Variant report

Variant	esv3348457
Chromosome Location	chr5:176995395-177020808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:610)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177019039-177019436	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:177015558-177015958	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:177003282-177003459	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:177008652-177008967	K562	blood:	n/a	n/a
5	ATF1	chr5:177015319-177016003	K562	blood:	n/a	n/a
6	ATF1	chr5:177018993-177019369	K562	blood:	n/a	n/a
7	ATF2	chr5:177018938-177019491	GM12878	blood:	n/a	n/a
8	ATF3	chr5:177019050-177019291	HepG2	liver:	n/a	chr5:177019159-177019179
9	ATF3	chr5:177019071-177019456	A549	lung:	n/a	chr5:177019159-177019179
10	ATF3	chr5:176995409-176995704	K562	blood:	n/a	n/a
11	ATF3	chr5:177019027-177019322	K562	blood:	n/a	chr5:177019159-177019179
12	BACH1	chr5:177019029-177019555	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:177015512-177015739	K562	blood:	n/a	n/a
14	BATF	chr5:176997755-176997922	GM12878	blood:	n/a	n/a
15	BCL3	chr5:177019095-177019518	A549	lung:	n/a	chr5:177019151-177019164 chr5:177019156-177019165 chr5:177019155-177019168 chr5:177019185-177019198
16	BCLAF1	chr5:177018861-177019568	GM12878	blood:	n/a	chr5:177019151-177019164 chr5:177019156-177019165 chr5:177019155-177019168 chr5:177019185-177019198
17	BHLHE40	chr5:177018820-177019853	GM12878	blood:	n/a	chr5:177019177-177019193 chr5:177019180-177019196
18	BHLHE40	chr5:177019232-177019557	A549	lung:	n/a	n/a
19	BHLHE40	chr5:177015653-177015896	K562	blood:	n/a	n/a
20	BHLHE40	chr5:177007521-177007570	A549	lung:	n/a	n/a
21	BHLHE40	chr5:177018943-177019662	HepG2	liver:	n/a	chr5:177019177-177019193 chr5:177019180-177019196
22	BHLHE40	chr5:177018850-177019869	K562	blood:	n/a	chr5:177019177-177019193 chr5:177019180-177019196
23	BRCA1	chr5:177019019-177019470	GM12878	blood:	n/a	n/a
24	BRCA1	chr5:177018577-177019316	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:177018851-177019323	HepG2	liver:	n/a	n/a
26	CBX3	chr5:177015403-177015822	K562	blood:	n/a	n/a
27	CBX3	chr5:176995267-176995729	K562	blood:	n/a	n/a
28	CBX3	chr5:177008540-177008922	K562	blood:	n/a	n/a
29	CCNT2	chr5:177019002-177019666	K562	blood:	n/a	n/a
30	CEBPB	chr5:177019025-177019320	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:177019080-177019377	K562	blood:	n/a	n/a
32	CEBPB	chr5:177000284-177000506	K562	blood:	n/a	n/a
33	CEBPB	chr5:177019001-177019429	Hela-S3	cervix:	n/a	n/a
34	CEBPD	chr5:177015543-177015866	HepG2	liver:	n/a	n/a
35	CEBPD	chr5:177018987-177019438	HepG2	liver:	n/a	n/a
36	CHD1	chr5:177018912-177019998	GM12878	blood:	n/a	n/a
37	CHD1	chr5:177019152-177019459	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr5:177018854-177019450	HepG2	liver:	n/a	n/a
39	CHD2	chr5:177018900-177019775	K562	blood:	n/a	n/a
40	CHD2	chr5:177018912-177019577	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr5:177018930-177019719	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr5:177018634-177019591	GM12878	blood:	n/a	n/a
43	CREB1	chr5:177018864-177019381	ECC-1	luminal epithelium:	n/a	n/a
44	CREB1	chr5:177018952-177019321	A549	lung:	n/a	n/a
45	CREB1	chr5:177018871-177019791	K562	blood:	n/a	n/a
46	CREB1	chr5:177018751-177019664	HepG2	liver:	n/a	n/a
47	CREB1	chr5:177018842-177019849	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr5:177018883-177019492	A549	lung:	n/a	n/a
49	CREB1	chr5:177018893-177019688	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr5:177018813-177019723	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177020109-177020159	BJ	skin:	n/a
2	chr5:177015777-177015827	H1-hESC	embryonic stem cell:	embryo
3	chr5:177019608-177019658	HIPEpiC	eye:	n/a
4	chr5:177019065-177019115	AG04450	lung:	fetal
5	chr5:177015777-177015827	BJ	skin:	n/a
6	chr5:177020109-177020159	AG04449	skin:	fetal
7	chr5:177020109-177020159	BE2_C	brain:	n/a
8	chr5:177019313-177019363	Caco-2	colon:	n/a
9	chr5:177018950-177019000	ECC-1	luminal epithelium:	n/a
10	chr5:177019044-177019094	MCF10A-Er-Src	breast:	n/a
11	chr5:177019313-177019363	LNCaP	prostate:	n/a
12	chr5:177018934-177018984	HEK293	kidney:	embryo
13	chr5:177019044-177019094	IMR90	lung:	fetal
14	chr5:177019608-177019658	AG09309	skin:	n/a
15	chr5:177018934-177018984	U87	brain:	n/a
16	chr5:177015777-177015827	SK-N-SH_RA	brain:	n/a
17	chr5:177018950-177019000	LNCaP	prostate:	n/a
18	chr5:177019608-177019658	SK-N-MC	brain:	n/a
19	chr5:177018950-177019000	ovcar-3	ovarian:	n/a
