Variant report

Variant	nsv524102
Chromosome Location	chr2:78221253-78562013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:667)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:78532952-78532953	K562	blood:	n/a	n/a
2	ARID3A	chr2:78413821-78414186	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:78389314-78389802	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:78336522-78336700	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:78361077-78361118	K562	blood:	n/a	n/a
6	ARID3A	chr2:78487915-78488675	HepG2	liver:	n/a	n/a
7	ATF1	chr2:78408127-78408325	K562	blood:	n/a	n/a
8	ATF1	chr2:78361002-78361126	K562	blood:	n/a	n/a
9	BACH1	chr2:78477710-78477711	K562	blood:	n/a	n/a
10	BACH1	chr2:78368178-78368199	K562	blood:	n/a	n/a
11	BATF	chr2:78508305-78508535	GM12878	blood:	n/a	n/a
12	BATF	chr2:78428253-78428380	GM12878	blood:	n/a	n/a
13	BATF	chr2:78508306-78508624	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:78508311-78508495	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:78263040-78263247	H1-hESC	embryonic stem cell:	n/a	n/a
16	BHLHE40	chr2:78389461-78389669	HepG2	liver:	n/a	n/a
17	BHLHE40	chr2:78508455-78508636	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:78490807-78490864	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:78487986-78488343	HepG2	liver:	n/a	n/a
20	CBX3	chr2:78256529-78256863	K562	blood:	n/a	n/a
21	CBX3	chr2:78273156-78273427	K562	blood:	n/a	n/a
22	CBX3	chr2:78256534-78256829	K562	blood:	n/a	n/a
23	CBX3	chr2:78273160-78273446	K562	blood:	n/a	n/a
24	CCNT2	chr2:78252676-78252871	K562	blood:	n/a	n/a
25	CEBPB	chr2:78537183-78537401	K562	blood:	n/a	n/a
26	CEBPB	chr2:78275962-78276210	IMR90	lung:	n/a	chr2:78276047-78276058
27	CEBPB	chr2:78445215-78445558	K562	blood:	n/a	chr2:78445380-78445391
28	CEBPB	chr2:78359289-78359640	MCF-7	breast:	n/a	n/a
29	CEBPB	chr2:78336457-78336742	K562	blood:	n/a	n/a
30	CEBPB	chr2:78336524-78336852	A549	lung:	n/a	n/a
31	CEBPB	chr2:78389426-78389688	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:78369163-78369459	HepG2	liver:	n/a	chr2:78369346-78369359 chr2:78369367-78369378
33	CEBPB	chr2:78445242-78445505	Hela-S3	cervix:	n/a	chr2:78445380-78445391
34	CEBPB	chr2:78359219-78359536	MCF-7	breast:	n/a	n/a
35	CEBPB	chr2:78518603-78518888	A549	lung:	n/a	chr2:78518707-78518718
36	CEBPB	chr2:78400416-78400616	HepG2	liver:	n/a	chr2:78400485-78400496
37	CEBPB	chr2:78420619-78420902	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:78518569-78518898	K562	blood:	n/a	chr2:78518707-78518718
39	CEBPB	chr2:78445211-78445551	A549	lung:	n/a	chr2:78445380-78445391
40	CEBPB	chr2:78445231-78445562	IMR90	lung:	n/a	chr2:78445380-78445391
41	CEBPB	chr2:78420652-78420781	K562	blood:	n/a	n/a
42	CEBPB	chr2:78278610-78278979	HepG2	liver:	n/a	chr2:78278787-78278798
43	CEBPB	chr2:78278617-78278979	IMR90	lung:	n/a	chr2:78278787-78278798
44	CEBPB	chr2:78278654-78278947	K562	blood:	n/a	chr2:78278787-78278798
45	CEBPB	chr2:78518559-78518875	IMR90	lung:	n/a	chr2:78518707-78518718
46	CEBPB	chr2:78221062-78221269	HepG2	liver:	n/a	chr2:78221170-78221181 chr2:78221168-78221179
47	CEBPB	chr2:78445231-78445483	H1-hESC	embryonic stem cell:	n/a	chr2:78445380-78445391
48	CEBPB	chr2:78288591-78288834	HepG2	liver:	n/a	chr2:78288709-78288720
49	CEBPB	chr2:78336473-78336839	IMR90	lung:	n/a	n/a
50	CEBPB	chr2:78278661-78278923	H1-hESC	embryonic stem cell:	n/a	chr2:78278787-78278798

