Variant report

Variant	nsv972041
Chromosome Location	chr11:71330518-71615123
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3987)
CpG islands
(count:3296)
Chromatin interactive
region (count:11)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3987 , 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	chr11:71423994-71424313	K562	blood:	n/a	n/a
2	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
3	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
4	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
5	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
6	ARID3A	chr11:71599388-71599657	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
8	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
10	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
11	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
12	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
13	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
14	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
15	ATF1	chr11:71575242-71575395	K562	blood:	n/a	n/a
16	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
17	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
18	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
19	ATF2	chr11:71540829-71541073	GM12878	blood:	n/a	n/a
20	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
21	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
22	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr11:71575077-71575386	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr11:71575100-71575329	K562	blood:	n/a	n/a
25	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
26	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr11:71376144-71376697	GM12878	blood:	n/a	n/a
28	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
29	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
30	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
31	BATF	chr11:71364018-71364247	GM12878	blood:	n/a	chr11:71364110-71364121
32	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
33	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
34	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
35	BATF	chr11:71574985-71575313	GM12878	blood:	n/a	n/a
36	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
37	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
38	BATF	chr11:71364307-71364538	GM12878	blood:	n/a	n/a
39	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
40	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
41	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
42	BATF	chr11:71575058-71575377	GM12878	blood:	n/a	n/a
43	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
44	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
45	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
46	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
47	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
48	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
49	BATF	chr11:71532357-71532883	GM12878	blood:	n/a	n/a
50	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890

(count:3296 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71597171-71597221	HAEpiC	amniotic membrane:	n/a
2	chr11:71350975-71351025	HNPCEpiC	eye:	n/a
3	chr11:71597171-71597221	HAEpiC	amniotic membrane:	n/a
4	chr11:71350975-71351025	HNPCEpiC	eye:	n/a
5	chr11:71524971-71525021	PFSK-1	brain:	n/a
6	chr11:71462149-71462199	HCM	heart:	n/a
7	chr11:71524971-71525021	AG04450	lung:	fetal
8	chr11:71462582-71462632	T-47D	breast:	n/a
9	chr11:71497552-71497602	K562	blood:	n/a
10	chr11:71340352-71340402	SK-N-MC	brain:	n/a
11	chr11:71524734-71524784	HNPCEpiC	eye:	n/a
12	chr11:71597171-71597221	ProgFib	skin:	n/a
13	chr11:71524734-71524784	HL-60	blood:	n/a
14	chr11:71524500-71524550	HIPEpiC	eye:	n/a
15	chr11:71340288-71340338	SK-N-SH_RA	brain:	n/a
16	chr11:71524540-71524590	HUVEC	blood vessel:	n/a
17	chr11:71524540-71524590	HCPEpiC	choroid plexus:	n/a
18	chr11:71543583-71543633	HCPEpiC	choroid plexus:	n/a
19	chr11:71417657-71417707	AoSMC	blood vessel:	n/a
20	chr11:71600961-71601011	GM12878	blood:	n/a
21	chr11:71497552-71497602	HepG2	liver:	n/a
22	chr11:71350888-71350938	NHBE	bronchial:	n/a
23	chr11:71485830-71485880	GM12892	blood:	n/a
24	chr11:71524500-71524550	HRCEpiC	kidney:	n/a
25	chr11:71457160-71457210	H1-hESC	embryonic stem cell:	embryo
26	chr11:71420485-71420535	A549	lung:	n/a
27	chr11:71497688-71497738	MCF-7	breast:	n/a
28	chr11:71597184-71597234	AG04449	skin:	fetal
29	chr11:71522461-71522511	GM12892	blood:	n/a
30	chr11:71346528-71346578	ovcar-3	ovarian:	n/a
31	chr11:71502816-71502866	SKMC	muscle:	n/a
32	chr11:71456947-71456997	Jurkat	blood:	n/a
33	chr11:71498202-71498252	Hepatocyte	liver:	n/a
34	chr11:71545243-71545293	IMR90	lung:	fetal
35	chr11:71567175-71567225	ovcar-3	ovarian:	n/a
36	chr11:71524734-71524784	RPTEC	kidney:	n/a
37	chr11:71350975-71351025	BE2_C	brain:	n/a
38	chr11:71498715-71498765	BE2_C	brain:	n/a
39	chr11:71346528-71346578	BE2_C	brain:	n/a
40	chr11:71351271-71351321	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:71498609-71498659	BE2_C	brain:	n/a
42	chr11:71597104-71597154	CMK	blood:	n/a
43	chr11:71350888-71350938	HL-60	blood:	n/a
44	chr11:71417713-71417763	NHBE	bronchial:	n/a
45	chr11:71524500-71524550	HepG2	liver:	n/a
46	chr11:71456947-71456997	Hela-S3	cervix:	n/a
47	chr11:71340352-71340402	AG09319	gingival:	n/a
48	chr11:71567175-71567225	HEK293	kidney:	embryo
49	chr11:71346528-71346578	Jurkat	blood:	n/a
50	chr11:71497552-71497602	MCF-7	breast:	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	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
3	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
4	chr11:71489714..71493464-chr11:71497648..71499552,3	MCF-7	breast:
5	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:
6	chr11:71502585..71504558-chr11:71523085..71525009,2	MCF-7	breast:
7	chr11:71498143..71498944-chr16:5147397..5148064,2	Hela-S3	cervix:
8	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
9	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
10	chr11:3442224..3443750-chr11:71497854..71499382,2	MCF-7	breast:
11	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:

