Variant report

Variant	esv3324611
Chromosome Location	chr7:66383817-66388015
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:681)
CpG islands
(count:611)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:681 , 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	chr7:66385864-66386220	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:66386606-66386710	HepG2	liver:	n/a	n/a
3	ATF1	chr7:66384388-66384664	K562	blood:	n/a	n/a
4	ATF2	chr7:66385771-66386323	GM12878	blood:	n/a	n/a
5	ATF2	chr7:66385679-66386383	GM12878	blood:	n/a	n/a
6	ATF3	chr7:66385745-66386246	A549	lung:	n/a	n/a
7	ATF3	chr7:66385848-66386331	A549	lung:	n/a	chr7:66386312-66386321
8	BACH1	chr7:66385825-66386278	K562	blood:	n/a	n/a
9	BACH1	chr7:66386756-66386769	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:66385825-66386372	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr7:66385761-66386158	GM12878	blood:	n/a	n/a
12	BCL3	chr7:66385626-66386276	A549	lung:	n/a	chr7:66386247-66386256 chr7:66385628-66385637 chr7:66386246-66386259
13	BCL3	chr7:66385637-66386299	A549	lung:	n/a	chr7:66386247-66386256 chr7:66386246-66386259
14	BCLAF1	chr7:66385693-66386379	GM12878	blood:	n/a	chr7:66386247-66386256 chr7:66386246-66386259
15	BCLAF1	chr7:66385669-66386385	GM12878	blood:	n/a	chr7:66386247-66386256 chr7:66386246-66386259
16	BCLAF1	chr7:66386723-66387514	GM12878	blood:	n/a	chr7:66386990-66386999
17	BHLHE40	chr7:66386635-66387560	K562	blood:	n/a	n/a
18	BHLHE40	chr7:66385702-66386353	GM12878	blood:	n/a	chr7:66386246-66386262 chr7:66386305-66386321
19	BHLHE40	chr7:66385762-66386393	HepG2	liver:	n/a	chr7:66386246-66386262 chr7:66386305-66386321
20	BHLHE40	chr7:66385672-66386407	K562	blood:	n/a	chr7:66386246-66386262 chr7:66386305-66386321
21	BRCA1	chr7:66385869-66386252	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr7:66386890-66387688	K562	blood:	n/a	n/a
23	CBX3	chr7:66385695-66386251	K562	blood:	n/a	n/a
24	CBX3	chr7:66385669-66386391	HCT-116	colon:	n/a	n/a
25	CBX3	chr7:66384335-66385056	K562	blood:	n/a	n/a
26	CBX3	chr7:66385281-66386301	K562	blood:	n/a	n/a
27	CCNT2	chr7:66384335-66384651	K562	blood:	n/a	n/a
28	CCNT2	chr7:66385838-66387627	K562	blood:	n/a	n/a
29	CEBPB	chr7:66385965-66386271	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:66386693-66387361	GM12878	blood:	n/a	n/a
31	CEBPB	chr7:66385664-66386251	K562	blood:	n/a	n/a
32	CEBPB	chr7:66385590-66386377	GM12878	blood:	n/a	n/a
33	CEBPB	chr7:66385839-66386320	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:66383763-66384021	K562	blood:	n/a	n/a
35	CEBPB	chr7:66385753-66386344	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:66385843-66386164	GM12878	blood:	n/a	n/a
37	CEBPD	chr7:66384234-66384767	K562	blood:	n/a	n/a
38	CEBPD	chr7:66385774-66386141	HepG2	liver:	n/a	n/a
39	CEBPD	chr7:66386956-66387629	K562	blood:	n/a	n/a
40	CEBPD	chr7:66384323-66384786	K562	blood:	n/a	n/a
41	CEBPD	chr7:66386595-66387667	K562	blood:	n/a	n/a
42	CHD2	chr7:66385789-66386337	K562	blood:	n/a	chr7:66386313-66386323
43	CHD2	chr7:66386605-66387440	K562	blood:	n/a	n/a
44	CHD2	chr7:66386631-66387377	GM12878	blood:	n/a	n/a
45	CHD2	chr7:66386749-66387203	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr7:66385870-66386355	Hela-S3	cervix:	n/a	chr7:66386313-66386323
47	CHD2	chr7:66385935-66386214	HepG2	liver:	n/a	n/a
48	CHD2	chr7:66385859-66386318	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr7:66385726-66386365	GM12878	blood:	n/a	chr7:66386313-66386323
50	CREB1	chr7:66385632-66386508	HepG2	liver:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66386859-66386909	Jurkat	blood:	n/a
2	chr7:66386859-66386909	Jurkat	blood:	n/a
3	chr7:66385256-66385306	H1-hESC	embryonic stem cell:	embryo
4	chr7:66385241-66385291	SK-N-MC	brain:	n/a
5	chr7:66387240-66387290	IMR90	lung:	fetal
6	chr7:66386797-66386847	U87	brain:	n/a
7	chr7:66386079-66386129	ProgFib	skin:	n/a
8	chr7:66387240-66387290	ECC-1	luminal epithelium:	n/a
9	chr7:66386045-66386095	HRE	kidney:	n/a
10	chr7:66386045-66386095	U87	brain:	n/a
