Variant report

Variant	nsv874339
Chromosome Location	chr2:77683562-77872197
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	chr2:77793763-77794055	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:77856705-77856971	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:77832125-77832532	HepG2	liver:	n/a	n/a
4	BACH1	chr2:77750117-77750320	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:77858291-77858408	K562	blood:	n/a	n/a
6	CEBPB	chr2:77866168-77866347	HepG2	liver:	n/a	chr2:77866208-77866219
7	CEBPB	chr2:77686883-77687193	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr2:77777482-77777812	HepG2	liver:	n/a	chr2:77777649-77777660
9	CEBPB	chr2:77735678-77735907	A549	lung:	n/a	chr2:77735834-77735845 chr2:77735832-77735849
10	CEBPB	chr2:77740493-77740504	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:77870309-77870701	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:77805386-77805678	H1-hESC	embryonic stem cell:	n/a	chr2:77805548-77805559
13	CEBPB	chr2:77807779-77808019	HepG2	liver:	n/a	chr2:77807874-77807885
14	CEBPB	chr2:77870443-77870684	A549	lung:	n/a	n/a
15	CEBPB	chr2:77861626-77861952	A549	lung:	n/a	chr2:77861765-77861776
16	CEBPB	chr2:77870422-77870629	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:77749105-77749135	HepG2	liver:	n/a	chr2:77749110-77749119
18	CEBPB	chr2:77802518-77802724	HepG2	liver:	n/a	chr2:77802613-77802624
19	CEBPB	chr2:77802542-77802758	A549	lung:	n/a	chr2:77802613-77802624
20	CEBPB	chr2:77735678-77735954	K562	blood:	n/a	chr2:77735834-77735845 chr2:77735832-77735849
21	CEBPB	chr2:77870317-77870489	K562	blood:	n/a	n/a
22	CEBPB	chr2:77861689-77861796	H1-hESC	embryonic stem cell:	n/a	chr2:77861765-77861776
23	CEBPB	chr2:77747356-77747682	IMR90	lung:	n/a	chr2:77747442-77747453 chr2:77747510-77747523 chr2:77747573-77747581 chr2:77747510-77747523
24	CEBPB	chr2:77793743-77794023	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:77832262-77832460	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:77805372-77805748	Hela-S3	cervix:	n/a	chr2:77805548-77805559
27	CEBPB	chr2:77733675-77734144	HepG2	liver:	n/a	chr2:77734044-77734055 chr2:77734043-77734054 chr2:77734043-77734056
28	CEBPB	chr2:77861610-77861945	HepG2	liver:	n/a	chr2:77861765-77861776
29	CEBPB	chr2:77861644-77861916	IMR90	lung:	n/a	chr2:77861765-77861776
30	CEBPB	chr2:77750079-77750314	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:77777488-77777779	A549	lung:	n/a	chr2:77777649-77777660
32	CEBPB	chr2:77835791-77835913	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:77735714-77735914	H1-hESC	embryonic stem cell:	n/a	chr2:77735834-77735845 chr2:77735832-77735849
34	CEBPB	chr2:77748991-77749319	H1-hESC	embryonic stem cell:	n/a	chr2:77749110-77749119
35	CEBPB	chr2:77855784-77856051	HepG2	liver:	n/a	chr2:77855924-77855935 chr2:77855922-77855939 chr2:77855923-77855936
36	CEBPB	chr2:77805397-77805727	HepG2	liver:	n/a	chr2:77805548-77805559
37	CEBPB	chr2:77857855-77858007	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:77735694-77735970	HepG2	liver:	n/a	chr2:77735834-77735845 chr2:77735832-77735849
39	CEBPB	chr2:77831047-77831112	HepG2	liver:	n/a	chr2:77831053-77831064 chr2:77831053-77831066
40	CEBPB	chr2:77866132-77866309	A549	lung:	n/a	chr2:77866208-77866219
41	CEBPB	chr2:77740319-77740722	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr2:77832211-77832570	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:77805466-77805710	A549	lung:	n/a	chr2:77805548-77805559
44	CEBPB	chr2:77705414-77705656	HepG2	liver:	n/a	chr2:77705476-77705487
45	CHD1	chr2:77749631-77750561	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr2:77708240-77708390	HPF	lung:	n/a	n/a
47	CTCF	chr2:77742885-77742896	LNCaP	prostate:	n/a	n/a
48	CTCF	chr2:77762061-77762113	HepG2	liver:	n/a	chr2:77762078-77762087
49	CTCF	chr2:77749420-77749570	HepG2	liver:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
50	CTCF	chr2:77749500-77749650	RPTEC	kidney:	n/a	chr2:77749505-77749518 chr2:77749503-77749521

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77856944-77856994	U87	brain:	n/a
2	chr2:77856944-77856994	U87	brain:	n/a
3	chr2:77750866-77750916	H1-hESC	embryonic stem cell:	embryo
4	chr2:77747049-77747099	NHBE	bronchial:	n/a
5	chr2:77856944-77856994	IMR90	lung:	fetal
6	chr2:77820248-77820298	AG04449	skin:	fetal
7	chr2:77747049-77747099	AG09309	skin:	n/a
8	chr2:77747049-77747099	HAEpiC	amniotic membrane:	n/a
9	chr2:77747049-77747099	HCM	heart:	n/a
10	chr2:77856944-77856994	HCF	heart:	n/a
11	chr2:77820248-77820298	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:77748917-77748967	HIPEpiC	eye:	n/a
13	chr2:77748917-77748967	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:77750866-77750916	PrEC	prostate:	n/a
15	chr2:77750866-77750916	AG09309	skin:	n/a
16	chr2:77747049-77747099	HEK293	kidney:	embryo
17	chr2:77750866-77750916	HCPEpiC	choroid plexus:	n/a
18	chr2:77747049-77747099	T-47D	breast:	n/a
19	chr2:77820248-77820298	H1-hESC	embryonic stem cell:	embryo
20	chr2:77748917-77748967	K562	blood:	n/a
21	chr2:77747049-77747099	PFSK-1	brain:	n/a
22	chr2:77856944-77856994	A549	lung:	n/a
23	chr2:77750866-77750916	SK-N-SH_RA	brain:	n/a
24	chr2:77750866-77750916	A549	lung:	n/a
25	chr2:77747049-77747099	HEEpiC	esophagus:	n/a
26	chr2:77747049-77747099	HL-60	blood:	n/a
