Variant report

Variant	esv1846202
Chromosome Location	chr5:77944003-77949565
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:550)
CpG islands
(count:488)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:77943329-77944203	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr5:77946095-77946330	GM12878	blood:	n/a	chr5:77946248-77946259
3	BCLAF1	chr5:77943183-77944315	GM12878	blood:	n/a	chr5:77944064-77944077 chr5:77943877-77943886 chr5:77944281-77944294 chr5:77944068-77944081 chr5:77944068-77944081
4	BCLAF1	chr5:77943246-77944248	GM12878	blood:	n/a	chr5:77944064-77944077 chr5:77943877-77943886 chr5:77944068-77944081 chr5:77944068-77944081
5	BHLHE40	chr5:77944778-77944985	GM12878	blood:	n/a	chr5:77944890-77944906 chr5:77944895-77944911
6	BHLHE40	chr5:77944357-77944668	HepG2	liver:	n/a	n/a
7	BRCA1	chr5:77943784-77944110	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr5:77943698-77945144	K562	blood:	n/a	n/a
9	CEBPB	chr5:77943833-77944035	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr5:77948651-77948661	A549	lung:	n/a	n/a
11	CEBPB	chr5:77946056-77946383	IMR90	lung:	n/a	n/a
12	CEBPB	chr5:77944302-77944476	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr5:77944264-77944761	HepG2	liver:	n/a	n/a
14	CHD1	chr5:77944075-77944256	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr5:77945675-77946014	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr5:77942547-77945482	IMR90	lung:	n/a	n/a
17	CHD1	chr5:77945063-77945402	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr5:77943257-77944553	GM12878	blood:	n/a	n/a
19	CHD1	chr5:77944979-77945152	GM12878	blood:	n/a	n/a
20	CHD2	chr5:77944170-77944205	HepG2	liver:	n/a	n/a
21	CHD2	chr5:77945965-77946157	HepG2	liver:	n/a	chr5:77946020-77946030
22	CHD2	chr5:77943939-77944073	GM12878	blood:	n/a	n/a
23	CHD2	chr5:77944483-77944673	HepG2	liver:	n/a	n/a
24	CHD2	chr5:77943828-77944774	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr5:77945707-77946074	H1-hESC	embryonic stem cell:	n/a	chr5:77946020-77946030
26	CHD2	chr5:77944340-77945022	GM12878	blood:	n/a	n/a
27	CHD2	chr5:77944946-77944949	HepG2	liver:	n/a	n/a
28	CREB1	chr5:77944031-77945157	A549	lung:	n/a	n/a
29	CTBP2	chr5:77943776-77945110	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr5:77945603-77946019	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr5:77944300-77944450	GM12865	blood:	n/a	n/a
32	CTCF	chr5:77943980-77944130	Caco-2	colon:	n/a	n/a
33	CTCF	chr5:77945140-77945290	HAc	cerebellar:	n/a	chr5:77945178-77945196
34	CTCF	chr5:77943780-77944566	GM12878	blood:	n/a	chr5:77943896-77943906
35	CTCF	chr5:77943937-77944092	GM10266	blood:	n/a	n/a
36	CTCF	chr5:77945160-77945310	BJ	skin:	n/a	chr5:77945178-77945196
37	CTCF	chr5:77944340-77944490	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr5:77943922-77944113	GM12891	blood:	n/a	n/a
39	CTCF	chr5:77944001-77944015	K562	blood:	n/a	n/a
40	CTCF	chr5:77945100-77945250	HCPEpiC	choroid plexus:	n/a	chr5:77945178-77945196
41	CTCF	chr5:77943980-77944130	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr5:77943912-77944438	K562	blood:	n/a	n/a
43	CTCF	chr5:77943940-77944090	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr5:77943906-77944086	GM19239	blood:	n/a	n/a
45	CTCF	chr5:77943980-77944130	AG10803	skin:	n/a	n/a
46	CTCF	chr5:77943980-77944130	NHEK	skin:	n/a	n/a
47	CTCF	chr5:77943940-77944090	GM12869	blood:	n/a	n/a
