Variant report

Variant	nsv825954
Chromosome Location	chr11:65792840-65803470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:427)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:65800502-65800794	HepG2	liver:	n/a	n/a
2	BHLHE40	chr11:65792622-65792860	K562	blood:	n/a	n/a
3	CEBPB	chr11:65798830-65798934	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr11:65800512-65800574	K562	blood:	n/a	n/a
5	CEBPB	chr11:65800481-65800617	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr11:65800394-65800702	MCF-7	breast:	n/a	n/a
7	CTCF	chr11:65800463-65800566	LNCaP	prostate:	n/a	n/a
8	CTCF	chr11:65803252-65803359	MCF-7	breast:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
9	CTCF	chr11:65803251-65803366	MCF-7	breast:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
10	CTCF	chr11:65803220-65803370	A549	lung:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
11	CTCF	chr11:65803200-65803350	Hela-S3	cervix:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
12	CTCF	chr11:65803192-65803444	MCF-7	breast:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
13	CTCF	chr11:65803180-65803330	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr11:65803280-65803430	A549	lung:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
15	CTCF	chr11:65803241-65803392	Hela-S3	cervix:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
16	CTCF	chr11:65793540-65793690	K562	blood:	n/a	n/a
17	CTCF	chr11:65803440-65803590	GM06990	blood:	n/a	n/a
18	CTCF	chr11:65803300-65803450	MCF-7	breast:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
19	CTCF	chr11:65803220-65803370	HCT-116	colon:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
20	CTCF	chr11:65803239-65803367	MCF-7	breast:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
21	CTCF	chr11:65803160-65803310	RPTEC	kidney:	n/a	n/a
22	CTCF	chr11:65803245-65803383	MCF-7	breast:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
23	CTCF	chr11:65803237-65803373	MCF-7	breast:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
24	CTCF	chr11:65803240-65803390	MCF-7	breast:	n/a	chr11:65803315-65803333 chr11:65803317-65803338
25	FOS	chr11:65798740-65799085	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr11:65798740-65799069	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr11:65798731-65799069	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr11:65798742-65799082	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL2	chr11:65798691-65799055	HepG2	liver:	n/a	n/a
30	FOXA1	chr11:65800461-65800812	HepG2	liver:	n/a	n/a
31	FOXA1	chr11:65800503-65800898	HepG2	liver:	n/a	n/a
32	FOXA2	chr11:65800538-65800794	HepG2	liver:	n/a	n/a
33	JUN	chr11:65798822-65798954	HepG2	liver:	n/a	n/a
34	JUND	chr11:65798752-65799066	HepG2	liver:	n/a	chr11:65798890-65798901
35	JUND	chr11:65798767-65799032	Hela-S3	cervix:	n/a	chr11:65798890-65798901
36	JUND	chr11:65798799-65798933	HepG2	liver:	n/a	chr11:65798890-65798901
37	JUND	chr11:65798784-65798986	HepG2	liver:	n/a	chr11:65798890-65798901
38	JUND	chr11:65798827-65799007	K562	blood:	n/a	chr11:65798890-65798901
39	MYC	chr11:65798796-65799033	MCF10A-Er-Src	breast:	n/a	n/a
40	MYC	chr11:65798779-65798979	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr11:65792918-65793014	MCF-7	breast:	n/a	n/a
42	POLR2A	chr11:65792919-65792968	MCF-7	breast:	n/a	n/a
43	POLR2A	chr11:65792903-65792915	MCF-7	breast:	n/a	n/a
44	POLR2A	chr11:65801755-65801852	K562	blood:	n/a	n/a
45	POLR2A	chr11:65792916-65793069	MCF-7	breast:	n/a	n/a
46	POLR2A	chr11:65803252-65803268	K562	blood:	n/a	n/a
47	POLR2A	chr11:65793150-65793178	MCF-7	breast:	n/a	n/a
48	POLR2A	chr11:65802828-65802845	K562	blood:	n/a	n/a
49	POLR2A	chr11:65793076-65793077	MCF-7	breast:	n/a	n/a
50	RAD21	chr11:65803170-65803419	MCF-7	breast:	n/a	chr11:65803316-65803335

