Variant report

Variant	nsv891291
Chromosome Location	chr8:111462136-111681660
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	chr8:111523582-111523674	K562	blood:	n/a	n/a
2	CEBPB	chr8:111663882-111664226	IMR90	lung:	n/a	n/a
3	CEBPB	chr8:111539037-111539369	IMR90	lung:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
4	CEBPB	chr8:111505352-111505461	HepG2	liver:	n/a	chr8:111505411-111505422
5	CEBPB	chr8:111551759-111552363	MCF-7	breast:	n/a	n/a
6	CEBPB	chr8:111655159-111655467	HepG2	liver:	n/a	chr8:111655308-111655319
7	CEBPB	chr8:111655239-111655443	H1-hESC	embryonic stem cell:	n/a	chr8:111655308-111655319
8	CEBPB	chr8:111470033-111470437	MCF-7	breast:	n/a	n/a
9	CEBPB	chr8:111630967-111631208	HepG2	liver:	n/a	chr8:111631031-111631042
10	CEBPB	chr8:111566370-111566428	HepG2	liver:	n/a	chr8:111566413-111566424
11	CEBPB	chr8:111520325-111520598	HepG2	liver:	n/a	chr8:111520458-111520471 chr8:111520458-111520471 chr8:111520460-111520471 chr8:111520460-111520469 chr8:111520458-111520469
12	CEBPB	chr8:111634949-111635197	IMR90	lung:	n/a	chr8:111635032-111635043
13	CEBPB	chr8:111617237-111617564	HepG2	liver:	n/a	chr8:111617393-111617404
14	CEBPB	chr8:111505335-111505447	A549	lung:	n/a	chr8:111505347-111505358 chr8:111505411-111505422
15	CEBPB	chr8:111573269-111573432	A549	lung:	n/a	n/a
16	CEBPB	chr8:111599775-111599936	K562	blood:	n/a	chr8:111599861-111599872
17	CEBPB	chr8:111563765-111564094	A549	lung:	n/a	chr8:111563940-111563951
18	CEBPB	chr8:111470060-111470420	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:111678139-111678458	HepG2	liver:	n/a	chr8:111678273-111678284
20	CEBPB	chr8:111634989-111635163	HepG2	liver:	n/a	chr8:111635032-111635043
21	CEBPB	chr8:111563470-111564178	MCF-7	breast:	n/a	chr8:111563940-111563951
22	CEBPB	chr8:111503841-111503896	K562	blood:	n/a	n/a
23	CEBPB	chr8:111539028-111539286	HepG2	liver:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
24	CEBPB	chr8:111503761-111504005	HepG2	liver:	n/a	chr8:111503888-111503901 chr8:111503888-111503899 chr8:111503889-111503900 chr8:111503888-111503901 chr8:111503888-111503901 chr8:111503888-111503899
25	CEBPB	chr8:111525002-111525202	HepG2	liver:	n/a	chr8:111525140-111525151 chr8:111525141-111525150 chr8:111525139-111525150
26	CEBPB	chr8:111678183-111678436	A549	lung:	n/a	chr8:111678273-111678284
27	CEBPB	chr8:111503758-111503941	H1-hESC	embryonic stem cell:	n/a	chr8:111503888-111503901 chr8:111503888-111503899 chr8:111503889-111503900 chr8:111503888-111503901 chr8:111503888-111503901 chr8:111503888-111503899
28	CEBPB	chr8:111566321-111566477	A549	lung:	n/a	chr8:111566413-111566424
29	CEBPB	chr8:111663840-111664346	MCF-7	breast:	n/a	n/a
30	CEBPB	chr8:111539090-111539260	H1-hESC	embryonic stem cell:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
31	CEBPB	chr8:111485063-111485373	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:111623432-111623641	MCF-7	breast:	n/a	n/a
33	CEBPB	chr8:111599789-111599997	HepG2	liver:	n/a	chr8:111599955-111599967 chr8:111599861-111599872
34	CEBPB	chr8:111469908-111470608	MCF-7	breast:	n/a	n/a
35	CEBPB	chr8:111605973-111606139	HepG2	liver:	n/a	chr8:111606013-111606024
36	CEBPB	chr8:111563640-111564025	MCF-7	breast:	n/a	chr8:111563940-111563951
37	CEBPB	chr8:111539099-111539344	A549	lung:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
38	CEBPB	chr8:111628707-111629028	HepG2	liver:	n/a	chr8:111628857-111628870 chr8:111628857-111628868 chr8:111628859-111628870 chr8:111628857-111628870 chr8:111628857-111628870 chr8:111628859-111628870
39	CEBPB	chr8:111539118-111539315	K562	blood:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
40	CEBPB	chr8:111485138-111485350	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:111673382-111673531	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:111580266-111580852	MCF-7	breast:	n/a	chr8:111580459-111580472
43	CEBPB	chr8:111563777-111564088	HepG2	liver:	n/a	chr8:111563940-111563951
44	CEBPB	chr8:111663794-111664226	MCF-7	breast:	n/a	n/a
45	CEBPB	chr8:111551859-111552317	MCF-7	breast:	n/a	n/a
46	CEBPZ	chr8:111561657-111561751	HepG2	liver:	n/a	n/a
47	CHD2	chr8:111571903-111572103	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr8:111571864-111572042	Gliobla	brain:	n/a	n/a
49	CTCF	chr8:111571960-111572110	HCT-116	colon:	n/a	n/a
50	CTCF	chr8:111610569-111610676	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:111564585..111566803-chr8:111570856..111572872,2	K562	blood:
2	chr8:111581974..111583484-chr8:111589126..111591939,2	MCF-7	breast:
3	chr8:111579951..111580480-chr8:111668750..111669442,2	MCF-7	breast:
4	chr8:111365043..111367620-chr8:111553595..111556957,3	MCF-7	breast:
5	chr7:153439451..153439951-chr8:111669137..111669684,2	MCF-7	breast:
6	chr8:111597648..111599475-chr8:111601535..111603940,2	MCF-7	breast:
7	chr8:111563289..111565363-chr8:111579783..111581298,2	MCF-7	breast:
8	chr8:111579951..111580480-chr8:111668750..111669442,2	MCF-7	breast:
9	chr2:189912462..189915135-chr8:111597995..111599883,2	MCF-7	breast:
10	chr8:111662012..111664592-chr8:111665712..111669617,3	MCF-7	breast:
11	chr8:111606860..111609172-chr8:111612437..111615361,2	K562	blood:
12	chr8:111594065..111596990-chr8:111668768..111671358,2	MCF-7	breast:
13	chr8:111564377..111566155-chr8:111573076..111575001,2	MCF-7	breast:
14	chr7:156803278..156804875-chr8:111542688..111545615,2	MCF-7	breast:
15	chr8:111554765..111555294-chr8:111669236..111669854,2	MCF-7	breast:
16	chr8:111629561..111631393-chr8:111634350..111636471,2	MCF-7	breast:
17	chr8:111676345..111679299-chr8:111684096..111685867,2	MCF-7	breast:
18	chr8:111606860..111609172-chr8:111612437..111615361,2	K562	blood:
19	chr8:111632530..111634212-chr8:111646106..111648334,2	MCF-7	breast:
20	chr8:111575672..111578651-chr8:111595648..111598231,2	MCF-7	breast:
21	chr8:111519159..111521111-chr8:111524177..111525688,2	MCF-7	breast:
22	chr8:111575672..111578651-chr8:111595648..111598231,2	MCF-7	breast:
23	chr22:21987659..21988468-chr8:111631630..111632515,2	MCF-7	breast:
24	chr8:111563289..111565363-chr8:111579783..111581298,2	MCF-7	breast:
25	chr8:111554765..111555294-chr8:111669236..111669854,2	MCF-7	breast:
26	chr8:111581974..111583484-chr8:111589126..111591939,2	MCF-7	breast:
27	chr8:111629561..111631393-chr8:111634350..111636471,2	MCF-7	breast:
28	chr8:111632530..111634212-chr8:111646106..111648334,2	MCF-7	breast:
29	chr15:38663825..38666657-chr8:111561522..111564455,2	MCF-7	breast:
30	chr8:111594065..111596990-chr8:111668768..111671358,2	MCF-7	breast:
31	chr8:111665338..111666843-chr8:111677219..111678888,2	K562	blood:
32	chr8:111564377..111566155-chr8:111573076..111575001,2	MCF-7	breast:
33	chr8:111662012..111664592-chr8:111665712..111669617,3	MCF-7	breast:
34	chr8:111667414..111669906-chr8:111688361..111690572,2	MCF-7	breast:
35	chr8:111663406..111666569-chr8:111666819..111669452,4	MCF-7	breast:
36	chr11:74302754..74304460-chr8:111676552..111678415,2	MCF-7	breast:
37	chr8:111618584..111620243-chr8:111621032..111622618,2	MCF-7	breast:
38	chr8:111551159..111553132-chr8:111554691..111557321,2	MCF-7	breast:
39	chr8:111668947..111669607-chr8:111877933..111878646,3	MCF-7	breast:
40	chr8:111597648..111599475-chr8:111601535..111603940,2	MCF-7	breast:
41	chr8:111551159..111553132-chr8:111554691..111557321,2	MCF-7	breast:
42	chr8:111563681..111564416-chr8:111663211..111663982,2	MCF-7	breast:
43	chr20:47537126..47538714-chr8:111554238..111556097,2	MCF-7	breast:
44	chr8:111669709..111671243-chr8:111673107..111675313,2	MCF-7	breast:
45	chr8:111564585..111566803-chr8:111570856..111572872,2	K562	blood:
46	chr8:111665338..111666843-chr8:111677219..111678888,2	K562	blood:
47	chr8:111561274..111563938-chr8:111668171..111670064,2	MCF-7	breast:
48	chr8:111661559..111663835-chr8:111734745..111737537,2	MCF-7	breast:
49	chr8:111663406..111666569-chr8:111666819..111669452,4	MCF-7	breast:
50	chr8:111563681..111564416-chr8:111663211..111663982,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-5	chr8:111567637-111568747	NONHSAT128309

Variant related genes	Relation type
ENSG00000253107	TF binding region
ENSG00000253122	TF binding region
ENSG00000124198	chromatin interactions
ENSG00000243479	chromatin interactions
ENSG00000130675	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000077514	chromatin interactions
ENSG00000253122	chromatin interactions

Extended variants
information (count: 3194 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3194 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192029531	chr8:111464334-111464335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540982605	chr8:111464370-111464371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374081711	chr8:111464371-111464372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183925719	chr8:111464400-111464401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77356729	chr8:111464412-111464413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs66481762	chr8:111464432-111464433	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs529936101	chr8:111464472-111464473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533837970	chr8:111464482-111464483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553510765	chr8:111464490-111464491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551269082	chr8:111464525-111464526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576739939	chr8:111464526-111464527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539424724	chr8:111464534-111464535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556922714	chr8:111464540-111464541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79211303	chr8:111464547-111464548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542482929	chr8:111464554-111464555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562266862	chr8:111464556-111464557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149979476	chr8:111464581-111464582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541484917	chr8:111464594-111464595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564337129	chr8:111464633-111464634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74565022	chr8:111464674-111464675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566462669	chr8:111464681-111464682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187630957	chr8:111464682-111464683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562484961	chr8:111464689-111464690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531462788	chr8:111464695-111464696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189666150	chr8:111464755-111464756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568219566	chr8:111464770-111464771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533667491	chr8:111464835-111464836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547503556	chr8:111464859-111464860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182287039	chr8:111464906-111464907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539485779	chr8:111464909-111464910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76271088	