Variant report

Variant	nsv873662
Chromosome Location	chr2:11035430-11061156
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1060)
CpG islands
(count:1099)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1060 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:11040452-11040652	HepG2	liver:	n/a	n/a
2	ATF3	chr2:11060352-11060492	K562	blood:	n/a	chr2:11060445-11060454
3	BACH1	chr2:11051644-11052076	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr2:11051636-11052221	A549	lung:	n/a	chr2:11051929-11051942 chr2:11052159-11052172 chr2:11052183-11052192 chr2:11051938-11051951
5	BHLHE40	chr2:11054509-11054746	A549	lung:	n/a	n/a
6	BHLHE40	chr2:11054444-11054778	HepG2	liver:	n/a	n/a
7	BHLHE40	chr2:11054461-11054830	K562	blood:	n/a	n/a
8	BHLHE40	chr2:11059237-11059702	K562	blood:	n/a	n/a
9	BHLHE40	chr2:11041394-11041682	A549	lung:	n/a	n/a
10	BHLHE40	chr2:11051905-11052116	A549	lung:	n/a	chr2:11051932-11051948 chr2:11051982-11051998
11	CCNT2	chr2:11059203-11059585	K562	blood:	n/a	n/a
12	CEBPB	chr2:11049203-11049518	MCF-7	breast:	n/a	n/a
13	CEBPB	chr2:11038015-11038316	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:11040460-11040660	K562	blood:	n/a	n/a
15	CEBPB	chr2:11041201-11041681	MCF-7	breast:	n/a	n/a
16	CEBPB	chr2:11049294-11049532	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:11041267-11041602	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:11041305-11041594	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:11049223-11049518	K562	blood:	n/a	n/a
20	CEBPB	chr2:11049236-11049538	K562	blood:	n/a	n/a
21	CEBPB	chr2:11041211-11041792	HCT-116	colon:	n/a	n/a
22	CEBPB	chr2:11049224-11049562	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:11049119-11049558	A549	lung:	n/a	n/a
24	CEBPB	chr2:11041259-11041634	A549	lung:	n/a	n/a
25	CEBPB	chr2:11049238-11049520	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:11040337-11040657	HepG2	liver:	n/a	chr2:11040340-11040353
27	CEBPB	chr2:11049205-11049543	A549	lung:	n/a	n/a
28	CEBPB	chr2:11041264-11041616	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:11041109-11041739	A549	lung:	n/a	chr2:11041132-11041145 chr2:11041132-11041143
30	CEBPB	chr2:11051049-11051059	K562	blood:	n/a	n/a
31	CEBPB	chr2:11041190-11041675	A549	lung:	n/a	n/a
32	CEBPB	chr2:11040250-11040558	IMR90	lung:	n/a	chr2:11040340-11040353
33	CEBPB	chr2:11040265-11040675	Hela-S3	cervix:	n/a	chr2:11040340-11040353
34	CEBPB	chr2:11049218-11049525	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:11040234-11040689	A549	lung:	n/a	chr2:11040340-11040353
36	CEBPB	chr2:11051871-11052064	A549	lung:	n/a	chr2:11051993-11052010
37	CHD1	chr2:11052102-11052105	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr2:11054519-11054681	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr2:11060115-11060325	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr2:11051582-11051992	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr2:11049901-11049924	K562	blood:	n/a	n/a
42	CREB1	chr2:11051707-11052236	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr2:11041230-11041631	A549	lung:	n/a	n/a
44	CREB1	chr2:11051746-11052236	A549	lung:	n/a	n/a
45	CREB1	chr2:11051852-11052156	A549	lung:	n/a	n/a
46	CTBP2	chr2:11051456-11052843	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr2:11051680-11051830	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr2:11050245-11050314	Medullo	brain:	n/a	chr2:11050275-11050283
49	CTCF	chr2:11054540-11054690	GM12864	blood:	n/a	chr2:11054583-11054601
50	CTCF	chr2:11051960-11052110	AG09319	gingival:	n/a	chr2:11052009-11052027 chr2:11052011-11052032

