Variant report

Variant	esv3432662
Chromosome Location	chr11:107877494-107880467
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	chr11:107879369-107880272	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:107880415-107881387	K562	blood:	n/a	n/a
3	ATF2	chr11:107879368-107880387	H1-hESC	embryonic stem cell:	n/a	chr11:107879925-107879939
4	ATF2	chr11:107879300-107880307	GM12878	blood:	n/a	chr11:107879925-107879939
5	ATF2	chr11:107879756-107880186	H1-hESC	embryonic stem cell:	n/a	chr11:107879925-107879939
6	ATF2	chr11:107879307-107880289	GM12878	blood:	n/a	chr11:107879925-107879939
7	ATF3	chr11:107879420-107879912	GM12878	blood:	n/a	chr11:107879642-107879662 chr11:107879642-107879651 chr11:107879631-107879651
8	ATF3	chr11:107879375-107879895	H1-hESC	embryonic stem cell:	n/a	chr11:107879642-107879662 chr11:107879642-107879651 chr11:107879631-107879651
9	ATF3	chr11:107879470-107879809	HepG2	liver:	n/a	chr11:107879642-107879662 chr11:107879642-107879651 chr11:107879631-107879651
10	ATF3	chr11:107879468-107880044	K562	blood:	n/a	chr11:107879642-107879662 chr11:107879642-107879651 chr11:107879631-107879651
11	BACH1	chr11:107879013-107879148	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:107879389-107880298	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr11:107879633-107880144	A549	lung:	n/a	chr11:107879707-107879716
14	BCLAF1	chr11:107879253-107880362	GM12878	blood:	n/a	chr11:107879707-107879716
15	BHLHE40	chr11:107879335-107880402	HepG2	liver:	n/a	chr11:107879640-107879653 chr11:107879643-107879652 chr11:107879641-107879650 chr11:107879636-107879657 chr11:107879642-107879651 chr11:107879642-107879651
16	BHLHE40	chr11:107879360-107880430	GM12878	blood:	n/a	chr11:107879640-107879653 chr11:107879643-107879652 chr11:107879641-107879650 chr11:107879636-107879657 chr11:107879642-107879651 chr11:107879642-107879651
17	BHLHE40	chr11:107879304-107880705	K562	blood:	n/a	chr11:107879640-107879653 chr11:107879643-107879652 chr11:107879641-107879650 chr11:107879636-107879657 chr11:107879642-107879651 chr11:107879642-107879651
18	BRCA1	chr11:107879218-107880299	Hela-S3	cervix:	n/a	chr11:107880049-107880058
19	BRCA1	chr11:107879497-107880287	HepG2	liver:	n/a	chr11:107880049-107880058
20	BRCA1	chr11:107879437-107880814	H1-hESC	embryonic stem cell:	n/a	chr11:107880049-107880058
21	BRCA1	chr11:107879497-107880374	GM12878	blood:	n/a	chr11:107880049-107880058
22	CBX3	chr11:107879289-107880291	K562	blood:	n/a	n/a
23	CBX3	chr11:107879332-107879914	K562	blood:	n/a	n/a
24	CCNT2	chr11:107879419-107880523	K562	blood:	n/a	n/a
25	CEBPB	chr11:107879816-107880206	K562	blood:	n/a	n/a
26	CEBPB	chr11:107879399-107879894	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:107879548-107879879	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:107879327-107879989	GM12878	blood:	n/a	n/a
29	CEBPD	chr11:107879566-107880096	HepG2	liver:	n/a	n/a
30	CEBPD	chr11:107879362-107880214	K562	blood:	n/a	n/a
31	CHD1	chr11:107879599-107880708	H1-hESC	embryonic stem cell:	n/a	chr11:107880049-107880058
32	CHD1	chr11:107879343-107880360	GM12878	blood:	n/a	chr11:107879515-107879525 chr11:107880049-107880058
33	CHD2	chr11:107879427-107880415	Hela-S3	cervix:	n/a	chr11:107879515-107879525 chr11:107880049-107880058
34	CHD2	chr11:107879385-107880429	HepG2	liver:	n/a	chr11:107879515-107879525 chr11:107880049-107880058
35	CHD2	chr11:107879358-107880747	K562	blood:	n/a	chr11:107879515-107879525 chr11:107880049-107880058
36	CHD2	chr11:107879380-107880677	GM12878	blood:	n/a	chr11:107879515-107879525 chr11:107880049-107880058
37	CHD2	chr11:107879358-107880701	H1-hESC	embryonic stem cell:	n/a	chr11:107879515-107879525 chr11:107880049-107880058
38	CREB1	chr11:107879279-107880460	HepG2	liver:	n/a	chr11:107879645-107879658
39	CREB1	chr11:107879336-107879820	A549	lung:	n/a	chr11:107879645-107879658
40	CREB1	chr11:107879329-107879936	H1-hESC	embryonic stem cell:	n/a	chr11:107879645-107879658
41	CREB1	chr11:107879839-107880229	A549	lung:	n/a	n/a
42	CTCF	chr11:107879500-107879650	AG09309	skin:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561
43	CTCF	chr11:107879480-107879630	NHEK	skin:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561
44	CTCF	chr11:107879480-107879630	AG04450	lung:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561
45	CTCF	chr11:107879420-107879570	AG04450	lung:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561
46	CTCF	chr11:107879460-107879610	A549	lung:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561
47	CTCF	chr11:107879443-107879656	HepG2	liver:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561
48	CTCF	chr11:107879415-107879695	H1-hESC	embryonic stem cell:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561
49	CTCF	chr11:107879405-107879715	ProgFib	skin:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561
50	CTCF	chr11:107879420-107879570	GM12801	blood:	n/a	chr11:107879544-107879560 chr11:107879546-107879559 chr11:107879545-107879566 chr11:107879543-107879561

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107879431-107879481	HL-60	blood:	n/a
2	chr11:107879431-107879481	HL-60	blood:	n/a
3	chr11:107879052-107879102	HAEpiC	amniotic membrane:	n/a
4	chr11:107880029-107880079	NHDF-neo	bronchial:	n/a
5	chr11:107880029-107880079	HRPEpiC	eye:	n/a
6	chr11:107879401-107879451	AoSMC	blood vessel:	n/a
7	chr11:107880418-107880468	HRCEpiC	kidney:	n/a
8	chr11:107879177-107879227	AoSMC	blood vessel:	n/a
9	chr11:107879501-107879551	GM12891	blood:	n/a
10	chr11:107879431-107879481	HepG2	liver:	n/a
