Variant report

Variant	nsv911776
Chromosome Location	chr19:42343526-42416056
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4643)
CpG islands
(count:3967)
Chromatin interactive
region (count:224)
LncRNA
region (count:10)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:4643 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:42387799-42388512	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:42363459-42364360	K562	blood:	n/a	n/a
3	ARID3A	chr19:42387458-42387503	K562	blood:	n/a	n/a
4	ARID3A	chr19:42387835-42388549	K562	blood:	n/a	n/a
5	ARID3A	chr19:42363525-42364394	HepG2	liver:	n/a	n/a
6	ARID3A	chr19:42347315-42347828	K562	blood:	n/a	n/a
7	ATF1	chr19:42387938-42388717	K562	blood:	n/a	n/a
8	ATF1	chr19:42363527-42364454	K562	blood:	n/a	n/a
9	ATF1	chr19:42347380-42347721	K562	blood:	n/a	n/a
10	ATF2	chr19:42375693-42377792	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr19:42363508-42364473	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr19:42380830-42381551	GM12878	blood:	n/a	n/a
13	ATF2	chr19:42376933-42377643	GM12878	blood:	n/a	n/a
14	ATF2	chr19:42371947-42372207	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr19:42366275-42366629	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr19:42366256-42366673	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr19:42386575-42388696	GM12878	blood:	n/a	n/a
18	ATF2	chr19:42379382-42379885	GM12878	blood:	n/a	n/a
19	ATF2	chr19:42375575-42376674	GM12878	blood:	n/a	n/a
20	ATF2	chr19:42363591-42364503	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr19:42390777-42392294	GM12878	blood:	n/a	n/a
22	ATF2	chr19:42376989-42377584	GM12878	blood:	n/a	n/a
23	ATF2	chr19:42380844-42382191	GM12878	blood:	n/a	n/a
24	ATF2	chr19:42363538-42364464	GM12878	blood:	n/a	n/a
25	ATF2	chr19:42376990-42377699	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr19:42375571-42376734	GM12878	blood:	n/a	n/a
27	ATF2	chr19:42363460-42364517	GM12878	blood:	n/a	n/a
28	ATF2	chr19:42370283-42370739	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr19:42387937-42388450	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr19:42368379-42368945	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr19:42387605-42388630	GM12878	blood:	n/a	n/a
32	ATF3	chr19:42387653-42388665	A549	lung:	n/a	n/a
33	ATF3	chr19:42363354-42364535	A549	lung:	n/a	n/a
34	ATF3	chr19:42364586-42366195	A549	lung:	n/a	n/a
35	ATF3	chr19:42363068-42364498	A549	lung:	n/a	n/a
36	ATF3	chr19:42376942-42377795	A549	lung:	n/a	n/a
37	ATF3	chr19:42375596-42377854	A549	lung:	n/a	n/a
38	ATF3	chr19:42364132-42364400	K562	blood:	n/a	n/a
39	ATF3	chr19:42387416-42389035	A549	lung:	n/a	n/a
40	BACH1	chr19:42377400-42377555	K562	blood:	n/a	n/a
41	BACH1	chr19:42361911-42361944	K562	blood:	n/a	n/a
42	BACH1	chr19:42387717-42388123	K562	blood:	n/a	n/a
43	BACH1	chr19:42388442-42388819	K562	blood:	n/a	n/a
44	BACH1	chr19:42391894-42392302	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr19:42363307-42364337	K562	blood:	n/a	n/a
46	BACH1	chr19:42388179-42388517	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr19:42363625-42364474	H1-hESC	embryonic stem cell:	n/a	n/a
48	BATF	chr19:42380947-42381336	GM12878	blood:	n/a	n/a
49	BATF	chr19:42375657-42375997	GM12878	blood:	n/a	n/a
50	BATF	chr19:42388179-42388562	GM12878	blood:	n/a	n/a

