Variant report

Variant	nsv1049467
Chromosome Location	chr11:93651025-93778717
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:893)
CpG islands
(count:427)
Chromatin interactive
region (count:48)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:93654954-93655197	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:93655005-93655286	K562	blood:	n/a	n/a
3	ARID3A	chr11:93685294-93686031	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:93706965-93707250	K562	blood:	n/a	n/a
5	ARID3A	chr11:93721682-93722075	K562	blood:	n/a	n/a
6	ARID3A	chr11:93757847-93758051	K562	blood:	n/a	n/a
7	ARID3A	chr11:93727028-93727190	K562	blood:	n/a	n/a
8	ATF1	chr11:93778579-93778710	K562	blood:	n/a	n/a
9	ATF1	chr11:93666368-93666727	K562	blood:	n/a	n/a
10	ATF1	chr11:93721674-93721940	K562	blood:	n/a	n/a
11	ATF1	chr11:93754009-93754142	K562	blood:	n/a	n/a
12	ATF1	chr11:93757089-93757299	K562	blood:	n/a	n/a
13	ATF1	chr11:93706547-93707226	K562	blood:	n/a	n/a
14	ATF2	chr11:93654907-93655245	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr11:93706772-93707275	K562	blood:	n/a	n/a
16	BACH1	chr11:93754699-93755013	K562	blood:	n/a	n/a
17	BACH1	chr11:93705430-93705460	K562	blood:	n/a	n/a
18	BHLHE40	chr11:93656077-93656420	HepG2	liver:	n/a	n/a
19	BHLHE40	chr11:93706624-93706753	K562	blood:	n/a	n/a
20	BHLHE40	chr11:93685434-93685948	HepG2	liver:	n/a	n/a
21	BHLHE40	chr11:93656163-93656222	K562	blood:	n/a	n/a
22	BHLHE40	chr11:93656211-93656310	GM12878	blood:	n/a	n/a
23	BHLHE40	chr11:93654989-93655206	K562	blood:	n/a	n/a
24	BHLHE40	chr11:93655396-93655543	GM12878	blood:	n/a	n/a
25	BHLHE40	chr11:93706958-93707199	K562	blood:	n/a	n/a
26	BRCA1	chr11:93655121-93655123	HepG2	liver:	n/a	n/a
27	CBX3	chr11:93706656-93708743	K562	blood:	n/a	n/a
28	CBX3	chr11:93706867-93707323	K562	blood:	n/a	n/a
29	CBX3	chr11:93654870-93655235	K562	blood:	n/a	n/a
30	CBX3	chr11:93726833-93727334	HCT-116	colon:	n/a	n/a
31	CBX3	chr11:93707335-93708411	K562	blood:	n/a	n/a
32	CBX3	chr11:93726896-93727284	K562	blood:	n/a	n/a
33	CBX3	chr11:93726921-93727267	K562	blood:	n/a	n/a
34	CCNT2	chr11:93706998-93707249	K562	blood:	n/a	n/a
35	CEBPB	chr11:93761715-93762104	IMR90	lung:	n/a	n/a
36	CEBPB	chr11:93714990-93715302	K562	blood:	n/a	n/a
37	CEBPB	chr11:93754252-93754526	K562	blood:	n/a	chr11:93754307-93754324
38	CEBPB	chr11:93706778-93707239	K562	blood:	n/a	n/a
39	CEBPB	chr11:93757077-93757345	HepG2	liver:	n/a	n/a
40	CEBPB	chr11:93719585-93720365	MCF-7	breast:	n/a	chr11:93720347-93720358
41	CEBPB	chr11:93719621-93720399	MCF-7	breast:	n/a	chr11:93720347-93720358
42	CEBPB	chr11:93675527-93675611	K562	blood:	n/a	chr11:93675571-93675582
43	CEBPB	chr11:93700459-93700810	K562	blood:	n/a	n/a
44	CEBPB	chr11:93675494-93675672	HepG2	liver:	n/a	chr11:93675571-93675582
45	CEBPB	chr11:93761812-93762014	K562	blood:	n/a	n/a
46	CEBPB	chr11:93681348-93681695	A549	lung:	n/a	n/a
47	CEBPB	chr11:93719980-93720265	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:93777358-93777562	K562	blood:	n/a	chr11:93777482-93777495
49	CEBPB	chr11:93700463-93700776	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:93700466-93700822	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93754390-93754440	AG09309	skin:	n/a
2	chr11:93753891-93753941	NH-A	brain:	n/a
3	chr11:93754223-93754273	HAEpiC	amniotic membrane:	n/a
4	chr11:93754288-93754338	K562	blood:	n/a
5	chr11:93754288-93754338	NHBE	bronchial:	n/a
6	chr11:93753891-93753941	MCF-7	breast:	n/a
7	chr11:93754223-93754273	ECC-1	luminal epithelium:	n/a
8	chr11:93754288-93754338	RPTEC	kidney:	n/a
9	chr11:93754390-93754440	HNPCEpiC	eye:	n/a
10	chr11:93753348-93753398	HMEC	breast:	n/a
11	chr11:93754094-93754144	HPAEpiC	pulmonary alveolar:	n/a
12	chr11:93754094-93754144	T-47D	breast:	n/a
13	chr11:93754288-93754338	AoSMC	blood vessel:	n/a
14	chr11:93754288-93754338	NB4	blood:	n/a
15	chr11:93753891-93753941	A549	lung:	n/a
16	chr11:93753891-93753941	AG04449	skin:	fetal
17	chr11:93754223-93754273	MCF-7	breast:	n/a
18	chr11:93754094-93754144	PrEC	prostate:	n/a
19	chr11:93753348-93753398	HCT-116	colon:	n/a
20	chr11:93754390-93754440	HepG2	liver:	n/a
21	chr11:93754347-93754397	HUVEC	blood vessel:	n/a
22	chr11:93754390-93754440	NHDF-neo	bronchial:	n/a
23	chr11:93754390-93754440	GM12892	blood:	n/a
24	chr11:93753891-93753941	AoSMC	blood vessel:	n/a
