Variant report

Variant	esv2754005
Chromosome Location	chr2:151753492-151840492
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	chr2:151793632-151793868	HepG2	liver:	n/a	n/a
2	BACH1	chr2:151768470-151768826	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:151838479-151838684	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr2:151768205-151768407	A549	lung:	n/a	n/a
5	BHLHE40	chr2:151768222-151768762	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:151761989-151762037	K562	blood:	n/a	chr2:151761998-151762009
7	CEBPB	chr2:151805274-151805445	H1-hESC	embryonic stem cell:	n/a	chr2:151805345-151805356
8	CEBPB	chr2:151768106-151768969	A549	lung:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
9	CEBPB	chr2:151768183-151768885	HepG2	liver:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
10	CEBPB	chr2:151761869-151762044	IMR90	lung:	n/a	chr2:151761998-151762009
11	CEBPB	chr2:151768168-151768881	A549	lung:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
12	CEBPB	chr2:151768246-151768514	MCF-7	breast:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
13	CEBPB	chr2:151805207-151805500	HepG2	liver:	n/a	chr2:151805345-151805356
14	CEBPB	chr2:151768555-151768849	MCF-7	breast:	n/a	n/a
15	CEBPB	chr2:151768118-151768648	MCF-7	breast:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
16	CEBPB	chr2:151793634-151793941	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:151768190-151768884	H1-hESC	embryonic stem cell:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
18	CEBPB	chr2:151805243-151805449	HepG2	liver:	n/a	chr2:151805345-151805356
19	CEBPB	chr2:151768230-151768494	ECC-1	luminal epithelium:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
20	CEBPB	chr2:151829994-151830332	HepG2	liver:	n/a	chr2:151830163-151830174 chr2:151830162-151830173 chr2:151830164-151830173
21	CEBPB	chr2:151805277-151805477	A549	lung:	n/a	chr2:151805345-151805356
22	CEBPB	chr2:151830022-151830302	A549	lung:	n/a	chr2:151830163-151830174 chr2:151830162-151830173 chr2:151830164-151830173
23	CEBPB	chr2:151768237-151768873	A549	lung:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
24	CEBPB	chr2:151768110-151768932	Hela-S3	cervix:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
25	CEBPB	chr2:151768202-151768453	HepG2	liver:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
26	CEBPB	chr2:151768174-151768838	HepG2	liver:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
27	CEBPB	chr2:151768136-151768920	IMR90	lung:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
28	CEBPB	chr2:151805263-151805445	HepG2	liver:	n/a	chr2:151805345-151805356
29	CEBPB	chr2:151768183-151768531	K562	blood:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
30	CEBPB	chr2:151761930-151762144	HepG2	liver:	n/a	chr2:151761998-151762009
31	CEBPB	chr2:151830025-151830297	IMR90	lung:	n/a	chr2:151830163-151830174 chr2:151830162-151830173 chr2:151830164-151830173
32	CHD2	chr2:151768314-151768904	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr2:151766200-151766350	AG10803	skin:	n/a	n/a
34	CTCF	chr2:151766240-151766390	AG09309	skin:	n/a	n/a
35	CTCF	chr2:151766240-151766390	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr2:151768274-151769016	A549	lung:	n/a	n/a
37	CTCF	chr2:151768600-151768750	RPTEC	kidney:	n/a	n/a
38	CTCF	chr2:151797920-151798070	GM12878	blood:	n/a	n/a
39	CTCF	chr2:151766280-151766430	A549	lung:	n/a	n/a
40	CTCF	chr2:151768560-151768710	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr2:151768640-151768790	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr2:151768600-151768750	AG09319	gingival:	n/a	n/a
43	CTCF	chr2:151768600-151768750	AG10803	skin:	n/a	n/a
44	CTCF	chr2:151766180-151766330	AG09319	gingival:	n/a	n/a
45	CTCF	chr2:151773100-151773198	LNCaP	prostate:	n/a	n/a
46	CTCF	chr2:151768600-151768750	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr2:151768600-151768750	AG04449	skin:	n/a	n/a
48	CTCF	chr2:151768576-151768832	Fibrobl	skin:	n/a	n/a
49	CTCF	chr2:151766100-151766250	GM12870	blood:	n/a	n/a
50	CTCF	chr2:151815087-151815170	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:151838548-151838598	HNPCEpiC	eye:	n/a
2	chr2:151768348-151768398	GM19239	blood:	n/a
3	chr2:151768348-151768398	AG04449	skin:	fetal
4	chr2:151768348-151768398	AG09309	skin:	n/a
5	chr2:151768348-151768398	NHDF-neo	bronchial:	n/a
6	chr2:151838548-151838598	RPTEC	kidney:	n/a
7	chr2:151768348-151768398	HCF	heart:	n/a
8	chr2:151838548-151838598	ProgFib	skin:	n/a
9	chr2:151788471-151788521	MCF10A-Er-Src	breast:	n/a
10	chr2:151838548-151838598	HCM	heart:	n/a
11	chr2:151838548-151838598	AG10803	skin:	n/a
12	chr2:151768348-151768398	PFSK-1	brain:	n/a
13	chr2:151788471-151788521	GM12892	blood:	n/a
14	chr2:151838548-151838598	CMK	blood:	n/a
15	chr2:151768348-151768398	Hela-S3	cervix:	n/a
16	chr2:151768348-151768398	SK-N-SH_RA	brain:	n/a
17	chr2:151788471-151788521	HNPCEpiC	eye:	n/a
18	chr2:151838548-151838598	PANC-1	pancreas:	n/a
