Variant report

Variant	esv3412283
Chromosome Location	chr8:124202171-124206869
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	ATF3	chr8:124203038-124203367	K562	blood:	n/a	n/a
2	BHLHE40	chr8:124203099-124203360	K562	blood:	n/a	n/a
3	CEBPB	chr8:124206589-124206732	IMR90	lung:	n/a	chr8:124206684-124206695
4	CEBPB	chr8:124206587-124206811	A549	lung:	n/a	chr8:124206684-124206695
5	CEBPB	chr8:124206597-124206815	HepG2	liver:	n/a	chr8:124206684-124206695
6	CTCF	chr8:124204880-124205030	GM12869	blood:	n/a	chr8:124204998-124205011 chr8:124204887-124204895
7	CTCF	chr8:124204953-124205083	K562	blood:	n/a	chr8:124204998-124205011
8	CTCF	chr8:124203520-124203670	HMEC	breast:	n/a	n/a
9	CTCF	chr8:124203500-124203650	MCF-7	breast:	n/a	n/a
10	CTCF	chr8:124204920-124205070	HBMEC	blood vessel:	n/a	chr8:124204998-124205011
11	CTCF	chr8:124204846-124205123	K562	blood:	n/a	chr8:124204998-124205011 chr8:124204887-124204895
12	CTCF	chr8:124204926-124205111	Hela-S3	cervix:	n/a	chr8:124204998-124205011
13	CTCF	chr8:124203594-124203773	K562	blood:	n/a	n/a
14	CTCF	chr8:124203547-124203699	HepG2	liver:	n/a	n/a
15	CTCF	chr8:124204880-124205030	BE2_C	brain:	n/a	chr8:124204998-124205011 chr8:124204887-124204895
16	CTCF	chr8:124204940-124205090	HEEpiC	esophagus:	n/a	chr8:124204998-124205011
17	CTCF	chr8:124204880-124205030	HepG2	liver:	n/a	chr8:124204998-124205011 chr8:124204887-124204895
18	CTCF	chr8:124204980-124205130	HCPEpiC	choroid plexus:	n/a	chr8:124204998-124205011
19	CTCF	chr8:124204974-124205040	GM12891	blood:	n/a	chr8:124204998-124205011
20	CTCF	chr8:124204840-124204990	HEEpiC	esophagus:	n/a	chr8:124204887-124204895
21	CTCF	chr8:124204863-124205225	K562	blood:	n/a	chr8:124204998-124205011 chr8:124204887-124204895
22	CTCF	chr8:124204995-124205037	ProgFib	skin:	n/a	chr8:124204998-124205011
23	CTCF	chr8:124204971-124205074	Fibrobl	skin:	n/a	chr8:124204998-124205011
24	CTCF	chr8:124205006-124205044	GM19238	blood:	n/a	n/a
25	CTCF	chr8:124204920-124205070	Hela-S3	cervix:	n/a	chr8:124204998-124205011
26	CTCF	chr8:124204880-124205030	SAEC	small airway:	n/a	chr8:124204998-124205011 chr8:124204887-124204895
27	CTCF	chr8:124205005-124205073	LNCaP	prostate:	n/a	n/a
28	CTCF	chr8:124203020-124203170	GM12864	blood:	n/a	n/a
29	CTCF	chr8:124204960-124205110	MCF-7	breast:	n/a	chr8:124204998-124205011
30	CTCF	chr8:124204979-124205040	H1-hESC	embryonic stem cell:	n/a	chr8:124204998-124205011
31	CTCF	chr8:124204864-124205093	K562	blood:	n/a	chr8:124204998-124205011 chr8:124204887-124204895
32	CTCF	chr8:124204960-124205110	SAEC	small airway:	n/a	chr8:124204998-124205011
33	CTCF	chr8:124204927-124205064	HepG2	liver:	n/a	chr8:124204998-124205011
34	CTCF	chr8:124204920-124205070	HMEC	breast:	n/a	chr8:124204998-124205011
35	CTCF	chr8:124204934-124205098	MCF-7	breast:	n/a	chr8:124204998-124205011
36	CTCF	chr8:124203600-124203750	GM12872	blood:	n/a	n/a
37	CTCF	chr8:124203582-124203705	HepG2	liver:	n/a	n/a
38	CTCF	chr8:124203373-124203829	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:124204900-124205050	HepG2	liver:	n/a	chr8:124204998-124205011
40	CTCF	chr8:124204943-124205052	HepG2	liver:	n/a	chr8:124204998-124205011
41	CTCF	chr8:124203594-124203705	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr8:124204925-124205112	MCF-7	breast:	n/a	chr8:124204998-124205011
43	CTCF	chr8:124203599-124203703	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:124204960-124205110	GM12864	blood:	n/a	chr8:124204998-124205011
45	CTCF	chr8:124204923-124205117	MCF-7	breast:	n/a	chr8:124204998-124205011
46	CTCF	chr8:124204980-124205130	WERI-Rb-1	eye:	n/a	chr8:124204998-124205011
47	CTCF	chr8:124204936-124205103	MCF-7	breast:	n/a	chr8:124204998-124205011
48	CTCF	chr8:124204900-124205050	HCPEpiC	choroid plexus:	n/a	chr8:124204998-124205011
49	CTCF	chr8:124204913-124205116	MCF-7	breast:	n/a	chr8:124204998-124205011
50	CTCF	chr8:124204967-124205074	NHEK	skin:	n/a	chr8:124204998-124205011