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:78545567-78545617	GM12892	blood:	n/a
2	chr2:78263008-78263058	HNPCEpiC	eye:	n/a
3	chr2:78263008-78263058	ECC-1	luminal epithelium:	n/a
4	chr2:78545567-78545617	MCF-7	breast:	n/a
5	chr2:78545567-78545617	A549	lung:	n/a
6	chr2:78263008-78263058	SK-N-MC	brain:	n/a
7	chr2:78263008-78263058	BJ	skin:	n/a
8	chr2:78545567-78545617	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:78545567-78545617	BJ	skin:	n/a
10	chr2:78545567-78545617	CMK	blood:	n/a
11	chr2:78263008-78263058	ovcar-3	ovarian:	n/a
12	chr2:78263008-78263058	SK-N-SH_RA	brain:	n/a
13	chr2:78545567-78545617	HEK293	kidney:	embryo
14	chr2:78545567-78545617	AoSMC	blood vessel:	n/a
15	chr2:78545567-78545617	HRE	kidney:	n/a
16	chr2:78263008-78263058	HRPEpiC	eye:	n/a
17	chr2:78545567-78545617	HMEC	breast:	n/a
18	chr2:78545567-78545617	RPTEC	kidney:	n/a
19	chr2:78263008-78263058	SKMC	muscle:	n/a
20	chr2:78545567-78545617	GM12878	blood:	n/a
21	chr2:78545567-78545617	PrEC	prostate:	n/a
22	chr2:78545567-78545617	K562	blood:	n/a
23	chr2:78263008-78263058	HRCEpiC	kidney:	n/a
24	chr2:78545567-78545617	Jurkat	blood:	n/a
25	chr2:78263008-78263058	LNCaP	prostate:	n/a
26	chr2:78545567-78545617	NHBE	bronchial:	n/a
27	chr2:78263008-78263058	NHDF-neo	bronchial:	n/a
28	chr2:78263008-78263058	NB4	blood:	n/a
29	chr2:78545567-78545617	T-47D	breast:	n/a
30	chr2:78263008-78263058	PANC-1	pancreas:	n/a
31	chr2:78545567-78545617	ECC-1	luminal epithelium:	n/a
32	chr2:78263008-78263058	PFSK-1	brain:	n/a
33	chr2:78545567-78545617	IMR90	lung:	fetal
34	chr2:78545567-78545617	HUVEC	blood vessel:	n/a
35	chr2:78545567-78545617	AG04449	skin:	fetal
36	chr2:78545567-78545617	NHDF-neo	bronchial:	n/a
37	chr2:78263008-78263058	SK-N-SH	brain:	n/a
38	chr2:78545567-78545617	HCM	heart:	n/a
39	chr2:78263008-78263058	AoSMC	blood vessel:	n/a
40	chr2:78545567-78545617	HRPEpiC	eye:	n/a
41	chr2:78545567-78545617	HRCEpiC	kidney:	n/a
42	chr2:78545567-78545617	HEEpiC	esophagus:	n/a
43	chr2:78545567-78545617	ovcar-3	ovarian:	n/a
44	chr2:78263008-78263058	GM12878	blood:	n/a
45	chr2:78545567-78545617	LNCaP	prostate:	n/a
46	chr2:78263008-78263058	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:78263008-78263058	AG04450	lung:	fetal
48	chr2:78545567-78545617	MCF10A-Er-Src	breast:	n/a
49	chr2:78263008-78263058	HEK293	kidney:	embryo
50	chr2:78545567-78545617	AG10803	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
2	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
3	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
4	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
5	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
6	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
7	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
8	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
9	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
10	chr17:59624355..59624932-chr2:78345304..78345966,2	MCF-7	breast:
11	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
12	chr2:78519747..78522682-chr2:78785137..78786876,2	K562	blood:
13	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
14	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
15	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
16	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
17	chr2:78215424..78217099-chr2:78219299..78221415,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-3	chr2:78339185-78339226	XLOC_001543
2	lnc-REG3G-3	chr2:78322790-78322968	XLOC_001543
3	lnc-REG3G-3	chr2:78321763-78321902	XLOC_001543
4	lnc-REG3G-3	chr2:78354625-78354877	XLOC_001543
5	lnc-LRRTM4-3	chr2:78225204-78225307	NONHSAT071835
6	lnc-REG3G-3	chr2:78320703-78320792	XLOC_001543
7	lnc-LRRTM4-3	chr2:78229100-78229271	NONHSAT071835
8	lnc-LRRTM4-8	chr2:78371022-78371323	ucscGeneNc_uc002snu_2
9	lnc-LRRTM4-3	chr2:78252450-78252550	NONHSAT071835
10	lnc-LRRTM4-3	chr2:78517514-78517857	NR_110288

