Variant report

Variant	nsv911743
Chromosome Location	chr19:41350039-41383828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:348)
CpG islands
(count:366)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41370633-41370945	K562	blood:	n/a	n/a
2	ARID3A	chr19:41378197-41378436	K562	blood:	n/a	n/a
3	ATF1	chr19:41370536-41370948	K562	blood:	n/a	n/a
4	ATF1	chr19:41378237-41378485	K562	blood:	n/a	n/a
5	ATF3	chr19:41370620-41370877	K562	blood:	n/a	n/a
6	ATF3	chr19:41378141-41378430	K562	blood:	n/a	n/a
7	CBX3	chr19:41370123-41371107	K562	blood:	n/a	n/a
8	CBX3	chr19:41381255-41381833	K562	blood:	n/a	n/a
9	CBX3	chr19:41379769-41380227	K562	blood:	n/a	n/a
10	CBX3	chr19:41349182-41350047	K562	blood:	n/a	n/a
11	CBX3	chr19:41379821-41380148	K562	blood:	n/a	n/a
12	CCNT2	chr19:41370582-41370786	K562	blood:	n/a	n/a
13	CEBPB	chr19:41368416-41368601	K562	blood:	n/a	n/a
14	CEBPB	chr19:41368480-41368982	A549	lung:	n/a	n/a
15	CEBPB	chr19:41373920-41374208	K562	blood:	n/a	n/a
16	CEBPB	chr19:41362024-41362201	K562	blood:	n/a	n/a
17	CEBPB	chr19:41378139-41378466	K562	blood:	n/a	n/a
18	CEBPB	chr19:41374056-41374100	A549	lung:	n/a	n/a
19	CEBPB	chr19:41378202-41378474	K562	blood:	n/a	n/a
20	CEBPB	chr19:41373834-41374300	A549	lung:	n/a	n/a
21	CEBPB	chr19:41370305-41370801	K562	blood:	n/a	chr19:41370433-41370441
22	CEBPB	chr19:41367289-41367476	A549	lung:	n/a	n/a
23	CEBPB	chr19:41370209-41371189	K562	blood:	n/a	chr19:41370433-41370441
24	CEBPB	chr19:41368761-41369068	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:41370543-41370910	K562	blood:	n/a	n/a
26	CEBPD	chr19:41370295-41371143	K562	blood:	n/a	n/a
27	CEBPD	chr19:41370661-41370862	K562	blood:	n/a	n/a
28	CTCF	chr19:41364176-41364245	MCF-7	breast:	n/a	n/a
29	CTCF	chr19:41360550-41360556	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr19:41364100-41364250	HEK293	kidney:	n/a	n/a
31	CTCF	chr19:41354540-41354690	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr19:41354437-41354750	K562	blood:	n/a	chr19:41354699-41354709
33	CTCF	chr19:41354540-41354690	AG04450	lung:	n/a	n/a
34	CTCF	chr19:41354459-41354759	K562	blood:	n/a	chr19:41354699-41354709
35	CTCF	chr19:41368380-41368530	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr19:41381740-41381820	GM13976	blood:	n/a	n/a
37	CTCF	chr19:41354511-41354642	K562	blood:	n/a	n/a
38	CTCF	chr19:41354620-41354770	HVMF	connective:	n/a	chr19:41354699-41354709
39	CTCF	chr19:41354359-41354806	A549	lung:	n/a	chr19:41354699-41354709
40	CTCF	chr19:41364120-41364270	K562	blood:	n/a	n/a
41	CTCF	chr19:41367440-41367590	K562	blood:	n/a	n/a
42	CTCF	chr19:41368380-41368530	A549	lung:	n/a	n/a
43	CTCF	chr19:41354660-41354810	A549	lung:	n/a	chr19:41354699-41354709
44	CTCF	chr19:41368340-41368490	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr19:41368360-41368510	AG10803	skin:	n/a	n/a
46	CTCF	chr19:41354312-41354785	K562	blood:	n/a	chr19:41354699-41354709