19	chr2:151788471-151788521	AG04450	lung:	fetal
20	chr2:151768348-151768398	HUVEC	blood vessel:	n/a
21	chr2:151768348-151768398	HAEpiC	amniotic membrane:	n/a
22	chr2:151768348-151768398	SK-N-SH	brain:	n/a
23	chr2:151768348-151768398	A549	lung:	n/a
24	chr2:151768348-151768398	K562	blood:	n/a
25	chr2:151838548-151838598	HRE	kidney:	n/a
26	chr2:151788471-151788521	ProgFib	skin:	n/a
27	chr2:151768348-151768398	GM12892	blood:	n/a
28	chr2:151788471-151788521	Jurkat	blood:	n/a
29	chr2:151838548-151838598	Hela-S3	cervix:	n/a
30	chr2:151768348-151768398	AG04450	lung:	fetal
31	chr2:151838548-151838598	SK-N-SH	brain:	n/a
32	chr2:151788471-151788521	HRE	kidney:	n/a
33	chr2:151788471-151788521	HIPEpiC	eye:	n/a
34	chr2:151838548-151838598	AG04450	lung:	fetal
35	chr2:151768348-151768398	HCT-116	colon:	n/a
36	chr2:151768348-151768398	HCM	heart:	n/a
37	chr2:151838548-151838598	NH-A	brain:	n/a
38	chr2:151838548-151838598	NB4	blood:	n/a
39	chr2:151788471-151788521	SK-N-SH	brain:	n/a
40	chr2:151768348-151768398	GM12891	blood:	n/a
41	chr2:151838548-151838598	PrEC	prostate:	n/a
42	chr2:151788471-151788521	CMK	blood:	n/a
43	chr2:151838548-151838598	HRPEpiC	eye:	n/a
44	chr2:151788471-151788521	GM19239	blood:	n/a
45	chr2:151768348-151768398	HRE	kidney:	n/a
46	chr2:151788471-151788521	ovcar-3	ovarian:	n/a
47	chr2:151838548-151838598	NT2-D1	testis:	n/a
48	chr2:151788471-151788521	MCF-7	breast:	n/a
49	chr2:151788471-151788521	PFSK-1	brain:	n/a
50	chr2:151788471-151788521	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:151768362..151769212-chr2:151907879..151908719,2	MCF-7	breast:
2	chr2:151834278..151835808-chr2:151846430..151849245,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC023469.1.1-1	chr2:151812105-151812299	NONHSAT074946
2	lnc-TNFAIP6-1	chr2:151839020-151839029	XLOC_001708
3	lnc-AC023469.1.1-1	chr2:151812442-151812560	NONHSAT074946

Variant related genes	Relation type
ENSG00000228064	TF binding region
ENSG00000228064	CpG island
ARID4B	miRNA target sites

Extended variants
information (count: 3288 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:3288 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534902640	chr2:151753527-151753528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558014993	chr2:151753538-151753539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs16828857	chr2:151753548-151753549	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs1014111	chr2:151753563-151753564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs557133143	chr2:151753618-151753619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573978348	chr2:151753644-151753645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546588833	chr2:151753657-151753658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144445152	chr2:151753707-151753708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73967470	chr2:151753713-151753714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573235037	chr2:151753742-151753743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568375530	chr2:151753758-151753759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545273344	chr2:151753780-151753781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6727140	chr2:151753807-151753808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs189030933	chr2:151753825-151753826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6727152	chr2:151753832-151753833	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs78009712	chr2:151753877-151753878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10188669	chr2:151753903-151753904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs549035901	chr2:151753923-151753924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537587674	chr2:151753928-151753929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565660916	chr2:151753937-151753938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370421437	chr2:151753958-151753959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551693529	chr2:151753959-151753960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571427264	chr2:151754024-151754025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536798102	chr2:151754030-151754031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551073062	chr2:151754057-151754058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145653193	chr2:151754091-151754092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536330395	chr2:151754121-151754122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77883921	chr2:151754131-151754132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572897760	chr2:151754169-151754170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6727663	chr2:151754242-151754243	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs181421021	chr2:151754264-151754265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185709132	chr2:151754270-151754271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147757965	