Variant report

Variant	nsv886925
Chromosome Location	chr6:165319631-165705488
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1692)
CpG islands
(count:549)
Chromatin interactive
region (count:25)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1692 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:165339529-165339854	K562	blood:	n/a	n/a
2	ATF1	chr6:165501047-165501063	K562	blood:	n/a	n/a
3	ATF1	chr6:165441073-165441114	K562	blood:	n/a	n/a
4	BCL3	chr6:165426595-165426923	GM12878	blood:	n/a	n/a
5	BCL3	chr6:165418145-165418452	GM12878	blood:	n/a	n/a
6	BCL3	chr6:165426681-165426931	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:165341085-165341390	K562	blood:	n/a	n/a
8	BHLHE40	chr6:165639608-165639621	K562	blood:	n/a	n/a
9	BHLHE40	chr6:165341057-165341386	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:165341052-165341377	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:165341191-165341391	HepG2	liver:	n/a	n/a
12	BRCA1	chr6:165341072-165341263	GM12878	blood:	n/a	n/a
13	CBX3	chr6:165462829-165463232	K562	blood:	n/a	n/a
14	CBX3	chr6:165462768-165463242	K562	blood:	n/a	n/a
15	CBX3	chr6:165462791-165463264	HCT-116	colon:	n/a	n/a
16	CEBPB	chr6:165673958-165674298	HepG2	liver:	n/a	chr6:165674134-165674145
17	CEBPB	chr6:165572815-165572909	H1-hESC	embryonic stem cell:	n/a	chr6:165572819-165572830 chr6:165572819-165572830 chr6:165572819-165572832 chr6:165572819-165572832
18	CEBPB	chr6:165327180-165327476	HepG2	liver:	n/a	chr6:165327326-165327337
19	CEBPB	chr6:165340967-165341396	H1-hESC	embryonic stem cell:	n/a	chr6:165341089-165341100 chr6:165341089-165341102 chr6:165341090-165341101
20	CEBPB	chr6:165533080-165533415	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr6:165491383-165491633	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:165595660-165595860	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr6:165426733-165426862	A549	lung:	n/a	n/a
24	CEBPB	chr6:165320320-165320636	HepG2	liver:	n/a	chr6:165320481-165320490 chr6:165320479-165320492 chr6:165320481-165320490 chr6:165320481-165320490 chr6:165320481-165320492 chr6:165320481-165320490 chr6:165320479-165320490 chr6:165320479-165320492
25	CEBPB	chr6:165340972-165341220	HepG2	liver:	n/a	chr6:165341089-165341100 chr6:165341089-165341102 chr6:165341090-165341101
26	CEBPB	chr6:165641184-165641536	IMR90	lung:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
27	CEBPB	chr6:165673976-165674309	IMR90	lung:	n/a	chr6:165674134-165674145
28	CEBPB	chr6:165440862-165440891	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:165595689-165595865	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr6:165641158-165641506	Hela-S3	cervix:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
31	CEBPB	chr6:165630086-165630271	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:165568927-165569218	HepG2	liver:	n/a	chr6:165569062-165569073
33	CEBPB	chr6:165556460-165556793	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:165673285-165673494	HepG2	liver:	n/a	chr6:165673335-165673346
35	CEBPB	chr6:165630165-165630323	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr6:165645810-165646083	HepG2	liver:	n/a	chr6:165645949-165645960
37	CEBPB	chr6:165533000-165533478	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr6:165641185-165641522	HepG2	liver:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
39	CEBPB	chr6:165340979-165341269	K562	blood:	n/a	chr6:165341089-165341100 chr6:165341089-165341102 chr6:165341090-165341101
40	CEBPB	chr6:165568950-165569240	A549	lung:	n/a	chr6:165569062-165569073
41	CEBPB	chr6:165674003-165674256	A549	lung:	n/a	chr6:165674134-165674145
42	CEBPB	chr6:165511782-165511924	K562	blood:	n/a	n/a
43	CEBPB	chr6:165556474-165556739	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:165327411-165327418	K562	blood:	n/a	n/a
45	CEBPB	chr6:165673289-165673478	Hela-S3	cervix:	n/a	chr6:165673335-165673346
46	CEBPB	chr6:165641184-165641505	A549	lung:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
47	CHD2	chr6:165463083-165463102	GM12878	blood:	n/a	n/a
48	CHD2	chr6:165341111-165341307	HepG2	liver:	n/a	n/a
49	CTCF	chr6:165645244-165645583	H1-hESC	embryonic stem cell:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
50	CTCF	chr6:165659240-165659390	HCM	heart:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165341382-165341432	HUVEC	blood vessel:	n/a
2	chr6:165341241-165341291	NT2-D1	testis:	n/a
