Variant report

Variant	nsv887643
Chromosome Location	chr7:13086613-13211263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:839)
CpG islands
(count:122)
Chromatin interactive
region (count:68)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:13097011-13097123	K562	blood:	n/a	n/a
2	ARID3A	chr7:13143855-13144055	K562	blood:	n/a	n/a
3	ARID3A	chr7:13176170-13176171	K562	blood:	n/a	n/a
4	ARID3A	chr7:13090394-13090680	K562	blood:	n/a	n/a
5	ARID3A	chr7:13138761-13139142	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:13156776-13157108	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:13090328-13090658	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:13143806-13144072	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:13131747-13132382	K562	blood:	n/a	n/a
10	ARID3A	chr7:13106506-13106882	K562	blood:	n/a	n/a
11	ARID3A	chr7:13156744-13157084	K562	blood:	n/a	n/a
12	ATF1	chr7:13187153-13187258	K562	blood:	n/a	n/a
13	ATF1	chr7:13158387-13158436	K562	blood:	n/a	n/a
14	ATF1	chr7:13090455-13090529	K562	blood:	n/a	n/a
15	ATF1	chr7:13143829-13144112	K562	blood:	n/a	n/a
16	ATF1	chr7:13172051-13172233	K562	blood:	n/a	n/a
17	ATF1	chr7:13131823-13132227	K562	blood:	n/a	n/a
18	ATF2	chr7:13097270-13097686	GM12878	blood:	n/a	n/a
19	ATF3	chr7:13191565-13191942	K562	blood:	n/a	n/a
20	ATF3	chr7:13131828-13132223	K562	blood:	n/a	n/a
21	BACH1	chr7:13089906-13090689	K562	blood:	n/a	n/a
22	BACH1	chr7:13094079-13094100	K562	blood:	n/a	n/a
23	BACH1	chr7:13112061-13112090	K562	blood:	n/a	n/a
24	BACH1	chr7:13090371-13090647	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr7:13138851-13139153	GM12878	blood:	n/a	chr7:13139007-13139018
26	BATF	chr7:13138876-13139164	GM12878	blood:	n/a	chr7:13139007-13139018
27	BHLHE40	chr7:13138780-13139161	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:13206129-13206138	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:13131711-13132161	K562	blood:	n/a	n/a
30	BHLHE40	chr7:13210877-13210897	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:13097430-13097605	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:13138027-13138202	K562	blood:	n/a	n/a
33	CBX3	chr7:13175950-13176286	K562	blood:	n/a	n/a
34	CBX3	chr7:13207821-13208141	K562	blood:	n/a	n/a
35	CBX3	chr7:13149470-13149761	K562	blood:	n/a	n/a
36	CBX3	chr7:13175978-13176252	K562	blood:	n/a	n/a
37	CBX3	chr7:13121526-13121869	K562	blood:	n/a	n/a
38	CBX3	chr7:13164235-13164595	K562	blood:	n/a	n/a
39	CCNT2	chr7:13106658-13106903	K562	blood:	n/a	n/a
40	CCNT2	chr7:13096980-13097278	K562	blood:	n/a	n/a
41	CCNT2	chr7:13131842-13132210	K562	blood:	n/a	n/a
42	CEBPB	chr7:13154952-13155171	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr7:13090308-13090657	A549	lung:	n/a	n/a
44	CEBPB	chr7:13100691-13101228	MCF-7	breast:	n/a	chr7:13101041-13101054
45	CEBPB	chr7:13194459-13194697	K562	blood:	n/a	n/a
46	CEBPB	chr7:13179227-13179427	K562	blood:	n/a	chr7:13179288-13179299
47	CEBPB	chr7:13179132-13179455	IMR90	lung:	n/a	chr7:13179288-13179299
48	CEBPB	chr7:13138823-13139120	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:13169983-13170271	A549	lung:	n/a	chr7:13170144-13170153 chr7:13170127-13170138 chr7:13170142-13170153 chr7:13170156-13170167
50	CEBPB	chr7:13137196-13137417	HepG2	liver:	n/a	chr7:13137277-13137288

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13141735-13141785	ovcar-3	ovarian:	n/a
2	chr7:13155344-13155394	NT2-D1	testis:	n/a
3	chr7:13141735-13141785	PrEC	prostate:	n/a
4	chr7:13141735-13141785	GM12878	blood:	n/a
5	chr7:13141735-13141785	K562	blood:	n/a
6	chr7:13155344-13155394	MCF10A-Er-Src	breast:	n/a
7	chr7:13141735-13141785	IMR90	lung:	fetal
8	chr7:13155344-13155394	Caco-2	colon:	n/a
9	chr7:13155344-13155394	HIPEpiC	eye:	n/a
10	chr7:13155344-13155394	H1-hESC	embryonic stem cell:	embryo
11	chr7:13155344-13155394	AG09309	skin:	n/a
12	chr7:13155344-13155394	HCT-116	colon:	n/a
13	chr7:13155344-13155394	BJ	skin:	n/a
14	chr7:13155344-13155394	HCF	heart:	n/a
15	chr7:13141735-13141785	ProgFib	skin:	n/a
16	chr7:13155344-13155394	T-47D	breast:	n/a
17	chr7:13141735-13141785	HRE	kidney:	n/a
18	chr7:13141735-13141785	GM19239	blood:	n/a
19	chr7:13155344-13155394	AG04449	skin:	fetal
20	chr7:13141735-13141785	HEEpiC	esophagus:	n/a
21	chr7:13155344-13155394	GM06990	blood:	n/a
