Variant report

Variant	esv3357299
Chromosome Location	chr11:87163584-87245523
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr11:87204621-87204917	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr11:87204640-87204899	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr11:87174607-87174838	HepG2	liver:	n/a	n/a
4	CEBPB	chr11:87180842-87181077	HepG2	liver:	n/a	chr11:87180927-87180938 chr11:87180926-87180937 chr11:87180926-87180939 chr11:87180926-87180937
5	CEBPB	chr11:87177314-87177627	IMR90	lung:	n/a	n/a
6	CEBPB	chr11:87184192-87185080	IMR90	lung:	n/a	n/a
7	CEBPB	chr11:87204666-87205419	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:87212560-87212680	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr11:87174640-87174790	GM12865	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
10	CTCF	chr11:87212560-87212710	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr11:87212579-87212654	GM13976	blood:	n/a	n/a
12	CTCF	chr11:87212540-87212690	SAEC	small airway:	n/a	n/a
13	CTCF	chr11:87212575-87212647	GM19238	blood:	n/a	n/a
14	CTCF	chr11:87174613-87174852	LNCaP	prostate:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
15	CTCF	chr11:87174660-87174810	GM12872	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
16	CTCF	chr11:87174680-87174830	GM12873	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
17	CTCF	chr11:87212580-87212730	HMEC	breast:	n/a	n/a
18	CTCF	chr11:87174620-87174859	GM12878	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
19	CTCF	chr11:87174860-87175010	HAc	cerebellar:	n/a	n/a
20	CTCF	chr11:87174557-87174907	K562	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
21	CTCF	chr11:87174680-87174830	HepG2	liver:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
22	CTCF	chr11:87174660-87174810	WERI-Rb-1	eye:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
23	CTCF	chr11:87212540-87212690	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr11:87174640-87174852	Fibrobl	skin:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
25	CTCF	chr11:87212611-87212691	Medullo	brain:	n/a	n/a
26	CTCF	chr11:87174680-87174830	GM12867	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
27	CTCF	chr11:87225320-87225470	HMEC	breast:	n/a	n/a
28	CTCF	chr11:87174680-87174830	HEEpiC	esophagus:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
29	CTCF	chr11:87174660-87174810	GM12866	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
30	CTCF	chr11:87212571-87212670	Gliobla	brain:	n/a	n/a
31	CTCF	chr11:87174660-87174810	HEK293	kidney:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
32	CTCF	chr11:87184369-87184489	NHEK	skin:	n/a	n/a
33	CTCF	chr11:87174675-87174771	GM13976	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
34	CTCF	chr11:87174680-87174830	NB4	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
35	CTCF	chr11:87212460-87212610	NHEK	skin:	n/a	n/a
36	CTCF	chr11:87174647-87174852	A549	lung:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
37	CTCF	chr11:87174610-87174872	MCF-7	breast:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
38	CTCF	chr11:87174811-87174824	GM12891	blood:	n/a	n/a
39	CTCF	chr11:87224000-87224150	GM12866	blood:	n/a	n/a
40	CTCF	chr11:87174640-87174790	RPTEC	kidney:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
41	CTCF	chr11:87212540-87212690	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr11:87174600-87174750	GM12868	blood:	n/a	chr11:87174731-87174747 chr11:87174730-87174748
43	CTCF	chr11:87174660-87174810	HMEC	breast:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
44	CTCF	chr11:87174640-87174790	HCT-116	colon:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
45	CTCF	chr11:87174660-87174795	SK-N-SH_RA	brain:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
46	CTCF	chr11:87174525-87175015	HCT-116	colon:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
47	CTCF	chr11:87184400-87184550	NHEK	skin:	n/a	n/a
48	CTCF	chr11:87174640-87174790	GM12871	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
49	CTCF	chr11:87174578-87174854	A549	lung:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
50	CTCF	chr11:87174600-87174750	HMF	breast:	n/a	chr11:87174731-87174747 chr11:87174730-87174748

