Variant report

Variant	nsv817836
Chromosome Location	chr19:41333284-41363765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:429)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41337675-41338160	HepG2	liver:	n/a	n/a
2	ATF1	chr19:41339642-41339915	K562	blood:	n/a	n/a
3	ATF3	chr19:41339727-41339986	K562	blood:	n/a	n/a
4	ATF3	chr19:41339265-41339474	K562	blood:	n/a	n/a
5	ATF3	chr19:41337642-41338304	A549	lung:	n/a	n/a
6	BCL3	chr19:41337399-41338400	A549	lung:	n/a	n/a
7	BCL3	chr19:41337271-41338291	A549	lung:	n/a	n/a
8	BHLHE40	chr19:41337704-41338087	A549	lung:	n/a	chr19:41337896-41337917
9	BHLHE40	chr19:41339813-41339844	K562	blood:	n/a	n/a
10	BHLHE40	chr19:41337595-41338254	HepG2	liver:	n/a	chr19:41337896-41337917
11	BHLHE40	chr19:41337763-41338048	HepG2	liver:	n/a	chr19:41337896-41337917
12	BHLHE40	chr19:41339267-41339464	K562	blood:	n/a	n/a
13	BHLHE40	chr19:41337685-41338115	K562	blood:	n/a	chr19:41337896-41337917
14	BHLHE40	chr19:41337782-41338177	HepG2	liver:	n/a	chr19:41337896-41337917
15	BRCA1	chr19:41337806-41338121	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr19:41347915-41348277	K562	blood:	n/a	n/a
17	CBX3	chr19:41349182-41350047	K562	blood:	n/a	n/a
18	CBX3	chr19:41347938-41348304	K562	blood:	n/a	n/a
19	CBX3	chr19:41337733-41338384	K562	blood:	n/a	n/a
20	CBX3	chr19:41333737-41334193	K562	blood:	n/a	n/a
21	CBX3	chr19:41333751-41334179	K562	blood:	n/a	n/a
22	CBX3	chr19:41339143-41339980	K562	blood:	n/a	n/a
23	CCNT2	chr19:41339675-41339875	K562	blood:	n/a	n/a
24	CEBPB	chr19:41342957-41343295	K562	blood:	n/a	chr19:41343121-41343132
25	CEBPB	chr19:41337708-41338253	MCF-7	breast:	n/a	n/a
26	CEBPB	chr19:41337643-41338329	HCT-116	colon:	n/a	n/a
27	CEBPB	chr19:41343011-41343287	HepG2	liver:	n/a	chr19:41343121-41343132
28	CEBPB	chr19:41337684-41338241	A549	lung:	n/a	n/a
29	CEBPB	chr19:41362024-41362201	K562	blood:	n/a	n/a
30	CEBPB	chr19:41337619-41338177	A549	lung:	n/a	n/a
31	CEBPB	chr19:41342862-41343338	A549	lung:	n/a	chr19:41343121-41343132
32	CEBPB	chr19:41334846-41335144	A549	lung:	n/a	chr19:41334912-41334923
33	CEBPB	chr19:41339647-41339931	K562	blood:	n/a	n/a
34	CEBPB	chr19:41343053-41343247	H1-hESC	embryonic stem cell:	n/a	chr19:41343121-41343132
35	CEBPB	chr19:41339359-41340046	K562	blood:	n/a	chr19:41339540-41339548
36	CEBPB	chr19:41337591-41338310	A549	lung:	n/a	n/a
37	CEBPB	chr19:41337608-41337699	K562	blood:	n/a	n/a
38	CEBPB	chr19:41337501-41338182	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:41337837-41338187	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:41339552-41339909	K562	blood:	n/a	n/a
41	CEBPB	chr19:41337713-41338232	IMR90	lung:	n/a	n/a
42	CEBPB	chr19:41337501-41338297	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr19:41343058-41343265	A549	lung:	n/a	chr19:41343121-41343132
44	CEBPB	chr19:41337605-41338263	MCF-7	breast:	n/a	n/a
45	CEBPB	chr19:41337683-41338182	HCT-116	colon:	n/a	n/a
46	CEBPB	chr19:41337826-41338039	HepG2	liver:	n/a	n/a
47	CEBPB	chr19:41343006-41343268	IMR90	lung:	n/a	chr19:41343121-41343132