22	chr7:13155344-13155394	SK-N-MC	brain:	n/a
23	chr7:13141735-13141785	Jurkat	blood:	n/a
24	chr7:13155344-13155394	U87	brain:	n/a
25	chr7:13141735-13141785	PFSK-1	brain:	n/a
26	chr7:13141735-13141785	AG04449	skin:	fetal
27	chr7:13141735-13141785	AG09319	gingival:	n/a
28	chr7:13155344-13155394	PANC-1	pancreas:	n/a
29	chr7:13141735-13141785	HL-60	blood:	n/a
30	chr7:13141735-13141785	SK-N-SH_RA	brain:	n/a
31	chr7:13155344-13155394	A549	lung:	n/a
32	chr7:13155344-13155394	NH-A	brain:	n/a
33	chr7:13155344-13155394	RPTEC	kidney:	n/a
34	chr7:13141735-13141785	RPTEC	kidney:	n/a
35	chr7:13141735-13141785	A549	lung:	n/a
36	chr7:13141735-13141785	SK-N-MC	brain:	n/a
37	chr7:13141735-13141785	GM06990	blood:	n/a
38	chr7:13141735-13141785	HepG2	liver:	n/a
39	chr7:13155344-13155394	Jurkat	blood:	n/a
40	chr7:13141735-13141785	HCF	heart:	n/a
41	chr7:13155344-13155394	HEK293	kidney:	embryo
42	chr7:13155344-13155394	MCF-7	breast:	n/a
43	chr7:13155344-13155394	Hepatocyte	liver:	n/a
44	chr7:13155344-13155394	HUVEC	blood vessel:	n/a
45	chr7:13155344-13155394	HRPEpiC	eye:	n/a
46	chr7:13155344-13155394	HEEpiC	esophagus:	n/a
47	chr7:13141735-13141785	AG04450	lung:	fetal
48	chr7:13141735-13141785	HRPEpiC	eye:	n/a
49	chr7:13155344-13155394	AG04450	lung:	fetal
50	chr7:13141735-13141785	NB4	blood:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:13195077..13196666-chr7:13196806..13198441,2	MCF-7	breast:
2	chr7:13129497..13132046-chr7:13137053..13139000,2	K562	blood:
3	chr7:13091634..13094570-chr7:13095004..13097471,2	K562	blood:
4	chr7:13081390..13084291-chr7:13084595..13087584,2	K562	blood:
5	chr7:13086829..13088462-chr7:13155188..13156937,2	K562	blood:
6	chr7:13104322..13106884-chr7:13107040..13109324,2	K562	blood:
7	chr7:13195077..13196666-chr7:13196806..13198441,2	MCF-7	breast:
8	chr7:13091224..13092839-chr7:13093299..13095856,2	K562	blood:
9	chr7:13093779..13096148-chr7:13099334..13101239,2	K562	blood:
10	chr7:12980961..12983258-chr7:13154370..13156023,2	MCF-7	breast:
11	chr7:13105294..13107639-chr7:13110167..13112332,4	K562	blood:
12	chr7:13085851..13087402-chr7:13106082..13107771,2	K562	blood:
13	chr7:13088931..13090663-chr7:13093892..13095543,2	K562	blood:
14	chr7:13081105..13083508-chr7:13090393..13094038,3	K562	blood:
15	chr7:12724403..12726396-chr7:13103717..13106545,2	K562	blood:
16	chr7:13056096..13059019-chr7:13091108..13093835,2	K562	blood:
17	chr7:12726572..12727399-chr7:13154701..13155615,3	MCF-7	breast:
18	chr7:13100363..13102009-chr7:13102221..13104284,2	K562	blood:
19	chr7:13195061..13198037-chr7:13199556..13201286,2	K562	blood:
20	chr7:12776917..12778957-chr7:13100732..13103715,2	MCF-7	breast:
21	chr7:13187144..13190009-chr7:13193078..13195345,2	K562	blood:
22	chr7:13099163..13101911-chr7:13106498..13108964,2	K562	blood:
23	chr7:12970290..12973079-chr7:13097205..13098974,2	K562	blood:
24	chr7:13091634..13094570-chr7:13095004..13097471,2	K562	blood:
25	chr20:52401294..52403111-chr7:13210219..13212096,2	MCF-7	breast:
26	chr7:13195061..13198037-chr7:13199556..13201286,2	K562	blood:
27	chr7:13080083..13082250-chr7:13086917..13089071,2	K562	blood:
28	chr7:13180182..13182648-chr7:13184471..13186941,2	K562	blood:
29	chr7:13180182..13182648-chr7:13184471..13186941,2	K562	blood:
30	chr7:13134342..13136300-chr7:13222418..13225299,2	MCF-7	breast:
31	chr7:13145074..13147493-chr7:13153724..13155360,2	MCF-7	breast:
32	chr7:13111805..13113325-chr7:13115222..13117599,2	K562	blood:
33	chr7:13145074..13147493-chr7:13153724..13155360,2	MCF-7	breast:
34	chr7:13086829..13088462-chr7:13155188..13156937,2	K562	blood:
35	chr7:13091224..13092839-chr7:13093299..13095856,2	K562	blood:
36	chr7:13130850..13133041-chr7:13136588..13139070,3	K562	blood:
37	chr7:13146440..13148600-chr7:13150373..13152655,2	K562	blood:
38	chr7:12730592..12732679-chr7:13123373..13125180,2	K562	blood:
39	chr7:13111805..13113325-chr7:13115222..13117599,2	K562	blood:
40	chr7:13189358..13191512-chr7:13195499..13197059,2	K562	blood:
41	chr7:13085851..13087402-chr7:13106082..13107771,2	K562	blood:
42	chr7:12726504..12729722-chr7:13092003..13095862,3	K562	blood:
43	chr7:12726190..12728016-chr7:13138204..13140895,2	K562	blood:
44	chr7:13146450..13148956-chr7:13151839..13153573,2	MCF-7	breast:
