Variant report

Variant	esv3347668
Chromosome Location	chr11:65770742-65771367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:35)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:35 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:65771273-65771460	Kidney_OC	kidney:	n/a	n/a
2	CTCF	chr11:65771180-65771529	Lung_OC	lung:	n/a	n/a
3	HCFC1	chr11:65768883-65771260	Hela-S3	cervix:	n/a	n/a
4	JUN	chr11:65768928-65770810	K562	blood:	n/a	chr11:65770266-65770275
5	MXI1	chr11:65768500-65771007	SK-N-SH	brain:	n/a	chr11:65769021-65769036
6	POLR2A	chr11:65770786-65772259	GM12892	blood:	n/a	n/a
7	POLR2A	chr11:65771138-65771150	MCF-7	breast:	n/a	n/a
8	POLR2A	chr11:65769003-65770744	HCT-116	colon:	n/a	n/a
9	POLR2A	chr11:65771280-65771640	GM12878	blood:	n/a	n/a
10	POLR2A	chr11:65771266-65771319	MCF-7	breast:	n/a	n/a
11	POLR2A	chr11:65769240-65770760	PANC-1	pancreas:	n/a	n/a
12	POLR2A	chr11:65771268-65771386	GM12878	blood:	n/a	n/a
13	POLR2A	chr11:65771154-65771174	MCF-7	breast:	n/a	n/a
14	POLR2A	chr11:65770998-65771999	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr11:65770814-65771136	ECC-1	luminal epithelium:	n/a	n/a
16	POLR2A	chr11:65771181-65771238	MCF-7	breast:	n/a	n/a
17	POLR2A	chr11:65771077-65771204	HUVEC	blood vessel:	n/a	n/a
18	POLR2A	chr11:65769184-65770807	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr11:65771193-65771257	MCF-7	breast:	n/a	n/a
20	POLR2A	chr11:65770832-65771510	K562	blood:	n/a	n/a
21	POLR2A	chr11:65769061-65771530	HepG2	liver:	n/a	n/a
22	POLR2A	chr11:65768720-65770765	K562	blood:	n/a	n/a
23	POLR2A	chr11:65771087-65771291	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr11:65771219-65771255	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:65770172-65770856	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:65768961-65771436	PANC-1	pancreas:	n/a	n/a
27	POLR2A	chr11:65770702-65770918	GM12891	blood:	n/a	n/a
28	POLR2A	chr11:65771154-65771264	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr11:65768990-65772628	GM12878	blood:	n/a	n/a
30	POLR2A	chr11:65771245-65771262	MCF-7	breast:	n/a	n/a
31	POLR2A	chr11:65770792-65771177	K562	blood:	n/a	n/a
32	POLR2A	chr11:65771022-65772233	GM12892	blood:	n/a	n/a
33	SIN3AK20	chr11:65768973-65770875	MCF-7	breast:	n/a	n/a
34	SREBP1	chr11:65768865-65770759	GM12878	blood:	n/a	chr11:65769022-65769036
35	ZBTB33	chr11:65771095-65771589	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65770987-65771037	ECC-1	luminal epithelium:	n/a
2	chr11:65770987-65771037	A549	lung:	n/a
3	chr11:65770987-65771037	NHDF-neo	bronchial:	n/a
4	chr11:65770987-65771037	ProgFib	skin:	n/a
5	chr11:65770987-65771037	HRE	kidney:	n/a
6	chr11:65770987-65771037	NT2-D1	testis:	n/a
7	chr11:65770987-65771037	NHBE	bronchial:	n/a
8	chr11:65770987-65771037	GM12892	blood:	n/a
9	chr11:65770987-65771037	Jurkat	blood:	n/a
10	chr11:65770987-65771037	HL-60	blood:	n/a
11	chr11:65770987-65771037	LNCaP	prostate:	n/a
12	chr11:65770987-65771037	HIPEpiC	eye:	n/a
13	chr11:65770987-65771037	Hepatocyte	liver:	n/a
14	chr11:65770987-65771037	HEK293	kidney:	embryo
15	chr11:65770987-65771037	ovcar-3	ovarian:	n/a
16	chr11:65770987-65771037	HEEpiC	esophagus:	n/a
17	chr11:65770987-65771037	HRCEpiC	kidney:	n/a
18	chr11:65770987-65771037	HUVEC	blood vessel:	n/a
19	chr11:65770987-65771037	Hela-S3	cervix:	n/a
20	chr11:65770987-65771037	HAEpiC	amniotic membrane:	n/a
21	chr11:65770987-65771037	Caco-2	colon:	n/a
22	chr11:65770987-65771037	AoSMC	blood vessel:	n/a
23	chr11:65770987-65771037	AG04450	lung:	fetal
24	chr11:65770987-65771037	GM06990	blood:	n/a
25	chr11:65770987-65771037	HCF	heart:	n/a
26	chr11:65770987-65771037	MCF10A-Er-Src	breast:	n/a
27	chr11:65770987-65771037	PrEC	prostate:	n/a
28	chr11:65770987-65771037	PANC-1	pancreas:	n/a
29	chr11:65770987-65771037	HepG2	liver:	n/a
30	chr11:65770987-65771037	SKMC	muscle:	n/a
31	chr11:65770987-65771037	MCF-7	breast:	n/a
32	chr11:65770987-65771037	U87	brain:	n/a
33	chr11:65770987-65771037	T-47D	breast:	n/a
34	chr11:65770987-65771037	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:65770987-65771037	GM12891	blood:	n/a
36	chr11:65770987-65771037	AG09319	gingival:	n/a
37	chr11:65770987-65771037	SAEC	small airway:	n/a
38	chr11:65770987-65771037	AG10803	skin:	n/a
39	chr11:65770987-65771037	CMK	blood:	n/a
40	chr11:65770987-65771037	BJ	skin:	n/a
41	chr11:65770987-65771037	HNPCEpiC	eye:	n/a
42	chr11:65770987-65771037	RPTEC	kidney:	n/a
43	chr11:65770987-65771037	HCM	heart:	n/a
44	chr11:65770987-65771037	SK-N-SH_RA	brain:	n/a
