Variant report

Variant	nsv458008
Chromosome Location	chr2:57626992-57671691
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	BCL3	chr2:57656947-57657199	GM12878	blood:	n/a	n/a
2	CEBPB	chr2:57635068-57635356	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:57671256-57671580	Hela-S3	cervix:	n/a	chr2:57671434-57671445
4	CEBPB	chr2:57653300-57653715	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:57644218-57644262	A549	lung:	n/a	n/a
6	CEBPB	chr2:57671064-57671644	HCT-116	colon:	n/a	chr2:57671434-57671445
7	CEBPB	chr2:57670883-57671690	HCT-116	colon:	n/a	chr2:57671434-57671445
8	CEBPB	chr2:57630938-57631021	A549	lung:	n/a	chr2:57630962-57630975
9	CEBPB	chr2:57671275-57671658	A549	lung:	n/a	chr2:57671434-57671445
10	CEBPB	chr2:57671313-57671586	IMR90	lung:	n/a	chr2:57671434-57671445
11	CEBPB	chr2:57671281-57671572	HepG2	liver:	n/a	chr2:57671434-57671445
12	E2F4	chr2:57641977-57642145	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr2:57670971-57671240	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr2:57657061-57657255	GM12878	blood:	n/a	n/a
15	EP300	chr2:57670897-57671693	SK-N-SH	brain:	n/a	n/a
16	EP300	chr2:57661785-57661845	GM12878	blood:	n/a	n/a
17	EP300	chr2:57670981-57671608	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr2:57671034-57671504	SK-N-SH_RA	brain:	n/a	n/a
19	FOS	chr2:57671103-57671649	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr2:57662110-57662426	MCF10A-Er-Src	breast:	n/a	chr2:57662249-57662257
21	FOS	chr2:57659821-57659982	MCF10A-Er-Src	breast:	n/a	chr2:57659822-57659829 chr2:57659821-57659831 chr2:57659822-57659830
22	FOS	chr2:57662114-57662426	MCF10A-Er-Src	breast:	n/a	chr2:57662249-57662257
23	FOS	chr2:57659818-57659959	MCF10A-Er-Src	breast:	n/a	chr2:57659822-57659829 chr2:57659821-57659831 chr2:57659822-57659830
24	FOS	chr2:57671355-57671608	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr2:57671252-57671525	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr2:57659796-57659996	MCF10A-Er-Src	breast:	n/a	chr2:57659822-57659829 chr2:57659821-57659831 chr2:57659822-57659830
27	FOS	chr2:57671303-57671561	MCF10A-Er-Src	breast:	n/a	n/a
28	FOSL1	chr2:57662150-57662490	HCT-116	colon:	n/a	chr2:57662249-57662257
29	FOSL1	chr2:57661997-57662428	HCT-116	colon:	n/a	chr2:57662249-57662257
30	FOSL2	chr2:57661987-57662533	SK-N-SH	brain:	n/a	chr2:57662249-57662257
31	FOSL2	chr2:57670922-57672647	SK-N-SH	brain:	n/a	n/a
32	FOSL2	chr2:57659610-57660143	SK-N-SH	brain:	n/a	chr2:57659822-57659829 chr2:57659770-57659779 chr2:57659821-57659831 chr2:57659822-57659830
33	FOXA1	chr2:57646122-57646426	HepG2	liver:	n/a	n/a
34	FOXA2	chr2:57646028-57646632	A549	lung:	n/a	n/a
35	FOXM1	chr2:57656909-57657355	GM12878	blood:	n/a	n/a
36	FOXP2	chr2:57634899-57635155	SK-N-MC	brain:	n/a	n/a
37	GATA3	chr2:57629136-57629509	SK-N-SH	brain:	n/a	chr2:57629263-57629272 chr2:57629285-57629294 chr2:57629256-57629277 chr2:57629259-57629275 chr2:57629259-57629275
38	GATA3	chr2:57629174-57629375	SH-SY5Y	brain:	n/a	chr2:57629263-57629272 chr2:57629285-57629294 chr2:57629256-57629277 chr2:57629259-57629275 chr2:57629259-57629275
39	GATA3	chr2:57670884-57672678	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr2:57670869-57672739	SK-N-SH	brain:	n/a	n/a
41	JUND	chr2:57662138-57662530	SK-N-SH	brain:	n/a	chr2:57662249-57662257
42	JUND	chr2:57653207-57653464	HepG2	liver:	n/a	n/a
43	JUND	chr2:57670895-57671559	HCT-116	colon:	n/a	n/a
44	JUND	chr2:57670934-57672655	SK-N-SH	brain:	n/a	chr2:57672033-57672044
45	JUND	chr2:57670920-57671595	SK-N-SH	brain:	n/a	n/a
46	JUND	chr2:57659581-57660024	SK-N-SH	brain:	n/a	chr2:57659822-57659829 chr2:57659770-57659779 chr2:57659821-57659831 chr2:57659822-57659830
47	JUND	chr2:57670719-57672659	SK-N-SH	brain:	n/a	chr2:57672033-57672044
48	JUND	chr2:57670915-57671630	HCT-116	colon:	n/a	n/a
49	MAFF	chr2:57671280-57671487	HepG2	liver:	n/a	chr2:57671386-57671404
50	MAFF	chr2:57668474-57668488	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:57634837-57634887	NB4	blood:	n/a
2	chr2:57634837-57634887	U87	brain:	n/a
3	chr2:57634837-57634887	HEEpiC	esophagus:	n/a
4	chr2:57634837-57634887	HCT-116	colon:	n/a
5	chr2:57634837-57634887	HNPCEpiC	eye:	n/a
6	chr2:57634837-57634887	HL-60	blood:	n/a
7	chr2:57634837-57634887	HIPEpiC	eye:	n/a
8	chr2:57634837-57634887	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:57634837-57634887	SKMC	muscle:	n/a
10	chr2:57634837-57634887	NT2-D1	testis:	n/a
11	chr2:57634837-57634887	GM06990	blood:	n/a
12	chr2:57634837-57634887	Hela-S3	cervix:	n/a
13	chr2:57634837-57634887	GM12891	blood:	n/a
14	chr2:57634837-57634887	A549	lung:	n/a
15	chr2:57634837-57634887	K562	blood:	n/a
16	chr2:57634837-57634887	SK-N-SH	brain:	n/a
17	chr2:57634837-57634887	HepG2	liver:	n/a
18	chr2:57634837-57634887	AG04449	skin:	fetal
19	chr2:57634837-57634887	BJ	skin:	n/a
20	chr2:57634837-57634887	HAEpiC	amniotic membrane:	n/a
21	chr2:57634837-57634887	GM12878	blood:	n/a
22	chr2:57634837-57634887	AG10803	skin:	n/a
23	chr2:57634837-57634887	ovcar-3	ovarian:	n/a
