Variant report

Variant	esv3369013
Chromosome Location	chr11:71338874-71612242
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3981)
CpG islands
(count:3298)
Chromatin interactive
region (count:11)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3981 , 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	chr11:71423449-71423649	K562	blood:	n/a	n/a
2	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
3	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
4	ARID3A	chr11:71599388-71599657	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
6	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
7	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
8	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
9	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
10	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
11	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
12	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
13	ATF1	chr11:71575242-71575395	K562	blood:	n/a	n/a
14	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
15	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
16	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
17	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
18	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
19	ATF2	chr11:71540829-71541073	GM12878	blood:	n/a	n/a
20	ATF3	chr11:71575100-71575329	K562	blood:	n/a	n/a
21	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
22	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
23	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
24	ATF3	chr11:71575077-71575386	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr11:71511455-71511719	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	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
28	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
29	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
30	BATF	chr11:71574985-71575313	GM12878	blood:	n/a	n/a
31	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
32	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
33	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
34	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
35	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
36	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
37	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
38	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
39	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
40	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
41	BATF	chr11:71376144-71376697	GM12878	blood:	n/a	n/a
42	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
43	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
44	BATF	chr11:71364307-71364538	GM12878	blood:	n/a	n/a
45	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890
46	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
47	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
48	BATF	chr11:71532357-71532883	GM12878	blood:	n/a	n/a
49	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
50	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a

(count:3298 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71554504-71554554	GM12878	blood:	n/a
2	chr11:71462582-71462632	HIPEpiC	eye:	n/a
3	chr11:71346528-71346578	ovcar-3	ovarian:	n/a
4	chr11:71524852-71524902	Hepatocyte	liver:	n/a
5	chr11:71554504-71554554	GM12878	blood:	n/a
6	chr11:71462582-71462632	HIPEpiC	eye:	n/a
7	chr11:71346528-71346578	ovcar-3	ovarian:	n/a
8	chr11:71524852-71524902	Hepatocyte	liver:	n/a
9	chr11:71353991-71354041	NHDF-neo	bronchial:	n/a
10	chr11:71524971-71525021	ovcar-3	ovarian:	n/a
11	chr11:71346528-71346578	HRPEpiC	eye:	n/a
12	chr11:71524540-71524590	GM12878	blood:	n/a
13	chr11:71545243-71545293	NH-A	brain:	n/a
14	chr11:71340352-71340402	AG04449	skin:	fetal
15	chr11:71522461-71522511	IMR90	lung:	fetal
16	chr11:71349753-71349803	RPTEC	kidney:	n/a
17	chr11:71420485-71420535	BJ	skin:	n/a
18	chr11:71350346-71350396	SAEC	small airway:	n/a
19	chr11:71502816-71502866	HCM	heart:	n/a
20	chr11:71524734-71524784	AG10803	skin:	n/a
21	chr11:71417657-71417707	Hela-S3	cervix:	n/a
22	chr11:71597184-71597234	T-47D	breast:	n/a
23	chr11:71462582-71462632	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:71522461-71522511	RPTEC	kidney:	n/a
25	chr11:71497552-71497602	RPTEC	kidney:	n/a
26	chr11:71417657-71417707	HUVEC	blood vessel:	n/a
27	chr11:71524500-71524550	GM12878	blood:	n/a
28	chr11:71417713-71417763	HCT-116	colon:	n/a
29	chr11:71417657-71417707	HMEC	breast:	n/a
30	chr11:71597104-71597154	NT2-D1	testis:	n/a
31	chr11:71418204-71418254	AG10803	skin:	n/a
32	chr11:71597184-71597234	IMR90	lung:	fetal
33	chr11:71457160-71457210	MCF-7	breast:	n/a
34	chr11:71340352-71340402	RPTEC	kidney:	n/a
35	chr11:71351271-71351321	IMR90	lung:	fetal
36	chr11:71457160-71457210	NH-A	brain:	n/a
37	chr11:71462149-71462199	SK-N-SH_RA	brain:	n/a
38	chr11:71350346-71350396	HMEC	breast:	n/a
39	chr11:71350975-71351025	HRPEpiC	eye:	n/a
40	chr11:71567175-71567225	AG10803	skin:	n/a
41	chr11:71524971-71525021	AG09309	skin:	n/a
42	chr11:71600961-71601011	HUVEC	blood vessel:	n/a
43	chr11:71340288-71340338	AG04449	skin:	fetal
44	chr11:71350888-71350938	HCM	heart:	n/a
45	chr11:71567175-71567225	LNCaP	prostate:	n/a
46	chr11:71597171-71597221	Hepatocyte	liver:	n/a
47	chr11:71421279-71421329	Jurkat	blood:	n/a
48	chr11:71502816-71502866	H1-hESC	embryonic stem cell:	embryo
49	chr11:71418204-71418254	Caco-2	colon:	n/a
50	chr11:71498715-71498765	HCF	heart:	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	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
3	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:
4	chr11:71489714..71493464-chr11:71497648..71499552,3	MCF-7	breast:
5	chr11:71498143..71498944-chr16:5147397..5148064,2	Hela-S3	cervix:
6	chr11:3442224..3443750-chr11:71497854..71499382,2	MCF-7	breast:
7	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
8	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
9	chr11:71502585..71504558-chr11:71523085..71525009,2	MCF-7	breast:
10	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
11	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:

