Variant report

Variant	esv2754051
Chromosome Location	chr19:40848081-40863842
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:686)
CpG islands
(count:1466)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40854921-40855228	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40854141-40854669	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40854326-40854851	K562	blood:	n/a	n/a
4	ATF1	chr19:40854854-40855352	K562	blood:	n/a	n/a
5	ATF2	chr19:40853959-40854742	GM12878	blood:	n/a	n/a
6	ATF2	chr19:40861767-40862254	GM12878	blood:	n/a	n/a
7	ATF2	chr19:40861703-40862360	GM12878	blood:	n/a	n/a
8	ATF3	chr19:40854269-40854686	K562	blood:	n/a	chr19:40854520-40854529 chr19:40854319-40854328
9	ATF3	chr19:40854291-40854755	H1-hESC	embryonic stem cell:	n/a	chr19:40854520-40854529 chr19:40854319-40854328 chr19:40854692-40854701
10	ATF3	chr19:40854264-40854605	HepG2	liver:	n/a	chr19:40854520-40854529 chr19:40854319-40854328
11	ATF3	chr19:40854240-40854648	K562	blood:	n/a	chr19:40854243-40854252 chr19:40854520-40854529 chr19:40854319-40854328
12	ATF3	chr19:40854100-40854753	A549	lung:	n/a	chr19:40854243-40854252 chr19:40854520-40854529 chr19:40854319-40854328 chr19:40854692-40854701
13	ATF3	chr19:40854947-40855374	K562	blood:	n/a	chr19:40855174-40855184 chr19:40855170-40855185 chr19:40855174-40855182
14	ATF3	chr19:40854131-40854758	HepG2	liver:	n/a	chr19:40854243-40854252 chr19:40854520-40854529 chr19:40854319-40854328 chr19:40854692-40854701
15	ATF3	chr19:40853772-40855604	A549	lung:	n/a	chr19:40855174-40855184 chr19:40855170-40855185 chr19:40854243-40854252 chr19:40855174-40855182 chr19:40854520-40854529 chr19:40854319-40854328 chr19:40854692-40854701
16	ATF3	chr19:40854294-40854650	H1-hESC	embryonic stem cell:	n/a	chr19:40854520-40854529 chr19:40854319-40854328
17	ATF3	chr19:40854126-40854724	GM12878	blood:	n/a	chr19:40854243-40854252 chr19:40854520-40854529 chr19:40854319-40854328 chr19:40854692-40854701
18	ATF3	chr19:40854290-40854606	GM12878	blood:	n/a	chr19:40854520-40854529 chr19:40854319-40854328
19	BACH1	chr19:40855035-40855136	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr19:40854058-40854812	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr19:40853516-40853672	K562	blood:	n/a	n/a
22	BATF	chr19:40861826-40862177	GM12878	blood:	n/a	n/a
23	BATF	chr19:40854226-40854481	GM12878	blood:	n/a	n/a
24	BCL11A	chr19:40861814-40862191	GM12878	blood:	n/a	n/a
25	BCL11A	chr19:40861872-40862183	GM12878	blood:	n/a	n/a
26	BCL3	chr19:40854078-40854771	A549	lung:	n/a	chr19:40854553-40854566 chr19:40854312-40854325
27	BCL3	chr19:40853516-40855436	A549	lung:	n/a	chr19:40854553-40854566 chr19:40854312-40854325
28	BCLAF1	chr19:40861740-40862348	GM12878	blood:	n/a	n/a
29	BCLAF1	chr19:40854100-40854753	GM12878	blood:	n/a	chr19:40854553-40854566 chr19:40854312-40854325
30	BHLHE40	chr19:40861856-40862280	GM12878	blood:	n/a	n/a
31	BHLHE40	chr19:40854078-40854743	HepG2	liver:	n/a	n/a
32	BHLHE40	chr19:40854987-40855395	K562	blood:	n/a	n/a
33	BHLHE40	chr19:40853924-40854735	K562	blood:	n/a	n/a
34	BHLHE40	chr19:40854890-40855090	GM12878	blood:	n/a	n/a
35	BHLHE40	chr19:40854264-40855032	A549	lung:	n/a	n/a
36	BHLHE40	chr19:40854179-40854669	GM12878	blood:	n/a	n/a
37	BRCA1	chr19:40854401-40854721	HepG2	liver:	n/a	n/a
38	BRCA1	chr19:40853876-40855370	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr19:40853933-40854779	K562	blood:	n/a	n/a
40	CCNT2	chr19:40854075-40854745	K562	blood:	n/a	n/a
41	CEBPB	chr19:40861737-40862337	GM12878	blood:	n/a	n/a
42	CEBPB	chr19:40854321-40854580	K562	blood:	n/a	n/a
43	CEBPB	chr19:40854972-40855431	MCF-7	breast:	n/a	n/a
44	CEBPB	chr19:40854951-40855391	K562	blood:	n/a	n/a
45	CEBPB	chr19:40854983-40855345	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr19:40854939-40855368	IMR90	lung:	n/a	n/a
47	CEBPB	chr19:40857308-40857484	K562	blood:	n/a	n/a
48	CEBPB	chr19:40854123-40855460	A549	lung:	n/a	n/a
49	CEBPB	chr19:40854839-40855363	A549	lung:	n/a	n/a
50	CEBPB	chr19:40854959-40855359	K562	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40853155-40853205	GM19239	blood:	n/a
2	chr19:40855502-40855552	HRPEpiC	eye:	n/a
3	chr19:40853155-40853205	GM19239	blood:	n/a
4	chr19:40855502-40855552	HRPEpiC	eye:	n/a
5	chr19:40854170-40854220	HNPCEpiC	eye:	n/a
