Variant report

Variant	nsv1057052
Chromosome Location	chr19:40776128-40789766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:429)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:13)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40789369-40789589	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40778392-40779106	K562	blood:	n/a	n/a
3	ATF1	chr19:40778758-40779057	K562	blood:	n/a	n/a
4	BACH1	chr19:40780681-40780685	K562	blood:	n/a	n/a
5	BHLHE40	chr19:40781026-40781347	K562	blood:	n/a	n/a
6	BHLHE40	chr19:40780502-40780719	K562	blood:	n/a	n/a
7	BHLHE40	chr19:40778193-40779131	K562	blood:	n/a	n/a
8	BHLHE40	chr19:40786194-40786488	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:40780462-40780858	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:40781087-40781345	GM12878	blood:	n/a	n/a
11	BRCA1	chr19:40783241-40783245	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr19:40781122-40781516	K562	blood:	n/a	n/a
13	CBX3	chr19:40781831-40782318	K562	blood:	n/a	n/a
14	CBX3	chr19:40778246-40779098	K562	blood:	n/a	n/a
15	CCNT2	chr19:40778633-40779035	K562	blood:	n/a	n/a
16	CEBPB	chr19:40778270-40779334	K562	blood:	n/a	n/a
17	CEBPB	chr19:40787778-40787948	A549	lung:	n/a	n/a
18	CEBPB	chr19:40789312-40789807	HepG2	liver:	n/a	n/a
19	CEBPB	chr19:40787820-40787910	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:40778379-40779154	K562	blood:	n/a	n/a
21	CEBPD	chr19:40778564-40779167	K562	blood:	n/a	n/a
22	CEBPD	chr19:40778558-40779143	K562	blood:	n/a	n/a
23	CHD1	chr19:40789452-40792116	IMR90	lung:	n/a	n/a
24	CHD2	chr19:40778196-40778944	K562	blood:	n/a	n/a
25	CHD2	chr19:40780645-40780923	K562	blood:	n/a	n/a
26	CHD2	chr19:40780572-40781350	GM12878	blood:	n/a	n/a
27	CHD2	chr19:40786311-40786381	GM12878	blood:	n/a	n/a
28	CHD2	chr19:40789629-40789952	HepG2	liver:	n/a	n/a
29	CTCF	chr19:40776400-40776725	K562	blood:	n/a	n/a
30	CTCF	chr19:40785200-40785350	AG10803	skin:	n/a	n/a
31	CTCF	chr19:40785280-40785430	AG10803	skin:	n/a	n/a
32	CTCF	chr19:40789080-40789230	HMF	breast:	n/a	n/a
33	CTCF	chr19:40785220-40785370	BJ	skin:	n/a	n/a
34	CTCF	chr19:40785120-40785270	HEK293	kidney:	n/a	n/a
35	CTCF	chr19:40789120-40789270	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr19:40776480-40776630	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr19:40785320-40785470	NHDF-neo	bronchial:	n/a	chr19:40785425-40785434
38	CTCF	chr19:40776440-40776590	K562	blood:	n/a	n/a
39	CTCF	chr19:40776480-40776630	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr19:40789260-40789410	AG10803	skin:	n/a	chr19:40789304-40789313
41	CTCF	chr19:40785280-40785430	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr19:40785280-40785430	HCM	heart:	n/a	n/a
43	CTCF	chr19:40789240-40789390	HAc	cerebellar:	n/a	chr19:40789304-40789313
44	CTCF	chr19:40785280-40785430	BJ	skin:	n/a	n/a
45	CTCF	chr19:40789420-40789570	GM12870	blood:	n/a	n/a
46	CTCF	chr19:40785300-40785450	HPF	lung:	n/a	chr19:40785425-40785434
47	CTCF	chr19:40776560-40776710	HRE	kidney:	n/a	n/a
48	CTCF	chr19:40785220-40785370	HPF	lung:	n/a	n/a
49	CTCF	chr19:40785240-40785390	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr19:40785240-40785390	HPAF	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40788787-40788837	HRE	kidney:	n/a
2	chr19:40788787-40788837	HRCEpiC	kidney:	n/a
3	chr19:40788787-40788837	Caco-2	colon:	n/a
4	chr19:40788787-40788837	PANC-1	pancreas:	n/a
5	chr19:40788926-40788976	HRE	kidney:	n/a
6	chr19:40788926-40788976	GM12878	blood:	n/a
7	chr19:40788787-40788837	HPAEpiC	pulmonary alveolar:	n/a
8	chr19:40788926-40788976	HCM	heart:	n/a
9	chr19:40788787-40788837	Hela-S3	cervix:	n/a
10	chr19:40788787-40788837	ECC-1	luminal epithelium:	n/a
11	chr19:40788926-40788976	ECC-1	luminal epithelium:	n/a
12	chr19:40788926-40788976	Hela-S3	cervix:	n/a
13	chr19:40788787-40788837	HCPEpiC	choroid plexus:	n/a
14	chr19:40788787-40788837	AG09319	gingival:	n/a
15	chr19:40788787-40788837	SK-N-SH_RA	brain:	n/a
16	chr19:40788787-40788837	NHBE	bronchial:	n/a
17	chr19:40788787-40788837	MCF-7	breast:	n/a
18	chr19:40788787-40788837	ProgFib	skin:	n/a
19	chr19:40788787-40788837	AG04450	lung:	fetal
20	chr19:40788926-40788976	SK-N-MC	brain:	n/a
21	chr19:40788787-40788837	AoSMC	blood vessel:	n/a