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

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

No data

Variant related genes	Relation type
OR7E128P	TF binding region
ENSG00000225805	TF binding region
ENSG00000248671	TF binding region
ENSG00000266859	TF binding region
ZNF705E	TF binding region
ENSG00000255157	TF binding region
ENSG00000264091	TF binding region
ENSG00000254805	TF binding region
ALG1L9P	TF binding region
ENPP7P8	TF binding region
ENSG00000221458	TF binding region
DEFB108B	TF binding region
FAM86C1	TF binding region
ENSG00000255415	TF binding region
ENSG00000223235	TF binding region
ENSG00000254972	TF binding region
RNA5SP342	TF binding region
OR7E126P	TF binding region
RPS3AP41	TF binding region
OR7E128P	CpG island
ENSG00000225805	CpG island
ENSG00000248671	CpG island
ENSG00000266859	CpG island
ZNF705E	CpG island
ENSG00000255157	CpG island
ENSG00000264091	CpG island
ENSG00000254805	CpG island
ALG1L9P	CpG island
ENPP7P8	CpG island
ENSG00000221458	CpG island
DEFB108B	CpG island
FAM86C1	CpG island
ENSG00000255415	CpG island
ENSG00000223235	CpG island
ENSG00000254972	CpG island
RNA5SP342	CpG island
OR7E126P	CpG island
RPS3AP41	CpG island
ENSG00000130522	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000160172	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000244026	chromatin interactions
ENSG00000118894	chromatin interactions
KIAA1217	miRNA target sites
OR11A1	miRNA target sites

Extended variants
information (count: 14106 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:14106 , 50 per page) page: 1 2 3 4 5 6 7 ... 283

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557126999	chr11:71338899-71338900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575711562	chr11:71338900-71338901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1815778	chr11:71338959-71338960	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs3934708	chr11:71338975-71338976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373764899	chr11:71339012-71339013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182505267	chr11:71339013-71339014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563366707	chr11:71339014-71339015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540525675	chr11:71339051-71339052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565189613	chr11:71339061-71339062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531965958	chr11:71339101-71339102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145044128	chr11:71339113-71339114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201614448	chr11:71339131-71339132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs398016588	chr11:71339146-71339147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562410078	chr11:71339157-71339158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1806494	chr11:71339163-71339164	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547909769	chr11:71339168-71339169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567516670	chr11:71339188-71339189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112308724	chr11:71339194-71339195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528700744	chr11:71339205-71339206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546847853	chr11:71339220-71339221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185454576	chr11:71339233-71339234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556822737	chr11:71339243-71339244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556573759	chr11:71339250-71339251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189509785	chr11:71339251-71339252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180708872	chr11:71339318-71339319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs386754825	chr11:71339344-71339345	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2077324	chr11:71339346-71339347	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572568159	chr11:71339451-71339452	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs185471348	chr11:71339452-71339453	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs370175370	chr11:71339461-71339462	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs558545455	chr11:71339493-71339494	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs577083826	chr11:71339501-71339502	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs115400040	chr11:71339511-71339512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190288033	chr11:71339513-71339514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75486794	chr11:71339526-71339527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561371901	chr11:71339549-71339550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181162814	chr11:71339554-71339555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2004160	chr11:71339561-71339562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559824751	chr11:71339565-71339566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185995143	chr11:71339572-71339573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546810703	chr11:71339627-71339628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3888289	chr11:71339667-71339668	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs375322994	chr11:71339670-71339671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113479926	chr11:71339692-71339693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562599654	chr11:71339721-71339722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4081430	chr11:71339730-71339731	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs111416419	chr11:71339804-71339805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199630840	chr11:71339814-71339815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191489318	chr11:71339819-71339820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9667092	chr11:71339831-71339832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
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

Chromatin state (count:1631 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71335200-71350400	Weak transcription	Right Atrium	heart
2	chr11:71338600-71339000	Enhancers	Duodenum Mucosa	Duodenum
3	chr11:71344200-71350600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:71346800-71347000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:71350000-71350200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
6	chr11:71350000-71350400	Enhancers	H9 Cell Line	embryonic stem cell
7	chr11:71350000-71350400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
8	chr11:71350000-71350400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr11:71350000-71350400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr11:71350000-71350400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
11	chr11:71350000-71350400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:71350000-71350400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
13	chr11:71350000-71350400	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr11:71350000-71350600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:71350000-71350600	Enhancers	Primary B cells from peripheral blood	blood
16	chr11:71350000-71350600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr11:71350000-71350600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
18	chr11:71350000-71350800	Enhancers	Primary B cells from cord blood	blood
19	chr11:71350000-71351400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
20	chr11:71350200-71350400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:71350200-71350400	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr11:71350200-71350400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:71350200-71350400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:71350200-71350400	Enhancers	Fetal Intestine Small	intestine
25	chr11:71350200-71350400	Enhancers	Right Ventricle	heart
26	chr11:71350200-71350600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:71350200-71350800	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr11:71350200-71350800	Active TSS	Fetal Brain Female	brain
29	chr11:71350200-71350800	Enhancers	Spleen	Spleen
30	chr11:71350200-71351200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr11:71350400-71350600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr11:71350400-71350600	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:71350400-71350600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:71350400-71350600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:71350400-71350600	Active TSS	Muscle Satellite Cultured Cells	--
36	chr11:71350400-71350600	Active TSS	Adipose Nuclei	Adipose
37	chr11:71350400-71350600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr11:71350400-71350600	Bivalent/Poised TSS	Colonic Mucosa	Colon
39	chr11:71350400-71350600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
40	chr11:71350400-71350600	Active TSS	Esophagus	oesophagus
41	chr11:71350400-71350600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr11:71350400-71350600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
43	chr11:71350400-71350600	Bivalent/Poised TSS	Placenta	Placenta
44	chr11:71350400-71350600	Active TSS	Pancreas	Pancrea
45	chr11:71350400-71350600	Active TSS	Placenta Amnion	Placenta Amnion
46	chr11:71350400-71350600	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr11:71350400-71350600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
48	chr11:71350400-71350600	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
49	chr11:71350400-71350800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr11:71350400-71350800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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