Variant report

Variant	nsv1041027
Chromosome Location	chr11:71299175-71527896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3959)
CpG islands
(count:4761)
Chromatin interactive
region (count:11)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3959 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
2	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
3	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
4	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
6	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
7	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
8	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
9	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
10	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
11	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
12	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
13	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
14	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
15	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
16	ATF1	chr11:71328834-71328851	K562	blood:	n/a	n/a
17	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
18	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
19	ATF3	chr11:71300244-71300497	K562	blood:	n/a	n/a
20	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
21	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
23	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890
25	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
26	BATF	chr11:71300267-71300538	GM12878	blood:	n/a	n/a
27	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
28	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
29	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
30	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
31	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
32	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
33	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
34	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
35	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
36	BATF	chr11:71376144-71376697	GM12878	blood:	n/a	n/a
37	BATF	chr11:71300267-71300512	GM12878	blood:	n/a	n/a
38	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
39	BATF	chr11:71364307-71364538	GM12878	blood:	n/a	n/a
40	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
41	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
42	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
43	BATF	chr11:71325884-71326044	GM12878	blood:	n/a	n/a
44	BATF	chr11:71315927-71316371	GM12878	blood:	n/a	n/a
45	BATF	chr11:71325819-71326075	GM12878	blood:	n/a	n/a
46	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
47	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
48	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
49	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
50	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a

(count:4761 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71324525-71324575	CMK	blood:	n/a
2	chr11:71324346-71324396	HIPEpiC	eye:	n/a
3	chr11:71301182-71301232	HepG2	liver:	n/a
4	chr11:71324525-71324575	CMK	blood:	n/a
5	chr11:71324346-71324396	HIPEpiC	eye:	n/a
6	chr11:71301182-71301232	HepG2	liver:	n/a
7	chr11:71324028-71324078	MCF10A-Er-Src	breast:	n/a
8	chr11:71418204-71418254	GM12878	blood:	n/a
9	chr11:71527895-71527945	HCT-116	colon:	n/a
10	chr11:71462549-71462599	HNPCEpiC	eye:	n/a
11	chr11:71524734-71524784	HIPEpiC	eye:	n/a
12	chr11:71420485-71420535	Hepatocyte	liver:	n/a
13	chr11:71420467-71420517	AG04450	lung:	fetal
14	chr11:71313838-71313888	HCM	heart:	n/a
15	chr11:71456947-71456997	Jurkat	blood:	n/a
16	chr11:71318057-71318107	NB4	blood:	n/a
17	chr11:71319400-71319450	PFSK-1	brain:	n/a
18	chr11:71301182-71301232	HL-60	blood:	n/a
19	chr11:71324525-71324575	HCPEpiC	choroid plexus:	n/a
20	chr11:71322699-71322749	K562	blood:	n/a
21	chr11:71346528-71346578	HCM	heart:	n/a
22	chr11:71527895-71527945	AG04450	lung:	fetal
23	chr11:71313232-71313282	MCF10A-Er-Src	breast:	n/a
24	chr11:71498202-71498252	HRCEpiC	kidney:	n/a
25	chr11:71318057-71318107	HIPEpiC	eye:	n/a
26	chr11:71327897-71327947	ovcar-3	ovarian:	n/a
27	chr11:71320766-71320816	HCT-116	colon:	n/a
28	chr11:71327897-71327947	GM06990	blood:	n/a
29	chr11:71524734-71524784	GM12892	blood:	n/a
30	chr11:71322699-71322749	NH-A	brain:	n/a
31	chr11:71322165-71322215	HL-60	blood:	n/a
32	chr11:71321226-71321276	K562	blood:	n/a
33	chr11:71417657-71417707	NB4	blood:	n/a
34	chr11:71524971-71525021	HCT-116	colon:	n/a
35	chr11:71324188-71324238	HRPEpiC	eye:	n/a
36	chr11:71421380-71421430	MCF10A-Er-Src	breast:	n/a
37	chr11:71524852-71524902	HCT-116	colon:	n/a
38	chr11:71324188-71324238	NHDF-neo	bronchial:	n/a
39	chr11:71524734-71524784	NT2-D1	testis:	n/a
40	chr11:71350888-71350938	SK-N-SH_RA	brain:	n/a
41	chr11:71315863-71315913	Caco-2	colon:	n/a
42	chr11:71497575-71497625	SAEC	small airway:	n/a
43	chr11:71340352-71340402	HL-60	blood:	n/a
44	chr11:71511486-71511536	ovcar-3	ovarian:	n/a
45	chr11:71311984-71312034	ProgFib	skin:	n/a
46	chr11:71327380-71327430	HEK293	kidney:	embryo
47	chr11:71320735-71320785	HAEpiC	amniotic membrane:	n/a
48	chr11:71350888-71350938	NHBE	bronchial:	n/a
49	chr11:71340288-71340338	HEEpiC	esophagus:	n/a
50	chr11:71340182-71340232	LNCaP	prostate:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
2	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
3	chr11:71498143..71498944-chr16:5147397..5148064,2	Hela-S3	cervix:
4	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
5	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
6	chr11:71489714..71493464-chr11:71497648..71499552,3	MCF-7	breast:
7	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
8	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:
9	chr11:3442224..3443750-chr11:71497854..71499382,2	MCF-7	breast:
10	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
11	chr11:71502585..71504558-chr11:71523085..71525009,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
2	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
3	lnc-AP000867.1-3	chr11:71310043-71310371	NONHSAT022693
4	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
5	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
6	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+
7	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
8	lnc-AP000867.1-3	chr11:71314349-71314399	NONHSAT022693
9	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
10	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
11	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
12	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
13	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
14	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
15	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
16	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3
17	lnc-AP000867.1-2	chr11:71383721-71384047	ENSG00000254504.1
18	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713

