Variant report

Variant	nsv831284
Chromosome Location	chr8:35018419-35193084
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	BACH1	chr8:35189339-35189377	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:35094403-35094433	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:35180822-35181005	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:35181721-35181921	K562	blood:	n/a	chr8:35181773-35181787 chr8:35181784-35181798
5	BACH1	chr8:35181513-35182272	H1-hESC	embryonic stem cell:	n/a	chr8:35181773-35181787 chr8:35181784-35181798
6	BRCA1	chr8:35055526-35055735	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr8:35184325-35184525	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr8:35080010-35080284	K562	blood:	n/a	n/a
9	CEBPB	chr8:35040497-35040798	IMR90	lung:	n/a	chr8:35040637-35040648
10	CEBPB	chr8:35156083-35156363	IMR90	lung:	n/a	chr8:35156207-35156218 chr8:35156209-35156220 chr8:35156209-35156218
11	CEBPB	chr8:35156041-35156392	HepG2	liver:	n/a	chr8:35156207-35156218 chr8:35156209-35156220 chr8:35156209-35156218
12	CEBPB	chr8:35040485-35040840	H1-hESC	embryonic stem cell:	n/a	chr8:35040637-35040648
13	CEBPB	chr8:35050356-35050623	HepG2	liver:	n/a	chr8:35050512-35050523
14	CEBPB	chr8:35184745-35185054	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr8:35040489-35040827	A549	lung:	n/a	chr8:35040637-35040648
16	CEBPB	chr8:35040511-35041061	Hela-S3	cervix:	n/a	chr8:35040637-35040648
17	CEBPB	chr8:35094185-35094219	K562	blood:	n/a	chr8:35094190-35094199
18	CEBPB	chr8:35050323-35050696	H1-hESC	embryonic stem cell:	n/a	chr8:35050512-35050523
19	CEBPB	chr8:35184658-35185589	ECC-1	luminal epithelium:	n/a	chr8:35184680-35184697
20	CEBPB	chr8:35094023-35094388	H1-hESC	embryonic stem cell:	n/a	chr8:35094190-35094199
21	CEBPB	chr8:35185121-35185532	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr8:35052896-35053164	H1-hESC	embryonic stem cell:	n/a	chr8:35053013-35053024 chr8:35052991-35053002
23	CEBPB	chr8:35094036-35094269	HepG2	liver:	n/a	chr8:35094190-35094199
24	CEBPB	chr8:35156126-35156359	A549	lung:	n/a	chr8:35156207-35156218 chr8:35156209-35156220 chr8:35156209-35156218
25	CEBPB	chr8:35050372-35050669	A549	lung:	n/a	chr8:35050512-35050523
26	CEBPB	chr8:35026649-35026651	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:35040493-35040829	HepG2	liver:	n/a	chr8:35040637-35040648
28	CEBPB	chr8:35092496-35092833	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr8:35052839-35053175	A549	lung:	n/a	chr8:35053013-35053024 chr8:35052991-35053002
30	CEBPB	chr8:35052840-35053176	HepG2	liver:	n/a	chr8:35053013-35053024 chr8:35052991-35053002
31	CEBPB	chr8:35040557-35040664	K562	blood:	n/a	chr8:35040637-35040648
32	CEBPB	chr8:35050354-35050674	IMR90	lung:	n/a	chr8:35050512-35050523
33	CHD1	chr8:35092304-35092718	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr8:35092997-35094795	H1-hESC	embryonic stem cell:	n/a	chr8:35093291-35093301
35	CHD2	chr8:35092757-35093136	H1-hESC	embryonic stem cell:	n/a	chr8:35092780-35092790 chr8:35092783-35092793
36	CREB1	chr8:35092684-35093151	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr8:35092640-35093190	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr8:35184240-35184390	NB4	blood:	n/a	chr8:35184364-35184373
39	CTCF	chr8:35184302-35184408	LNCaP	prostate:	n/a	chr8:35184364-35184373
40	CTCF	chr8:35184200-35184350	GM12872	blood:	n/a	n/a
41	CTCF	chr8:35184370-35184391	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:35184300-35184450	Caco-2	colon:	n/a	chr8:35184364-35184373
43	CTCF	chr8:35184280-35184430	WERI-Rb-1	eye:	n/a	chr8:35184364-35184373
44	CTCF	chr8:35132100-35132250	HRE	kidney:	n/a	n/a
45	CTCF	chr8:35184320-35184470	SAEC	small airway:	n/a	chr8:35184364-35184373
46	CTCF	chr8:35184255-35184398	HepG2	liver:	n/a	chr8:35184364-35184373
47	CTCF	chr8:35184288-35184475	H1-hESC	embryonic stem cell:	n/a	chr8:35184364-35184373
48	CTCF	chr8:35184360-35184510	HEK293	kidney:	n/a	chr8:35184364-35184373
49	CTCF	chr8:35184320-35184470	HRE	kidney:	n/a	chr8:35184364-35184373
50	CTCF	chr8:35046130-35046199	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:35094001-35094051	BE2_C	brain:	n/a
2	chr8:35092687-35092737	HIPEpiC	eye:	n/a
3	chr8:35092687-35092737	ProgFib	skin:	n/a
4	chr8:35094001-35094051	BE2_C	brain:	n/a
5	chr8:35092687-35092737	HIPEpiC	eye:	n/a
6	chr8:35092687-35092737	ProgFib	skin:	n/a
7	chr8:35090128-35090178	HCF	heart:	n/a
8	chr8:35097798-35097848	A549	lung:	n/a
9	chr8:35094053-35094103	LNCaP	prostate:	n/a
10	chr8:35090128-35090178	HCPEpiC	choroid plexus:	n/a
11	chr8:35092876-35092926	HRE	kidney:	n/a
12	chr8:35090128-35090178	GM12891	blood:	n/a
13	chr8:35091536-35091586	Hela-S3	cervix:	n/a
14	chr8:35095362-35095412	BE2_C	brain:	n/a
15	chr8:35186363-35186413	GM06990	blood:	n/a
16	chr8:35091430-35091480	HepG2	liver:	n/a
17	chr8:35093411-35093461	NH-A	brain:	n/a
18	chr8:35093411-35093461	SAEC	small airway:	n/a
19	chr8:35092870-35092920	Caco-2	colon:	n/a
20	chr8:35092870-35092920	BE2_C	brain:	n/a