25	chr11:93754390-93754440	NHBE	bronchial:	n/a
26	chr11:93754288-93754338	A549	lung:	n/a
27	chr11:93754094-93754144	NH-A	brain:	n/a
28	chr11:93754288-93754338	HCT-116	colon:	n/a
29	chr11:93753348-93753398	GM19239	blood:	n/a
30	chr11:93754223-93754273	HCM	heart:	n/a
31	chr11:93754288-93754338	GM19239	blood:	n/a
32	chr11:93754094-93754144	HL-60	blood:	n/a
33	chr11:93754347-93754397	SAEC	small airway:	n/a
34	chr11:93753348-93753398	SK-N-SH_RA	brain:	n/a
35	chr11:93754288-93754338	PFSK-1	brain:	n/a
36	chr11:93754288-93754338	Jurkat	blood:	n/a
37	chr11:93754347-93754397	CMK	blood:	n/a
38	chr11:93754347-93754397	RPTEC	kidney:	n/a
39	chr11:93753891-93753941	HepG2	liver:	n/a
40	chr11:93754347-93754397	K562	blood:	n/a
41	chr11:93754288-93754338	AG04450	lung:	fetal
42	chr11:93754094-93754144	AG09319	gingival:	n/a
43	chr11:93754223-93754273	BE2_C	brain:	n/a
44	chr11:93753348-93753398	U87	brain:	n/a
45	chr11:93754347-93754397	MCF-7	breast:	n/a
46	chr11:93754390-93754440	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:93753891-93753941	GM12878	blood:	n/a
48	chr11:93753891-93753941	NHBE	bronchial:	n/a
49	chr11:93754288-93754338	HCPEpiC	choroid plexus:	n/a
50	chr11:93754288-93754338	ovcar-3	ovarian:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:93667177..93668967-chr11:93861410..93863273,2	K562	blood:
2	chr11:93667365..93670015-chr11:93861067..93863754,2	MCF-7	breast:
3	chr11:93654234..93656516-chr11:93799480..93801603,2	K562	blood:
4	chr11:93654636..93655438-chr11:93916836..93917602,2	MCF-7	breast:
5	chr11:93687985..93689849-chr11:93692203..93693783,2	K562	blood:
6	chr11:93741108..93743362-chr11:93748550..93751276,2	K562	blood:
7	chr11:93741108..93743362-chr11:93748550..93751276,2	K562	blood:
8	chr11:93699154..93702139-chr11:93715372..93717196,2	K562	blood:
9	chr11:93718444..93721972-chr11:93724685..93727460,3	K562	blood:
10	chr11:93700752..93703504-chr11:93704529..93706599,2	K562	blood:
11	chr11:93730828..93732331-chr11:93734323..93737196,2	MCF-7	breast:
12	chr11:93700752..93703504-chr11:93704529..93706599,2	K562	blood:
13	chr11:93654497..93655291-chr11:93768975..93769708,2	MCF-7	breast:
14	chr11:93654633..93655604-chr11:93769016..93769927,3	K562	blood:
15	chr11:93710125..93711813-chr11:93711990..93713968,2	K562	blood:
16	chr11:93691026..93692794-chr11:93694188..93696052,2	K562	blood:
17	chr11:93687985..93689849-chr11:93692203..93693783,2	K562	blood:
18	chr11:93654633..93655604-chr11:93769016..93769927,3	K562	blood:
19	chr11:93698163..93699732-chr11:93702050..93703572,2	K562	blood:
20	chr11:93724420..93726827-chr11:93860849..93862959,2	MCF-7	breast:
21	chr11:93718654..93721406-chr11:93860779..93862683,2	MCF-7	breast:
22	chr11:93725136..93726953-chr11:93730088..93732138,2	K562	blood:
23	chr11:93710125..93711813-chr11:93711990..93713968,2	K562	blood:
24	chr11:93715164..93717058-chr11:93768133..93770763,2	K562	blood:
25	chr11:93710641..93712864-chr11:93716292..93719148,2	K562	blood:
26	chr11:93715164..93717058-chr11:93768133..93770763,2	K562	blood:
27	chr11:93718251..93719933-chr11:93722882..93724386,2	K562	blood:
28	chr1:145200270..145202766-chr11:93677416..93679121,2	K562	blood:
29	chr11:93698163..93699732-chr11:93702050..93703572,2	K562	blood:
30	chr11:93652951..93654960-chr11:93861223..93864128,2	MCF-7	breast:
31	chr11:93753591..93755146-chr11:93763747..93766351,2	K562	blood:
32	chr11:93710641..93712864-chr11:93716292..93719148,2	K562	blood:
33	chr11:93691026..93692794-chr11:93694188..93696052,2	K562	blood:
34	chr11:93730828..93732331-chr11:93734323..93737196,2	MCF-7	breast:
35	chr11:93699154..93702139-chr11:93715372..93717196,2	K562	blood:
36	chr11:93718251..93719933-chr11:93722882..93724386,2	K562	blood:
37	chr11:93710641..93713058-chr11:93716292..93719864,4	K562	blood:
38	chr11:93718444..93721972-chr11:93724685..93727460,3	K562	blood:
39	chr11:93700458..93703504-chr11:93704523..93708049,5	K562	blood:
40	chr11:93654497..93655291-chr11:93768975..93769708,2	MCF-7	breast:
41	chr11:93700458..93703504-chr11:93704523..93708049,5	K562	blood:
42	chr11:93680099..93683642-chr11:93684474..93688848,4	K562	blood:
43	chr11:93725136..93726953-chr11:93730088..93732138,2	K562	blood:
44	chr11:93710641..93713058-chr11:93716292..93719864,4	K562	blood:
45	chr11:93684701..93687298-chr11:93690286..93693320,3	K562	blood:
46	chr11:93684701..93687298-chr11:93690286..93693320,3	K562	blood:
47	chr11:93720101..93721932-chr11:93723597..93725188,2	MCF-7	breast:
48	chr11:93680099..93683642-chr11:93684474..93688848,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VSTM5-3	chr11:93760135-93761825	NONHSAT023702
2	lnc-VSTM5-2	chr11:93731809-93732384	NONHSAT023700

No data

Variant related genes	Relation type
HPRTP3	TF binding region
HEPHL1	TF binding region
HPRTP4	TF binding region
HPRTP3	CpG island
HEPHL1	CpG island
HPRTP4	CpG island
ENSG00000272709	chromatin interactions
ENSG00000181333	chromatin interactions
ENSG00000255995	chromatin interactions
ENSG00000110218	chromatin interactions

Extended variants
information (count: 4439 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4439 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550455682	chr11:93651028-93651029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139261410	chr11:93651046-93651047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs908754	chr11:93651071-93651072	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs79271888	chr11:93651097-93651098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566256531	chr11:93651102-93651103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533909533	chr11:93651164-93651165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558677272	chr11:93651177-93651178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565491249	chr11:93651222-93651223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71480694	chr11:93651236-93651237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200764194	chr11:93651276-93651277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556429881	chr11:93651300-93651301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574610520	chr11:93651317-93651318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569142584	chr11:93651328-93651329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9888266	chr11:93651355-93651356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs11020595	chr11:93651425-93651426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79436418	chr11:93651426-93651427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75474675	chr11:93651427-93651428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559941693	chr11:93651440-93651441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571892049	chr11:93651468-93651469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545932199	chr11:93651469-93651470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149554999	chr11:93651487-93651488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77055996	chr11:93651502-93651503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs80150451	chr11:93651515-93651516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562429825	chr11:93651555-93651556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529588272	chr11:93651603-93651604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186264093	chr11:93651623-93651624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147239129	chr11:93651662-93651663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76559256	chr11:93651690-93651691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552303257	chr11:93651722-93651723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570410986	chr11:93651730-93651731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115725571	chr11:93651752-93651753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189277060	chr11:93651761-93651762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374439959	chr11:93651822-93651823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9888143	chr11:93651823-93651824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs553638659	chr11:93651837-93651838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs908753	chr11:93651883-93651884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs75401647	chr11:93651907-93651908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564258605	chr11:93651917-93651918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576433408	chr11:93651919-93651920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374891768	chr11:93651922-93651923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79161905	chr11:93651974-93651975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114774174	