Variant report

Variant	esv33175
Chromosome Location	chr19:52002098-52010839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:736)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:52009630-52009736	K562	blood:	n/a	n/a
2	ATF1	chr19:52004930-52005237	K562	blood:	n/a	n/a
3	BHLHE40	chr19:52010493-52012020	K562	blood:	n/a	n/a
4	CBX3	chr19:52010361-52012240	K562	blood:	n/a	n/a
5	CBX3	chr19:52007578-52007932	K562	blood:	n/a	n/a
6	CEBPB	chr19:52010837-52011736	K562	blood:	n/a	n/a
7	CEBPB	chr19:52002024-52002259	K562	blood:	n/a	chr19:52002134-52002147
8	CEBPB	chr19:52009695-52009905	HepG2	liver:	n/a	chr19:52009784-52009795
9	CEBPB	chr19:52009670-52009938	IMR90	lung:	n/a	chr19:52009784-52009795
10	CTCF	chr19:52005320-52005470	NB4	blood:	n/a	n/a
11	CTCF	chr19:52004258-52004314	GM20000	blood:	n/a	n/a
12	CTCF	chr19:52005260-52005410	GM12874	blood:	n/a	n/a
13	CTCF	chr19:52005160-52005310	GM12867	blood:	n/a	n/a
14	CTCF	chr19:52005140-52005290	GM12871	blood:	n/a	n/a
15	CUX1	chr19:52009748-52009830	K562	blood:	n/a	n/a
16	CUX1	chr19:52010569-52011664	K562	blood:	n/a	n/a
17	ELF1	chr19:52010526-52011351	K562	blood:	n/a	n/a
18	EP300	chr19:52009926-52009934	K562	blood:	n/a	n/a
19	EP300	chr19:52010509-52012049	K562	blood:	n/a	n/a
20	GATA1	chr19:52009384-52012121	K562	blood:	n/a	chr19:52011791-52011801 chr19:52011555-52011562 chr19:52011553-52011562 chr19:52011177-52011187
21	HMGN3	chr19:52010839-52011855	K562	blood:	n/a	chr19:52011554-52011561
22	IRF1	chr19:52010571-52011722	K562	blood:	n/a	chr19:52011192-52011201 chr19:52011686-52011695
23	IRF1	chr19:52010489-52011803	K562	blood:	n/a	chr19:52011192-52011201 chr19:52011686-52011695
24	JUND	chr19:52004990-52005201	K562	blood:	n/a	n/a
25	JUND	chr19:52010512-52011828	K562	blood:	n/a	n/a
26	MAFF	chr19:52004842-52005079	K562	blood:	n/a	n/a
27	MAFK	chr19:52004892-52005011	HepG2	liver:	n/a	n/a
28	MAFK	chr19:52004788-52005014	HepG2	liver:	n/a	n/a
29	MAFK	chr19:52004747-52004973	K562	blood:	n/a	n/a
30	MAX	chr19:52009234-52009502	K562	blood:	n/a	n/a
31	MAX	chr19:52010417-52011378	K562	blood:	n/a	chr19:52011273-52011282
32	MAX	chr19:52006620-52007028	NB4	blood:	n/a	n/a
33	MAX	chr19:52009211-52009610	K562	blood:	n/a	n/a
34	MAZ	chr19:52004932-52005080	K562	blood:	n/a	n/a
35	MAZ	chr19:52010625-52012202	K562	blood:	n/a	chr19:52011273-52011282
36	MAZ	chr19:52005419-52005428	K562	blood:	n/a	n/a
37	MYC	chr19:52006883-52006915	NB4	blood:	n/a	n/a
38	MYC	chr19:52010503-52011959	K562	blood:	n/a	chr19:52011273-52011282
39	MYC	chr19:52010453-52012039	K562	blood:	n/a	chr19:52011273-52011282
40	NR2F2	chr19:52010537-52011764	K562	blood:	n/a	n/a
41	NR2F2	chr19:52010568-52012132	K562	blood:	n/a	n/a
42	PML	chr19:52010539-52011920	K562	blood:	n/a	n/a
43	POLR2A	chr19:52003926-52003930	MCF-7	breast:	n/a	n/a
44	POLR2A	chr19:52004196-52004357	MCF-7	breast:	n/a	n/a
45	POLR2A	chr19:52002736-52002745	MCF-7	breast:	n/a	n/a
46	POLR2A	chr19:52003949-52003962	MCF-7	breast:	n/a	n/a
47	POLR2A	chr19:52003866-52004166	MCF-7	breast:	n/a	n/a
48	POLR2A	chr19:52004328-52004330	MCF-7	breast:	n/a	n/a
49	POLR2A	chr19:52004337-52004345	MCF-7	breast:	n/a	n/a
50	POLR2A	chr19:52010620-52010789	K562	blood:	n/a	n/a

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52005176-52005226	A549	lung:	n/a
2	chr19:52005108-52005158	BE2_C	brain:	n/a
3	chr19:52005990-52006040	HepG2	liver:	n/a
4	chr19:52005070-52005120	T-47D	breast:	n/a
5	chr19:52005176-52005226	A549	lung:	n/a
6	chr19:52005108-52005158	BE2_C	brain:	n/a
7	chr19:52005990-52006040	HepG2	liver:	n/a
8	chr19:52005070-52005120	T-47D	breast:	n/a
9	chr19:52005176-52005226	HCM	heart:	n/a
10	chr19:52005982-52006032	HUVEC	blood vessel:	n/a
11	chr19:52006105-52006155	HMEC	breast:	n/a
12	chr19:52003566-52003616	IMR90	lung:	fetal
13	chr19:52005188-52005238	HMEC	breast:	n/a
14	chr19:52003566-52003616	HMEC	breast:	n/a
15	chr19:52006105-52006155	BJ	skin:	n/a
16	chr19:52005990-52006040	PFSK-1	brain:	n/a
17	chr19:52005651-52005701	HIPEpiC	eye:	n/a
18	chr19:52005070-52005120	GM19239	blood:	n/a
19	chr19:52006105-52006155	MCF10A-Er-Src	breast:	n/a
20	chr19:52003566-52003616	T-47D	breast:	n/a
21	chr19:52005188-52005238	GM12878	blood:	n/a
22	chr19:52004992-52005042	Jurkat	blood:	n/a
23	chr19:52005982-52006032	ECC-1	luminal epithelium:	n/a
24	chr19:52005070-52005120	SK-N-SH_RA	brain:	n/a
25	chr19:52004630-52004680	SK-N-MC	brain:	n/a
26	chr19:52005188-52005238	IMR90	lung:	fetal
27	chr19:52005108-52005158	HRPEpiC	eye:	n/a
28	chr19:52005153-52005203	PANC-1	pancreas:	n/a
29	chr19:52005651-52005701	GM12878	blood:	n/a
30	chr19:52005651-52005701	Caco-2	colon:	n/a
31	chr19:52005982-52006032	HepG2	liver:	n/a
32	chr19:52005990-52006040	HNPCEpiC	eye:	n/a
33	chr19:52005176-52005226	HIPEpiC	eye:	n/a
34	chr19:52005108-52005158	SAEC	small airway:	n/a
35	chr19:52004630-52004680	U87	brain:	n/a
36	chr19:52004630-52004680	AG09319	gingival:	n/a