27	chr2:77748917-77748967	H1-hESC	embryonic stem cell:	embryo
28	chr2:77820248-77820298	A549	lung:	n/a
29	chr2:77747049-77747099	NT2-D1	testis:	n/a
30	chr2:77747049-77747099	K562	blood:	n/a
31	chr2:77856944-77856994	H1-hESC	embryonic stem cell:	embryo
32	chr2:77820248-77820298	SKMC	muscle:	n/a
33	chr2:77820248-77820298	SK-N-SH	brain:	n/a
34	chr2:77820248-77820298	AG04450	lung:	fetal
35	chr2:77747049-77747099	MCF-7	breast:	n/a
36	chr2:77820248-77820298	MCF-7	breast:	n/a
37	chr2:77820248-77820298	CMK	blood:	n/a
38	chr2:77750866-77750916	HRE	kidney:	n/a
39	chr2:77856944-77856994	ECC-1	luminal epithelium:	n/a
40	chr2:77748917-77748967	HEK293	kidney:	embryo
41	chr2:77747049-77747099	Caco-2	colon:	n/a
42	chr2:77747049-77747099	GM12878	blood:	n/a
43	chr2:77820248-77820298	GM19239	blood:	n/a
44	chr2:77856944-77856994	HMEC	breast:	n/a
45	chr2:77750866-77750916	SK-N-SH	brain:	n/a
46	chr2:77750866-77750916	NH-A	brain:	n/a
47	chr2:77747049-77747099	ovcar-3	ovarian:	n/a
48	chr2:77747049-77747099	IMR90	lung:	fetal
49	chr2:77856944-77856994	HCPEpiC	choroid plexus:	n/a
50	chr2:77747049-77747099	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:77833265..77836018-chr2:77837658..77839973,2	MCF-7	breast:
2	chr2:77833883..77835543-chr2:77837670..77840066,2	K562	blood:
3	chr2:77726699..77728852-chr2:77733118..77735865,2	MCF-7	breast:
4	chr2:77697026..77699297-chr2:77719458..77722284,2	MCF-7	breast:
5	chr2:77833883..77835543-chr2:77837670..77840066,2	K562	blood:
6	chr2:77747263..77749621-chr20:52208634..52211022,2	MCF-7	breast:
7	chr2:77833265..77836018-chr2:77837658..77839973,2	MCF-7	breast:
8	chr2:77794457..77797155-chr2:77797930..77800616,2	K562	blood:
9	chr17:57922805..57924826-chr2:77850689..77852567,2	MCF-7	breast:
10	chr2:77726699..77728852-chr2:77733118..77735865,2	MCF-7	breast:
11	chr17:74349617..74350377-chr2:77809788..77810706,2	HCT-116	colon:
12	chr2:77794457..77797155-chr2:77797930..77800616,2	K562	blood:
13	chr2:77697026..77699297-chr2:77719458..77722284,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-11	chr2:77753685-77754426	NONHSAT071828
2	lnc-REG1B-8	chr2:77733047-77733243	NONHSAT071827
3	lnc-REG3G-11	chr2:77752849-77752903	NONHSAT071828
4	lnc-REG1B-8	chr2:77735216-77735302	NONHSAT071827

Variant related genes	Relation type
LRRTM4	TF binding region
LRRTM4	CpG island
ENSG00000161542	chromatin interactions
ENSG00000171940	chromatin interactions

Extended variants
information (count: 5125 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5125 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1882681	chr2:77683562-77683563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543699899	chr2:77683585-77683586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563589484	chr2:77683588-77683589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62162583	chr2:77683591-77683592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187043290	chr2:77683613-77683614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573912601	chr2:77683638-77683639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535156752	chr2:77683725-77683726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72811236	chr2:77683755-77683756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192438511	chr2:77683880-77683881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141491173	chr2:77683891-77683892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568276555	chr2:77683934-77683935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537265530	chr2:77683950-77683951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201320498	chr2:77684080-77684081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372166999	chr2:77684119-77684120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376316571	chr2:77684126-77684127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199614882	chr2:77684129-77684130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6146817	chr2:77684130-77684131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374485222	chr2:77684145-77684146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs60120009	chr2:77684149-77684150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558119454	chr2:77684152-77684153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs5002968	chr2:77684178-77684179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182484977	chr2:77684191-77684192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550836885	chr2:77684203-77684204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146275426	chr2:77684232-77684233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34535249	chr2:77684236-77684237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539777777	chr2:77684321-77684322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139198840	chr2:77684344-77684345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186273641	chr2:77684449-77684450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79464568	chr2:77684451-77684452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554714730	chr2:77684565-77684566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35232455	chr2:77684596-77684597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190071148	chr2:77684599-77684600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543663931	