Variant report

Variant	esv997362
Chromosome Location	chr1:113234820-113243297
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:183)
Chromatin interactive
region (count:21)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:113241408-113241950	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:113243153-113243661	K562	blood:	n/a	n/a
3	ARID3A	chr1:113241656-113241875	K562	blood:	n/a	n/a
4	ATF1	chr1:113243103-113243860	K562	blood:	n/a	n/a
5	ATF2	chr1:113242970-113243867	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:113243158-113243903	GM12878	blood:	n/a	n/a
7	ATF2	chr1:113243218-113243836	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:113243025-113244165	GM12878	blood:	n/a	n/a
9	ATF3	chr1:113243005-113243807	K562	blood:	n/a	n/a
10	BACH1	chr1:113243210-113243852	K562	blood:	n/a	n/a
11	BCL3	chr1:113242793-113245886	A549	lung:	n/a	n/a
12	BCL3	chr1:113241235-113241675	A549	lung:	n/a	n/a
13	BCL3	chr1:113242980-113244427	A549	lung:	n/a	n/a
14	BCL3	chr1:113243104-113243739	GM12878	blood:	n/a	n/a
15	BCLAF1	chr1:113243017-113243811	K562	blood:	n/a	n/a
16	BCLAF1	chr1:113242981-113243806	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:113243039-113243964	K562	blood:	n/a	n/a
18	BHLHE40	chr1:113241120-113241754	K562	blood:	n/a	n/a
19	BHLHE40	chr1:113241112-113241824	HepG2	liver:	n/a	n/a
20	BHLHE40	chr1:113242164-113242545	K562	blood:	n/a	n/a
21	BHLHE40	chr1:113242867-113244011	K562	blood:	n/a	n/a
22	BHLHE40	chr1:113243176-113243728	HepG2	liver:	n/a	n/a
23	BHLHE40	chr1:113243286-113243714	GM12878	blood:	n/a	n/a
24	BRCA1	chr1:113243160-113243771	HepG2	liver:	n/a	n/a
25	BRCA1	chr1:113240996-113241200	HepG2	liver:	n/a	n/a
26	CBX3	chr1:113242817-113243845	K562	blood:	n/a	n/a
27	CCNT2	chr1:113239491-113239790	K562	blood:	n/a	n/a
28	CCNT2	chr1:113242999-113243955	K562	blood:	n/a	n/a
29	CCNT2	chr1:113241567-113241778	K562	blood:	n/a	n/a
30	CEBPB	chr1:113241233-113241359	K562	blood:	n/a	n/a
31	CEBPB	chr1:113243135-113243761	K562	blood:	n/a	n/a
32	CEBPB	chr1:113243038-113243780	K562	blood:	n/a	n/a
33	CEBPB	chr1:113242978-113243021	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:113243017-113243885	GM12878	blood:	n/a	n/a
35	CEBPD	chr1:113241466-113241723	HepG2	liver:	n/a	n/a
36	CEBPD	chr1:113242955-113243906	K562	blood:	n/a	n/a
37	CHD2	chr1:113243137-113243826	HepG2	liver:	n/a	n/a
38	CHD2	chr1:113241815-113241840	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr1:113242974-113243737	GM12878	blood:	n/a	n/a
40	CHD2	chr1:113242644-113243920	K562	blood:	n/a	n/a
41	CHD2	chr1:113241180-113241897	HepG2	liver:	n/a	n/a
42	CHD2	chr1:113242204-113242247	K562	blood:	n/a	n/a
43	CHD2	chr1:113241145-113241689	K562	blood:	n/a	n/a
44	CHD2	chr1:113242956-113243794	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr1:113242160-113242310	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr1:113243160-113243310	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr1:113243220-113243370	HEK293	kidney:	n/a	n/a
48	CTCF	chr1:113241120-113241270	HEK293	kidney:	n/a	n/a
49	CTCF	chr1:113243260-113243410	HVMF	connective:	n/a	n/a
50	CTCF	chr1:113243211-113243831	K562	blood:	n/a	chr1:113243509-113243522

