Variant report

Variant	nsv891322
Chromosome Location	chr8:112978128-113267916
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	chr8:113038752-113039444	HepG2	liver:	n/a	n/a
2	ATF1	chr8:113041124-113041245	K562	blood:	n/a	n/a
3	BACH1	chr8:113114422-113114764	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr8:112980773-112980798	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:113219629-113219873	H1-hESC	embryonic stem cell:	n/a	chr8:113219724-113219733 chr8:113219723-113219734 chr8:113219722-113219733 chr8:113219722-113219735 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219722-113219735 chr8:113219689-113219697
6	CEBPB	chr8:113130499-113130817	IMR90	lung:	n/a	n/a
7	CEBPB	chr8:113122867-113123167	HepG2	liver:	n/a	chr8:113123001-113123012
8	CEBPB	chr8:113022271-113022547	HepG2	liver:	n/a	chr8:113022392-113022403
9	CEBPB	chr8:113134941-113135208	HepG2	liver:	n/a	chr8:113135033-113135042 chr8:113135032-113135043
10	CEBPB	chr8:113016873-113017172	IMR90	lung:	n/a	n/a
11	CEBPB	chr8:113124344-113124674	K562	blood:	n/a	n/a
12	CEBPB	chr8:113215823-113215968	H1-hESC	embryonic stem cell:	n/a	chr8:113215919-113215928 chr8:113215919-113215928 chr8:113215918-113215929 chr8:113215917-113215930 chr8:113215919-113215928 chr8:113215917-113215928 chr8:113215919-113215928
13	CEBPB	chr8:112979512-112979823	HepG2	liver:	n/a	chr8:112979671-112979682
14	CEBPB	chr8:112979515-112979804	K562	blood:	n/a	chr8:112979671-112979682
15	CEBPB	chr8:113200266-113200580	HepG2	liver:	n/a	chr8:113200412-113200423 chr8:113200411-113200424
16	CEBPB	chr8:113206405-113206718	HepG2	liver:	n/a	chr8:113206547-113206558
17	CEBPB	chr8:113016885-113017171	A549	lung:	n/a	n/a
18	CEBPB	chr8:113124393-113124693	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:113162725-113163296	MCF-7	breast:	n/a	n/a
20	CEBPB	chr8:113249290-113249512	A549	lung:	n/a	chr8:113249323-113249336
21	CEBPB	chr8:113219601-113219895	K562	blood:	n/a	chr8:113219724-113219733 chr8:113219723-113219734 chr8:113219722-113219733 chr8:113219722-113219735 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219722-113219735 chr8:113219689-113219697
22	CEBPB	chr8:113038782-113039266	HepG2	liver:	n/a	chr8:113039120-113039133
23	CEBPB	chr8:113158356-113158618	HepG2	liver:	n/a	chr8:113158502-113158513
24	CEBPB	chr8:113148585-113148957	HepG2	liver:	n/a	chr8:113148765-113148776
25	CEBPB	chr8:113124360-113124710	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:113200322-113200587	A549	lung:	n/a	chr8:113200412-113200423 chr8:113200411-113200424
27	CEBPB	chr8:113124365-113124706	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr8:113219563-113219901	IMR90	lung:	n/a	chr8:113219724-113219733 chr8:113219723-113219734 chr8:113219722-113219733 chr8:113219722-113219735 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219722-113219735 chr8:113219689-113219697
29	CEBPB	chr8:112979559-112979838	A549	lung:	n/a	chr8:112979671-112979682
30	CEBPB	chr8:113215733-113216060	A549	lung:	n/a	chr8:113215919-113215928 chr8:113215919-113215928 chr8:113215918-113215929 chr8:113215917-113215930 chr8:113215998-113216009 chr8:113215919-113215928 chr8:113215917-113215928 chr8:113215919-113215928
31	CEBPB	chr8:113177658-113177980	HepG2	liver:	n/a	chr8:113177817-113177828
32	CEBPB	chr8:113016889-113017172	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:113038704-113039417	MCF-7	breast:	n/a	chr8:113039120-113039133
34	CEBPB	chr8:113200327-113200529	K562	blood:	n/a	chr8:113200412-113200423 chr8:113200411-113200424
35	CEBPB	chr8:113215559-113216077	HepG2	liver:	n/a	chr8:113215919-113215928 chr8:113215919-113215928 chr8:113215918-113215929 chr8:113215917-113215930 chr8:113215998-113216009 chr8:113215919-113215928 chr8:113215917-113215928 chr8:113215919-113215928
36	CEBPB	chr8:113242212-113242350	A549	lung:	n/a	n/a
37	CEBPB	chr8:113130509-113130814	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:113219571-113219907	A549	lung:	n/a	chr8:113219724-113219733 chr8:113219723-113219734 chr8:113219722-113219733 chr8:113219722-113219735 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219722-113219735 chr8:113219689-113219697
39	CEBPB	chr8:113061491-113061642	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:113059099-113059288	A549	lung:	n/a	chr8:113059194-113059207
41	CEBPB	chr8:113161150-113161370	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:113124367-113124716	IMR90	lung:	n/a	n/a
43	CEBPB	chr8:113124347-113124676	A549	lung:	n/a	n/a
44	CEBPB	chr8:113162974-113163124	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:113162912-113163153	A549	lung:	n/a	n/a
46	CEBPB	chr8:113177713-113177962	IMR90	lung:	n/a	chr8:113177817-113177828
47	CEBPB	chr8:113022244-113022537	IMR90	lung:	n/a	chr8:113022392-113022403
48	CEBPB	chr8:113219552-113219914	HepG2	liver:	n/a	chr8:113219724-113219733 chr8:113219723-113219734 chr8:113219722-113219733 chr8:113219722-113219735 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219722-113219735 chr8:113219689-113219697
49	CEBPB	chr8:113162870-113163178	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr8:112979542-112979859	IMR90	lung:	n/a	chr8:112979671-112979682

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:113113972-113114022	SKMC	muscle:	n/a
2	chr8:113049519-113049569	AG09309	skin:	n/a
3	chr8:113113972-113114022	HCM	heart:	n/a
4	chr8:113113972-113114022	AG04449	skin:	fetal
5	chr8:113145005-113145055	HAEpiC	amniotic membrane:	n/a
6	chr8:113113972-113114022	AG04450	lung:	fetal
7	chr8:113049519-113049569	AoSMC	blood vessel:	n/a
8	chr8:113113972-113114022	NB4	blood:	n/a
