Variant report

Variant	esv3398259
Chromosome Location	chr5:179717146-179721444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:949)
CpG islands
(count:613)
Chromatin interactive
region (count:35)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179717554-179717711	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:179720477-179720778	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:179720502-179720795	K562	blood:	n/a	n/a
4	ATF2	chr5:179720348-179720900	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:179720267-179720956	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr5:179720392-179720963	A549	lung:	n/a	n/a
7	BCL3	chr5:179720340-179721023	A549	lung:	n/a	n/a
8	BCLAF1	chr5:179720327-179720896	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:179718950-179719809	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:179720495-179720872	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:179719365-179719686	K562	blood:	n/a	n/a
12	BHLHE40	chr5:179720388-179720831	K562	blood:	n/a	n/a
13	BRCA1	chr5:179720366-179720851	HepG2	liver:	n/a	n/a
14	BRCA1	chr5:179720396-179720674	GM12878	blood:	n/a	n/a
15	BRCA1	chr5:179720359-179720856	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr5:179719185-179719237	HepG2	liver:	n/a	n/a
17	BRCA1	chr5:179719675-179719818	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr5:179720346-179720922	K562	blood:	n/a	n/a
19	CCNT2	chr5:179718487-179718688	K562	blood:	n/a	n/a
20	CCNT2	chr5:179720510-179720724	K562	blood:	n/a	chr5:179720640-179720649
21	CCNT2	chr5:179718911-179719770	K562	blood:	n/a	chr5:179719683-179719692
22	CEBPB	chr5:179719933-179720172	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:179719936-179720171	K562	blood:	n/a	n/a
24	CEBPB	chr5:179719930-179720257	K562	blood:	n/a	n/a
25	CEBPB	chr5:179719571-179720846	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:179720438-179720758	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPD	chr5:179718894-179719537	HepG2	liver:	n/a	n/a
28	CHD1	chr5:179718413-179719826	IMR90	lung:	n/a	chr5:179719149-179719159
29	CHD1	chr5:179719304-179719476	GM12878	blood:	n/a	n/a
30	CHD2	chr5:179720452-179720625	K562	blood:	n/a	n/a
31	CHD2	chr5:179718122-179718125	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr5:179718471-179718561	GM12878	blood:	n/a	n/a
33	CHD2	chr5:179718946-179719864	GM12878	blood:	n/a	chr5:179719149-179719159
34	CHD2	chr5:179717383-179717390	K562	blood:	n/a	n/a
35	CHD2	chr5:179719528-179719702	HepG2	liver:	n/a	n/a
36	CHD2	chr5:179720220-179720789	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr5:179720516-179720825	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr5:179719079-179719183	HepG2	liver:	n/a	chr5:179719149-179719159
39	CHD2	chr5:179719565-179719743	K562	blood:	n/a	n/a
40	CHD2	chr5:179718953-179719317	K562	blood:	n/a	chr5:179719149-179719159
41	CHD2	chr5:179720504-179720777	HepG2	liver:	n/a	n/a
42	CHD2	chr5:179718926-179719872	Hela-S3	cervix:	n/a	chr5:179719149-179719159
43	CHD2	chr5:179718942-179719772	H1-hESC	embryonic stem cell:	n/a	chr5:179719149-179719159
44	CHD2	chr5:179718570-179718610	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr5:179720142-179720766	GM12878	blood:	n/a	chr5:179720169-179720179 chr5:179720164-179720174
46	CREB1	chr5:179720500-179720942	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr5:179720453-179720978	GM12878	blood:	n/a	n/a
48	CREB1	chr5:179718828-179719977	HepG2	liver:	n/a	n/a
49	CREB1	chr5:179720442-179720965	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr5:179720527-179720859	A549	lung:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179719416-179719466	NHDF-neo	bronchial:	n/a
2	chr5:179719756-179719806	K562	blood:	n/a
3	chr5:179720254-179720304	PrEC	prostate:	n/a
4	chr5:179719416-179719466	NHDF-neo	bronchial:	n/a
5	chr5:179719756-179719806	K562	blood:	n/a
6	chr5:179720254-179720304	PrEC	prostate:	n/a
7	chr5:179718531-179718581	MCF-7	breast:	n/a
8	chr5:179719199-179719249	AG09319	gingival:	n/a
9	chr5:179719190-179719240	NHDF-neo	bronchial:	n/a
10	chr5:179720254-179720304	LNCaP	prostate:	n/a
11	chr5:179718531-179718581	NHBE	bronchial:	n/a
12	chr5:179718685-179718735	GM12878	blood:	n/a
13	chr5:179720254-179720304	HCPEpiC	choroid plexus:	n/a
14	chr5:179719171-179719221	RPTEC	kidney:	n/a
15	chr5:179718685-179718735	U87	brain:	n/a
16	chr5:179719756-179719806	HRE	kidney:	n/a
17	chr5:179718531-179718581	LNCaP	prostate:	n/a