No data

Variant related genes	Relation type
OR7E87P	TF binding region
OR7E4P	TF binding region
ENSG00000248671	TF binding region
ENSG00000264091	TF binding region
ENSG00000254805	TF binding region
ALG1L9P	TF binding region
ENPP7P8	TF binding region
ENSG00000221458	TF binding region
FAM86C1	TF binding region
ENSG00000255415	TF binding region
ENSG00000223235	TF binding region
ENSG00000254972	TF binding region
ENSG00000187811	TF binding region
KRTAP5-11	TF binding region
UNC93B6	TF binding region
RPS3AP41	TF binding region
OR7E87P	CpG island
OR7E4P	CpG island
ENSG00000248671	CpG island
ENSG00000264091	CpG island
ENSG00000254805	CpG island
ALG1L9P	CpG island
ENPP7P8	CpG island
ENSG00000221458	CpG island
FAM86C1	CpG island
ENSG00000255415	CpG island
ENSG00000223235	CpG island
ENSG00000254972	CpG island
ENSG00000187811	CpG island
KRTAP5-11	CpG island
UNC93B6	CpG island
RPS3AP41	CpG island
ENSG00000248671	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000118894	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000244026	chromatin interactions
ENSG00000160172	chromatin interactions

Extended variants
information (count: 11575 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:11575 , 50 per page) page: 1 2 3 4 5 6 7 ... 232

