Variant report

Variant	nsv831344
Chromosome Location	chr8:64658229-64712338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:64663736-64664361	GM12878	blood:	n/a	n/a
2	BATF	chr8:64671496-64671744	GM12878	blood:	n/a	n/a
3	BATF	chr8:64671799-64672147	GM12878	blood:	n/a	n/a
4	BATF	chr8:64670790-64671070	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:64706949-64707278	IMR90	lung:	n/a	n/a
6	CEBPB	chr8:64706944-64707246	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:64665252-64665290	HepG2	liver:	n/a	chr8:64665271-64665282
8	CEBPB	chr8:64694489-64694534	HepG2	liver:	n/a	chr8:64694518-64694529
9	CEBPB	chr8:64693108-64693314	A549	lung:	n/a	chr8:64693246-64693257
10	CEBPB	chr8:64693103-64693398	HepG2	liver:	n/a	chr8:64693246-64693257
11	CEBPB	chr8:64706953-64707265	A549	lung:	n/a	n/a
12	CEBPB	chr8:64706958-64707302	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr8:64659104-64659172	Fibrobl	skin:	n/a	n/a
14	CTCF	chr8:64662620-64662770	GM12873	blood:	n/a	n/a
15	CTCF	chr8:64669985-64670059	GM10248	blood:	n/a	n/a
16	CTCF	chr8:64662680-64662830	GM06990	blood:	n/a	n/a
17	CTCF	chr8:64662592-64662842	GM12878	blood:	n/a	n/a
18	CTCF	chr8:64662580-64662730	HRE	kidney:	n/a	n/a
19	CTCF	chr8:64662180-64662330	GM06990	blood:	n/a	n/a
20	CTCF	chr8:64662560-64662710	RPTEC	kidney:	n/a	n/a
21	CTCF	chr8:64671820-64671859	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr8:64703062-64703184	K562	blood:	n/a	n/a
23	CTCF	chr8:64694882-64694952	GM13976	blood:	n/a	n/a
24	CTCF	chr8:64662520-64662670	RPTEC	kidney:	n/a	n/a
25	CTCF	chr8:64671584-64671664	GM13976	blood:	n/a	n/a
26	CTCF	chr8:64662600-64662750	GM06990	blood:	n/a	n/a
27	CTCF	chr8:64697360-64697510	GM12867	blood:	n/a	n/a
28	CTCF	chr8:64662600-64662750	GM12873	blood:	n/a	n/a
29	JUN	chr8:64684567-64684617	H1-hESC	embryonic stem cell:	n/a	n/a
30	JUND	chr8:64693173-64693286	HepG2	liver:	n/a	n/a
31	MAFF	chr8:64672579-64672809	K562	blood:	n/a	chr8:64672722-64672740
32	MAFF	chr8:64672546-64672869	HepG2	liver:	n/a	chr8:64672722-64672740
33	MAFK	chr8:64672661-64672796	Hela-S3	cervix:	n/a	chr8:64672723-64672738
34	MAFK	chr8:64672561-64672759	K562	blood:	n/a	chr8:64672723-64672738
35	MAFK	chr8:64673452-64673565	HepG2	liver:	n/a	chr8:64673495-64673510
36	MAFK	chr8:64672551-64672879	IMR90	lung:	n/a	chr8:64672723-64672738
37	MAFK	chr8:64699819-64699876	HepG2	liver:	n/a	chr8:64699823-64699839 chr8:64699824-64699844 chr8:64699826-64699842 chr8:64699823-64699838 chr8:64699824-64699835
38	MAFK	chr8:64699721-64699947	HepG2	liver:	n/a	chr8:64699823-64699839 chr8:64699824-64699844 chr8:64699826-64699842 chr8:64699823-64699838 chr8:64699824-64699835
39	MAFK	chr8:64672563-64672890	HepG2	liver:	n/a	chr8:64672723-64672738
40	MAFK	chr8:64672544-64672911	HepG2	liver:	n/a	chr8:64672723-64672738
41	MAFK	chr8:64705125-64705188	HepG2	liver:	n/a	chr8:64705164-64705179
42	MAFK	chr8:64672562-64672748	H1-hESC	embryonic stem cell:	n/a	chr8:64672723-64672738
43	MEF2A	chr8:64663791-64664427	GM12878	blood:	n/a	chr8:64664062-64664083 chr8:64664069-64664080 chr8:64663902-64663911 chr8:64663898-64663914 chr8:64664326-64664334 chr8:64664067-64664081 chr8:64664066-64664081 chr8:64663899-64663914 chr8:64663902-64663913
44	MEF2A	chr8:64675020-64675340	GM12878	blood:	n/a	n/a
45	MEF2A	chr8:64676582-64676935	GM12878	blood:	n/a	n/a
46	MEF2A	chr8:64671596-64672047	GM12878	blood:	n/a	n/a
47	MXI1	chr8:64662331-64662343	GM12878	blood:	n/a	n/a
48	MYC	chr8:64667794-64667805	MCF-7	breast:	n/a	n/a
49	NFIC	chr8:64663827-64664357	GM12878	blood:	n/a	n/a
50	NFIC	chr8:64671529-64672291	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:64681200-64681250	HEEpiC	esophagus:	n/a
2	chr8:64681840-64681890	NHDF-neo	bronchial:	n/a
3	chr8:64681200-64681250	NB4	blood:	n/a
4	chr8:64681840-64681890	Hepatocyte	liver:	n/a
5	chr8:64681200-64681250	H1-hESC	embryonic stem cell:	embryo
6	chr8:64681840-64681890	BJ	skin:	n/a
7	chr8:64681200-64681250	GM19239	blood:	n/a
8	chr8:64681840-64681890	RPTEC	kidney:	n/a
9	chr8:64681200-64681250	CMK	blood:	n/a
10	chr8:64681200-64681250	MCF10A-Er-Src	breast:	n/a
11	chr8:64681200-64681250	U87	brain:	n/a
12	chr8:64681840-64681890	HRPEpiC	eye:	n/a
13	chr8:64681840-64681890	BE2_C	brain:	n/a
14	chr8:64681840-64681890	GM12892	blood:	n/a
15	chr8:64681200-64681250	HRE	kidney:	n/a
16	chr8:64681200-64681250	SK-N-SH	brain:	n/a
17	chr8:64681840-64681890	GM12878	blood:	n/a
18	chr8:64681840-64681890	K562	blood:	n/a
19	chr8:64681840-64681890	HCM	heart:	n/a
20	chr8:64681840-64681890	SK-N-SH	brain:	n/a
21	chr8:64681200-64681250	HPAEpiC	pulmonary alveolar:	n/a
22	chr8:64681840-64681890	H1-hESC	embryonic stem cell:	embryo
