Variant report

Variant	nsv1021815
Chromosome Location	chr6:113703567-113799956
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1048)
CpG islands
(count:245)
Chromatin interactive
region (count:25)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1048 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:113754672-113754879	HepG2	liver:	n/a	n/a
2	ATF1	chr6:113768318-113768514	K562	blood:	n/a	n/a
3	ATF1	chr6:113732307-113732507	K562	blood:	n/a	n/a
4	ATF3	chr6:113754522-113754958	A549	lung:	n/a	n/a
5	BACH1	chr6:113733978-113734537	H1-hESC	embryonic stem cell:	n/a	chr6:113734363-113734377
6	BACH1	chr6:113734213-113734508	K562	blood:	n/a	chr6:113734363-113734377
7	BACH1	chr6:113750054-113750124	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:113711021-113711060	K562	blood:	n/a	n/a
9	BCL3	chr6:113761249-113761562	GM12878	blood:	n/a	n/a
10	BCL3	chr6:113753888-113755123	A549	lung:	n/a	n/a
11	BCL3	chr6:113743661-113743984	GM12878	blood:	n/a	n/a
12	BCL3	chr6:113754122-113754485	GM12878	blood:	n/a	n/a
13	BCL3	chr6:113754514-113755014	A549	lung:	n/a	n/a
14	BHLHE40	chr6:113768305-113768578	K562	blood:	n/a	n/a
15	BHLHE40	chr6:113768323-113768567	HepG2	liver:	n/a	n/a
16	BRCA1	chr6:113753980-113755089	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr6:113786063-113786678	HCT-116	colon:	n/a	n/a
18	CBX3	chr6:113786094-113786655	HCT-116	colon:	n/a	n/a
19	CEBPB	chr6:113768192-113768722	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr6:113786105-113786668	HCT-116	colon:	n/a	n/a
21	CEBPB	chr6:113768256-113768665	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr6:113768278-113768620	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:113768204-113768702	A549	lung:	n/a	n/a
24	CEBPB	chr6:113768265-113768689	MCF-7	breast:	n/a	n/a
25	CEBPB	chr6:113754718-113755037	HepG2	liver:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
26	CEBPB	chr6:113768082-113768823	HCT-116	colon:	n/a	n/a
27	CEBPB	chr6:113786170-113786478	MCF-7	breast:	n/a	n/a
28	CEBPB	chr6:113754482-113755075	A549	lung:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
29	CEBPB	chr6:113716041-113716297	HepG2	liver:	n/a	chr6:113716141-113716152 chr6:113716139-113716150 chr6:113716141-113716152
30	CEBPB	chr6:113754780-113754993	H1-hESC	embryonic stem cell:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
31	CEBPB	chr6:113753852-113755255	A549	lung:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
32	CEBPB	chr6:113770078-113770639	HCT-116	colon:	n/a	n/a
33	CEBPB	chr6:113753887-113755234	Hela-S3	cervix:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
34	CEBPB	chr6:113768353-113768690	A549	lung:	n/a	n/a
35	CEBPB	chr6:113771207-113771457	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr6:113726450-113727392	MCF-7	breast:	n/a	chr6:113727348-113727361
37	CEBPB	chr6:113765415-113765592	A549	lung:	n/a	n/a
38	CEBPB	chr6:113754665-113755068	ECC-1	luminal epithelium:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
39	CEBPB	chr6:113753789-113755513	MCF-7	breast:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
40	CEBPB	chr6:113768273-113768695	MCF-7	breast:	n/a	n/a
41	CEBPB	chr6:113754657-113755006	HepG2	liver:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
42	CEBPB	chr6:113754654-113755021	ECC-1	luminal epithelium:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
43	CEBPB	chr6:113754634-113755024	HepG2	liver:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
44	CEBPB	chr6:113716074-113716244	IMR90	lung:	n/a	chr6:113716141-113716152 chr6:113716139-113716150 chr6:113716141-113716152
45	CEBPB	chr6:113768171-113768679	HCT-116	colon:	n/a	n/a
46	CEBPB	chr6:113753888-113754477	MCF-7	breast:	n/a	n/a
47	CEBPB	chr6:113753928-113755259	IMR90	lung:	n/a	chr6:113754871-113754882 chr6:113754869-113754882
48	CEBPB	chr6:113727510-113727794	IMR90	lung:	n/a	chr6:113727649-113727658 chr6:113727648-113727659
49	CEBPB	chr6:113786096-113786564	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:113727496-113727815	HepG2	liver:	n/a	chr6:113727649-113727658 chr6:113727648-113727659

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:113717752-113717802	NH-A	brain:	n/a
2	chr6:113717752-113717802	NH-A	brain:	n/a
3	chr6:113717752-113717802	U87	brain:	n/a
4	chr6:113755716-113755766	GM12878	blood:	n/a