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10792801	chr11:71299175-71299176	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10792802	chr11:71299186-71299187	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs544991553	chr11:71299205-71299206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184261647	chr11:71299240-71299241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563184510	chr11:71299241-71299242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544595293	chr11:71299243-71299244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188541864	chr11:71299283-71299284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562698632	chr11:71299284-71299285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111737851	chr11:71299288-71299289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561924378	chr11:71299295-71299296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533354170	chr11:71299296-71299297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10792803	chr11:71299332-71299333	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs10792804	chr11:71299358-71299359	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs533129530	chr11:71299379-71299380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551740191	chr11:71299411-71299412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369441117	chr11:71299438-71299439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537517902	chr11:71299449-71299450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7934017	chr11:71299455-71299456	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs567434656	chr11:71299456-71299457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199918769	chr11:71299487-71299488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534820677	chr11:71299502-71299503	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs7944847	chr11:71299525-71299526	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs577865160	chr11:71299526-71299527	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs543165698	chr11:71299531-71299532	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs545017099	chr11:71299554-71299555	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs193164515	chr11:71299557-71299558	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs11234290	chr11:71299567-71299568	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs7943994	chr11:71299568-71299569	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs36040018	chr11:71299577-71299578	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs560668956	chr11:71299614-71299615	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs12574459	chr11:71299629-71299630	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs184982337	chr11:71299635-71299636	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs549190482	chr11:71299636-71299637	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs541617772	chr11:71299638-71299639	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs559745141	chr11:71299640-71299641	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs533659751	chr11:71299652-71299653	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs150570572	chr11:71299683-71299684	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs570036220	chr11:71299685-71299686	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs530944173	chr11:71299743-71299744	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs549457773	chr11:71299761-71299762	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs528935742	chr11:71299766-71299767	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs550560797	chr11:71299784-71299785	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs117123331	chr11:71299826-71299827	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs535170199	chr11:71299839-71299840	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs139514052	chr11:71299867-71299868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571387851	chr11:71299878-71299879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538903967	chr11:71299890-71299891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575004047	chr11:71299901-71299902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139968535	chr11:71299902-71299903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574862240	chr11:71299905-71299906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD

Chromatin state (count:1568 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71293600-71300000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:71297000-71301000	Enhancers	Fetal Intestine Small	intestine
3	chr11:71298800-71299800	Enhancers	HepG2	liver
4	chr11:71299000-71299200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:71299000-71299200	Enhancers	Stomach Mucosa	stomach
6	chr11:71299000-71299600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:71299000-71299800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr11:71299000-71300200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr11:71299000-71300200	Enhancers	Fetal Intestine Large	intestine
10	chr11:71299000-71300200	Enhancers	Gastric	stomach
11	chr11:71299000-71300400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr11:71299000-71300800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:71299000-71301000	Enhancers	Duodenum Mucosa	Duodenum
14	chr11:71299000-71301000	Enhancers	Placenta	Placenta
15	chr11:71299000-71301000	Enhancers	Pancreas	Pancrea
16	chr11:71299200-71299800	Weak transcription	Stomach Mucosa	stomach
17	chr11:71299200-71300000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:71299600-71300200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr11:71299800-71300000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:71299800-71300600	Enhancers	Stomach Mucosa	stomach
21	chr11:71300000-71300200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr11:71300000-71300600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr11:71314200-71314600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:71314400-71314600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr11:71315200-71316000	Enhancers	Fetal Thymus	thymus
26	chr11:71316400-71316600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
27	chr11:71316400-71316600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr11:71317800-71318000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:71317800-71319000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
30	chr11:71317800-71319000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:71317800-71319600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
32	chr11:71318000-71318200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
33	chr11:71318000-71318200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
34	chr11:71318000-71318200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:71318000-71318200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr11:71318000-71318400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:71318000-71318600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
38	chr11:71318000-71318600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
39	chr11:71318000-71318600	Bivalent Enhancer	Placenta	Placenta
40	chr11:71318000-71318600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
41	chr11:71318000-71318800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:71318000-71318800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
43	chr11:71318000-71319000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr11:71318000-71319000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr11:71318000-71319000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr11:71318000-71319000	Bivalent Enhancer	Stomach Mucosa	stomach
47	chr11:71318000-71319000	Bivalent Enhancer	HMEC	breast
48	chr11:71318000-71319600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
49	chr11:71318000-71319600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
50	chr11:71318200-71318400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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