9	chr8:113113972-113114022	HMEC	breast:	n/a
10	chr8:113049519-113049569	GM12878	blood:	n/a
11	chr8:113113972-113114022	SK-N-SH	brain:	n/a
12	chr8:113113972-113114022	HepG2	liver:	n/a
13	chr8:113145005-113145055	MCF10A-Er-Src	breast:	n/a
14	chr8:113113972-113114022	IMR90	lung:	fetal
15	chr8:113113972-113114022	NH-A	brain:	n/a
16	chr8:113049519-113049569	IMR90	lung:	fetal
17	chr8:113145005-113145055	NT2-D1	testis:	n/a
18	chr8:113145005-113145055	Hela-S3	cervix:	n/a
19	chr8:113049519-113049569	GM19239	blood:	n/a
20	chr8:113049519-113049569	BJ	skin:	n/a
21	chr8:113113972-113114022	GM19239	blood:	n/a
22	chr8:113049519-113049569	HCT-116	colon:	n/a
23	chr8:113113972-113114022	GM12878	blood:	n/a
24	chr8:113145005-113145055	Jurkat	blood:	n/a
25	chr8:113113972-113114022	HEEpiC	esophagus:	n/a
26	chr8:113145005-113145055	NHDF-neo	bronchial:	n/a
27	chr8:113113972-113114022	HRCEpiC	kidney:	n/a
28	chr8:113145005-113145055	U87	brain:	n/a
29	chr8:113145005-113145055	HRE	kidney:	n/a
30	chr8:113113972-113114022	ECC-1	luminal epithelium:	n/a
31	chr8:113145005-113145055	AG04449	skin:	fetal
32	chr8:113145005-113145055	PFSK-1	brain:	n/a
33	chr8:113113972-113114022	AoSMC	blood vessel:	n/a
34	chr8:113145005-113145055	H1-hESC	embryonic stem cell:	embryo
35	chr8:113113972-113114022	CMK	blood:	n/a
36	chr8:113145005-113145055	HEEpiC	esophagus:	n/a
37	chr8:113145005-113145055	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:113145005-113145055	ovcar-3	ovarian:	n/a
39	chr8:113049519-113049569	NB4	blood:	n/a
40	chr8:113145005-113145055	HCT-116	colon:	n/a
41	chr8:113049519-113049569	HIPEpiC	eye:	n/a
42	chr8:113049519-113049569	Hela-S3	cervix:	n/a
43	chr8:113113972-113114022	SAEC	small airway:	n/a
44	chr8:113113972-113114022	SK-N-SH_RA	brain:	n/a
45	chr8:113145005-113145055	AG09309	skin:	n/a
46	chr8:113113972-113114022	GM06990	blood:	n/a
47	chr8:113113972-113114022	NHDF-neo	bronchial:	n/a
48	chr8:113113972-113114022	HCF	heart:	n/a
49	chr8:113145005-113145055	K562	blood:	n/a
50	chr8:113049519-113049569	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:113123396..113125846-chr8:113130246..113132854,2	MCF-7	breast:
2	chr8:113121132..113122642-chr8:113123330..113125697,2	MCF-7	breast:
3	chr8:113123396..113125846-chr8:113130246..113132854,2	MCF-7	breast:
4	chr8:113057607..113060468-chr8:113062471..113064373,2	MCF-7	breast:
5	chr8:113057607..113060468-chr8:113062471..113064373,2	MCF-7	breast:
6	chr8:113234003..113236007-chr8:113240691..113242262,2	MCF-7	breast:
7	chr8:113121132..113122642-chr8:113123330..113125697,2	MCF-7	breast:
8	chr8:112980405..112982694-chr8:112982938..112985443,2	MCF-7	breast:
9	chr8:112980405..112982694-chr8:112982938..112985443,2	MCF-7	breast:
10	chr8:113036903..113039112-chr8:113145309..113148146,2	K562	blood:
11	chr8:113234003..113236007-chr8:113240691..113242262,2	MCF-7	breast:
12	chr8:113036903..113039112-chr8:113145309..113148146,2	K562	blood:

Variant related genes	Relation type
RNU4-37P	TF binding region
RNU4-37P	CpG island

Extended variants
information (count: 3863 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3863 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs716312	chr8:112978128-112978129	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577007115	chr8:112978141-112978142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539481847	chr8:112978172-112978173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138718600	chr8:112978197-112978198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557864441	chr8:112978220-112978221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190053454	chr8:112978221-112978222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541474958	chr8:112978232-112978233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10505166	chr8:112978248-112978249	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572035109	chr8:112978249-112978250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540823787	chr8:112978311-112978312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10505167	chr8:112978384-112978385	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs532989543	chr8:112978530-112978531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114777117	chr8:112978636-112978637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562859105	chr8:112978709-112978710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531717087	chr8:112978721-112978722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548630234	chr8:112978734-112978735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568768318	chr8:112978758-112978759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534541634	chr8:112978775-112978776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561502618	chr8:112986493-112986494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527484258	chr8:112986495-112986496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547041653	chr8:112986516-112986517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142204727	chr8:112986534-112986535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532521072	chr8:112986538-112986539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544433832	chr8:112986560-112986561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545325018	chr8:112986612-112986613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181816192	chr8:112986638-112986639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs57991593	chr8:112986668-112986669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565213572	chr8:112986697-112986698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548902944	