Variant report

Variant	esv2829956
Chromosome Location	chr11:86872504-87025059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:956)
CpG islands
(count:61)
Chromatin interactive
region (count:43)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:86884421-86884672	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:87011415-87011637	K562	blood:	n/a	n/a
3	ARID3A	chr11:86904903-86905110	K562	blood:	n/a	n/a
4	ARID3A	chr11:86944770-86944904	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:87001268-87001774	K562	blood:	n/a	chr11:87001403-87001419
6	ARID3A	chr11:87001358-87001863	HepG2	liver:	n/a	chr11:87001403-87001419
7	ARID3A	chr11:86901984-86902332	K562	blood:	n/a	n/a
8	ATF1	chr11:86902082-86902330	K562	blood:	n/a	n/a
9	ATF1	chr11:86977830-86978145	K562	blood:	n/a	n/a
10	ATF1	chr11:86926393-86926477	K562	blood:	n/a	n/a
11	ATF1	chr11:86992567-86992847	K562	blood:	n/a	n/a
12	ATF1	chr11:87001481-87001810	K562	blood:	n/a	n/a
13	ATF3	chr11:86977766-86978150	K562	blood:	n/a	n/a
14	BACH1	chr11:86950832-86950861	K562	blood:	n/a	n/a
15	BACH1	chr11:87013438-87013541	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr11:87006356-87006585	GM12878	blood:	n/a	n/a
17	BCL3	chr11:86884209-86884921	A549	lung:	n/a	n/a
18	BHLHE40	chr11:86902070-86902395	K562	blood:	n/a	n/a
19	BRCA1	chr11:86884212-86885082	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr11:86943417-86943753	K562	blood:	n/a	n/a
21	CBX3	chr11:86901982-86902385	K562	blood:	n/a	n/a
22	CBX3	chr11:86884234-86885151	HCT-116	colon:	n/a	n/a
23	CBX3	chr11:86884217-86885173	HCT-116	colon:	n/a	n/a
24	CCNT2	chr11:86885754-86886111	K562	blood:	n/a	n/a
25	CCNT2	chr11:87011981-87012237	K562	blood:	n/a	n/a
26	CEBPB	chr11:86977749-86978195	K562	blood:	n/a	n/a
27	CEBPB	chr11:86884318-86885021	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:86977736-86978248	HCT-116	colon:	n/a	n/a
29	CEBPB	chr11:86977783-86978174	K562	blood:	n/a	n/a
30	CEBPB	chr11:86992567-86992933	K562	blood:	n/a	n/a
31	CEBPB	chr11:86915350-86915531	Hela-S3	cervix:	n/a	chr11:86915439-86915450
32	CEBPB	chr11:87001596-87001812	H1-hESC	embryonic stem cell:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
33	CEBPB	chr11:86974550-86974809	A549	lung:	n/a	chr11:86974644-86974655
34	CEBPB	chr11:86915333-86915574	HepG2	liver:	n/a	chr11:86915439-86915450
35	CEBPB	chr11:87001609-87001929	HepG2	liver:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
36	CEBPB	chr11:86974570-86974776	H1-hESC	embryonic stem cell:	n/a	chr11:86974644-86974655
37	CEBPB	chr11:86992591-86992884	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr11:86991276-86991459	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:86993269-86993392	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr11:87008716-87009063	A549	lung:	n/a	n/a
41	CEBPB	chr11:86915337-86915548	HepG2	liver:	n/a	chr11:86915439-86915450
42	CEBPB	chr11:86974537-86974813	HepG2	liver:	n/a	chr11:86974644-86974655
43	CEBPB	chr11:86992611-86992934	A549	lung:	n/a	n/a
44	CEBPB	chr11:87018244-87018529	A549	lung:	n/a	chr11:87018359-87018372 chr11:87018361-87018370 chr11:87018360-87018371
45	CEBPB	chr11:86977861-86978136	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:87018185-87018519	HepG2	liver:	n/a	chr11:87018359-87018372 chr11:87018361-87018370 chr11:87018360-87018371
47	CEBPB	chr11:86992557-86993003	MCF-7	breast:	n/a	n/a
48	CEBPB	chr11:86915290-86915613	HepG2	liver:	n/a	chr11:86915439-86915450 chr11:86915318-86915329
49	CEBPB	chr11:86977827-86978105	MCF-7	breast:	n/a	n/a
50	CEBPB	chr11:87001595-87001911	A549	lung:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:87002864-87002914	U87	brain:	n/a
2	chr11:87002864-87002914	ProgFib	skin:	n/a
3	chr11:87002864-87002914	HCF	heart:	n/a
4	chr11:87002864-87002914	AG10803	skin:	n/a
5	chr11:87002864-87002914	MCF-7	breast:	n/a
6	chr11:87002864-87002914	HMEC	breast:	n/a
7	chr11:87002864-87002914	AG09319	gingival:	n/a
8	chr11:87002864-87002914	HCM	heart:	n/a
9	chr11:87002864-87002914	BE2_C	brain:	n/a
10	chr11:87002864-87002914	CMK	blood:	n/a
11	chr11:87002864-87002914	PANC-1	pancreas:	n/a
12	chr11:87002864-87002914	PFSK-1	brain:	n/a
13	chr11:87002864-87002914	NB4	blood:	n/a
14	chr11:87002864-87002914	Hepatocyte	liver:	n/a
15	chr11:87002864-87002914	NT2-D1	testis:	n/a