3	chr6:165679873-165679923	PrEC	prostate:	n/a
4	chr6:165341320-165341370	GM12891	blood:	n/a
5	chr6:165658423-165658473	AG09309	skin:	n/a
6	chr6:165679873-165679923	SK-N-SH_RA	brain:	n/a
7	chr6:165679873-165679923	HRCEpiC	kidney:	n/a
8	chr6:165341382-165341432	GM12878	blood:	n/a
9	chr6:165324747-165324797	ProgFib	skin:	n/a
10	chr6:165341320-165341370	AG10803	skin:	n/a
11	chr6:165384599-165384649	HCF	heart:	n/a
12	chr6:165679873-165679923	AoSMC	blood vessel:	n/a
13	chr6:165341320-165341370	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:165341382-165341432	ECC-1	luminal epithelium:	n/a
15	chr6:165679873-165679923	HAEpiC	amniotic membrane:	n/a
16	chr6:165384599-165384649	A549	lung:	n/a
17	chr6:165341382-165341432	GM12892	blood:	n/a
18	chr6:165384599-165384649	GM12891	blood:	n/a
19	chr6:165324747-165324797	Hepatocyte	liver:	n/a
20	chr6:165658423-165658473	HNPCEpiC	eye:	n/a
21	chr6:165348000-165348050	AG09309	skin:	n/a
22	chr6:165324747-165324797	ovcar-3	ovarian:	n/a
23	chr6:165324747-165324797	ECC-1	luminal epithelium:	n/a
24	chr6:165679873-165679923	IMR90	lung:	fetal
25	chr6:165341320-165341370	HIPEpiC	eye:	n/a
26	chr6:165658423-165658473	AG09319	gingival:	n/a
27	chr6:165341382-165341432	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:165341241-165341291	HCT-116	colon:	n/a
29	chr6:165679873-165679923	NHBE	bronchial:	n/a
30	chr6:165341382-165341432	RPTEC	kidney:	n/a
31	chr6:165415258-165415308	AG04449	skin:	fetal
32	chr6:165324747-165324797	BE2_C	brain:	n/a
33	chr6:165658423-165658473	NHBE	bronchial:	n/a
34	chr6:165324747-165324797	AoSMC	blood vessel:	n/a
35	chr6:165341382-165341432	K562	blood:	n/a
36	chr6:165341382-165341432	CMK	blood:	n/a
37	chr6:165658423-165658473	NHDF-neo	bronchial:	n/a
38	chr6:165415258-165415308	MCF10A-Er-Src	breast:	n/a
39	chr6:165415258-165415308	SK-N-SH_RA	brain:	n/a
40	chr6:165341241-165341291	ProgFib	skin:	n/a
41	chr6:165341320-165341370	SK-N-SH	brain:	n/a
42	chr6:165341241-165341291	LNCaP	prostate:	n/a
43	chr6:165348000-165348050	A549	lung:	n/a
44	chr6:165384599-165384649	PrEC	prostate:	n/a
45	chr6:165341382-165341432	ovcar-3	ovarian:	n/a
46	chr6:165341382-165341432	AG09319	gingival:	n/a
47	chr6:165348000-165348050	H1-hESC	embryonic stem cell:	embryo
48	chr6:165384599-165384649	SKMC	muscle:	n/a
49	chr6:165324747-165324797	HepG2	liver:	n/a
50	chr6:165341320-165341370	SKMC	muscle:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:165632737..165634730-chr6:165637289..165639668,2	K562	blood:
2	chr6:165271396..165272279-chr6:165462865..165463466,2	MCF-7	breast:
3	chr6:165539543..165541848-chr6:165544518..165546207,2	K562	blood:
4	chr6:165375696..165377875-chr6:165438259..165440436,2	K562	blood:
5	chr6:165577753..165580449-chr6:165583004..165584853,2	K562	blood:
6	chr6:165566946..165568457-chr6:165571126..165572931,2	K562	blood:
7	chr6:165447524..165449382-chr6:165456045..165457781,2	K562	blood:
8	chr6:165632737..165634730-chr6:165637289..165639668,2	K562	blood:
9	chr6:164768200..164769032-chr6:165340931..165341635,2	MCF-7	breast:
10	chr6:165566946..165568457-chr6:165571126..165572931,2	K562	blood:
11	chr6:165375696..165377875-chr6:165438259..165440436,2	K562	blood:
12	chr6:164767711..164769131-chr6:165340232..165341669,7	MCF-7	breast:
13	chr6:165641887..165643835-chr6:165647824..165649680,2	K562	blood:
14	chr6:165610948..165613240-chr6:165614979..165616709,2	K562	blood:
15	chr6:165539543..165541848-chr6:165544518..165546207,2	K562	blood:
16	chr6:165447524..165449382-chr6:165456045..165457781,2	K562	blood:
17	chr6:165549550..165552338-chr6:165552859..165555355,2	K562	blood:
18	chr6:165577753..165580449-chr6:165583004..165584853,2	K562	blood:
19	chr6:165693401..165693973-chr6:165739529..165740029,2	K562	blood:
20	chr6:165549550..165552338-chr6:165552859..165555355,2	K562	blood:
21	chr6:165335824..165337632-chr6:165338882..165340730,2	K562	blood:
22	chr6:164637205..164638102-chr6:165340164..165340958,2	MCF-7	breast:
23	chr6:165610948..165613240-chr6:165614979..165616709,2	K562	blood:
24	chr6:165335824..165337632-chr6:165338882..165340730,2	K562	blood:
25	chr6:165641887..165643835-chr6:165647824..165649680,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-QKI-5	chr6:165341449-165341714	FPKM1_group_28841_transcript_1
2	lnc-C6orf118-4	chr6:165530684-165531013	NONHSAT115999
3	lnc-QKI-5	chr6:165341827-165342092	NONHSAT115997