chr2:77684602-77684603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182395037	chr2:77684635-77684636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577057673	chr2:77684659-77684660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545827204	chr2:77684665-77684666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149942495	chr2:77684694-77684695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13030574	chr2:77684710-77684711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113451237	chr2:77684722-77684723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528488074	chr2:77684734-77684735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13030949	chr2:77684774-77684775	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs78179765	chr2:77684810-77684811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530943567	chr2:77684814-77684815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374579919	chr2:77684815-77684816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371856029	chr2:77684833-77684834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187033271	chr2:77684859-77684860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191983278	chr2:77684866-77684867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144025815	chr2:77684951-77684952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75931691	chr2:77684975-77684976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565628109	chr2:77684979-77684980	Enhancers 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
Lung cancer	18438408	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
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	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77675400-77687000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:77681800-77688600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:77681800-77689000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:77683800-77685800	Enhancers	Fetal Heart	heart
5	chr2:77684600-77685200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:77684800-77690200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr2:77685000-77686200	Enhancers	Brain Anterior Caudate	brain
8	chr2:77685200-77688600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:77685800-77686800	Weak transcription	Fetal Heart	heart
10	chr2:77686200-77687000	Weak transcription	Brain Anterior Caudate	brain
11	chr2:77687000-77687200	Enhancers	Brain Germinal Matrix	brain
12	chr2:77687000-77687200	Enhancers	Fetal Heart	heart
13	chr2:77687000-77687400	Active TSS	Brain Hippocampus Middle	brain
14	chr2:77687000-77687600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:77687000-77687600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr2:77687000-77687600	Enhancers	Brain Angular Gyrus	brain
17	chr2:77687000-77687600	Active TSS	Brain Anterior Caudate	brain
18	chr2:77687000-77689200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:77687000-77689800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:77687200-77687400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr2:77687200-77687400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr2:77687200-77687600	Active TSS	NHLF	lung
23	chr2:77687200-77688800	Weak transcription	Brain Germinal Matrix	brain
24	chr2:77687400-77688800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr2:77687400-77689200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:77687600-77689000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr2:77688600-77688800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:77688600-77689600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:77688600-77690000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:77688800-77689600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr2:77688800-77689600	Enhancers	Brain Germinal Matrix	brain
32	chr2:77688800-77690000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr2:77688800-77690000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr2:77689000-77689400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:77689000-77689400	Enhancers	Fetal Brain Male	brain
36	chr2:77689000-77690000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:77689000-77690000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:77689200-77690000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:77689200-77692800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:77689400-77690000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr2:77689400-77693000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr2:77689600-77690000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:77689600-77693200	Weak transcription	Brain Germinal Matrix	brain
44	chr2:77689800-77693000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:77690200-77693000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr2:77691200-77692600	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr2:77692400-77692600	Active TSS	Brain Hippocampus Middle	brain
48	chr2:77692600-77692800	Flanking Active TSS	Brain Hippocampus Middle	brain
49	chr2:77692600-77693000	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr2:77692600-77693200	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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