22	chr19:40788787-40788837	LNCaP	prostate:	n/a
23	chr19:40788926-40788976	HL-60	blood:	n/a
24	chr19:40788787-40788837	HAEpiC	amniotic membrane:	n/a
25	chr19:40788926-40788976	IMR90	lung:	fetal
26	chr19:40788926-40788976	HRPEpiC	eye:	n/a
27	chr19:40788926-40788976	A549	lung:	n/a
28	chr19:40788926-40788976	AG09319	gingival:	n/a
29	chr19:40788926-40788976	BE2_C	brain:	n/a
30	chr19:40788926-40788976	K562	blood:	n/a
31	chr19:40788787-40788837	CMK	blood:	n/a
32	chr19:40788926-40788976	AG10803	skin:	n/a
33	chr19:40788926-40788976	PFSK-1	brain:	n/a
34	chr19:40788787-40788837	T-47D	breast:	n/a
35	chr19:40788926-40788976	HCF	heart:	n/a
36	chr19:40788787-40788837	U87	brain:	n/a
37	chr19:40788787-40788837	AG10803	skin:	n/a
38	chr19:40788787-40788837	HNPCEpiC	eye:	n/a
39	chr19:40788787-40788837	SK-N-MC	brain:	n/a
40	chr19:40788926-40788976	SKMC	muscle:	n/a
41	chr19:40788787-40788837	HepG2	liver:	n/a
42	chr19:40788926-40788976	Hepatocyte	liver:	n/a
43	chr19:40788926-40788976	PANC-1	pancreas:	n/a
44	chr19:40788926-40788976	HNPCEpiC	eye:	n/a
45	chr19:40788787-40788837	HUVEC	blood vessel:	n/a
46	chr19:40788787-40788837	SAEC	small airway:	n/a
47	chr19:40788926-40788976	ovcar-3	ovarian:	n/a
48	chr19:40788926-40788976	HEEpiC	esophagus:	n/a
49	chr19:40788926-40788976	NHDF-neo	bronchial:	n/a
50	chr19:40788926-40788976	AG09309	skin:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40768260..40771807-chr19:40783478..40786593,4	K562	blood:
2	chr19:40776409..40778614-chr19:40779445..40781045,2	K562	blood:
3	chr19:40776878..40778500-chr19:40970454..40972142,2	K562	blood:
4	chr19:40770481..40772610-chr19:40774016..40777021,3	K562	blood:
5	chr19:40769216..40771181-chr19:40778063..40779733,2	K562	blood:
6	chr19:40774152..40777118-chr19:40779107..40782198,3	MCF-7	breast:
7	chr19:40773358..40775863-chr19:40778274..40780379,3	K562	blood:
8	chr19:40788680..40791212-chr19:40852795..40854366,2	K562	blood:
9	chr19:40776468..40779839-chr19:40784717..40787633,5	MCF-7	breast:
10	chr19:40776468..40779839-chr19:40784717..40787633,5	MCF-7	breast:
11	chr19:40783887..40786272-chr19:41107076..41108731,2	K562	blood:
12	chr19:40731324..40733318-chr19:40786434..40789035,2	MCF-7	breast:
13	chr17:56708147..56710537-chr19:40780894..40783062,2	MCF-7	breast:
14	chr19:40761210..40764143-chr19:40782426..40783993,2	MCF-7	breast:
15	chr19:40778844..40781132-chr19:41035904..41037926,2	K562	blood:
16	chr19:40787579..40789839-chr19:40846986..40849835,2	MCF-7	breast:
17	chr19:40774152..40777118-chr19:40779107..40782198,3	MCF-7	breast:
18	chr19:40695407..40698481-chr19:40788292..40792778,5	K562	blood:
19	chr19:40776186..40778648-chr19:40782455..40784190,2	MCF-7	breast:
20	chr19:40780031..40782205-chr19:40949064..40951116,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC118344.1-3	chr19:40788155-40788351	NONHSAT066363
2	lnc-MAP3K10-1	chr19:40784047-40784243	NONHSAT066362
3	lnc-MAP3K10-1	chr19:40780649-40780699	NONHSAT066362
4	lnc-AC118344.1-3	chr19:40788615-40789072	NONHSAT066363
5	lnc-MAP3K10-1	chr19:40783383-40783496	l_1686_chr19:40779415-40784234_testes
6	lnc-MAP3K10-1	chr19:40780043-40780172	l_1686_chr19:40779415-40784234_testes
7	lnc-MAP3K10-1	chr19:40780617-40780699	l_1686_chr19:40779415-40784234_testes
8	lnc-AC118344.1-1	chr19:40779396-40779537	ENSG00000205041.1
9	lnc-MAP3K10-1	chr19:40783383-40783496	NONHSAT066362
10	lnc-AC118344.1-1	chr19:40780067-40781386	ENSG00000205041.1
11	lnc-MAP3K10-1	chr19:40784047-40784234	l_1686_chr19:40779415-40784234_testes
12	lnc-AC118344.1-2	chr19:40785014-40785131	NONHSAT066360
13	lnc-MAP3K10-1	chr19:40779416-40780009	l_1686_chr19:40779415-40784234_testes

miRNA name	Chromosome Location	mirBase accession
hsa-miR-641	chr19:40788510-40788533	MIMAT0003311

No data

Variant related genes	Relation type
MIR641	TF binding region
ENSG00000205041	TF binding region
AKT2	TF binding region
MIR641	CpG island
ENSG00000205041	CpG island
AKT2	CpG island
ENSG00000090006	chromatin interactions
ENSG00000206925	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000160460	chromatin interactions
ENSG00000167565	chromatin interactions
ENSG00000090013	chromatin interactions
ENSG00000160392	chromatin interactions
ENSG00000205041	chromatin interactions