45	chr7:12726944..12729146-chr7:13085985..13088167,2	K562	blood:
46	chr7:13099163..13101911-chr7:13106498..13108964,2	K562	blood:
47	chr7:13146440..13148600-chr7:13150373..13152655,2	K562	blood:
48	chr7:13100363..13102009-chr7:13102221..13104284,2	K562	blood:
49	chr7:13088931..13090663-chr7:13093892..13095543,2	K562	blood:
50	chr7:13094404..13096720-chr7:13097474..13099748,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL4A-7	chr7:13107541-13107733	NONHSAT119247
2	lnc-ARL4A-1	chr7:13141097-13141208	XLOC_005988
3	lnc-ARL4A-7	chr7:13107622-13107733	NONHSAT119248
4	lnc-ARL4A-7	chr7:13108158-13108539	NONHSAT119247

No data

Variant related genes	Relation type
ENSG00000229618	TF binding region
ENSG00000229618	CpG island
ENSG00000271253	chromatin interactions
ENSG00000122644	chromatin interactions

Extended variants
information (count: 4361 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4361 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10227653	chr7:13086613-13086614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374054584	chr7:13086643-13086644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548298637	chr7:13086655-13086656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs562113278	chr7:13086667-13086668	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535446573	chr7:13086690-13086691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527822232	chr7:13086718-13086719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183951099	chr7:13086729-13086730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149185005	chr7:13086745-13086746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs78580287	chr7:13086748-13086749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115418579	chr7:13086781-13086782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs367602615	chr7:13086825-13086826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536099302	chr7:13086912-13086913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369480409	chr7:13086949-13086950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs554260087	chr7:13086962-13086963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372735661	chr7:13086989-13086990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs189194852	chr7:13087006-13087007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs192454872	chr7:13087068-13087069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs17166658	chr7:13087201-13087202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs543209500	chr7:13087227-13087228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577781976	chr7:13087233-13087234	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541390572	chr7:13087246-13087247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540862313	chr7:13087277-13087278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs142414836	chr7:13087332-13087333	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75779727	chr7:13087334-13087335	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184720490	chr7:13087367-13087368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369431823	chr7:13087388-13087389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs56317384	chr7:13087403-13087404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs398085583	chr7:13087412-13087413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542899728	chr7:13087430-13087431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561782341	chr7:13087444-13087445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs151316669	chr7:13087445-13087446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs540999991	chr7:13087522-13087523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577700565	chr7:13087599-13087600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564256394	chr7:13087607-13087608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35896937	chr7:13087643-13087644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187497476	chr7:13087727-13087728	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543537719	chr7:13087731-13087732	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141867475	chr7:13087742-13087743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs145716572	chr7:13087758-13087759	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs73678973	