21	chr8:35092823-35092873	HIPEpiC	eye:	n/a
22	chr8:35091165-35091215	BJ	skin:	n/a
23	chr8:35092687-35092737	LNCaP	prostate:	n/a
24	chr8:35092876-35092926	AG09309	skin:	n/a
25	chr8:35092876-35092926	Hela-S3	cervix:	n/a
26	chr8:35101074-35101124	LNCaP	prostate:	n/a
27	chr8:35092876-35092926	HL-60	blood:	n/a
28	chr8:35135754-35135804	NHDF-neo	bronchial:	n/a
29	chr8:35092823-35092873	AG10803	skin:	n/a
30	chr8:35092870-35092920	HEK293	kidney:	embryo
31	chr8:35091430-35091480	T-47D	breast:	n/a
32	chr8:35090128-35090178	AG04449	skin:	fetal
33	chr8:35092823-35092873	U87	brain:	n/a
34	chr8:35135754-35135804	GM12892	blood:	n/a
35	chr8:35097798-35097848	H1-hESC	embryonic stem cell:	embryo
36	chr8:35135754-35135804	MCF-7	breast:	n/a
37	chr8:35094053-35094103	AG04450	lung:	fetal
38	chr8:35092876-35092926	Jurkat	blood:	n/a
39	chr8:35093411-35093461	MCF10A-Er-Src	breast:	n/a
40	chr8:35091165-35091215	GM19239	blood:	n/a
41	chr8:35091536-35091586	MCF-7	breast:	n/a
42	chr8:35095362-35095412	NHDF-neo	bronchial:	n/a
43	chr8:35101074-35101124	GM12892	blood:	n/a
44	chr8:35091548-35091598	Caco-2	colon:	n/a
45	chr8:35135754-35135804	SK-N-SH	brain:	n/a
46	chr8:35097798-35097848	MCF-7	breast:	n/a
47	chr8:35092823-35092873	HEK293	kidney:	embryo
48	chr8:35092687-35092737	HepG2	liver:	n/a
49	chr8:35092876-35092926	AG04449	skin:	fetal
50	chr8:35101074-35101124	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:35018612..35019300-chr8:35998668..35999178,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC5D-4	chr8:35057929-35058030	l_3577_chr8:35057575-35070873_testes
2	lnc-UNC5D-4	chr8:35070198-35070873	l_3577_chr8:35057575-35070873_testes
3	lnc-UNC5D-4	chr8:35057576-35057769	l_3577_chr8:35057575-35070873_testes

Variant related genes	Relation type
UNC5D	TF binding region
UNC5D	CpG island

Extended variants
information (count: 5170 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:5170 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141437933	chr8:35018452-35018453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142643621	chr8:35018482-35018483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551448185	chr8:35018483-35018484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555318805	chr8:35018541-35018542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189717514	chr8:35018589-35018590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150985640	chr8:35018596-35018597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375402068	chr8:35018616-35018617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567928419	chr8:35018621-35018622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201051809	chr8:35018657-35018658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140810273	chr8:35018690-35018691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551915753	chr8:35018706-35018707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148614649	chr8:35018707-35018708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs71910000	chr8:35018709-35018710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs57974910	chr8:35018741-35018742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74886503	chr8:35018753-35018754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114692183	chr8:35018813-35018814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs578120841	chr8:35018824-35018825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538794895	chr8:35018850-35018851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569040241	chr8:35018863-35018864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554221347	chr8:35018878-35018879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572374090	chr8:35018934-35018935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542584160	chr8:35018958-35018959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561662273	chr8:35019087-35019088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534562242	chr8:35019111-35019112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573557248	chr8:35019157-35019158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552863802	chr8:35019158-35019159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544004331	chr8:35019179-35019180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539747414	chr8:35019209-35019210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533136287	chr8:35019240-35019241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544805479	chr8:35019260-35019261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560165649	chr8:35019274-35019275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111449881	chr8:35019299-35019300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs67724435	chr8:35019303-35019304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200367041	chr8:35019306-35019307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527301827	chr8:35019338-35019339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557639404	