6	chr19:40854313-40854363	HIPEpiC	eye:	n/a
7	chr19:40854424-40854474	Hepatocyte	liver:	n/a
8	chr19:40853908-40853958	T-47D	breast:	n/a
9	chr19:40854525-40854575	Hepatocyte	liver:	n/a
10	chr19:40854523-40854573	Hela-S3	cervix:	n/a
11	chr19:40854347-40854397	HRPEpiC	eye:	n/a
12	chr19:40850441-40850491	AG04450	lung:	fetal
13	chr19:40854020-40854070	HRPEpiC	eye:	n/a
14	chr19:40854069-40854119	ECC-1	luminal epithelium:	n/a
15	chr19:40853164-40853214	HMEC	breast:	n/a
16	chr19:40853155-40853205	HUVEC	blood vessel:	n/a
17	chr19:40854718-40854768	BJ	skin:	n/a
18	chr19:40857787-40857837	SAEC	small airway:	n/a
19	chr19:40855502-40855552	BJ	skin:	n/a
20	chr19:40854347-40854397	Hela-S3	cervix:	n/a
21	chr19:40853908-40853958	ProgFib	skin:	n/a
22	chr19:40854151-40854201	H1-hESC	embryonic stem cell:	embryo
23	chr19:40854430-40854480	SAEC	small airway:	n/a
24	chr19:40853164-40853214	LNCaP	prostate:	n/a
25	chr19:40854409-40854459	PFSK-1	brain:	n/a
26	chr19:40854718-40854768	NHBE	bronchial:	n/a
27	chr19:40855502-40855552	GM06990	blood:	n/a
28	chr19:40854424-40854474	AG04450	lung:	fetal
29	chr19:40853155-40853205	GM12878	blood:	n/a
30	chr19:40854069-40854119	H1-hESC	embryonic stem cell:	embryo
31	chr19:40854525-40854575	HMEC	breast:	n/a
32	chr19:40854523-40854573	AG09319	gingival:	n/a
33	chr19:40854664-40854714	BJ	skin:	n/a
34	chr19:40854313-40854363	LNCaP	prostate:	n/a
35	chr19:40850441-40850491	HCT-116	colon:	n/a
36	chr19:40855329-40855379	A549	lung:	n/a
37	chr19:40853164-40853214	GM12891	blood:	n/a
38	chr19:40854151-40854201	HL-60	blood:	n/a
39	chr19:40854190-40854240	PrEC	prostate:	n/a
40	chr19:40853155-40853205	HRCEpiC	kidney:	n/a
41	chr19:40854190-40854240	ECC-1	luminal epithelium:	n/a
42	chr19:40854718-40854768	H1-hESC	embryonic stem cell:	embryo
43	chr19:40854718-40854768	AG09309	skin:	n/a
44	chr19:40854151-40854201	LNCaP	prostate:	n/a
45	chr19:40854144-40854194	BE2_C	brain:	n/a
46	chr19:40854664-40854714	NT2-D1	testis:	n/a
47	chr19:40854525-40854575	HCM	heart:	n/a
48	chr19:40854424-40854474	GM06990	blood:	n/a
49	chr19:40855329-40855379	SAEC	small airway:	n/a
50	chr19:40854424-40854474	AG04449	skin:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40853841..40855507-chr19:41105833..41108523,2	K562	blood:
2	chr19:40853920..40856703-chr19:40862603..40866302,4	K562	blood:
3	chr19:40861491..40863430-chr19:40866543..40869308,2	K562	blood:
4	chr19:40853787..40856715-chr19:40882110..40885015,2	K562	blood:
5	chr19:40858935..40867508-chr19:40870167..40875772,11	K562	blood:
6	chr19:40853028..40855563-chr19:40876148..40878218,2	K562	blood:
7	chr19:40788680..40791212-chr19:40852795..40854366,2	K562	blood:
8	chr19:40852692..40855852-chr19:40948280..40952207,5	K562	blood:
9	chr19:40846921..40852460-chr19:40852861..40856555,6	K562	blood:
10	chr19:40854558..40856307-chr19:40856338..40858284,2	MCF-7	breast:
11	chr19:40854582..40856444-chr19:40862603..40865437,3	K562	blood:
12	chr19:40854917..40856679-chr19:40945662..40948462,2	MCF-7	breast:
13	chr19:40855052..40856726-chr19:40865449..40867831,2	MCF-7	breast:
14	chr19:40846573..40849159-chr19:40852803..40855284,3	K562	blood:
15	chr19:40853920..40856703-chr19:40862603..40866302,4	K562	blood:
16	chr19:40825864..40828845-chr19:40848574..40850485,2	K562	blood:
17	chr19:40853192..40856646-chr19:40870044..40873206,4	K562	blood:
18	chr19:40787579..40789839-chr19:40846986..40849835,2	MCF-7	breast:
19	chr19:40846573..40849159-chr19:40852803..40855284,3	K562	blood:
20	chr19:40855517..40857078-chr19:40875905..40878728,2	K562	blood:
21	chr19:40857735..40859819-chr19:40860082..40862864,2	K562	blood:
22	chr19:40851351..40853152-chr19:40892640..40895401,2	K562	blood:
23	chr19:40846921..40852460-chr19:40852861..40856555,6	K562	blood:
24	chr19:40853951..40856077-chr19:40931313..40932883,2	MCF-7	breast:
25	chr19:40857735..40859819-chr19:40860082..40862864,2	K562	blood:
26	chr19:40853029..40856025-chr19:41082472..41085390,2	K562	blood:
27	chr19:40851266..40855955-chr19:40945466..40950850,6	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLD3-1	chr19:40854597-40854675	NONHSAT066375
2	lnc-PLD3-1	chr19:40854414-40854631	NONHSAT066374

No data

Variant related genes	Relation type
ENSG00000207281	TF binding region
ENSG00000206925	TF binding region
C19orf47	TF binding region
PLD3	TF binding region
