Variant report

Variant	nsv911695
Chromosome Location	chr19:40217794-40235008
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	ATF2	chr19:40217452-40218159	GM12878	blood:	n/a	n/a
2	BACH1	chr19:40220520-40220648	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr19:40222311-40222662	GM12878	blood:	n/a	n/a
4	BCL3	chr19:40222329-40222619	GM12878	blood:	n/a	n/a
5	BCL3	chr19:40227965-40228346	GM12878	blood:	n/a	n/a
6	BCLAF1	chr19:40217620-40218132	GM12878	blood:	n/a	n/a
7	BHLHE40	chr19:40217720-40218075	GM12878	blood:	n/a	n/a
8	CTCF	chr19:40218160-40218310	GM12864	blood:	n/a	n/a
9	CTCF	chr19:40233909-40233920	GM10266	blood:	n/a	n/a
10	CTCF	chr19:40234350-40234364	Lung_OC	lung:	n/a	n/a
11	CUX1	chr19:40217661-40217959	GM12878	blood:	n/a	n/a
12	EBF1	chr19:40217671-40218059	GM12878	blood:	n/a	n/a
13	EBF1	chr19:40217667-40217966	GM12878	blood:	n/a	n/a
14	EGR1	chr19:40226809-40227006	GM12878	blood:	n/a	chr19:40226904-40226926 chr19:40226910-40226920 chr19:40226910-40226920 chr19:40226909-40226923 chr19:40226908-40226921 chr19:40226908-40226922 chr19:40226909-40226920 chr19:40226909-40226920
15	EGR1	chr19:40226800-40227011	K562	blood:	n/a	chr19:40226904-40226926 chr19:40226910-40226920 chr19:40226910-40226920 chr19:40226909-40226923 chr19:40226908-40226921 chr19:40226908-40226922 chr19:40226909-40226920 chr19:40226909-40226920
16	EGR1	chr19:40226829-40227000	GM12878	blood:	n/a	chr19:40226904-40226926 chr19:40226910-40226920 chr19:40226910-40226920 chr19:40226909-40226923 chr19:40226908-40226921 chr19:40226908-40226922 chr19:40226909-40226920 chr19:40226909-40226920
17	EGR1	chr19:40226813-40227024	K562	blood:	n/a	chr19:40226904-40226926 chr19:40226910-40226920 chr19:40226910-40226920 chr19:40226909-40226923 chr19:40226908-40226921 chr19:40226908-40226922 chr19:40226909-40226920 chr19:40226909-40226920
18	EP300	chr19:40217657-40218068	GM12878	blood:	n/a	n/a
19	EP300	chr19:40217589-40218081	GM12878	blood:	n/a	n/a
20	IKZF1	chr19:40217711-40218039	GM12878	blood:	n/a	n/a
21	MAFF	chr19:40233381-40233592	HepG2	liver:	n/a	n/a
22	MAFK	chr19:40233448-40233502	HepG2	liver:	n/a	n/a
23	MAFK	chr19:40233367-40233597	HepG2	liver:	n/a	n/a
24	MAZ	chr19:40229864-40229874	HepG2	liver:	n/a	n/a
25	MTA3	chr19:40217397-40218194	GM12878	blood:	n/a	n/a
26	MYC	chr19:40228033-40228100	MCF-7	breast:	n/a	n/a
27	PBX3	chr19:40222409-40222633	GM12878	blood:	n/a	n/a
28	PBX3	chr19:40218774-40218964	GM12878	blood:	n/a	n/a
29	PBX3	chr19:40228058-40228295	GM12878	blood:	n/a	n/a
30	POLR2A	chr19:40230709-40231139	H1-neurons	neurons:	n/a	n/a
31	POLR2A	chr19:40222153-40222668	HL-60	blood:	n/a	n/a
32	POLR2A	chr19:40218823-40218905	A549	lung:	n/a	n/a
33	POLR2A	chr19:40218642-40218682	GM12878	blood:	n/a	n/a
34	POLR2A	chr19:40230510-40231120	H1-neurons	neurons:	n/a	n/a
35	POLR2A	chr19:40218687-40218703	GM12878	blood:	n/a	n/a
36	POU2F2	chr19:40217716-40218221	GM12891	blood:	n/a	chr19:40217994-40218004 chr19:40217987-40218008 chr19:40217989-40218003 chr19:40217994-40218002 chr19:40217992-40218005 chr19:40217993-40218003 chr19:40217989-40218007 chr19:40217987-40218009 chr19:40217988-40218001 chr19:40217992-40218003 chr19:40217992-40218003 chr19:40217994-40218004 chr19:40217995-40218002 chr19:40217988-40218001 chr19:40217994-40218003 chr19:40217991-40218005 chr19:40217988-40218001 chr19:40217993-40218005 chr19:40217991-40218006
37	POU2F2	chr19:40217583-40218216	GM12878	blood:	n/a	chr19:40217994-40218004 chr19:40217987-40218008 chr19:40217989-40218003 chr19:40217994-40218002 chr19:40217992-40218005 chr19:40217993-40218003 chr19:40217989-40218007 chr19:40217987-40218009 chr19:40217988-40218001 chr19:40217992-40218003 chr19:40217992-40218003 chr19:40217994-40218004 chr19:40217995-40218002 chr19:40217988-40218001 chr19:40217994-40218003 chr19:40217991-40218005 chr19:40217988-40218001 chr19:40217993-40218005 chr19:40217991-40218006
38	POU2F2	chr19:40217667-40218175	GM12878	blood:	n/a	chr19:40217994-40218004 chr19:40217987-40218008 chr19:40217989-40218003 chr19:40217994-40218002 chr19:40217992-40218005 chr19:40217993-40218003 chr19:40217989-40218007 chr19:40217987-40218009 chr19:40217988-40218001 chr19:40217992-40218003 chr19:40217992-40218003 chr19:40217994-40218004 chr19:40217995-40218002 chr19:40217988-40218001 chr19:40217994-40218003 chr19:40217991-40218005 chr19:40217988-40218001 chr19:40217993-40218005 chr19:40217991-40218006
39	RCOR1	chr19:40217664-40218153	GM12878	blood:	n/a	n/a
40	REST	chr19:40230243-40231278	H1-neurons	neurons:	n/a	n/a
41	RUNX3	chr19:40217634-40218047	GM12878	blood:	n/a	n/a
42	RUNX3	chr19:40217617-40218037	GM12878	blood:	n/a	n/a
43	RUNX3	chr19:40226707-40227037	GM12878	blood:	n/a	n/a
44	SMC3	chr19:40217514-40217935	GM12878	blood:	n/a	n/a
45	SPI1	chr19:40229558-40229737	K562	blood:	n/a	n/a
46	SPI1	chr19:40229461-40229816	GM12891	blood:	n/a	n/a
47	SPI1	chr19:40229404-40229916	GM12891	blood:	n/a	n/a
48	SPI1	chr19:40229516-40229803	GM12878	blood:	n/a	n/a
49	SPI1	chr19:40229390-40229979	HL-60	blood:	n/a	n/a
50	SPI1	chr19:40229539-40229770	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40229366-40229416	HL-60	blood:	n/a
2	chr19:40228820-40228870	GM12892	blood:	n/a
3	chr19:40229266-40229316	Hepatocyte	liver:	n/a