chr8:35019339-35019340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567965125	chr8:35019348-35019349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532088560	chr8:35019413-35019414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182416873	chr8:35019452-35019453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs16883597	chr8:35019465-35019466	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs186363506	chr8:35019476-35019477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539198419	chr8:35019482-35019483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192121761	chr8:35019483-35019484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183619546	chr8:35019494-35019495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573009692	chr8:35019572-35019573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536254784	chr8:35019602-35019603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370388835	chr8:35019648-35019649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372663462	chr8:35019658-35019659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554494735	chr8:35019677-35019678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188202491	chr8:35019680-35019681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:768 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35010200-35020000	Weak transcription	Fetal Kidney	kidney
2	chr8:35019400-35019800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr8:35020000-35020200	Enhancers	Fetal Kidney	kidney
4	chr8:35026400-35027600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr8:35036000-35036200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr8:35036200-35040000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:35039800-35040200	Enhancers	HMEC	breast
8	chr8:35040000-35040800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:35040000-35041000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr8:35040000-35041000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:35040000-35041200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:35040000-35041400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr8:35040200-35040800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:35040200-35040800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr8:35040200-35041000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:35040200-35041800	Enhancers	H9 Cell Line	embryonic stem cell
17	chr8:35040400-35041000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr8:35040400-35041200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:35040800-35042200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr8:35040800-35045000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr8:35040800-35048400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr8:35041200-35043000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr8:35041200-35048600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:35041400-35047800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr8:35042200-35042400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr8:35045000-35047600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr8:35047600-35050200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr8:35047800-35049800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr8:35048200-35049800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr8:35048400-35049600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:35048400-35050000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr8:35048400-35051000	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr8:35048400-35051200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:35048400-35052200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr8:35048600-35048800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:35048600-35051400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:35049200-35050400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:35049800-35050400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr8:35049800-35051000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr8:35050200-35050600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr8:35050400-35051200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:35050400-35052000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr8:35050600-35051200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr8:35051000-35052600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr8:35051400-35056600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr8:35052200-35052600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr8:35052600-35053000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:35054200-35054400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
49	chr8:35060400-35061600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr8:35061200-35062400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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