Variant report

Variant	nsv1006036
Chromosome Location	chr1:144895697-144950969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1661)
CpG islands
(count:1345)
Chromatin interactive
region (count:109)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1661 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:144931963-144932828	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:144937109-144937725	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:144931414-144931602	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:144923974-144924494	HepG2	liver:	n/a	chr1:144924178-144924194
5	ARID3A	chr1:144938874-144939338	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:144918079-144918361	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:144921610-144922130	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:144938243-144938360	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:144918090-144918310	K562	blood:	n/a	n/a
10	ATF1	chr1:144918124-144918317	K562	blood:	n/a	n/a
11	ATF2	chr1:144931771-144932702	GM12878	blood:	n/a	n/a
12	ATF2	chr1:144908048-144908805	GM12878	blood:	n/a	n/a
13	ATF2	chr1:144931922-144932867	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr1:144908134-144908746	GM12878	blood:	n/a	n/a
15	ATF2	chr1:144931876-144932753	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:144931477-144932093	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:144924377-144924386	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr1:144908154-144908914	GM12878	blood:	n/a	n/a
19	BATF	chr1:144918063-144918340	GM12878	blood:	n/a	n/a
20	BATF	chr1:144908200-144908921	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:144908224-144908540	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:144908211-144908941	GM12878	blood:	n/a	n/a
23	BCL3	chr1:144931803-144933017	A549	lung:	n/a	chr1:144932014-144932027 chr1:144932069-144932082 chr1:144931862-144931875 chr1:144932058-144932071 chr1:144932171-144932179
24	BCLAF1	chr1:144931095-144932686	GM12878	blood:	n/a	chr1:144932014-144932027 chr1:144931744-144931753 chr1:144932069-144932082 chr1:144931862-144931875 chr1:144931747-144931756 chr1:144931740-144931753 chr1:144931749-144931762 chr1:144931743-144931756 chr1:144932058-144932071 chr1:144931741-144931750 chr1:144931742-144931755 chr1:144932171-144932179
25	BHLHE40	chr1:144935383-144935704	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:144918068-144918289	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:144907946-144908684	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:144921698-144922064	HepG2	liver:	n/a	n/a
29	BHLHE40	chr1:144931358-144932896	GM12878	blood:	n/a	chr1:144931851-144931867 chr1:144931740-144931756 chr1:144932069-144932085
30	BRCA1	chr1:144932346-144932836	GM12878	blood:	n/a	n/a
31	BRCA1	chr1:144938833-144938875	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr1:144932110-144933073	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr1:144916619-144916671	GM12878	blood:	n/a	n/a
34	BRCA1	chr1:144931904-144933128	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr1:144938742-144938911	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr1:144912899-144912910	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr1:144931824-144932592	HepG2	liver:	n/a	n/a
38	CBX3	chr1:144931897-144932645	K562	blood:	n/a	n/a
39	CCNT2	chr1:144931633-144932040	K562	blood:	n/a	chr1:144931905-144931914
40	CCNT2	chr1:144932320-144932515	K562	blood:	n/a	n/a
41	CEBPB	chr1:144914532-144914875	A549	lung:	n/a	chr1:144914701-144914712
42	CEBPB	chr1:144914541-144914847	H1-hESC	embryonic stem cell:	n/a	chr1:144914701-144914712
43	CEBPB	chr1:144941257-144941624	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:144936386-144937168	H1-hESC	embryonic stem cell:	n/a	chr1:144936754-144936767
45	CEBPB	chr1:144934021-144934315	IMR90	lung:	n/a	chr1:144934170-144934183 chr1:144934170-144934183
46	CEBPB	chr1:144927282-144927658	Hela-S3	cervix:	n/a	chr1:144927468-144927477 chr1:144927468-144927479 chr1:144927466-144927477
47	CEBPB	chr1:144936951-144937274	IMR90	lung:	n/a	n/a
48	CEBPB	chr1:144944549-144944889	K562	blood:	n/a	chr1:144944788-144944799 chr1:144944820-144944832 chr1:144944789-144944798 chr1:144944784-144944801 chr1:144944789-144944798 chr1:144944830-144944841
49	CEBPB	chr1:144918083-144918206	K562	blood:	n/a	n/a
50	CEBPB	chr1:144927281-144927655	HepG2	liver:	n/a	chr1:144927468-144927477 chr1:144927468-144927479 chr1:144927466-144927477

