Variant report

Variant	esv1791841
Chromosome Location	chr2:189811074-189864582
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	ATF2	chr2:189843359-189843871	GM12878	blood:	n/a	n/a
2	ATF2	chr2:189843358-189843943	GM12878	blood:	n/a	n/a
3	BACH1	chr2:189849679-189849710	K562	blood:	n/a	n/a
4	BATF	chr2:189843499-189843807	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:189843396-189843873	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:189843520-189843778	GM12878	blood:	n/a	n/a
7	BCL3	chr2:189843444-189843804	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:189843031-189843813	GM12878	blood:	n/a	n/a
9	CCNT2	chr2:189814185-189814456	K562	blood:	n/a	n/a
10	CEBPB	chr2:189827410-189827675	HepG2	liver:	n/a	chr2:189827520-189827531
11	CEBPB	chr2:189837469-189837706	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr2:189817691-189817963	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:189822399-189822740	HepG2	liver:	n/a	chr2:189822561-189822572
14	CEBPB	chr2:189822384-189822731	IMR90	lung:	n/a	chr2:189822561-189822572
15	CEBPB	chr2:189862109-189862340	HepG2	liver:	n/a	chr2:189862184-189862195 chr2:189862182-189862195
16	CEBPB	chr2:189834071-189834731	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:189834976-189835579	IMR90	lung:	n/a	chr2:189835050-189835063
18	CEBPB	chr2:189849485-189849678	A549	lung:	n/a	n/a
19	CEBPB	chr2:189822393-189822712	A549	lung:	n/a	chr2:189822561-189822572
20	CEBPB	chr2:189848532-189849169	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:189837555-189837665	K562	blood:	n/a	n/a
22	CTCF	chr2:189848260-189848410	NHDF-neo	bronchial:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
23	CTCF	chr2:189843082-189843239	GM19238	blood:	n/a	n/a
24	CTCF	chr2:189849040-189849190	HA-sp	spinal cord:	n/a	chr2:189849095-189849116
25	CTCF	chr2:189843120-189843270	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr2:189849000-189849150	HCT-116	colon:	n/a	chr2:189849095-189849116
27	CTCF	chr2:189848880-189849030	A549	lung:	n/a	n/a
28	CTCF	chr2:189843079-189843317	A549	lung:	n/a	n/a
29	CTCF	chr2:189848300-189848450	NHEK	skin:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
30	CTCF	chr2:189840640-189840790	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr2:189848300-189848450	HRPEpiC	eye:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
32	CTCF	chr2:189849000-189849150	HCPEpiC	choroid plexus:	n/a	chr2:189849095-189849116
33	CTCF	chr2:189848240-189848390	GM12873	blood:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
34	CTCF	chr2:189843120-189843270	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr2:189848320-189848470	GM12872	blood:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
36	CTCF	chr2:189841480-189841630	HMF	breast:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
37	CTCF	chr2:189843120-189843270	Caco-2	colon:	n/a	n/a
38	CTCF	chr2:189841500-189841650	HPF	lung:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
39	CTCF	chr2:189841298-189841868	HCT-116	colon:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
40	CTCF	chr2:189848240-189848390	WERI-Rb-1	eye:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
41	CTCF	chr2:189849060-189849210	AG04450	lung:	n/a	chr2:189849095-189849116
42	CTCF	chr2:189843120-189843270	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr2:189841500-189841650	AG09319	gingival:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
44	CTCF	chr2:189843092-189843243	GM19239	blood:	n/a	n/a
45	CTCF	chr2:189843100-189843250	HRE	kidney:	n/a	n/a
46	CTCF	chr2:189848218-189848445	MCF-7	breast:	n/a	chr2:189848338-189848354 chr2:189848337-189848355
47	CTCF	chr2:189841495-189841703	MCF-7	breast:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
48	CTCF	chr2:189848160-189848310	WI-38	lung:	n/a	n/a
49	CTCF	chr2:189841506-189841688	Lung_OC	lung:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597
50	CTCF	chr2:189841560-189841710	AG04450	lung:	n/a	chr2:189841574-189841595 chr2:189841586-189841593 chr2:189841580-189841596 chr2:189841579-189841597

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:189859022-189859072	SK-N-SH_RA	brain:	n/a