45	chr11:65770987-65771037	AG09309	skin:	n/a
46	chr11:65770987-65771037	PFSK-1	brain:	n/a
47	chr11:65770987-65771037	SK-N-MC	brain:	n/a
48	chr11:65770987-65771037	HRPEpiC	eye:	n/a
49	chr11:65770987-65771037	SK-N-SH	brain:	n/a
50	chr11:65770987-65771037	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:65380602..65383246-chr11:65768678..65771455,2	K562	blood:
2	chr11:65727706..65730705-chr11:65767958..65771448,5	K562	blood:
3	chr11:65771026..65774019-chr11:65782878..65784960,2	MCF-7	breast:
4	chr11:65727757..65730728-chr11:65768462..65771270,6	MCF-7	breast:
5	chr11:65768713..65771187-chr11:65815106..65817250,2	MCF-7	breast:
6	chr11:65727817..65730505-chr11:65769706..65771571,3	MCF-7	breast:
7	chr11:65768250..65771590-chr11:65817294..65821421,6	K562	blood:
8	chr11:65767772..65771693-chr11:65812597..65815090,3	MCF-7	breast:
9	chr11:65623413..65628719-chr11:65768360..65773657,11	MCF-7	breast:
10	chr11:65728631..65731213-chr11:65769693..65771448,3	K562	blood:
11	chr11:65631727..65633927-chr11:65768782..65771616,2	MCF-7	breast:
12	chr11:65745204..65747160-chr11:65768458..65770932,2	MCF-7	breast:
13	chr11:65767679..65771369-chr11:65818165..65822112,6	MCF-7	breast:
14	chr11:65769812..65778104-chr11:65786537..65794453,15	K562	blood:
15	chr11:65626233..65629168-chr11:65768411..65771473,3	MCF-7	breast:
16	chr11:65769145..65771135-chr11:65826724..65830064,3	MCF-7	breast:
17	chr11:65768250..65771110-chr11:65819143..65821313,2	K562	blood:
18	chr11:65635925..65638559-chr11:65769134..65770863,2	MCF-7	breast:
19	chr11:65768121..65772581-chr11:65835630..65838620,4	MCF-7	breast:
20	chr11:65428607..65430796-chr11:65768393..65771088,2	K562	blood:
21	chr11:65652640..65657924-chr11:65769844..65772901,4	MCF-7	breast:

No data

Variant related genes	Relation type
EIF1AD	TF binding region
EIF1AD	CpG island
ENSG00000175229	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000175294	chromatin interactions
ENSG00000175115	chromatin interactions
ENSG00000172638	chromatin interactions
ENSG00000172500	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000255038	chromatin interactions
ENSG00000087365	chromatin interactions
ENSG00000173327	chromatin interactions
ENSG00000173039	chromatin interactions
ENSG00000175467	chromatin interactions
ENSG00000175602	chromatin interactions
ENSG00000197136	chromatin interactions
ENSG00000238752	chromatin interactions

Extended variants
information (count: 32 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373827318	chr11:65770746-65770747	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
2	rs387906871	chr11:65770755-65770756	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
3	rs34305777	chr11:65770772-65770773	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
4	rs137937738	chr11:65770793-65770794	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
5	rs11604921	chr11:65770840-65770841	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
6	rs533253708	chr11:65770877-65770878	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
7	rs544313647	chr11:65770880-65770881	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
8	rs372318769	chr11:65770893-65770894	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
9	rs553789168	chr11:65770907-65770908	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
10	rs557802364	chr11:65770919-65770920	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
11	rs549758169	chr11:65770945-65770946	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs577419542	chr11:65770950-65770951	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
13	rs72930967	chr11:65770953-65770954	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs186931511	chr11:65771006-65771007	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
15	rs191905461	chr11:65771031-65771032	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
16	rs147010511	chr11:65771051-65771052	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
17	rs542636194	chr11:65771052-65771053	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
18	rs56984820	chr11:65771053-65771054	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
19	rs398016452	chr11:65771060-65771061	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
20	rs201016838	chr11:65771078-65771079	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
21	rs372591003	chr11:65771084-65771085	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
22	rs377026745	chr11:65771087-65771088	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
