Variant report

Variant	nsv975401
Chromosome Location	chr11:93364502-93390549
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	ARID3A	chr11:93385273-93385580	HepG2	liver:	n/a	n/a
2	BACH1	chr11:93376114-93376223	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr11:93386189-93386528	GM12878	blood:	n/a	chr11:93386343-93386354
4	BATF	chr11:93386137-93386525	GM12878	blood:	n/a	chr11:93386343-93386354
5	BHLHE40	chr11:93386339-93386484	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:93378604-93378929	HepG2	liver:	n/a	n/a
7	BRCA1	chr11:93384967-93384999	GM12878	blood:	n/a	n/a
8	CEBPB	chr11:93375713-93375933	K562	blood:	n/a	chr11:93375789-93375800 chr11:93375787-93375800 chr11:93375787-93375800
9	CEBPB	chr11:93367585-93367691	HepG2	liver:	n/a	chr11:93367628-93367639
10	CEBPB	chr11:93383817-93384017	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:93375650-93375857	Hela-S3	cervix:	n/a	chr11:93375789-93375800 chr11:93375787-93375800 chr11:93375787-93375800
12	CEBPB	chr11:93375624-93375949	H1-hESC	embryonic stem cell:	n/a	chr11:93375789-93375800 chr11:93375787-93375800 chr11:93375787-93375800
13	CTCF	chr11:93381420-93381570	HVMF	connective:	n/a	chr11:93381517-93381538
14	CTCF	chr11:93385272-93385528	HepG2	liver:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
15	CTCF	chr11:93385352-93385513	SK-N-SH_RA	brain:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
16	CTCF	chr11:93381540-93381690	HVMF	connective:	n/a	n/a
17	CTCF	chr11:93381407-93381607	SK-N-SH_RA	brain:	n/a	chr11:93381517-93381538
18	CTCF	chr11:93381446-93381560	A549	lung:	n/a	chr11:93381517-93381538
19	CTCF	chr11:93385660-93385810	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr11:93385360-93385510	HEK293	kidney:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
21	CTCF	chr11:93381435-93381659	HUVEC	blood vessel:	n/a	chr11:93381517-93381538
22	CTCF	chr11:93385340-93385490	AG04449	skin:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
23	CTCF	chr11:93384960-93385110	GM12873	blood:	n/a	n/a
24	CTCF	chr11:93381460-93381610	Caco-2	colon:	n/a	chr11:93381517-93381538
25	CTCF	chr11:93381460-93381610	Hela-S3	cervix:	n/a	chr11:93381517-93381538
26	CTCF	chr11:93385416-93385477	MCF-7	breast:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432
27	CTCF	chr11:93385300-93385450	HVMF	connective:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
28	CTCF	chr11:93385760-93385910	NHLF	lung:	n/a	n/a
29	CTCF	chr11:93385380-93385530	HA-sp	spinal cord:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
30	CTCF	chr11:93385360-93385510	HPF	lung:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
31	CTCF	chr11:93385655-93385802	GM19238	blood:	n/a	n/a
32	CTCF	chr11:93381440-93381590	GM12864	blood:	n/a	chr11:93381517-93381538
33	CTCF	chr11:93384920-93385070	GM12872	blood:	n/a	n/a
34	CTCF	chr11:93385620-93385770	HPF	lung:	n/a	n/a
35	CTCF	chr11:93381500-93381650	HAc	cerebellar:	n/a	chr11:93381517-93381538
36	CTCF	chr11:93381480-93381630	HMEC	breast:	n/a	chr11:93381517-93381538
37	CTCF	chr11:93381459-93381639	GM10266	blood:	n/a	chr11:93381517-93381538
38	CTCF	chr11:93381420-93381570	GM12868	blood:	n/a	chr11:93381517-93381538
39	CTCF	chr11:93385340-93385490	HEEpiC	esophagus:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
40	CTCF	chr11:93385360-93385510	GM12869	blood:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
41	CTCF	chr11:93385232-93385527	SK-N-SH_RA	brain:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
42	CTCF	chr11:93385701-93385756	Fibrobl	skin:	n/a	n/a
43	CTCF	chr11:93381420-93381570	HUVEC	blood vessel:	n/a	chr11:93381517-93381538
44	CTCF	chr11:93381440-93381590	WERI-Rb-1	eye:	n/a	chr11:93381517-93381538
45	CTCF	chr11:93385340-93385490	RPTEC	kidney:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
46	CTCF	chr11:93381460-93381610	HMF	breast:	n/a	chr11:93381517-93381538
47	CTCF	chr11:93385380-93385530	AG09309	skin:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433
48	CTCF	chr11:93381400-93381550	GM12874	blood:	n/a	chr11:93381517-93381538
49	CTCF	chr11:93381359-93381716	K562	blood:	n/a	chr11:93381517-93381538
50	CTCF	chr11:93385360-93385510	GM12867	blood:	n/a	chr11:93385420-93385430 chr11:93385418-93385434 chr11:93385417-93385435 chr11:93385419-93385432 chr11:93385419-93385432 chr11:93385423-93385432 chr11:93385412-93385433