18	chr5:179719416-179719466	Caco-2	colon:	n/a
19	chr5:179718685-179718735	ProgFib	skin:	n/a
20	chr5:179719416-179719466	GM06990	blood:	n/a
21	chr5:179718685-179718735	HL-60	blood:	n/a
22	chr5:179718531-179718581	GM12891	blood:	n/a
23	chr5:179718685-179718735	T-47D	breast:	n/a
24	chr5:179717478-179717528	HCT-116	colon:	n/a
25	chr5:179720254-179720304	HRE	kidney:	n/a
26	chr5:179719416-179719466	K562	blood:	n/a
27	chr5:179718685-179718735	SAEC	small airway:	n/a
28	chr5:179718685-179718735	ECC-1	luminal epithelium:	n/a
29	chr5:179719416-179719466	NB4	blood:	n/a
30	chr5:179719171-179719221	HepG2	liver:	n/a
31	chr5:179719199-179719249	SKMC	muscle:	n/a
32	chr5:179719756-179719806	AG09319	gingival:	n/a
33	chr5:179718531-179718581	BJ	skin:	n/a
34	chr5:179719756-179719806	NHBE	bronchial:	n/a
35	chr5:179719190-179719240	HEEpiC	esophagus:	n/a
36	chr5:179718531-179718581	ovcar-3	ovarian:	n/a
37	chr5:179718531-179718581	Hela-S3	cervix:	n/a
38	chr5:179719190-179719240	AG10803	skin:	n/a
39	chr5:179720254-179720304	PFSK-1	brain:	n/a
40	chr5:179719199-179719249	NT2-D1	testis:	n/a
41	chr5:179719199-179719249	U87	brain:	n/a
42	chr5:179717478-179717528	GM19239	blood:	n/a
43	chr5:179720254-179720304	GM12878	blood:	n/a
44	chr5:179719171-179719221	GM06990	blood:	n/a
45	chr5:179719171-179719221	A549	lung:	n/a
46	chr5:179718531-179718581	NH-A	brain:	n/a
47	chr5:179719502-179719552	H1-hESC	embryonic stem cell:	embryo
48	chr5:179719756-179719806	BJ	skin:	n/a
49	chr5:179719190-179719240	SKMC	muscle:	n/a
50	chr5:179719171-179719221	ProgFib	skin:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179717698..179720150-chr5:179758033..179760822,3	MCF-7	breast:
2	chr5:179628129..179628639-chr5:179720355..179721073,2	MCF-7	breast:
3	chr5:179720972..179723069-chr5:179918796..179921248,2	MCF-7	breast:
4	chr5:179715674..179717304-chr5:179721521..179723626,2	K562	blood:
5	chr5:179718232..179719781-chr5:179756949..179759059,2	MCF-7	breast:
6	chr20:46275666..46278048-chr5:179716451..179718791,2	MCF-7	breast:
7	chr5:179716385..179718922-chr5:179921407..179923351,3	MCF-7	breast:
8	chr5:179716091..179718097-chr5:179718228..179720650,3	MCF-7	breast:
9	chr5:179683447..179685223-chr5:179718038..179720496,2	MCF-7	breast:
10	chr16:9123624..9124124-chr5:179718416..179718917,2	Hela-S3	cervix:
11	chr5:179720435..179721221-chr5:179897609..179898164,2	MCF-7	breast:
12	chr5:179718262..179720717-chr5:180237170..180239607,2	MCF-7	breast:
13	chr5:179712494..179714081-chr5:179717178..179718692,2	K562	blood:
14	chr5:179720287..179721046-chr5:179740621..179741577,2	MCF-7	breast:
15	chr5:179718755..179721306-chr5:179919977..179922949,4	MCF-7	breast:
16	chr5:179720249..179721437-chr5:179755481..179756336,5	K562	blood:
17	chr5:179635600..179638547-chr5:179713821..179718130,5	MCF-7	breast:
18	chr5:179720303..179721088-chr5:179756913..179757480,2	MCF-7	breast:
19	chr5:179715940..179718137-chr5:179891672..179893899,2	MCF-7	breast:
20	chr5:179616220..179617824-chr5:179714865..179717440,2	MCF-7	breast:
21	chr5:179716694..179718257-chr5:179740990..179742816,2	MCF-7	breast:
22	chr5:179716122..179718666-chr5:179757910..179760029,2	K562	blood:
23	chr5:179720624..179723530-chr5:179725711..179728473,2	K562	blood:
24	chr17:56708811..56709431-chr5:179718614..179719163,2	MCF-7	breast:
25	chr5:179707659..179712077-chr5:179712622..179717997,8	MCF-7	breast:
26	chr5:179720392..179721373-chr5:179895885..179896410,2	MCF-7	breast:
27	chr5:179718120..179720283-chr5:180227933..180230146,2	MCF-7	breast:
28	chr5:179721389..179723686-chr5:179731790..179733996,2	K562	blood:
29	chr19:1747829..1748422-chr5:179718198..179718965,2	Hela-S3	cervix:
30	chr5:179695378..179696983-chr5:179716689..179718636,2	K562	blood:
31	chr2:178298391..178298891-chr5:179720979..179721480,2	Hela-S3	cervix:
32	chr5:179720259..179720769-chrX:4912894..4913414,2	MCF-7	breast:
33	chr5:179633482..179636303-chr5:179718045..179719781,2	K562	blood:
34	chr5:179715141..179717166-chr5:179896710..179898786,2	MCF-7	breast:
35	chr5:179720585..179721111-chr5:179742335..179742892,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNOT6-4	chr5:179720245-179720418	XLOC_004678
2	lnc-CNOT6-4	chr5:179719184-179722539	NONHSAT105673
3	lnc-CNOT6-4	chr5:179719195-179719481	XLOC_004678

No data

Variant related genes	Relation type
ENSG00000248367	TF binding region
MAPK9	TF binding region
ENSG00000248367	CpG island
MAPK9	CpG island
