Variant report

Variant	esv1851354
Chromosome Location	chr10:94414263-94450386
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:784)
CpG islands
(count:793)
Chromatin interactive
region (count:28)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94448575-94448749	K562	blood:	n/a	n/a
2	ARID3A	chr10:94422716-94422926	K562	blood:	n/a	n/a
3	ARID3A	chr10:94449623-94449834	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:94449642-94449923	K562	blood:	n/a	n/a
5	BACH1	chr10:94449756-94450595	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr10:94450119-94450426	GM12878	blood:	n/a	chr10:94450279-94450290
7	BHLHE40	chr10:94448577-94448982	K562	blood:	n/a	n/a
8	BHLHE40	chr10:94449290-94449318	K562	blood:	n/a	n/a
9	BHLHE40	chr10:94450084-94450434	GM12878	blood:	n/a	chr10:94450146-94450162
10	BHLHE40	chr10:94448540-94450445	HepG2	liver:	n/a	chr10:94449270-94449286 chr10:94450146-94450162 chr10:94449642-94449658
11	BHLHE40	chr10:94449745-94450830	K562	blood:	n/a	chr10:94450146-94450162
12	BRCA1	chr10:94450090-94450104	HepG2	liver:	n/a	n/a
13	CBX3	chr10:94422559-94423000	K562	blood:	n/a	n/a
14	CBX3	chr10:94448327-94449135	K562	blood:	n/a	n/a
15	CBX3	chr10:94445139-94445451	K562	blood:	n/a	n/a
16	CBX3	chr10:94422636-94423056	HCT-116	colon:	n/a	n/a
17	CBX3	chr10:94422489-94423015	K562	blood:	n/a	n/a
18	CCNT2	chr10:94448631-94451909	K562	blood:	n/a	chr10:94449521-94449530 chr10:94451255-94451264
19	CEBPB	chr10:94440455-94440734	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr10:94445970-94446248	K562	blood:	n/a	chr10:94446100-94446111
21	CEBPB	chr10:94448399-94448626	HepG2	liver:	n/a	n/a
22	CEBPB	chr10:94440478-94440712	MCF-7	breast:	n/a	n/a
23	CEBPB	chr10:94416810-94417148	Hela-S3	cervix:	n/a	chr10:94416963-94416974
24	CEBPB	chr10:94428684-94428915	IMR90	lung:	n/a	chr10:94428810-94428821
25	CEBPB	chr10:94416811-94417069	HepG2	liver:	n/a	chr10:94416963-94416974
26	CEBPB	chr10:94440480-94440865	MCF-7	breast:	n/a	n/a
27	CEBPB	chr10:94445969-94446189	HepG2	liver:	n/a	chr10:94446100-94446111
28	CEBPB	chr10:94440427-94440721	K562	blood:	n/a	n/a
29	CEBPB	chr10:94428769-94428854	K562	blood:	n/a	chr10:94428810-94428821
30	CEBPB	chr10:94416795-94417153	HepG2	liver:	n/a	chr10:94416963-94416974
31	CEBPB	chr10:94440405-94440764	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr10:94416861-94417074	MCF-7	breast:	n/a	chr10:94416963-94416974
33	CEBPB	chr10:94428690-94428986	A549	lung:	n/a	chr10:94428810-94428821
34	CEBPB	chr10:94440400-94440763	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:94450133-94450542	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr10:94416739-94417100	HepG2	liver:	n/a	chr10:94416963-94416974
37	CEBPB	chr10:94440451-94440703	A549	lung:	n/a	n/a
38	CEBPB	chr10:94416859-94417057	K562	blood:	n/a	chr10:94416963-94416974
39	CEBPB	chr10:94416790-94417202	A549	lung:	n/a	chr10:94416963-94416974
40	CEBPB	chr10:94424449-94424613	HepG2	liver:	n/a	chr10:94424496-94424507
41	CEBPB	chr10:94450237-94450353	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:94440410-94440763	A549	lung:	n/a	n/a
43	CEBPB	chr10:94428676-94428982	HepG2	liver:	n/a	chr10:94428810-94428821
44	CEBPB	chr10:94416811-94417139	H1-hESC	embryonic stem cell:	n/a	chr10:94416963-94416974
45	CEBPB	chr10:94428693-94428805	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr10:94422603-94422900	K562	blood:	n/a	n/a
47	CEBPB	chr10:94416819-94417133	A549	lung:	n/a	chr10:94416963-94416974
48	CEBPB	chr10:94440396-94440767	IMR90	lung:	n/a	n/a
49	CEBPB	chr10:94416779-94417152	HepG2	liver:	n/a	chr10:94416963-94416974
50	CEBPB	chr10:94440427-94440833	A549	lung:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94429569-94429619	HAEpiC	amniotic membrane:	n/a
2	chr10:94429530-94429580	H1-hESC	embryonic stem cell:	embryo
3	chr10:94450056-94450106	SK-N-MC	brain:	n/a
4	chr10:94445035-94445085	SK-N-MC	brain:	n/a
5	chr10:94449567-94449617	MCF10A-Er-Src	breast:	n/a
6	chr10:94429569-94429619	GM12878	blood:	n/a
7	chr10:94429506-94429556	HCF	heart:	n/a
8	chr10:94449797-94449847	SK-N-MC	brain:	n/a
9	chr10:94429542-94429592	HAEpiC	amniotic membrane:	n/a
10	chr10:94429542-94429592	SK-N-MC	brain:	n/a
11	chr10:94429506-94429556	HCT-116	colon:	n/a
12	chr10:94448532-94448582	HRCEpiC	kidney:	n/a
13	chr10:94449797-94449847	AoSMC	blood vessel:	n/a