4	lnc-C6orf118-3	chr6:165694970-165695025	NONHSAT116000
5	lnc-C6orf118-3	chr6:165695129-165695184	NONHSAT116000
6	lnc-QKI-5	chr6:165341509-165341544	XLOC_005534
7	lnc-QKI-5	chr6:165341407-165341431	FPKM1_group_28841_transcript_1
8	lnc-C6orf118-3	chr6:165695129-165695511	NONHSAT116001
9	lnc-C6orf118-3	chr6:165693522-165693599	NONHSAT116001
10	lnc-C6orf118-3	chr6:165693153-165693522	NONHSAT116000
11	lnc-QKI-5	chr6:165341827-165342411	XLOC_005534
12	lnc-QKI-5	chr6:165341407-165341431	NONHSAT115997
13	lnc-C6orf118-3	chr6:165694970-165695025	NONHSAT116001

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C6orf118	hsa-miR-1	chr6:165693446-165693473

Variant related genes	Relation type
ENSG00000217878	TF binding region
C6orf118	TF binding region
ENSG00000217878	CpG island
C6orf118	CpG island

Extended variants
information (count: 11047 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:11047 , 50 per page) page: 1 2 3 4 5 6 7 ... 221

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1227990	chr6:165319631-165319632	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540659191	chr6:165319647-165319648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186736898	chr6:165319648-165319649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75053631	chr6:165319732-165319733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138101675	chr6:165319762-165319763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562938110	chr6:165319773-165319774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377751741	chr6:165319867-165319868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142643267	chr6:165319884-165319885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143203659	chr6:165319939-165319940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560441416	chr6:165319955-165319956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528051958	chr6:165319985-165319986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75088316	chr6:165320057-165320058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550391037	chr6:165320060-165320061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578109088	chr6:165320079-165320080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76535834	chr6:165320084-165320085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535203596	chr6:165320093-165320094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141290727	chr6:165320095-165320096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569061947	chr6:165320157-165320158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539676703	chr6:165320165-165320166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113751086	chr6:165320206-165320207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114064109	chr6:165320207-165320208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555484788	chr6:165320315-165320316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9347944	chr6:165320379-165320380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138021091	chr6:165320384-165320385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116433330	chr6:165320451-165320452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76896550	chr6:165320461-165320462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367921902	chr6:165320486-165320487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545220016	chr6:165320500-165320501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs60545455	chr6:165320513-165320514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560382123	chr6:165320564-165320565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527990382	chr6:165320579-165320580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114239720	chr6:165320586-165320587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79875850	chr6:165320587-165320588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79505272	chr6:165320618-165320619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550385736	chr6:165320648-165320649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs58801628	chr6:165320682-165320683	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs533131014	chr6:165320683-165320684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561623095	chr6:165320698-165320699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551618137	chr6:165320706-165320707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566730277	