5	chr6:113755716-113755766	ProgFib	skin:	n/a
6	chr6:113779374-113779424	NB4	blood:	n/a
7	chr6:113717752-113717802	SK-N-MC	brain:	n/a
8	chr6:113779374-113779424	PANC-1	pancreas:	n/a
9	chr6:113717752-113717802	Hela-S3	cervix:	n/a
10	chr6:113786051-113786101	IMR90	lung:	fetal
11	chr6:113717752-113717802	HNPCEpiC	eye:	n/a
12	chr6:113779374-113779424	MCF-7	breast:	n/a
13	chr6:113786051-113786101	H1-hESC	embryonic stem cell:	embryo
14	chr6:113786051-113786101	PFSK-1	brain:	n/a
15	chr6:113755716-113755766	SK-N-SH	brain:	n/a
16	chr6:113786051-113786101	HCF	heart:	n/a
17	chr6:113755716-113755766	GM12892	blood:	n/a
18	chr6:113717752-113717802	GM19239	blood:	n/a
19	chr6:113717752-113717802	BJ	skin:	n/a
20	chr6:113786051-113786101	A549	lung:	n/a
21	chr6:113755716-113755766	PrEC	prostate:	n/a
22	chr6:113755716-113755766	HEK293	kidney:	embryo
23	chr6:113717752-113717802	A549	lung:	n/a
24	chr6:113786051-113786101	HepG2	liver:	n/a
25	chr6:113755716-113755766	A549	lung:	n/a
26	chr6:113786051-113786101	ovcar-3	ovarian:	n/a
27	chr6:113779374-113779424	K562	blood:	n/a
28	chr6:113755716-113755766	CMK	blood:	n/a
29	chr6:113779374-113779424	GM12878	blood:	n/a
30	chr6:113755716-113755766	HCPEpiC	choroid plexus:	n/a
31	chr6:113755716-113755766	HL-60	blood:	n/a
32	chr6:113786051-113786101	AoSMC	blood vessel:	n/a
33	chr6:113786051-113786101	HUVEC	blood vessel:	n/a
34	chr6:113779374-113779424	ovcar-3	ovarian:	n/a
35	chr6:113755716-113755766	AG10803	skin:	n/a
36	chr6:113717752-113717802	HIPEpiC	eye:	n/a
37	chr6:113786051-113786101	U87	brain:	n/a
38	chr6:113786051-113786101	PANC-1	pancreas:	n/a
39	chr6:113755716-113755766	HRCEpiC	kidney:	n/a
40	chr6:113786051-113786101	HCPEpiC	choroid plexus:	n/a
41	chr6:113755716-113755766	HIPEpiC	eye:	n/a
42	chr6:113786051-113786101	SK-N-SH_RA	brain:	n/a
43	chr6:113779374-113779424	H1-hESC	embryonic stem cell:	embryo
44	chr6:113779374-113779424	CMK	blood:	n/a
45	chr6:113779374-113779424	U87	brain:	n/a
46	chr6:113779374-113779424	HMEC	breast:	n/a
47	chr6:113786051-113786101	NHDF-neo	bronchial:	n/a
48	chr6:113779374-113779424	AG04450	lung:	fetal
49	chr6:113786051-113786101	HL-60	blood:	n/a
50	chr6:113717752-113717802	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr6:113710899..113713233-chr6:113713434..113715224,2	K562	blood:
2	chr6:113753938..113755617-chr6:113771103..113773814,2	MCF-7	breast:
3	chr6:113753712..113755714-chr6:114178275..114180113,2	MCF-7	breast:
4	chr6:113732055..113735601-chr6:114178607..114183451,4	MCF-7	breast:
5	chr6:113799640..113802302-chr6:113802740..113805019,2	K562	blood:
6	chr6:113748365..113749941-chr6:113754582..113756807,2	MCF-7	breast:
7	chr6:113750617..113753339-chr6:113755230..113758094,2	MCF-7	breast:
8	chr6:113696986..113699351-chr6:113701475..113704316,2	MCF-7	breast:
9	chr6:113701651..113703892-chr6:113706663..113709047,2	K562	blood:
10	chr6:113750617..113753339-chr6:113755230..113758094,2	MCF-7	breast:
11	chr6:113701651..113703892-chr6:113706663..113709047,2	K562	blood:
12	chr6:113754604..113756824-chr6:113757687..113759351,2	MCF-7	breast:
13	chr6:113735341..113737235-chr6:113752412..113754611,2	MCF-7	breast:
14	chr6:113753088..113757268-chr6:113951584..113954499,3	MCF-7	breast:
15	chr6:113763198..113764987-chr6:114177471..114180396,2	MCF-7	breast:
16	chr6:113752685..113754255-chr6:113760032..113762327,2	MCF-7	breast:
17	chr6:113745322..113747163-chr6:114177770..114179887,2	MCF-7	breast:
18	chr6:113710899..113713233-chr6:113713434..113715224,2	K562	blood:
19	chr6:113753759..113754729-chr6:113767071..113767994,2	MCF-7	breast:
20	chr6:113748860..113752704-chr6:114177965..114181213,3	MCF-7	breast:
21	chr6:113753858..113756059-chr6:113770303..113773626,3	MCF-7	breast:
22	chr6:113753134..113757391-chr6:113759557..113761652,4	MCF-7	breast:
23	chr6:113741733..113746480-chr6:113749879..113754068,4	MCF-7	breast:
24	chr6:113755353..113757884-chr6:113758152..113760628,2	MCF-7	breast:
25	chr6:113755353..113757884-chr6:113758152..113760628,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC2-13	chr6:113795769-113795839	NONHSAT114543
2	lnc-HDAC2-3	chr6:113749742-113750180	XLOC_005809
3	lnc-HDAC2-13	chr6:113784898-113785193	NONHSAT114543
4	lnc-HDAC2-3	chr6:113754539-113754623	XLOC_005809
5	lnc-HDAC2-13	chr6:113790426-113790565	NONHSAT114543