11	chr11:107880029-107880079	MCF10A-Er-Src	breast:	n/a
12	chr11:107880372-107880422	BJ	skin:	n/a
13	chr11:107880418-107880468	MCF-7	breast:	n/a
14	chr11:107880372-107880422	SKMC	muscle:	n/a
15	chr11:107880372-107880422	HAEpiC	amniotic membrane:	n/a
16	chr11:107879431-107879481	HCT-116	colon:	n/a
17	chr11:107880418-107880468	NHBE	bronchial:	n/a
18	chr11:107880052-107880102	NH-A	brain:	n/a
19	chr11:107880418-107880468	NH-A	brain:	n/a
20	chr11:107879431-107879481	ovcar-3	ovarian:	n/a
21	chr11:107880418-107880468	SAEC	small airway:	n/a
22	chr11:107879431-107879481	NB4	blood:	n/a
23	chr11:107879063-107879113	PFSK-1	brain:	n/a
24	chr11:107879063-107879113	NHDF-neo	bronchial:	n/a
25	chr11:107879401-107879451	HMEC	breast:	n/a
26	chr11:107879052-107879102	U87	brain:	n/a
27	chr11:107879177-107879227	HCT-116	colon:	n/a
28	chr11:107880029-107880079	RPTEC	kidney:	n/a
29	chr11:107879501-107879551	NHBE	bronchial:	n/a
30	chr11:107879177-107879227	A549	lung:	n/a
31	chr11:107880372-107880422	SK-N-MC	brain:	n/a
32	chr11:107879052-107879102	Caco-2	colon:	n/a
33	chr11:107879177-107879227	HCF	heart:	n/a
34	chr11:107880418-107880468	HEEpiC	esophagus:	n/a
35	chr11:107879501-107879551	SK-N-MC	brain:	n/a
36	chr11:107879177-107879227	BJ	skin:	n/a
37	chr11:107879052-107879102	GM19239	blood:	n/a
38	chr11:107880052-107880102	IMR90	lung:	fetal
39	chr11:107879063-107879113	Caco-2	colon:	n/a
40	chr11:107880372-107880422	ECC-1	luminal epithelium:	n/a
41	chr11:107879063-107879113	HNPCEpiC	eye:	n/a
42	chr11:107880372-107880422	PANC-1	pancreas:	n/a
43	chr11:107879431-107879481	NHDF-neo	bronchial:	n/a
44	chr11:107880029-107880079	U87	brain:	n/a
45	chr11:107880082-107880132	AoSMC	blood vessel:	n/a
46	chr11:107879063-107879113	GM19239	blood:	n/a
47	chr11:107879052-107879102	K562	blood:	n/a
48	chr11:107879501-107879551	BJ	skin:	n/a
49	chr11:107880082-107880132	HRE	kidney:	n/a
50	chr11:107879063-107879113	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr11:107879008..107882817-chr11:107991227..107994837,4	K562	blood:
2	chr11:107879008..107882104-chr11:107991227..107994837,4	K562	blood:
3	chr11:107878949..107881765-chr11:111797372..111799123,2	K562	blood:
4	chr11:107879542..107880211-chr14:24740204..24740754,2	NB4	blood:
5	chr11:107871230..107872781-chr11:107876755..107878294,2	K562	blood:
6	chr11:107728941..107731899-chr11:107878493..107880123,2	K562	blood:
7	chr11:107858533..107861411-chr11:107880096..107882320,2	K562	blood:
8	chr11:107879617..107881507-chr11:108535769..108537352,2	K562	blood:
9	chr11:107879595..107880498-chr17:5322749..5323427,2	NB4	blood:

Variant related genes	Relation type
CUL5	TF binding region
CUL5	CpG island
ENSG00000178105	chromatin interactions
ENSG00000129197	chromatin interactions
ENSG00000108559	chromatin interactions
ENSG00000150764	chromatin interactions
ENSG00000075239	chromatin interactions
ENSG00000100949	chromatin interactions
ENSG00000255467	chromatin interactions
ENSG00000110660	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545343000	chr11:107877519-107877520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537067806	chr11:107877539-107877540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553937483	chr11:107877560-107877561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572589103	chr11:107877643-107877644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543087888	chr11:107877700-107877701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183028808	chr11:107877763-107877764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566982513	chr11:107877836-107877837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187129748	chr11:107877842-107877843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191910719	chr11:107877859-107877860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75582793	chr11:107877861-107877862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114378212	chr11:107877869-107877870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543789530	chr11:107877929-107877930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144268936	chr11:107877951-107877952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533253483	chr11:107877982-107877983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79713500	chr11:107878032-107878033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs117953901	chr11:107878115-107878116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557022079	chr11:107878120-107878121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549176258	chr11:107878221-107878222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567209570	chr11:107878236-107878237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537552414	chr11:107878262-107878263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141732754	chr11:107878269-107878270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184156612	chr11:107878278-107878279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150572929	chr11:107878280-107878281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554073870	chr11:107878299-107878300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140594110	chr11:107878394-107878395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542822455	chr11:107878423-107878424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555146019	chr11:107878433-107878434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201663425	chr11:107878479-107878480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141065532	chr11:107878481-107878482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79502322	