Variant report

Variant	esv3373922
Chromosome Location	chr7:140371933-140374031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:333)
CpG islands
(count:549)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:140372787-140372978	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:140373579-140373779	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:140372954-140373392	K562	blood:	n/a	chr7:140372973-140372989
4	BHLHE40	chr7:140372764-140373272	GM12878	blood:	n/a	chr7:140372800-140372816 chr7:140372789-140372805 chr7:140372973-140372989
5	CBX3	chr7:140372988-140373477	K562	blood:	n/a	n/a
6	CCNT2	chr7:140372736-140373840	K562	blood:	n/a	n/a
7	CEBPD	chr7:140372637-140372956	HepG2	liver:	n/a	n/a
8	CHD1	chr7:140372757-140373439	GM12878	blood:	n/a	n/a
9	CHD1	chr7:140373811-140373821	GM12878	blood:	n/a	n/a
10	CHD2	chr7:140372876-140372929	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr7:140371945-140372228	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr7:140372897-140373638	GM12878	blood:	n/a	n/a
13	CHD2	chr7:140373165-140373347	K562	blood:	n/a	n/a
14	CREB1	chr7:140372680-140372996	A549	lung:	n/a	n/a
15	CREB1	chr7:140372523-140373445	HepG2	liver:	n/a	n/a
16	CTCF	chr7:140373220-140373490	K562	blood:	n/a	n/a
17	CTCF	chr7:140373300-140373450	GM12873	blood:	n/a	n/a
18	CTCF	chr7:140373082-140373173	GM10248	blood:	n/a	n/a
19	CTCF	chr7:140373320-140373470	NHEK	skin:	n/a	n/a
20	CTCF	chr7:140373000-140373150	GM12873	blood:	n/a	n/a
21	CTCF	chr7:140373380-140373530	SAEC	small airway:	n/a	n/a
22	CTCF	chr7:140373384-140373438	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr7:140373140-140373290	BJ	skin:	n/a	n/a
24	CTCF	chr7:140373360-140373510	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr7:140373400-140373494	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:140373340-140373490	GM12873	blood:	n/a	n/a
27	CTCF	chr7:140373380-140373530	GM12874	blood:	n/a	n/a
28	CTCF	chr7:140373126-140373148	HepG2	liver:	n/a	n/a
29	CTCF	chr7:140372978-140373238	K562	blood:	n/a	n/a
30	CTCF	chr7:140373020-140373170	GM12869	blood:	n/a	n/a
31	CTCF	chr7:140373094-140373186	NHEK	skin:	n/a	n/a
32	CTCF	chr7:140373300-140373450	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr7:140373140-140373290	SAEC	small airway:	n/a	n/a
34	CTCF	chr7:140373280-140373430	HMF	breast:	n/a	n/a
35	CTCF	chr7:140373020-140373170	GM12865	blood:	n/a	n/a
36	CTCF	chr7:140373320-140373470	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr7:140373060-140373210	HEK293	kidney:	n/a	n/a
38	CTCF	chr7:140373103-140373208	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:140373320-140373470	RPTEC	kidney:	n/a	n/a
40	CTCF	chr7:140373340-140373490	AG10803	skin:	n/a	n/a
41	CTCF	chr7:140373020-140373170	HCM	heart:	n/a	n/a
42	CTCF	chr7:140373080-140373230	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr7:140373047-140373293	GM12892	blood:	n/a	n/a
44	CTCF	chr7:140373100-140373250	GM12873	blood:	n/a	n/a
45	CTCF	chr7:140373000-140373150	GM12874	blood:	n/a	n/a
46	CTCF	chr7:140373066-140373271	GM19239	blood:	n/a	n/a
47	CTCF	chr7:140373091-140373217	GM19240	blood:	n/a	n/a
48	CTCF	chr7:140373180-140373330	GM12864	blood:	n/a	n/a
