Variant report

Variant	nsv831210
Chromosome Location	chr8:2867572-2929922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:488)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:2916177-2916545	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:2916230-2916576	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:2918202-2918564	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:2922469-2922529	K562	blood:	n/a	n/a
5	BATF	chr8:2882522-2882786	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:2882534-2882878	GM12878	blood:	n/a	n/a
7	CEBPB	chr8:2916260-2916546	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr8:2926963-2927222	K562	blood:	n/a	n/a
9	CEBPB	chr8:2915827-2915913	HepG2	liver:	n/a	n/a
10	CEBPB	chr8:2886397-2886623	IMR90	lung:	n/a	n/a
11	CTCF	chr8:2877400-2877550	AG04450	lung:	n/a	n/a
12	CTCF	chr8:2877500-2877650	HRE	kidney:	n/a	n/a
13	CTCF	chr8:2877464-2877646	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr8:2877460-2877610	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr8:2877414-2877649	K562	blood:	n/a	n/a
16	CTCF	chr8:2877482-2877609	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr8:2877391-2877743	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr8:2877514-2877543	A549	lung:	n/a	n/a
19	CTCF	chr8:2877480-2877630	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr8:2877540-2877690	HRE	kidney:	n/a	n/a
21	CTCF	chr8:2877494-2877627	K562	blood:	n/a	n/a
22	CTCF	chr8:2877520-2877670	HL-60	blood:	n/a	n/a
23	CTCF	chr8:2877481-2877625	LNCaP	prostate:	n/a	n/a
24	CTCF	chr8:2877480-2877630	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr8:2877520-2877670	MCF-7	breast:	n/a	n/a
26	CTCF	chr8:2877460-2877610	GM12869	blood:	n/a	n/a
27	CTCF	chr8:2877510-2877619	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:2877504-2877636	LNCaP	prostate:	n/a	n/a
29	CTCF	chr8:2877460-2877610	RPTEC	kidney:	n/a	n/a
30	CTCF	chr8:2877560-2877710	K562	blood:	n/a	n/a
31	CTCF	chr8:2877440-2877590	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr8:2885553-2885612	Fibrobl	skin:	n/a	n/a
33	CTCF	chr8:2877460-2877610	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr8:2877420-2877570	GM12869	blood:	n/a	n/a
35	CTCF	chr8:2879808-2879927	GM13976	blood:	n/a	n/a
36	CTCF	chr8:2926420-2926464	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr8:2877480-2877630	Caco-2	colon:	n/a	n/a
38	CTCF	chr8:2870524-2870610	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr8:2877460-2877610	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr8:2898217-2898301	Fibrobl	skin:	n/a	n/a
41	CTCF	chr8:2877580-2877730	RPTEC	kidney:	n/a	n/a
42	CTCF	chr8:2883968-2884041	Fibrobl	skin:	n/a	n/a
43	CTCF	chr8:2877352-2877643	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:2877498-2877624	Medullo	brain:	n/a	n/a
45	CTCF	chr8:2884055-2884129	Fibrobl	skin:	n/a	n/a
46	E2F4	chr8:2929323-2929523	MCF10A-Er-Src	breast:	n/a	n/a
47	ELF1	chr8:2877430-2877614	K562	blood:	n/a	n/a
48	EP300	chr8:2914767-2914867	K562	blood:	n/a	n/a
49	GABPA	chr8:2882512-2882722	Hela-S3	cervix:	n/a	n/a
50	GATA2	chr8:2896298-2896786	SH-SY5Y	brain:	n/a	chr8:2896481-2896502 chr8:2896486-2896496 chr8:2896483-2896499 chr8:2896483-2896499