20	chr5:177018950-177019000	GM06990	blood:	n/a
21	chr5:177019065-177019115	HEEpiC	esophagus:	n/a
22	chr5:177018950-177019000	GM19239	blood:	n/a
23	chr5:177018929-177018979	Hepatocyte	liver:	n/a
24	chr5:177019065-177019115	MCF-7	breast:	n/a
25	chr5:177018950-177019000	AG10803	skin:	n/a
26	chr5:177019065-177019115	HRCEpiC	kidney:	n/a
27	chr5:177019065-177019115	RPTEC	kidney:	n/a
28	chr5:177019313-177019363	HIPEpiC	eye:	n/a
29	chr5:177015777-177015827	HL-60	blood:	n/a
30	chr5:177018929-177018979	HCT-116	colon:	n/a
31	chr5:177018929-177018979	GM19239	blood:	n/a
32	chr5:177018934-177018984	MCF10A-Er-Src	breast:	n/a
33	chr5:177015777-177015827	HCF	heart:	n/a
34	chr5:177019065-177019115	HCF	heart:	n/a
35	chr5:177018929-177018979	CMK	blood:	n/a
36	chr5:177020109-177020159	SK-N-MC	brain:	n/a
37	chr5:177020109-177020159	AoSMC	blood vessel:	n/a
38	chr5:177018934-177018984	ECC-1	luminal epithelium:	n/a
39	chr5:177020109-177020159	HCT-116	colon:	n/a
40	chr5:177018929-177018979	HRCEpiC	kidney:	n/a
41	chr5:177018986-177019036	HCT-116	colon:	n/a
42	chr5:177019044-177019094	NB4	blood:	n/a
43	chr5:177018986-177019036	HCM	heart:	n/a
44	chr5:177018934-177018984	AG04450	lung:	fetal
45	chr5:177019608-177019658	Caco-2	colon:	n/a
46	chr5:177019313-177019363	SKMC	muscle:	n/a
47	chr5:177019313-177019363	AG04449	skin:	fetal
48	chr5:177018986-177019036	HCF	heart:	n/a
49	chr5:177019065-177019115	AG04449	skin:	fetal
50	chr5:177018934-177018984	BJ	skin:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:177004473..177006959-chr5:177017181..177019392,2	MCF-7	breast:
2	chr5:176980076..176982423-chr5:177017925..177021146,3	K562	blood:
3	chr5:177010327..177013689-chr5:177016648..177020930,5	MCF-7	breast:
4	chr5:176986861..176989577-chr5:176994718..176996708,3	K562	blood:
5	chr5:176994952..176997019-chr5:177017562..177019894,2	K562	blood:
6	chr5:176994608..176996221-chr5:176998430..177000511,2	K562	blood:
7	chr5:177019232..177020994-chr5:177656791..177659399,2	K562	blood:
8	chr5:177014696..177016221-chr5:177020591..177022587,2	K562	blood:
9	chr5:177017384..177019488-chr5:177631001..177633000,2	MCF-7	breast:
10	chr5:176923602..176926182-chr5:177017999..177019710,2	K562	blood:
11	chr5:176990906..176992861-chr5:176995527..176997623,2	MCF-7	breast:
12	chr5:176994913..176997833-chr5:177022408..177024826,2	K562	blood:
13	chr5:177011986..177013740-chr5:177018078..177019628,2	K562	blood:
14	chr5:176943414..176949809-chr5:177018256..177021226,8	MCF-7	breast:
15	chr5:176923095..176925209-chr5:177019148..177022259,3	MCF-7	breast:
16	chr5:176936816..176938708-chr5:177019651..177022498,2	MCF-7	breast:
17	chr5:176996104..176998748-chr5:177012032..177013974,2	MCF-7	breast:
18	chr5:176994090..176995971-chr5:177025849..177027352,2	K562	blood:
19	chr5:176978290..176981747-chr5:177017313..177020640,7	MCF-7	breast:
20	chr5:176983331..176986206-chr5:177001141..177003444,2	MCF-7	breast:
21	chr5:177014696..177016221-chr5:177020591..177022587,2	K562	blood:
22	chr5:177008572..177010603-chr5:177022660..177024180,2	K562	blood:
23	chr5:176994608..176996221-chr5:176998430..177000511,2	K562	blood:
24	chr5:176939485..176941829-chr5:177017923..177020658,4	MCF-7	breast:
25	chr5:176928239..176929895-chr5:177020806..177023092,2	MCF-7	breast:
26	chr5:176996104..176998748-chr5:177012032..177013974,2	MCF-7	breast:
27	chr5:176979031..176980967-chr5:177019678..177022578,2	MCF-7	breast:
28	chr5:176933337..176935861-chr5:177015983..177018322,2	K562	blood:
29	chr5:176946312..176949197-chr5:177018379..177020484,2	K562	blood:
30	chr5:177010880..177013120-chr5:177024317..177026904,2	K562	blood:
31	chr5:176922040..176925610-chr5:177017064..177019499,4	K562	blood:
32	chr12:32112363..32113149-chr5:177019226..177020019,2	NB4	blood:
33	chr5:176994783..176996833-chr5:177031297..177033294,2	K562	blood:
34	chr12:46383645..46384386-chr5:177019349..177019927,2	Hela-S3	cervix:
35	chr5:176977384..176979109-chr5:177015440..177017120,2	K562	blood:
36	chr5:176994399..176996378-chr5:177006435..177008467,2	MCF-7	breast:
37	chr5:176942293..176944420-chr5:177019101..177021147,2	MCF-7	breast:
38	chr5:176980966..176983175-chr5:176993425..176995860,2	K562	blood:
39	chr1:93297145..93297889-chr5:177019241..177019876,2	HCT-116	colon:
40	chr5:176951222..176953772-chr5:177019144..177020770,2	MCF-7	breast:
41	chr5:176959784..176964247-chr5:177018558..177022874,5	MCF-7	breast:
42	chr5:177018435..177020960-chr5:177539226..177540753,2	MCF-7	breast:
43	chr5:176994399..176996378-chr5:177006435..177008467,2	MCF-7	breast:
