Variant report

Variant	nsv526043
Chromosome Location	chr7:126985158-126998210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:601)
CpG islands
(count:427)
Chromatin interactive
region (count:33)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:601 , 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	chr7:126989412-126989672	K562	blood:	n/a	n/a
2	ATF3	chr7:126987603-126988067	K562	blood:	n/a	n/a
3	BACH1	chr7:126995773-126996154	K562	blood:	n/a	n/a
4	BACH1	chr7:126987734-126988023	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr7:126987748-126988175	GM12878	blood:	n/a	n/a
6	BCLAF1	chr7:126987623-126988049	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:126987792-126988212	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:126987588-126988333	K562	blood:	n/a	n/a
9	BRCA1	chr7:126987644-126987923	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:126987712-126988010	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr7:126987442-126988067	K562	blood:	n/a	n/a
12	CCNT2	chr7:126987613-126988330	K562	blood:	n/a	n/a
13	CCNT2	chr7:126986497-126986697	K562	blood:	n/a	n/a
14	CCNT2	chr7:126993812-126994004	K562	blood:	n/a	n/a
15	CCNT2	chr7:126990973-126991160	K562	blood:	n/a	n/a
16	CEBPB	chr7:126987664-126987912	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:126994611-126994999	K562	blood:	n/a	n/a
18	CHD2	chr7:126987857-126987961	HepG2	liver:	n/a	n/a
19	CHD2	chr7:126987698-126988060	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr7:126987706-126988036	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr7:126991378-126991391	K562	blood:	n/a	n/a
22	CHD2	chr7:126987726-126987876	K562	blood:	n/a	n/a
23	CREB1	chr7:126987748-126988232	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr7:126987741-126988222	A549	lung:	n/a	n/a
25	CREB1	chr7:126987580-126988211	K562	blood:	n/a	n/a
26	CTCF	chr7:126987820-126987970	AG04450	lung:	n/a	n/a
27	CTCF	chr7:126988160-126988310	AG04450	lung:	n/a	n/a
28	CTCF	chr7:126988160-126988310	GM12878	blood:	n/a	n/a
29	CTCF	chr7:126987800-126987950	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr7:126987584-126988045	A549	lung:	n/a	n/a
31	CTCF	chr7:126988140-126988290	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr7:126987640-126988257	GM12892	blood:	n/a	n/a
33	CTCF	chr7:126987626-126988089	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:126987800-126987950	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr7:126988215-126988235	GM19239	blood:	n/a	n/a
36	CTCF	chr7:126988211-126988232	HepG2	liver:	n/a	n/a
37	CTCF	chr7:126993600-126993750	AG04450	lung:	n/a	n/a
38	CTCF	chr7:126987700-126987850	GM06990	blood:	n/a	n/a
39	CTCF	chr7:126987560-126987710	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr7:126987680-126987830	GM12870	blood:	n/a	n/a
41	CTCF	chr7:126987554-126988697	K562	blood:	n/a	n/a
42	CTCF	chr7:126988180-126988330	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr7:126987787-126988024	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr7:126987840-126987990	HCM	heart:	n/a	n/a
45	CTCF	chr7:126987820-126987970	GM12865	blood:	n/a	n/a
46	CTCF	chr7:126987728-126987996	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr7:126987652-126988286	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:126987840-126987990	GM12875	blood:	n/a	n/a
49	CTCF	chr7:126987840-126987990	GM12874	blood:	n/a	n/a
50	CTCF	chr7:126988203-126988207	Medullo	brain:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126988262-126988312	HRPEpiC	eye:	n/a
2	chr7:126987042-126987092	NB4	blood:	n/a
3	chr7:126988262-126988312	AG04450	lung:	fetal
4	chr7:126988262-126988312	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:126987042-126987092	NHDF-neo	bronchial:	n/a
6	chr7:126988120-126988170	AoSMC	blood vessel:	n/a
7	chr7:126990845-126990895	ProgFib	skin:	n/a
8	chr7:126990845-126990895	HUVEC	blood vessel:	n/a
9	chr7:126988120-126988170	SK-N-SH	brain:	n/a
10	chr7:126988262-126988312	HCT-116	colon:	n/a
11	chr7:126988262-126988312	HMEC	breast:	n/a
12	chr7:126988232-126988282	GM06990	blood:	n/a
13	chr7:126987840-126987890	NHBE	bronchial:	n/a
14	chr7:126987042-126987092	U87	brain:	n/a
15	chr7:126987682-126987732	HCPEpiC	choroid plexus:	n/a