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

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

No data

Variant related genes	Relation type
DEFB108B	TF binding region
FAM86C1	TF binding region
OR7E128P	TF binding region
OR7E4P	TF binding region
ENSG00000255415	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
OR7E4P	CpG island
ENSG00000255415	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
ENSG00000158483	chromatin interactions
ENSG00000118894	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000160172	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000244026	chromatin interactions
OR11A1	miRNA target sites
KIAA1217	miRNA target sites

Extended variants
information (count: 14492 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:14492 , 50 per page) page: 1 2 3 4 5 6 7 ... 290

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79239918	chr11:71335241-71335242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575638204	chr11:71335248-71335249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542755009	chr11:71335268-71335269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373346983	chr11:71335283-71335284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572914740	chr11:71335284-71335285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79788829	chr11:71335292-71335293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6592248	chr11:71335294-71335295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs565128575	chr11:71335295-71335296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111938595	chr11:71335320-71335321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532457160	chr11:71335369-71335370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550933597	chr11:71335402-71335403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138931017	chr11:71335465-71335466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529720967	chr11:71335479-71335480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547962448	chr11:71335485-71335486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568476199	chr11:71335529-71335530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534862188	chr11:71335538-71335539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149018731	chr11:71335542-71335543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28859366	chr11:71335563-71335564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs538939910	chr11:71335592-71335593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557685126	chr11:71335649-71335650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569138631	chr11:71335657-71335658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547888862	chr11:71335676-71335677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187129032	chr11:71335678-71335679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10898390	chr11:71335695-71335696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573376061	chr11:71335703-71335704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147264484	chr11:71335732-71335733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189006676	chr11:71335786-71335787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs28849968	chr11:71335820-71335821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540912423	chr11:71335850-71335851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562296025	chr11:71335871-71335872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530560770	chr11:71335885-71335886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370437221	chr11:71335889-71335890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544495677	chr11:71335895-71335896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181990155	chr11:71335904-71335905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs60667648	chr11:71335913-71335914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs141403193	chr11:71335914-71335915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559946276	chr11:71335935-71335936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186327673	chr11:71336022-71336023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150837119	chr11:71336031-71336032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530446548	chr11:71336042-71336043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552117143	chr11:71336043-71336044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571506133	chr11:71336056-71336057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189885062	chr11:71336075-71336076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550955186	chr11:71336076-71336077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569553827	chr11:71336094-71336095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182104551	chr11:71336098-71336099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554956285	chr11:71336104-71336105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28516412	chr11:71336123-71336124	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534283737	chr11:71336129-71336130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559122200	chr11:71336132-71336133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Non-syndromic sensorineural hearing loss	17122850	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:1684 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71335200-71350400	Weak transcription	Right Atrium	heart
2	chr11:71336800-71337000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:71338600-71339000	Enhancers	Duodenum Mucosa	Duodenum
4	chr11:71344200-71350600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr11:71346800-71347000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:71350000-71350200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
7	chr11:71350000-71350400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr11:71350000-71350400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
9	chr11:71350000-71350400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
10	chr11:71350000-71350400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr11:71350000-71350400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
12	chr11:71350000-71350400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr11:71350000-71350400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
14	chr11:71350000-71350400	Bivalent Enhancer	Fetal Muscle Leg	muscle
15	chr11:71350000-71350600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:71350000-71350600	Enhancers	Primary B cells from peripheral blood	blood
17	chr11:71350000-71350600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr11:71350000-71350600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
19	chr11:71350000-71350800	Enhancers	Primary B cells from cord blood	blood
20	chr11:71350000-71351400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
21	chr11:71350200-71350400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr11:71350200-71350400	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr11:71350200-71350400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:71350200-71350400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr11:71350200-71350400	Enhancers	Fetal Intestine Small	intestine
26	chr11:71350200-71350400	Enhancers	Right Ventricle	heart
27	chr11:71350200-71350600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:71350200-71350800	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr11:71350200-71350800	Active TSS	Fetal Brain Female	brain
30	chr11:71350200-71350800	Enhancers	Spleen	Spleen
31	chr11:71350200-71351200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr11:71350400-71350600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr11:71350400-71350600	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr11:71350400-71350600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
35	chr11:71350400-71350600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:71350400-71350600	Active TSS	Muscle Satellite Cultured Cells	--
37	chr11:71350400-71350600	Active TSS	Adipose Nuclei	Adipose
38	chr11:71350400-71350600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr11:71350400-71350600	Bivalent/Poised TSS	Colonic Mucosa	Colon
40	chr11:71350400-71350600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
41	chr11:71350400-71350600	Active TSS	Esophagus	oesophagus
42	chr11:71350400-71350600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr11:71350400-71350600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
44	chr11:71350400-71350600	Bivalent/Poised TSS	Placenta	Placenta
45	chr11:71350400-71350600	Active TSS	Pancreas	Pancrea
46	chr11:71350400-71350600	Active TSS	Placenta Amnion	Placenta Amnion
47	chr11:71350400-71350600	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr11:71350400-71350600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
49	chr11:71350400-71350600	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
50	chr11:71350400-71350800	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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