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:87184120-87184170	HUVEC	blood vessel:	n/a
2	chr11:87224821-87224871	SKMC	muscle:	n/a
3	chr11:87224821-87224871	BJ	skin:	n/a
4	chr11:87224821-87224871	HEEpiC	esophagus:	n/a
5	chr11:87184120-87184170	SK-N-MC	brain:	n/a
6	chr11:87204675-87204725	K562	blood:	n/a
7	chr11:87204675-87204725	LNCaP	prostate:	n/a
8	chr11:87204675-87204725	HCM	heart:	n/a
9	chr11:87204675-87204725	GM06990	blood:	n/a
10	chr11:87204675-87204725	NHDF-neo	bronchial:	n/a
11	chr11:87204675-87204725	ProgFib	skin:	n/a
12	chr11:87224821-87224871	MCF-7	breast:	n/a
13	chr11:87184120-87184170	BJ	skin:	n/a
14	chr11:87184120-87184170	PFSK-1	brain:	n/a
15	chr11:87224821-87224871	PANC-1	pancreas:	n/a
16	chr11:87204675-87204725	T-47D	breast:	n/a
17	chr11:87204675-87204725	HIPEpiC	eye:	n/a
18	chr11:87224821-87224871	NB4	blood:	n/a
19	chr11:87224821-87224871	AG10803	skin:	n/a
20	chr11:87224821-87224871	AoSMC	blood vessel:	n/a
21	chr11:87204675-87204725	HCPEpiC	choroid plexus:	n/a
22	chr11:87184120-87184170	NHBE	bronchial:	n/a
23	chr11:87224821-87224871	NHBE	bronchial:	n/a
24	chr11:87204675-87204725	NH-A	brain:	n/a
25	chr11:87184120-87184170	A549	lung:	n/a
26	chr11:87224821-87224871	HRPEpiC	eye:	n/a
27	chr11:87184120-87184170	ECC-1	luminal epithelium:	n/a
28	chr11:87204675-87204725	HCF	heart:	n/a
29	chr11:87204675-87204725	NHBE	bronchial:	n/a
30	chr11:87204675-87204725	SKMC	muscle:	n/a
31	chr11:87204675-87204725	RPTEC	kidney:	n/a
32	chr11:87204675-87204725	AG04450	lung:	fetal
33	chr11:87204675-87204725	MCF-7	breast:	n/a
34	chr11:87224821-87224871	HMEC	breast:	n/a
35	chr11:87204675-87204725	AG04449	skin:	fetal
36	chr11:87184120-87184170	Hela-S3	cervix:	n/a
37	chr11:87224821-87224871	K562	blood:	n/a
38	chr11:87224821-87224871	Caco-2	colon:	n/a
39	chr11:87224821-87224871	PFSK-1	brain:	n/a
40	chr11:87184120-87184170	HMEC	breast:	n/a
41	chr11:87224821-87224871	SAEC	small airway:	n/a
42	chr11:87184120-87184170	HRE	kidney:	n/a
43	chr11:87184120-87184170	GM06990	blood:	n/a
44	chr11:87224821-87224871	ECC-1	luminal epithelium:	n/a
45	chr11:87204675-87204725	HEK293	kidney:	embryo
46	chr11:87184120-87184170	AG09319	gingival:	n/a
47	chr11:87224821-87224871	NH-A	brain:	n/a
48	chr11:87184120-87184170	HEEpiC	esophagus:	n/a
49	chr11:87224821-87224871	GM12891	blood:	n/a
50	chr11:87224821-87224871	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:87174299..87174869-chr11:87433363..87434025,2	MCF-7	breast:
2	chr11:87134513..87137251-chr11:87164100..87165972,2	K562	blood:
3	chr11:87241708..87244193-chr11:87247237..87248940,2	K562	blood:
4	chr11:87228574..87230526-chr11:87233558..87236260,2	K562	blood:
5	chr11:87228574..87230526-chr11:87233558..87236260,2	K562	blood:
6	chr11:87157048..87159158-chr11:87161561..87163817,3	K562	blood:
7	chr11:87197219..87198779-chr11:87200306..87201927,2	K562	blood:
8	chr11:87174249..87175551-chr11:88277215..88277965,4	K562	blood:
9	chr11:87220063..87221996-chr11:87226594..87228726,2	K562	blood:
10	chr11:87162800..87163602-chr11:87174227..87174795,2	K562	blood:
11	chr11:87197219..87198779-chr11:87200306..87201927,2	K562	blood:
12	chr11:87162800..87163602-chr11:87174227..87174795,2	K562	blood:
13	chr11:87220063..87221996-chr11:87226594..87228726,2	K562	blood:

Variant related genes	Relation type
ENSG00000255391	TF binding region
ENSG00000255391	CpG island