6	lnc-HDAC2-3	chr6:113749753-113750180	XLOC_005809
7	lnc-HDAC2-3	chr6:113753761-113753843	XLOC_005809

No data

Variant related genes	Relation type
ENSG00000232316	TF binding region
ENSG00000232316	CpG island
ENSG00000155130	chromatin interactions
ENSG00000232316	chromatin interactions
ENSG00000230943	chromatin interactions
CCDC86	miRNA target sites
TMEFF2	miRNA target sites

Extended variants
information (count: 3878 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:3878 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540391	chr6:113703567-113703568	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200734057	chr6:113703577-113703578	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547725702	chr6:113703618-113703619	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs376393478	chr6:113703667-113703668	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs77502417	chr6:113703698-113703699	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs536267320	chr6:113703750-113703751	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs376873846	chr6:113703768-113703769	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs145579928	chr6:113703769-113703770	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs570763097	chr6:113703840-113703841	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs576123151	chr6:113703876-113703877	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs537227625	chr6:113703898-113703899	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs113133719	chr6:113703924-113703925	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs376457927	chr6:113703934-113703935	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs586040	chr6:113703939-113703940	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs586027	chr6:113703944-113703945	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs9387140	chr6:113703947-113703948	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs574705663	chr6:113703975-113703976	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs542240906	chr6:113704000-113704001	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs186915583	chr6:113704007-113704008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531082674	chr6:113704031-113704032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191746179	chr6:113704057-113704058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147708577	chr6:113704079-113704080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183096084	chr6:113704110-113704111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547687053	chr6:113704122-113704123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565996391	chr6:113704132-113704133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535856153	chr6:113704175-113704176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545530812	chr6:113704204-113704205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187041626	chr6:113704220-113704221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191469471	chr6:113704253-113704254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537108779	chr6:113704310-113704311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182109462	chr6:113704339-113704340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576994792	chr6:113704356-113704357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534903912	chr6:113704383-113704384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371875026	chr6:113704404-113704405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371685943	chr6:113704441-113704442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186790482	chr6:113704450-113704451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141060240	chr6:113704468-113704469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541852844	chr6:113704527-113704528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536322338	chr6:113704540-113704541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192674257	chr6:113704595-113704596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144919472	chr6:113704606-113704607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564592807	chr6:113704654-113704655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532315200	chr6:113704697-113704698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185636548	chr6:113704719-113704720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73539771	chr6:113704762-113704763	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530052956	chr6:113704774-113704775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150937963	chr6:113704824-113704825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76222402	chr6:113704825-113704826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554512395	chr6:113704850-113704851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369809354	chr6:113704884-113704885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
