Variant report

Variant	nsv897905
Chromosome Location	chr11:71371354-71615727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3539)
CpG islands
(count:2564)
Chromatin interactive
region (count:10)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3539 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
2	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
3	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
4	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
6	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
7	ARID3A	chr11:71599388-71599657	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
9	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
10	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
11	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
12	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
13	ATF1	chr11:71575242-71575395	K562	blood:	n/a	n/a
14	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
15	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
16	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
17	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
18	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
19	ATF2	chr11:71540829-71541073	GM12878	blood:	n/a	n/a
20	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
21	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
22	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
24	ATF3	chr11:71575100-71575329	K562	blood:	n/a	n/a
25	ATF3	chr11:71575077-71575386	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
28	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
29	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
30	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
31	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
32	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
33	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
34	BATF	chr11:71532357-71532883	GM12878	blood:	n/a	n/a
35	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
36	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
37	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
38	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
39	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
40	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
41	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
42	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
43	BATF	chr11:71575058-71575377	GM12878	blood:	n/a	n/a
44	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
45	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
46	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
47	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
48	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
49	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
50	BATF	chr11:71574985-71575313	GM12878	blood:	n/a	n/a

(count:2564 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71421380-71421430	K562	blood:	n/a
2	chr11:71457160-71457210	SKMC	muscle:	n/a
3	chr11:71421380-71421430	K562	blood:	n/a
4	chr11:71457160-71457210	SKMC	muscle:	n/a
5	chr11:71601069-71601119	Jurkat	blood:	n/a
6	chr11:71545243-71545293	Hela-S3	cervix:	n/a
7	chr11:71457160-71457210	HRCEpiC	kidney:	n/a
8	chr11:71524500-71524550	HepG2	liver:	n/a
9	chr11:71485830-71485880	HCF	heart:	n/a
10	chr11:71485830-71485880	HIPEpiC	eye:	n/a
11	chr11:71524734-71524784	HCM	heart:	n/a
12	chr11:71524500-71524550	HRE	kidney:	n/a
13	chr11:71502816-71502866	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:71497688-71497738	SKMC	muscle:	n/a
15	chr11:71597171-71597221	H1-hESC	embryonic stem cell:	embryo
16	chr11:71527895-71527945	BE2_C	brain:	n/a
17	chr11:71417713-71417763	GM12878	blood:	n/a
18	chr11:71497575-71497625	A549	lung:	n/a
19	chr11:71420947-71420997	PrEC	prostate:	n/a
20	chr11:71524540-71524590	MCF10A-Er-Src	breast:	n/a
21	chr11:71554504-71554554	A549	lung:	n/a
22	chr11:71421380-71421430	LNCaP	prostate:	n/a
23	chr11:71524734-71524784	HEEpiC	esophagus:	n/a
24	chr11:71597104-71597154	IMR90	lung:	fetal
25	chr11:71524500-71524550	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:71524852-71524902	GM12891	blood:	n/a
27	chr11:71420947-71420997	NHBE	bronchial:	n/a
28	chr11:71418204-71418254	HCF	heart:	n/a
29	chr11:71601069-71601119	AG09319	gingival:	n/a
30	chr11:71421279-71421329	HL-60	blood:	n/a
31	chr11:71524500-71524550	HEEpiC	esophagus:	n/a
32	chr11:71420485-71420535	HCT-116	colon:	n/a
33	chr11:71524971-71525021	SKMC	muscle:	n/a
34	chr11:71462549-71462599	AG09319	gingival:	n/a
35	chr11:71457160-71457210	HCT-116	colon:	n/a
36	chr11:71522461-71522511	Hela-S3	cervix:	n/a
37	chr11:71600961-71601011	GM12878	blood:	n/a
38	chr11:71597184-71597234	NB4	blood:	n/a
39	chr11:71601069-71601119	PANC-1	pancreas:	n/a
40	chr11:71462149-71462199	SK-N-MC	brain:	n/a
41	chr11:71417713-71417763	HCPEpiC	choroid plexus:	n/a
42	chr11:71527895-71527945	ovcar-3	ovarian:	n/a
43	chr11:71554504-71554554	GM12878	blood:	n/a
44	chr11:71418204-71418254	SAEC	small airway:	n/a
45	chr11:71421380-71421430	GM12892	blood:	n/a
46	chr11:71456947-71456997	NHBE	bronchial:	n/a
47	chr11:71498202-71498252	NT2-D1	testis:	n/a
48	chr11:71462149-71462199	MCF10A-Er-Src	breast:	n/a
49	chr11:71527895-71527945	AG10803	skin:	n/a
50	chr11:71420485-71420535	HL-60	blood:	n/a