4	chr19:40229366-40229416	ovcar-3	ovarian:	n/a
5	chr19:40228820-40228870	A549	lung:	n/a
6	chr19:40229266-40229316	GM12892	blood:	n/a
7	chr19:40229266-40229316	BJ	skin:	n/a
8	chr19:40227949-40227999	Jurkat	blood:	n/a
9	chr19:40227949-40227999	HUVEC	blood vessel:	n/a
10	chr19:40227949-40227999	Caco-2	colon:	n/a
11	chr19:40229215-40229265	T-47D	breast:	n/a
12	chr19:40229766-40229816	HCPEpiC	choroid plexus:	n/a
13	chr19:40227949-40227999	HRE	kidney:	n/a
14	chr19:40229266-40229316	SKMC	muscle:	n/a
15	chr19:40227949-40227999	SK-N-SH	brain:	n/a
16	chr19:40228820-40228870	PFSK-1	brain:	n/a
17	chr19:40229766-40229816	AG04449	skin:	fetal
18	chr19:40229366-40229416	GM19239	blood:	n/a
19	chr19:40229766-40229816	ProgFib	skin:	n/a
20	chr19:40229215-40229265	HCT-116	colon:	n/a
21	chr19:40229266-40229316	NHDF-neo	bronchial:	n/a
22	chr19:40229766-40229816	RPTEC	kidney:	n/a
23	chr19:40229366-40229416	CMK	blood:	n/a
24	chr19:40229366-40229416	AG09309	skin:	n/a
25	chr19:40229266-40229316	HPAEpiC	pulmonary alveolar:	n/a
26	chr19:40228820-40228870	CMK	blood:	n/a
27	chr19:40229266-40229316	AG09309	skin:	n/a
28	chr19:40228820-40228870	SK-N-SH	brain:	n/a
29	chr19:40229215-40229265	PFSK-1	brain:	n/a
30	chr19:40229766-40229816	HEEpiC	esophagus:	n/a
31	chr19:40229266-40229316	NH-A	brain:	n/a
32	chr19:40229215-40229265	AG09309	skin:	n/a
33	chr19:40229215-40229265	HPAEpiC	pulmonary alveolar:	n/a
34	chr19:40229766-40229816	PANC-1	pancreas:	n/a
35	chr19:40229266-40229316	HL-60	blood:	n/a
36	chr19:40229215-40229265	BJ	skin:	n/a
37	chr19:40228820-40228870	PANC-1	pancreas:	n/a
38	chr19:40229266-40229316	HEK293	kidney:	embryo
39	chr19:40229766-40229816	Hela-S3	cervix:	n/a
40	chr19:40228820-40228870	BJ	skin:	n/a
41	chr19:40228820-40228870	PrEC	prostate:	n/a
42	chr19:40229366-40229416	A549	lung:	n/a
43	chr19:40229366-40229416	HIPEpiC	eye:	n/a
44	chr19:40229766-40229816	NB4	blood:	n/a
45	chr19:40228820-40228870	SK-N-MC	brain:	n/a
46	chr19:40229766-40229816	T-47D	breast:	n/a
47	chr19:40229266-40229316	Jurkat	blood:	n/a
48	chr19:40229215-40229265	HCF	heart:	n/a
49	chr19:40229366-40229416	HRPEpiC	eye:	n/a
50	chr19:40229366-40229416	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:40219606..40222689-chr19:40225665..40231232,5	K562	blood:
2	chr19:40218825..40222024-chr19:40225949..40228732,3	K562	blood:

Variant related genes	Relation type
CLC	TF binding region
CLC	CpG island
ENSG00000105205	chromatin interactions

Extended variants
information (count: 773 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs385563	chr19:40217794-40217795	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187054368	chr19:40217798-40217799	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs535235652	chr19:40217816-40217817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7249932	chr19:40217820-40217821	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575187403	chr19:40217904-40217905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs385895	chr19:40217907-40217908	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs564977036	chr19:40217924-40217925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554628514	chr19:40217925-40217926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191123836	chr19:40217977-40217978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201658583	chr19:40218007-40218008	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs182868663	chr19:40218009-40218010	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs577259638	chr19:40218016-40218017	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs150577662	chr19:40218029-40218030	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs530194228	chr19:40218039-40218040	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs548829748	chr19:40218068-40218069	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs553689461	chr19:40218095-40218096	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs386545	chr19:40218097-40218098	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531274407	chr19:40218098-40218099	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs552864733	chr19:40218144-40218145	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs556718984	chr19:40218146-40218147	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs186138803	chr19:40218166-40218167	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs138753823	chr19:40218188-40218189	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs546688161	chr19:40218189-40218190	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs190217394	chr19:40218199-40218200	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs542430309	chr19:40218216-40218217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535154838	chr19:40218227-40218228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570291969	chr19:40218262-40218263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556782419	chr19:40218281-40218282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs58565953	chr19:40218291-40218292	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs183227225	chr19:40218295-40218296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141900878	chr19:40218371-40218372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573097573	