Variant report

Variant	nsv891292
Chromosome Location	chr8:111478321-111673039
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	chr8:111539037-111539369	IMR90	lung:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
3	CEBPB	chr8:111655239-111655443	H1-hESC	embryonic stem cell:	n/a	chr8:111655308-111655319
4	CEBPB	chr8:111655159-111655467	HepG2	liver:	n/a	chr8:111655308-111655319
5	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
6	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
7	CEBPB	chr8:111599775-111599936	K562	blood:	n/a	chr8:111599861-111599872
8	CEBPB	chr8:111663882-111664226	IMR90	lung:	n/a	n/a
9	CEBPB	chr8:111485063-111485373	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:111539118-111539315	K562	blood:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
11	CEBPB	chr8:111599789-111599997	HepG2	liver:	n/a	chr8:111599955-111599967 chr8:111599861-111599872
12	CEBPB	chr8:111617237-111617564	HepG2	liver:	n/a	chr8:111617393-111617404
13	CEBPB	chr8:111663840-111664346	MCF-7	breast:	n/a	n/a
14	CEBPB	chr8:111580266-111580852	MCF-7	breast:	n/a	chr8:111580459-111580472
15	CEBPB	chr8:111563640-111564025	MCF-7	breast:	n/a	chr8:111563940-111563951
16	CEBPB	chr8:111563777-111564088	HepG2	liver:	n/a	chr8:111563940-111563951
17	CEBPB	chr8:111563470-111564178	MCF-7	breast:	n/a	chr8:111563940-111563951
18	CEBPB	chr8:111623432-111623641	MCF-7	breast:	n/a	n/a
19	CEBPB	chr8:111566321-111566477	A549	lung:	n/a	chr8:111566413-111566424
20	CEBPB	chr8:111551759-111552363	MCF-7	breast:	n/a	n/a
21	CEBPB	chr8:111605973-111606139	HepG2	liver:	n/a	chr8:111606013-111606024
22	CEBPB	chr8:111563765-111564094	A549	lung:	n/a	chr8:111563940-111563951
23	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
24	CEBPB	chr8:111573269-111573432	A549	lung:	n/a	n/a
25	CEBPB	chr8:111539028-111539286	HepG2	liver:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
26	CEBPB	chr8:111551859-111552317	MCF-7	breast:	n/a	n/a
27	CEBPB	chr8:111634949-111635197	IMR90	lung:	n/a	chr8:111635032-111635043
28	CEBPB	chr8:111505352-111505461	HepG2	liver:	n/a	chr8:111505411-111505422
29	CEBPB	chr8:111503841-111503896	K562	blood:	n/a	n/a
30	CEBPB	chr8:111566370-111566428	HepG2	liver:	n/a	chr8:111566413-111566424
31	CEBPB	chr8:111539099-111539344	A549	lung:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
32	CEBPB	chr8:111505335-111505447	A549	lung:	n/a	chr8:111505347-111505358 chr8:111505411-111505422
33	CEBPB	chr8:111634989-111635163	HepG2	liver:	n/a	chr8:111635032-111635043
34	CEBPB	chr8:111539090-111539260	H1-hESC	embryonic stem cell:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
35	CEBPB	chr8:111485138-111485350	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:111630967-111631208	HepG2	liver:	n/a	chr8:111631031-111631042
37	CEBPB	chr8:111663794-111664226	MCF-7	breast:	n/a	n/a
38	CEBPB	chr8:111525002-111525202	HepG2	liver:	n/a	chr8:111525140-111525151 chr8:111525141-111525150 chr8:111525139-111525150
39	CEBPB	chr8:111520325-111520598	HepG2	liver:	n/a	chr8:111520458-111520471 chr8:111520458-111520471 chr8:111520460-111520471 chr8:111520460-111520469 chr8:111520458-111520469
40	CEBPZ	chr8:111561657-111561751	HepG2	liver:	n/a	n/a
41	CHD2	chr8:111571903-111572103	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:111571898-111571965	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr8:111571880-111572030	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:111571847-111572055	T-47D	breast:	n/a	n/a
45	CTCF	chr8:111616060-111616210	BE2_C	brain:	n/a	n/a
46	CTCF	chr8:111571820-111571970	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr8:111571831-111572102	LNCaP	prostate:	n/a	n/a
48	CTCF	chr8:111571813-111572151	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr8:111597260-111597410	GM12801	blood:	n/a	n/a
50	CTCF	chr8:111571860-111572010	NHEK	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:111519159..111521111-chr8:111524177..111525688,2	MCF-7	breast:
2	chr8:111669709..111671243-chr8:111673107..111675313,2	MCF-7	breast:
3	chr8:111667414..111669906-chr8:111688361..111690572,2	MCF-7	breast:
4	chr8:111663406..111666569-chr8:111666819..111669452,4	MCF-7	breast:
5	chr8:111663406..111666569-chr8:111666819..111669452,4	MCF-7	breast:
6	chr8:111563289..111565363-chr8:111579783..111581298,2	MCF-7	breast:
7	chr8:111564377..111566155-chr8:111573076..111575001,2	MCF-7	breast:
8	chr15:38663825..38666657-chr8:111561522..111564455,2	MCF-7	breast:
9	chr8:111563681..111564416-chr8:111663211..111663982,2	MCF-7	breast:
10	chr8:111665338..111666843-chr8:111677219..111678888,2	K562	blood:
11	chr7:153439451..153439951-chr8:111669137..111669684,2	MCF-7	breast:
12	chr8:111563289..111565363-chr8:111579783..111581298,2	MCF-7	breast:
13	chr8:111629561..111631393-chr8:111634350..111636471,2	MCF-7	breast:
14	chr8:111579951..111580480-chr8:111668750..111669442,2	MCF-7	breast:
15	chr8:111564585..111566803-chr8:111570856..111572872,2	K562	blood:
16	chr8:111594065..111596990-chr8:111668768..111671358,2	MCF-7	breast:
17	chr8:111632530..111634212-chr8:111646106..111648334,2	MCF-7	breast:
18	chr8:111597648..111599475-chr8:111601535..111603940,2	MCF-7	breast:
19	chr8:111597648..111599475-chr8:111601535..111603940,2	MCF-7	breast:
20	chr8:111561274..111563938-chr8:111668171..111670064,2	MCF-7	breast:
21	chr8:111551159..111553132-chr8:111554691..111557321,2	MCF-7	breast:
22	chr8:111554765..111555294-chr8:111669236..111669854,2	MCF-7	breast:
23	chr8:111519159..111521111-chr8:111524177..111525688,2	MCF-7	breast:
24	chr8:111579951..111580480-chr8:111668750..111669442,2	MCF-7	breast:
25	chr8:111629561..111631393-chr8:111634350..111636471,2	MCF-7	breast:
26	chr8:111632530..111634212-chr8:111646106..111648334,2	MCF-7	breast:
27	chr8:111594065..111596990-chr8:111668768..111671358,2	MCF-7	breast:
28	chr8:111554765..111555294-chr8:111669236..111669854,2	MCF-7	breast:
29	chr22:21987659..21988468-chr8:111631630..111632515,2	MCF-7	breast:
30	chr8:111662012..111664592-chr8:111665712..111669617,3	MCF-7	breast:
31	chr8:111575672..111578651-chr8:111595648..111598231,2	MCF-7	breast:
32	chr2:189912462..189915135-chr8:111597995..111599883,2	MCF-7	breast:
33	chr8:111606860..111609172-chr8:111612437..111615361,2	K562	blood:
34	chr8:111563681..111564416-chr8:111663211..111663982,2	MCF-7	breast:
35	chr8:111564585..111566803-chr8:111570856..111572872,2	K562	blood:
36	chr8:111581974..111583484-chr8:111589126..111591939,2	MCF-7	breast:
37	chr17:41466208..41468149-chr8:111587283..111588803,2	K562	blood:
38	chr8:111581974..111583484-chr8:111589126..111591939,2	MCF-7	breast:
39	chr8:111618584..111620243-chr8:111621032..111622618,2	MCF-7	breast:
40	chr8:111662012..111664592-chr8:111665712..111669617,3	MCF-7	breast:
41	chr8:111606860..111609172-chr8:111612437..111615361,2	K562	blood:
42	chr8:111575672..111578651-chr8:111595648..111598231,2	MCF-7	breast:
43	chr8:111668947..111669607-chr8:111877933..111878646,3	MCF-7	breast:
44	chr8:111614672..111616882-chr8:111628243..111630115,2	MCF-7	breast:
45	chr7:156803278..156804875-chr8:111542688..111545615,2	MCF-7	breast:
46	chr8:111614672..111616882-chr8:111628243..111630115,2	MCF-7	breast:
47	chr8:111551159..111553132-chr8:111554691..111557321,2	MCF-7	breast:
48	chr8:111365043..111367620-chr8:111553595..111556957,3	MCF-7	breast:
49	chr8:111661559..111663835-chr8:111734745..111737537,2	MCF-7	breast:
50	chr8:111561274..111563938-chr8:111668171..111670064,2	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
ENSG00000253122	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000130675	chromatin interactions
ENSG00000243479	chromatin interactions

Extended variants
information (count: 2549 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2549 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138710805	chr8:111496865-111496866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539391885	chr8:111496869-111496870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534325825	chr8:111496929-111496930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547482730	chr8:111496960-111496961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373129853	chr8:111497001-111497002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113458834	chr8:111497036-111497037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570551471	chr8:111497037-111497038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4386953	chr8:111497055-111497056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539407726	chr8:111497062-111497063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558431331	chr8:111497085-111497086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575469256	chr8:111497093-111497094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537661002	chr8:111497125-111497126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10706793	chr8:111497164-111497165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368681063	chr8:111497234-111497235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574524925	chr8:111497244-111497245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540379763	chr8:111497245-111497246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142723864	chr8:111497268-111497269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560282408	chr8:111497294-111497295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576926412	chr8:111497351-111497352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146928630	chr8:111497371-111497372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575107860	chr8:111497415-111497416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562553899	chr8:111497423-111497424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs193110438	chr8:111497433-111497434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148170235	chr8:111497468-111497469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562350560	chr8:111497469-111497470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527871156	chr8:111497473-111497474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141975406	chr8:111497488-111497489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111626107	chr8:111497564-111497565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544977605	chr8:111497581-111497582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563973362	chr8:111497585-111497586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564772620	chr8:111497603-111497604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527563862	chr8:111497610-111497611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549730819	