Variant report

Variant	nsv933654
Chromosome Location	chr11:71153638-71156067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:24)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:24 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:71155417-71155657	HepG2	liver:	n/a	n/a
2	MYC	chr11:71154748-71154890	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr11:71156061-71156495	HepG2	liver:	n/a	n/a
4	POLR2A	chr11:71154559-71154797	K562	blood:	n/a	n/a
5	POLR2A	chr11:71151944-71156747	K562	blood:	n/a	n/a
6	POLR2A	chr11:71154830-71155558	K562	blood:	n/a	n/a
7	POLR2A	chr11:71155832-71156314	HepG2	liver:	n/a	n/a
8	POLR2A	chr11:71154921-71155049	GM12878	blood:	n/a	n/a
9	POLR2A	chr11:71154555-71155619	HepG2	liver:	n/a	n/a
10	POLR2A	chr11:71154354-71154698	K562	blood:	n/a	n/a
11	POLR2A	chr11:71155904-71156521	K562	blood:	n/a	n/a
12	POLR2A	chr11:71155332-71155464	K562	blood:	n/a	n/a
13	POLR2A	chr11:71154973-71155299	K562	blood:	n/a	n/a
14	POLR2A	chr11:71154751-71155205	ECC-1	luminal epithelium:	n/a	n/a
15	POLR2A	chr11:71155500-71155679	K562	blood:	n/a	n/a
16	POLR2A	chr11:71153912-71154233	K562	blood:	n/a	n/a
17	POLR2A	chr11:71155864-71156478	K562	blood:	n/a	n/a
18	POLR2A	chr11:71154345-71154893	K562	blood:	n/a	n/a
19	POLR2A	chr11:71155781-71155817	HepG2	liver:	n/a	n/a
20	POLR2A	chr11:71155069-71155402	HepG2	liver:	n/a	n/a
21	POLR2A	chr11:71153241-71154120	K562	blood:	n/a	n/a
22	POLR2A	chr11:71154953-71154971	K562	blood:	n/a	n/a
23	POLR2A	chr11:71153728-71154345	HepG2	liver:	n/a	n/a
24	USF2	chr11:71154614-71154684	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71155081-71155131	SK-N-SH	brain:	n/a
2	chr11:71155081-71155131	HCT-116	colon:	n/a
3	chr11:71155081-71155131	T-47D	breast:	n/a
4	chr11:71155081-71155131	SK-N-MC	brain:	n/a
5	chr11:71155081-71155131	MCF-7	breast:	n/a
6	chr11:71155081-71155131	HRE	kidney:	n/a
7	chr11:71155081-71155131	HEK293	kidney:	embryo
8	chr11:71155081-71155131	NT2-D1	testis:	n/a
9	chr11:71155081-71155131	Hepatocyte	liver:	n/a
10	chr11:71155081-71155131	HRCEpiC	kidney:	n/a
11	chr11:71155081-71155131	AG10803	skin:	n/a
12	chr11:71155081-71155131	HUVEC	blood vessel:	n/a
13	chr11:71155081-71155131	Hela-S3	cervix:	n/a
14	chr11:71155081-71155131	SAEC	small airway:	n/a
15	chr11:71155081-71155131	SK-N-SH_RA	brain:	n/a
16	chr11:71155081-71155131	AG04449	skin:	fetal
17	chr11:71155081-71155131	NH-A	brain:	n/a
18	chr11:71155081-71155131	NB4	blood:	n/a
19	chr11:71155081-71155131	HNPCEpiC	eye:	n/a
20	chr11:71155081-71155131	SKMC	muscle:	n/a
21	chr11:71155081-71155131	U87	brain:	n/a
22	chr11:71155081-71155131	PrEC	prostate:	n/a
23	chr11:71155081-71155131	HepG2	liver:	n/a
24	chr11:71155081-71155131	GM19239	blood:	n/a
25	chr11:71155081-71155131	MCF10A-Er-Src	breast:	n/a
26	chr11:71155081-71155131	HCM	heart:	n/a
27	chr11:71155081-71155131	HIPEpiC	eye:	n/a
28	chr11:71155081-71155131	HAEpiC	amniotic membrane:	n/a
29	chr11:71155081-71155131	AG09309	skin:	n/a
30	chr11:71155081-71155131	NHDF-neo	bronchial:	n/a
31	chr11:71155081-71155131	HL-60	blood:	n/a
32	chr11:71155081-71155131	AoSMC	blood vessel:	n/a
33	chr11:71155081-71155131	GM12892	blood:	n/a
34	chr11:71155081-71155131	CMK	blood:	n/a
35	chr11:71155081-71155131	Jurkat	blood:	n/a
36	chr11:71155081-71155131	GM12878	blood:	n/a
37	chr11:71155081-71155131	HEEpiC	esophagus:	n/a
38	chr11:71155081-71155131	GM12891	blood:	n/a
39	chr11:71155081-71155131	HMEC	breast:	n/a
40	chr11:71155081-71155131	PFSK-1	brain:	n/a
41	chr11:71155081-71155131	ECC-1	luminal epithelium:	n/a
42	chr11:71155081-71155131	IMR90	lung:	fetal
43	chr11:71155081-71155131	AG09319	gingival:	n/a
44	chr11:71155081-71155131	RPTEC	kidney:	n/a
45	chr11:71155081-71155131	K562	blood:	n/a
46	chr11:71155081-71155131	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:71155081-71155131	HCF	heart:	n/a
48	chr11:71155081-71155131	A549	lung:	n/a
49	chr11:71155081-71155131	HRPEpiC	eye:	n/a
50	chr11:71155081-71155131	LNCaP	prostate:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71154436..71156970-chr11:71198755..71201662,2	MCF-7	breast:
2	chr11:71144398..71146962-chr11:71155881..71158329,2	K562	blood:
3	chr11:71138911..71140880-chr11:71154532..71157322,2	K562	blood:
4	chr11:71146059..71148297-chr11:71153188..71155860,2	K562	blood:
5	chr11:71137158..71140424-chr11:71155885..71157748,3	K562	blood:
6	chr11:71155911..71156698-chr3:193498553..193499213,2	MCF-7	breast:
7	chr11:71150692..71153685-chr11:71157371..71159231,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254682	TF binding region
DHCR7	TF binding region
ENSG00000254682	CpG island
DHCR7	CpG island
ENSG00000172893	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370073658	chr11:71153638-71153639	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs547282679	chr11:71153643-71153644	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs571366047	chr11:71153678-71153679	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs188474369	chr11:71153684-71153685	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534072582	chr11:71153753-71153754	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs1792223	chr11:71153757-71153758	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs34405099	chr11:71153855-71153856	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs576893086	chr11:71153875-71153876	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs537875271	chr11:71153899-71153900	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs538404244	chr11:71153900-71153901	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs12294879	chr11:71154021-71154022	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs180898058	chr11:71154037-71154038	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542502521	chr11:71154039-71154040	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs370739983	chr11:71154076-71154077	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs113845968	chr11:71154109-71154110	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185547354	chr11:71154141-71154142	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572653187	chr11:71154170-71154171	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs11606033	chr11:71154204-71154205	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs2852851	chr11:71154243-71154244	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs564183405	chr11:71154298-71154299	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs189645623	