Variant report

Variant	nsv533642
Chromosome Location	chr8:3104559-3250929
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	ARID3A	chr8:3141618-3141628	K562	blood:	n/a	n/a
2	BACH1	chr8:3243732-3243769	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr8:3166862-3167033	GM12878	blood:	n/a	chr8:3166959-3166972 chr8:3166944-3166955
4	BATF	chr8:3192435-3192715	GM12878	blood:	n/a	chr8:3192592-3192602 chr8:3192591-3192602
5	BCL11A	chr8:3181323-3181510	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:3142129-3142341	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:3181325-3182184	GM12878	blood:	n/a	n/a
8	BRCA1	chr8:3142211-3142538	Hela-S3	cervix:	n/a	chr8:3142419-3142426
9	CEBPB	chr8:3119754-3120007	A549	lung:	n/a	n/a
10	CEBPB	chr8:3120563-3120733	HepG2	liver:	n/a	chr8:3120612-3120623
11	CEBPB	chr8:3220332-3220556	A549	lung:	n/a	n/a
12	CEBPB	chr8:3159558-3159842	A549	lung:	n/a	n/a
13	CEBPB	chr8:3242964-3243198	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:3220252-3220565	IMR90	lung:	n/a	n/a
15	CEBPB	chr8:3242893-3243173	K562	blood:	n/a	n/a
16	CEBPB	chr8:3119734-3120051	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:3120608-3120683	A549	lung:	n/a	chr8:3120612-3120623
18	CEBPB	chr8:3119761-3119974	K562	blood:	n/a	n/a
19	CEBPB	chr8:3242976-3243214	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:3220251-3220570	HepG2	liver:	n/a	n/a
21	CHD2	chr8:3142082-3142314	GM12878	blood:	n/a	n/a
22	CHD2	chr8:3183890-3183998	GM12878	blood:	n/a	n/a
23	CHD2	chr8:3181180-3182258	GM12878	blood:	n/a	n/a
24	CTCF	chr8:3237997-3238028	GM10248	blood:	n/a	n/a
25	CTCF	chr8:3141600-3141750	HepG2	liver:	n/a	n/a
26	CTCF	chr8:3141603-3141743	GM10266	blood:	n/a	n/a
27	CTCF	chr8:3141860-3142010	WI-38	lung:	n/a	n/a
28	CTCF	chr8:3142104-3142455	T-47D	breast:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
29	CTCF	chr8:3141660-3141810	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:3142200-3142350	A549	lung:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
31	CTCF	chr8:3141651-3141742	GM19238	blood:	n/a	n/a
32	CTCF	chr8:3142106-3142418	K562	blood:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
33	CTCF	chr8:3142180-3142330	AG09309	skin:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
34	CTCF	chr8:3141620-3141770	GM12878	blood:	n/a	n/a
35	CTCF	chr8:3141610-3141836	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:3142240-3142390	HMF	breast:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
37	CTCF	chr8:3142240-3142390	GM12865	blood:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
38	CTCF	chr8:3142200-3142350	AG04449	skin:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
39	CTCF	chr8:3141908-3142653	A549	lung:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
40	CTCF	chr8:3142155-3142416	GM19238	blood:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
41	CTCF	chr8:3142149-3142413	Spleen_OC	spleen:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
42	CTCF	chr8:3192280-3192430	GM12869	blood:	n/a	chr8:3192368-3192376
43	CTCF	chr8:3142220-3142370	HBMEC	blood vessel:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
44	CTCF	chr8:3175430-3175432	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr8:3142140-3142290	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr8:3141580-3141730	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr8:3142170-3142456	MCF-7	breast:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
48	CTCF	chr8:3142594-3142597	GM10266	blood:	n/a	n/a
49	CTCF	chr8:3142200-3142350	BE2_C	brain:	n/a	chr8:3142281-3142302 chr8:3142279-3142297
50	CTCF	chr8:3142149-3142407	ProgFib	skin:	n/a	chr8:3142281-3142302 chr8:3142279-3142297