48	CEBPD	chr19:41339436-41340105	K562	blood:	n/a	n/a
49	CHD2	chr19:41337774-41338104	HepG2	liver:	n/a	n/a
50	CHD2	chr19:41337773-41338158	Hela-S3	cervix:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41354682-41354732	ECC-1	luminal epithelium:	n/a
2	chr19:41354142-41354192	AG09309	skin:	n/a
3	chr19:41354682-41354732	HCM	heart:	n/a
4	chr19:41354553-41354603	HRPEpiC	eye:	n/a
5	chr19:41355973-41356023	AoSMC	blood vessel:	n/a
6	chr19:41354682-41354732	HL-60	blood:	n/a
7	chr19:41354142-41354192	SAEC	small airway:	n/a
8	chr19:41354682-41354732	ProgFib	skin:	n/a
9	chr19:41354553-41354603	HIPEpiC	eye:	n/a
10	chr19:41355973-41356023	HPAEpiC	pulmonary alveolar:	n/a
11	chr19:41354682-41354732	MCF10A-Er-Src	breast:	n/a
12	chr19:41354553-41354603	Caco-2	colon:	n/a
13	chr19:41355973-41356023	HEEpiC	esophagus:	n/a
14	chr19:41354682-41354732	SKMC	muscle:	n/a
15	chr19:41354682-41354732	HEK293	kidney:	embryo
16	chr19:41355973-41356023	AG09309	skin:	n/a
17	chr19:41354553-41354603	AG09309	skin:	n/a
18	chr19:41351924-41351974	SAEC	small airway:	n/a
19	chr19:41354682-41354732	HCPEpiC	choroid plexus:	n/a
20	chr19:41354682-41354732	H1-hESC	embryonic stem cell:	embryo
21	chr19:41354142-41354192	RPTEC	kidney:	n/a
22	chr19:41354142-41354192	AG09319	gingival:	n/a
23	chr19:41354682-41354732	PANC-1	pancreas:	n/a
24	chr19:41354553-41354603	HCM	heart:	n/a
25	chr19:41354142-41354192	CMK	blood:	n/a
26	chr19:41354142-41354192	HCF	heart:	n/a
27	chr19:41355973-41356023	Jurkat	blood:	n/a
28	chr19:41354553-41354603	HCPEpiC	choroid plexus:	n/a
29	chr19:41355973-41356023	HRCEpiC	kidney:	n/a
30	chr19:41355973-41356023	AG10803	skin:	n/a
31	chr19:41355973-41356023	HIPEpiC	eye:	n/a
32	chr19:41354142-41354192	HRPEpiC	eye:	n/a
33	chr19:41354682-41354732	AG04450	lung:	fetal
34	chr19:41354682-41354732	HCF	heart:	n/a
35	chr19:41354682-41354732	HUVEC	blood vessel:	n/a
36	chr19:41351924-41351974	NH-A	brain:	n/a
37	chr19:41351924-41351974	MCF-7	breast:	n/a
38	chr19:41354682-41354732	NHBE	bronchial:	n/a
39	chr19:41355973-41356023	BJ	skin:	n/a
40	chr19:41354142-41354192	HRE	kidney:	n/a
41	chr19:41355973-41356023	HepG2	liver:	n/a
42	chr19:41355973-41356023	PrEC	prostate:	n/a
43	chr19:41354142-41354192	LNCaP	prostate:	n/a
44	chr19:41354142-41354192	U87	brain:	n/a
45	chr19:41351924-41351974	Caco-2	colon:	n/a
46	chr19:41351924-41351974	HRPEpiC	eye:	n/a
47	chr19:41355973-41356023	A549	lung:	n/a
48	chr19:41354142-41354192	GM06990	blood:	n/a
49	chr19:41354682-41354732	HMEC	breast:	n/a
50	chr19:41355973-41356023	NHDF-neo	bronchial:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41333069..41334753-chr19:41334934..41336779,2	K562	blood:
2	chr19:41309668..41312632-chr19:41335922..41337729,2	MCF-7	breast:
3	chr19:41333069..41334753-chr19:41334934..41336779,2	K562	blood:
4	chr19:41168873..41171001-chr19:41337568..41339858,2	MCF-7	breast:
5	chr16:4474827..4477394-chr19:41351022..41353007,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2A6-1	chr19:41342991-41343115	ENSG00000269843.1
2	lnc-CYP2A6-1	chr19:41337126-41337482	ENSG00000269843.1