chr7:13087842-13087843	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs74561051	chr7:13087859-13087860	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565705873	chr7:13087886-13087887	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs80185222	chr7:13087940-13087941	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138656917	chr7:13087953-13087954	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs28666742	chr7:13087981-13087982	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559506950	chr7:13087982-13087983	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs75047973	chr7:13087986-13087987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114838874	chr7:13087994-13087995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs75876111	chr7:13088018-13088019	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530071176	chr7:13088027-13088028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	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
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
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13082800-13089800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:13083200-13089400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr7:13085800-13086800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:13085800-13089400	Weak transcription	NHLF	lung
5	chr7:13086000-13089200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:13086000-13089400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:13086400-13087200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr7:13086600-13087600	Enhancers	A549	lung
9	chr7:13086600-13089400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:13086600-13089400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:13086800-13087000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:13087000-13087200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:13087200-13089600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:13087600-13089200	Weak transcription	A549	lung
15	chr7:13089200-13089600	Enhancers	A549	lung
16	chr7:13089200-13090600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:13089400-13090000	Enhancers	NHLF	lung
18	chr7:13089400-13090200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:13089400-13090200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:13089400-13090600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:13089400-13090600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:13089400-13091000	Enhancers	K562	blood
23	chr7:13089400-13091200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:13089400-13091800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr7:13089600-13089800	Flanking Active TSS	A549	lung
26	chr7:13089600-13090000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:13089600-13090000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr7:13089600-13090000	Enhancers	Colon Smooth Muscle	Colon
29	chr7:13089800-13090200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr7:13089800-13090200	Enhancers	A549	lung
31	chr7:13089800-13090400	Enhancers	Osteobl	bone
32	chr7:13089800-13090600	Enhancers	HMEC	breast
33	chr7:13089800-13090800	Enhancers	NH-A	brain
34	chr7:13089800-13091000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:13089800-13091400	Enhancers	HUVEC	blood vessel
36	chr7:13090000-13090600	Enhancers	HepG2	liver
37	chr7:13090000-13090800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr7:13090000-13090800	Weak transcription	NHLF	lung
39	chr7:13090200-13090800	Flanking Active TSS	A549	lung
40	chr7:13090200-13090800	Enhancers	NHEK	skin
41	chr7:13090200-13091400	Enhancers	Hela-S3	cervix
42	chr7:13090200-13102600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:13090400-13091200	Weak transcription	Osteobl	bone
44	chr7:13090800-13091000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:13090800-13091600	Enhancers	A549	lung
46	chr7:13090800-13091600	Enhancers	NHLF	lung
47	chr7:13091000-13097000	Weak transcription	K562	blood
48	chr7:13091200-13091400	Enhancers	Osteobl	bone
49	chr7:13091400-13091800	Weak transcription	Osteobl	bone
50	chr7:13091400-13095800	Weak transcription	HUVEC	blood vessel

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