ENSG00000130758	chromatin interactions
ENSG00000268366	chromatin interactions
ENSG00000105219	chromatin interactions
ENSG00000105223	chromatin interactions
ENSG00000105221	chromatin interactions
TOB1	Mature miRNA region

Extended variants
information (count: 541 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547692731	chr19:40776132-40776133	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs374074657	chr19:40776133-40776134	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs565730149	chr19:40776134-40776135	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs529859512	chr19:40776185-40776186	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs73555594	chr19:40776194-40776195	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs569700834	chr19:40776275-40776276	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs537317524	chr19:40776305-40776306	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs149397268	chr19:40776309-40776310	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs386809249	chr19:40776310-40776311	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs375629047	chr19:40776314-40776315	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs201196129	chr19:40776316-40776317	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs369223871	chr19:40776317-40776318	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs570670857	chr19:40776342-40776343	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs8111561	chr19:40776408-40776409	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs552894625	chr19:40776425-40776426	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs572205864	chr19:40776448-40776449	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs563294713	chr19:40776467-40776468	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs542754171	chr19:40776493-40776494	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554527553	chr19:40776501-40776502	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs576056886	chr19:40776513-40776514	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs543476150	chr19:40776523-40776524	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs565541251	chr19:40776530-40776531	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs201450513	chr19:40776558-40776559	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs532707533	chr19:40776562-40776563	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs530599838	chr19:40776592-40776593	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs559734837	chr19:40776599-40776600	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs529795244	chr19:40776645-40776646	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs117187898	chr19:40776649-40776650	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs151186267	chr19:40776650-40776651	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs530483165	chr19:40776658-40776659	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs140319446	chr19:40776661-40776662	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs570679402	chr19:40776672-40776673	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs534657476	chr19:40776717-40776718	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs150357248	chr19:40776725-40776726	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs182459042	chr19:40776796-40776797	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs555969832	chr19:40776884-40776885	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs144804672	chr19:40776928-40776929	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs376542958	chr19:40776929-40776930	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs569708630	chr19:40776954-40776955	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs549133687	chr19:40776989-40776990	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs137997072	chr19:40776990-40776991	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs142104695	chr19:40777042-40777043	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs543761959	chr19:40777091-40777092	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs373178827	chr19:40777099-40777100	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs546879870	chr19:40777104-40777105	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs558686939	chr19:40777109-40777110	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs12461508	chr19:40777117-40777118	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs139585487	chr19:40777118-40777119	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs202024724	chr19:40777119-40777120	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs577466029	chr19:40777120-40777121	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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

