Variant report

Variant	nsv890372
Chromosome Location	chr8:11840071-11951168
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	chr8:11872669-11872691	HepG2	liver:	n/a	n/a
2	BATF	chr8:11921283-11921507	GM12878	blood:	n/a	n/a
3	BATF	chr8:11921281-11921530	GM12878	blood:	n/a	n/a
4	BATF	chr8:11895971-11896326	GM12878	blood:	n/a	n/a
5	CBX3	chr8:11839401-11840135	HCT-116	colon:	n/a	n/a
6	CCNT2	chr8:11872580-11872794	K562	blood:	n/a	n/a
7	CCNT2	chr8:11843856-11844050	K562	blood:	n/a	n/a
8	CEBPB	chr8:11852501-11853120	HCT-116	colon:	n/a	chr8:11852980-11852993
9	CEBPB	chr8:11854319-11854398	H1-hESC	embryonic stem cell:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
10	CEBPB	chr8:11909083-11909117	A549	lung:	n/a	chr8:11909099-11909108 chr8:11909099-11909108 chr8:11909097-11909110 chr8:11909097-11909110 chr8:11909099-11909108
11	CEBPB	chr8:11908914-11909287	Hela-S3	cervix:	n/a	chr8:11909099-11909108 chr8:11909099-11909108 chr8:11909097-11909110 chr8:11909097-11909110 chr8:11909099-11909108
12	CEBPB	chr8:11854282-11854495	HepG2	liver:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
13	CEBPB	chr8:11858214-11858439	A549	lung:	n/a	n/a
14	CEBPB	chr8:11858214-11858354	IMR90	lung:	n/a	n/a
15	CEBPB	chr8:11858243-11858418	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:11852658-11853061	IMR90	lung:	n/a	chr8:11852980-11852993
17	CEBPB	chr8:11854216-11854508	IMR90	lung:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
18	CEBPB	chr8:11854194-11854540	K562	blood:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
19	CHD2	chr8:11844195-11844527	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:11872640-11872790	AG09319	gingival:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
21	CTCF	chr8:11872629-11872866	MCF-7	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
22	CTCF	chr8:11921308-11921399	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr8:11872740-11872890	GM06990	blood:	n/a	n/a
24	CTCF	chr8:11921282-11921450	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:11872613-11872890	Gliobla	brain:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
26	CTCF	chr8:11921149-11921625	A549	lung:	n/a	n/a
27	CTCF	chr8:11872630-11872837	HUVEC	blood vessel:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
28	CTCF	chr8:11872800-11872950	A549	lung:	n/a	n/a
29	CTCF	chr8:11844040-11844190	HMF	breast:	n/a	n/a
30	CTCF	chr8:11844060-11844210	HFF	foreskin:	n/a	n/a
31	CTCF	chr8:11872481-11872951	A549	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
32	CTCF	chr8:11872859-11872860	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr8:11872623-11872861	Kidney_OC	kidney:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
34	CTCF	chr8:11844260-11844410	HCM	heart:	n/a	n/a
35	CTCF	chr8:11872660-11872810	NB4	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
36	CTCF	chr8:11872618-11872868	GM13977	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
37	CTCF	chr8:11872591-11872933	K562	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
38	CTCF	chr8:11872660-11872810	NHDF-neo	bronchial:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
39	CTCF	chr8:11933196-11933217	GM10248	blood:	n/a	n/a
40	CTCF	chr8:11872660-11872810	GM12868	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
41	CTCF	chr8:11872548-11872789	T-47D	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
42	CTCF	chr8:11912601-11912655	LNCaP	prostate:	n/a	n/a
43	CTCF	chr8:11844080-11844230	Caco-2	colon:	n/a	n/a
44	CTCF	chr8:11901063-11901078	LNCaP	prostate:	n/a	n/a
45	CTCF	chr8:11872583-11872907	GM12892	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
46	CTCF	chr8:11872660-11872810	WI-38	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
47	CTCF	chr8:11872760-11872910	HPF	lung:	n/a	n/a
48	CTCF	chr8:11924589-11924699	GM13977	blood:	n/a	n/a
49	CTCF	chr8:11948674-11948722	LNCaP	prostate:	n/a	n/a
50	CTCF	chr8:11921336-11921462	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11872659-11872709	T-47D	breast:	n/a
2	chr8:11872659-11872709	T-47D	breast:	n/a
3	chr8:11872778-11872828	GM19239	blood:	n/a
4	chr8:11895252-11895302	HL-60	blood:	n/a
5	chr8:11853121-11853171	SAEC	small airway:	n/a
6	chr8:11882982-11883032	GM12892	blood:	n/a
7	chr8:11882962-11883012	HCPEpiC	choroid plexus:	n/a
8	chr8:11876646-11876696	GM06990	blood:	n/a
9	chr8:11876646-11876696	HNPCEpiC	eye:	n/a
10	chr8:11843816-11843866	H1-hESC	embryonic stem cell:	embryo
11	chr8:11882897-11882947	HCPEpiC	choroid plexus:	n/a
12	chr8:11876646-11876696	HRPEpiC	eye:	n/a
13	chr8:11872659-11872709	HRE	kidney:	n/a
14	chr8:11882962-11883012	HCM	heart:	n/a
15	chr8:11853878-11853928	Hela-S3	cervix:	n/a
16	chr8:11843971-11844021	GM12892	blood:	n/a
17	chr8:11872141-11872191	PrEC	prostate:	n/a
18	chr8:11872882-11872932	PANC-1	pancreas:	n/a
19	chr8:11843971-11844021	AG04450	lung:	fetal
20	chr8:11872778-11872828	HCF	heart:	n/a
21	chr8:11872659-11872709	MCF10A-Er-Src	breast:	n/a
22	chr8:11947722-11947772	HEEpiC	esophagus:	n/a
23	chr8:11872778-11872828	Hela-S3	cervix:	n/a
24	chr8:11947722-11947772	SK-N-SH	brain:	n/a
25	chr8:11872141-11872191	GM12878	blood:	n/a
26	chr8:11872659-11872709	HEEpiC	esophagus:	n/a
27	chr8:11841980-11842030	NT2-D1	testis:	n/a