(count:3967 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42414972-42415022	U87	brain:	n/a
2	chr19:42388160-42388210	PrEC	prostate:	n/a
3	chr19:42414972-42415022	U87	brain:	n/a
4	chr19:42388160-42388210	PrEC	prostate:	n/a
5	chr19:42364661-42364711	CMK	blood:	n/a
6	chr19:42388160-42388210	LNCaP	prostate:	n/a
7	chr19:42363800-42363850	GM12891	blood:	n/a
8	chr19:42348902-42348952	Caco-2	colon:	n/a
9	chr19:42351841-42351891	HNPCEpiC	eye:	n/a
10	chr19:42381258-42381308	IMR90	lung:	fetal
11	chr19:42409117-42409167	HUVEC	blood vessel:	n/a
12	chr19:42379710-42379760	BE2_C	brain:	n/a
13	chr19:42348686-42348736	Hela-S3	cervix:	n/a
14	chr19:42383292-42383342	HCT-116	colon:	n/a
15	chr19:42405234-42405284	HCF	heart:	n/a
16	chr19:42363626-42363676	HepG2	liver:	n/a
17	chr19:42348947-42348997	HepG2	liver:	n/a
18	chr19:42385074-42385124	HIPEpiC	eye:	n/a
19	chr19:42360913-42360963	Hepatocyte	liver:	n/a
20	chr19:42414972-42415022	GM12891	blood:	n/a
21	chr19:42388290-42388340	MCF10A-Er-Src	breast:	n/a
22	chr19:42388476-42388526	HEK293	kidney:	embryo
23	chr19:42390475-42390525	NH-A	brain:	n/a
24	chr19:42364661-42364711	HAEpiC	amniotic membrane:	n/a
25	chr19:42409117-42409167	CMK	blood:	n/a
26	chr19:42348822-42348872	HCPEpiC	choroid plexus:	n/a
27	chr19:42388471-42388521	HNPCEpiC	eye:	n/a
28	chr19:42364667-42364717	ProgFib	skin:	n/a
29	chr19:42408458-42408508	NHBE	bronchial:	n/a
30	chr19:42363800-42363850	HIPEpiC	eye:	n/a
31	chr19:42388284-42388334	HCM	heart:	n/a
32	chr19:42367976-42368026	SAEC	small airway:	n/a
33	chr19:42386382-42386432	AG04449	skin:	fetal
34	chr19:42385074-42385124	NT2-D1	testis:	n/a
35	chr19:42388284-42388334	T-47D	breast:	n/a
36	chr19:42348327-42348377	HMEC	breast:	n/a
37	chr19:42356072-42356122	ovcar-3	ovarian:	n/a
38	chr19:42364661-42364711	BJ	skin:	n/a
39	chr19:42364667-42364717	HCT-116	colon:	n/a
40	chr19:42365024-42365074	CMK	blood:	n/a
41	chr19:42365024-42365074	NHBE	bronchial:	n/a
42	chr19:42364667-42364717	HRE	kidney:	n/a
43	chr19:42349032-42349082	HepG2	liver:	n/a
44	chr19:42388476-42388526	ECC-1	luminal epithelium:	n/a
45	chr19:42390475-42390525	SK-N-MC	brain:	n/a
46	chr19:42386872-42386922	NT2-D1	testis:	n/a
47	chr19:42346176-42346226	AG04450	lung:	fetal
48	chr19:42360913-42360963	MCF-7	breast:	n/a
49	chr19:42363949-42363999	HNPCEpiC	eye:	n/a
50	chr19:42407471-42407521	HL-60	blood:	n/a