chr2:151754274-151754275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561517413	chr2:151754284-151754285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573685306	chr2:151754306-151754307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79123328	chr2:151754338-151754339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397814880	chr2:151754339-151754340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200786739	chr2:151754340-151754341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201794616	chr2:151754341-151754342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542743404	chr2:151754352-151754353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4664809	chr2:151754368-151754369	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs72862941	chr2:151754400-151754401	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs144858580	chr2:151754446-151754447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6724697	chr2:151754448-151754449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs112914651	chr2:151754465-151754466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574839647	chr2:151754480-151754481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76805860	chr2:151754494-151754495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6737835	chr2:151754507-151754508	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs536393279	chr2:151754526-151754527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191251305	chr2:151754536-151754537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151735200-151770600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:151756600-151758000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr2:151757400-151757600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:151758000-151758200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:151759800-151760600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:151759800-151760800	Enhancers	Osteobl	bone
7	chr2:151760800-151767400	Weak transcription	Osteobl	bone
8	chr2:151762600-151765600	Enhancers	Fetal Heart	heart
9	chr2:151764000-151768200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:151765000-151766400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:151765400-151766200	Enhancers	HMEC	breast
12	chr2:151765400-151766200	Enhancers	NHEK	skin
13	chr2:151765400-151766400	Enhancers	GM12878-XiMat	blood
14	chr2:151765600-151766000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:151765600-151766200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:151765800-151766200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:151766200-151768200	Weak transcription	HMEC	breast
18	chr2:151766200-151768200	Weak transcription	NHEK	skin
19	chr2:151766200-151769000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr2:151766400-151767800	Weak transcription	GM12878-XiMat	blood
21	chr2:151766400-151773000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:151767200-151768200	Enhancers	NHDF-Ad	bronchial
23	chr2:151767200-151768400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:151767400-151768200	Enhancers	Osteobl	bone
25	chr2:151767600-151768000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:151767600-151768200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:151767600-151768600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr2:151767600-151769000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr2:151767600-151769000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr2:151767600-151769000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:151767800-151768000	Enhancers	GM12878-XiMat	blood
32	chr2:151767800-151768200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:151767800-151768200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:151767800-151768400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr2:151767800-151768400	Enhancers	Hela-S3	cervix
36	chr2:151767800-151768400	Enhancers	HSMM	muscle
37	chr2:151767800-151768800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr2:151767800-151768800	Enhancers	Fetal Muscle Leg	muscle
39	chr2:151767800-151769000	Enhancers	HSMMtube	muscle
40	chr2:151767800-151769200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr2:151767800-151769200	Enhancers	NHLF	lung
42	chr2:151768000-151768600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:151768200-151768400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr2:151768200-151768400	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr2:151768200-151768600	Active TSS	Adipose Nuclei	Adipose
46	chr2:151768200-151768600	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr2:151768200-151768600	Enhancers	Fetal Lung	lung
48	chr2:151768200-151768800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:151768200-151768800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr2:151768200-151768800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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