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:113242047-113242097	H1-hESC	embryonic stem cell:	embryo
2	chr1:113242047-113242097	HCF	heart:	n/a
3	chr1:113239645-113239695	SKMC	muscle:	n/a
4	chr1:113239645-113239695	U87	brain:	n/a
5	chr1:113240710-113240760	ProgFib	skin:	n/a
6	chr1:113242047-113242097	HRCEpiC	kidney:	n/a
7	chr1:113240710-113240760	AoSMC	blood vessel:	n/a
8	chr1:113239645-113239695	K562	blood:	n/a
9	chr1:113239645-113239695	SK-N-MC	brain:	n/a
10	chr1:113242047-113242097	T-47D	breast:	n/a
11	chr1:113239645-113239695	Jurkat	blood:	n/a
12	chr1:113242047-113242097	IMR90	lung:	fetal
13	chr1:113242047-113242097	AG04449	skin:	fetal
14	chr1:113239645-113239695	ProgFib	skin:	n/a
15	chr1:113239645-113239695	SAEC	small airway:	n/a
16	chr1:113240710-113240760	GM19239	blood:	n/a
17	chr1:113239645-113239695	HL-60	blood:	n/a
18	chr1:113239645-113239695	RPTEC	kidney:	n/a
19	chr1:113239645-113239695	PANC-1	pancreas:	n/a
20	chr1:113240710-113240760	SK-N-SH_RA	brain:	n/a
21	chr1:113242047-113242097	SK-N-MC	brain:	n/a
22	chr1:113240710-113240760	ovcar-3	ovarian:	n/a
23	chr1:113242047-113242097	SK-N-SH	brain:	n/a
24	chr1:113240710-113240760	HepG2	liver:	n/a
25	chr1:113242047-113242097	NHDF-neo	bronchial:	n/a
26	chr1:113239645-113239695	Hela-S3	cervix:	n/a
27	chr1:113239645-113239695	GM06990	blood:	n/a
28	chr1:113239645-113239695	HPAEpiC	pulmonary alveolar:	n/a
29	chr1:113242047-113242097	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:113239645-113239695	MCF10A-Er-Src	breast:	n/a
31	chr1:113239645-113239695	HRE	kidney:	n/a
32	chr1:113239645-113239695	SK-N-SH	brain:	n/a
33	chr1:113242047-113242097	A549	lung:	n/a
34	chr1:113239645-113239695	A549	lung:	n/a
35	chr1:113239645-113239695	HepG2	liver:	n/a
36	chr1:113240710-113240760	HEEpiC	esophagus:	n/a
37	chr1:113242047-113242097	HRPEpiC	eye:	n/a
38	chr1:113242047-113242097	HCM	heart:	n/a
39	chr1:113242047-113242097	HepG2	liver:	n/a
40	chr1:113242047-113242097	Jurkat	blood:	n/a
41	chr1:113242047-113242097	AG09319	gingival:	n/a
42	chr1:113240710-113240760	MCF-7	breast:	n/a
43	chr1:113242047-113242097	GM06990	blood:	n/a
44	chr1:113242047-113242097	SK-N-SH_RA	brain:	n/a
45	chr1:113240710-113240760	A549	lung:	n/a
46	chr1:113240710-113240760	HRPEpiC	eye:	n/a
47	chr1:113239645-113239695	SK-N-SH_RA	brain:	n/a
48	chr1:113239645-113239695	LNCaP	prostate:	n/a
49	chr1:113240710-113240760	HMEC	breast:	n/a
50	chr1:113239645-113239695	CMK	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:112937855..112940278-chr1:113239914..113242532,2	MCF-7	breast:
2	chr1:113214002..113222947-chr1:113236890..113251579,47	MCF-7	breast:
3	chr1:113160443..113165363-chr1:113242054..113245654,5	K562	blood:
4	chr1:113240296..113243095-chr1:113496225..113498995,2	K562	blood:
5	chr1:113160176..113163931-chr1:113238020..113242018,6	K562	blood:
6	chr1:113160402..113162739-chr1:113234192..113237024,2	K562	blood:
7	chr1:113214866..113222565-chr1:113237012..113253952,54	K562	blood:
8	chr1:113184100..113185954-chr1:113242899..113245081,2	K562	blood:
9	chr1:113226102..113228407-chr1:113233460..113235950,2	MCF-7	breast:
10	chr1:113214782..113217536-chr1:113235013..113236894,2	K562	blood:
11	chr1:113215224..113219998-chr1:113238829..113244717,20	MCF-7	breast:
12	chr1:113239573..113244483-chr1:113252369..113259292,10	K562	blood:
13	chr1:113229049..113232047-chr1:113233162..113235859,4	MCF-7	breast:
14	chr1:112937481..112939065-chr1:113242426..113245199,2	MCF-7	breast:
15	chr1:113156746..113166477-chr1:113240630..113253423,46	MCF-7	breast:
16	chr1:113159779..113171222-chr1:113238237..113251191,41	K562	blood:
17	chr1:113242660..113244199-chr17:59477359..59479903,2	MCF-7	breast:
18	chr1:113156399..113165396-chr1:113241191..113253782,55	MCF-7	breast:
19	chr1:113163032..113164854-chr1:113235920..113238010,2	K562	blood:
20	chr1:113193973..113196320-chr1:113243250..113245358,2	K562	blood:
21	chr1:113193696..113198407-chr1:113243250..113250056,8	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RHOC-1	chr1:113237123-113237386	ENSG00000225075.1
2	lnc-FAM19A3-3	chr1:113241279-113241597	NONHSAT005275
3	lnc-RHOC-1	chr1:113239222-113239243	ENSG00000225075.1
4	lnc-FAM19A3-3	chr1:113240930-113240989	NONHSAT005275
5	lnc-RHOC-1	chr1:113236310-113236472	ENSG00000225075.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MOV10	hsa-miR-16-5p	chr1:113243281-113243302

Variant related genes	Relation type
MOV10	TF binding region
ENSG00000225075	TF binding region
MOV10	CpG island
ENSG00000225075	CpG island
ENSG00000235299	chromatin interactions
ENSG00000271810	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000116489	chromatin interactions
ENSG00000155367	chromatin interactions
ENSG00000261595	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000143079	chromatin interactions
ENSG00000155363	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000238975	chromatin interactions
ENSG00000007341	chromatin interactions