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr19:42377383..42379799-chr19:42454565..42456876,2	MCF-7	breast:
2	chr19:42347384..42349576-chr19:42363024..42365083,2	K562	blood:
3	chr19:42373255..42375761-chr19:42417935..42419997,2	K562	blood:
4	chr19:42386808..42388903-chr19:42409471..42412143,2	K562	blood:
5	chr19:42364123..42365765-chr19:42410876..42413809,2	K562	blood:
6	chr19:42382515..42384277-chr19:42396659..42398289,2	MCF-7	breast:
7	chr19:42398848..42401100-chr19:42409902..42411983,2	MCF-7	breast:
8	chr19:42377202..42377808-chr19:42438762..42439328,2	MCF-7	breast:
9	chr19:42377260..42377774-chr19:42455449..42456424,2	MCF-7	breast:
10	chr19:42407772..42411584-chr19:42411987..42415149,3	MCF-7	breast:
11	chr19:42370231..42372294-chr19:42382726..42385087,2	MCF-7	breast:
12	chr19:42387549..42389204-chr19:42401111..42402879,2	MCF-7	breast:
13	chr19:42388358..42390538-chr19:42579521..42581745,2	MCF-7	breast:
14	chr19:42344282..42346616-chr19:42346629..42348983,3	MCF-7	breast:
15	chr19:42378499..42381176-chr19:42422747..42425494,2	MCF-7	breast:
16	chr19:42385706..42396512-chr19:42423854..42433641,19	K562	blood:
17	chr19:42392649..42394240-chr19:42444125..42445799,2	K562	blood:
18	chr19:42389226..42390893-chr19:42441627..42443907,2	MCF-7	breast:
19	chr19:42362466..42365153-chr19:42745908..42747542,2	K562	blood:
20	chr19:42390448..42392513-chr19:42434205..42436040,2	MCF-7	breast:
21	chr19:42392300..42393961-chr19:42403075..42405096,2	K562	blood:
22	chr19:42403036..42406958-chr19:42407264..42409613,3	MCF-7	breast:
23	chr19:42346920..42348959-chr19:42369071..42372047,3	K562	blood:
24	chr19:42354940..42358615-chr19:42368975..42372693,4	K562	blood:
25	chr19:42385733..42387603-chr19:42407160..42410354,3	MCF-7	breast:
26	chr12:54678901..54681605-chr19:42364228..42365826,2	K562	blood:
27	chr19:42385266..42389164-chr19:42392215..42397025,5	MCF-7	breast:
28	chr19:42386056..42389793-chr19:42407267..42411147,5	MCF-7	breast:
29	chr19:42408977..42410880-chr19:42415090..42416805,2	MCF-7	breast:
30	chr19:42387920..42390020-chr19:42392761..42394560,2	K562	blood:
31	chr19:42361079..42367934-chr19:42431466..42436133,8	K562	blood:
32	chr19:42386109..42390387-chr19:42411996..42416642,6	K562	blood:
33	chr19:42399993..42402789-chr19:42426992..42429764,2	MCF-7	breast:
34	chr19:42392300..42393961-chr19:42403075..42405096,2	K562	blood:
35	chr19:42347384..42349429-chr19:42363024..42365795,2	K562	blood:
36	chr19:42362135..42368129-chr19:42461941..42464761,7	MCF-7	breast:
37	chr19:42362802..42365669-chr19:42579542..42583856,4	MCF-7	breast:
38	chr19:42375885..42381575-chr19:42432655..42439530,9	K562	blood:
39	chr19:42376370..42377844-chr19:42455348..42456066,5	K562	blood:
40	chr19:42337138..42340110-chr19:42342013..42344959,2	MCF-7	breast:
41	chr19:42404537..42406482-chr19:42420163..42422046,2	K562	blood:
42	chr19:42379146..42381960-chr19:42461841..42465419,3	MCF-7	breast:
43	chr19:42391577..42392478-chr19:42455568..42456267,3	MCF-7	breast:
44	chr19:42374454..42377744-chr19:42431362..42433284,5	K562	blood:
45	chr19:42390499..42394130-chr19:42395488..42398499,5	MCF-7	breast:
46	chr19:42371817..42374747-chr19:42545510..42548368,2	K562	blood:
47	chr1:207503537..207504067-chr19:42368282..42368782,2	Hela-S3	cervix:
48	chr19:42368937..42370473-chr19:42375983..42377700,2	MCF-7	breast:
49	chr19:42370513..42373649-chr19:42375625..42377894,4	MCF-7	breast:
50	chr19:42311416..42313552-chr19:42366859..42369350,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD79A-2	chr19:42409952-42409979	NONHSAT066500
2	lnc-LYPD4-2	chr19:42400853-42400876	NONHSAT066499
3	lnc-LYPD4-2	chr19:42400972-42402807	NONHSAT066497
4	lnc-LYPD4-2	chr19:42401027-42401182	NONHSAT066498
5	lnc-LYPD4-2	chr19:42400176-42400914	NONHSAT066497
6	lnc-LYPD4-2	chr19:42400991-42402843	NONHSAT066499
7	lnc-RPS19-1	chr19:42354312-42354768	NONHSAT066493
8	lnc-RPS19-1	chr19:42355652-42355716	NONHSAT066493
9	lnc-LYPD4-2	chr19:42400449-42400876	NONHSAT066498
10	lnc-CD79A-2	chr19:42410091-42410487	NONHSAT066500

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6797-3p	chr19:42373745-42373766	MIMAT0027495
hsa-miR-6797-5p	chr19:42373702-42373726	MIMAT0027494

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ARHGEF1	hsa-miR-124-3p	chr19:42411237-42411243
2	ARHGEF1	hsa-miR-124-3p	chr19:42411526-42411545

Variant related genes	Relation type
CD79A	TF binding region
ARHGEF1	TF binding region
ENSG00000267839	TF binding region
LYPD4	TF binding region
DMRTC2	TF binding region
RPS19	TF binding region
ENSG00000268041	TF binding region
CD79A	CpG island
ARHGEF1	CpG island
ENSG00000267839	CpG island
LYPD4	CpG island
DMRTC2	CpG island
RPS19	CpG island
ENSG00000268041	CpG island
ENSG00000086061	chromatin interactions
ENSG00000135486	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000268041	chromatin interactions
ENSG00000170956	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000267839	chromatin interactions
ENSG00000267549	chromatin interactions
ENSG00000137074	chromatin interactions
ENSG00000173334	chromatin interactions
ENSG00000079432	chromatin interactions
ENSG00000105732	chromatin interactions
ENSG00000105737	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000076928	chromatin interactions
ENSG00000162236	chromatin interactions
ENSG00000183103	chromatin interactions
ENSG00000204957	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000105369	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000256690	chromatin interactions
ENSG00000105372	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000142025	chromatin interactions
ENSG00000269119	chromatin interactions
ENSG00000105404	chromatin interactions
ENSG00000105723	chromatin interactions
ENSG00000079462	chromatin interactions