(count:10 , 50 per page) page: 1

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

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB108B-1	chr11:71580800-71580844	XLOC_009200
2	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
3	lnc-DEFB108B-2	chr11:71548445-71548756	NONHSAT022717
4	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
5	lnc-DEFB108B-1	chr11:71595453-71596531	XLOC_009200
6	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
7	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
8	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
9	lnc-AP000867.1-2	chr11:71383721-71384047	ENSG00000254504.1
10	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
11	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713
12	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
13	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+
14	lnc-NUMA1-1	chr11:71589418-71589551	XLOC_009494
15	lnc-DEFB108B-1	chr11:71589499-71589564	NONHSAT022724
16	lnc-DEFB108B-1	chr11:71595455-71595604	NONHSAT022724
17	lnc-DEFB108B-2	chr11:71545758-71545904	NONHSAT022717
18	lnc-DEFB108B-1	chr11:71578414-71578614	XLOC_009200
19	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
20	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3
21	lnc-NUMA1-1	chr11:71581076-71581470	XLOC_009494
22	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
23	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
24	lnc-RNF121-6	chr11:71612764-71612976	expReg_chr11_7433_+
25	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
26	lnc-RP11-849H4.2.1-1	chr11:71527956-71528142	ENSG00000248671.3
27	lnc-RP11-849H4.2.1-1	chr11:71529199-71529284	ENSG00000248671.3
28	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
29	lnc-DEFB108B-2	chr11:71548070-71548218	NONHSAT022717

No data

Variant related genes	Relation type
DEFB108B	TF binding region
FAM86C1	TF binding region
OR7E128P	TF binding region
ENSG00000225805	TF binding region
ENSG00000248671	TF binding region
ENSG00000266859	TF binding region
ZNF705E	TF binding region
ENSG00000255157	TF binding region
ENSG00000223235	TF binding region
ENSG00000264091	TF binding region
ENSG00000254805	TF binding region
ALG1L9P	TF binding region
ENPP7P8	TF binding region
ENSG00000254972	TF binding region
RNA5SP342	TF binding region
OR7E126P	TF binding region
ENSG00000221458	TF binding region
RPS3AP41	TF binding region
DEFB108B	CpG island
FAM86C1	CpG island
OR7E128P	CpG island
ENSG00000225805	CpG island
ENSG00000248671	CpG island
ENSG00000266859	CpG island
ZNF705E	CpG island
ENSG00000255157	CpG island
ENSG00000223235	CpG island
ENSG00000264091	CpG island
ENSG00000254805	CpG island
ALG1L9P	CpG island
ENPP7P8	CpG island
ENSG00000254972	CpG island
RNA5SP342	CpG island
OR7E126P	CpG island
ENSG00000221458	CpG island
RPS3AP41	CpG island
ENSG00000166492	chromatin interactions
ENSG00000118894	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000244026	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000160172	chromatin interactions
OR11A1	miRNA target sites
KIAA1217	miRNA target sites

Extended variants
information (count: 12366 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:12366 , 50 per page) page: 1 2 3 4 5 6 7 ... 248