24	chr2:57634837-57634887	GM19239	blood:	n/a
25	chr2:57634837-57634887	MCF10A-Er-Src	breast:	n/a
26	chr2:57634837-57634887	Jurkat	blood:	n/a
27	chr2:57634837-57634887	GM12892	blood:	n/a
28	chr2:57634837-57634887	PFSK-1	brain:	n/a
29	chr2:57634837-57634887	IMR90	lung:	fetal
30	chr2:57634837-57634887	T-47D	breast:	n/a
31	chr2:57634837-57634887	Hepatocyte	liver:	n/a
32	chr2:57634837-57634887	SK-N-SH_RA	brain:	n/a
33	chr2:57634837-57634887	HCF	heart:	n/a
34	chr2:57634837-57634887	RPTEC	kidney:	n/a
35	chr2:57634837-57634887	BE2_C	brain:	n/a
36	chr2:57634837-57634887	HEK293	kidney:	embryo
37	chr2:57634837-57634887	AG04450	lung:	fetal
38	chr2:57634837-57634887	AG09309	skin:	n/a
39	chr2:57634837-57634887	SK-N-MC	brain:	n/a
40	chr2:57634837-57634887	AoSMC	blood vessel:	n/a
41	chr2:57634837-57634887	SAEC	small airway:	n/a
42	chr2:57634837-57634887	HRE	kidney:	n/a
43	chr2:57634837-57634887	NH-A	brain:	n/a
44	chr2:57634837-57634887	HRCEpiC	kidney:	n/a
45	chr2:57634837-57634887	HCM	heart:	n/a
46	chr2:57634837-57634887	PANC-1	pancreas:	n/a
47	chr2:57634837-57634887	HRPEpiC	eye:	n/a
48	chr2:57634837-57634887	NHBE	bronchial:	n/a
49	chr2:57634837-57634887	Caco-2	colon:	n/a
50	chr2:57634837-57634887	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:57631506..57633055-chr2:57645760..57647304,2	MCF-7	breast:
2	chr2:57670502..57672263-chr2:57675373..57678104,2	MCF-7	breast:
3	chr2:57633446..57635721-chr2:57643662..57645382,2	MCF-7	breast:
4	chr2:57627476..57629537-chr2:57644280..57646195,2	MCF-7	breast:
5	chr2:57633446..57635721-chr2:57643662..57645382,2	MCF-7	breast:
6	chr2:57627476..57629537-chr2:57644280..57646195,2	MCF-7	breast:
7	chr2:57631506..57633055-chr2:57645760..57647304,2	MCF-7	breast:
8	chr2:57669021..57671005-chr2:57673900..57675904,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCL-8	chr2:57656683-57656947	NONHSAT070833
2	lnc-VRK2-16	chr2:57659475-57659520	NONHSAT070834
3	lnc-FANCL-8	chr2:57657781-57657828	NONHSAT070833
4	lnc-FANCL-8	chr2:57657275-57657340	NONHSAT070833

Variant related genes	Relation type
ENSG00000270569	TF binding region
ENSG00000270569	CpG island

Extended variants
information (count: 925 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1401257	chr2:57626992-57626993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180995009	chr2:57627005-57627006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199953176	chr2:57627073-57627074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544710026	chr2:57627075-57627076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564508029	chr2:57627083-57627084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183855284	chr2:57627100-57627101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200544793	chr2:57627101-57627102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540558059	chr2:57627136-57627137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs60795666	chr2:57627239-57627240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs529097750	chr2:57627247-57627248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548855313	chr2:57627256-57627257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372230987	chr2:57627293-57627294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188576464	chr2:57627296-57627297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531345230	chr2:57627328-57627329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375569666	chr2:57627355-57627356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56350320	chr2:57627397-57627398	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs1518684	chr2:57627453-57627454	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs146136095	chr2:57627526-57627527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75078323	chr2:57627547-57627548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567012677	chr2:57627559-57627560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536142884	chr2:57627588-57627589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140173936	chr2:57627613-57627614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35559147	chr2:57627623-57627624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575779407	chr2:57627629-57627630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375785564	chr2:57627631-57627632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538371255	chr2:57627671-57627672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558256448	chr2:57627715-57627716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs578083291	chr2:57627735-57627736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541049457	chr2:57627855-57627856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149438780	chr2:57627879-57627880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554041333	chr2:57627885-57627886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573896333	chr2:57627887-57627888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561532156	chr2:57627897-57627898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530264846	