Variant report

Variant	nsv873371
Chromosome Location	chr1:241667244-241747838
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1325)
CpG islands
(count:977)
Chromatin interactive
region (count:81)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1325 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:241683097-241684070	K562	blood:	n/a	n/a
2	ARID3A	chr1:241694493-241695661	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:241714852-241715643	K562	blood:	n/a	n/a
4	ARID3A	chr1:241690257-241691274	K562	blood:	n/a	n/a
5	ARID3A	chr1:241694536-241695353	K562	blood:	n/a	n/a
6	ARID3A	chr1:241682922-241683657	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:241685036-241685352	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:241686056-241686075	K562	blood:	n/a	n/a
9	ATF1	chr1:241697083-241697492	K562	blood:	n/a	n/a
10	ATF1	chr1:241715030-241715741	K562	blood:	n/a	n/a
11	ATF1	chr1:241682963-241683569	K562	blood:	n/a	n/a
12	ATF2	chr1:241695968-241696944	GM12878	blood:	n/a	chr1:241696382-241696393
13	ATF2	chr1:241714951-241715844	GM12878	blood:	n/a	n/a
14	ATF2	chr1:241694560-241695898	GM12878	blood:	n/a	n/a
15	ATF2	chr1:241715190-241715785	GM12878	blood:	n/a	n/a
16	ATF2	chr1:241694596-241695663	GM12878	blood:	n/a	n/a
17	ATF2	chr1:241682785-241683603	GM12878	blood:	n/a	n/a
18	ATF3	chr1:241715257-241715543	K562	blood:	n/a	n/a
19	ATF3	chr1:241696169-241696628	GM12878	blood:	n/a	chr1:241696382-241696393 chr1:241696381-241696391 chr1:241696380-241696393 chr1:241696382-241696393 chr1:241696383-241696391
20	ATF3	chr1:241694523-241695264	A549	lung:	n/a	n/a
21	BACH1	chr1:241682658-241683183	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr1:241681762-241682263	K562	blood:	n/a	n/a
23	BACH1	chr1:241690370-241690931	K562	blood:	n/a	n/a
24	BACH1	chr1:241682783-241683376	K562	blood:	n/a	n/a
25	BATF	chr1:241715317-241715652	GM12878	blood:	n/a	n/a
26	BATF	chr1:241715327-241715639	GM12878	blood:	n/a	n/a
27	BATF	chr1:241696116-241696500	GM12878	blood:	n/a	chr1:241696276-241696287
28	BCL11A	chr1:241715268-241715717	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:241715316-241715617	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:241715243-241715708	GM12878	blood:	n/a	n/a
31	BCLAF1	chr1:241682675-241683423	GM12878	blood:	n/a	n/a
32	BCLAF1	chr1:241696089-241696746	GM12878	blood:	n/a	chr1:241696400-241696409
33	BCLAF1	chr1:241694508-241695854	GM12878	blood:	n/a	chr1:241694855-241694864
34	BCLAF1	chr1:241715048-241715796	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:241682415-241683500	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:241714878-241715622	K562	blood:	n/a	n/a
37	BHLHE40	chr1:241681890-241683384	K562	blood:	n/a	n/a
38	BHLHE40	chr1:241715281-241715643	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:241694463-241695736	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:241696035-241696664	GM12878	blood:	n/a	chr1:241696378-241696387 chr1:241696378-241696387 chr1:241696379-241696388 chr1:241696376-241696389
41	BRCA1	chr1:241682758-241684056	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr1:241714827-241715676	K562	blood:	n/a	n/a
43	CBX3	chr1:241682907-241683425	K562	blood:	n/a	n/a
44	CBX3	chr1:241682673-241683553	K562	blood:	n/a	n/a
45	CBX3	chr1:241690310-241690989	K562	blood:	n/a	n/a
46	CCNT2	chr1:241681980-241683195	K562	blood:	n/a	n/a
47	CCNT2	chr1:241715128-241715690	K562	blood:	n/a	n/a
48	CCNT2	chr1:241694674-241695140	K562	blood:	n/a	n/a
49	CCNT2	chr1:241690455-241690704	K562	blood:	n/a	n/a
50	CEBPB	chr1:241674099-241674365	A549	lung:	n/a	chr1:241674244-241674255

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:241683161-241683211	AoSMC	blood vessel:	n/a
2	chr1:241683161-241683211	AoSMC	blood vessel:	n/a
3	chr1:241695616-241695666	NHBE	bronchial:	n/a
4	chr1:241683111-241683161	HepG2	liver:	n/a
5	chr1:241696246-241696296	K562	blood:	n/a
6	chr1:241676975-241677025	HRE	kidney:	n/a
7	chr1:241679938-241679988	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:241715378-241715428	IMR90	lung:	fetal
9	chr1:241676975-241677025	AG09309	skin:	n/a
10	chr1:241683075-241683125	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:241683111-241683161	HEK293	kidney:	embryo
12	chr1:241694934-241694984	HL-60	blood:	n/a
13	chr1:241694934-241694984	HRPEpiC	eye:	n/a
14	chr1:241694605-241694655	SK-N-SH	brain:	n/a
15	chr1:241682243-241682293	NHBE	bronchial:	n/a
16	chr1:241683161-241683211	AG10803	skin:	n/a
17	chr1:241683161-241683211	HCPEpiC	choroid plexus:	n/a
18	chr1:241682627-241682677	PrEC	prostate:	n/a
19	chr1:241694934-241694984	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:241683161-241683211	NHBE	bronchial:	n/a