37	chr19:52005990-52006040	LNCaP	prostate:	n/a
38	chr19:52005153-52005203	ovcar-3	ovarian:	n/a
39	chr19:52005990-52006040	GM12878	blood:	n/a
40	chr19:52005153-52005203	NHBE	bronchial:	n/a
41	chr19:52006105-52006155	SAEC	small airway:	n/a
42	chr19:52003566-52003616	PrEC	prostate:	n/a
43	chr19:52005070-52005120	Hela-S3	cervix:	n/a
44	chr19:52005153-52005203	HIPEpiC	eye:	n/a
45	chr19:52005070-52005120	HPAEpiC	pulmonary alveolar:	n/a
46	chr19:52005108-52005158	NHDF-neo	bronchial:	n/a
47	chr19:52005176-52005226	Caco-2	colon:	n/a
48	chr19:52005153-52005203	HRE	kidney:	n/a
49	chr19:52003566-52003616	AoSMC	blood vessel:	n/a
50	chr19:52005153-52005203	ProgFib	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52004923..52007446-chr19:52009404..52012427,3	K562	blood:
2	chr19:51895053..51897765-chr19:52007493..52009642,2	K562	blood:
3	chr19:52005541..52007329-chr19:52009799..52012427,3	K562	blood:
4	chr19:52000624..52003424-chr19:52007284..52010665,4	K562	blood:
5	chr19:51985395..51986977-chr19:52005149..52007708,2	K562	blood:
6	chr19:52009466..52011500-chr19:52096366..52099744,3	K562	blood:
7	chr19:52001211..52003424-chr19:52007284..52009327,3	K562	blood:
8	chr19:52005076..52007479-chr19:52052391..52054693,2	K562	blood:
9	chr19:52004923..52007446-chr19:52009404..52012427,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000268839	TF binding region
SIGLEC12	TF binding region
SIGLEC27P	TF binding region
ENSG00000268839	CpG island
SIGLEC12	CpG island
SIGLEC27P	CpG island
ENSG00000269580	chromatin interactions
ENSG00000269388	chromatin interactions
ENSG00000254521	chromatin interactions
ENSG00000268889	chromatin interactions
ENSG00000268839	chromatin interactions
ENSG00000167765	chromatin interactions

Extended variants
information (count: 467 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16982740	chr19:52002110-52002111	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191811181	chr19:52002122-52002123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs113724739	chr19:52002149-52002150	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs141075666	chr19:52002154-52002155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184340235	chr19:52002209-52002210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562988374	chr19:52002215-52002216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs533720315	chr19:52002234-52002235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577999635	chr19:52002263-52002264	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs73051351	chr19:52002291-52002292	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs369987765	chr19:52002312-52002313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4801871	chr19:52002317-52002318	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs111229073	chr19:52002319-52002320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188597022	chr19:52002320-52002321	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs528291230	chr19:52002328-52002329	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546844501	chr19:52002340-52002341	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115077666	chr19:52002351-52002352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200668316	chr19:52002361-52002362	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374368191	chr19:52002364-52002365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539778485	chr19:52002385-52002386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs199796873	chr19:52002408-52002409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201806540	chr19:52002417-52002418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538969850	chr19:52002452-52002453	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558174294	chr19:52002454-52002455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs968491	chr19:52002488-52002489	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs59372820	chr19:52002493-52002494	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs375879393	chr19:52002508-52002509	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555586981	chr19:52002525-52002526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113543312	chr19:52002532-52002533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs10414259	chr19:52002535-52002536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs76072416	chr19:52002545-52002546	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184169588	chr19:52002546-52002547	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372786026	chr19:52002647-52002648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373613023	chr19:52002656-52002657	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs377152692	chr19:52002657-52002658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs77857273	chr19:52002673-52002674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201270349	