2	chr2:189859022-189859072	SK-N-SH_RA	brain:	n/a
3	chr2:189834269-189834319	A549	lung:	n/a
4	chr2:189839474-189839524	AG04449	skin:	fetal
5	chr2:189834269-189834319	HIPEpiC	eye:	n/a
6	chr2:189850571-189850621	AG04450	lung:	fetal
7	chr2:189839015-189839065	HepG2	liver:	n/a
8	chr2:189839015-189839065	PFSK-1	brain:	n/a
9	chr2:189837928-189837978	PFSK-1	brain:	n/a
10	chr2:189834269-189834319	HepG2	liver:	n/a
11	chr2:189839474-189839524	MCF-7	breast:	n/a
12	chr2:189839015-189839065	HEEpiC	esophagus:	n/a
13	chr2:189834269-189834319	HRPEpiC	eye:	n/a
14	chr2:189839015-189839065	HCT-116	colon:	n/a
15	chr2:189837928-189837978	Hela-S3	cervix:	n/a
16	chr2:189834269-189834319	GM12892	blood:	n/a
17	chr2:189850571-189850621	HCPEpiC	choroid plexus:	n/a
18	chr2:189837928-189837978	HEEpiC	esophagus:	n/a
19	chr2:189834269-189834319	LNCaP	prostate:	n/a
20	chr2:189850571-189850621	AG10803	skin:	n/a
21	chr2:189859022-189859072	AG10803	skin:	n/a
22	chr2:189839474-189839524	HMEC	breast:	n/a
23	chr2:189839120-189839170	AoSMC	blood vessel:	n/a
24	chr2:189859022-189859072	NHBE	bronchial:	n/a
25	chr2:189839474-189839524	AG09309	skin:	n/a
26	chr2:189839120-189839170	GM12878	blood:	n/a
27	chr2:189859022-189859072	NB4	blood:	n/a
28	chr2:189839474-189839524	GM06990	blood:	n/a
29	chr2:189839120-189839170	MCF-7	breast:	n/a
30	chr2:189834269-189834319	AG04449	skin:	fetal
31	chr2:189839015-189839065	HL-60	blood:	n/a
32	chr2:189859022-189859072	HCPEpiC	choroid plexus:	n/a
33	chr2:189837928-189837978	SAEC	small airway:	n/a
34	chr2:189839120-189839170	HL-60	blood:	n/a
35	chr2:189859022-189859072	HNPCEpiC	eye:	n/a
36	chr2:189839120-189839170	SK-N-MC	brain:	n/a
37	chr2:189850571-189850621	HRCEpiC	kidney:	n/a
38	chr2:189839474-189839524	HUVEC	blood vessel:	n/a
39	chr2:189850571-189850621	HRE	kidney:	n/a
40	chr2:189834269-189834319	MCF-7	breast:	n/a
41	chr2:189850571-189850621	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:189839015-189839065	HCM	heart:	n/a
43	chr2:189859022-189859072	AG04449	skin:	fetal
44	chr2:189839120-189839170	SAEC	small airway:	n/a
45	chr2:189859022-189859072	HCM	heart:	n/a
46	chr2:189850571-189850621	HRPEpiC	eye:	n/a
47	chr2:189834269-189834319	RPTEC	kidney:	n/a
48	chr2:189850571-189850621	NT2-D1	testis:	n/a
49	chr2:189839015-189839065	GM19239	blood:	n/a
50	chr2:189839474-189839524	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:189822907..189823896-chr8:96619389..96620128,2	MCF-7	breast:
2	chr2:189840465..189844920-chr2:189846827..189849857,3	MCF-7	breast:
3	chr2:189847939..189848875-chr2:190211912..190212800,2	MCF-7	breast:
4	chr2:189378368..189379278-chr2:189848607..189850003,3	MCF-7	breast:
5	chr2:189465598..189467415-chr2:189847399..189849894,2	MCF-7	breast:
6	chr2:189630030..189631002-chr2:189840905..189842141,9	MCF-7	breast:
7	chr2:189467608..189469705-chr2:189839952..189841474,2	MCF-7	breast:
8	chr2:189843846..189845833-chr2:189848371..189850816,2	K562	blood:
9	chr2:189388967..189389813-chr2:189842832..189843620,3	MCF-7	breast:
10	chr2:188459276..188460160-chr2:189841055..189841647,2	MCF-7	breast:
11	chr2:189848219..189848800-chr2:190276497..190277312,2	MCF-7	breast:
12	chr2:189849262..189851265-chr2:189851542..189854419,2	MCF-7	breast:
13	chr2:189468604..189471181-chr2:189847592..189850287,2	MCF-7	breast:
14	chr2:189460620..189463074-chr2:189843714..189846986,3	MCF-7	breast:
15	chr2:189652355..189655667-chr2:189836980..189839231,3	MCF-7	breast:
16	chr2:189849262..189851265-chr2:189851542..189854419,2	MCF-7	breast:
17	chr2:189389424..189389930-chr2:189841189..189841702,2	MCF-7	breast:
18	chr2:189843846..189845833-chr2:189848371..189850816,2	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1245b-3p	chr2:189842825-189842846	MIMAT0019951
hsa-miR-3606-3p	chr2:189860397-189860417	MIMAT0022965
hsa-miR-3606-5p	chr2:189860371-189860391	MIMAT0017983
hsa-miR-1245b-5p	chr2:189842859-189842879	MIMAT0019950
hsa-miR-1245a	chr2:189842862-189842882	MIMAT0005897

No.	miRNA target gene	miRNA name	Chromosome Location
1	COL3A1	hsa-miR-29b-3p	chr2:189857643-189857664
2	COL3A1	hsa-miR-29c-3p	chr2:189857643-189857664
3	COL3A1	hsa-miR-29b-3p	chr2:189859016-189859038