ENSG00000248367	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000113300	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000267073	chromatin interactions
ENSG00000253908	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000146090	chromatin interactions
ENSG00000131459	chromatin interactions
TGFBR1	miRNA target sites

Extended variants
information (count: 151 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:151 , 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	rs149748774	chr5:179717152-179717153	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs145594879	chr5:179717155-179717156	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs576007819	chr5:179717169-179717170	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs554544476	chr5:179717203-179717204	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs574120810	chr5:179717218-179717219	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs533625140	chr5:179717229-179717230	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs553466475	chr5:179717236-179717237	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs576600401	chr5:179717237-179717238	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs185202988	chr5:179717350-179717351	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs545602963	chr5:179717353-179717354	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs562581997	chr5:179717376-179717377	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs35075037	chr5:179717383-179717384	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs538569220	chr5:179717392-179717393	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs576283900	chr5:179717400-179717401	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs35703820	chr5:179717446-179717447	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs148455818	chr5:179717452-179717453	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs142614566	chr5:179717460-179717461	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs61255050	chr5:179717498-179717499	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs188471469	chr5:179717518-179717519	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs12658400	chr5:179717643-179717644	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550337175	chr5:179717720-179717721	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs570199667	chr5:179717740-179717741	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs374932869	chr5:179717828-179717829	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs536122500	chr5:179717849-179717850	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs549444879	chr5:179717907-179717908	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs567682812	chr5:179717908-179717909	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs77251925	chr5:179717943-179717944	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs192793596	chr5:179717981-179717982	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs35115810	chr5:179718001-179718002	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs576520995	chr5:179718007-179718008	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs540631519	chr5:179718027-179718028	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs560590089	chr5:179718071-179718072	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs556302625	chr5:179718115-179718116	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs184844236	chr5:179718131-179718132	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs145618038	chr5:179718135-179718136	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs577306856	chr5:179718162-179718163	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs527871599	chr5:179718173-179718174	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs4274946	chr5:179718189-179718190	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs555723981	chr5:179718208-179718209	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs572425743	chr5:179718220-179718221	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs541448958	chr5:179718228-179718229	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs564509963	chr5:179718279-179718280	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs565988124	chr5:179718293-179718294	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs188276588	chr5:179718330-179718331	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs563889781	chr5:179718332-179718333	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs529478163	chr5:179718395-179718396	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs142416325	chr5:179718396-179718397	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs566035356	chr5:179718409-179718410	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs180752640	chr5:179718475-179718476	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs546986692	chr5:179718478-179718479	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