23	chr8:64681200-64681250	NT2-D1	testis:	n/a
24	chr8:64681200-64681250	HUVEC	blood vessel:	n/a
25	chr8:64681840-64681890	Jurkat	blood:	n/a
26	chr8:64681200-64681250	HEK293	kidney:	embryo
27	chr8:64681200-64681250	HRCEpiC	kidney:	n/a
28	chr8:64681200-64681250	T-47D	breast:	n/a
29	chr8:64681200-64681250	HCT-116	colon:	n/a
30	chr8:64681840-64681890	SK-N-SH_RA	brain:	n/a
31	chr8:64681200-64681250	Hepatocyte	liver:	n/a
32	chr8:64681200-64681250	ECC-1	luminal epithelium:	n/a
33	chr8:64681840-64681890	MCF10A-Er-Src	breast:	n/a
34	chr8:64681840-64681890	GM06990	blood:	n/a
35	chr8:64681200-64681250	Hela-S3	cervix:	n/a
36	chr8:64681840-64681890	HCT-116	colon:	n/a
37	chr8:64681840-64681890	MCF-7	breast:	n/a
38	chr8:64681840-64681890	AG09319	gingival:	n/a
39	chr8:64681840-64681890	PrEC	prostate:	n/a
40	chr8:64681200-64681250	GM12892	blood:	n/a
41	chr8:64681200-64681250	NHDF-neo	bronchial:	n/a
42	chr8:64681840-64681890	AG10803	skin:	n/a
43	chr8:64681840-64681890	GM19239	blood:	n/a
44	chr8:64681200-64681250	A549	lung:	n/a
45	chr8:64681200-64681250	PFSK-1	brain:	n/a
46	chr8:64681200-64681250	BE2_C	brain:	n/a
47	chr8:64681200-64681250	GM06990	blood:	n/a
48	chr8:64681840-64681890	PANC-1	pancreas:	n/a
49	chr8:64681840-64681890	T-47D	breast:	n/a
50	chr8:64681840-64681890	NHBE	bronchial:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:64662934..64664651-chr8:64673638..64676203,2	K562	blood:
2	chr8:64662235..64663084-chr8:65176753..65177365,3	MCF-7	breast:
3	chr8:64662291..64663069-chr8:65294420..65295295,2	MCF-7	breast:
4	chr17:61903864..61904600-chr8:64662891..64663391,2	MCF-7	breast:
5	chr8:64662934..64664651-chr8:64673638..64676203,2	K562	blood:
6	chr8:64692440..64694258-chr8:64697965..64699703,2	MCF-7	breast:
7	chr8:64662682..64663203-chr8:65176721..65177303,2	MCF-7	breast:
8	chr8:64692440..64694258-chr8:64697965..64699703,2	MCF-7	breast:
9	chr17:61903672..61905628-chr8:64662891..64664391,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-32K4.2.1-2	chr8:64660164-64660313	ENSG00000253762
2	lnc-RP11-32K4.2.1-2	chr8:64664133-64664235	ENSG00000253762
3	lnc-RP11-32K4.2.1-1	chr8:64681988-64682403	NR_038875
4	lnc-RP11-32K4.2.1-1	chr8:64697237-64698058	ENSG00000253734
5	lnc-RP11-32K4.2.1-1	chr8:64697237-64698054	NR_038875
6	lnc-RP11-32K4.2.1-1	chr8:64691006-64693479	ENSG00000253734
7	lnc-RP11-32K4.2.1-1	chr8:64681988-64682403	ENSG00000253734
8	lnc-RP11-32K4.2.1-1	chr8:64691006-64693479	NR_038875
9	lnc-RP11-32K4.2.1-1	chr8:64686472-64686494	NONHSAT126951
10	lnc-RP11-32K4.2.1-1	chr8:64691006-64691560	NONHSAT126951

No data

Variant related genes	Relation type
ENSG00000253734	TF binding region
ENSG00000253734	CpG island
ENSG00000108592	chromatin interactions
ENSG00000087191	chromatin interactions

Extended variants
information (count: 1313 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1313 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28542151	chr8:64658276-64658277	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369639574	chr8:64658294-64658295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544510613	chr8:64658319-64658320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73686538	chr8:64658320-64658321	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs560099270	chr8:64658385-64658386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530270479	chr8:64658423-64658424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77732479	chr8:64658430-64658431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531565907	chr8:64658500-64658501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563337645	chr8:64658530-64658531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144796009	chr8:64658545-64658546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547944437	chr8:64658546-64658547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552127369	chr8:64658580-64658581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570397250	chr8:64658595-64658596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114505847	chr8:64658633-64658634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546445712	chr8:64658674-64658675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568039180	chr8:64658709-64658710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140291632	chr8:64658711-64658712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185657500	chr8:64658737-64658738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188588756	chr8:64658739-64658740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537196920	