ENSG00000207281	CpG island
ENSG00000206925	CpG island
C19orf47	CpG island
PLD3	CpG island
ENSG00000105223	chromatin interactions
ENSG00000160410	chromatin interactions
ENSG00000105221	chromatin interactions
ENSG00000167565	chromatin interactions
ENSG00000206925	chromatin interactions
ENSG00000207631	chromatin interactions
ENSG00000090006	chromatin interactions
ENSG00000160392	chromatin interactions
ENSG00000268366	chromatin interactions
ENSG00000197019	chromatin interactions

Extended variants
information (count: 596 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4802074	chr19:40848081-40848082	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374493736	chr19:40848093-40848094	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs8104162	chr19:40848145-40848146	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs578252631	chr19:40848156-40848157	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs563106685	chr19:40848211-40848212	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs556321003	chr19:40848226-40848227	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs118130471	chr19:40848240-40848241	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs115957552	chr19:40848278-40848279	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs545946879	chr19:40848346-40848347	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs372557590	chr19:40848368-40848369	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs142484708	chr19:40848373-40848374	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs189510352	chr19:40848412-40848413	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs201570788	chr19:40848502-40848503	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs149760084	chr19:40848509-40848510	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs145715014	chr19:40848515-40848516	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs571163733	chr19:40848536-40848537	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs538571770	chr19:40848545-40848546	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs181496767	chr19:40848557-40848558	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs148894784	chr19:40848612-40848613	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs534279135	chr19:40848648-40848649	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs143615784	chr19:40848677-40848678	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs573969725	chr19:40848698-40848699	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs538203322	chr19:40848719-40848720	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs556600044	chr19:40848731-40848732	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs35513131	chr19:40848781-40848782	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs578242942	chr19:40848823-40848824	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs148067201	chr19:40848826-40848827	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs372065487	chr19:40848873-40848874	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs554327411	chr19:40848879-40848880	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs572578813	chr19:40848894-40848895	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs542703209	chr19:40848907-40848908	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs117004636	chr19:40848914-40848915	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs572033221	chr19:40848939-40848940	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs140990023	chr19:40848980-40848981	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs542988908	chr19:40848983-40848984	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs55954198	chr19:40848994-40848995	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs561276319	chr19:40849001-40849002	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs547317922	chr19:40849037-40849038	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs565865327	chr19:40849063-40849064	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs529888486	chr19:40849106-40849107	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs574629038	chr19:40849139-40849140	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs548375532	chr19:40849144-40849145	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs567606675	