chr11:93651985-93651986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541793032	chr11:93652055-93652056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181982073	chr11:93652103-93652104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116494714	chr11:93652124-93652125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79588111	chr11:93652128-93652129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186368398	chr11:93652175-93652176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs67549397	chr11:93652213-93652214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs541500323	chr11:93652218-93652219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549830366	chr11:93652251-93652252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	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
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	18852474	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93641600-93652800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:93642000-93655200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:93653000-93653200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:93655000-93655400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:93655000-93655400	Enhancers	GM12878-XiMat	blood
6	chr11:93655000-93655600	Enhancers	NHEK	skin
7	chr11:93655000-93656400	Enhancers	HMEC	breast
8	chr11:93655200-93655400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:93655200-93655800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:93655200-93656400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:93655200-93656800	Enhancers	HepG2	liver
12	chr11:93655600-93656600	Enhancers	Fetal Intestine Small	intestine
13	chr11:93656000-93656200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:93656200-93656400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:93656200-93656600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr11:93656400-93669000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:93669000-93670400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:93669400-93670200	Enhancers	Fetal Brain Female	brain
19	chr11:93669400-93670400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr11:93669400-93670400	Enhancers	NHEK	skin
21	chr11:93669400-93671800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr11:93669600-93669800	Enhancers	HMEC	breast
23	chr11:93669600-93670000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:93669600-93670400	Enhancers	Fetal Brain Male	brain
25	chr11:93669800-93670200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:93670000-93671200	Weak transcription	HMEC	breast
27	chr11:93670400-93671400	Weak transcription	NHEK	skin
28	chr11:93670400-93671600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr11:93670400-93671600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:93670400-93671600	Weak transcription	Fetal Brain Male	brain
31	chr11:93671200-93675600	Enhancers	HMEC	breast
32	chr11:93671400-93672200	Enhancers	NHEK	skin
33	chr11:93671600-93672200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr11:93671600-93675600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr11:93671800-93672600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr11:93672000-93672400	Enhancers	NH-A	brain
37	chr11:93672000-93673400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr11:93672000-93673400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr11:93672200-93672600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
40	chr11:93672200-93672600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr11:93672200-93672600	Flanking Active TSS	NHEK	skin
42	chr11:93672200-93673200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr11:93672600-93674800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:93672600-93675400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr11:93672600-93675600	Enhancers	NHEK	skin
46	chr11:93673400-93674800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:93674200-93675200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr11:93674800-93675400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr11:93675400-93678600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:93675600-93678400	Weak transcription	HMEC	breast

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