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10898408	chr11:71371354-71371355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558854803	chr11:71371355-71371356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567582599	chr11:71371374-71371375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377310795	chr11:71371377-71371378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138475539	chr11:71371404-71371405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181219631	chr11:71371427-71371428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549986846	chr11:71371444-71371445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530371316	chr11:71371446-71371447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369542608	chr11:71371464-71371465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372501086	chr11:71371477-71371478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571501790	chr11:71371485-71371486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72475695	chr11:71371527-71371528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185388181	chr11:71371626-71371627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201704190	chr11:71371633-71371634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527754692	chr11:71371646-71371647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552233287	chr11:71371695-71371696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200212042	chr11:71371729-71371730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541519056	chr11:71371734-71371735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570892835	chr11:71371738-71371739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74609818	chr11:71371739-71371740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78561184	chr11:71371745-71371746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549758244	chr11:71371755-71371756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182441695	chr11:71371781-71371782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17160374	chr11:71371785-71371786	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553768666	chr11:71371818-71371819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565701743	chr11:71371824-71371825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533756210	chr11:71371860-71371861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539467363	chr11:71371878-71371879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187027099	chr11:71371899-71371900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576095665	chr11:71371903-71371904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71052811	chr11:71371934-71371935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189871007	chr11:71371961-71371962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556480209	chr11:71371984-71371985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200014367	chr11:71371989-71371990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574747753	chr11:71372021-71372022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181074839	chr11:71372029-71372030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560443408	chr11:71372030-71372031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144724840	chr11:71372038-71372039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185285117	chr11:71372074-71372075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564603254	chr11:71372078-71372079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531715981	chr11:71372087-71372088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574018767	chr11:71372092-71372093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148541524	chr11:71372106-71372107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190385486	chr11:71372119-71372120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529174236	chr11:71372121-71372122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182903722	chr11:71372131-71372132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188748057	chr11:71372132-71372133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142786661	chr11:71372145-71372146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551135031	chr11:71372164-71372165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191447644	chr11:71372171-71372172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:1490 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71360400-71373000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:71368200-71395600	Weak transcription	Fetal Intestine Small	intestine
3	chr11:71385800-71386000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
4	chr11:71394000-71396800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:71395600-71396200	Enhancers	Fetal Intestine Large	intestine
6	chr11:71395600-71396200	Enhancers	Fetal Intestine Small	intestine
7	chr11:71396200-71396400	Weak transcription	Fetal Intestine Large	intestine
8	chr11:71396200-71398000	Active TSS	Fetal Intestine Small	intestine
9	chr11:71396400-71398000	Active TSS	Fetal Intestine Large	intestine
10	chr11:71396800-71404000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:71400200-71400600	Enhancers	K562	blood
12	chr11:71400600-71403400	Weak transcription	K562	blood
13	chr11:71403400-71403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr11:71403400-71404400	Enhancers	K562	blood
15	chr11:71404000-71404800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:71404200-71404400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr11:71404200-71404600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr11:71404200-71405000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr11:71404400-71404800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:71404800-71409200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:71406400-71411400	Weak transcription	Fetal Intestine Small	intestine
22	chr11:71409200-71409800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:71409800-71411400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:71411400-71412400	Enhancers	Fetal Intestine Small	intestine
25	chr11:71411400-71412600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:71411400-71412600	Enhancers	Fetal Intestine Large	intestine
27	chr11:71412400-71413200	Weak transcription	Fetal Intestine Small	intestine
28	chr11:71413200-71415800	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr11:71414800-71416000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:71415400-71415600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr11:71415400-71416000	Enhancers	K562	blood
32	chr11:71415400-71416400	Enhancers	Fetal Intestine Large	intestine
33	chr11:71415600-71416200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr11:71415800-71416000	Weak transcription	Fetal Intestine Small	intestine
35	chr11:71416000-71416400	Flanking Active TSS	K562	blood
36	chr11:71416000-71416600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:71416000-71417000	Enhancers	Fetal Intestine Small	intestine
38	chr11:71416200-71416400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr11:71416400-71417400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr11:71416400-71417400	Weak transcription	Fetal Intestine Large	intestine
41	chr11:71416400-71417400	Enhancers	K562	blood
42	chr11:71416600-71417400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:71417000-71417400	Weak transcription	Fetal Intestine Small	intestine
44	chr11:71417000-71418400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr11:71417200-71417600	Enhancers	Fetal Lung	lung
46	chr11:71417200-71417800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr11:71417200-71418400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:71417400-71417600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:71417400-71417800	Flanking Active TSS	K562	blood
50	chr11:71417400-71418000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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