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65794191-65794241	H1-hESC	embryonic stem cell:	embryo
2	chr11:65793986-65794036	HRCEpiC	kidney:	n/a
3	chr11:65794191-65794241	NH-A	brain:	n/a
4	chr11:65793525-65793575	CMK	blood:	n/a
5	chr11:65794191-65794241	ovcar-3	ovarian:	n/a
6	chr11:65794062-65794112	A549	lung:	n/a
7	chr11:65794352-65794402	BE2_C	brain:	n/a
8	chr11:65794062-65794112	HRE	kidney:	n/a
9	chr11:65793706-65793756	H1-hESC	embryonic stem cell:	embryo
10	chr11:65794352-65794402	NT2-D1	testis:	n/a
11	chr11:65794191-65794241	HAEpiC	amniotic membrane:	n/a
12	chr11:65794191-65794241	NT2-D1	testis:	n/a
13	chr11:65793706-65793756	MCF-7	breast:	n/a
14	chr11:65793238-65793288	CMK	blood:	n/a
15	chr11:65793238-65793288	HepG2	liver:	n/a
16	chr11:65794062-65794112	Caco-2	colon:	n/a
17	chr11:65793986-65794036	NHBE	bronchial:	n/a
18	chr11:65793525-65793575	PANC-1	pancreas:	n/a
19	chr11:65793525-65793575	ECC-1	luminal epithelium:	n/a
20	chr11:65794062-65794112	GM19239	blood:	n/a
21	chr11:65793706-65793756	HCT-116	colon:	n/a
22	chr11:65793525-65793575	HAEpiC	amniotic membrane:	n/a
23	chr11:65793706-65793756	SK-N-MC	brain:	n/a
24	chr11:65794352-65794402	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:65793525-65793575	PrEC	prostate:	n/a
26	chr11:65793238-65793288	GM19239	blood:	n/a
27	chr11:65794191-65794241	ProgFib	skin:	n/a
28	chr11:65793986-65794036	ECC-1	luminal epithelium:	n/a
29	chr11:65794352-65794402	Hela-S3	cervix:	n/a
30	chr11:65794062-65794112	HAEpiC	amniotic membrane:	n/a
31	chr11:65794191-65794241	HIPEpiC	eye:	n/a
32	chr11:65793238-65793288	SKMC	muscle:	n/a
33	chr11:65793525-65793575	AoSMC	blood vessel:	n/a
34	chr11:65793706-65793756	ProgFib	skin:	n/a
35	chr11:65794352-65794402	Jurkat	blood:	n/a
36	chr11:65793238-65793288	HCT-116	colon:	n/a
37	chr11:65793986-65794036	AG09319	gingival:	n/a
38	chr11:65794062-65794112	AG09319	gingival:	n/a
39	chr11:65793525-65793575	GM12878	blood:	n/a
40	chr11:65794191-65794241	SK-N-MC	brain:	n/a
41	chr11:65793525-65793575	SK-N-MC	brain:	n/a
42	chr11:65793986-65794036	IMR90	lung:	fetal
43	chr11:65794352-65794402	GM12892	blood:	n/a
44	chr11:65793238-65793288	ovcar-3	ovarian:	n/a
45	chr11:65794352-65794402	SKMC	muscle:	n/a
46	chr11:65794191-65794241	NHDF-neo	bronchial:	n/a
47	chr11:65794062-65794112	GM06990	blood:	n/a
48	chr11:65793986-65794036	GM12891	blood:	n/a
49	chr11:65793238-65793288	HNPCEpiC	eye:	n/a
50	chr11:65793706-65793756	CMK	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65802624..65805080-chr11:65807648..65810087,2	K562	blood:
2	chr11:65657179..65659552-chr11:65792099..65795097,2	MCF-7	breast:
3	chr11:65778738..65782540-chr11:65791690..65794306,3	MCF-7	breast:
4	chr11:65774540..65776396-chr11:65801301..65804263,2	MCF-7	breast:
5	chr11:65657243..65659691-chr11:65793625..65795769,2	K562	blood:
6	chr11:65762816..65765321-chr11:65799547..65802531,2	MCF-7	breast:
7	chr11:65791115..65793279-chr11:65800928..65803391,2	MCF-7	breast:
8	chr11:65802871..65803569-chr11:65812357..65812898,2	MCF-7	breast:
9	chr11:65799174..65802005-chr11:65821311..65824271,2	MCF-7	breast:
10	chr11:65790800..65793677-chr11:65804088..65806843,2	MCF-7	breast:
11	chr11:65769812..65778104-chr11:65786537..65794453,15	K562	blood:
12	chr11:65791225..65793923-chr11:65817959..65820856,2	K562	blood:
13	chr11:65801882..65803649-chr11:65821378..65823730,2	K562	blood:
14	chr11:65791115..65793279-chr11:65800928..65803391,2	MCF-7	breast:
15	chr11:65792938..65795924-chr11:65797637..65800432,2	MCF-7	breast:
16	chr11:65792176..65796965-chr11:65812595..65817477,5	MCF-7	breast:
17	chr11:65788506..65790955-chr11:65792237..65795353,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST6-2	chr11:65796622-65796862	expReg_chr11_6351_+

