Variant report

Variant	nsv1019357
Chromosome Location	chr6:118731468-118860705
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:684)
CpG islands
(count:366)
Chromatin interactive
region (count:45)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:118827198-118827857	K562	blood:	n/a	n/a
2	ARID3A	chr6:118823438-118823630	K562	blood:	n/a	n/a
3	ARID3A	chr6:118858668-118859424	K562	blood:	n/a	n/a
4	ARID3A	chr6:118830184-118830599	K562	blood:	n/a	n/a
5	ARID3A	chr6:118789925-118790949	HepG2	liver:	n/a	n/a
6	ATF1	chr6:118858821-118859136	K562	blood:	n/a	n/a
7	ATF1	chr6:118857664-118857956	K562	blood:	n/a	n/a
8	ATF2	chr6:118844367-118844780	GM12878	blood:	n/a	n/a
9	ATF2	chr6:118788378-118788709	GM12878	blood:	n/a	n/a
10	ATF3	chr6:118790642-118790921	K562	blood:	n/a	n/a
11	ATF3	chr6:118827141-118827527	K562	blood:	n/a	n/a
12	ATF3	chr6:118858885-118859169	K562	blood:	n/a	n/a
13	BATF	chr6:118806735-118807083	GM12878	blood:	n/a	chr6:118806904-118806914 chr6:118806903-118806914
14	BATF	chr6:118844451-118844653	GM12878	blood:	n/a	n/a
15	BATF	chr6:118844430-118844743	GM12878	blood:	n/a	n/a
16	BATF	chr6:118806716-118807107	GM12878	blood:	n/a	chr6:118806904-118806914 chr6:118806903-118806914
17	BHLHE40	chr6:118858863-118859144	K562	blood:	n/a	n/a
18	BHLHE40	chr6:118790184-118790852	HepG2	liver:	n/a	n/a
19	BHLHE40	chr6:118826979-118827557	K562	blood:	n/a	n/a
20	BHLHE40	chr6:118806741-118807388	GM12878	blood:	n/a	n/a
21	CBX3	chr6:118809816-118810159	K562	blood:	n/a	n/a
22	CBX3	chr6:118809864-118810120	K562	blood:	n/a	n/a
23	CBX3	chr6:118809874-118810172	HCT-116	colon:	n/a	n/a
24	CBX3	chr6:118852098-118852469	HCT-116	colon:	n/a	n/a
25	CBX3	chr6:118852090-118852382	K562	blood:	n/a	n/a
26	CBX3	chr6:118816720-118817275	HCT-116	colon:	n/a	n/a
27	CCNT2	chr6:118857653-118857969	K562	blood:	n/a	n/a
28	CCNT2	chr6:118858773-118859317	K562	blood:	n/a	n/a
29	CCNT2	chr6:118827176-118827545	K562	blood:	n/a	n/a
30	CEBPB	chr6:118807394-118807584	K562	blood:	n/a	chr6:118807509-118807520
31	CEBPB	chr6:118816703-118817336	HCT-116	colon:	n/a	n/a
32	CEBPB	chr6:118758682-118758919	HepG2	liver:	n/a	chr6:118758789-118758800
33	CEBPB	chr6:118741797-118741903	A549	lung:	n/a	n/a
34	CEBPB	chr6:118790076-118790981	Hela-S3	cervix:	n/a	chr6:118790816-118790827
35	CEBPB	chr6:118790309-118791032	HepG2	liver:	n/a	chr6:118790816-118790827
36	CEBPB	chr6:118758660-118758932	IMR90	lung:	n/a	chr6:118758789-118758800
37	CEBPB	chr6:118858766-118859165	K562	blood:	n/a	n/a
38	CEBPB	chr6:118790642-118790962	K562	blood:	n/a	chr6:118790816-118790827
39	CEBPB	chr6:118790202-118791017	IMR90	lung:	n/a	chr6:118790816-118790827
40	CEBPB	chr6:118790697-118790886	H1-hESC	embryonic stem cell:	n/a	chr6:118790816-118790827
41	CEBPB	chr6:118850957-118851173	A549	lung:	n/a	chr6:118851113-118851124 chr6:118851111-118851124 chr6:118851111-118851122
42	CEBPB	chr6:118816801-118817338	IMR90	lung:	n/a	n/a
43	CEBPB	chr6:118807323-118807703	IMR90	lung:	n/a	chr6:118807509-118807520
44	CEBPB	chr6:118826847-118827174	HepG2	liver:	n/a	chr6:118827005-118827016
45	CEBPB	chr6:118790676-118791047	MCF-7	breast:	n/a	chr6:118790816-118790827
46	CEBPB	chr6:118823417-118823791	K562	blood:	n/a	n/a
47	CEBPB	chr6:118807313-118807756	MCF-7	breast:	n/a	chr6:118807509-118807520
48	CEBPB	chr6:118850942-118851291	HepG2	liver:	n/a	chr6:118851113-118851124 chr6:118851111-118851124 chr6:118851111-118851122
49	CEBPB	chr6:118816873-118817089	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:118826803-118827596	K562	blood:	n/a	chr6:118827005-118827016

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:118821449-118821499	GM19239	blood:	n/a
2	chr6:118822505-118822555	AG09309	skin:	n/a
3	chr6:118823964-118824014	Hela-S3	cervix:	n/a
4	chr6:118822466-118822516	HRCEpiC	kidney:	n/a
5	chr6:118822131-118822181	LNCaP	prostate:	n/a
6	chr6:118822505-118822555	HRCEpiC	kidney:	n/a
7	chr6:118823964-118824014	HEK293	kidney:	embryo
8	chr6:118821449-118821499	ProgFib	skin:	n/a
9	chr6:118821449-118821499	HAEpiC	amniotic membrane:	n/a
10	chr6:118821449-118821499	K562	blood:	n/a
11	chr6:118823964-118824014	PrEC	prostate:	n/a
12	chr6:118776527-118776577	K562	blood:	n/a
13	chr6:118822505-118822555	Jurkat	blood:	n/a
14	chr6:118823964-118824014	NHDF-neo	bronchial:	n/a
15	chr6:118822466-118822516	Jurkat	blood:	n/a
16	chr6:118776527-118776577	ProgFib	skin:	n/a
17	chr6:118822505-118822555	HEK293	kidney:	embryo
18	chr6:118822131-118822181	RPTEC	kidney:	n/a