21	chr1:241679938-241679988	HRCEpiC	kidney:	n/a
22	chr1:241679938-241679988	HEK293	kidney:	embryo
23	chr1:241682994-241683044	HAEpiC	amniotic membrane:	n/a
24	chr1:241676975-241677025	K562	blood:	n/a
25	chr1:241682243-241682293	HCPEpiC	choroid plexus:	n/a
26	chr1:241682994-241683044	HL-60	blood:	n/a
27	chr1:241682627-241682677	PANC-1	pancreas:	n/a
28	chr1:241715378-241715428	BJ	skin:	n/a
29	chr1:241683075-241683125	A549	lung:	n/a
30	chr1:241695164-241695214	ovcar-3	ovarian:	n/a
31	chr1:241682627-241682677	GM12892	blood:	n/a
32	chr1:241695164-241695214	K562	blood:	n/a
33	chr1:241695616-241695666	HCT-116	colon:	n/a
34	chr1:241679938-241679988	GM06990	blood:	n/a
35	chr1:241683111-241683161	MCF10A-Er-Src	breast:	n/a
36	chr1:241694934-241694984	Hela-S3	cervix:	n/a
37	chr1:241695616-241695666	HCPEpiC	choroid plexus:	n/a
38	chr1:241682884-241682934	HRE	kidney:	n/a
39	chr1:241695164-241695214	SAEC	small airway:	n/a
40	chr1:241683075-241683125	SK-N-MC	brain:	n/a
41	chr1:241695164-241695214	HRCEpiC	kidney:	n/a
42	chr1:241682884-241682934	Hela-S3	cervix:	n/a
43	chr1:241694605-241694655	NHDF-neo	bronchial:	n/a
44	chr1:241682243-241682293	CMK	blood:	n/a
45	chr1:241683161-241683211	Jurkat	blood:	n/a
46	chr1:241683161-241683211	Caco-2	colon:	n/a
47	chr1:241694605-241694655	NH-A	brain:	n/a
48	chr1:241683075-241683125	Hela-S3	cervix:	n/a
49	chr1:241695616-241695666	Caco-2	colon:	n/a
50	chr1:241676975-241677025	BE2_C	brain:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:241695478..241697074-chr1:241703546..241705289,2	MCF-7	breast:
2	chr1:241671168..241675196-chr1:241680746..241684260,5	MCF-7	breast:
3	chr1:241673338..241676303-chr1:241690156..241692248,2	K562	blood:
4	chr1:241686849..241688415-chr1:241693556..241695270,2	MCF-7	breast:
5	chr1:241745082..241748095-chr1:241752482..241756598,4	MCF-7	breast:
6	chr1:241653862..241656906-chr1:241669771..241671642,4	K562	blood:
7	chr1:241694345..241694856-chr1:241790996..241791500,2	K562	blood:
8	chr1:241714129..241716798-chr1:241717149..241719743,2	K562	blood:
9	chr1:241694037..241696144-chr1:241714939..241716744,2	K562	blood:
10	chr1:241682514..241683274-chr10:38299405..38300057,2	Hela-S3	cervix:
11	chr1:241680902..241684541-chr1:242009942..242012706,4	K562	blood:
12	chr1:241665859..241668124-chr1:241670823..241673465,2	K562	blood:
13	chr1:241655406..241657552-chr1:241670142..241672034,2	K562	blood:
14	chr1:241746264..241748164-chr1:241770315..241772018,2	MCF-7	breast:
15	chr1:241694305..241695206-chr1:242161362..242162044,2	K562	blood:
16	chr1:241705464..241707473-chr1:241746825..241749623,2	MCF-7	breast:
17	chr1:241693526..241696085-chr1:241801417..241805051,3	MCF-7	breast:
18	chr1:241678718..241680701-chr1:241800665..241802574,2	K562	blood:
19	chr1:241725906..241728962-chr1:241730720..241733854,3	K562	blood:
20	chr1:241698010..241700668-chr1:241801760..241804733,2	MCF-7	breast:
21	chr1:241694273..241697777-chr1:241702428..241708800,6	K562	blood:
22	chr1:241681788..241683367-chr1:241706494..241709376,2	K562	blood:
23	chr1:241709734..241712050-chr1:241802730..241804987,2	K562	blood:
24	chr1:241697671..241700441-chr1:241723434..241725631,2	K562	blood:
25	chr1:241702260..241709454-chr1:241751164..241757390,11	MCF-7	breast:
26	chr1:241627488..241629959-chr1:241677113..241679217,2	K562	blood:
27	chr1:241698161..241701033-chr1:241703578..241707173,3	MCF-7	breast:
28	chr1:241701584..241703559-chr1:241703570..241706365,2	MCF-7	breast:
29	chr1:241703983..241707059-chr1:241753583..241756935,3	MCF-7	breast:
30	chr1:241677220..241680834-chr1:241684726..241688550,4	K562	blood:
31	chr1:241726042..241727666-chr1:241749650..241751469,2	K562	blood:
32	chr1:241705868..241707677-chr1:241764709..241766650,3	MCF-7	breast:
33	chr1:241745713..241748645-chr1:241790250..241792527,2	K562	blood:
34	chr1:241698161..241701033-chr1:241703578..241707173,3	MCF-7	breast:
35	chr1:241714129..241716798-chr1:241717149..241719743,2	K562	blood:
36	chr1:241660405..241662938-chr1:241668854..241671757,2	K562	blood:
37	chr1:241695089..241697622-chr1:241705840..241708838,3	MCF-7	breast:
38	chr1:241740414..241742828-chr1:241751126..241752757,2	MCF-7	breast:
39	chr1:241677220..241680834-chr1:241684726..241688550,4	K562	blood:
40	chr1:241697913..241700856-chr1:241791206..241793471,2	MCF-7	breast:
41	chr1:241676840..241679427-chr1:241681305..241683481,5	MCF-7	breast:
42	chr1:241713534..241716005-chr1:241800890..241804792,3	K562	blood:
43	chr1:241705724..241709431-chr1:241710439..241713347,4	MCF-7	breast:
44	chr1:241693547..241697485-chr1:242010276..242012986,4	K562	blood:
45	chr1:241694248..241695217-chr1:241997845..241998483,2	K562	blood:
46	chr1:241683433..241685881-chr1:241689141..241691385,3	MCF-7	breast:
47	chr1:241692902..241697485-chr1:242010276..242014432,6	K562	blood:
48	chr1:241719444..241722973-chr1:241723572..241727553,5	K562	blood:
49	chr1:241665518..241668923-chr1:241674331..241676931,3	MCF-7	breast:
50	chr1:241657615..241659200-chr1:241678785..241681032,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR64-2	chr1:241712977-241713387	NONHSAT010548
2	lnc-WDR64-2	chr1:241712129-241712198	NONHSAT010548
3	lnc-WDR64-2	chr1:241695679-241695798	NONHSAT010548

No data

Variant related genes	Relation type
FH	TF binding region
KMO	TF binding region
FH	CpG island
KMO	CpG island
ENSG00000117009	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000054277	chromatin interactions
ENSG00000091483	chromatin interactions
ENSG00000189180	chromatin interactions

Extended variants
information (count: 3155 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3155 , 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	rs4659607	chr1:241667244-241667245	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190353292	chr1:241667245-241667246	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs539449056	chr1:241667246-241667247	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555908729	chr1:241667278-241667279	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368482304	chr1:241667311-241667312	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs200550559	chr1:241667313-241667314	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576072868	chr1:241667329-241667330	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201513242	chr1:241667332-241667333	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200118475	chr1:241667339-241667340	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs121913119	chr1:241667366-241667367	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs121913122	chr1:241667423-241667424	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201383596	chr1:241667425-241667426	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11545655	chr1:241667429-241667430	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs398123159	chr1:241667430-241667431	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201975537	chr1:241667437-241667438	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201652136	chr1:241667440-241667441	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200028270	chr1:241667461-241667462	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs1049719	chr1:241667463-241667464	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146816517	chr1:241667468-241667469	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs201124581	chr1:241667477-241667478	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs202147731	chr1:241667491-241667492	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146751488	chr1:241667493-241667494	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs398123168	chr1:241667498-241667499	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549087719	chr1:241667520-241667521	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs61737760	chr1:241667523-241667524	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs368849989	chr1:241667525-241667526	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs121913118	chr1:241667528-241667529	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs147991516	chr1:241667533-241667534	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200491078	chr1:241667539-241667540	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201502246	chr1:241667542-241667543	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182531846	chr1:241667566-241667567	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs199539806	chr1:241667573-241667574	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs367887305	chr1:241667575-241667576	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200809528	chr1:241667584-241667585	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs553516187	chr1:241667589-241667590	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs144597860	chr1:241667590-241667591	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs201168038	chr1:241667593-241667594	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs115081518	chr1:241667621-241667622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373514084	chr1:241667623-241667624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571824927	chr1:241667628-241667629	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185874443	chr1:241667729-241667730	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550019175	chr1:241667784-241667785	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs563354611	