chr11:71154313-71154314	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs531405133	chr11:71154315-71154316	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs77872619	chr11:71154361-71154362	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201344213	chr11:71154389-71154390	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs561683678	chr11:71154407-71154408	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs117901692	chr11:71154408-71154409	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs181698101	chr11:71154487-71154488	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs147830399	chr11:71154492-71154493	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs554700181	chr11:71154546-71154547	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs77202975	chr11:71154558-71154559	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs551133432	chr11:71154577-71154578	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs570860137	chr11:71154593-71154594	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs17161531	chr11:71154615-71154616	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs186915587	chr11:71154617-71154618	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs368124125	chr11:71154621-71154622	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs556325764	chr11:71154692-71154693	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs117488879	chr11:71154698-71154699	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs576363566	chr11:71154732-71154733	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs554489379	chr11:71154761-71154762	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs529516351	chr11:71154781-71154782	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs12422045	chr11:71154820-71154821	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs148838369	chr11:71154836-71154837	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs546439671	chr11:71154848-71154849	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs564620383	chr11:71154861-71154862	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs576065593	chr11:71154907-71154908	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs2851691	chr11:71154924-71154925	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs543494118	chr11:71154928-71154929	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs561574250	chr11:71154957-71154958	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs557737952	chr11:71154961-71154962	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs192249049	chr11:71154993-71154994	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Breast cancer	21785460	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71140600-71158200	Weak transcription	Fetal Brain Male	brain
2	chr11:71140800-71154000	Weak transcription	Fetal Lung	lung
3	chr11:71140800-71154000	Weak transcription	HSMM	muscle
4	chr11:71144000-71156200	Strong transcription	Fetal Brain Female	brain
5	chr11:71144200-71158200	Weak transcription	Small Intestine	intestine
6	chr11:71144400-71156200	Strong transcription	Primary T cells from cord blood	blood
7	chr11:71144600-71157800	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr11:71144800-71156600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:71144800-71156800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:71144800-71156800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr11:71144800-71157800	Strong transcription	H9 Cell Line	embryonic stem cell
12	chr11:71145000-71155400	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr11:71145000-71156400	Strong transcription	Brain Germinal Matrix	brain
14	chr11:71145000-71156600	Strong transcription	Fetal Stomach	stomach
15	chr11:71145000-71157000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:71145000-71157000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr11:71145000-71157400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:71145000-71157800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr11:71145000-71158600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr11:71145200-71156200	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr11:71145200-71157000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr11:71145200-71157000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr11:71145200-71157200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr11:71145200-71157400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr11:71145200-71157400	Strong transcription	HMEC	breast
26	chr11:71145200-71157800	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr11:71145400-71157800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:71145400-71158000	Weak transcription	Stomach Mucosa	stomach
29	chr11:71145600-71157000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr11:71145600-71157000	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr11:71145600-71158000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:71145800-71155400	Strong transcription	Left Ventricle	heart
33	chr11:71145800-71156200	Strong transcription	Lung	lung
34	chr11:71145800-71156400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:71145800-71156600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:71145800-71156600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:71145800-71156800	Strong transcription	Duodenum Mucosa	Duodenum
38	chr11:71145800-71156800	Strong transcription	Fetal Muscle Trunk	muscle
39	chr11:71145800-71157000	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr11:71145800-71157200	Strong transcription	HSMMtube	muscle
41	chr11:71145800-71157400	Strong transcription	Fetal Intestine Large	intestine
42	chr11:71145800-71157800	Strong transcription	Fetal Intestine Small	intestine
43	chr11:71146000-71153800	Strong transcription	Brain Cingulate Gyrus	brain
44	chr11:71146000-71155800	Strong transcription	HepG2	liver
45	chr11:71146000-71156200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:71146000-71156800	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr11:71146000-71156800	Strong transcription	Fetal Muscle Leg	muscle
48	chr11:71146000-71157000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr11:71146000-71157000	Strong transcription	Dnd41	blood
50	chr11:71146000-71158000	Strong transcription	HUES48 Cell Line	embryonic stem cell

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