Acute lymphoblastic leukemia	17443227	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
Leukemia	18688285	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
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	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
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:113698800-113705800	Weak transcription	NH-A	brain
2	chr6:113699000-113704600	Weak transcription	Osteobl	bone
3	chr6:113699200-113706400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:113701800-113703600	Enhancers	NHDF-Ad	bronchial
5	chr6:113702200-113703600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr6:113702200-113703800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:113702200-113704000	Enhancers	NHLF	lung
8	chr6:113702200-113705000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:113702400-113703600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr6:113702600-113703600	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr6:113702800-113703800	Enhancers	Fetal Lung	lung
12	chr6:113703000-113703600	Enhancers	Fetal Brain Female	brain
13	chr6:113703000-113704000	Bivalent Enhancer	Primary B cells from cord blood	blood
14	chr6:113703200-113703600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:113703200-113703600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:113703200-113703600	Enhancers	Adipose Nuclei	Adipose
17	chr6:113703200-113703600	Enhancers	Fetal Brain Male	brain
18	chr6:113703200-113703600	Enhancers	HUVEC	blood vessel
19	chr6:113703200-113703800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr6:113703400-113704000	Enhancers	Fetal Stomach	stomach
21	chr6:113703400-113704400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:113703400-113706200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:113703600-113705000	Weak transcription	NHDF-Ad	bronchial
24	chr6:113703600-113705800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr6:113703600-113706000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr6:113703600-113706200	Weak transcription	HUVEC	blood vessel
27	chr6:113703600-113706400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr6:113703800-113704400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr6:113703800-113705800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:113703800-113706400	Weak transcription	Fetal Lung	lung
31	chr6:113704000-113704400	Weak transcription	Fetal Stomach	stomach
32	chr6:113704000-113704400	Weak transcription	NHLF	lung
33	chr6:113704400-113704600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:113704400-113704600	Enhancers	Fetal Stomach	stomach
35	chr6:113704400-113704800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:113704400-113704800	Enhancers	Ovary	ovary
37	chr6:113704400-113705000	Enhancers	NHLF	lung
38	chr6:113704600-113705000	Enhancers	Osteobl	bone
39	chr6:113704600-113712000	Weak transcription	Fetal Stomach	stomach
40	chr6:113704800-113705800	Weak transcription	Ovary	ovary
41	chr6:113704800-113706600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr6:113705000-113705200	Enhancers	NHDF-Ad	bronchial
43	chr6:113705000-113706000	Weak transcription	NHLF	lung
44	chr6:113705000-113706200	Weak transcription	Osteobl	bone
45	chr6:113705000-113708600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:113705200-113705600	Weak transcription	NHDF-Ad	bronchial
47	chr6:113705600-113705800	Weak transcription	HSMM	muscle
48	chr6:113705600-113707400	Enhancers	NHDF-Ad	bronchial
49	chr6:113705800-113706400	Enhancers	Muscle Satellite Cultured Cells	--
50	chr6:113705800-113707000	Enhancers	NH-A	brain

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