28	chr8:11946867-11946917	HNPCEpiC	eye:	n/a
29	chr8:11882897-11882947	PFSK-1	brain:	n/a
30	chr8:11853121-11853171	PFSK-1	brain:	n/a
31	chr8:11907551-11907601	Hepatocyte	liver:	n/a
32	chr8:11872882-11872932	SK-N-MC	brain:	n/a
33	chr8:11853878-11853928	BJ	skin:	n/a
34	chr8:11870063-11870113	GM06990	blood:	n/a
35	chr8:11853121-11853171	PANC-1	pancreas:	n/a
36	chr8:11870063-11870113	MCF-7	breast:	n/a
37	chr8:11841980-11842030	SK-N-SH	brain:	n/a
38	chr8:11853121-11853171	AG04449	skin:	fetal
39	chr8:11872778-11872828	CMK	blood:	n/a
40	chr8:11841980-11842030	H1-hESC	embryonic stem cell:	embryo
41	chr8:11946498-11946548	T-47D	breast:	n/a
42	chr8:11843971-11844021	NH-A	brain:	n/a
43	chr8:11895252-11895302	AG04449	skin:	fetal
44	chr8:11843971-11844021	HCM	heart:	n/a
45	chr8:11853878-11853928	ProgFib	skin:	n/a
46	chr8:11882982-11883032	AG04449	skin:	fetal
47	chr8:11841980-11842030	AG04450	lung:	fetal
48	chr8:11872659-11872709	IMR90	lung:	fetal
49	chr8:11895252-11895302	HMEC	breast:	n/a
50	chr8:11907551-11907601	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
2	chr10:101006536..101007134-chr8:11906757..11907257,2	MCF-7	breast:
3	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
4	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:
5	chr8:11836841..11840054-chr8:11842955..11845395,3	MCF-7	breast:
6	chr8:11838617..11840884-chr8:11844089..11846019,2	K562	blood:
7	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
8	chr8:11851923..11853652-chr8:11853797..11856578,2	K562	blood:
9	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB134-1	chr8:11860909-11861591	NONHSAT125106
2	lnc-DEFB135-1	chr8:11856596-11856977	NONHSAT125105

Variant related genes	Relation type
RNA5SP253	TF binding region
ENSG00000255016	TF binding region
ENSG00000255174	TF binding region
DEFB134	TF binding region
ENSG00000254507	TF binding region
ENSG00000233050	TF binding region
ENSG00000255098	TF binding region
OR7E160P	TF binding region
ENSG00000254700	TF binding region
RNA5SP253	CpG island
ENSG00000255016	CpG island
ENSG00000255174	CpG island
DEFB134	CpG island
ENSG00000254507	CpG island
ENSG00000233050	CpG island
ENSG00000255098	CpG island
OR7E160P	CpG island
ENSG00000254700	CpG island
ENSG00000205883	chromatin interactions
ENSG00000205882	chromatin interactions
ENSG00000149823	chromatin interactions

Extended variants
information (count: 2204 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:2204 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6985349	chr8:11840071-11840072	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs13256786	chr8:11840095-11840096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533129512	chr8:11840109-11840110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552113718	chr8:11840133-11840134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555222009	chr8:11840139-11840140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187549250	chr8:11840163-11840164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568583244	chr8:11840166-11840167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs13257076	chr8:11840172-11840173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549580353	chr8:11840178-11840179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537618464	chr8:11840195-11840196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371688476	chr8:11840196-11840197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139091402	chr8:11840266-11840267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535529528	chr8:11840291-11840292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570228306	chr8:11840330-11840331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556732840	chr8:11840346-11840347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568842625	chr8:11840350-11840351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539011388	chr8:11840369-11840370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542586103	chr8:11840375-11840376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572779218	chr8:11840383-11840384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184694019	chr8:11840388-11840389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555529783	chr8:11840412-11840413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4458916	chr8:11840431-11840432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs367624898	chr8:11840466-11840467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562802170	chr8:11840469-11840470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28524834	chr8:11840500-11840501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs545394515	chr8:11840505-11840506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560798727	chr8:11840508-11840509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527977352	chr8:11840517-11840518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145266328	chr8:11840531-11840532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563634083	chr8:11840542-11840543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4458915	chr8:11840551-11840552	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs4455884	chr8:11840575-11840576	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs189141630	