16	chr11:87002864-87002914	HUVEC	blood vessel:	n/a
17	chr11:87002864-87002914	RPTEC	kidney:	n/a
18	chr11:87002864-87002914	Jurkat	blood:	n/a
19	chr11:87002864-87002914	K562	blood:	n/a
20	chr11:87002864-87002914	SKMC	muscle:	n/a
21	chr11:87002864-87002914	Caco-2	colon:	n/a
22	chr11:87002864-87002914	T-47D	breast:	n/a
23	chr11:87002864-87002914	HCPEpiC	choroid plexus:	n/a
24	chr11:87002864-87002914	HRCEpiC	kidney:	n/a
25	chr11:87002864-87002914	GM12891	blood:	n/a
26	chr11:87002864-87002914	HCT-116	colon:	n/a
27	chr11:87002864-87002914	NH-A	brain:	n/a
28	chr11:87002864-87002914	BJ	skin:	n/a
29	chr11:87002864-87002914	SK-N-SH_RA	brain:	n/a
30	chr11:87002864-87002914	AG04450	lung:	fetal
31	chr11:87002864-87002914	HIPEpiC	eye:	n/a
32	chr11:87002864-87002914	ovcar-3	ovarian:	n/a
33	chr11:87002864-87002914	GM19239	blood:	n/a
34	chr11:87002864-87002914	GM12892	blood:	n/a
35	chr11:87002864-87002914	HRE	kidney:	n/a
36	chr11:87002864-87002914	MCF10A-Er-Src	breast:	n/a
37	chr11:87002864-87002914	HEEpiC	esophagus:	n/a
38	chr11:87002864-87002914	ECC-1	luminal epithelium:	n/a
39	chr11:87002864-87002914	HRPEpiC	eye:	n/a
40	chr11:87002864-87002914	HL-60	blood:	n/a
41	chr11:87002864-87002914	GM06990	blood:	n/a
42	chr11:87002864-87002914	SK-N-MC	brain:	n/a
43	chr11:87002864-87002914	NHDF-neo	bronchial:	n/a
44	chr11:87002864-87002914	HEK293	kidney:	embryo
45	chr11:87002864-87002914	SAEC	small airway:	n/a
46	chr11:87002864-87002914	AG04449	skin:	fetal
47	chr11:87002864-87002914	SK-N-SH	brain:	n/a
48	chr11:87002864-87002914	HNPCEpiC	eye:	n/a
49	chr11:87002864-87002914	HepG2	liver:	n/a
50	chr11:87002864-87002914	Hela-S3	cervix:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:86641346..86643236-chr11:86990430..86992858,2	K562	blood:
2	chr11:86710137..86711956-chr11:86990366..86992245,2	MCF-7	breast:
3	chr11:86899712..86901382-chr11:86903626..86906084,2	K562	blood:
4	chr11:86895352..86897026-chr11:86899805..86901720,2	K562	blood:
5	chr11:86920351..86922677-chr11:86924131..86926585,2	K562	blood:
6	chr11:86664855..86666701-chr11:87000839..87002926,2	MCF-7	breast:
7	chr11:86895352..86897026-chr11:86899805..86901720,2	K562	blood:
8	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
9	chr11:86936889..86939702-chr11:86940206..86942335,2	K562	blood:
10	chr11:86936889..86939702-chr11:86940206..86942335,2	K562	blood:
11	chr11:86921997..86924234-chr11:86927310..86928877,2	K562	blood:
12	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
13	chr11:86805484..86807360-chr11:87007311..87009404,2	MCF-7	breast:
14	chr11:86900182..86903492-chr11:86905711..86910083,4	K562	blood:
15	chr11:86806619..86807569-chr11:86992272..86993052,3	MCF-7	breast:
16	chr11:86650138..86651130-chr11:87001040..87002269,8	K562	blood:
17	chr11:87019923..87022315-chr11:87031348..87034093,2	K562	blood:
18	chr11:86580752..86581690-chr11:87001116..87001998,4	K562	blood:
19	chr11:86166836..86167387-chr11:87001058..87001771,2	K562	blood:
20	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
21	chr11:87006858..87009141-chr11:87011283..87013131,2	K562	blood:
22	chr11:86889371..86892096-chr11:86895507..86898091,3	K562	blood:
23	chr11:86924206..86926245-chr11:86930378..86932580,2	K562	blood:
24	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
25	chr11:86664990..86667056-chr11:86996903..86999848,2	K562	blood:
26	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
27	chr11:86921997..86925633-chr11:86926619..86929927,5	K562	blood:
28	chr11:86924206..86926245-chr11:86930378..86932580,2	K562	blood:
29	chr11:87025025..87027495-chr11:87031919..87033616,2	K562	blood:
30	chr11:86991946..86992672-chr5:176296643..176297235,2	MCF-7	breast:
31	chr11:86664953..86668319-chr11:86999800..87002548,3	MCF-7	breast:
32	chr11:86921997..86925633-chr11:86926619..86929927,5	K562	blood:
33	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
34	chr11:87006858..87009141-chr11:87011283..87013131,2	K562	blood:
35	chr11:86899712..86901382-chr11:86903626..86906084,2	K562	blood:
36	chr11:86921997..86924234-chr11:86927310..86928877,2	K562	blood:
37	chr11:86665223..86667347-chr11:87003604..87005762,3	MCF-7	breast:
38	chr11:86689677..86690529-chr11:87011689..87012195,2	MCF-7	breast:
39	chr11:86867900..86869412-chr11:86871775..86874240,2	K562	blood:
40	chr11:87001464..87002001-chr7:75943410..75944161,2	K562	blood:
41	chr11:86900182..86903492-chr11:86905711..86910083,4	K562	blood:
42	chr11:86920351..86922677-chr11:86924131..86926585,2	K562	blood:
43	chr11:86889371..86892096-chr11:86895507..86898091,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FZD4-8	chr11:86969893-86970301	NONHSAT023515

No data

Variant related genes	Relation type
ENSG00000213287	TF binding region
TMEM135	TF binding region
ENSG00000213287	CpG island
TMEM135	CpG island
ENSG00000246523	chromatin interactions
ENSG00000174804	chromatin interactions

Extended variants
information (count: 5996 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:5996 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546229	chr11:86872504-86872505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187613603	chr11:86872530-86872531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570163158	chr11:86872539-86872540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541532214	chr11:86872576-86872577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367665690	chr11:86872585-86872586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537937638	chr11:86872586-86872587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192949077	chr11:86872588-86872589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571199094	chr11:86872594-86872595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558789514	chr11:86872609-86872610	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547867	chr11:86872647-86872648	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553366337	chr11:86872761-86872762	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573554906	chr11:86872845-86872846	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576592946	chr11:86872869-86872870	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185150914	chr11:86872901-86872902	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549932	chr11:86872908-86872909	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs485113	chr11:86872913-86872914	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs371765179	chr11:86872915-86872916	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375057735	chr11:86872947-86872948	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545463218	chr11:86872981-86872982	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565271485	chr11:86872987-86872988	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139259840	chr11:86873028-86873029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189627149	chr11:86873036-86873037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561269013	chr11:86873062-86873063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577014590	chr11:86873120-86873121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116462327	chr11:86873121-86873122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78339496	chr11:86873124-86873125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563904110	chr11:86873164-86873165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551570292	chr11:86873169-86873170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141567417	chr11:86873200-86873201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532845811	chr11:86873202-86873203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201740288	chr11:86873239-86873240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200532217	chr11:86873240-86873241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74987316	chr11:86873249-86873250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201480061	chr11:86873268-86873269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181109443	chr11:86873322-86873323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559443856	chr11:86873328-86873329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530236565	chr11:86873370-86873371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533660977	chr11:86873378-86873379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546949925	chr11:86873402-86873403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566966304	chr11:86873414-86873415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536140360	chr11:86873423-86873424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556213144	