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:3245076-3245126	HCPEpiC	choroid plexus:	n/a
2	chr8:3245076-3245126	HCPEpiC	choroid plexus:	n/a
3	chr8:3244626-3244676	GM19239	blood:	n/a
4	chr8:3245147-3245197	GM12892	blood:	n/a
5	chr8:3141907-3141957	GM12892	blood:	n/a
6	chr8:3244626-3244676	HEK293	kidney:	embryo
7	chr8:3141844-3141894	HCF	heart:	n/a
8	chr8:3244912-3244962	AG09319	gingival:	n/a
9	chr8:3141844-3141894	PFSK-1	brain:	n/a
10	chr8:3244912-3244962	HNPCEpiC	eye:	n/a
11	chr8:3141844-3141894	PANC-1	pancreas:	n/a
12	chr8:3245076-3245126	HUVEC	blood vessel:	n/a
13	chr8:3141844-3141894	AoSMC	blood vessel:	n/a
14	chr8:3141907-3141957	ECC-1	luminal epithelium:	n/a
15	chr8:3245147-3245197	H1-hESC	embryonic stem cell:	embryo
16	chr8:3141844-3141894	LNCaP	prostate:	n/a
17	chr8:3141844-3141894	BE2_C	brain:	n/a
18	chr8:3141844-3141894	HEEpiC	esophagus:	n/a
19	chr8:3245076-3245126	HIPEpiC	eye:	n/a
20	chr8:3245147-3245197	AoSMC	blood vessel:	n/a
21	chr8:3245076-3245126	LNCaP	prostate:	n/a
22	chr8:3141844-3141894	A549	lung:	n/a
23	chr8:3141907-3141957	LNCaP	prostate:	n/a
24	chr8:3245076-3245126	SK-N-MC	brain:	n/a
25	chr8:3245147-3245197	HEEpiC	esophagus:	n/a
26	chr8:3141844-3141894	U87	brain:	n/a
27	chr8:3245076-3245126	PFSK-1	brain:	n/a
28	chr8:3245147-3245197	PFSK-1	brain:	n/a
29	chr8:3141907-3141957	HAEpiC	amniotic membrane:	n/a
30	chr8:3244626-3244676	HL-60	blood:	n/a
31	chr8:3245147-3245197	RPTEC	kidney:	n/a
32	chr8:3141907-3141957	SAEC	small airway:	n/a
33	chr8:3141907-3141957	NB4	blood:	n/a
34	chr8:3141844-3141894	HCPEpiC	choroid plexus:	n/a
35	chr8:3244626-3244676	Hepatocyte	liver:	n/a
36	chr8:3244912-3244962	HUVEC	blood vessel:	n/a
37	chr8:3244912-3244962	HCPEpiC	choroid plexus:	n/a
38	chr8:3141907-3141957	Caco-2	colon:	n/a
39	chr8:3244912-3244962	PFSK-1	brain:	n/a
40	chr8:3245147-3245197	HCM	heart:	n/a
41	chr8:3245147-3245197	IMR90	lung:	fetal
42	chr8:3244626-3244676	ECC-1	luminal epithelium:	n/a
43	chr8:3245076-3245126	GM06990	blood:	n/a
44	chr8:3141844-3141894	GM12892	blood:	n/a
45	chr8:3244626-3244676	ovcar-3	ovarian:	n/a
46	chr8:3244912-3244962	A549	lung:	n/a
47	chr8:3244912-3244962	SAEC	small airway:	n/a
48	chr8:3244912-3244962	HRPEpiC	eye:	n/a
49	chr8:3245076-3245126	Hela-S3	cervix:	n/a
50	chr8:3245076-3245126	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:3208152..3210922-chr8:3213074..3214852,2	K562	blood:
2	chr8:3121428..3123841-chr8:3126010..3128450,2	K562	blood:
3	chr8:3121428..3123841-chr8:3126010..3128450,2	K562	blood:
4	chr8:3208152..3210922-chr8:3213074..3214852,2	K562	blood:
5	chr8:3239734..3241510-chr8:3243012..3245362,2	K562	blood:
6	chr8:3142221..3142747-chr8:3393835..3394631,2	MCF-7	breast:
7	chr8:3239734..3241510-chr8:3243012..3245362,2	K562	blood:
8	chr10:127849492..127850062-chr8:3194741..3195243,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERICH1-8	chr8:3230875-3231250	ENSG00000253162.1
2	lnc-ERICH1-8	chr8:3232662-3232748	ENSG00000253162.1

Variant related genes	Relation type
CSMD1	TF binding region
ENSG00000253162	TF binding region
CSMD1	CpG island
ENSG00000253162	CpG island