chr8:111497611-111497612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185508804	chr8:111497618-111497619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538169575	chr8:111497661-111497662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547323914	chr8:111497665-111497666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554565598	chr8:111497676-111497677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs58173160	chr8:111497681-111497682	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs372910858	chr8:111497732-111497733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533936557	chr8:111497734-111497735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187726078	chr8:111520419-111520420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532842589	chr8:111520476-111520477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77871740	chr8:111520528-111520529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77928448	chr8:111520533-111520534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141249427	chr8:111520556-111520557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4439100	chr8:111520670-111520671	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549363820	chr8:111520682-111520683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566271307	chr8:111520707-111520708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578194484	chr8:111520732-111520733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534870938	chr8:111520769-111520770	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:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111496800-111497800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr8:111520400-111521600	Enhancers	HUVEC	blood vessel
3	chr8:111521200-111522000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:111521400-111521800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:111521400-111521800	Enhancers	Colon Smooth Muscle	Colon
6	chr8:111521400-111522000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:111521400-111522000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:111521400-111522000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr8:111521600-111522000	Flanking Active TSS	HUVEC	blood vessel
10	chr8:111522000-111522400	Enhancers	HUVEC	blood vessel
11	chr8:111533400-111533800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:111535000-111535400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr8:111535000-111535400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:111535200-111535600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:111537800-111538400	Enhancers	Placenta Amnion	Placenta Amnion
16	chr8:111538400-111538800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr8:111538800-111539200	Enhancers	Placenta Amnion	Placenta Amnion
18	chr8:111548600-111550200	Active TSS	Right Atrium	heart
19	chr8:111550600-111550800	Enhancers	Pancreas	Pancrea
20	chr8:111556000-111556400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:111556200-111556600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:111556400-111556600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr8:111556600-111562200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:111563400-111564600	Enhancers	HMEC	breast
25	chr8:111563800-111564200	Enhancers	Muscle Satellite Cultured Cells	--
26	chr8:111563800-111564600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr8:111564000-111564600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:111564200-111564600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:111564200-111564600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:111570000-111570600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr8:111570600-111571600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr8:111571800-111572600	Enhancers	Fetal Brain Male	brain
33	chr8:111572000-111572200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr8:111572000-111572600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr8:111572400-111572600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:111591400-111591600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:111591800-111592400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr8:111592400-111592600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:111592600-111597200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr8:111594600-111597400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:111597200-111597600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr8:111597400-111598000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr8:111597400-111598200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:111606400-111606800	Enhancers	Fetal Brain Male	brain
45	chr8:111606600-111607200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:111628600-111629000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:111641400-111641800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:111641400-111642000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr8:111641600-111642000	Enhancers	Fetal Brain Female	brain
50	chr8:111641800-111648200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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