No data

Variant related genes	Relation type
CATSPER1	TF binding region
CATSPER1	CpG island
ENSG00000087365	chromatin interactions
ENSG00000175315	chromatin interactions
ENSG00000238752	chromatin interactions
ENSG00000175229	chromatin interactions
ENSG00000175334	chromatin interactions
ENSG00000175602	chromatin interactions
ENSG00000175294	chromatin interactions

Extended variants
information (count: 478 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114764419	chr11:65792855-65792856	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs142296641	chr11:65792856-65792857	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs201390042	chr11:65792861-65792862	Enhancers Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs375751217	chr11:65792862-65792863	Enhancers Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs200608739	chr11:65792897-65792898	Enhancers Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs193929391	chr11:65792902-65792903	Enhancers Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs199848950	chr11:65792903-65792904	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs148686517	chr11:65792904-65792905	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs113730172	chr11:65792911-65792912	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs368165391	chr11:65792924-65792925	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs138686285	chr11:65792927-65792928	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs141376441	chr11:65792928-65792929	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs370786090	chr11:65792929-65792930	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs570358467	chr11:65792930-65792931	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs143520345	chr11:65792932-65792933	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs148010566	chr11:65792933-65792934	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs370635615	chr11:65792961-65792962	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs374112491	chr11:65792962-65792963	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs141659121	chr11:65792967-65792968	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs150803613	chr11:65792968-65792969	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs150884482	chr11:65793011-65793012	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs534823391	chr11:65793013-65793014	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs201195978	chr11:65793016-65793017	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs576829972	chr11:65793028-65793029	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs371489713	chr11:65793038-65793039	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs368688295	chr11:65793053-65793054	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs138388451	chr11:65793055-65793056	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs139056553	chr11:65793056-65793057	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs372082637	chr11:65793078-65793079	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs375184637	chr11:65793079-65793080	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs199940038	chr11:65793090-65793091	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs79062509	chr11:65793121-65793122	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs200806107	chr11:65793127-65793128	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs192856378	chr11:65793140-65793141	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs149769183	chr11:65793156-65793157	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs74794071	chr11:65793162-65793163	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs113202862	chr11:65793163-65793164	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs202130764	chr11:65793168-65793169	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs372432257	chr11:65793173-65793174	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs370358531	chr11:65793176-65793177	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs201253357	chr11:65793208-65793209	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs369397065	chr11:65793238-65793239	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs372650214	chr11:65793241-65793242	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs142855965	chr11:65793251-65793252	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs199771570	chr11:65793255-65793256	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs375411792	chr11:65793269-65793270	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs369936891	chr11:65793311-65793312	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs150987227	chr11:65793336-65793337	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs142151431	chr11:65793343-65793344	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs543744984	chr11:65793355-65793356	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65783400-65811200	Weak transcription	Aorta	Aorta
2	chr11:65790000-65800800	Weak transcription	HSMMtube	muscle
3	chr11:65790400-65812600	Weak transcription	Right Atrium	heart
4	chr11:65790400-65818600	Weak transcription	HSMM	muscle
5	chr11:65792600-65793000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:65792600-65793200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr11:65793000-65793200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:65793200-65793600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:65793200-65794400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:65793600-65793800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr11:65794400-65804400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:65795200-65795600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:65798600-65799400	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr11:65799000-65799200	Enhancers	Lung	lung
15	chr11:65799200-65799400	Weak transcription	Lung	lung
16	chr11:65800400-65801000	Enhancers	A549	lung
17	chr11:65802200-65802400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr11:65803200-65804000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr11:65803400-65803600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:65803400-65803800	Enhancers	Adipose Nuclei	Adipose
21	chr11:65803400-65804000	Enhancers	Cortex derived primary cultured neurospheres	brain

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