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144932136-144932186	PrEC	prostate:	n/a
2	chr1:144928806-144928856	AG04449	skin:	fetal
3	chr1:144928806-144928856	HCPEpiC	choroid plexus:	n/a
4	chr1:144932136-144932186	PrEC	prostate:	n/a
5	chr1:144928806-144928856	AG04449	skin:	fetal
6	chr1:144928806-144928856	HCPEpiC	choroid plexus:	n/a
7	chr1:144931379-144931429	CMK	blood:	n/a
8	chr1:144935409-144935459	HNPCEpiC	eye:	n/a
9	chr1:144931975-144932025	GM06990	blood:	n/a
10	chr1:144932473-144932523	AG09309	skin:	n/a
11	chr1:144932311-144932361	IMR90	lung:	fetal
12	chr1:144935409-144935459	Jurkat	blood:	n/a
13	chr1:144932476-144932526	IMR90	lung:	fetal
14	chr1:144931966-144932016	PANC-1	pancreas:	n/a
15	chr1:144932207-144932257	HMEC	breast:	n/a
16	chr1:144931379-144931429	HRCEpiC	kidney:	n/a
17	chr1:144932473-144932523	HEEpiC	esophagus:	n/a
18	chr1:144928806-144928856	GM06990	blood:	n/a
19	chr1:144930964-144931014	NH-A	brain:	n/a
20	chr1:144931980-144932030	SKMC	muscle:	n/a
21	chr1:144930964-144931014	MCF10A-Er-Src	breast:	n/a
22	chr1:144937317-144937367	SK-N-MC	brain:	n/a
23	chr1:144931862-144931912	HAEpiC	amniotic membrane:	n/a
24	chr1:144913803-144913853	ECC-1	luminal epithelium:	n/a
25	chr1:144931966-144932016	AG04450	lung:	fetal
26	chr1:144932311-144932361	SK-N-SH_RA	brain:	n/a
27	chr1:144931862-144931912	T-47D	breast:	n/a
28	chr1:144931862-144931912	BJ	skin:	n/a
29	chr1:144930964-144931014	NHBE	bronchial:	n/a
30	chr1:144932476-144932526	Hepatocyte	liver:	n/a
31	chr1:144932476-144932526	AG09309	skin:	n/a
32	chr1:144931966-144932016	HepG2	liver:	n/a
33	chr1:144932227-144932277	GM06990	blood:	n/a
34	chr1:144931975-144932025	LNCaP	prostate:	n/a
35	chr1:144932207-144932257	SAEC	small airway:	n/a
36	chr1:144937317-144937367	SK-N-SH	brain:	n/a
37	chr1:144931966-144932016	HEK293	kidney:	embryo
38	chr1:144937317-144937367	NHDF-neo	bronchial:	n/a
39	chr1:144942354-144942404	AoSMC	blood vessel:	n/a
40	chr1:144932136-144932186	HUVEC	blood vessel:	n/a
41	chr1:144930572-144930622	Caco-2	colon:	n/a
42	chr1:144932207-144932257	HAEpiC	amniotic membrane:	n/a
43	chr1:144930964-144931014	ovcar-3	ovarian:	n/a
44	chr1:144935409-144935459	HRE	kidney:	n/a
45	chr1:144930572-144930622	AG10803	skin:	n/a
46	chr1:144928806-144928856	HCM	heart:	n/a
47	chr1:144932476-144932526	CMK	blood:	n/a
48	chr1:144930572-144930622	AoSMC	blood vessel:	n/a
49	chr1:144930572-144930622	HCT-116	colon:	n/a
50	chr1:144932227-144932277	HL-60	blood:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:144933330..144935038-chr1:144937428..144939924,2	K562	blood:
2	chr1:144917778..144918636-chr1:147553160..147554160,3	MCF-7	breast:
3	chr1:144908995..144910553-chr1:144913596..144915672,2	K562	blood:
4	chr1:144911399..144913167-chr1:144914593..144916227,2	MCF-7	breast:
5	chr1:144941413..144943372-chr1:144947098..144949301,2	MCF-7	breast:
6	chr1:144925446..144929176-chr1:145057629..145060761,3	MCF-7	breast:
7	chr1:144925900..144930140-chr1:144930950..144934648,7	K562	blood:
8	chr1:144924927..144926596-chr1:145062250..145064152,2	MCF-7	breast:
9	chr1:144925057..144927728-chr1:145381929..145384283,2	MCF-7	breast:
10	chr1:144891214..144893695-chr1:144896100..144898968,2	MCF-7	breast:
11	chr1:144931832..144934351-chr1:145043528..145045220,3	K562	blood:
12	chr1:144921855..144924116-chr1:144941489..144944232,2	K562	blood:
13	chr1:144935150..144939379-chr1:144940271..144942978,9	K562	blood:
14	chr1:144913721..144916057-chr1:144919209..144920985,3	K562	blood:
15	chr1:144895341..144897404-chr1:144905462..144906982,2	MCF-7	breast:
16	chr1:144916772..144918364-chr1:145096684..145098671,2	MCF-7	breast:
17	chr1:144932935..144935038-chr1:144937428..144939924,3	K562	blood:
18	chr1:144931784..144933992-chr8:86374827..86377261,2	MCF-7	breast:
19	chr1:144912685..144914252-chr1:144947438..144950034,2	K562	blood:
20	chr1:144933246..144935275-chr11:64863413..64865438,2	MCF-7	breast:
21	chr1:144894819..144897241-chr1:144898698..144901682,2	K562	blood:
22	chr1:144933330..144935038-chr1:144937428..144939924,2	K562	blood:
23	chr1:144938052..144939993-chr1:145041831..145044190,2	K562	blood:
24	chr1:144943493..144945510-chr1:145439161..145441032,2	MCF-7	breast:
25	chr1:144913721..144916057-chr1:144919209..144920985,3	K562	blood:
26	chr1:144930770..144933506-chr20:52490207..52493077,2	MCF-7	breast:
27	chr1:144892599..144896749-chr1:144930798..144933879,5	MCF-7	breast:
28	chr1:144929981..144935077-chr1:145095230..145100493,10	MCF-7	breast:
29	chr1:144916627..144918753-chr1:144920547..144922373,2	K562	blood:
30	chr1:144917479..144918148-chr1:145066148..145066847,2	K562	blood:
31	chr1:144906087..144908086-chr1:144911253..144912912,2	K562	blood:
32	chr1:144932649..144934258-chr15:98503922..98505541,2	MCF-7	breast:
33	chr1:144931059..144933605-chr1:149223782..149225455,2	MCF-7	breast:
34	chr1:144920944..144925051-chr1:144925584..144929146,5	K562	blood:
35	chr1:144929958..144931521-chr17:48748229..48750387,2	MCF-7	breast:
36	chr1:144938723..144940543-chr1:144954443..144955999,2	K562	blood:
37	chr1:144928885..144930474-chr1:144935425..144937244,2	K562	blood:
38	chr1:144928278..144930809-chr1:145113028..145115664,2	MCF-7	breast:
39	chr1:144923461..144926279-chr1:144929594..144932453,4	K562	blood:
40	chr1:144934978..144937918-chr1:145018510..145021156,2	K562	blood:
41	chr1:144932256..144932802-chr2:8821849..8822771,2	HCT-116	colon:
42	chr1:144926859..144928442-chr1:145074988..145077339,2	K562	blood:
43	chr1:144919025..144921038-chr1:145058900..145061668,2	K562	blood:
44	chr1:144937739..144940161-chr1:145039312..145041037,2	K562	blood:
45	chr1:144912685..144914252-chr1:144947438..144950034,2	K562	blood:
46	chr1:144932935..144935038-chr1:144937428..144939924,3	K562	blood:
47	chr1:144928885..144930474-chr1:144935425..144937244,2	K562	blood:
48	chr1:144930971..144932699-chr1:145382569..145384639,2	MCF-7	breast:
49	chr1:144930600..144932534-chr1:145038038..145040681,2	MCF-7	breast:
50	chr1:144926702..144928514-chr1:144928774..144930808,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR3GL-8	chr1:144940359-144940515	NONHSAT005866
2	lnc-POLR3GL-8	chr1:144941080-144941374	NONHSAT005865
3	lnc-POLR3GL-8	chr1:144941080-144941367	NONHSAT005866
4	lnc-POLR3GL-8	chr1:144940123-144940515	NONHSAT005865
5	lnc-POLR3GL-8	chr1:144941764-144941802	NONHSAT005865
6	lnc-POLR3GL-8	chr1:144940612-144940760	NONHSAT005866