No data

Variant related genes	Relation type
ENSG00000229494	TF binding region
ENSG00000229494	CpG island

Extended variants
information (count: 6786 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:6786 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534240128	chr2:78225237-78225238	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs185359161	chr2:78225239-78225240	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs115601971	chr2:78225284-78225285	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs542721181	chr2:78225301-78225302	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs376916113	chr2:78226224-78226225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551411123	chr2:78226279-78226280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564943084	chr2:78226288-78226289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149769648	chr2:78226294-78226295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147969585	chr2:78226308-78226309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190402506	chr2:78226406-78226407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182664648	chr2:78226420-78226421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536281124	chr2:78226425-78226426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549752994	chr2:78226438-78226439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569859073	chr2:78226469-78226470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538757929	chr2:78226484-78226485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558967847	chr2:78226522-78226523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548237771	chr2:78226547-78226548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535200842	chr2:78226565-78226566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12991380	chr2:78226578-78226579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188481552	chr2:78226653-78226654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191762236	chr2:78226658-78226659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575204369	chr2:78226664-78226665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141836362	chr2:78226695-78226696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183933650	chr2:78226731-78226732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147097425	chr2:78226733-78226734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373626672	chr2:78226753-78226754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188878602	chr2:78226836-78226837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138488807	chr2:78226854-78226855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375980061	chr2:78226979-78226980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35198361	chr2:78226996-78226997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370043624	chr2:78227044-78227045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78479809	chr2:78227114-78227115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547171477	chr2:78227142-78227143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111740642	chr2:78227194-78227195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149184588	chr2:78227200-78227201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372669052	chr2:78227202-78227203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75884667	chr2:78227231-78227232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76803466	chr2:78227233-78227234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201236210	chr2:78227245-78227246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538987533	chr2:78227273-78227274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552420406	chr2:78227289-78227290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566150138	chr2:78227316-78227317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534947058	chr2:78227339-78227340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143082313	chr2:78227349-78227350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111245837	chr2:78227357-78227358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568625750	chr2:78227397-78227398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191328751	chr2:78227421-78227422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557654878	chr2:78227483-78227484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183767711	chr2:78227529-78227530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544965227	chr2:78227621-78227622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78226200-78226800	Enhancers	Muscle Satellite Cultured Cells	--
2	chr2:78226200-78227000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:78226600-78227400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:78226800-78227200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr2:78227200-78227400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr2:78227400-78229200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:78229200-78229400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr2:78229400-78229800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr2:78229800-78230200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr2:78237000-78237200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:78237200-78238200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:78238000-78238400	Active TSS	Brain Substantia Nigra	brain
13	chr2:78238200-78238400	Enhancers	Brain Cingulate Gyrus	brain
14	chr2:78238200-78238600	Active TSS	Brain Angular Gyrus	brain
15	chr2:78238200-78240800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:78238400-78238800	Active TSS	Brain Cingulate Gyrus	brain
17	chr2:78239400-78239600	Enhancers	Brain Cingulate Gyrus	brain
18	chr2:78243000-78253200	Weak transcription	HepG2	liver
19	chr2:78250400-78251000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr2:78251800-78254000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr2:78254000-78254200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
22	chr2:78255800-78257600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:78259000-78259800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
24	chr2:78259800-78262400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr2:78260600-78261600	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:78261600-78261800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr2:78261800-78262400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr2:78261800-78263600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr2:78261800-78263800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:78261800-78263800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:78261800-78263800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:78262000-78263000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr2:78262400-78262800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr2:78262400-78263200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:78262600-78263600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:78262800-78263000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr2:78262800-78263400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr2:78263000-78263400	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr2:78263200-78263600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
40	chr2:78263400-78263800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr2:78263600-78263800	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr2:78263800-78264000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr2:78263800-78264800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr2:78265000-78265200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:78270800-78271000	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr2:78271000-78272200	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr2:78272800-78274200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:78282400-78284000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:78286000-78289600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr2:78288200-78288600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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