chr11:107878482-107878483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377022965	chr11:107878483-107878484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200763751	chr11:107878491-107878492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529976832	chr11:107878498-107878499	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543983289	chr11:107878499-107878500	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs75750062	chr11:107878501-107878502	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs76082777	chr11:107878504-107878505	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs565258624	chr11:107878523-107878524	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs572954673	chr11:107878544-107878545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188851612	chr11:107878579-107878580	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs541453102	chr11:107878594-107878595	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560159421	chr11:107878595-107878596	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs527586948	chr11:107878641-107878642	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs147855445	chr11:107878709-107878710	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs139415234	chr11:107878710-107878711	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs368255549	chr11:107878715-107878716	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs549491568	chr11:107878761-107878762	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570892403	chr11:107878768-107878769	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs191136837	chr11:107878802-107878803	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs182241311	chr11:107878803-107878804	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs186845489	chr11:107878804-107878805	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	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
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107863600-107879400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:107871200-107879200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:107871200-107879400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:107873600-107879000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:107875800-107878800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:107875800-107879000	Weak transcription	A549	lung
7	chr11:107876000-107879000	Weak transcription	K562	blood
8	chr11:107878200-107878400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr11:107878800-107879000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:107878800-107879000	Enhancers	Colon Smooth Muscle	Colon
11	chr11:107878800-107879000	Enhancers	Stomach Smooth Muscle	stomach
12	chr11:107878800-107879000	Enhancers	Dnd41	blood
13	chr11:107878800-107879000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr11:107878800-107879200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:107878800-107879200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr11:107878800-107881200	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr11:107879000-107879200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr11:107879000-107879200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr11:107879000-107879200	Enhancers	Primary B cells from cord blood	blood
20	chr11:107879000-107879200	Enhancers	Primary B cells from peripheral blood	blood
21	chr11:107879000-107879200	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr11:107879000-107879200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr11:107879000-107879200	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr11:107879000-107879200	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr11:107879000-107879200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr11:107879000-107879200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:107879000-107879200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr11:107879000-107879200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr11:107879000-107879200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr11:107879000-107879200	Enhancers	Liver	Liver
31	chr11:107879000-107879200	Flanking Active TSS	A549	lung
32	chr11:107879000-107879200	Enhancers	HMEC	breast
33	chr11:107879000-107879200	Enhancers	K562	blood
34	chr11:107879000-107879200	Enhancers	NH-A	brain
35	chr11:107879000-107879200	Enhancers	NHDF-Ad	bronchial
36	chr11:107879000-107879200	Enhancers	Osteobl	bone
37	chr11:107879000-107879400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:107879000-107879400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:107879000-107879400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr11:107879000-107879400	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr11:107879000-107879400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:107879000-107879400	Enhancers	Aorta	Aorta
43	chr11:107879000-107879400	Flanking Active TSS	Colon Smooth Muscle	Colon
44	chr11:107879000-107879400	Enhancers	Placenta	Placenta
45	chr11:107879000-107879400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr11:107879000-107879600	Enhancers	Small Intestine	intestine
47	chr11:107879000-107879600	Flanking Active TSS	Dnd41	blood
48	chr11:107879000-107880400	Active TSS	Fetal Brain Female	brain
49	chr11:107879000-107880800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:107879000-107881000	Active TSS	Stomach Smooth Muscle	stomach

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