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:11052081-11052131	SK-N-MC	brain:	n/a
2	chr2:11052081-11052131	SK-N-MC	brain:	n/a
3	chr2:11054229-11054279	AG09319	gingival:	n/a
4	chr2:11053801-11053851	NT2-D1	testis:	n/a
5	chr2:11052558-11052608	U87	brain:	n/a
6	chr2:11052081-11052131	BJ	skin:	n/a
7	chr2:11059462-11059512	Jurkat	blood:	n/a
8	chr2:11053801-11053851	AG04450	lung:	fetal
9	chr2:11059462-11059512	GM06990	blood:	n/a
10	chr2:11055702-11055752	AG09309	skin:	n/a
11	chr2:11051953-11052003	SK-N-SH_RA	brain:	n/a
12	chr2:11049855-11049905	Hepatocyte	liver:	n/a
13	chr2:11051728-11051778	SK-N-SH	brain:	n/a
14	chr2:11052081-11052131	NHBE	bronchial:	n/a
15	chr2:11051728-11051778	MCF10A-Er-Src	breast:	n/a
16	chr2:11049855-11049905	NB4	blood:	n/a
17	chr2:11051973-11052023	GM12892	blood:	n/a
18	chr2:11051135-11051185	H1-hESC	embryonic stem cell:	embryo
19	chr2:11059462-11059512	HCPEpiC	choroid plexus:	n/a
20	chr2:11052081-11052131	SKMC	muscle:	n/a
21	chr2:11051802-11051852	AG09309	skin:	n/a
22	chr2:11053937-11053987	GM12892	blood:	n/a
23	chr2:11053694-11053744	HCF	heart:	n/a
24	chr2:11053694-11053744	SK-N-SH	brain:	n/a
25	chr2:11051973-11052023	ProgFib	skin:	n/a
26	chr2:11059462-11059512	AG04449	skin:	fetal
27	chr2:11051802-11051852	HEK293	kidney:	embryo
28	chr2:11052558-11052608	HUVEC	blood vessel:	n/a
29	chr2:11059462-11059512	K562	blood:	n/a
30	chr2:11059462-11059512	HCT-116	colon:	n/a
31	chr2:11053801-11053851	BJ	skin:	n/a
32	chr2:11054229-11054279	HCM	heart:	n/a
33	chr2:11052102-11052152	HEEpiC	esophagus:	n/a
34	chr2:11056425-11056475	LNCaP	prostate:	n/a
35	chr2:11056425-11056475	AG10803	skin:	n/a
36	chr2:11051802-11051852	SK-N-MC	brain:	n/a
37	chr2:11055702-11055752	BE2_C	brain:	n/a
38	chr2:11052102-11052152	GM19239	blood:	n/a
39	chr2:11051135-11051185	HEK293	kidney:	embryo
40	chr2:11053801-11053851	H1-hESC	embryonic stem cell:	embryo
41	chr2:11055702-11055752	AG04450	lung:	fetal
42	chr2:11053801-11053851	SAEC	small airway:	n/a
43	chr2:11051135-11051185	HNPCEpiC	eye:	n/a
44	chr2:11052885-11052935	A549	lung:	n/a
45	chr2:11049855-11049905	GM12891	blood:	n/a
46	chr2:11051728-11051778	HMEC	breast:	n/a
47	chr2:11051135-11051185	BE2_C	brain:	n/a
48	chr2:11051802-11051852	Caco-2	colon:	n/a
49	chr2:11053937-11053987	SKMC	muscle:	n/a
50	chr2:11056425-11056475	HCPEpiC	choroid plexus:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:11037226..11040023-chr2:11050517..11054085,3	K562	blood:
2	chr2:11054479..11055033-chr2:11168295..11169158,2	MCF-7	breast:
3	chr2:11055046..11056818-chr2:11058961..11061152,2	MCF-7	breast:
4	chr2:11034858..11036763-chr2:11049175..11051034,2	MCF-7	breast:
5	chr2:11059744..11063370-chr2:11065035..11067309,5	K562	blood:
6	chr2:11040441..11043101-chr2:11053459..11055088,2	MCF-7	breast:
7	chr2:11040441..11043101-chr2:11053459..11055088,2	MCF-7	breast:
8	chr2:10975120..10976125-chr2:11039348..11040908,7	MCF-7	breast:
9	chr2:11038977..11043256-chr2:11044026..11047628,4	MCF-7	breast:
10	chr2:11051947..11053779-chr2:11056308..11059546,3	MCF-7	breast:
11	chr2:11031969..11033770-chr2:11036500..11039498,2	K562	blood:
12	chr2:11049134..11051684-chr2:11064717..11067313,2	K562	blood:
13	chr2:11031810..11033770-chr2:11036437..11038000,2	K562	blood:
14	chr2:10977377..10978983-chr2:11051588..11054422,2	MCF-7	breast:
15	chr2:11057377..11060185-chr2:11071124..11073413,3	MCF-7	breast:
16	chr2:11053891..11056006-chr2:11074074..11075819,2	MCF-7	breast:
17	chr2:10972705..10973216-chr2:11040003..11040608,2	MCF-7	breast:
18	chr2:11035883..11038116-chr2:11040212..11042118,2	K562	blood:
19	chr2:11052090..11054765-chr2:11077274..11080049,2	K562	blood:
20	chr2:10972202..10972851-chr2:11049568..11050477,2	MCF-7	breast:
21	chr2:11060369..11062715-chr2:11069853..11071919,2	MCF-7	breast:
22	chr2:11049631..11050251-chr2:11168175..11168739,2	MCF-7	breast:
23	chr2:11035883..11038116-chr2:11040212..11042118,2	K562	blood:
24	chr2:11005078..11005780-chr2:11040335..11040915,2	MCF-7	breast:
25	chr2:10975612..10976184-chr2:11054131..11054669,2	K562	blood:
26	chr2:11056290..11057062-chr2:11066095..11066758,2	K562	blood:
27	chr2:11044742..11047538-chr2:11051544..11053203,2	MCF-7	breast:
28	chr2:10975313..10976101-chr2:11040499..11041194,2	K562	blood:
29	chr2:11045162..11047241-chr2:11052527..11054468,2	K562	blood:
30	chr2:11034858..11036763-chr2:11049175..11051034,2	MCF-7	breast:
31	chr2:11055046..11056818-chr2:11058961..11061152,2	MCF-7	breast:
32	chr2:11053991..11056052-chr2:11065201..11067671,2	MCF-7	breast:
33	chr2:11054784..11057728-chr2:11061728..11064590,3	MCF-7	breast:
34	chr2:11045162..11047241-chr2:11052527..11054468,2	K562	blood:
35	chr2:10975563..10976087-chr2:11049930..11050449,2	K562	blood:
36	chr2:11054478..11056999-chr2:11265255..11267127,2	MCF-7	breast:
37	chr2:11049420..11051539-chr2:11073823..11076217,2	MCF-7	breast:
38	chr2:11038977..11043256-chr2:11044026..11047628,4	MCF-7	breast:
39	chr2:11029425..11031490-chr2:11033562..11035622,2	MCF-7	breast:

No data

Variant related genes	Relation type
KCNF1	TF binding region
KCNF1	CpG island
ENSG00000143870	chromatin interactions
ENSG00000162975	chromatin interactions

Extended variants
information (count: 1057 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1057 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2884316	chr2:11035430-11035431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373947953	chr2:11035448-11035449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377087240	chr2:11035450-11035451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368595126	chr2:11035458-11035459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555870651	chr2:11035480-11035481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574182950	chr2:11035498-11035499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372864779	chr2:11035532-11035533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528634728	chr2:11035554-11035555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138344295	chr2:11035558-11035559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116458110	chr2:11035572-11035573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564375478	chr2:11035578-11035579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142345202	chr2:11035594-11035595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190550285	chr2:11035628-11035629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562203803	chr2:11035634-11035635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529401828	chr2:11035648-11035649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146471866	chr2:11035691-11035692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557065824	chr2:11035777-11035778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567779074	chr2:11035779-11035780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536325166	chr2:11035780-11035781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139162390	chr2:11035789-11035790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183112326	chr2:11035798-11035799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570309329	chr2:11035823-11035824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187756152	chr2:11035837-11035838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115938840	chr2:11035868-11035869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72781455	chr2:11035871-11035872	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs141508828	chr2:11035956-11035957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150886535	chr2:11036014-11036015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138321528	chr2:11036030-11036031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539596887	chr2:11036031-11036032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557801335	chr2:11036045-11036046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182626700	chr2:11036046-11036047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534806083	chr2:11036052-11036053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543883998	chr2:11036077-11036078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149652520	chr2:11036107-11036108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528912326	chr2:11036125-11036126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541183050	chr2:11036130-11036131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374928182	chr2:11036138-11036139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187592703	chr2:11036161-11036162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533390659	chr2:11036171-11036172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545570980	chr2:11036173-11036174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563682790	chr2:11036193-11036194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531110726	chr2:11036244-11036245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549222235	chr2:11036247-11036248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567731170	chr2:11036251-11036252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528850804	chr2:11036253-11036254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558090526	chr2:11036257-11036258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547201488	chr2:11036300-11036301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368980146	chr2:11036303-11036304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553339015	chr2:11036335-11036336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539295362	chr2:11036361-11036362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD

Chromatin state (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11031200-11044800	Weak transcription	Right Ventricle	heart
2	chr2:11034800-11041400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:11035200-11041400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:11036000-11037000	Enhancers	Placenta	Placenta
5	chr2:11036400-11036600	Enhancers	HMEC	breast
6	chr2:11037000-11040600	Weak transcription	Placenta	Placenta
7	chr2:11037200-11040400	Weak transcription	HMEC	breast
8	chr2:11037800-11038800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:11038200-11038400	Enhancers	Small Intestine	intestine
10	chr2:11038400-11038600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:11038400-11041800	Weak transcription	Small Intestine	intestine
12	chr2:11038800-11040400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:11038800-11041200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:11040400-11041200	Enhancers	A549	lung
15	chr2:11040400-11041800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:11040400-11041800	Enhancers	HMEC	breast
17	chr2:11040400-11042000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr2:11040400-11042000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr2:11040600-11041600	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr2:11040600-11042000	Enhancers	Placenta	Placenta
21	chr2:11040800-11041000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:11040800-11041600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:11040800-11041600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:11040800-11041800	Enhancers	Stomach Mucosa	stomach
25	chr2:11040800-11041800	Enhancers	Hela-S3	cervix
26	chr2:11040800-11042000	Enhancers	Duodenum Mucosa	Duodenum
27	chr2:11041000-11044600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:11041200-11041600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
29	chr2:11041200-11041600	Enhancers	Left Ventricle	heart
30	chr2:11041200-11041800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:11041200-11041800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr2:11041200-11041800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr2:11041200-11041800	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr2:11041200-11041800	Flanking Active TSS	A549	lung
35	chr2:11041200-11042000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr2:11041200-11042000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:11041200-11042000	Enhancers	HUVEC	blood vessel
38	chr2:11041200-11042000	Enhancers	NHEK	skin
39	chr2:11041400-11041600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:11041400-11041600	Enhancers	Right Atrium	heart
41	chr2:11041400-11041800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr2:11041400-11041800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr2:11041400-11042000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:11041400-11042000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:11041400-11042000	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr2:11041400-11042000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr2:11041600-11041800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:11041600-11042000	Enhancers	HepG2	liver
49	chr2:11041800-11042000	Enhancers	A549	lung
50	chr2:11041800-11042200	Enhancers	Small Intestine	intestine

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