chr19:52002694-52002695	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373503153	chr19:52002698-52002699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377017791	chr19:52002706-52002707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201756364	chr19:52002717-52002718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs144437495	chr19:52002720-52002721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370144797	chr19:52002722-52002723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2009362	chr19:52002729-52002730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs372626174	chr19:52002732-52002733	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145810003	chr19:52002739-52002740	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375646481	chr19:52002749-52002750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146928756	chr19:52002757-52002758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs144920279	chr19:52002759-52002760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs546800905	chr19:52002761-52002762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs370592510	chr19:52002773-52002774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs373987989	chr19:52002783-52002784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51996400-52002600	Weak transcription	Spleen	Spleen
2	chr19:51997800-52002600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr19:51997800-52002800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr19:52000000-52002800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:52001800-52004400	Weak transcription	K562	blood
6	chr19:52002600-52002800	Enhancers	Spleen	Spleen
7	chr19:52002600-52015000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr19:52002800-52003600	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr19:52002800-52003800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:52002800-52004600	Weak transcription	Spleen	Spleen
11	chr19:52003000-52003200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
12	chr19:52003200-52003400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr19:52003400-52003600	Enhancers	Colonic Mucosa	Colon
14	chr19:52003400-52004600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr19:52003600-52003800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr19:52003600-52004600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr19:52003600-52004600	Weak transcription	Colonic Mucosa	Colon
18	chr19:52003600-52004800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr19:52003800-52004200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr19:52003800-52004800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:52004200-52005000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr19:52004200-52007000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr19:52004200-52007400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr19:52004400-52004600	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr19:52004400-52005600	Enhancers	Primary B cells from peripheral blood	blood
26	chr19:52004400-52005600	Enhancers	Primary hematopoietic stem cells	blood
27	chr19:52004400-52006000	Enhancers	K562	blood
28	chr19:52004600-52004800	Enhancers	Primary T cells from cord blood	blood
29	chr19:52004600-52004800	Bivalent Enhancer	Adipose Nuclei	Adipose
30	chr19:52004600-52005000	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr19:52004600-52005000	Enhancers	Colonic Mucosa	Colon
32	chr19:52004600-52005000	Active TSS	Duodenum Mucosa	Duodenum
33	chr19:52004600-52005000	Enhancers	Fetal Thymus	thymus
34	chr19:52004600-52005000	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr19:52004600-52005200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr19:52004600-52005200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
37	chr19:52004600-52005200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
38	chr19:52004600-52005200	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr19:52004600-52005200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr19:52004600-52005400	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr19:52004600-52005800	Enhancers	Primary B cells from cord blood	blood
42	chr19:52004600-52005800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr19:52004600-52005800	Enhancers	Placenta	Placenta
44	chr19:52004600-52006000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr19:52004600-52006000	Enhancers	Spleen	Spleen
46	chr19:52004800-52005000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr19:52004800-52005000	Bivalent Enhancer	Primary T cells from cord blood	blood
48	chr19:52004800-52005000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
49	chr19:52004800-52005000	Enhancers	Dnd41	blood
50	chr19:52004800-52005200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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