No.	Distal block	Cell Line	Cell type
1	chr8:124172226..124173291-chr8:124203205..124204142,6	MCF-7	breast:
2	chr8:124172170..124173373-chr8:124203108..124203740,5	MCF-7	breast:
3	chr8:124034586..124035350-chr8:124203347..124204148,2	MCF-7	breast:
4	chr8:124205722..124208237-chr8:124217531..124219104,2	K562	blood:
5	chr8:124202911..124204464-chr8:124210784..124212515,2	K562	blood:
6	chr8:124202642..124205088-chr8:124211959..124213771,2	MCF-7	breast:
7	chr8:124193731..124198397-chr8:124202096..124205086,5	MCF-7	breast:
8	chr8:124197444..124199510-chr8:124205893..124207940,2	MCF-7	breast:
9	chr8:124202410..124205099-chr8:124250791..124252752,2	K562	blood:
10	chr8:124202299..124204634-chr8:124227331..124230067,2	K562	blood:
11	chr8:124202196..124205513-chr8:124205556..124208969,4	K562	blood:
12	chr8:124205866..124208638-chr8:124223387..124226315,2	K562	blood:

Variant related genes	Relation type
ENSG00000253410	TF binding region
ENSG00000253410	chromatin interactions
ENSG00000266324	chromatin interactions
ENSG00000147689	chromatin interactions
ENSG00000189376	chromatin interactions
ENSG00000253258	chromatin interactions

Extended variants
information (count: 199 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:199 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11783554	chr8:124202184-124202185	Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540428370	chr8:124202210-124202211	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs11779903	chr8:124202219-124202220	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs11779971	chr8:124202236-124202237	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs367759173	chr8:124202261-124202262	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs529186579	chr8:124202293-124202294	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs533539587	chr8:124202336-124202337	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs140667630	chr8:124202352-124202353	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs186538036	chr8:124202419-124202420	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs56070700	chr8:124202421-124202422	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs531443273	chr8:124202524-124202525	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs375633053	chr8:124202525-124202526	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs558494156	chr8:124202526-124202527	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs191344314	chr8:124202570-124202571	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs372733145	chr8:124202588-124202589	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs182643274	chr8:124202651-124202652	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs7812683	chr8:124202659-124202660	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs567254834	chr8:124202668-124202669	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs112663814	chr8:124202693-124202694	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs150172330	chr8:124202705-124202706	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs536515552	chr8:124202768-124202769	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs138618040	chr8:124202903-124202904	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs544199971	chr8:124202973-124202974	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs576319998	chr8:124202998-124202999	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs545489342	chr8:124203074-124203075	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs559142902	chr8:124203148-124203149	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs572565763	chr8:124203161-124203162	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs540468142	chr8:124203186-124203187	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs369511248	chr8:124203187-124203188	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs114369657	chr8:124203203-124203204	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs7833092	chr8:124203215-124203216	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs542523715	chr8:124203225-124203226	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs149299969	chr8:124203226-124203227	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs551347766	chr8:124203251-124203252	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs34947160	chr8:124203307-124203308	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs527361416	chr8:124203322-124203323	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs563605443	chr8:124203393-124203394	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs192167009	chr8:124203434-124203435	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs147402059	chr8:124203508-124203509	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs7003842	chr8:124203514-124203515	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564458619	chr8:124203515-124203516	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs75131087	chr8:124203536-124203537	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs570327220	chr8:124203537-124203538	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs183419492	chr8:124203544-124203545	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs558978503	chr8:124203593-124203594	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs572601048	chr8:124203641-124203642	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs17377283	chr8:124203663-124203664	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs139189774	chr8:124203696-124203697	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs573705966	chr8:124203705-124203706	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs542803504	chr8:124203718-124203719	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:144)

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
Acute myeloid leukemia	20729466	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	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
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	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
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124193400-124241200	Weak transcription	Right Atrium	heart
2	chr8:124199800-124206400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:124199800-124216600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr8:124201000-124205200	Genic enhancers	K562	blood
5	chr8:124201400-124202200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:124201600-124202800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr8:124201600-124202800	Weak transcription	HMEC	breast
8	chr8:124201600-124203000	Weak transcription	Hela-S3	cervix
9	chr8:124201600-124205000	Weak transcription	Esophagus	oesophagus
10	chr8:124201600-124212600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:124201600-124216000	Strong transcription	NHEK	skin
12	chr8:124201600-124216800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:124202200-124203400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:124202800-124203000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr8:124202800-124211600	Strong transcription	HMEC	breast
16	chr8:124203000-124205200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:124203000-124206200	Genic enhancers	Hela-S3	cervix
18	chr8:124204400-124205800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr8:124205000-124205200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:124205000-124205200	ZNF genes & repeats	Esophagus	oesophagus
21	chr8:124205000-124205200	Enhancers	Gastric	stomach
22	chr8:124205000-124205400	Enhancers	Pancreas	Pancrea
23	chr8:124205000-124205800	Enhancers	Fetal Muscle Trunk	muscle
24	chr8:124205200-124205400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:124205200-124209000	Strong transcription	K562	blood
26	chr8:124205200-124209200	Weak transcription	Esophagus	oesophagus
27	chr8:124205200-124217600	Weak transcription	Gastric	stomach
28	chr8:124205400-124209200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:124206000-124206600	Enhancers	Adipose Nuclei	Adipose
30	chr8:124206200-124215200	Strong transcription	Hela-S3	cervix
31	chr8:124206600-124207200	Weak transcription	Adipose Nuclei	Adipose

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