No.	Distal block	Cell Line	Cell type
1	chr11:93370422..93373225-chr11:93388885..93391216,2	K562	blood:
2	chr11:93385405..93388385-chr17:41464736..41467755,3	K562	blood:
3	chr11:93370422..93373225-chr11:93388885..93391216,2	K562	blood:
4	chr11:92967543..92968491-chr11:93381050..93382178,5	MCF-7	breast:
5	chr11:93360947..93363200-chr11:93376219..93378928,2	K562	blood:
6	chr11:92967484..92968450-chr11:93381041..93381968,2	MCF-7	breast:
7	chr11:93276494..93277057-chr11:93381157..93382010,2	MCF-7	breast:
8	chr11:93373748..93375964-chr11:93381168..93383462,2	K562	blood:
9	chr11:93276243..93277171-chr11:93385273..93385858,2	MCF-7	breast:
10	chr11:93366738..93368495-chr11:93376329..93377877,2	K562	blood:
11	chr11:93384857..93386804-chr11:93393751..93396000,2	MCF-7	breast:
12	chr11:93372093..93374223-chr11:93472267..93473882,2	K562	blood:
13	chr11:93386929..93389387-chr11:93393075..93395163,2	MCF-7	breast:
14	chr11:92967849..92968562-chr11:93381285..93382522,3	K562	blood:
15	chr11:93373748..93375964-chr11:93381168..93383462,2	K562	blood:
16	chr11:93366738..93368495-chr11:93376329..93377877,2	K562	blood:
17	chr11:93384737..93386704-chr11:93387448..93389310,2	K562	blood:
18	chr11:92967004..92969255-chr11:93384967..93385922,6	K562	blood:
19	chr11:93384737..93386704-chr11:93387448..93389310,2	K562	blood:

Variant related genes	Relation type
KIAA1731	TF binding region
ENSG00000188825	chromatin interactions
ENSG00000166002	chromatin interactions
ENSG00000166004	chromatin interactions

Extended variants
information (count: 721 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61918530	chr11:93364502-93364503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568519435	chr11:93364526-93364527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1939575	chr11:93364531-93364532	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs554197317	chr11:93364533-93364534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11823769	chr11:93364583-93364584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370217001	chr11:93364600-93364601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34949293	chr11:93365036-93365037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78234664	chr11:93365045-93365046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148835641	chr11:93365102-93365103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559716102	chr11:93365116-93365117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527317112	chr11:93365155-93365156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117236106	chr11:93365169-93365170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143425484	chr11:93365190-93365191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558857042	chr11:93365191-93365192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531950857	chr11:93371208-93371209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4515928	chr11:93371223-93371224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552264026	chr11:93371233-93371234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562117654	chr11:93371234-93371235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117378898	chr11:93371261-93371262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375047730	chr11:93371284-93371285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs71064767	chr11:93371287-93371288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78401701	chr11:93371310-93371311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4595504	chr11:93371325-93371326	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs139602628	chr11:93371334-93371335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565597209	chr11:93371356-93371357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551693898	chr11:93371378-93371379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570032517	chr11:93371414-93371415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537222920	chr11:93371419-93371420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369435405	chr11:93371457-93371458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534818292	chr11:93371476-93371477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555547354	chr11:93371526-93371527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574409040	chr11:93371538-93371539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149720448	chr11:93371576-93371577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553486270	chr11:93371581-93371582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572040016	chr11:93371613-93371614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545829490	chr11:93371615-93371616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564343893	chr11:93371642-93371643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs58172303	chr11:93371676-93371677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs374415843	chr11:93371723-93371724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543599149	chr11:93371773-93371774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561956798	chr11:93371855-93371856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529363357	chr11:93371940-93371941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111561037	chr11:93371950-93371951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556719372	chr11:93371958-93371959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568403374	chr11:93371967-93371968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs60410024	chr11:93372107-93372108	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs77896058	chr11:93372147-93372148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12290661	chr11:93372152-93372153	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs61229806	chr11:93372183-93372184	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182494911	chr11:93372237-93372238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Schizophrenia	23813976	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93356600-93364600	Weak transcription	Pancreas	Pancrea
2	chr11:93365000-93365200	Enhancers	Pancreas	Pancrea
3	chr11:93371200-93371600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr11:93371600-93375800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr11:93371800-93372200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:93375600-93376200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr11:93375800-93376200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr11:93375800-93376200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr11:93375800-93376200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:93375800-93376200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr11:93375800-93376400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr11:93376600-93377200	Active TSS	Lung	lung
13	chr11:93377600-93378000	Enhancers	HSMMtube	muscle
14	chr11:93377800-93378400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr11:93377800-93378400	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr11:93377800-93379000	Enhancers	HepG2	liver
17	chr11:93378000-93378200	Flanking Active TSS	HSMMtube	muscle
18	chr11:93378000-93378200	Enhancers	Osteobl	bone
19	chr11:93378000-93378400	Enhancers	Primary T cells from cord blood	blood
20	chr11:93378000-93378400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:93378000-93378400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr11:93378000-93378400	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr11:93378000-93378400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr11:93378000-93378400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr11:93378000-93378400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:93378000-93378400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr11:93378000-93378600	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr11:93378000-93378800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr11:93378200-93378400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:93378200-93379000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr11:93378400-93378600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
32	chr11:93378400-93378800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr11:93378400-93378800	Active TSS	Primary T cells from cord blood	blood
34	chr11:93378400-93378800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
35	chr11:93378400-93378800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
36	chr11:93378400-93378800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
37	chr11:93378400-93378800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr11:93378400-93378800	Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr11:93378400-93378800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr11:93378400-93378800	Active TSS	Monocytes-CD14+_RO01746	blood
41	chr11:93378400-93379000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr11:93378400-93379000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr11:93378400-93379000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:93378400-93379000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr11:93378600-93378800	Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr11:93378600-93378800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:93378600-93379000	Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr11:93378600-93379000	Enhancers	GM12878-XiMat	blood
49	chr11:93378600-93379000	Active TSS	Osteobl	bone
50	chr11:93378800-93379000	Enhancers	Primary T cells fromperipheralblood	blood

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