Extended variants
information (count: 2350 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2350 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143059238	chr11:87163615-87163616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147487732	chr11:87163617-87163618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562206391	chr11:87163638-87163639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115122002	chr11:87163682-87163683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375985625	chr11:87163684-87163685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368392653	chr11:87163686-87163687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112960295	chr11:87163690-87163691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56750299	chr11:87163699-87163700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201773332	chr11:87163700-87163701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200569082	chr11:87163701-87163702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34521519	chr11:87163705-87163706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79884848	chr11:87163709-87163710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139857731	chr11:87163722-87163723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557061615	chr11:87163733-87163734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138086899	chr11:87163872-87163873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149517694	chr11:87163892-87163893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551847687	chr11:87163995-87163996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73537967	chr11:87164003-87164004	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376409508	chr11:87164029-87164030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11235152	chr11:87164046-87164047	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs79480544	chr11:87164069-87164070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79337497	chr11:87164074-87164075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529449530	chr11:87164080-87164081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537272426	chr11:87164142-87164143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73537969	chr11:87164167-87164168	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs559613407	chr11:87164175-87164176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74641509	chr11:87164187-87164188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191528028	chr11:87164188-87164189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148702144	chr11:87164195-87164196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373227665	chr11:87164217-87164218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376570159	chr11:87164258-87164259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556048891	chr11:87164290-87164291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539994455	chr11:87164309-87164310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575877731	chr11:87164377-87164378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562062854	chr11:87164425-87164426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529168928	chr11:87164430-87164431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146169776	chr11:87164431-87164432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183717614	chr11:87164470-87164471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533346873	chr11:87164513-87164514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76706887	chr11:87164525-87164526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371026528	chr11:87164536-87164537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188147816	chr11:87164554-87164555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144022576	chr11:87164602-87164603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528104490	chr11:87164621-87164622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547847273	chr11:87164638-87164639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78838270	chr11:87164690-87164691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530746517	chr11:87164704-87164705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76941929	chr11:87164735-87164736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570704030	chr11:87164743-87164744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs193274145	chr11:87164758-87164759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:87151600-87165200	Weak transcription	Colon Smooth Muscle	Colon
2	chr11:87156400-87165000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:87156800-87164000	Weak transcription	Fetal Heart	heart
4	chr11:87156800-87164800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:87157000-87165000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:87157800-87164600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:87162800-87164600	Weak transcription	Fetal Muscle Leg	muscle
8	chr11:87162800-87164800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr11:87162800-87164800	Weak transcription	Fetal Kidney	kidney
10	chr11:87163000-87164400	Weak transcription	HSMMtube	muscle
11	chr11:87163000-87164800	Weak transcription	NHDF-Ad	bronchial
12	chr11:87163000-87165000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:87163200-87165000	Weak transcription	Osteobl	bone
14	chr11:87163400-87164600	Weak transcription	HSMM	muscle
15	chr11:87164000-87165400	Enhancers	Psoas Muscle	Psoas
16	chr11:87164000-87165800	Enhancers	Fetal Heart	heart
17	chr11:87164400-87165400	Enhancers	HSMMtube	muscle
18	chr11:87164600-87165400	Enhancers	Fetal Muscle Leg	muscle
19	chr11:87164600-87165400	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr11:87164600-87165600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:87164600-87165800	Enhancers	HSMM	muscle
22	chr11:87164800-87165000	Enhancers	Fetal Kidney	kidney
23	chr11:87164800-87165400	Enhancers	NHDF-Ad	bronchial
24	chr11:87164800-87165600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:87164800-87165600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:87164800-87165600	Enhancers	Pancreas	Pancrea
27	chr11:87165000-87165200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:87165000-87165400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr11:87165000-87165400	Weak transcription	Fetal Kidney	kidney
30	chr11:87165000-87165400	Flanking Active TSS	GM12878-XiMat	blood
31	chr11:87165000-87165600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:87165000-87165600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:87165000-87165600	Enhancers	Osteobl	bone
34	chr11:87165000-87165800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:87165200-87165400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr11:87165200-87165600	Enhancers	Colon Smooth Muscle	Colon
37	chr11:87165400-87165800	Enhancers	Fetal Kidney	kidney
38	chr11:87165400-87166800	Enhancers	GM12878-XiMat	blood
39	chr11:87165600-87167400	Weak transcription	Pancreas	Pancrea
40	chr11:87165800-87173200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:87166800-87167200	Weak transcription	GM12878-XiMat	blood
42	chr11:87167200-87167800	Enhancers	GM12878-XiMat	blood
43	chr11:87167800-87170200	Weak transcription	GM12878-XiMat	blood
44	chr11:87170200-87170600	Enhancers	Spleen	Spleen
45	chr11:87170200-87170600	Enhancers	GM12878-XiMat	blood
46	chr11:87173200-87173600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:87175600-87176200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:87175600-87177800	Enhancers	Fetal Stomach	stomach
49	chr11:87176000-87179000	Enhancers	Colon Smooth Muscle	Colon
50	chr11:87176600-87177600	Enhancers	Fetal Muscle Leg	muscle

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