47	CTCF	chr19:41364080-41364230	A549	lung:	n/a	n/a
48	CTCF	chr19:41368320-41368470	AG09309	skin:	n/a	n/a
49	CTCF	chr19:41367560-41367710	HEK293	kidney:	n/a	n/a
50	CTCF	chr19:41354500-41354650	HCM	heart:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41351924-41351974	MCF10A-Er-Src	breast:	n/a
2	chr19:41354682-41354732	PrEC	prostate:	n/a
3	chr19:41355973-41356023	GM19239	blood:	n/a
4	chr19:41351924-41351974	HIPEpiC	eye:	n/a
5	chr19:41354142-41354192	AG04450	lung:	fetal
6	chr19:41351924-41351974	SK-N-SH	brain:	n/a
7	chr19:41383654-41383704	AoSMC	blood vessel:	n/a
8	chr19:41354142-41354192	ECC-1	luminal epithelium:	n/a
9	chr19:41354142-41354192	HCM	heart:	n/a
10	chr19:41354142-41354192	Hepatocyte	liver:	n/a
11	chr19:41354682-41354732	T-47D	breast:	n/a
12	chr19:41354142-41354192	HCF	heart:	n/a
13	chr19:41351924-41351974	MCF-7	breast:	n/a
14	chr19:41354682-41354732	ProgFib	skin:	n/a
15	chr19:41354553-41354603	PrEC	prostate:	n/a
16	chr19:41351924-41351974	NB4	blood:	n/a
17	chr19:41354142-41354192	HNPCEpiC	eye:	n/a
18	chr19:41354142-41354192	HEEpiC	esophagus:	n/a
19	chr19:41355973-41356023	AG04450	lung:	fetal
20	chr19:41383654-41383704	HCF	heart:	n/a
21	chr19:41351924-41351974	ProgFib	skin:	n/a
22	chr19:41354142-41354192	PrEC	prostate:	n/a
23	chr19:41354553-41354603	AG09309	skin:	n/a
24	chr19:41354553-41354603	AG04450	lung:	fetal
25	chr19:41354553-41354603	ovcar-3	ovarian:	n/a
26	chr19:41354142-41354192	SAEC	small airway:	n/a
27	chr19:41351924-41351974	T-47D	breast:	n/a
28	chr19:41354553-41354603	HCF	heart:	n/a
29	chr19:41383654-41383704	MCF-7	breast:	n/a
30	chr19:41354553-41354603	NHDF-neo	bronchial:	n/a
31	chr19:41355973-41356023	AG10803	skin:	n/a
32	chr19:41383654-41383704	HUVEC	blood vessel:	n/a
33	chr19:41351924-41351974	NHBE	bronchial:	n/a
34	chr19:41354553-41354603	HAEpiC	amniotic membrane:	n/a
35	chr19:41351924-41351974	GM06990	blood:	n/a
36	chr19:41355973-41356023	U87	brain:	n/a
37	chr19:41354682-41354732	PANC-1	pancreas:	n/a
38	chr19:41355973-41356023	H1-hESC	embryonic stem cell:	embryo
39	chr19:41351924-41351974	Hela-S3	cervix:	n/a
40	chr19:41355973-41356023	NH-A	brain:	n/a
41	chr19:41383654-41383704	LNCaP	prostate:	n/a
42	chr19:41355973-41356023	A549	lung:	n/a
43	chr19:41354682-41354732	GM06990	blood:	n/a
44	chr19:41354682-41354732	LNCaP	prostate:	n/a
45	chr19:41351924-41351974	BE2_C	brain:	n/a
46	chr19:41354553-41354603	K562	blood:	n/a
47	chr19:41351924-41351974	ECC-1	luminal epithelium:	n/a
48	chr19:41351924-41351974	H1-hESC	embryonic stem cell:	embryo
49	chr19:41355973-41356023	Hela-S3	cervix:	n/a
50	chr19:41354553-41354603	HRPEpiC	eye:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41195484..41197379-chr19:41368669..41371255,2	K562	blood:
2	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
3	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
4	chr16:4474827..4477394-chr19:41351022..41353007,2	MCF-7	breast:

No data

Variant related genes	Relation type
CYP2A6	TF binding region
CYP2A7	TF binding region
CYP2A6	CpG island
CYP2A7	CpG island
ENSG00000103423	chromatin interactions
ENSG00000262246	chromatin interactions
ENSG00000105245	chromatin interactions

Extended variants
information (count: 1764 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1764 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2431414	chr19:41350039-41350040	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72547581	chr19:41350050-41350051	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560172971	chr19:41350056-41350057	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572409121	chr19:41350086-41350087	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542939658	chr19:41350098-41350099	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570351602	chr19:41350114-41350115	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561117972	chr19:41350173-41350174	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531467589	chr19:41350189-41350190	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531414040	chr19:41350191-41350192	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549914213	chr19:41350211-41350212	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145026630	chr19:41350217-41350218	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386809287	chr19:41350232-41350233	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2644908	chr19:41350241-41350242	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533443716	chr19:41350272-41350273	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551519233	chr19:41350284-41350285	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566521623	chr19:41350349-41350350	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549865604	chr19:41350361-41350362	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs60708866	chr19:41350383-41350384	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534270874	chr19:41350439-41350440	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186833314	chr19:41350448-41350449	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567580611	chr19:41350460-41350461	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72549446	chr19:41350475-41350476	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2002975	chr19:41350489-41350490	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs571285801	chr19:41350502-41350503	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113368210	chr19:41350505-41350506	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374380841	chr19:41350506-41350507	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs56164728	chr19:41350507-41350508	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs2002976	chr19:41350509-41350510	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs373592802	chr19:41350527-41350528	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151062237	chr19:41350537-41350538	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554920226	chr19:41350575-41350576	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs8192730	chr19:41350582-41350583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28399463	chr19:41350587-41350588	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs367713420	chr19:41350590-41350591	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2002977	chr19:41350594-41350595	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs143336165	chr19:41350600-41350601	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371553133	chr19:41350611-41350612	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150476660	chr19:41350612-41350613	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59505316	chr19:41350613-41350614	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28399462	chr19:41350615-41350616	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs56314118	chr19:41350630-41350631	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs143984220	chr19:41350642-41350643	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560168395	chr19:41350645-41350646	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28399461	chr19:41350648-41350649	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1809810	chr19:41350664-41350665	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376817657	chr19:41350671-41350672	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs59389036	chr19:41350672-41350673	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369346633	chr19:41350682-41350683	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372324955	chr19:41350684-41350685	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550145221	chr19:41350696-41350697	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
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
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	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
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41349200-41350200	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr19:41349200-41350200	Active TSS	Primary B cells from cord blood	blood
3	chr19:41349200-41350200	Enhancers	Primary T cells from cord blood	blood
4	chr19:41349200-41350400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr19:41349200-41350400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr19:41349200-41350800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr19:41349400-41350200	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr19:41349400-41350200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
9	chr19:41349400-41350200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
10	chr19:41349400-41350200	Enhancers	K562	blood
11	chr19:41349400-41350400	Enhancers	Stomach Mucosa	stomach
12	chr19:41349600-41350200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr19:41349600-41350200	Active TSS	Duodenum Mucosa	Duodenum
14	chr19:41349600-41350600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr19:41349600-41351200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr19:41349600-41351200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr19:41349800-41350200	Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr19:41349800-41350200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr19:41349800-41350400	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr19:41349800-41350400	Weak transcription	Esophagus	oesophagus
21	chr19:41349800-41350600	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr19:41349800-41350600	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr19:41349800-41350800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr19:41349800-41351200	Weak transcription	Right Ventricle	heart
25	chr19:41349800-41353800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr19:41350000-41350200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr19:41350000-41350200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
28	chr19:41350000-41350200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
29	chr19:41350000-41350200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr19:41350000-41350800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr19:41350000-41350800	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr19:41350000-41351000	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr19:41350000-41351000	Weak transcription	Pancreas	Pancrea
34	chr19:41350000-41351400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr19:41350000-41352600	Weak transcription	Lung	lung
36	chr19:41350000-41353000	Strong transcription	Liver	Liver
37	chr19:41350200-41350400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr19:41350200-41350600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr19:41350200-41350800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr19:41350200-41350800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr19:41350200-41351000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr19:41350200-41351200	Enhancers	Primary T cells fromperipheralblood	blood
43	chr19:41350400-41351200	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr19:41350600-41354400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr19:41350800-41354400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr19:41351000-41354600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr19:41351200-41354400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr19:41351200-41354400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr19:41351400-41351600	Enhancers	Esophagus	oesophagus
50	chr19:41351400-41351600	Enhancers	Right Ventricle	heart

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