chr1:241667819-241667820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529207374	chr1:241667842-241667843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114103037	chr1:241667932-241667933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs147909642	chr1:241667938-241667939	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs6689999	chr1:241667958-241667959	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs188046831	chr1:241668011-241668012	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs571787005	chr1:241668066-241668067	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs537359913	chr1:241668076-241668077	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	17989066	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	22291905	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma	18772890	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Brain overgrowth syndrome	24179207	CNVD

Chromatin state (count:1559 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241655800-241677200	Strong transcription	Liver	Liver
2	chr1:241656800-241670000	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr1:241656800-241677000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:241656800-241678200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:241657000-241669800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:241657000-241670000	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr1:241657000-241675800	Strong transcription	Stomach Smooth Muscle	stomach
8	chr1:241657000-241676000	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr1:241657000-241676200	Strong transcription	Duodenum Smooth Muscle	Duodenum
10	chr1:241657000-241676400	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr1:241657000-241677000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr1:241657000-241677200	Strong transcription	Adipose Nuclei	Adipose
13	chr1:241657000-241677400	Strong transcription	Fetal Thymus	thymus
14	chr1:241657000-241680000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr1:241657200-241668400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr1:241657200-241669800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:241657200-241677000	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr1:241657200-241677200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:241657200-241677400	Strong transcription	Duodenum Mucosa	Duodenum
20	chr1:241657400-241676600	Strong transcription	Primary B cells from peripheral blood	blood
21	chr1:241657400-241676800	Strong transcription	K562	blood
22	chr1:241657400-241678600	Strong transcription	Dnd41	blood
23	chr1:241657400-241680000	Strong transcription	Primary B cells from cord blood	blood
24	chr1:241657600-241667800	Strong transcription	Rectal Mucosa Donor 31	rectum
25	chr1:241657600-241668200	Strong transcription	NH-A	brain
26	chr1:241657600-241672000	Strong transcription	HSMM	muscle
27	chr1:241657600-241676600	Strong transcription	Placenta	Placenta
28	chr1:241657600-241677000	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr1:241657800-241667800	Strong transcription	Primary hematopoietic stem cells	blood
30	chr1:241657800-241671400	Weak transcription	Stomach Mucosa	stomach
31	chr1:241658200-241671200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr1:241659000-241682000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:241659200-241679800	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:241659600-241679000	Strong transcription	HMEC	breast
35	chr1:241660000-241675800	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr1:241661200-241681400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr1:241662800-241667800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr1:241662800-241676000	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr1:241663000-241675200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr1:241663200-241671000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:241663600-241669400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr1:241663800-241669800	Strong transcription	Osteobl	bone
43	chr1:241663800-241675800	Strong transcription	Left Ventricle	heart
44	chr1:241663800-241676000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr1:241663800-241676000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr1:241663800-241677000	Strong transcription	Fetal Muscle Trunk	muscle
47	chr1:241664000-241668800	Strong transcription	HepG2	liver
48	chr1:241664000-241669200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:241664000-241676800	Strong transcription	GM12878-XiMat	blood
50	chr1:241664000-241677200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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