Variant report

Variant	nsv1022670
Chromosome Location	chr8:8561196-8613387
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8563551..8565890-chr8:8569428..8571116,2	K562	blood:
2	chr8:8559280..8561948-chr8:8563852..8566020,2	MCF-7	breast:
3	chr8:8560907..8563057-chr8:8567449..8569715,2	MCF-7	breast:
4	chr8:8608085..8608900-chr8:8846417..8847265,2	MCF-7	breast:
5	chr8:8608326..8608981-chr8:9195964..9196742,2	MCF-7	breast:
6	chr8:8528173..8528908-chr8:8567698..8568456,2	MCF-7	breast:
7	chr8:8558670..8561637-chr8:8568317..8570904,3	K562	blood:
8	chr8:8607965..8608861-chr8:8846540..8847483,5	K562	blood:
9	chr8:8527332..8529283-chr8:8594084..8595110,9	K562	blood:
10	chr8:8556386..8558383-chr8:8560900..8563538,2	K562	blood:
11	chr8:8527839..8528754-chr8:8592246..8592999,2	K562	blood:
12	chr8:8538997..8539534-chr8:8594174..8595039,2	MCF-7	breast:
13	chr8:8527493..8529178-chr8:8594079..8595134,11	MCF-7	breast:
14	chr8:8527797..8529806-chr8:8592444..8595839,3	MCF-7	breast:
15	chr8:8559423..8561174-chr8:8562199..8564616,2	MCF-7	breast:
16	chr8:8242378..8243902-chr8:8594357..8596139,2	MCF-7	breast:
17	chr8:8557473..8560405-chr8:8562361..8564009,2	K562	blood:
18	chr8:8579801..8581466-chr8:8590103..8593043,2	MCF-7	breast:
19	chr8:8553226..8556449-chr8:8563078..8566145,3	MCF-7	breast:
20	chr8:8608069..8609942-chr8:8861282..8862933,2	MCF-7	breast:
21	chr8:8563551..8565890-chr8:8569428..8571116,2	K562	blood:
22	chr8:8527809..8528658-chr8:8569477..8570252,2	MCF-7	breast:
23	chr8:8607923..8608592-chr8:9007837..9008750,3	K562	blood:
24	chr8:8599224..8601341-chr8:8748933..8751645,2	MCF-7	breast:
25	chr8:8607817..8608748-chr8:9007897..9008818,2	MCF-7	breast:
26	chr8:8607912..8608860-chr8:8887402..8888108,2	K562	blood:
27	chr8:8560907..8563057-chr8:8567449..8569715,2	MCF-7	breast:
28	chr8:8579801..8581466-chr8:8590103..8593043,2	MCF-7	breast:
29	chr8:8558568..8560739-chr8:8564922..8567226,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MFHAS1-1	chr8:8611510-8611618	ENSG00000254367
2	lnc-MFHAS1-1	chr8:8581203-8581244	ENSG00000254367

No data

Variant related genes	Relation type
ENSG00000253958	chromatin interactions
ENSG00000147324	chromatin interactions
ENSG00000173281	chromatin interactions
ENSG00000176305	chromatin interactions