14	chr10:94448532-94448582	GM12891	blood:	n/a
15	chr10:94429530-94429580	GM06990	blood:	n/a
16	chr10:94449250-94449300	GM06990	blood:	n/a
17	chr10:94429506-94429556	ovcar-3	ovarian:	n/a
18	chr10:94445035-94445085	LNCaP	prostate:	n/a
19	chr10:94429526-94429576	NHDF-neo	bronchial:	n/a
20	chr10:94445035-94445085	AG09319	gingival:	n/a
21	chr10:94449797-94449847	AG04450	lung:	fetal
22	chr10:94429542-94429592	IMR90	lung:	fetal
23	chr10:94448728-94448778	PFSK-1	brain:	n/a
24	chr10:94429506-94429556	LNCaP	prostate:	n/a
25	chr10:94429530-94429580	IMR90	lung:	fetal
26	chr10:94448702-94448752	BJ	skin:	n/a
27	chr10:94449250-94449300	GM12891	blood:	n/a
28	chr10:94449567-94449617	GM19239	blood:	n/a
29	chr10:94449250-94449300	A549	lung:	n/a
30	chr10:94429542-94429592	HNPCEpiC	eye:	n/a
31	chr10:94449250-94449300	BE2_C	brain:	n/a
32	chr10:94429542-94429592	MCF10A-Er-Src	breast:	n/a
33	chr10:94445035-94445085	AG04449	skin:	fetal
34	chr10:94448532-94448582	GM06990	blood:	n/a
35	chr10:94449250-94449300	ovcar-3	ovarian:	n/a
36	chr10:94429569-94429619	U87	brain:	n/a
37	chr10:94429542-94429592	NH-A	brain:	n/a
38	chr10:94450056-94450106	SK-N-SH_RA	brain:	n/a
39	chr10:94450056-94450106	HPAEpiC	pulmonary alveolar:	n/a
40	chr10:94449567-94449617	CMK	blood:	n/a
41	chr10:94450056-94450106	AoSMC	blood vessel:	n/a
42	chr10:94448532-94448582	BJ	skin:	n/a
43	chr10:94449567-94449617	K562	blood:	n/a
44	chr10:94449797-94449847	NH-A	brain:	n/a
45	chr10:94449797-94449847	GM12892	blood:	n/a
46	chr10:94429569-94429619	AoSMC	blood vessel:	n/a
47	chr10:94449567-94449617	ProgFib	skin:	n/a
48	chr10:94429569-94429619	NB4	blood:	n/a
49	chr10:94429530-94429580	NB4	blood:	n/a
50	chr10:94445035-94445085	Hepatocyte	liver:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94449314..94450224-chr16:30388710..30389229,2	NB4	blood:
2	chr10:94449635..94450319-chr15:59396946..59397778,2	NB4	blood:
3	chr10:94449913..94450519-chr18:12990641..12991585,2	Hela-S3	cervix:
4	chr10:94441256..94444670-chr10:94449156..94451252,3	MCF-7	breast:
5	chr10:94415353..94417803-chr10:94419120..94421104,2	K562	blood:
6	chr10:94448193..94452899-chr10:94604769..94609293,6	K562	blood:
7	chr10:94334145..94336156-chr10:94441112..94444728,3	K562	blood:
8	chr10:94434850..94438940-chr10:94446699..94450647,3	K562	blood:
9	chr10:94439735..94442066-chr10:94601811..94604673,2	K562	blood:
10	chr10:94332371..94335153-chr10:94446165..94448467,2	K562	blood:
11	chr10:94449475..94450112-chr19:14529907..14530785,2	Hela-S3	cervix:
12	chr10:94449678..94450357-chr11:62359130..62359860,2	Hela-S3	cervix:
13	chr10:94449237..94450232-chr6:27805942..27806496,2	NB4	blood:
14	chr10:94430325..94433160-chr10:94453394..94455547,2	K562	blood:
15	chr10:94333616..94336720-chr10:94448718..94451044,3	K562	blood:
16	chr10:94437792..94440441-chr10:94441307..94443434,2	K562	blood:
17	chr10:94450024..94450724-chr19:12901932..12902636,2	Hela-S3	cervix:
18	chr10:94353767..94355428-chr10:94415113..94417602,2	MCF-7	breast:
19	chr10:94449758..94450309-chr20:30192485..30193219,2	Hela-S3	cervix:
20	chr10:94349533..94354628-chr10:94448059..94453493,12	K562	blood:
21	chr10:94440739..94442413-chr10:94446603..94449404,2	K562	blood:
22	chr10:94407828..94410112-chr10:94420940..94422860,2	K562	blood:
23	chr10:94349533..94356622-chr10:94447410..94453498,11	K562	blood:
24	chr10:94434338..94436350-chr10:94446810..94449570,2	K562	blood:
25	chr10:94449603..94452740-chr10:94589464..94592452,3	K562	blood:
26	chr10:94439547..94442442-chr10:94446922..94448732,2	MCF-7	breast:
27	chr10:94437792..94440441-chr10:94441307..94443434,2	K562	blood:
28	chr10:94415353..94417803-chr10:94419120..94421104,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HHEX-1	chr10:94440775-94440994	expReg_chr10_6169_+
2	lnc-HHEX-2	chr10:94440441-94440641	expReg_chr10_6166_+
3	lnc-KIF11-2	chr10:94418801-94419055	NONHSAT015671

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KIF11	hsa-miR-186-5p	chr10:94414695-94414716
2	KIF11	hsa-miR-30a-5p	chr10:94414702-94414723

Variant related genes	Relation type
RN7SL644P	TF binding region
EIF2S2P3	TF binding region
HHEX	TF binding region
RN7SL644P	CpG island
EIF2S2P3	CpG island
HHEX	CpG island
ENSG00000266969	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000171223	chromatin interactions
ENSG00000152804	chromatin interactions
ENSG00000119912	chromatin interactions