49	CTCF	chr7:140373360-140373510	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:140372980-140373130	GM12874	blood:	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	chr7:140373029-140373079	MCF10A-Er-Src	breast:	n/a
2	chr7:140372755-140372805	PFSK-1	brain:	n/a
3	chr7:140372727-140372777	GM12892	blood:	n/a
4	chr7:140373033-140373083	HMEC	breast:	n/a
5	chr7:140372755-140372805	HAEpiC	amniotic membrane:	n/a
6	chr7:140372727-140372777	PrEC	prostate:	n/a
7	chr7:140373596-140373646	SAEC	small airway:	n/a
8	chr7:140372725-140372775	CMK	blood:	n/a
9	chr7:140373292-140373342	NHDF-neo	bronchial:	n/a
10	chr7:140372864-140372914	HepG2	liver:	n/a
11	chr7:140373596-140373646	HRCEpiC	kidney:	n/a
12	chr7:140373292-140373342	HRE	kidney:	n/a
13	chr7:140373235-140373285	HRPEpiC	eye:	n/a
14	chr7:140373029-140373079	HL-60	blood:	n/a
15	chr7:140373596-140373646	ProgFib	skin:	n/a
16	chr7:140372755-140372805	AG04449	skin:	fetal
17	chr7:140372755-140372805	GM12891	blood:	n/a
18	chr7:140372864-140372914	BE2_C	brain:	n/a
19	chr7:140373033-140373083	NB4	blood:	n/a
20	chr7:140373235-140373285	U87	brain:	n/a
21	chr7:140373033-140373083	GM12878	blood:	n/a
22	chr7:140372755-140372805	Hepatocyte	liver:	n/a
23	chr7:140373235-140373285	HCPEpiC	choroid plexus:	n/a
24	chr7:140373033-140373083	NH-A	brain:	n/a
25	chr7:140373029-140373079	GM12892	blood:	n/a
26	chr7:140373029-140373079	SK-N-SH_RA	brain:	n/a
27	chr7:140373596-140373646	HCF	heart:	n/a
28	chr7:140373235-140373285	GM12878	blood:	n/a
29	chr7:140373596-140373646	NT2-D1	testis:	n/a
30	chr7:140373235-140373285	ProgFib	skin:	n/a
31	chr7:140373292-140373342	HIPEpiC	eye:	n/a
32	chr7:140372725-140372775	HepG2	liver:	n/a
33	chr7:140373596-140373646	SK-N-SH_RA	brain:	n/a
34	chr7:140372725-140372775	MCF-7	breast:	n/a
35	chr7:140373292-140373342	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:140372864-140372914	HAEpiC	amniotic membrane:	n/a
37	chr7:140373033-140373083	GM12892	blood:	n/a
38	chr7:140372755-140372805	RPTEC	kidney:	n/a
39	chr7:140373033-140373083	RPTEC	kidney:	n/a
40	chr7:140373029-140373079	U87	brain:	n/a
41	chr7:140372725-140372775	ovcar-3	ovarian:	n/a
42	chr7:140373033-140373083	ProgFib	skin:	n/a
43	chr7:140372727-140372777	AG10803	skin:	n/a
44	chr7:140373235-140373285	HRCEpiC	kidney:	n/a
45	chr7:140372725-140372775	A549	lung:	n/a
46	chr7:140373235-140373285	AG09309	skin:	n/a
47	chr7:140372755-140372805	CMK	blood:	n/a
48	chr7:140373292-140373342	HCPEpiC	choroid plexus:	n/a
49	chr7:140372725-140372775	K562	blood:	n/a
50	chr7:140373029-140373079	SK-N-MC	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:140358444..140360553-chr7:140370671..140372780,2	MCF-7	breast:
2	chr7:140370275..140375389-chr7:140393210..140401279,16	MCF-7	breast:
3	chr7:140371506..140376729-chr7:140377280..140380130,6	K562	blood:
4	chr7:140372637..140375611-chr7:140394231..140397834,5	K562	blood:
5	chr7:140366280..140367939-chr7:140371289..140372844,2	MCF-7	breast:
6	chr7:140370608..140383131-chr7:140387718..140398587,28	MCF-7	breast:
7	chr7:140371193..140374993-chr7:140376654..140380151,6	MCF-7	breast:
8	chr7:140371233..140372859-chr7:140417535..140420248,2	MCF-7	breast:
9	chr7:140372831..140374417-chr7:140400299..140402616,2	MCF-7	breast:
10	chr7:140371560..140374067-chr7:140396511..140398663,2	K562	blood:
11	chr7:140177294..140179711-chr7:140373712..140375545,2	K562	blood:

No data

Variant related genes	Relation type
DENND2A	TF binding region
ADCK2	TF binding region
DENND2A	CpG island
ADCK2	CpG island
ENSG00000133606	chromatin interactions
ENSG00000240889	chromatin interactions
ENSG00000090266	chromatin interactions
ENSG00000133597	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537309818	chr7:140371968-140371969	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs569301576	chr7:140372007-140372008	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs556286182	chr7:140372108-140372109	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs73505647	chr7:140372161-140372162	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs535913125	chr7:140372169-140372170	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs35020037	chr7:140372238-140372239	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs269267	chr7:140372299-140372300	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs115842892	chr7:140372343-140372344	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs28517771	chr7:140372378-140372379	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs182303776	chr7:140372383-140372384	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs543663620	chr7:140372393-140372394	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs143378587	chr7:140372533-140372534	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs529445272	chr7:140372566-140372567	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs6464937	chr7:140372579-140372580	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs375522274	chr7:140372621-140372622	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs560280474	chr7:140372679-140372680	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs186697162	chr7:140372704-140372705	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs552156648	chr7:140372715-140372716	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs570771524	chr7:140372745-140372746	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs538112104	chr7:140372800-140372801	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs549735595	chr7:140372857-140372858	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs11540284	chr7:140372889-140372890	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs535275841	chr7:140372901-140372902	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs553887467	chr7:140372908-140372909	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs569845382	chr7:140372917-140372918	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs374248592	chr7:140372932-140372933	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs572203720	chr7:140372998-140372999	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs151015312	chr7:140373183-140373184	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs539450262	chr7:140373194-140373195	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs374452342	chr7:140373226-140373227	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs557689792	chr7:140373235-140373236	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs368494131	chr7:140373239-140373240	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs140971515	chr7:140373254-140373255	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs370797181	chr7:140373307-140373308	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs2968558	chr7:140373326-140373327	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs147151212	chr7:140373330-140373331	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs574217210	chr7:140373347-140373348	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs553849506	chr7:140373356-140373357	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs375366072	chr7:140373359-140373360	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs140313292	chr7:140373381-140373382	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs541642479	chr7:140373382-140373383	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs367917022	chr7:140373386-140373387	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs371950297	chr7:140373388-140373389	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs376611609	chr7:140373389-140373390	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs560294528	chr7:140373406-140373407	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs145231926	chr7:140373423-140373424	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs201013665	chr7:140373438-140373439	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs368706879	chr7:140373440-140373441	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs372972431	chr7:140373452-140373453	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs137941874	chr7:140373480-140373481	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Glioblastoma multiforme	21525872	CNVD

Chromatin state (count:494 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140365800-140372000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr7:140369600-140372000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr7:140370400-140372000	Weak transcription	A549	lung
4	chr7:140370600-140372200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:140370800-140372000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr7:140370800-140372000	Weak transcription	K562	blood
7	chr7:140371000-140372400	Weak transcription	NHLF	lung
8	chr7:140371600-140372000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
9	chr7:140371600-140372000	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr7:140371600-140372200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:140371600-140372200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:140371600-140372200	Enhancers	Spleen	Spleen
13	chr7:140371600-140372200	Active TSS	HepG2	liver
14	chr7:140371600-140372400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:140371800-140372000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:140371800-140372000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:140371800-140372000	Enhancers	H9 Cell Line	embryonic stem cell
18	chr7:140371800-140372000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:140371800-140372000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:140371800-140372000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
21	chr7:140371800-140372000	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr7:140371800-140372000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:140371800-140372000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr7:140371800-140372000	Enhancers	Brain Anterior Caudate	brain
25	chr7:140371800-140372000	Enhancers	Brain Substantia Nigra	brain
26	chr7:140371800-140372000	Enhancers	Fetal Kidney	kidney
27	chr7:140371800-140372000	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr7:140371800-140372000	Enhancers	Hela-S3	cervix
29	chr7:140371800-140372200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr7:140371800-140372200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr7:140371800-140372200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:140371800-140372200	Enhancers	Brain Cingulate Gyrus	brain
33	chr7:140371800-140372200	Enhancers	Placenta	Placenta
34	chr7:140371800-140372200	Enhancers	Dnd41	blood
35	chr7:140371800-140372400	Enhancers	Fetal Heart	heart
36	chr7:140371800-140372400	Weak transcription	Ovary	ovary
37	chr7:140371800-140372400	Enhancers	Pancreas	Pancrea
38	chr7:140371800-140372400	Enhancers	Placenta Amnion	Placenta Amnion
39	chr7:140371800-140372400	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr7:140371800-140372400	Enhancers	Stomach Mucosa	stomach
41	chr7:140372000-140372200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr7:140372000-140372200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
43	chr7:140372000-140372200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:140372000-140372200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:140372000-140372200	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr7:140372000-140372200	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr7:140372000-140372200	Enhancers	Primary B cells from cord blood	blood
48	chr7:140372000-140372200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr7:140372000-140372200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr7:140372000-140372200	Enhancers	Cortex derived primary cultured neurospheres	brain

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