23	rs370432107	chr11:65771138-65771139	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs143413856	chr11:65771144-65771145	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs140057395	chr11:65771177-65771178	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs564929774	chr11:65771182-65771183	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs374456907	chr11:65771183-65771184	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs140412018	chr11:65771188-65771189	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs181035066	chr11:65771278-65771279	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs546873462	chr11:65771335-65771336	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs145574018	chr11:65771343-65771344	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs535755968	chr11:65771355-65771356	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65768000-65770800	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr11:65768000-65770800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:65768000-65770800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:65768000-65771200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:65768200-65770800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:65768400-65771000	Active TSS	H1 Cell Line	embryonic stem cell
7	chr11:65768400-65771000	Active TSS	H9 Cell Line	embryonic stem cell
8	chr11:65768400-65771200	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr11:65768400-65771200	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr11:65768600-65770800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:65768600-65770800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:65768600-65770800	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr11:65768600-65770800	Active TSS	Ovary	ovary
14	chr11:65768600-65771000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:65768600-65771000	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr11:65768600-65771000	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr11:65768600-65771000	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr11:65768600-65771000	Active TSS	A549	lung
19	chr11:65768600-65771200	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr11:65768600-65771200	Active TSS	NHDF-Ad	bronchial
21	chr11:65768800-65770800	Active TSS	Aorta	Aorta
22	chr11:65768800-65770800	Active TSS	Esophagus	oesophagus
23	chr11:65768800-65770800	Active TSS	Psoas Muscle	Psoas
24	chr11:65768800-65771000	Active TSS	Fetal Kidney	kidney
25	chr11:65769000-65770800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
26	chr11:65769000-65770800	Active TSS	Gastric	stomach
27	chr11:65769000-65770800	Active TSS	Pancreas	Pancrea
28	chr11:65769000-65770800	Active TSS	Sigmoid Colon	Sigmoid Colon
29	chr11:65769600-65770800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:65770200-65770800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr11:65770200-65771000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr11:65770400-65770800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:65770400-65770800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:65770400-65770800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
35	chr11:65770400-65770800	Flanking Active TSS	Primary B cells from cord blood	blood
36	chr11:65770400-65770800	Flanking Active TSS	Primary B cells from peripheral blood	blood
37	chr11:65770400-65770800	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr11:65770400-65770800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
39	chr11:65770400-65770800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr11:65770400-65770800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
41	chr11:65770400-65770800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr11:65770400-65770800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr11:65770400-65770800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr11:65770400-65770800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr11:65770400-65770800	Flanking Active TSS	Fetal Lung	lung
46	chr11:65770400-65770800	Flanking Active TSS	Placenta	Placenta
47	chr11:65770400-65770800	Active TSS	Right Atrium	heart
48	chr11:65770400-65770800	Flanking Active TSS	Stomach Smooth Muscle	stomach
49	chr11:65770400-65770800	Flanking Active TSS	Thymus	Thymus
50	chr11:65770400-65771000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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