chr19:40849151-40849152	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs538362992	chr19:40849158-40849159	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs144820432	chr19:40849193-40849194	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs571703092	chr19:40849255-40849256	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs138586595	chr19:40849275-40849276	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs554212182	chr19:40849312-40849313	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs141641074	chr19:40849341-40849342	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs542812080	chr19:40849349-40849350	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40820800-40848400	Strong transcription	Dnd41	blood
2	chr19:40822000-40851000	Strong transcription	Fetal Stomach	stomach
3	chr19:40824200-40848600	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr19:40824200-40849600	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr19:40826600-40853000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:40832200-40852800	Weak transcription	NHDF-Ad	bronchial
7	chr19:40834400-40853400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr19:40834800-40853600	Weak transcription	Small Intestine	intestine
9	chr19:40836000-40853600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:40837200-40848400	Weak transcription	Psoas Muscle	Psoas
11	chr19:40837400-40853400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr19:40837400-40853600	Weak transcription	Stomach Mucosa	stomach
13	chr19:40839800-40852800	Weak transcription	Hela-S3	cervix
14	chr19:40839800-40853400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr19:40840000-40852800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr19:40840000-40852800	Weak transcription	HUVEC	blood vessel
17	chr19:40840000-40853400	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr19:40840000-40853600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr19:40840200-40850400	Weak transcription	Osteobl	bone
20	chr19:40840200-40852800	Weak transcription	HepG2	liver
21	chr19:40840400-40850800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr19:40840400-40852800	Weak transcription	Fetal Kidney	kidney
23	chr19:40840400-40853000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr19:40840400-40853000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr19:40840400-40853000	Weak transcription	Fetal Brain Male	brain
26	chr19:40840400-40853400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr19:40841400-40853000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr19:40842200-40848600	Weak transcription	Gastric	stomach
29	chr19:40842200-40852800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr19:40842200-40853200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr19:40842200-40853600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr19:40842200-40853600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr19:40842400-40848800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr19:40842400-40849000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr19:40842400-40850600	Weak transcription	Brain Substantia Nigra	brain
36	chr19:40842400-40852800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr19:40842400-40853000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr19:40842400-40853000	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr19:40842400-40853400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr19:40842400-40853600	Weak transcription	Fetal Intestine Large	intestine
41	chr19:40842400-40853600	Weak transcription	Ovary	ovary
42	chr19:40842600-40853400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr19:40842800-40848400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr19:40842800-40850400	Weak transcription	Esophagus	oesophagus
45	chr19:40842800-40853000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr19:40842800-40853600	Weak transcription	Pancreas	Pancrea
47	chr19:40843000-40850400	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr19:40843000-40853000	Weak transcription	NH-A	brain
49	chr19:40843000-40853400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr19:40844000-40848400	Weak transcription	Spleen	Spleen

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