11	chr7:66385829-66385879	MCF10A-Er-Src	breast:	n/a
12	chr7:66386859-66386909	BE2_C	brain:	n/a
13	chr7:66386079-66386129	NB4	blood:	n/a
14	chr7:66386499-66386549	SK-N-SH_RA	brain:	n/a
15	chr7:66386079-66386129	MCF-7	breast:	n/a
16	chr7:66386489-66386539	ECC-1	luminal epithelium:	n/a
17	chr7:66385829-66385879	HEEpiC	esophagus:	n/a
18	chr7:66386797-66386847	HCF	heart:	n/a
19	chr7:66386859-66386909	GM06990	blood:	n/a
20	chr7:66385256-66385306	RPTEC	kidney:	n/a
21	chr7:66386797-66386847	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:66386489-66386539	BJ	skin:	n/a
23	chr7:66387240-66387290	BE2_C	brain:	n/a
24	chr7:66385241-66385291	BJ	skin:	n/a
25	chr7:66386499-66386549	HCPEpiC	choroid plexus:	n/a
26	chr7:66386499-66386549	A549	lung:	n/a
27	chr7:66386859-66386909	GM19239	blood:	n/a
28	chr7:66387240-66387290	PFSK-1	brain:	n/a
29	chr7:66386499-66386549	HCM	heart:	n/a
30	chr7:66386859-66386909	MCF-7	breast:	n/a
31	chr7:66386499-66386549	U87	brain:	n/a
32	chr7:66385256-66385306	HEEpiC	esophagus:	n/a
33	chr7:66386859-66386909	HCM	heart:	n/a
34	chr7:66386079-66386129	Hepatocyte	liver:	n/a
35	chr7:66386045-66386095	AoSMC	blood vessel:	n/a
36	chr7:66385256-66385306	SAEC	small airway:	n/a
37	chr7:66386045-66386095	SK-N-SH	brain:	n/a
38	chr7:66386797-66386847	AoSMC	blood vessel:	n/a
39	chr7:66385241-66385291	PANC-1	pancreas:	n/a
40	chr7:66385829-66385879	A549	lung:	n/a
41	chr7:66385241-66385291	AG04449	skin:	fetal
42	chr7:66385256-66385306	HRPEpiC	eye:	n/a
43	chr7:66386489-66386539	K562	blood:	n/a
44	chr7:66386859-66386909	HCPEpiC	choroid plexus:	n/a
45	chr7:66385256-66385306	LNCaP	prostate:	n/a
46	chr7:66387240-66387290	ovcar-3	ovarian:	n/a
47	chr7:66386489-66386539	A549	lung:	n/a
48	chr7:66386499-66386549	HCT-116	colon:	n/a
49	chr7:66386079-66386129	HRE	kidney:	n/a
50	chr7:66386079-66386129	BE2_C	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:66385651..66388919-chr7:66460114..66462403,3	MCF-7	breast:
2	chr7:66147119..66147718-chr7:66386034..66386593,2	Hela-S3	cervix:
3	chr7:66312126..66314998-chr7:66385416..66387725,2	MCF-7	breast:
4	chr7:66118570..66121104-chr7:66386256..66388029,2	K562	blood:
5	chr7:66308191..66311276-chr7:66384066..66387492,7	MCF-7	breast:
6	chr7:66309154..66310879-chr7:66385975..66387792,2	MCF-7	breast:
7	chr12:110939415..110940003-chr7:66385750..66386337,2	NB4	blood:
8	chr7:66361028..66363688-chr7:66387186..66389228,2	K562	blood:
9	chr7:66384799..66388848-chr7:66389441..66396879,12	K562	blood:
10	chr7:66309510..66310213-chr7:66385838..66386579,2	MCF-7	breast:
11	chr7:66308297..66310076-chr7:66385373..66388075,2	K562	blood:
12	chr7:66204784..66206359-chr7:66385620..66388278,2	MCF-7	breast:
13	chr7:66385188..66388317-chr7:66459133..66463010,3	K562	blood:
14	chr7:66385080..66386736-chr7:66393610..66396808,3	MCF-7	breast:
15	chr1:228353195..228353730-chr7:66385183..66386076,2	NB4	blood:
16	chr7:66385169..66388074-chr7:66392898..66397062,6	MCF-7	breast:
17	chr7:66378566..66381625-chr7:66385153..66387745,3	MCF-7	breast:
18	chr7:66385883..66386781-chr7:66459948..66460665,2	Hela-S3	cervix:
19	chr7:66092683..66094985-chr7:66385486..66387762,2	K562	blood:
20	chr7:66384595..66388317-chr7:66459135..66463010,5	K562	blood:
21	chr7:66379191..66382749-chr7:66384574..66388642,5	K562	blood:
22	chr7:66386885..66388455-chr7:66393635..66395755,2	MCF-7	breast:
23	chr16:777428..780278-chr7:66386006..66387525,2	MCF-7	breast:

No data

Variant related genes	Relation type
TMEM248	TF binding region
TMEM248	CpG island
ENSG00000198874	chromatin interactions
ENSG00000232546	chromatin interactions
ENSG00000243335	chromatin interactions
ENSG00000181873	chromatin interactions
ENSG00000179131	chromatin interactions
ENSG00000103253	chromatin interactions
ENSG00000151164	chromatin interactions
ENSG00000226824	chromatin interactions
ENSG00000230583	chromatin interactions
ENSG00000203684	chromatin interactions
ENSG00000106609	chromatin interactions
ENSG00000111237	chromatin interactions