48	CTCF	chr5:77944300-77944450	GM12873	blood:	n/a	n/a
49	CTCF	chr5:77943940-77944090	AG10803	skin:	n/a	n/a
50	CTCF	chr5:77943952-77944134	LNCaP	prostate:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:77949077-77949127	HEK293	kidney:	embryo
2	chr5:77945219-77945269	U87	brain:	n/a
3	chr5:77945347-77945397	HCF	heart:	n/a
4	chr5:77945178-77945228	HepG2	liver:	n/a
5	chr5:77946110-77946160	HCF	heart:	n/a
6	chr5:77945178-77945228	HRCEpiC	kidney:	n/a
7	chr5:77945178-77945228	NHBE	bronchial:	n/a
8	chr5:77945347-77945397	GM12892	blood:	n/a
9	chr5:77945347-77945397	HUVEC	blood vessel:	n/a
10	chr5:77944851-77944901	HEK293	kidney:	embryo
11	chr5:77945347-77945397	AG04449	skin:	fetal
12	chr5:77945739-77945789	PrEC	prostate:	n/a
13	chr5:77944851-77944901	AG09309	skin:	n/a
14	chr5:77945347-77945397	HRCEpiC	kidney:	n/a
15	chr5:77945178-77945228	MCF-7	breast:	n/a
16	chr5:77945347-77945397	Hepatocyte	liver:	n/a
17	chr5:77945739-77945789	AG04450	lung:	fetal
18	chr5:77945178-77945228	HCM	heart:	n/a
19	chr5:77945219-77945269	H1-hESC	embryonic stem cell:	embryo
20	chr5:77944851-77944901	AG10803	skin:	n/a
21	chr5:77945347-77945397	Caco-2	colon:	n/a
22	chr5:77945739-77945789	HCPEpiC	choroid plexus:	n/a
23	chr5:77945219-77945269	Hela-S3	cervix:	n/a
24	chr5:77949077-77949127	ProgFib	skin:	n/a
25	chr5:77945178-77945228	NT2-D1	testis:	n/a
26	chr5:77945219-77945269	AoSMC	blood vessel:	n/a
27	chr5:77946110-77946160	GM12891	blood:	n/a
28	chr5:77949077-77949127	PFSK-1	brain:	n/a
29	chr5:77944343-77944393	T-47D	breast:	n/a
30	chr5:77944343-77944393	GM06990	blood:	n/a
31	chr5:77946110-77946160	ECC-1	luminal epithelium:	n/a
32	chr5:77945347-77945397	GM19239	blood:	n/a
33	chr5:77944343-77944393	BJ	skin:	n/a
34	chr5:77944343-77944393	HMEC	breast:	n/a
35	chr5:77945347-77945397	HCT-116	colon:	n/a
36	chr5:77944851-77944901	NHBE	bronchial:	n/a
37	chr5:77949077-77949127	Caco-2	colon:	n/a
38	chr5:77944851-77944901	LNCaP	prostate:	n/a
39	chr5:77944343-77944393	HEK293	kidney:	embryo
40	chr5:77945347-77945397	AG09319	gingival:	n/a
41	chr5:77944851-77944901	AoSMC	blood vessel:	n/a
42	chr5:77945739-77945789	K562	blood:	n/a
43	chr5:77946110-77946160	SK-N-SH	brain:	n/a
44	chr5:77946110-77946160	SKMC	muscle:	n/a
45	chr5:77945739-77945789	GM12891	blood:	n/a
46	chr5:77945347-77945397	SAEC	small airway:	n/a
47	chr5:77949077-77949127	HCF	heart:	n/a
48	chr5:77944851-77944901	MCF10A-Er-Src	breast:	n/a
49	chr5:77949077-77949127	PrEC	prostate:	n/a
50	chr5:77944343-77944393	HCM	heart:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:77948053..77949941-chr5:77952156..77953774,2	K562	blood:
2	chr5:77936618..77938171-chr5:77943031..77945738,2	K562	blood:
3	chr5:77943633..77945471-chr5:77948483..77951262,3	MCF-7	breast:
4	chr5:77932938..77939935-chr5:77942023..77946135,10	MCF-7	breast:
5	chr5:77947585..77950288-chr5:77961353..77964094,3	K562	blood:
6	chr5:77943376..77944358-chr9:107509480..107510026,2	Hela-S3	cervix:
7	chr5:77935628..77937313-chr5:77945519..77948138,2	MCF-7	breast:
8	chr5:77949562..77953709-chr5:77953710..77956487,4	K562	blood:
9	chr5:77945458..77947369-chr5:77973307..77975636,2	K562	blood:
10	chr5:77945339..77947011-chr5:77970962..77972578,2	K562	blood:
11	chr5:77947982..77950288-chr5:77962264..77964094,2	K562	blood:
12	chr5:77940516..77942352-chr5:77943015..77944536,2	MCF-7	breast:
13	chr5:77944860..77948164-chr5:77958771..77961486,4	MCF-7	breast:

No data

Variant related genes	Relation type
HMGB1P21	TF binding region
LHFPL2	TF binding region
HMGB1P21	CpG island
LHFPL2	CpG island
ENSG00000136783	chromatin interactions
ENSG00000145685	chromatin interactions
ENSG00000248909	chromatin interactions

Extended variants
information (count: 183 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:183 , 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	rs374796105	chr5:77944019-77944020	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs543787730	chr5:77944020-77944021	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs554392195	chr5:77944029-77944030	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs574444176	chr5:77944104-77944105	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs540066807	chr5:77944121-77944122	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs560252999	chr5:77944203-77944204	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs532306667	chr5:77944217-77944218	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs546165892	chr5:77944218-77944219	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs562760893	chr5:77944284-77944285	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs150087159	chr5:77944305-77944306	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs550972423	chr5:77944339-77944340	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs561249055	chr5:77944348-77944349	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs530175870	chr5:77944413-77944414	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs546890036	chr5:77944414-77944415	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs567009231	chr5:77944417-77944418	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs559274490	chr5:77944418-77944419	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs552495149	chr5:77944433-77944434	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs569183929	chr5:77944556-77944557	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs537468610	chr5:77944614-77944615	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs341924	chr5:77944618-77944619	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs112451911	chr5:77944653-77944654	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574457307	chr5:77944761-77944762	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs533836033	chr5:77944823-77944824	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs553582280	chr5:77944828-77944829	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs577149354	chr5:77944834-77944835	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs546005529	chr5:77944851-77944852	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs549578968	chr5:77944856-77944857	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs562799085	chr5:77944905-77944906	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs576377517	chr5:77944974-77944975	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs544295923	chr5:77945022-77945023	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs561296799	chr5:77945077-77945078	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs530141933	chr5:77945099-77945100	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs148824713	chr5:77945167-77945168	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs560376734	chr5:77945221-77945222	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs532593634	chr5:77945258-77945259	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs73769044	chr5:77945276-77945277	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569223590	chr5:77945318-77945319	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs547267674	chr5:77945339-77945340	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs78941363	chr5:77945407-77945408	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs115939333	chr5:77945412-77945413	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs72762908	chr5:77945435-77945436	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs533545551	chr5:77945438-77945439	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs553866157	chr5:77945485-77945486	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs146827144	chr5:77945536-77945537	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs201935781	chr5:77945537-77945538	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs341923	chr5:77945540-77945541	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs576991149	chr5:77945598-77945599	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs535339512	chr5:77945678-77945679	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs370740716	chr5:77945748-77945749	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs188799007	chr5:77945782-77945783	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Breast cancer	21858162	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:77941600-77945200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:77942200-77945000	Active TSS	GM12878-XiMat	blood
3	chr5:77942200-77945200	Active TSS	HSMMtube	muscle
4	chr5:77942200-77945400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:77942200-77945400	Active TSS	Rectal Smooth Muscle	rectum
6	chr5:77942200-77945600	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr5:77942200-77945800	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr5:77942600-77945200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:77942600-77945200	Active TSS	Fetal Stomach	stomach
10	chr5:77942600-77945400	Active TSS	Aorta	Aorta
11	chr5:77942600-77945400	Active TSS	Ovary	ovary
12	chr5:77942800-77945000	Active TSS	HMEC	breast
13	chr5:77942800-77945200	Active TSS	HSMM	muscle
14	chr5:77942800-77945200	Active TSS	NHLF	lung
15	chr5:77942800-77945400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr5:77942800-77945400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:77942800-77945400	Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr5:77942800-77945400	Active TSS	NHDF-Ad	bronchial
19	chr5:77942800-77945600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:77942800-77945600	Active TSS	Breast Myoepithelial Primary Cells	Breast
21	chr5:77942800-77945800	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr5:77943000-77944200	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
23	chr5:77943000-77944200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
24	chr5:77943000-77944200	Active TSS	Stomach Mucosa	stomach
25	chr5:77943000-77944400	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr5:77943000-77944400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:77943000-77945000	Active TSS	Muscle Satellite Cultured Cells	--
28	chr5:77943000-77945000	Active TSS	Fetal Intestine Small	intestine
29	chr5:77943000-77945200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:77943000-77945200	Active TSS	A549	lung
31	chr5:77943000-77945400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr5:77943000-77945400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr5:77943000-77945400	Active TSS	Fetal Intestine Large	intestine
34	chr5:77943000-77945400	Active TSS	Sigmoid Colon	Sigmoid Colon
35	chr5:77943000-77945600	Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr5:77943000-77945800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
37	chr5:77943000-77945800	Active TSS	H9 Cell Line	embryonic stem cell
38	chr5:77943000-77946000	Active TSS	Fetal Kidney	kidney
39	chr5:77943200-77944200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
40	chr5:77943200-77944200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
41	chr5:77943200-77944200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr5:77943200-77944200	Flanking Active TSS	Spleen	Spleen
43	chr5:77943200-77945200	Active TSS	Lung	lung
44	chr5:77943200-77945400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr5:77943200-77945400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:77943200-77945400	Active TSS	Colon Smooth Muscle	Colon
47	chr5:77943200-77945600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr5:77943200-77945600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr5:77943200-77945600	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr5:77943200-77945600	Active TSS	HepG2	liver

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