44	chr5:177013361..177016176-chr5:177017373..177019237,2	MCF-7	breast:
45	chr5:176805970..176807499-chr5:177018005..177019768,2	K562	blood:
46	chr5:177002606..177004367-chr5:177025618..177028461,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM193B-1	chr5:176999986-177000002	NONHSAT105437

No data

Variant related genes	Relation type
TMED9	TF binding region
TMED9	CpG island
ENSG00000196923	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000184840	chromatin interactions
ENSG00000139218	chromatin interactions
ENSG00000027847	chromatin interactions
ENSG00000131183	chromatin interactions
ENSG00000145911	chromatin interactions
ENSG00000272459	chromatin interactions
ENSG00000174718	chromatin interactions
ENSG00000146094	chromatin interactions
ENSG00000146067	chromatin interactions
ENSG00000175309	chromatin interactions
ENSG00000183258	chromatin interactions
ENSG00000197451	chromatin interactions

Extended variants
information (count: 697 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:697 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373990182	chr5:176995407-176995408	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs201005336	chr5:176995411-176995412	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs149688311	chr5:176995448-176995449	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs568954884	chr5:176995449-176995450	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs555371726	chr5:176995518-176995519	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs573794212	chr5:176995520-176995521	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs4582294	chr5:176995611-176995612	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs576967728	chr5:176995616-176995617	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs541078688	chr5:176995734-176995735	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs145527582	chr5:176995792-176995793	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs577814376	chr5:176995805-176995806	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs148823160	chr5:176995838-176995839	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs563634906	chr5:176995842-176995843	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs111447312	chr5:176995919-176995920	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs530694009	chr5:176995935-176995936	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs549786342	chr5:176995940-176995941	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs561714523	chr5:176995947-176995948	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529357733	chr5:176995975-176995976	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs28688762	chr5:176996001-176996002	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs368975450	chr5:176996037-176996038	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547825595	chr5:176996045-176996046	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566040686	chr5:176996053-176996054	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs184702156	chr5:176996061-176996062	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs551658225	chr5:176996062-176996063	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562930733	chr5:176996066-176996067	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs556397288	chr5:176996100-176996101	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570381842	chr5:176996139-176996140	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs537703397	chr5:176996173-176996174	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576369462	chr5:176996175-176996176	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs190652898	chr5:176996181-176996182	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs367759723	chr5:176996207-176996208	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs28738071	chr5:176996218-176996219	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs577648686	chr5:176996272-176996273	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs545215721	chr5:176996305-176996306	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556710770	chr5:176996315-176996316	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs575185080	chr5:176996519-176996520	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs79894546	chr5:176996633-176996634	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs28661084	chr5:176996640-176996641	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs335487	chr5:176996670-176996671	