16	chr7:126987682-126987732	CMK	blood:	n/a
17	chr7:126987682-126987732	AG09309	skin:	n/a
18	chr7:126987042-126987092	Jurkat	blood:	n/a
19	chr7:126988232-126988282	HepG2	liver:	n/a
20	chr7:126990845-126990895	U87	brain:	n/a
21	chr7:126988232-126988282	NB4	blood:	n/a
22	chr7:126988120-126988170	H1-hESC	embryonic stem cell:	embryo
23	chr7:126987840-126987890	HUVEC	blood vessel:	n/a
24	chr7:126987682-126987732	SKMC	muscle:	n/a
25	chr7:126987042-126987092	HepG2	liver:	n/a
26	chr7:126988120-126988170	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:126987840-126987890	NB4	blood:	n/a
28	chr7:126988232-126988282	AoSMC	blood vessel:	n/a
29	chr7:126988262-126988312	AG10803	skin:	n/a
30	chr7:126988120-126988170	NT2-D1	testis:	n/a
31	chr7:126988262-126988312	SK-N-SH_RA	brain:	n/a
32	chr7:126987042-126987092	HCPEpiC	choroid plexus:	n/a
33	chr7:126987840-126987890	HCPEpiC	choroid plexus:	n/a
34	chr7:126987042-126987092	ProgFib	skin:	n/a
35	chr7:126988120-126988170	HUVEC	blood vessel:	n/a
36	chr7:126987042-126987092	HUVEC	blood vessel:	n/a
37	chr7:126987682-126987732	Jurkat	blood:	n/a
38	chr7:126987042-126987092	AG04450	lung:	fetal
39	chr7:126988262-126988312	GM12878	blood:	n/a
40	chr7:126990845-126990895	AG04449	skin:	fetal
41	chr7:126987840-126987890	HRPEpiC	eye:	n/a
42	chr7:126990845-126990895	GM12891	blood:	n/a
43	chr7:126987042-126987092	GM19239	blood:	n/a
44	chr7:126987682-126987732	GM12891	blood:	n/a
45	chr7:126988232-126988282	U87	brain:	n/a
46	chr7:126987840-126987890	HCF	heart:	n/a
47	chr7:126988232-126988282	T-47D	breast:	n/a
48	chr7:126988232-126988282	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:126987042-126987092	HRE	kidney:	n/a
50	chr7:126987682-126987732	PANC-1	pancreas:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:126992195..126994598-chr7:127031831..127034380,2	K562	blood:
2	chr7:126987100..126989492-chr7:127030062..127031935,2	K562	blood:
3	chr7:126987414..126988399-chr7:127154646..127155519,3	MCF-7	breast:
4	chr7:126987640..126988151-chr7:127849704..127850461,2	MCF-7	breast:
5	chr7:126983343..126987079-chr7:126991252..126994803,3	K562	blood:
6	chr7:126994441..126996750-chr7:126997785..127000283,3	K562	blood:
7	chr7:126983343..126987079-chr7:126991252..126994803,3	K562	blood:
8	chr7:126894392..126896260-chr7:126987799..126989472,2	K562	blood:
9	chr7:126993441..126998972-chr7:127031083..127033725,7	MCF-7	breast:
10	chr7:126977128..126979944-chr7:126984146..126986183,2	K562	blood:
11	chr7:126987395..126988347-chr7:127156521..127157053,2	K562	blood:
12	chr7:126985770..126989525-chr7:127030949..127034199,6	MCF-7	breast:
13	chr7:126985529..126987852-chr7:126995561..126998469,2	K562	blood:
14	chr7:126991047..126993006-chr7:127034690..127037263,2	K562	blood:
15	chr7:126986612..126990415-chr7:127030676..127033732,5	MCF-7	breast:
16	chr7:126987087..126990445-chr7:126991275..126994232,5	K562	blood:
17	chr7:126987461..126988081-chr7:127049072..127050341,3	MCF-7	breast:
18	chr7:126986399..126988206-chr7:127024325..127027237,2	K562	blood:
19	chr7:126987864..126988465-chr7:127847991..127848717,2	MCF-7	breast:
20	chr7:126982960..126985576-chr7:127008832..127010898,2	K562	blood:
21	chr7:126994441..126996750-chr7:126997785..127000283,3	K562	blood:
22	chr7:126985529..126987852-chr7:126995561..126998469,2	K562	blood:
23	chr7:126985955..126988348-chr7:127020622..127023787,3	K562	blood:
24	chr7:126987666..126988359-chr7:127047527..127048847,7	MCF-7	breast:
25	chr7:126983674..126985378-chr7:126988409..126990765,2	K562	blood:
26	chr7:126985549..126992875-chr7:127029251..127034121,12	K562	blood:
27	chr7:126986706..126988243-chr7:127024325..127027268,2	K562	blood:
28	chr7:126985391..126987885-chr7:127220985..127222536,2	MCF-7	breast:
29	chr7:126987125..126989269-chr7:127032034..127034121,3	K562	blood:
30	chr7:126979918..126982217-chr7:126984570..126987487,3	K562	blood:
31	chr7:126992206..126994276-chr7:126998893..127000633,3	K562	blood:
32	chr7:126975549..126977117-chr7:126985194..126987625,2	MCF-7	breast:
33	chr7:126985498..126988348-chr7:127020185..127023787,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-2	chr7:126990182-126990571	XLOC_006237
2	lnc-ARF5-2	chr7:126991452-126991577	XLOC_006237