19	chr6:118823964-118824014	K562	blood:	n/a
20	chr6:118823964-118824014	SK-N-SH	brain:	n/a
21	chr6:118822131-118822181	CMK	blood:	n/a
22	chr6:118822505-118822555	RPTEC	kidney:	n/a
23	chr6:118822131-118822181	HRE	kidney:	n/a
24	chr6:118822505-118822555	ECC-1	luminal epithelium:	n/a
25	chr6:118823964-118824014	ECC-1	luminal epithelium:	n/a
26	chr6:118776527-118776577	T-47D	breast:	n/a
27	chr6:118823964-118824014	BJ	skin:	n/a
28	chr6:118821449-118821499	BJ	skin:	n/a
29	chr6:118822466-118822516	NB4	blood:	n/a
30	chr6:118776527-118776577	RPTEC	kidney:	n/a
31	chr6:118822466-118822516	A549	lung:	n/a
32	chr6:118822466-118822516	AG04450	lung:	fetal
33	chr6:118822505-118822555	ovcar-3	ovarian:	n/a
34	chr6:118823964-118824014	MCF10A-Er-Src	breast:	n/a
35	chr6:118776527-118776577	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:118822131-118822181	GM12878	blood:	n/a
37	chr6:118822505-118822555	SAEC	small airway:	n/a
38	chr6:118823964-118824014	A549	lung:	n/a
39	chr6:118822131-118822181	SKMC	muscle:	n/a
40	chr6:118821449-118821499	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:118821449-118821499	HepG2	liver:	n/a
42	chr6:118776527-118776577	PANC-1	pancreas:	n/a
43	chr6:118822131-118822181	AoSMC	blood vessel:	n/a
44	chr6:118821449-118821499	HIPEpiC	eye:	n/a
45	chr6:118822505-118822555	Caco-2	colon:	n/a
46	chr6:118823964-118824014	HCM	heart:	n/a
47	chr6:118776527-118776577	AG04449	skin:	fetal
48	chr6:118822466-118822516	NHBE	bronchial:	n/a
49	chr6:118822505-118822555	NB4	blood:	n/a
50	chr6:118822505-118822555	SK-N-SH_RA	brain:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:118787172..118789058-chr6:118799160..118802134,2	MCF-7	breast:
2	chr6:118604757..118606576-chr6:118829465..118831114,11	MCF-7	breast:
3	chr6:118827080..118828715-chr6:118830473..118832709,2	K562	blood:
4	chr6:118729437..118730312-chr6:118828228..118829001,2	MCF-7	breast:
5	chr6:118790912..118793638-chr6:118795834..118798403,2	K562	blood:
6	chr6:118807810..118810020-chr6:118811825..118813344,2	K562	blood:
7	chr6:118826989..118829311-chr6:118938215..118940660,2	K562	blood:
8	chr6:118797218..118799094-chr6:118801502..118803823,2	K562	blood:
9	chr6:118830553..118833464-chr6:118833711..118836187,2	K562	blood:
10	chr6:118839207..118841504-chr6:119214917..119216766,2	MCF-7	breast:
11	chr6:118824560..118826306-chr6:118830401..118832913,2	K562	blood:
12	chr6:118785192..118787598-chr6:118787814..118790088,2	K562	blood:
13	chr6:118785192..118787598-chr6:118787814..118790088,2	K562	blood:
14	chr6:118827080..118828715-chr6:118830473..118832709,2	K562	blood:
15	chr6:118787172..118789058-chr6:118799160..118802134,2	MCF-7	breast:
16	chr6:118836380..118838045-chr6:118841416..118842970,2	K562	blood:
17	chr6:118766414..118769352-chr6:118774128..118777684,3	K562	blood:
18	chr6:118807810..118810020-chr6:118811825..118813344,2	K562	blood:
19	chr6:118845234..118848026-chr6:118887537..118889460,2	K562	blood:
20	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
21	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
22	chr6:118824560..118826306-chr6:118830401..118832913,2	K562	blood:
23	chr6:118836380..118838045-chr6:118841416..118842970,2	K562	blood:
24	chr6:118830553..118833373-chr6:118834538..118836187,2	K562	blood:
25	chr6:118840065..118842365-chr6:118844866..118846753,2	K562	blood:
26	chr6:118807029..118809570-chr6:118811844..118815669,3	K562	blood:
27	chr6:118830553..118833464-chr6:118833711..118836187,2	K562	blood:
28	chr6:118840065..118842365-chr6:118844866..118846753,2	K562	blood:
29	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
30	chr6:118790912..118793638-chr6:118795834..118798403,2	K562	blood:
31	chr6:118604657..118606544-chr6:118829791..118831020,17	MCF-7	breast:
32	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:
33	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
34	chr6:118630135..118632500-chr6:118803686..118805267,2	K562	blood:
35	chr6:118829900..118830527-chr6:118872009..118872536,2	MCF-7	breast:
36	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
37	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:
38	chr6:118605631..118606342-chr6:118829971..118830837,2	K562	blood:
39	chr6:118830553..118833373-chr6:118834538..118836187,2	K562	blood:
40	chr6:118807029..118809570-chr6:118811844..118815669,3	K562	blood:
41	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
42	chr6:118829899..118830781-chr6:118901492..118902427,2	MCF-7	breast:
43	chr6:118858794..118860547-chr6:118861810..118864378,3	K562	blood:
44	chr6:118797218..118799094-chr6:118801502..118803823,2	K562	blood:
45	chr6:118829745..118830555-chr6:118939535..118940562,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLN-1	chr6:118822536-118824996	NR_002730
2	lnc-PLN-2	chr6:118772307-118773627	NONHSAT114692

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C6orf204	hsa-miR-335-5p	chr6:118812647-118812669

Variant related genes	Relation type
ENSG00000216809	TF binding region
BRD7P3	TF binding region
ENSG00000216809	CpG island
BRD7P3	CpG island
ENSG00000111877	chromatin interactions
ENSG00000216809	chromatin interactions
ENSG00000111875	chromatin interactions

Extended variants
information (count: 4461 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:4461 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10457330	chr6:118731468-118731469	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550893470	chr6:118731503-118731504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188673308	chr6:118731560-118731561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201604820	chr6:118731562-118731563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142847829	chr6:118731563-118731564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533159453	chr6:118731599-118731600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546662352	chr6:118731750-118731751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566642051	chr6:118731819-118731820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571734608	chr6:118731881-118731882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12663066	chr6:118731926-118731927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569479133	chr6:118732007-118732008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552481155	chr6:118732036-118732037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538145893	chr6:118732106-118732107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151039202	chr6:118732113-118732114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576860644	chr6:118732119-118732120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140931162	chr6:118732124-118732125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553069246	chr6:118732129-118732130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537262869	chr6:118732139-118732140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541955872	chr6:118732153-118732154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561723966	chr6:118732215-118732216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575407708	chr6:118732228-118732229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374898479	chr6:118732242-118732243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544132260	chr6:118732291-118732292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185941519	chr6:118732312-118732313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533123790	chr6:118732321-118732322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546576442	chr6:118732333-118732334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201751296	chr6:118732359-118732360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374188654	chr6:118732362-118732363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529363282	chr6:118732367-118732368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188794708	chr6:118732411-118732412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182419402	chr6:118732435-118732436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs117487940	chr6:118732444-118732445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371963914	chr6:118732445-118732446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs578202287	chr6:118732471-118732472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551758699	chr6:118732474-118732475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146872168	chr6:118732494-118732495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534530679	chr6:118732573-118732574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574221574	chr6:118732581-118732582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374368224	chr6:118732620-118732621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34880874	chr6:118732662-118732663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548666721	chr6:118732663-118732664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552981376	