Extended variants
information (count: 397 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11102520	chr1:113234886-113234887	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529154012	chr1:113234887-113234888	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552005766	chr1:113234899-113234900	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs143578103	chr1:113234910-113234911	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558876888	chr1:113234920-113234921	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528073250	chr1:113234929-113234930	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs150560681	chr1:113234955-113234956	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs182335433	chr1:113234976-113234977	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs571303197	chr1:113234994-113234995	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530547108	chr1:113234997-113234998	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs550318936	chr1:113235034-113235035	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs114941412	chr1:113235045-113235046	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs186638440	chr1:113235174-113235175	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs4285696	chr1:113235191-113235192	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs536112955	chr1:113235247-113235248	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs139654538	chr1:113235252-113235253	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs6537750	chr1:113235256-113235257	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs6537751	chr1:113235259-113235260	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs149318798	chr1:113235284-113235285	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs535002386	chr1:113235354-113235355	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs370364431	chr1:113235381-113235382	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs377289045	chr1:113235412-113235413	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs192758588	chr1:113235422-113235423	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs4448516	chr1:113235433-113235434	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs578026200	chr1:113235452-113235453	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs373947278	chr1:113235469-113235470	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs199993555	chr1:113235496-113235497	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs141446785	chr1:113235497-113235498	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs201675777	chr1:113235539-113235540	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs114735246	chr1:113235545-113235546	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs573758185	chr1:113235576-113235577	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs377335991	chr1:113235591-113235592	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs113286998	chr1:113235617-113235618	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs538046973	chr1:113235629-113235630	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs147849362	chr1:113235673-113235674	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs183219041	chr1:113235675-113235676	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs144691388	chr1:113235719-113235720	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs572834599	chr1:113235720-113235721	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs544581768	chr1:113235751-113235752	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs116194843	chr1:113235844-113235845	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs530591538	chr1:113235859-113235860	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs550410476	chr1:113235892-113235893	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs113191264	chr1:113235895-113235896	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs563855357	chr1:113235899-113235900	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs529503796	chr1:113235902-113235903	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs139480550	chr1:113235939-113235940	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs556450667	chr1:113235972-113235973	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs75362158	chr1:113235990-113235991	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs370085231	chr1:113236048-113236049	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs571560834	chr1:113236062-113236063	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113218600-113235000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:113218600-113235400	Weak transcription	HSMM	muscle
3	chr1:113218600-113240800	Weak transcription	Right Atrium	heart
4	chr1:113219000-113235400	Weak transcription	A549	lung
5	chr1:113219000-113242200	Weak transcription	NHDF-Ad	bronchial
6	chr1:113219000-113243800	Weak transcription	Fetal Brain Male	brain
7	chr1:113222000-113243000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr1:113224800-113235000	Weak transcription	HSMMtube	muscle
9	chr1:113228400-113239000	Strong transcription	Fetal Intestine Small	intestine
10	chr1:113228600-113242800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:113228600-113242800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr1:113229000-113235200	Weak transcription	Stomach Mucosa	stomach
13	chr1:113229000-113242200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr1:113229200-113237200	Weak transcription	Brain Germinal Matrix	brain
15	chr1:113229200-113248000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr1:113229600-113243200	Strong transcription	Dnd41	blood
17	chr1:113230200-113238000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:113230200-113239400	Strong transcription	Fetal Intestine Large	intestine
19	chr1:113230200-113239800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:113230200-113240200	Weak transcription	Fetal Heart	heart
21	chr1:113230200-113240600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:113230200-113240800	Strong transcription	Adipose Nuclei	Adipose
23	chr1:113230200-113241200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:113230200-113242600	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr1:113230200-113243000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:113230200-113243200	Strong transcription	Primary T cells from cord blood	blood
27	chr1:113230400-113240400	Strong transcription	HepG2	liver
28	chr1:113230400-113240600	Strong transcription	Stomach Smooth Muscle	stomach
29	chr1:113230400-113241200	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:113230600-113240800	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr1:113230600-113241000	Strong transcription	Gastric	stomach
32	chr1:113230600-113241400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:113230600-113242000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:113230600-113242000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:113230600-113242200	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr1:113230600-113242600	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr1:113230800-113239800	Strong transcription	Liver	Liver
38	chr1:113230800-113240000	Strong transcription	Duodenum Mucosa	Duodenum
39	chr1:113230800-113241400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:113231000-113236400	Weak transcription	Brain Angular Gyrus	brain
41	chr1:113231200-113241400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:113231400-113236600	Strong transcription	NHEK	skin
43	chr1:113231400-113241800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr1:113231600-113241200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:113231600-113243000	Weak transcription	Psoas Muscle	Psoas
46	chr1:113231600-113243200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr1:113231800-113237000	Strong transcription	Spleen	Spleen
48	chr1:113231800-113238800	Strong transcription	Placenta Amnion	Placenta Amnion
49	chr1:113231800-113239200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:113231800-113239800	Strong transcription	HMEC	breast

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