chr8:64658770-64658771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143424638	chr8:64658771-64658772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10090496	chr8:64658778-64658779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs541440629	chr8:64658779-64658780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560059086	chr8:64658797-64658798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373722168	chr8:64658798-64658799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575225601	chr8:64658809-64658810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542425807	chr8:64658812-64658813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547379499	chr8:64658814-64658815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570505913	chr8:64658829-64658830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376856633	chr8:64658852-64658853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563898757	chr8:64658877-64658878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370564797	chr8:64658893-64658894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374588569	chr8:64658919-64658920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548378220	chr8:64658942-64658943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572496167	chr8:64658964-64658965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201267115	chr8:64658973-64658974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59070811	chr8:64658975-64658976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs397738447	chr8:64658978-64658979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552024145	chr8:64658980-64658981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192928561	chr8:64659041-64659042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564215431	chr8:64659044-64659045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376700221	chr8:64659064-64659065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528025444	chr8:64659075-64659076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535101761	chr8:64659097-64659098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568001119	chr8:64659146-64659147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535391322	chr8:64659214-64659215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184794040	chr8:64659222-64659223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568999448	chr8:64659261-64659262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368005301	chr8:64659264-64659265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562743565	chr8:64659316-64659317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64654400-64663400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:64659400-64659600	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr8:64661800-64664200	Enhancers	Fetal Brain Male	brain
4	chr8:64662800-64663800	Enhancers	GM12878-XiMat	blood
5	chr8:64663000-64663400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:64663000-64663400	Active TSS	Fetal Brain Female	brain
7	chr8:64663400-64663600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:64663800-64665000	Flanking Active TSS	GM12878-XiMat	blood
9	chr8:64665000-64665400	Enhancers	GM12878-XiMat	blood
10	chr8:64665400-64666200	Weak transcription	GM12878-XiMat	blood
11	chr8:64666200-64666400	Enhancers	GM12878-XiMat	blood
12	chr8:64666400-64671200	Weak transcription	GM12878-XiMat	blood
13	chr8:64671200-64673000	Enhancers	GM12878-XiMat	blood
14	chr8:64675200-64675400	Enhancers	GM12878-XiMat	blood
15	chr8:64675400-64676400	Weak transcription	GM12878-XiMat	blood
16	chr8:64676400-64677200	Enhancers	GM12878-XiMat	blood
17	chr8:64680000-64680600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:64680200-64680400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:64680400-64681000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr8:64680400-64681200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:64680400-64681200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:64680600-64680800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:64680600-64681200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:64681200-64681800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr8:64690800-64691200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:64691200-64700800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr8:64700800-64701000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:64701000-64706000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:64706000-64706200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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