211697	chr7:27844326-27844327	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576489451	chr7:27844328-27844329	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543524992	chr7:27844351-27844352	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184534429	chr7:27844377-27844378	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35343536	chr7:27844435-27844436	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs12375192	chr7:27844477-27844478	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs560138703	chr7:27844498-27844499	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6462050	chr7:27844503-27844504	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs142154064	chr7:27844561-27844562	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151207695	chr7:27844595-27844596	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116945162	chr7:27844610-27844611	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185536295	chr7:27844656-27844657	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181926029	chr7:27844660-27844661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6462051	chr7:27844661-27844662	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs553546448	chr7:27844669-27844670	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572344797	chr7:27844747-27844748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139547296	chr7:27844758-27844759	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558135214	chr7:27844801-27844802	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555389093	chr7:27844821-27844822	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539257878	chr7:27844834-27844835	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145140232	chr7:27844875-27844876	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562193461	chr7:27844896-27844897	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147549981	chr7:27844942-27844943	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182214383	chr7:27844954-27844955	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186578143	chr7:27844959-27844960	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189024594	chr7:27844973-27844974	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367747479	chr7:27845017-27845018	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141111323	chr7:27845055-27845056	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186500147	chr7:27845057-27845058	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192689434	chr7:27845063-27845064	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545352230	chr7:27845068-27845069	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111299011	chr7:27845133-27845134	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117905849	chr7:27845193-27845194	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113882679	chr7:27845231-27845232	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549342799	chr7:27845285-27845286	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567860344	chr7:27845326-27845327	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112094788	chr7:27845333-27845334	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150097211	chr7:27845345-27845346	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182108640	chr7:27845379-27845380	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376935298	chr7:27845453-27845454	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Cancer	17440070	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1514 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27781000-27861800	Weak transcription	Aorta	Aorta
2	chr7:27784800-27878400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:27790600-27857400	Weak transcription	Colonic Mucosa	Colon
4	chr7:27798600-27847800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr7:27798600-27874000	Weak transcription	Brain Angular Gyrus	brain
6	chr7:27801200-27851800	Weak transcription	Fetal Brain Male	brain
7	chr7:27801600-27852800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr7:27805800-27857600	Weak transcription	Esophagus	oesophagus
9	chr7:27806000-27882600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:27806400-27878600	Weak transcription	Right Ventricle	heart
11	chr7:27815600-27874000	Weak transcription	Pancreas	Pancrea
12	chr7:27820400-27847400	Weak transcription	Fetal Heart	heart
13	chr7:27823800-27878000	Weak transcription	Spleen	Spleen
14	chr7:27824200-27876800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr7:27825600-27848000	Weak transcription	NHLF	lung
16	chr7:27825600-27874000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr7:27826000-27870000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr7:27826600-27852800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:27827000-27881800	Weak transcription	Small Intestine	intestine
20	chr7:27827600-27878400	Weak transcription	Fetal Kidney	kidney
21	chr7:27831200-27844800	Strong transcription	HSMM	muscle
22	chr7:27832600-27852800	Weak transcription	Lung	lung
23	chr7:27832600-27852800	Weak transcription	Thymus	Thymus
24	chr7:27832600-27856000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr7:27832800-27853200	Weak transcription	Fetal Muscle Leg	muscle
26	chr7:27833000-27858000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:27833600-27856000	Weak transcription	Brain Anterior Caudate	brain
28	chr7:27833600-27858400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:27834200-27845600	Weak transcription	Brain Germinal Matrix	brain
30	chr7:27834200-27847800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr7:27834400-27873600	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr7:27834800-27848000	Weak transcription	HMEC	breast
33	chr7:27834800-27855600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr7:27835000-27856000	Weak transcription	GM12878-XiMat	blood
35	chr7:27835200-27848000	Weak transcription	NHEK	skin
36	chr7:27835200-27856000	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr7:27835200-27857600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr7:27835200-27878200	Weak transcription	Gastric	stomach
39	chr7:27835800-27847600	Weak transcription	NH-A	brain
40	chr7:27836000-27847600	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr7:27836000-27847800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr7:27836000-27856400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr7:27836200-27847600	Weak transcription	HSMMtube	muscle
44	chr7:27836200-27848000	Weak transcription	K562	blood
45	chr7:27836400-27856000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr7:27836400-27856000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr7:27836400-27867400	Weak transcription	HUVEC	blood vessel
48	chr7:27836400-27878000	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr7:27836400-27882200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr7:27836600-27852600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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