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2879687-2879737	Caco-2	colon:	n/a
2	chr8:2877217-2877267	Hela-S3	cervix:	n/a
3	chr8:2879917-2879967	SK-N-SH_RA	brain:	n/a
4	chr8:2885516-2885566	NH-A	brain:	n/a
5	chr8:2916814-2916864	HL-60	blood:	n/a
6	chr8:2885627-2885677	PFSK-1	brain:	n/a
7	chr8:2877217-2877267	HRE	kidney:	n/a
8	chr8:2885516-2885566	HRCEpiC	kidney:	n/a
9	chr8:2885516-2885566	HCF	heart:	n/a
10	chr8:2879687-2879737	HCM	heart:	n/a
11	chr8:2879687-2879737	SKMC	muscle:	n/a
12	chr8:2879687-2879737	GM12892	blood:	n/a
13	chr8:2877217-2877267	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:2879687-2879737	ProgFib	skin:	n/a
15	chr8:2883914-2883964	HIPEpiC	eye:	n/a
16	chr8:2879687-2879737	GM12891	blood:	n/a
17	chr8:2885537-2885587	HMEC	breast:	n/a
18	chr8:2877217-2877267	H1-hESC	embryonic stem cell:	embryo
19	chr8:2916814-2916864	AG04450	lung:	fetal
20	chr8:2879687-2879737	H1-hESC	embryonic stem cell:	embryo
21	chr8:2885537-2885587	AG09319	gingival:	n/a
22	chr8:2916814-2916864	H1-hESC	embryonic stem cell:	embryo
23	chr8:2916814-2916864	GM12891	blood:	n/a
24	chr8:2879917-2879967	PrEC	prostate:	n/a
25	chr8:2885627-2885677	NHDF-neo	bronchial:	n/a
26	chr8:2883914-2883964	Hepatocyte	liver:	n/a
27	chr8:2879917-2879967	SKMC	muscle:	n/a
28	chr8:2879687-2879737	LNCaP	prostate:	n/a
29	chr8:2885516-2885566	HCT-116	colon:	n/a
30	chr8:2885516-2885566	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:2883914-2883964	MCF10A-Er-Src	breast:	n/a
32	chr8:2877217-2877267	BJ	skin:	n/a
33	chr8:2883914-2883964	RPTEC	kidney:	n/a
34	chr8:2879687-2879737	AG09309	skin:	n/a
35	chr8:2883914-2883964	Hela-S3	cervix:	n/a
36	chr8:2885516-2885566	AG04449	skin:	fetal
37	chr8:2885516-2885566	HepG2	liver:	n/a
38	chr8:2885537-2885587	T-47D	breast:	n/a
39	chr8:2885537-2885587	Jurkat	blood:	n/a
40	chr8:2885627-2885677	H1-hESC	embryonic stem cell:	embryo
41	chr8:2879687-2879737	AG04450	lung:	fetal
42	chr8:2885537-2885587	GM06990	blood:	n/a
43	chr8:2885516-2885566	K562	blood:	n/a
44	chr8:2885537-2885587	BJ	skin:	n/a
45	chr8:2916814-2916864	MCF10A-Er-Src	breast:	n/a
46	chr8:2885516-2885566	HRPEpiC	eye:	n/a
47	chr8:2877217-2877267	NB4	blood:	n/a
48	chr8:2877217-2877267	BE2_C	brain:	n/a
49	chr8:2885537-2885587	HEK293	kidney:	embryo
50	chr8:2879917-2879967	AG04450	lung:	fetal

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:2924503..2926165-chr8:2927948..2929693,2	K562	blood:
2	chr8:2920157..2922787-chr8:2924910..2926529,2	K562	blood:
3	chr8:2917024..2919683-chr8:2921100..2923818,2	K562	blood:
4	chr8:2910108..2911963-chr8:2912249..2914943,2	K562	blood:
5	chr8:2893385..2895332-chr8:2897701..2899292,2	K562	blood:
6	chr8:2920157..2922787-chr8:2924910..2926529,2	K562	blood:
7	chr8:2923421..2926165-chr8:2927948..2929676,2	K562	blood:
8	chr8:2865247..2867969-chr8:2868176..2872126,4	K562	blood:
9	chr8:2910108..2911963-chr8:2912249..2914943,2	K562	blood:
10	chr8:2865247..2867969-chr8:2868176..2872126,4	K562	blood:
11	chr8:2923421..2926165-chr8:2927948..2929676,2	K562	blood:
12	chr8:2917024..2919683-chr8:2921100..2923818,2	K562	blood:
13	chr8:2893385..2895332-chr8:2897701..2899292,2	K562	blood:
14	chr12:56367505..56368235-chr8:2894157..2894798,2	MCF-7	breast:
15	chr8:2913080..2916209-chr8:2916693..2920762,3	K562	blood:
16	chr8:2884129..2886374-chr8:2888333..2890117,2	K562	blood:
17	chr8:2924503..2926165-chr8:2927948..2929693,2	K562	blood:
18	chr8:2913080..2916209-chr8:2916693..2920762,3	K562	blood:
19	chr8:2884129..2886374-chr8:2888333..2890117,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOM2-14	chr8:2877373-2877426	NONHSAT124740
2	lnc-MYOM2-14	chr8:2879062-2880003	NONHSAT124740

No data

Variant related genes	Relation type
CSMD1	TF binding region
CSMD1	CpG island
ENSG00000111540	chromatin interactions