ENSG00000138160	chromatin interactions
ENSG00000149016	chromatin interactions
ENSG00000138190	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000101639	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000157456	chromatin interactions
ENSG00000123136	chromatin interactions

Extended variants
information (count: 1101 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7078243	chr10:94414263-94414264	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535457060	chr10:94414268-94414269	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs80332631	chr10:94414286-94414287	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs527713532	chr10:94414290-94414291	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs577963479	chr10:94414313-94414314	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546490974	chr10:94414370-94414371	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs11187119	chr10:94414390-94414391	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs191655591	chr10:94414404-94414405	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs36107638	chr10:94414410-94414411	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs559578777	chr10:94414429-94414430	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs181135385	chr10:94414565-94414566	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs4933734	chr10:94414567-94414568	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs17875347	chr10:94414638-94414639	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs540084475	chr10:94414645-94414646	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs376518815	chr10:94414655-94414656	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs74151679	chr10:94414674-94414675	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs550639908	chr10:94414679-94414680	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs563970874	chr10:94414712-94414713	Weak transcription Strong transcription Genic enhancers	TF binding region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
19	rs189660821	chr10:94414717-94414718	Weak transcription Strong transcription Genic enhancers	TF binding region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
20	rs532919775	chr10:94414732-94414733	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs149623261	chr10:94414764-94414765	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs566790700	chr10:94414776-94414777	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs564779267	chr10:94414781-94414782	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs183803262	chr10:94414786-94414787	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs549120162	chr10:94414796-94414797	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs187509052	chr10:94414844-94414845	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs144378344	chr10:94414914-94414915	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs537991933	chr10:94414931-94414932	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200057635	chr10:94414937-94414938	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs571583424	chr10:94414994-94414995	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs187812016	chr10:94415004-94415005	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs558983534	chr10:94415032-94415033	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs558386414	chr10:94415056-94415057	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs1044153	chr10:94415078-94415079	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs553011391	chr10:94415095-94415096	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs573124430	chr10:94415114-94415115	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs542054234	chr10:94415116-94415117	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs555640772	chr10:94415133-94415134	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs543827625	chr10:94415155-94415156	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs575505912	chr10:94415222-94415223	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs544003735	chr10:94415248-94415249	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs564192889	chr10:94415276-94415277	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs375231512	chr10:94415384-94415385	