Variant report

Variant	nsv1020360
Chromosome Location	chr8:132068287-132195108
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	BHLHE40	chr8:132165657-132165768	GM12878	blood:	n/a	n/a
2	CEBPB	chr8:132084318-132084535	IMR90	lung:	n/a	n/a
3	CEBPB	chr8:132104782-132105016	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:132068058-132068391	HepG2	liver:	n/a	chr8:132068257-132068268
5	CEBPB	chr8:132068089-132068367	A549	lung:	n/a	chr8:132068257-132068268
6	CHD2	chr8:132129803-132130003	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr8:132138580-132138730	GM12864	blood:	n/a	n/a
8	CTCF	chr8:132138640-132138790	GM06990	blood:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
9	CTCF	chr8:132104506-132104531	GM20000	blood:	n/a	n/a
10	CTCF	chr8:132138720-132138870	BE2_C	brain:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
11	CTCF	chr8:132129668-132129967	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr8:132138620-132138770	GM12865	blood:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
13	CTCF	chr8:132138694-132138819	LNCaP	prostate:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
14	CTCF	chr8:132175100-132175250	GM12869	blood:	n/a	n/a
15	CTCF	chr8:132129760-132129910	RPTEC	kidney:	n/a	n/a
16	CTCF	chr8:132138620-132138770	HEK293	kidney:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
17	CTCF	chr8:132106127-132106188	H1-hESC	embryonic stem cell:	n/a	chr8:132106152-132106170
18	CTCF	chr8:132138760-132138910	HMEC	breast:	n/a	n/a
19	CTCF	chr8:132138640-132138790	HCT-116	colon:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
20	CTCF	chr8:132138640-132138790	AG04449	skin:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
21	CTCF	chr8:132129800-132129950	HMEC	breast:	n/a	n/a
22	CTCF	chr8:132165360-132165510	GM12875	blood:	n/a	n/a
23	CTCF	chr8:132138699-132138752	Medullo	brain:	n/a	n/a
24	CTCF	chr8:132147120-132147270	GM06990	blood:	n/a	n/a
25	CTCF	chr8:132138800-132138950	GM12865	blood:	n/a	n/a
26	CTCF	chr8:132138580-132138730	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr8:132138720-132138870	RPTEC	kidney:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
28	CTCF	chr8:132138680-132138830	RPTEC	kidney:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
29	CTCF	chr8:132138680-132138830	HL-60	blood:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
30	CTCF	chr8:132138720-132138870	MCF-7	breast:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
31	CTCF	chr8:132138820-132138970	NHEK	skin:	n/a	n/a
32	CTCF	chr8:132129740-132129890	HMEC	breast:	n/a	n/a
33	CTCF	chr8:132138640-132138790	Hela-S3	cervix:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
34	CTCF	chr8:132138680-132138830	HMEC	breast:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
35	CTCF	chr8:132138742-132138789	HepG2	liver:	n/a	chr8:132138748-132138761
36	CTCF	chr8:132138555-132138948	HCT-116	colon:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
37	CTCF	chr8:132098300-132098450	HL-60	blood:	n/a	n/a
38	CTCF	chr8:132138680-132138830	HepG2	liver:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
39	CTCF	chr8:132138701-132138784	MCF-7	breast:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
40	CTCF	chr8:132129840-132129990	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr8:132138700-132138850	SK-N-SH_RA	brain:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
42	CTCF	chr8:132138600-132138750	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:132135448-132135512	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr8:132138707-132138785	MCF-7	breast:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
45	CTCF	chr8:132129861-132129901	GM12878	blood:	n/a	n/a
46	CTCF	chr8:132138620-132138770	GM12872	blood:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
47	CTCF	chr8:132138740-132138890	HCT-116	colon:	n/a	chr8:132138748-132138761 chr8:132138741-132138762
48	CTCF	chr8:132129820-132129970	GM06990	blood:	n/a	n/a
49	CTCF	chr8:132107644-132107840	K562	blood:	n/a	n/a
50	CTCF	chr8:132138660-132138810	HMF	breast:	n/a	chr8:132138748-132138761 chr8:132138741-132138762

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:132151006..132153588-chr8:132157450..132159845,2	MCF-7	breast:
2	chr8:132151006..132153588-chr8:132157450..132159845,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADCY8-1	chr8:132157081-132157128	ENSG00000253407
2	lnc-EFR3A-2	chr8:132101581-132101711	NONHSAT129164
3	lnc-EFR3A-2	chr8:132142125-132142145	NONHSAT129164
4	lnc-EFR3A-2	chr8:132089368-132089479	XLOC_006928
5	lnc-EFR3A-2	chr8:132089368-132089479	XLOC_006928
6	lnc-EFR3A-2	chr8:132089367-132089479	NONHSAT129164
7	lnc-ADCY8-1	chr8:132142635-132142935	ENSG00000253407
8	lnc-EFR3A-2	chr8:132101582-132101711	XLOC_006928
9	lnc-EFR3A-2	chr8:132142126-132142145	XLOC_006928
10	lnc-ADCY8-1	chr8:132143323-132143464	ENSG00000253407