No data

Variant related genes	Relation type
PDE4DIP	TF binding region
RNU2-38P	TF binding region
PDE4DIP	CpG island
RNU2-38P	CpG island
ENSG00000115738	chromatin interactions
ENSG00000149823	chromatin interactions
ENSG00000272755	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000108846	chromatin interactions
ENSG00000222788	chromatin interactions
ENSG00000235092	chromatin interactions
ENSG00000241721	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000140450	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000269900	chromatin interactions
ENSG00000198517	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000144355	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000159884	chromatin interactions
ENSG00000117289	chromatin interactions

Extended variants
information (count: 2370 )
Associated
traits (count: 168 )

Variant overlapped rSNPs/rCNVs (count:2370 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587644943	chr1:144895704-144895705	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs370000532	chr1:144895715-144895716	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587600599	chr1:144895747-144895748	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587658597	chr1:144895803-144895804	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587711826	chr1:144895835-144895836	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs587594901	chr1:144895991-144895992	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587693127	chr1:144896134-144896135	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs587750189	chr1:144896190-144896191	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs587649762	chr1:144896237-144896238	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587657491	chr1:144896244-144896245	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587746094	chr1:144896293-144896294	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs199532787	chr1:144896294-144896295	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs111506914	chr1:144896298-144896299	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587743525	chr1:144896315-144896316	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12124527	chr1:144896319-144896320	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs587698667	chr1:144896349-144896350	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs373132988	chr1:144896551-144896552	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587735023	chr1:144896578-144896579	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587632839	chr1:144896671-144896672	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587691738	chr1:144896726-144896727	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs587770627	chr1:144896740-144896741	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs56735472	chr1:144896748-144896749	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587646423	chr1:144896806-144896807	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376128222	chr1:144896861-144896862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587761220	chr1:144896880-144896881	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs367576209	chr1:144896940-144896941	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150067299	chr1:144896960-144896961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111549448	chr1:144897002-144897003	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs587596830	chr1:144897003-144897004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587671085	chr1:144897018-144897019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587729550	chr1:144897031-144897032	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143114071	chr1:144897034-144897035	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs587619398	chr1:144897056-144897057	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587678015	chr1:144897062-144897063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs587627229	chr1:144897102-144897103	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182769837	chr1:144897112-144897113	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587664617	chr1:144897186-144897187	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587738545	chr1:144897303-144897304	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34512789	chr1:144897365-144897366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368272399	chr1:144897370-144897371	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs17842348	chr1:144897380-144897381	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs587736653	chr1:144897410-144897411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs587634515	chr1:144897424-144897425	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142295341	chr1:144897475-144897476	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587691859	chr1:144897547-144897548	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187454210	chr1:144897584-144897585	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192318599	chr1:144897652-144897653	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587682165	chr1:144897682-144897683	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185731337	chr1:144897692-144897693	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187575458	chr1:144897695-144897696	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:168)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Autism	20858243	CNVD

Chromatin state (count:2898 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144852200-144913200	Weak transcription	Stomach Mucosa	stomach
2	chr1:144869400-144905000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:144874600-144901600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:144874800-144906600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr1:144875000-144911000	Weak transcription	Thymus	Thymus
6	chr1:144877400-144902200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:144881400-144904800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr1:144883000-144902600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr1:144883000-144902800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:144883000-144911600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:144883200-144902600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:144887200-144904400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:144887800-144902600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr1:144888000-144902000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:144888000-144902400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr1:144888000-144902800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr1:144888000-144908800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:144888200-144903800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr1:144888200-144914400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr1:144889000-144896200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr1:144889200-144896200	Strong transcription	Brain Anterior Caudate	brain
22	chr1:144890400-144896200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr1:144892600-144897400	Weak transcription	Hela-S3	cervix
24	chr1:144892600-144900800	Weak transcription	Primary B cells from cord blood	blood
25	chr1:144892600-144902800	Weak transcription	Ovary	ovary
26	chr1:144892600-144903000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:144892600-144903000	Weak transcription	Small Intestine	intestine
28	chr1:144892600-144903200	Weak transcription	Gastric	stomach
29	chr1:144892800-144896600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:144892800-144902400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr1:144892800-144902600	Weak transcription	Colon Smooth Muscle	Colon
32	chr1:144892800-144902800	Weak transcription	Fetal Lung	lung
33	chr1:144892800-144905000	Weak transcription	Fetal Brain Male	brain
34	chr1:144892800-144907400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:144893000-144902800	Weak transcription	Spleen	Spleen
36	chr1:144893200-144901400	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr1:144893400-144901400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr1:144893400-144902400	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr1:144893400-144902600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr1:144893400-144902600	Weak transcription	Psoas Muscle	Psoas
41	chr1:144893400-144902800	Weak transcription	Lung	lung
42	chr1:144893400-144904800	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr1:144893400-144906800	Weak transcription	Pancreas	Pancrea
44	chr1:144893600-144902600	Weak transcription	Colonic Mucosa	Colon
45	chr1:144893800-144898400	Strong transcription	HSMMtube	muscle
46	chr1:144893800-144901200	Weak transcription	Fetal Intestine Large	intestine
47	chr1:144894000-144896000	Weak transcription	NHEK	skin
48	chr1:144894000-144896200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr1:144894000-144897000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:144894000-144901000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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