chr11:86873424-86873425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545163905	chr11:86873482-86873483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150495712	chr11:86873497-86873498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563841289	chr11:86873505-86873506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548361157	chr11:86873508-86873509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563789712	chr11:86873509-86873510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376535896	chr11:86873516-86873517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577329	chr11:86873570-86873571	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs146959550	chr11:86873599-86873600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	18194544	CNVD

Chromatin state (count:1069 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86809000-86876000	Weak transcription	Left Ventricle	heart
2	chr11:86836800-86877200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:86851200-86872600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:86867000-86888600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:86867600-86884200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:86868200-86881800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:86868200-86884200	Weak transcription	HepG2	liver
8	chr11:86870400-86884600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:86872600-86873000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:86872600-86873000	Enhancers	Fetal Heart	heart
11	chr11:86872600-86873000	Enhancers	Osteobl	bone
12	chr11:86872600-86873200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr11:86872800-86873200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr11:86872800-86873200	Enhancers	HSMMtube	muscle
15	chr11:86873000-86873400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr11:86873200-86884200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr11:86873600-86874000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:86874000-86876800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:86876800-86880000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:86880000-86884800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:86880600-86891800	Weak transcription	Aorta	Aorta
22	chr11:86880800-86881200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr11:86880800-86892600	Weak transcription	Liver	Liver
24	chr11:86881000-86889000	Weak transcription	Fetal Intestine Small	intestine
25	chr11:86881200-86886600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr11:86881400-86881600	Weak transcription	Left Ventricle	heart
27	chr11:86881400-86881600	Enhancers	Thymus	Thymus
28	chr11:86881400-86884600	Weak transcription	Adipose Nuclei	Adipose
29	chr11:86881600-86881800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:86881600-86882000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr11:86881600-86882000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
32	chr11:86881600-86882000	ZNF genes & repeats	Fetal Stomach	stomach
33	chr11:86881600-86882000	Enhancers	Left Ventricle	heart
34	chr11:86881600-86882000	Enhancers	Lung	lung
35	chr11:86881600-86882000	Enhancers	Pancreas	Pancrea
36	chr11:86881600-86882400	Enhancers	Right Ventricle	heart
37	chr11:86881600-86884800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr11:86881800-86882000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr11:86881800-86884600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr11:86881800-86884800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr11:86881800-86891000	Weak transcription	Thymus	Thymus
42	chr11:86882000-86882800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:86882000-86884200	Weak transcription	Lung	lung
44	chr11:86882000-86884400	Weak transcription	Primary hematopoietic stem cells	blood
45	chr11:86882000-86928000	Weak transcription	Left Ventricle	heart
46	chr11:86882400-86883000	Weak transcription	Right Ventricle	heart
47	chr11:86882400-86883000	Enhancers	K562	blood
48	chr11:86882800-86883200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:86882800-86883200	Enhancers	Psoas Muscle	Psoas
50	chr11:86883000-86883200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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