No data

Variant related genes	Relation type
ENSG00000224138	TF binding region
ENSG00000224138	CpG island
ENSG00000224138	chromatin interactions
ENSG00000048405	chromatin interactions
NUFIP2	miRNA target sites

Extended variants
information (count: 441 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6973848	chr7:126985158-126985159	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146691690	chr7:126985192-126985193	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs17869704	chr7:126985197-126985198	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555740137	chr7:126985215-126985216	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570979936	chr7:126985242-126985243	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538332996	chr7:126985250-126985251	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576142580	chr7:126985314-126985315	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34510825	chr7:126985349-126985350	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs397890500	chr7:126985350-126985351	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189997083	chr7:126985357-126985358	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs398006189	chr7:126985359-126985360	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554924974	chr7:126985403-126985404	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140150307	chr7:126985404-126985405	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs193122308	chr7:126985439-126985440	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs4731349	chr7:126985478-126985479	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs542683651	chr7:126985495-126985496	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377338741	chr7:126985540-126985541	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs115470846	chr7:126985543-126985544	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150303715	chr7:126985568-126985569	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs17866185	chr7:126985573-126985574	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs527483968	chr7:126985652-126985653	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs184306955	chr7:126985666-126985667	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs12706780	chr7:126985682-126985683	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs563466584	chr7:126985698-126985699	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs531521470	chr7:126985705-126985706	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs551855166	chr7:126985746-126985747	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549328727	chr7:126985752-126985753	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs570892064	chr7:126985809-126985810	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs112014091	chr7:126985812-126985813	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs77250396	chr7:126985835-126985836	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs149121423	chr7:126985932-126985933	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs73445345	chr7:126985935-126985936	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs188608776	chr7:126985959-126985960	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs536031834	chr7:126986067-126986068	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs180963256	chr7:126986092-126986093	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183860582	chr7:126986110-126986111	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs374858437	chr7:126986113-126986114	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs376858489	chr7:126986126-126986127	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs6959198	chr7:126986135-126986136	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs6959473	chr7:126986199-126986200	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541477405	chr7:126986200-126986201	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs138875530	chr7:126986211-126986212	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530213347	chr7:126986251-126986252	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs6959255	chr7:126986276-126986277	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs561149987	chr7:126986382-126986383	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs28952014	chr7:126986438-126986439	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549665110	chr7:126986472-126986473	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142800647	chr7:126986502-126986503	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs535827209	chr7:126986539-126986540	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs189302331	chr7:126986544-126986545	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126982000-126987000	Weak transcription	HSMM	muscle
2	chr7:126984400-126987600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr7:126984400-127000800	Weak transcription	HSMMtube	muscle
4	chr7:126984600-126987600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr7:126984800-126987600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:126984800-126987600	Weak transcription	K562	blood
7	chr7:126985600-126987600	Weak transcription	Thymus	Thymus
8	chr7:126985800-126987600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr7:126986000-126986200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
10	chr7:126986000-126987600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:126986200-126986400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:126986200-126987600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr7:126986400-126988000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:126986600-126987600	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr7:126986600-126987600	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr7:126986800-126987600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:126986800-126987600	Enhancers	Adipose Nuclei	Adipose
18	chr7:126986800-126987600	Enhancers	Aorta	Aorta
19	chr7:126986800-126987600	Enhancers	Colonic Mucosa	Colon
20	chr7:126987000-126987200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
21	chr7:126987000-126987600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:126987000-126987600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr7:126987000-126987600	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr7:126987000-126987600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr7:126987000-126987600	Enhancers	Esophagus	oesophagus
26	chr7:126987000-126987600	Enhancers	Lung	lung
27	chr7:126987000-126987600	Enhancers	Pancreas	Pancrea
28	chr7:126987000-126987600	Strong transcription	HSMM	muscle
29	chr7:126987000-126988200	Enhancers	Gastric	stomach
30	chr7:126987000-126988400	Enhancers	Primary T cells fromperipheralblood	blood
31	chr7:126987000-126988400	Enhancers	Placenta	Placenta
32	chr7:126987000-126988600	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr7:126987200-126987600	Enhancers	Primary B cells from peripheral blood	blood
34	chr7:126987200-126988800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr7:126987200-126995400	Weak transcription	Dnd41	blood
36	chr7:126987400-126987600	Enhancers	Primary T cells from cord blood	blood
37	chr7:126987400-126987600	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr7:126987400-126987600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
39	chr7:126987400-126987600	Enhancers	Ovary	ovary
40	chr7:126987400-126987600	Enhancers	Right Ventricle	heart
41	chr7:126987400-126987600	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr7:126987400-126987600	Enhancers	HMEC	breast
43	chr7:126987600-126987800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr7:126987600-126987800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
45	chr7:126987600-126987800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:126987600-126987800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr7:126987600-126987800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr7:126987600-126987800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:126987600-126987800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:126987600-126987800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood

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