No data

Variant related genes	Relation type
ENSG00000269843	TF binding region
CYP2F2P	TF binding region
CYP2A6	TF binding region
ENSG00000269843	CpG island
CYP2F2P	CpG island
CYP2A6	CpG island
ENSG00000262246	chromatin interactions
ENSG00000269858	chromatin interactions
ENSG00000103423	chromatin interactions

Extended variants
information (count: 1550 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1550 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11878604	chr19:41333284-41333285	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34410235	chr19:41333286-41333287	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs141014591	chr19:41333318-41333319	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541124463	chr19:41333327-41333328	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369618581	chr19:41333395-41333396	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs559945412	chr19:41333405-41333406	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369841557	chr19:41333422-41333423	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150190242	chr19:41333436-41333437	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4803378	chr19:41333441-41333442	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs532437661	chr19:41333443-41333444	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547411751	chr19:41333456-41333457	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565915234	chr19:41333460-41333461	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536988858	chr19:41333524-41333525	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548593495	chr19:41333593-41333594	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545713168	chr19:41333594-41333595	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557094287	chr19:41333607-41333608	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs564357199	chr19:41333615-41333616	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs559160192	chr19:41333625-41333626	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs185403711	chr19:41333681-41333682	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs549787579	chr19:41333682-41333683	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs567957584	chr19:41333715-41333716	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs577034516	chr19:41333718-41333719	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs116921376	chr19:41333726-41333727	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs138738866	chr19:41333741-41333742	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189890137	chr19:41333753-41333754	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs553036538	chr19:41333805-41333806	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs574340337	chr19:41333814-41333815	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs547498083	chr19:41333836-41333837	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs149317932	chr19:41333842-41333843	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs181460083	chr19:41333845-41333846	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs557947673	chr19:41333852-41333853	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs563435857	chr19:41333871-41333872	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs575452747	chr19:41333875-41333876	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs545612811	chr19:41333878-41333879	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs563913917	chr19:41333879-41333880	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs147423621	chr19:41333900-41333901	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs185295507	chr19:41333903-41333904	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs547472475	chr19:41333907-41333908	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs559740149	chr19:41333915-41333916	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs577130492	chr19:41333965-41333966	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs138214136	chr19:41334007-41334008	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570263014	chr19:41334036-41334037	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs544980882	chr19:41334039-41334040	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs552831900	chr19:41334052-41334053	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs571040883	chr19:41334065-41334066	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs534748692	chr19:41334091-41334092	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs578081413	chr19:41334100-41334101	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs189714282	chr19:41334117-41334118	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558813813	chr19:41334136-41334137	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371027026	chr19:41334169-41334170	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41324800-41337400	Weak transcription	Colonic Mucosa	Colon
2	chr19:41324800-41339200	Weak transcription	Brain Germinal Matrix	brain
3	chr19:41325000-41337400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr19:41325600-41337400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr19:41326000-41339800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr19:41328000-41334000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr19:41328800-41337400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr19:41329000-41335400	Weak transcription	Fetal Muscle Leg	muscle
9	chr19:41329200-41334000	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr19:41329200-41335000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr19:41329200-41337200	Weak transcription	A549	lung
12	chr19:41329400-41334200	Weak transcription	Brain Hippocampus Middle	brain
13	chr19:41329800-41334000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr19:41329800-41334200	Enhancers	Primary T cells fromperipheralblood	blood
15	chr19:41330000-41337800	Weak transcription	Colon Smooth Muscle	Colon
16	chr19:41330000-41339800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr19:41330200-41333600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr19:41330200-41335000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr19:41330200-41349400	Weak transcription	Right Ventricle	heart
20	chr19:41330400-41337200	Weak transcription	HepG2	liver
21	chr19:41331000-41334000	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr19:41331000-41334200	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr19:41331000-41335000	Weak transcription	Lung	lung
24	chr19:41331600-41337800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr19:41331600-41339800	Weak transcription	Fetal Lung	lung
26	chr19:41331800-41334400	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr19:41332000-41333400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr19:41332000-41333800	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr19:41332400-41333400	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr19:41332600-41333400	Strong transcription	Primary B cells from cord blood	blood
31	chr19:41332600-41333400	Enhancers	Primary T cells from cord blood	blood
32	chr19:41332600-41333400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr19:41332600-41333400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr19:41332600-41333400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr19:41332600-41333400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr19:41332600-41333400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr19:41332600-41333400	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr19:41332600-41333400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr19:41332600-41333400	Strong transcription	Duodenum Mucosa	Duodenum
40	chr19:41332600-41333400	Strong transcription	Fetal Brain Male	brain
41	chr19:41332600-41333400	Strong transcription	Pancreatic Islets	Pancreatic Islet
42	chr19:41332600-41333400	Strong transcription	Pancreas	Pancrea
43	chr19:41332600-41333400	Strong transcription	HSMM	muscle
44	chr19:41332600-41333600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr19:41332600-41333600	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr19:41332600-41333800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr19:41332600-41334000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr19:41332600-41334000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr19:41332600-41334000	Strong transcription	Aorta	Aorta
50	chr19:41332600-41334000	Strong transcription	Fetal Stomach	stomach

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