chr6:165320711-165320712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533846412	chr6:165320751-165320752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115826508	chr6:165320771-165320772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567538050	chr6:165320773-165320774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538266379	chr6:165320806-165320807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140334627	chr6:165320865-165320866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577733526	chr6:165320899-165320900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545158818	chr6:165320913-165320914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528792377	chr6:165320926-165320927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34564357	chr6:165320992-165320993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572353255	chr6:165321066-165321067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165319000-165320000	Weak transcription	Fetal Brain Female	brain
2	chr6:165319600-165321000	Weak transcription	Gastric	stomach
3	chr6:165320000-165321000	Enhancers	Fetal Brain Female	brain
4	chr6:165320600-165321400	Enhancers	Fetal Brain Male	brain
5	chr6:165321000-165321200	Enhancers	Gastric	stomach
6	chr6:165321000-165325800	Weak transcription	Fetal Brain Female	brain
7	chr6:165321400-165326000	Weak transcription	Fetal Brain Male	brain
8	chr6:165323800-165326400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:165324400-165324600	Enhancers	Fetal Heart	heart
10	chr6:165324400-165324800	Enhancers	Brain Anterior Caudate	brain
11	chr6:165324400-165325400	Enhancers	Brain Germinal Matrix	brain
12	chr6:165324400-165326000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr6:165324600-165324800	Flanking Active TSS	Fetal Heart	heart
14	chr6:165324600-165325000	Enhancers	HSMM	muscle
15	chr6:165324600-165325800	Active TSS	Brain Cingulate Gyrus	brain
16	chr6:165324600-165325800	Active TSS	Brain Hippocampus Middle	brain
17	chr6:165324600-165325800	Active TSS	Brain Substantia Nigra	brain
18	chr6:165324800-165325000	Enhancers	Fetal Heart	heart
19	chr6:165324800-165325400	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr6:165324800-165325600	Active TSS	Right Ventricle	heart
21	chr6:165324800-165325800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr6:165324800-165325800	Active TSS	Brain Angular Gyrus	brain
23	chr6:165324800-165325800	Active TSS	Brain Anterior Caudate	brain
24	chr6:165324800-165325800	Active TSS	Right Atrium	heart
25	chr6:165324800-165326000	Active TSS	Brain Inferior Temporal Lobe	brain
26	chr6:165324800-165326000	Active TSS	Stomach Smooth Muscle	stomach
27	chr6:165324800-165326200	Enhancers	Adipose Nuclei	Adipose
28	chr6:165325000-165325200	Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr6:165325000-165325400	Active TSS	Colon Smooth Muscle	Colon
30	chr6:165325000-165325400	Flanking Active TSS	Fetal Heart	heart
31	chr6:165325000-165325400	Weak transcription	HSMM	muscle
32	chr6:165325000-165325800	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr6:165325200-165325400	Flanking Active TSS	HSMMtube	muscle
34	chr6:165325200-165325600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr6:165325200-165325600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr6:165325200-165326000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr6:165325200-165326400	Enhancers	Fetal Stomach	stomach
38	chr6:165325400-165325600	Flanking Active TSS	Colon Smooth Muscle	Colon
39	chr6:165325400-165325600	Flanking Active TSS	Psoas Muscle	Psoas
40	chr6:165325400-165325600	Active TSS	HSMMtube	muscle
41	chr6:165325400-165325800	Flanking Active TSS	Brain Germinal Matrix	brain
42	chr6:165325400-165325800	Active TSS	Fetal Muscle Trunk	muscle
43	chr6:165325400-165325800	Enhancers	Left Ventricle	heart
44	chr6:165325400-165325800	Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr6:165325400-165326000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr6:165325400-165326200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr6:165325400-165326200	Enhancers	Fetal Heart	heart
48	chr6:165325400-165326200	Enhancers	HSMM	muscle
49	chr6:165325400-165326400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr6:165325400-165326400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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