Variant report

Variant	nsv609556
Chromosome Location	chr8:1948888-1951163
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:1945649..1948332-chr8:1948376..1949994,2	MCF-7	breast:
2	chr8:1906659..1908488-chr8:1948019..1949630,2	MCF-7	breast:
3	chr8:1920209..1923568-chr8:1948553..1950993,3	MCF-7	breast:
4	chr17:8339151..8339685-chr8:1949081..1949841,2	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000253764	chromatin interactions
ENSG00000176595	chromatin interactions
ENSG00000270988	chromatin interactions
ENSG00000166579	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3824143	chr8:1948888-1948889	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12676812	chr8:1948895-1948896	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs567829482	chr8:1948896-1948897	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs36027367	chr8:1948916-1948917	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs191111990	chr8:1948917-1948918	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs113389737	chr8:1948920-1948921	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs183820656	chr8:1948921-1948922	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs568175698	chr8:1948927-1948928	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs533404267	chr8:1948933-1948934	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs536817988	chr8:1948953-1948954	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs540891447	chr8:1948970-1948971	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs560878191	chr8:1948975-1948976	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs188363109	chr8:1948981-1948982	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs4322044	chr8:1949126-1949127	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs116649895	chr8:1949137-1949138	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs531786142	chr8:1949196-1949197	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs34006337	chr8:1949200-1949201	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs141713602	chr8:1949207-1949208	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs35165869	chr8:1949209-1949210	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs551595877	chr8:1949210-1949211	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs375699885	chr8:1949214-1949215	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs201386090	chr8:1949215-1949216	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs78769493	chr8:1949220-1949221	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs569423757	chr8:1949231-1949232	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs527706957	chr8:1949246-1949247	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs548085013	chr8:1949247-1949248	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs567991723	chr8:1949248-1949249	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs536828995	chr8:1949270-1949271	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs143973546	chr8:1949293-1949294	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs570156978	chr8:1949337-1949338	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs112371239	chr8:1949350-1949351	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs192520338	chr8:1949354-1949355	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs111590613	chr8:1949382-1949383	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs571687633	chr8:1949397-1949398	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs534350763	chr8:1949415-1949416	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs560567428	chr8:1949418-1949419	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs554435260	chr8:1949444-1949445	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs574439513	chr8:1949445-1949446	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs375293379	chr8:1949481-1949482	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs183228973	chr8:1949499-1949500	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs369319088	chr8:1949505-1949506	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs551938929	chr8:1949512-1949513	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs563459707	chr8:1949593-1949594	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs576981949	chr8:1949764-1949765	Bivalent/Poised TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs13252213	chr8:1949824-1949825	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs545459005	chr8:1949841-1949842	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs565404310	chr8:1949908-1949909	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs527668395	chr8:1949915-1949916	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs541475533	chr8:1949919-1949920	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs561562641	chr8:1950015-1950016	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	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
Breast cancer	21364760	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
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1940400-1949000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:1946000-1949000	Weak transcription	Psoas Muscle	Psoas
3	chr8:1946400-1949000	Enhancers	Fetal Lung	lung
4	chr8:1947600-1949200	Enhancers	Spleen	Spleen
5	chr8:1948200-1949000	Enhancers	Pancreas	Pancrea
6	chr8:1948200-1949000	Bivalent Enhancer	Thymus	Thymus
7	chr8:1948400-1949000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:1948400-1949000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:1948400-1949000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:1948400-1949000	Enhancers	Liver	Liver
11	chr8:1948400-1949000	Enhancers	Brain Hippocampus Middle	brain
12	chr8:1948400-1949000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr8:1948400-1949200	Bivalent Enhancer	Placenta	Placenta
14	chr8:1948400-1949200	Enhancers	Left Ventricle	heart
15	chr8:1948400-1949200	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr8:1948400-1949400	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr8:1948400-1949400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
18	chr8:1948400-1949400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr8:1948400-1951600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr8:1948600-1949000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:1948600-1949000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
22	chr8:1948600-1949000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
23	chr8:1948600-1949000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
24	chr8:1948600-1949000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr8:1948600-1949000	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr8:1948600-1949000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
27	chr8:1948600-1949000	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr8:1948600-1949000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr8:1948600-1949000	Bivalent Enhancer	Fetal Stomach	stomach
30	chr8:1948600-1949000	Bivalent Enhancer	Stomach Mucosa	stomach
31	chr8:1948600-1949200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:1948600-1949200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
33	chr8:1948600-1949200	Enhancers	Small Intestine	intestine
34	chr8:1948600-1949400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:1948600-1949400	Enhancers	Fetal Heart	heart
36	chr8:1948600-1949400	Flanking Active TSS	Fetal Muscle Leg	muscle
37	chr8:1948600-1949400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
38	chr8:1948600-1949400	Flanking Active TSS	HSMM	muscle
39	chr8:1948600-1949600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr8:1948800-1949000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr8:1948800-1949000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:1948800-1949000	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr8:1948800-1949000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
44	chr8:1948800-1949000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
45	chr8:1948800-1949000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
46	chr8:1948800-1949000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
47	chr8:1948800-1949000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr8:1948800-1949000	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
49	chr8:1948800-1949000	Flanking Active TSS	Primary T cells from cord blood	blood
50	chr8:1948800-1949000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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