Chromatin state (count:1251 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40759800-40780600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr19:40762000-40779800	Weak transcription	Stomach Mucosa	stomach
3	chr19:40762800-40777600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr19:40762800-40780800	Weak transcription	Small Intestine	intestine
5	chr19:40763600-40777800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr19:40763800-40777600	Weak transcription	Hela-S3	cervix
7	chr19:40763800-40777600	Weak transcription	HMEC	breast
8	chr19:40765400-40777800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr19:40766200-40788600	Weak transcription	HSMMtube	muscle
10	chr19:40766800-40776600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr19:40767000-40776200	Strong transcription	Primary T cells from cord blood	blood
12	chr19:40767600-40779600	Strong transcription	Fetal Stomach	stomach
13	chr19:40767800-40780400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr19:40768200-40780400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr19:40769000-40776600	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr19:40769000-40778200	Weak transcription	HSMM	muscle
17	chr19:40769000-40779600	Strong transcription	Fetal Intestine Small	intestine
18	chr19:40769400-40777400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr19:40769600-40776200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr19:40769600-40783600	Weak transcription	Fetal Kidney	kidney
21	chr19:40770000-40789600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr19:40770000-40789600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr19:40770200-40776200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr19:40770200-40789600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr19:40770200-40790200	Weak transcription	Aorta	Aorta
26	chr19:40770400-40784000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr19:40771000-40777600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr19:40771000-40780400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr19:40771000-40780800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr19:40771000-40783600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr19:40771200-40776200	Enhancers	Brain Anterior Caudate	brain
32	chr19:40771200-40776200	Weak transcription	Fetal Thymus	thymus
33	chr19:40771200-40776200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr19:40771200-40776400	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr19:40771200-40777600	Weak transcription	Osteobl	bone
36	chr19:40771200-40778000	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr19:40771400-40776200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr19:40771400-40776600	Enhancers	Pancreas	Pancrea
39	chr19:40771400-40776800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr19:40771400-40778200	Enhancers	Left Ventricle	heart
41	chr19:40771400-40779400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr19:40771400-40789400	Weak transcription	HUVEC	blood vessel
43	chr19:40771600-40778000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr19:40771600-40780400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr19:40771600-40786000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr19:40772000-40776800	Enhancers	Brain Cingulate Gyrus	brain
47	chr19:40772000-40778200	Weak transcription	Dnd41	blood
48	chr19:40772200-40776200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr19:40772400-40776200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr19:40772400-40776400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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