Variant related genes	Relation type
ENSG00000253407	TF binding region
WASL	miRNA target sites

Extended variants
information (count: 1703 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544249559	chr8:132079630-132079631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556288867	chr8:132079652-132079653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1888083	chr8:132079687-132079688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541971199	chr8:132079691-132079692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189190346	chr8:132079731-132079732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192711550	chr8:132079732-132079733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73350501	chr8:132079769-132079770	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs529147465	chr8:132079783-132079784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147546041	chr8:132079789-132079790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184938965	chr8:132079793-132079794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561545637	chr8:132079794-132079795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78048829	chr8:132079897-132079898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189787366	chr8:132079974-132079975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565853672	chr8:132079978-132079979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539291000	chr8:132080003-132080004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551260776	chr8:132080032-132080033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181629496	chr8:132080033-132080034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547207390	chr8:132080036-132080037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12677297	chr8:132080062-132080063	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs556484547	chr8:132080077-132080078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533255255	chr8:132080086-132080087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185950968	chr8:132080098-132080099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535921176	chr8:132080107-132080108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188798479	chr8:132080109-132080110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572665637	chr8:132080127-132080128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73352503	chr8:132080140-132080141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs181900484	chr8:132080172-132080173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564672837	chr8:132080173-132080174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140078839	chr8:132080180-132080181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75098247	chr8:132080235-132080236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187193735	chr8:132080246-132080247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12679474	chr8:132080247-132080248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528917107	chr8:132080270-132080271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547462660	chr8:132080273-132080274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190955957	chr8:132080295-132080296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202053380	chr8:132080299-132080300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145501965	chr8:132080323-132080324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551123145	chr8:132080365-132080366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182782773	chr8:132080381-132080382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548817071	chr8:132080382-132080383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536915986	chr8:132080391-132080392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535459070	chr8:132080396-132080397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147302198	chr8:132080415-132080416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186488554	chr8:132080436-132080437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535519892	chr8:132080439-132080440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148735146	chr8:132080517-132080518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572525005	chr8:132080518-132080519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78599354	chr8:132080536-132080537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191518920	chr8:132080542-132080543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182561608	chr8:132080579-132080580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
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
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	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
Acute myeloid leukemia	20729466	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
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
Endometrioid adenocarcinoma	16974079	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
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastric cancer	16891809	CNVD
Colorectal cancer	19455253	CNVD
Pregnancies with abnormal ultrasound findings	21110858	CNVD
Breast cancer	19181860	CNVD
Brain cancer	19584924	CNVD
Medulloblastoma	19584924	CNVD
Follicular lymphoma	17699855	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164919	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:132079600-132093600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:132082000-132082400	Active TSS	Aorta	Aorta
3	chr8:132085000-132085200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:132089800-132091600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:132090400-132090800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:132090400-132090800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:132117400-132118600	Enhancers	Fetal Brain Male	brain
8	chr8:132123000-132123200	Enhancers	Brain Hippocampus Middle	brain
9	chr8:132123000-132124200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:132123000-132124200	Enhancers	Brain Substantia Nigra	brain
11	chr8:132123000-132124600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr8:132123200-132123600	Enhancers	Brain Angular Gyrus	brain
13	chr8:132123200-132123600	Enhancers	Brain Anterior Caudate	brain
14	chr8:132123200-132123600	Flanking Active TSS	Brain Hippocampus Middle	brain
15	chr8:132123200-132124000	Enhancers	Brain Cingulate Gyrus	brain
16	chr8:132123600-132123800	Enhancers	Brain Hippocampus Middle	brain
17	chr8:132130000-132130400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:132130400-132131400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:132131200-132132200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:132131400-132132000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr8:132131400-132132000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:132137000-132137800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:132140600-132140800	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr8:132141000-132142200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr8:132142200-132143200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr8:132143200-132144200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr8:132144200-132145200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr8:132148000-132148400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:132148400-132153800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:132153800-132154000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:132160400-132162000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:132160800-132161800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:132160800-132161800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:132161200-132161400	Enhancers	Left Ventricle	heart
35	chr8:132161800-132162200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr8:132161800-132162200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:132161800-132162400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:132161800-132162400	Enhancers	Fetal Heart	heart
39	chr8:132162000-132162400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr8:132162200-132162800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr8:132162400-132162800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:132162800-132167400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:132177600-132178600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:132177600-132178600	Enhancers	HMEC	breast
45	chr8:132178200-132178600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:132189800-132190000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:132190200-132192200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:132192200-132192800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr8:132192200-132193200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr8:132192200-132193600	Enhancers	HMEC	breast

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