Extended variants
information (count: 6485 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:6485 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192827580	chr8:3104570-3104571	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs547485275	chr8:3104582-3104583	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs537882272	chr8:3104589-3104590	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs17319596	chr8:3104594-3104595	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs529650955	chr8:3104598-3104599	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs549357065	chr8:3104616-3104617	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs569258051	chr8:3104640-3104641	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs538128016	chr8:3104642-3104643	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs577816736	chr8:3104646-3104647	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs558104146	chr8:3104656-3104657	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs183014138	chr8:3104658-3104659	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs188449810	chr8:3104661-3104662	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs34020985	chr8:3104678-3104679	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs34435098	chr8:3104691-3104692	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs553703609	chr8:3104719-3104720	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs554325123	chr8:3104755-3104756	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs73185559	chr8:3104767-3104768	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs542437897	chr8:3104800-3104801	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs35927143	chr8:3104817-3104818	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs35047073	chr8:3104829-3104830	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs17063092	chr8:3104832-3104833	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs540821329	chr8:3104840-3104841	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs560691453	chr8:3104841-3104842	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs529737661	chr8:3104851-3104852	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs549395417	chr8:3104854-3104855	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs7834606	chr8:3104856-3104857	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs531980123	chr8:3104860-3104861	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs191241151	chr8:3104861-3104862	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs183739532	chr8:3104871-3104872	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs534411437	chr8:3104872-3104873	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs547663634	chr8:3104875-3104876	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs7846442	chr8:3104884-3104885	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs536720538	chr8:3104889-3104890	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs370720018	chr8:3104893-3104894	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs35729878	chr8:3104896-3104897	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs189244992	chr8:3104918-3104919	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs13269927	chr8:3104920-3104921	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs558816010	chr8:3104921-3104922	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs192595243	chr8:3104933-3104934	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs142086851	chr8:3104934-3104935	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs185146467	chr8:3104944-3104945	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs370842934	chr8:3104947-3104948	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs13269978	chr8:3104967-3104968	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs372718620	chr8:3104985-3104986	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs532140370	chr8:3104992-3104993	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs551849020	chr8:3104997-3104998	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs565610378	chr8:3105032-3105033	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs561343725	chr8:3105034-3105035	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs17319617	chr8:3105038-3105039	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs367556282	chr8:3105050-3105051	Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

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
Schizophrenia	23813976	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3103400-3104800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
2	chr8:3103400-3105200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
3	chr8:3103400-3105200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:3103400-3105400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
5	chr8:3103600-3105200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:3103800-3105600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr8:3104600-3104800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
8	chr8:3104600-3105000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr8:3104600-3105200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr8:3104600-3105200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
11	chr8:3105000-3105200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
12	chr8:3105000-3105200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
13	chr8:3105000-3105200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr8:3106400-3106600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
15	chr8:3112200-3112400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:3112600-3113400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:3125200-3125400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:3126200-3127000	Enhancers	Fetal Muscle Leg	muscle
19	chr8:3141200-3141600	Enhancers	Fetal Kidney	kidney
20	chr8:3141400-3141600	Enhancers	Fetal Muscle Trunk	muscle
21	chr8:3141400-3142200	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr8:3141600-3141800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr8:3141600-3141800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr8:3141600-3141800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
25	chr8:3141600-3141800	Active TSS	Brain Cingulate Gyrus	brain
26	chr8:3141600-3141800	Enhancers	Brain Hippocampus Middle	brain
27	chr8:3141600-3141800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr8:3141600-3141800	Enhancers	Fetal Brain Male	brain
29	chr8:3141600-3141800	Active TSS	Fetal Brain Female	brain
30	chr8:3141600-3141800	Active TSS	Fetal Lung	lung
31	chr8:3141600-3142000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr8:3141600-3142000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:3141600-3142000	Active TSS	Brain Germinal Matrix	brain
34	chr8:3141600-3142000	Active TSS	Duodenum Mucosa	Duodenum
35	chr8:3141600-3142000	Flanking Active TSS	Fetal Muscle Trunk	muscle
36	chr8:3141600-3142200	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr8:3141600-3142200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr8:3141600-3142200	Flanking Active TSS	Fetal Kidney	kidney
39	chr8:3141800-3142000	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr8:3141800-3142000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
41	chr8:3141800-3142000	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr8:3141800-3142000	Active TSS	Brain Anterior Caudate	brain
43	chr8:3141800-3142000	Active TSS	Brain Substantia Nigra	brain
44	chr8:3141800-3142000	Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr8:3141800-3142000	Flanking Active TSS	Fetal Stomach	stomach
46	chr8:3141800-3142000	Enhancers	Pancreas	Pancrea
47	chr8:3141800-3142000	Enhancers	HMEC	breast
48	chr8:3141800-3142000	Enhancers	K562	blood
49	chr8:3141800-3142200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr8:3141800-3142200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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