Variant report

Variant	nsv568824
Chromosome Location	chr15:31776343-31787108
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:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr15:31728928..31731704-chr15:31776995..31778781,2	MCF-7	breast:
2	chr15:31729614..31735490-chr15:31778794..31782835,6	MCF-7	breast:
3	chr15:31753960..31755078-chr15:31780591..31781425,3	MCF-7	breast:
4	chr15:31748477..31753108-chr15:31776889..31783172,7	MCF-7	breast:
5	chr15:31507689..31508257-chr15:31779754..31780346,2	K562	blood:
6	chr15:31780894..31782465-chr15:31785232..31787543,2	MCF-7	breast:
7	chr15:31492707..31493313-chr15:31780465..31781069,2	MCF-7	breast:
8	chr15:31507301..31508500-chr15:31780431..31781449,6	K562	blood:
9	chr15:31492924..31493816-chr15:31781800..31782800,3	K562	blood:
10	chr15:31780894..31782465-chr15:31785232..31787543,2	MCF-7	breast:
11	chr15:31727262..31728165-chr15:31780632..31781327,2	MCF-7	breast:
12	chr15:31731222..31732109-chr15:31780643..31781604,3	MCF-7	breast:
13	chr15:31731428..31732434-chr15:31780398..31781184,5	K562	blood:
14	chr15:31730666..31732248-chr15:31779741..31781482,12	MCF-7	breast:
15	chr15:31489768..31490355-chr15:31780489..31781405,2	K562	blood:
16	chr15:31507500..31508054-chr15:31782035..31782545,2	K562	blood:
17	chr15:31492529..31493483-chr15:31780441..31781476,6	MCF-7	breast:
18	chr15:31775112..31777688-chr15:31780214..31782887,2	K562	blood:
19	chr15:31775112..31777688-chr15:31780214..31782887,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000259448	chromatin interactions

Extended variants
information (count: 400 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375289192	chr15:31776364-31776365	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs80021613	chr15:31776370-31776371	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs368655642	chr15:31776376-31776377	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs546365883	chr15:31776396-31776397	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs371889770	chr15:31776418-31776419	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs375688748	chr15:31776434-31776435	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs530871959	chr15:31776468-31776469	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs77376353	chr15:31776469-31776470	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs570970882	chr15:31776476-31776477	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs201183526	chr15:31776484-31776485	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs547007498	chr15:31776490-31776491	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs372960314	chr15:31776511-31776512	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs200515947	chr15:31776530-31776531	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs372490862	chr15:31776534-31776535	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs373551661	chr15:31776545-31776546	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs141917827	chr15:31776551-31776552	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs199588939	chr15:31776557-31776558	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs202059339	chr15:31776558-31776559	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs150629417	chr15:31776562-31776563	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs542041260	chr15:31776570-31776571	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs377720188	chr15:31776600-31776601	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200619668	chr15:31776604-31776605	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139698222	chr15:31776633-31776634	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376166961	chr15:31776637-31776638	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547619116	chr15:31776652-31776653	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143552707	chr15:31776657-31776658	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369730464	chr15:31776706-31776707	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201681150	chr15:31776717-31776718	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376362683	chr15:31776721-31776722	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146885561	chr15:31776751-31776752	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139774758	chr15:31776763-31776764	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377421686	chr15:31776802-31776803	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371211492	chr15:31776811-31776812	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148643263	chr15:31776814-31776815	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76704217	chr15:31776837-31776838	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552445976	chr15:31776847-31776848	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573163595	chr15:31776852-31776853	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149179005	chr15:31776865-31776866	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373899339	chr15:31776897-31776898	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377185847	chr15:31776901-31776902	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201934783	chr15:31776934-31776935	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79947648	chr15:31776994-31776995	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531004599	chr15:31777010-31777011	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551196926	chr15:31777031-31777032	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564409236	chr15:31777036-31777037	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142042011	chr15:31777093-31777094	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546649040	chr15:31777099-31777100	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12439310	chr15:31777104-31777105	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535709841	chr15:31777117-31777118	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549303498	chr15:31777141-31777142	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31765600-31779200	Weak transcription	Brain Angular Gyrus	brain
2	chr15:31766000-31776400	Weak transcription	Brain Hippocampus Middle	brain
3	chr15:31769000-31776400	Weak transcription	Brain Substantia Nigra	brain
4	chr15:31774600-31776600	Bivalent/Poised TSS	Thymus	Thymus
5	chr15:31775000-31777200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
6	chr15:31775200-31776400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
7	chr15:31775200-31776400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr15:31775200-31776400	Active TSS	Primary T helper cells PMA-I stimulated	--
9	chr15:31775200-31776400	Flanking Active TSS	Right Ventricle	heart
10	chr15:31775200-31776600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
11	chr15:31775200-31776600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr15:31775200-31776600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:31775400-31776400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
14	chr15:31775400-31776400	Active TSS	Primary T cells from cord blood	blood
15	chr15:31775400-31776400	Flanking Active TSS	Primary hematopoietic stem cells	blood
16	chr15:31775400-31776400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
17	chr15:31775400-31776400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr15:31775400-31776400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr15:31775400-31776400	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
20	chr15:31775400-31776400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
21	chr15:31775400-31776400	Active TSS	Fetal Brain Female	brain
22	chr15:31775400-31776400	Bivalent/Poised TSS	Psoas Muscle	Psoas
23	chr15:31775400-31776600	Active TSS	Primary B cells from cord blood	blood
24	chr15:31775400-31776600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr15:31775400-31776600	Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr15:31775400-31776600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr15:31775400-31780400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr15:31775600-31776600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
29	chr15:31775600-31777000	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr15:31775800-31776400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
31	chr15:31775800-31776400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr15:31775800-31776600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr15:31775800-31776600	Weak transcription	Brain Anterior Caudate	brain
34	chr15:31775800-31779000	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr15:31775800-31779600	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr15:31776000-31776400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr15:31776000-31776400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr15:31776000-31776400	Weak transcription	Colonic Mucosa	Colon
39	chr15:31776000-31776400	Weak transcription	Gastric	stomach
40	chr15:31776000-31776400	Weak transcription	Pancreas	Pancrea
41	chr15:31776000-31776600	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr15:31776000-31777000	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr15:31776000-31777200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:31776000-31777400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr15:31776000-31777400	Enhancers	Esophagus	oesophagus
46	chr15:31776000-31780000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr15:31776000-31780000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr15:31776000-31780200	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr15:31776000-31780600	Weak transcription	Left Ventricle	heart
50	chr15:31776200-31776400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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