Extended variants
information (count: 3199 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3199 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3922888	chr19:42343526-42343527	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545603770	chr19:42343527-42343528	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs560336042	chr19:42343598-42343599	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs527792357	chr19:42343636-42343637	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs549096228	chr19:42343641-42343642	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs146676575	chr19:42343643-42343644	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372288679	chr19:42343655-42343656	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs74728743	chr19:42343731-42343732	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs371794265	chr19:42343747-42343748	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs397724191	chr19:42343754-42343755	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs374135020	chr19:42343755-42343756	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs5828130	chr19:42343759-42343760	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs60674548	chr19:42343799-42343800	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs187598617	chr19:42343812-42343813	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs538791906	chr19:42343820-42343821	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs553942703	chr19:42343864-42343865	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs140224390	chr19:42343884-42343885	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs534648977	chr19:42343988-42343989	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs536396492	chr19:42343996-42343997	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs192964425	chr19:42344012-42344013	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs74386560	chr19:42344049-42344050	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs543031992	chr19:42344085-42344086	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs556410295	chr19:42344110-42344111	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs577918402	chr19:42344119-42344120	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs545227453	chr19:42344136-42344137	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs7508460	chr19:42344240-42344241	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs368982850	chr19:42344241-42344242	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs7508359	chr19:42344242-42344243	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs527780560	chr19:42344259-42344260	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs543134877	chr19:42344260-42344261	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs561250428	chr19:42344318-42344319	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs541553993	chr19:42344340-42344341	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs561845191	chr19:42344349-42344350	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs115611601	chr19:42344426-42344427	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs532490351	chr19:42344448-42344449	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs189755565	chr19:42344459-42344460	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs140664991	chr19:42344501-42344502	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs143788556	chr19:42344529-42344530	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs148137259	chr19:42344539-42344540	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs569436452	chr19:42344543-42344544	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs552840802	chr19:42344572-42344573	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs372804481	chr19:42344577-42344578	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs181340631	chr19:42344581-42344582	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs577904275	chr19:42344669-42344670	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs183635492	chr19:42344670-42344671	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs539363524	chr19:42344791-42344792	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs554050272	chr19:42344792-42344793	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs568891185	chr19:42344797-42344798	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs542867475	chr19:42344798-42344799	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs8113780	chr19:42344819-42344820	Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

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
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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3192 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42340400-42344600	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr19:42340600-42344800	Weak transcription	Right Atrium	heart
3	chr19:42342400-42343800	Enhancers	K562	blood
4	chr19:42343400-42344800	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr19:42344000-42345000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr19:42344600-42344800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr19:42346000-42347200	Enhancers	K562	blood
8	chr19:42347000-42347800	Enhancers	HepG2	liver
9	chr19:42347200-42347600	Enhancers	Duodenum Mucosa	Duodenum
10	chr19:42347200-42348000	Enhancers	Stomach Mucosa	stomach
11	chr19:42347200-42348000	Flanking Active TSS	K562	blood
12	chr19:42347600-42347800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:42348000-42349200	Enhancers	K562	blood
14	chr19:42348400-42349000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:42348600-42349000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr19:42351400-42351600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:42351600-42351800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:42351600-42351800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr19:42351800-42352000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:42352000-42363800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:42355200-42355800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr19:42355200-42356000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr19:42355400-42355800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr19:42355400-42355800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr19:42355400-42355800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr19:42355400-42355800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr19:42355400-42356000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
28	chr19:42355400-42356000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr19:42355400-42356000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr19:42355600-42355800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr19:42357800-42359400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr19:42358000-42358400	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr19:42358400-42363200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr19:42362000-42362600	Enhancers	K562	blood
35	chr19:42362600-42363000	Weak transcription	K562	blood
36	chr19:42363000-42363200	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr19:42363000-42363200	Enhancers	Primary B cells from cord blood	blood
38	chr19:42363000-42363200	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr19:42363000-42363200	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr19:42363000-42363200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr19:42363000-42363200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr19:42363000-42363200	Enhancers	Liver	Liver
43	chr19:42363000-42363200	Enhancers	Brain Anterior Caudate	brain
44	chr19:42363000-42363200	Enhancers	Colon Smooth Muscle	Colon
45	chr19:42363000-42363200	Enhancers	Duodenum Mucosa	Duodenum
46	chr19:42363000-42363200	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr19:42363000-42363200	Enhancers	Dnd41	blood
48	chr19:42363000-42363200	Enhancers	Hela-S3	cervix
49	chr19:42363000-42363200	Enhancers	HepG2	liver
50	chr19:42363000-42363200	Enhancers	K562	blood

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