chr6:118732664-118732665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556783316	chr6:118732690-118732691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568577329	chr6:118732693-118732694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534343268	chr6:118732744-118732745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557094643	chr6:118732753-118732754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572917621	chr6:118732754-118732755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71554901	chr6:118732758-118732759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9489376	chr6:118732779-118732780	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs140698745	chr6:118732812-118732813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	22522925	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118715800-118731800	Weak transcription	Pancreas	Pancrea
2	chr6:118730400-118745000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:118737000-118737800	Enhancers	Aorta	Aorta
4	chr6:118737800-118738800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:118737800-118748000	Weak transcription	Aorta	Aorta
6	chr6:118740600-118741200	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr6:118740800-118741400	Enhancers	Fetal Heart	heart
8	chr6:118742400-118742600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:118742400-118743000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:118742400-118743000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:118742400-118743000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:118742400-118743000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:118742400-118743000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:118742400-118743000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:118742400-118743400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:118748000-118748200	ZNF genes & repeats	Aorta	Aorta
17	chr6:118757400-118757800	Enhancers	HSMMtube	muscle
18	chr6:118757600-118757800	Enhancers	Psoas Muscle	Psoas
19	chr6:118757800-118758000	ZNF genes & repeats	Psoas Muscle	Psoas
20	chr6:118763000-118770600	Weak transcription	HSMM	muscle
21	chr6:118763600-118772600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr6:118763800-118770200	Weak transcription	Brain Substantia Nigra	brain
23	chr6:118764600-118766400	Weak transcription	Primary T cells from cord blood	blood
24	chr6:118764800-118765200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr6:118764800-118772000	Weak transcription	Ovary	ovary
26	chr6:118765200-118765600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr6:118765400-118769200	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr6:118765600-118766200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:118765600-118769000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:118766200-118767000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:118766400-118766800	Strong transcription	Primary T cells from cord blood	blood
32	chr6:118766600-118769600	Weak transcription	Gastric	stomach
33	chr6:118766600-118771800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr6:118766800-118767200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
35	chr6:118766800-118767600	Weak transcription	NH-A	brain
36	chr6:118766800-118769400	ZNF genes & repeats	Primary T cells from cord blood	blood
37	chr6:118767000-118771600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:118767200-118767400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:118767400-118771200	Weak transcription	Left Ventricle	heart
40	chr6:118768000-118768600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:118768800-118769200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr6:118769000-118771200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr6:118769400-118769800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr6:118772600-118774000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:118773200-118775000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:118773400-118776200	ZNF genes & repeats	Adipose Nuclei	Adipose
47	chr6:118774400-118808600	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr6:118775000-118779600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:118775600-118784600	Weak transcription	HSMM	muscle
50	chr6:118776000-118792400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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