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs541060439	chr5:176996743-176996744	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs114544201	chr5:176996852-176996853	Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572815550	chr5:176996860-176996861	Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181518841	chr5:176996863-176996864	Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551965085	chr5:176996880-176996881	Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187049489	chr5:176996883-176996884	Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537970233	chr5:176996962-176996963	Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146941790	chr5:176996985-176996986	Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs147630931	chr5:176996999-176997000	Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534647644	chr5:176997011-176997012	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552672131	chr5:176997014-176997015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Autism	20841430	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:176989600-176997600	Weak transcription	Right Atrium	heart
2	chr5:176991600-176995800	Enhancers	K562	blood
3	chr5:176994600-176995600	Enhancers	NHEK	skin
4	chr5:176995400-176995800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:176996000-176996600	Bivalent Enhancer	HepG2	liver
6	chr5:176996200-176996400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr5:176996200-176996400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr5:176996200-176996400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr5:176996400-176996800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:176996800-176997000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:177001600-177001800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:177001600-177003400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:177001600-177003600	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr5:177001600-177003600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr5:177001800-177002000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr5:177001800-177003000	Enhancers	H9 Cell Line	embryonic stem cell
17	chr5:177001800-177003000	Enhancers	Esophagus	oesophagus
18	chr5:177001800-177003600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr5:177001800-177003600	Enhancers	HMEC	breast
20	chr5:177001800-177003600	Enhancers	NHEK	skin
21	chr5:177002000-177002800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:177003600-177005400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:177005400-177005600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:177013200-177014200	Enhancers	Primary B cells from peripheral blood	blood
25	chr5:177013400-177013800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr5:177013400-177013800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr5:177014200-177018600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr5:177015200-177015400	Enhancers	HepG2	liver
29	chr5:177015400-177015800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:177015400-177016000	Flanking Active TSS	HepG2	liver
31	chr5:177015400-177016000	Flanking Active TSS	K562	blood
32	chr5:177015400-177016200	Enhancers	Stomach Mucosa	stomach
33	chr5:177015600-177015800	Enhancers	Gastric	stomach
34	chr5:177015800-177016200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:177016000-177016800	Enhancers	HepG2	liver
36	chr5:177016000-177018400	Weak transcription	K562	blood
37	chr5:177016200-177016400	Enhancers	Fetal Intestine Small	intestine
38	chr5:177016400-177018600	Weak transcription	Fetal Intestine Small	intestine
39	chr5:177016600-177016800	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr5:177016800-177018600	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr5:177016800-177018600	Weak transcription	HepG2	liver
42	chr5:177018400-177018600	Enhancers	Liver	Liver
43	chr5:177018400-177018600	Weak transcription	Gastric	stomach
44	chr5:177018400-177018600	Bivalent Enhancer	Dnd41	blood
45	chr5:177018400-177018600	Enhancers	K562	blood
46	chr5:177018600-177018800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr5:177018600-177018800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr5:177018600-177018800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:177018600-177018800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
50	chr5:177018600-177018800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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