ENSG00000154710	chromatin interactions
ENSG00000126524	chromatin interactions
ENSG00000272831	chromatin interactions

Extended variants
information (count: 154 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:154 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572507769	chr7:66383872-66383873	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs541226241	chr7:66383893-66383894	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs10280816	chr7:66383943-66383944	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs374899380	chr7:66383963-66383964	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs111296513	chr7:66383964-66383965	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536925690	chr7:66383965-66383966	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs34309546	chr7:66383985-66383986	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs533639865	chr7:66384012-66384013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs550529389	chr7:66384046-66384047	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs10232188	chr7:66384063-66384064	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs367837646	chr7:66384085-66384086	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371729816	chr7:66384092-66384093	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs548965259	chr7:66384093-66384094	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs565597086	chr7:66384097-66384098	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367915164	chr7:66384120-66384121	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201420396	chr7:66384155-66384156	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs10281090	chr7:66384208-66384209	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs138135342	chr7:66384219-66384220	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs113615283	chr7:66384243-66384244	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571118053	chr7:66384299-66384300	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs10235423	chr7:66384315-66384316	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs187398835	chr7:66384322-66384323	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs192186531	chr7:66384328-66384329	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs149077064	chr7:66384370-66384371	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs75393189	chr7:66384516-66384517	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564654311	chr7:66384534-66384535	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546410330	chr7:66384592-66384593	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs77026721	chr7:66384614-66384615	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs62465750	chr7:66384617-66384618	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs184733517	chr7:66384634-66384635	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs28501161	chr7:66384706-66384707	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs570807250	chr7:66384707-66384708	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs28641990	chr7:66384855-66384856	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs189452506	chr7:66384897-66384898	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs199664566	chr7:66384898-66384899	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs561307059	chr7:66384917-66384918	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs148267860	chr7:66385004-66385005	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs536893576	chr7:66385033-66385034	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs373066150	chr7:66385177-66385178	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs550366508	chr7:66385180-66385181	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs79440965	chr7:66385189-66385190	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs552935360	chr7:66385212-66385213	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs111644894	chr7:66385279-66385280	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs555447796	