chr19:40218376-40218377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577188917	chr19:40218394-40218395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541101396	chr19:40218432-40218433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556095781	chr19:40218442-40218443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187791690	chr19:40218490-40218491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574884029	chr19:40218539-40218540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542335964	chr19:40218540-40218541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369813818	chr19:40218553-40218554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563884174	chr19:40218615-40218616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146236622	chr19:40218638-40218639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192445538	chr19:40218647-40218648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564587892	chr19:40218662-40218663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576085146	chr19:40218681-40218682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528764623	chr19:40218686-40218687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546305355	chr19:40218690-40218691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs410034	chr19:40218709-40218710	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs373803143	chr19:40218724-40218725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528994298	chr19:40218730-40218731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182900361	chr19:40218750-40218751	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40217200-40219200	Enhancers	Placenta	Placenta
2	chr19:40217400-40217800	Flanking Active TSS	GM12878-XiMat	blood
3	chr19:40217800-40218000	Enhancers	GM12878-XiMat	blood
4	chr19:40218000-40218200	Flanking Active TSS	GM12878-XiMat	blood
5	chr19:40218200-40219200	Enhancers	GM12878-XiMat	blood
6	chr19:40218400-40219000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr19:40219200-40221800	Weak transcription	GM12878-XiMat	blood
8	chr19:40219200-40225200	Weak transcription	Placenta	Placenta
9	chr19:40221800-40222200	Enhancers	GM12878-XiMat	blood
10	chr19:40222000-40222600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr19:40222200-40225600	Weak transcription	GM12878-XiMat	blood
12	chr19:40224600-40226600	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr19:40225200-40226000	Enhancers	Placenta	Placenta
14	chr19:40225600-40229400	Enhancers	GM12878-XiMat	blood
15	chr19:40226000-40228600	Weak transcription	Placenta	Placenta
16	chr19:40226000-40228800	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr19:40226200-40229200	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr19:40226400-40227000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr19:40226400-40228200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr19:40226600-40227800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr19:40226800-40228800	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr19:40227000-40227400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr19:40227400-40228200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr19:40227800-40228200	Active TSS	Rectal Mucosa Donor 29	rectum
25	chr19:40227800-40229600	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr19:40228000-40228200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:40228000-40228400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr19:40228200-40229000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr19:40228200-40229000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr19:40228600-40230200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr19:40228800-40229400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr19:40228800-40230000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr19:40228800-40230600	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr19:40228800-40231200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr19:40229000-40229200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr19:40229000-40229200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:40229000-40229200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr19:40229200-40230600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr19:40229200-40230800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr19:40229200-40237400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr19:40229400-40229800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr19:40229400-40236200	Weak transcription	GM12878-XiMat	blood
43	chr19:40229600-40230600	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr19:40230600-40231000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr19:40230600-40231000	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr19:40230600-40231000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr19:40230600-40231000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr19:40230800-40231000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr19:40230800-40231200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr19:40231000-40231200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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