Extended variants
information (count: 2389 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:2389 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556995689	chr8:8561203-8561204	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs542843864	chr8:8561247-8561248	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs10105591	chr8:8561311-8561312	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs187839059	chr8:8561370-8561371	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs11403457	chr8:8561391-8561392	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs192926090	chr8:8561393-8561394	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs397942859	chr8:8561396-8561397	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs71286005	chr8:8561397-8561398	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs1060107	chr8:8561399-8561400	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs554469050	chr8:8561419-8561420	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs4840350	chr8:8561442-8561443	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs1060106	chr8:8561452-8561453	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs184100360	chr8:8561467-8561468	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs564784949	chr8:8561501-8561502	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs187841496	chr8:8561502-8561503	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs560962049	chr8:8561510-8561511	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs372332994	chr8:8561536-8561537	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs11249883	chr8:8561537-8561538	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs11249884	chr8:8561552-8561553	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs143580227	chr8:8561605-8561606	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs10106836	chr8:8561619-8561620	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs12681925	chr8:8561649-8561650	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs148037387	chr8:8561683-8561684	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs13272181	chr8:8561688-8561689	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs12680019	chr8:8561698-8561699	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs536240308	chr8:8561704-8561705	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs117834625	chr8:8561719-8561720	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs547255106	chr8:8561751-8561752	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs573455580	chr8:8561753-8561754	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs545638368	chr8:8561766-8561767	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs558894876	chr8:8561780-8561781	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs374028058	chr8:8561795-8561796	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs199657506	chr8:8561797-8561798	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs369017421	chr8:8561831-8561832	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs529120420	chr8:8561853-8561854	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs113996999	chr8:8561895-8561896	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs184833971	chr8:8561896-8561897	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs574525445	chr8:8561909-8561910	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs540221143	chr8:8561914-8561915	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs11249885	chr8:8562008-8562009	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs11249886	chr8:8562021-8562022	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs551608763	chr8:8562065-8562066	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs35731820	chr8:8562139-8562140	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs71537849	chr8:8562140-8562141	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs564957317	chr8:8562142-8562143	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs373350578	chr8:8562143-8562144	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs11249887	chr8:8562184-8562185	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs150541138	chr8:8562230-8562231	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs115225175	chr8:8562254-8562255	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs12550057	chr8:8562268-8562269	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:140)

Disease	PMID	Source
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
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
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
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
Colorectal cancer	16774939	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
Bladder cancer	21909424	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
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8558400-8562800	Active TSS	Rectal Mucosa Donor 29	rectum
2	chr8:8559200-8562000	Bivalent/Poised TSS	Fetal Stomach	stomach
3	chr8:8559400-8561400	Bivalent Enhancer	Fetal Brain Male	brain
4	chr8:8560000-8561200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr8:8560000-8561200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:8560000-8561200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
7	chr8:8560000-8561600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr8:8560000-8562000	Weak transcription	Fetal Lung	lung
9	chr8:8560000-8562600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr8:8560000-8563600	Enhancers	GM12878-XiMat	blood
11	chr8:8560000-8563600	Weak transcription	Hela-S3	cervix
12	chr8:8560200-8562000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:8560200-8562200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:8560200-8562600	Weak transcription	NHLF	lung
15	chr8:8560400-8561200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:8560400-8561400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
17	chr8:8560400-8561800	Bivalent Enhancer	Fetal Intestine Large	intestine
18	chr8:8560400-8562000	Enhancers	Adipose Nuclei	Adipose
19	chr8:8560400-8562200	Active TSS	Duodenum Mucosa	Duodenum
20	chr8:8560400-8563000	ZNF genes & repeats	Fetal Intestine Small	intestine
21	chr8:8560400-8564400	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr8:8560600-8562000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr8:8560600-8562600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr8:8560800-8561800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr8:8560800-8562200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:8560800-8562200	Enhancers	Liver	Liver
27	chr8:8560800-8562400	Active TSS	Gastric	stomach
28	chr8:8560800-8562600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:8560800-8563000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr8:8560800-8563600	Weak transcription	Esophagus	oesophagus
31	chr8:8561000-8561400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr8:8561000-8561400	Active TSS	Colonic Mucosa	Colon
33	chr8:8561000-8561600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr8:8561000-8561600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:8561000-8561800	Weak transcription	Rectal Smooth Muscle	rectum
36	chr8:8561000-8561800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr8:8561000-8561800	Enhancers	Stomach Mucosa	stomach
38	chr8:8561000-8562000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr8:8561000-8562800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr8:8561000-8562800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:8561000-8563400	Weak transcription	Placenta	Placenta
42	chr8:8561000-8563800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:8561200-8561400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr8:8561200-8562200	Active TSS	Rectal Mucosa Donor 31	rectum
45	chr8:8561200-8562800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:8561200-8562800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:8561400-8561600	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr8:8561400-8561800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:8561400-8561800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:8561400-8561800	Weak transcription	Colonic Mucosa	Colon

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