chr7:66385288-66385289	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs182551087	chr7:66385290-66385291	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs116035902	chr7:66385322-66385323	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs184248183	chr7:66385323-66385324	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs578146135	chr7:66385438-66385439	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs189561868	chr7:66385473-66385474	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs535866537	chr7:66385495-66385496	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD

Chromatin state (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66311000-66385200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr7:66311200-66385200	Weak transcription	Brain Angular Gyrus	brain
3	chr7:66350600-66385200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:66364400-66385400	Weak transcription	HSMMtube	muscle
5	chr7:66364800-66385000	Weak transcription	Brain Anterior Caudate	brain
6	chr7:66366400-66385600	Weak transcription	Brain Substantia Nigra	brain
7	chr7:66368000-66385400	Weak transcription	Adipose Nuclei	Adipose
8	chr7:66369000-66385400	Weak transcription	Thymus	Thymus
9	chr7:66369000-66385600	Weak transcription	Ovary	ovary
10	chr7:66370000-66385200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:66370200-66385400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr7:66370800-66385000	Weak transcription	Brain Hippocampus Middle	brain
13	chr7:66371000-66385200	Weak transcription	Fetal Muscle Leg	muscle
14	chr7:66371200-66385400	Weak transcription	Fetal Intestine Small	intestine
15	chr7:66371200-66385600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr7:66371800-66385400	Weak transcription	Fetal Stomach	stomach
17	chr7:66379000-66385200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:66379400-66384200	Weak transcription	K562	blood
19	chr7:66380800-66384800	Weak transcription	GM12878-XiMat	blood
20	chr7:66381200-66385000	Weak transcription	HepG2	liver
21	chr7:66383000-66385000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr7:66383000-66385200	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr7:66383000-66385200	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr7:66383000-66385400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:66383000-66385400	Weak transcription	Osteobl	bone
26	chr7:66383200-66385200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr7:66383400-66385200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:66383400-66385200	Weak transcription	Psoas Muscle	Psoas
29	chr7:66383400-66385400	Weak transcription	Liver	Liver
30	chr7:66384200-66384400	Enhancers	K562	blood
31	chr7:66384400-66384800	Enhancers	Dnd41	blood
32	chr7:66384400-66385000	Flanking Active TSS	K562	blood
33	chr7:66384800-66385000	Flanking Active TSS	GM12878-XiMat	blood
34	chr7:66384800-66385600	Flanking Active TSS	Dnd41	blood
35	chr7:66384800-66387400	Active TSS	NHDF-Ad	bronchial
36	chr7:66385000-66385200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr7:66385000-66385200	Active TSS	GM12878-XiMat	blood
38	chr7:66385000-66385200	Enhancers	Hela-S3	cervix
39	chr7:66385000-66385200	Enhancers	NHEK	skin
40	chr7:66385000-66385200	Enhancers	NHLF	lung
41	chr7:66385000-66385400	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr7:66385000-66385400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr7:66385000-66385400	Enhancers	Colon Smooth Muscle	Colon
44	chr7:66385000-66385400	Enhancers	HepG2	liver
45	chr7:66385000-66385400	Transcr. at gene 5' and 3'	K562	blood
46	chr7:66385000-66385600	Enhancers	Brain Anterior Caudate	brain
47	chr7:66385000-66385600	Enhancers	Brain Hippocampus Middle	brain
48	chr7:66385000-66387000	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr7:66385000-66387200	Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr7:66385000-66388000	Active TSS	A549	lung

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