Extended variants
information (count: 2550 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:2550 , 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	rs372868920	chr8:2867574-2867575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115482378	chr8:2867590-2867591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375785229	chr8:2867596-2867597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562102018	chr8:2867604-2867605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531014986	chr8:2867640-2867641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544299274	chr8:2867641-2867642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564283049	chr8:2867648-2867649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145595483	chr8:2867671-2867672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191360983	chr8:2867679-2867680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546647027	chr8:2867716-2867717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184317071	chr8:2867717-2867718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529132771	chr8:2867731-2867732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557002704	chr8:2867780-2867781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576952997	chr8:2867781-2867782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116753038	chr8:2867782-2867783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569069979	chr8:2867803-2867804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538077939	chr8:2867813-2867814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35664211	chr8:2867844-2867845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367878823	chr8:2867860-2867861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571392557	chr8:2867884-2867885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189831330	chr8:2867924-2867925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76346084	chr8:2867928-2867929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117225590	chr8:2867930-2867931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181131390	chr8:2867940-2867941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187032090	chr8:2867962-2867963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575426706	chr8:2867988-2867989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544440568	chr8:2867990-2867991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564221416	chr8:2867996-2867997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149522388	chr8:2868000-2868001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540728861	chr8:2868016-2868017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79659080	chr8:2868019-2868020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75715896	chr8:2868043-2868044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189884148	chr8:2868057-2868058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562805123	chr8:2868065-2868066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561836046	chr8:2868068-2868069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531510936	chr8:2868095-2868096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373181094	chr8:2868127-2868128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79937003	chr8:2868158-2868159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571483477	chr8:2868159-2868160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75257001	chr8:2868183-2868184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370738127	chr8:2868207-2868208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375863030	chr8:2868214-2868215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34404492	chr8:2868268-2868269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182503461	chr8:2868286-2868287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116824693	chr8:2868300-2868301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544507538	chr8:2868330-2868331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567148635	chr8:2868334-2868335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536288020	chr8:2868349-2868350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186205087	chr8:2868368-2868369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34649095	chr8:2868379-2868380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2858600-2887600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr8:2868800-2869600	Enhancers	Dnd41	blood
3	chr8:2868800-2870200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:2869200-2869600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:2869200-2869600	Enhancers	Primary hematopoietic stem cells	blood
6	chr8:2869600-2870000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr8:2869600-2870200	Enhancers	Fetal Heart	heart
8	chr8:2872800-2873600	Enhancers	Fetal Brain Male	brain
9	chr8:2873200-2873600	Enhancers	Brain Germinal Matrix	brain
10	chr8:2879200-2879600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:2883800-2884200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:2883800-2884200	ZNF genes & repeats	Lung	lung
13	chr8:2884200-2886800	Weak transcription	Lung	lung
14	chr8:2885400-2885600	Enhancers	Pancreas	Pancrea
15	chr8:2885600-2886600	Weak transcription	Pancreas	Pancrea
16	chr8:2886600-2887000	ZNF genes & repeats	Pancreas	Pancrea
17	chr8:2886800-2887000	ZNF genes & repeats	Lung	lung
18	chr8:2887000-2892400	Weak transcription	Pancreas	Pancrea
19	chr8:2891400-2891600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:2891400-2893000	Enhancers	Fetal Lung	lung
21	chr8:2892400-2892600	Enhancers	Pancreas	Pancrea
22	chr8:2893000-2893800	Weak transcription	Fetal Lung	lung
23	chr8:2893800-2894000	Enhancers	Fetal Lung	lung
24	chr8:2894000-2894400	Weak transcription	Fetal Lung	lung
25	chr8:2901600-2902200	Enhancers	Fetal Lung	lung
26	chr8:2902200-2902600	Weak transcription	Fetal Lung	lung
27	chr8:2902600-2903000	Enhancers	Fetal Lung	lung
28	chr8:2903600-2903800	Enhancers	Spleen	Spleen
29	chr8:2907000-2907400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
30	chr8:2907400-2911400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr8:2915800-2917200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:2916000-2916400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
33	chr8:2916000-2916600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
34	chr8:2916000-2916800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:2916000-2916800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:2916000-2917000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr8:2916000-2917400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
38	chr8:2916000-2917400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
39	chr8:2916200-2916600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:2916200-2917200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
41	chr8:2916400-2916600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
42	chr8:2916600-2917000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
43	chr8:2916600-2917200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
44	chr8:2916600-2917600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
45	chr8:2916800-2917000	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:2916800-2917200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
47	chr8:2917000-2917200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
48	chr8:2917000-2917200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:2919800-2920000	Enhancers	Fetal Lung	lung
50	chr8:2920000-2920800	Enhancers	Cortex derived primary cultured neurospheres	brain

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