4	COL3A1	hsa-miR-29c-3p	chr2:189859018-189859038

Variant related genes	Relation type
MIR1245A	TF binding region
COL3A1	TF binding region
MIR1245A	CpG island
COL3A1	CpG island
ENSG00000174325	chromatin interactions
ENSG00000221502	chromatin interactions
BRCA2	Mature miRNA region

Extended variants
information (count: 1988 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1988 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10931389	chr2:189811074-189811075	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564924058	chr2:189811080-189811081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532567919	chr2:189811158-189811159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373662530	chr2:189811170-189811171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547773693	chr2:189811198-189811199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs180956220	chr2:189811247-189811248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76088839	chr2:189811294-189811295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548753566	chr2:189811308-189811309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185950307	chr2:189811359-189811360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537110003	chr2:189811379-189811380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190928626	chr2:189811406-189811407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576885131	chr2:189811416-189811417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556348084	chr2:189811463-189811464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568590239	chr2:189811505-189811506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571422705	chr2:189811552-189811553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34738801	chr2:189811605-189811606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534660405	chr2:189811612-189811613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552982646	chr2:189811649-189811650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140886389	chr2:189811678-189811679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539093726	chr2:189811686-189811687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541758609	chr2:189811763-189811764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563113586	chr2:189811764-189811765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79043098	chr2:189811829-189811830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138039822	chr2:189811895-189811896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535802718	chr2:189811898-189811899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370821254	chr2:189811913-189811914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543491340	chr2:189811914-189811915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565087216	chr2:189811919-189811920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532394690	chr2:189811920-189811921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375206696	chr2:189811926-189811927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149738794	chr2:189812010-189812011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572768510	chr2:189812020-189812021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182029809	chr2:189812040-189812041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112215531	chr2:189812041-189812042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59937878	chr2:189812067-189812068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373537828	chr2:189812068-189812069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186219088	chr2:189812090-189812091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187206990	chr2:189812116-189812117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113821626	chr2:189812137-189812138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7568409	chr2:189812145-189812146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs183573927	chr2:189812148-189812149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145574508	chr2:189812149-189812150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544013539	