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
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
Autism	20808228	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD

Chromatin state (count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179692800-179718000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:179694800-179717600	Weak transcription	HUVEC	blood vessel
3	chr5:179703000-179717400	Weak transcription	NHLF	lung
4	chr5:179704600-179717200	Weak transcription	Small Intestine	intestine
5	chr5:179704600-179718000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:179705200-179717200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr5:179705600-179717600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:179706600-179717200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:179706600-179717200	Weak transcription	Colon Smooth Muscle	Colon
10	chr5:179706800-179718400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr5:179707200-179717200	Weak transcription	NHDF-Ad	bronchial
12	chr5:179707400-179717200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr5:179707600-179717600	Weak transcription	Fetal Kidney	kidney
14	chr5:179708000-179717200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr5:179708200-179717200	Weak transcription	HSMM	muscle
16	chr5:179708400-179717400	Weak transcription	Osteobl	bone
17	chr5:179708400-179717800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:179710000-179717400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr5:179710000-179717800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr5:179710400-179717200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr5:179710400-179717200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr5:179710400-179717800	Weak transcription	Right Ventricle	heart
23	chr5:179710600-179717200	Weak transcription	Adipose Nuclei	Adipose
24	chr5:179710600-179717200	Weak transcription	Brain Germinal Matrix	brain
25	chr5:179710600-179717200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr5:179710600-179717400	Weak transcription	Fetal Intestine Large	intestine
27	chr5:179710800-179717200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr5:179710800-179717200	Weak transcription	Placenta	Placenta
29	chr5:179711400-179717200	Weak transcription	Fetal Thymus	thymus
30	chr5:179711400-179717200	Weak transcription	Right Atrium	heart
31	chr5:179711600-179717200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:179711600-179717600	Weak transcription	Aorta	Aorta
33	chr5:179711600-179718000	Weak transcription	Lung	lung
34	chr5:179712200-179717200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr5:179712400-179717400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr5:179712400-179717600	Weak transcription	NH-A	brain
37	chr5:179712400-179717800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:179712600-179717200	Weak transcription	Brain Angular Gyrus	brain
39	chr5:179712600-179717200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr5:179712600-179717200	Weak transcription	Brain Hippocampus Middle	brain
41	chr5:179712600-179717200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr5:179712600-179717600	Weak transcription	Brain Substantia Nigra	brain
43	chr5:179712800-179717200	Weak transcription	Fetal Muscle Leg	muscle
44	chr5:179713800-179717200	Weak transcription	Fetal Stomach	stomach
45	chr5:179713800-179717200	Weak transcription	Hela-S3	cervix
46	chr5:179714000-179717200	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr5:179714000-179717200	Weak transcription	Thymus	Thymus
48	chr5:179714000-179717400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:179714000-179717600	Weak transcription	Primary B cells from cord blood	blood
50	chr5:179714200-179717200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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