chr8:112986730-112986731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568642470	chr8:112986744-112986745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534146660	chr8:112986749-112986750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556669680	chr8:112986792-112986793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62520458	chr8:112986827-112986828	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs186115548	chr8:112986838-112986839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547600380	chr8:112986839-112986840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555929255	chr8:112986900-112986901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567479540	chr8:112986971-112986972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575639675	chr8:112986978-112986979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115453530	chr8:112987049-112987050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs62520459	chr8:112987059-112987060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141910424	chr8:112987068-112987069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372643178	chr8:112987115-112987116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150635441	chr8:112987154-112987155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560612300	chr8:112987246-112987247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532544559	chr8:112987311-112987312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190858499	chr8:112987321-112987322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569593100	chr8:112987339-112987340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144609153	chr8:112992861-112992862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574353327	chr8:112992878-112992879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540493701	chr8:112992891-112992892	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112976000-112978800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr8:112977000-112978200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:112977000-112978200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr8:112977000-112978600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr8:112977600-112978200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:112986400-112987200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:112986600-112987200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:112987000-112987400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:112992800-112993200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:112993200-112993600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:112993600-112994200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:113003800-113006400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:113004000-113006400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr8:113005200-113005600	Enhancers	Primary hematopoietic stem cells	blood
15	chr8:113006400-113011600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:113006400-113011800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:113007800-113009400	Enhancers	Fetal Lung	lung
18	chr8:113011200-113012000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:113011600-113013200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:113011800-113013000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:113013000-113013800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:113013800-113014000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:113021200-113021400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:113021400-113021600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:113021600-113024400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:113027600-113030600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:113028600-113029000	Active TSS	Fetal Heart	heart
28	chr8:113035000-113036000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:113038600-113039000	Enhancers	HepG2	liver
30	chr8:113040600-113041000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr8:113044000-113046400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr8:113049200-113049800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr8:113049400-113050000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:113049600-113050400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr8:113049600-113050600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr8:113074200-113074800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:113075800-113076000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:113077600-113078000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:113077600-113078000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:113084400-113084800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr8:113086000-113086200	Enhancers	Gastric	stomach
42	chr8:113086000-113086400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:113086000-113086400	Active TSS	Skeletal Muscle Male	skeletal muscle
44	chr8:113086400-113095200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:113086600-113087400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:113087400-113087600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:113087600-113087800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:113087800-113088000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr8:113088000-113089600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr8:113089600-113090600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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