chr8:111464912-111464913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549693665	chr8:111464935-111464936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576815991	chr8:111464955-111464956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533738374	chr8:111464973-111464974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555702717	chr8:111465001-111465002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187329244	chr8:111465039-111465040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113227728	chr8:111465050-111465051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77269919	chr8:111465107-111465108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558280235	chr8:111465158-111465159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139765713	chr8:111465164-111465165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543424009	chr8:111465224-111465225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191735347	chr8:111465242-111465243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531523316	chr8:111465248-111465249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569500072	chr8:111465260-111465261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185289915	chr8:111465307-111465308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567657077	chr8:111465325-111465326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561820098	chr8:111465336-111465337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573732050	chr8:111465346-111465347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527507452	chr8:111465355-111465356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532147973	chr8:111465376-111465377	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Glioblastoma multiforme	21080181	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
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
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111464200-111464600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr8:111464200-111464800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr8:111464200-111464800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr8:111464200-111464800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr8:111464600-111465400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:111465400-111466600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:111466600-111467200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:111466800-111467200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
9	chr8:111469200-111469400	Enhancers	Placenta Amnion	Placenta Amnion
10	chr8:111469600-111470600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr8:111469800-111470400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:111469800-111470600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr8:111469800-111471000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:111469800-111471000	Enhancers	HMEC	breast
15	chr8:111469800-111471200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:111470000-111470600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr8:111470200-111470600	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr8:111470400-111471200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:111470600-111471000	Enhancers	Placenta Amnion	Placenta Amnion
20	chr8:111472000-111472800	Enhancers	Fetal Heart	heart
21	chr8:111472400-111472600	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr8:111472600-111472800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:111472600-111473400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:111473000-111474000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:111473200-111474200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:111474000-111474400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr8:111496800-111497800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:111520400-111521600	Enhancers	HUVEC	blood vessel
29	chr8:111521200-111522000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:111521400-111521800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:111521400-111521800	Enhancers	Colon Smooth Muscle	Colon
32	chr8:111521400-111522000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:111521400-111522000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr8:111521400-111522000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr8:111521600-111522000	Flanking Active TSS	HUVEC	blood vessel
36	chr8:111522000-111522400	Enhancers	HUVEC	blood vessel
37	chr8:111533400-111533800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:111535000-111535400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr8:111535000-111535400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr8:111535200-111535600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr8:111537800-111538400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr8:111538400-111538800	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr8:111538800-111539200	Enhancers	Placenta Amnion	Placenta Amnion
44	chr8:111548600-111550200	Active TSS	Right Atrium	heart
45	chr8:111550600-111550800	Enhancers	Pancreas	Pancrea
46	chr8:111556000-111556400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:111556200-111556600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr8:111556400-111556600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr8:111556600-111562200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr8:111563400-111564600	Enhancers	HMEC	breast

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