chr2:189812159-189812160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562194955	chr2:189812192-189812193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574201038	chr2:189812200-189812201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188060563	chr2:189812261-189812262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7609210	chr2:189812267-189812268	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs199733246	chr2:189812329-189812330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373593152	chr2:189812372-189812373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191279497	chr2:189812387-189812388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Colorectal cancer	16912164	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:189807600-189817600	Weak transcription	Aorta	Aorta
2	chr2:189809600-189813800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:189811000-189811400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:189813600-189813800	Weak transcription	Pancreas	Pancrea
5	chr2:189813800-189814000	ZNF genes & repeats	Pancreas	Pancrea
6	chr2:189813800-189814400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:189814000-189814400	Bivalent Enhancer	HepG2	liver
8	chr2:189814000-189830800	Weak transcription	Pancreas	Pancrea
9	chr2:189821800-189822400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:189822400-189823800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:189826400-189828600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:189828000-189828400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:189828000-189828800	Enhancers	Adipose Nuclei	Adipose
14	chr2:189828000-189828800	Enhancers	Fetal Lung	lung
15	chr2:189828200-189828400	Enhancers	Fetal Kidney	kidney
16	chr2:189828400-189829200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr2:189828400-189838400	Weak transcription	Fetal Kidney	kidney
18	chr2:189828600-189828800	Enhancers	Colon Smooth Muscle	Colon
19	chr2:189828600-189828800	Enhancers	Fetal Stomach	stomach
20	chr2:189828600-189830600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:189828800-189829000	Enhancers	NHDF-Ad	bronchial
22	chr2:189828800-189829400	Weak transcription	Adipose Nuclei	Adipose
23	chr2:189828800-189829800	Weak transcription	Fetal Lung	lung
24	chr2:189829000-189830800	Weak transcription	NHDF-Ad	bronchial
25	chr2:189829000-189833600	Weak transcription	Fetal Stomach	stomach
26	chr2:189829200-189830400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:189829200-189833600	Weak transcription	NHLF	lung
28	chr2:189829400-189829600	Enhancers	Adipose Nuclei	Adipose
29	chr2:189829600-189830600	Weak transcription	Adipose Nuclei	Adipose
30	chr2:189829800-189830800	Enhancers	Fetal Lung	lung
31	chr2:189830200-189830800	Weak transcription	Colon Smooth Muscle	Colon
32	chr2:189830400-189830600	Enhancers	Aorta	Aorta
33	chr2:189830400-189830600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr2:189830400-189831200	Enhancers	Ovary	ovary
35	chr2:189830400-189832000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:189830600-189831200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:189830600-189831600	Weak transcription	Aorta	Aorta
38	chr2:189830600-189832000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr2:189830600-189832200	Enhancers	Adipose Nuclei	Adipose
40	chr2:189830800-189831000	Enhancers	Pancreas	Pancrea
41	chr2:189830800-189831200	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr2:189830800-189831200	Flanking Active TSS	Fetal Lung	lung
43	chr2:189830800-189831200	Enhancers	Fetal Muscle Leg	muscle
44	chr2:189830800-189831400	Enhancers	Colon Smooth Muscle	Colon
45	chr2:189830800-189832000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr2:189830800-189832000	Enhancers	Rectal Smooth Muscle	rectum
47	chr2:189830800-189833600	Enhancers	NHDF-Ad	bronchial
48	chr2:189830800-189839000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr2:189831200-189831600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr2:189831200-189831600	Weak transcription	Fetal Muscle Leg	muscle

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