chr8:11840587-11840588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181573385	chr8:11840631-11840632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566470163	chr8:11840656-11840657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147603483	chr8:11840666-11840667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116644862	chr8:11840673-11840674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573790550	chr8:11840701-11840702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372666193	chr8:11840731-11840732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185029722	chr8:11840753-11840754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375015675	chr8:11840771-11840772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189924400	chr8:11840776-11840777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114271144	chr8:11840786-11840787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560488837	chr8:11840789-11840790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572419338	chr8:11840791-11840792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543313849	chr8:11840846-11840847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561386734	chr8:11840851-11840852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531222955	chr8:11840853-11840854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531953854	chr8:11840867-11840868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140611018	chr8:11840874-11840875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Osteosarcoma	21215367	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11838600-11843600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:11838600-11843600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:11839400-11840200	Enhancers	NH-A	brain
4	chr8:11843400-11843600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
5	chr8:11843400-11843600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
6	chr8:11843400-11843600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
7	chr8:11843400-11843600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
8	chr8:11843400-11843600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr8:11843400-11843600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
10	chr8:11843400-11843600	Bivalent Enhancer	HepG2	liver
11	chr8:11843400-11843800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:11843400-11844000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:11843400-11844600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:11843400-11844600	Active TSS	H9 Cell Line	embryonic stem cell
15	chr8:11843400-11844600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
16	chr8:11843400-11844600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
17	chr8:11843600-11843800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:11843600-11843800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:11843600-11843800	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:11843600-11843800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:11843600-11843800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:11843600-11843800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr8:11843600-11843800	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr8:11843600-11843800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr8:11843600-11843800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
26	chr8:11843600-11843800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr8:11843600-11843800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:11843600-11843800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr8:11843600-11843800	Enhancers	Liver	Liver
30	chr8:11843600-11843800	Enhancers	Brain Angular Gyrus	brain
31	chr8:11843600-11843800	Flanking Active TSS	Brain Anterior Caudate	brain
32	chr8:11843600-11843800	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr8:11843600-11843800	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
34	chr8:11843600-11843800	Bivalent/Poised TSS	Fetal Brain Female	brain
35	chr8:11843600-11843800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr8:11843600-11843800	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr8:11843600-11843800	Bivalent Enhancer	Fetal Stomach	stomach
38	chr8:11843600-11843800	Active TSS	Gastric	stomach
39	chr8:11843600-11843800	Bivalent Enhancer	Left Ventricle	heart
40	chr8:11843600-11843800	Enhancers	Pancreas	Pancrea
41	chr8:11843600-11843800	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
42	chr8:11843600-11843800	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
43	chr8:11843600-11843800	Active TSS	Right Atrium	heart
44	chr8:11843600-11843800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr8:11843600-11843800	Flanking Bivalent TSS/Enh	HepG2	liver
46	chr8:11843600-11843800	Flanking Active TSS	NH-A	brain
47	chr8:11843600-11844000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:11843600-11844000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:11843600-11844000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr8:11843600-11844000	Bivalent Enhancer	Placenta	Placenta

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