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs192699495	chr10:94415391-94415392	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs560670956	chr10:94415407-94415408	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs532805897	chr10:94415443-94415444	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529693717	chr10:94415465-94415466	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560418584	chr10:94415539-94415540	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs376375593	chr10:94415561-94415562	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs529505242	chr10:94415621-94415622	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94354000-94420000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:94354200-94416000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr10:94364000-94416400	Strong transcription	Dnd41	blood
4	chr10:94364200-94417400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr10:94364400-94415200	Weak transcription	Fetal Heart	heart
6	chr10:94365600-94415600	Strong transcription	Fetal Thymus	thymus
7	chr10:94371000-94414600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr10:94371000-94417000	Weak transcription	Primary B cells from cord blood	blood
9	chr10:94374800-94416000	Weak transcription	Placenta	Placenta
10	chr10:94374800-94418600	Weak transcription	Brain Germinal Matrix	brain
11	chr10:94383000-94414600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr10:94384000-94416400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr10:94389000-94416400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr10:94391400-94415000	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr10:94391400-94415400	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr10:94391400-94415400	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr10:94391400-94415400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
18	chr10:94391400-94415400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:94391400-94415800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr10:94392000-94415400	Weak transcription	Small Intestine	intestine
21	chr10:94395000-94414800	Weak transcription	Fetal Brain Male	brain
22	chr10:94396400-94418200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:94398400-94421200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr10:94400200-94416800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr10:94403600-94415600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr10:94403600-94416200	Strong transcription	GM12878-XiMat	blood
27	chr10:94404400-94415200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr10:94404400-94416800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr10:94404600-94415000	Strong transcription	H1 Cell Line	embryonic stem cell
30	chr10:94404600-94416000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr10:94404800-94414400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:94404800-94415600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr10:94404800-94415800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr10:94405200-94415800	Strong transcription	NHDF-Ad	bronchial
35	chr10:94406000-94415800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr10:94406200-94415800	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr10:94407400-94415600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr10:94409800-94417000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr10:94410800-94414600	Weak transcription	Fetal Kidney	kidney
40	chr10:94410800-94414600	Weak transcription	Osteobl	bone
41	chr10:94410800-94416200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr10:94410800-94416200	Weak transcription	NHEK	skin
43	chr10:94411000-94415200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr10:94411000-94416600	Strong transcription	Thymus	Thymus
45	chr10:94411000-94417400	Weak transcription	Fetal Lung	lung
46	chr10:94411200-94416200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr10:94412000-94415400	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr10:94412200-94415800	Weak transcription	Fetal Intestine Small	intestine
49	chr10:94412200-94416000	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr10:94412400-94415400	Strong transcription	Cortex derived primary cultured neurospheres	brain

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