chr2:57627933-57627934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562573866	chr2:57627993-57627994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531379643	chr2:57628016-57628017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs33999009	chr2:57628029-57628030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs564604146	chr2:57628063-57628064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551518357	chr2:57628121-57628122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527300633	chr2:57628126-57628127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547036394	chr2:57628247-57628248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567245537	chr2:57628256-57628257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376249385	chr2:57628286-57628287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181296855	chr2:57628287-57628288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144663293	chr2:57628318-57628319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550525179	chr2:57628327-57628328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538409911	chr2:57628383-57628384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74722777	chr2:57628388-57628389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571726540	chr2:57628392-57628393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs59619330	chr2:57628401-57628402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57624000-57634800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr2:57629000-57629400	Enhancers	Fetal Brain Female	brain
3	chr2:57629000-57630400	Enhancers	Fetal Lung	lung
4	chr2:57633400-57633600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:57633400-57636000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:57633600-57633800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr2:57633800-57634800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:57634200-57636000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:57634400-57635800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr2:57634600-57635200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr2:57634600-57635600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:57634600-57635800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:57634600-57636000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr2:57634600-57636000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:57634800-57635200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:57634800-57635200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr2:57634800-57635400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:57634800-57635600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:57634800-57635800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr2:57634800-57635800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr2:57634800-57635800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr2:57634800-57636000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:57635000-57635400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:57635000-57635400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr2:57635000-57635400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:57635400-57637600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:57644200-57644400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:57645400-57645800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr2:57645800-57646200	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr2:57645800-57646400	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr2:57654800-57655200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr2:57656400-57658000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr2:57656600-57658000	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr2:57657000-57657800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:57657800-57658000	Enhancers	Pancreas	Pancrea
36	chr2:57658000-57661800	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr2:57658000-57661800	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr2:57659000-57659200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr2:57659000-57659600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:57659200-57660400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:57659200-57660800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:57659400-57660000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:57659600-57660600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:57660400-57660800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:57660600-57662000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:57661600-57662200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:57661800-57662200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:57661800-57662400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr2:57661800-57662600	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr2:57662000-57662200	Enhancers	Pancreatic Islets	Pancreatic Islet

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