Variant report

Variant	nsv510766
Chromosome Location	chr19:40344356-40453018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1705)
CpG islands
(count:3176)
Chromatin interactive
region (count:41)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1705 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40372209-40372386	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40388564-40388584	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40449962-40450371	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:40377903-40377918	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:40415611-40415775	HepG2	liver:	n/a	n/a
6	ATF1	chr19:40447904-40447932	K562	blood:	n/a	n/a
7	ATF1	chr19:40372283-40372483	K562	blood:	n/a	n/a
8	ATF2	chr19:40372199-40372449	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr19:40447416-40448147	GM12878	blood:	n/a	n/a
10	ATF2	chr19:40372203-40372491	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr19:40415366-40416097	A549	lung:	n/a	n/a
12	ATF3	chr19:40449763-40450424	A549	lung:	n/a	n/a
13	ATF3	chr19:40415390-40416029	A549	lung:	n/a	n/a
14	BCL11A	chr19:40404210-40404647	GM12878	blood:	n/a	chr19:40404401-40404414
15	BCL11A	chr19:40372229-40372663	GM12878	blood:	n/a	chr19:40372417-40372430
16	BCL11A	chr19:40447638-40448040	GM12878	blood:	n/a	chr19:40447863-40447872
17	BCL3	chr19:40412289-40412518	GM12878	blood:	n/a	n/a
18	BCL3	chr19:40449550-40450626	A549	lung:	n/a	n/a
19	BCL3	chr19:40411970-40412242	GM12878	blood:	n/a	n/a
20	BCL3	chr19:40415371-40416066	A549	lung:	n/a	n/a
21	BCL3	chr19:40414546-40416122	A549	lung:	n/a	n/a
22	BCL3	chr19:40440742-40441792	A549	lung:	n/a	n/a
23	BCL3	chr19:40412323-40412529	GM12878	blood:	n/a	n/a
24	BCL3	chr19:40452447-40452751	GM12878	blood:	n/a	n/a
25	BCL3	chr19:40412032-40412240	GM12878	blood:	n/a	n/a
26	BCLAF1	chr19:40447419-40448094	GM12878	blood:	n/a	chr19:40447863-40447872
27	BHLHE40	chr19:40372341-40372378	HepG2	liver:	n/a	n/a
28	BHLHE40	chr19:40450012-40450239	GM12878	blood:	n/a	n/a
29	BHLHE40	chr19:40372174-40372382	GM12878	blood:	n/a	n/a
30	BHLHE40	chr19:40393689-40394027	HepG2	liver:	n/a	n/a
31	BHLHE40	chr19:40353783-40353941	K562	blood:	n/a	chr19:40353876-40353885 chr19:40353876-40353885 chr19:40353874-40353887 chr19:40353870-40353891 chr19:40353877-40353886
32	BHLHE40	chr19:40372310-40372375	K562	blood:	n/a	n/a
33	BHLHE40	chr19:40378004-40378342	HepG2	liver:	n/a	n/a
34	BHLHE40	chr19:40404194-40404362	GM12878	blood:	n/a	n/a
35	CBX3	chr19:40372094-40372533	K562	blood:	n/a	n/a
36	CBX3	chr19:40404078-40404473	K562	blood:	n/a	n/a
37	CBX3	chr19:40446407-40446710	K562	blood:	n/a	n/a
38	CEBPB	chr19:40443774-40444069	K562	blood:	n/a	n/a
39	CEBPB	chr19:40452409-40452740	K562	blood:	n/a	chr19:40452606-40452617
40	CEBPB	chr19:40443562-40444602	A549	lung:	n/a	n/a
41	CEBPB	chr19:40402641-40402841	A549	lung:	n/a	chr19:40402707-40402718
42	CEBPB	chr19:40452375-40452761	HepG2	liver:	n/a	chr19:40452606-40452617
43	CEBPB	chr19:40415410-40415896	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr19:40402564-40402888	HepG2	liver:	n/a	chr19:40402707-40402718
45	CEBPB	chr19:40354800-40355128	K562	blood:	n/a	n/a
46	CEBPB	chr19:40450036-40450314	HepG2	liver:	n/a	chr19:40450188-40450199
47	CEBPB	chr19:40452432-40452801	K562	blood:	n/a	chr19:40452606-40452617
48	CEBPB	chr19:40415381-40416017	A549	lung:	n/a	n/a
49	CEBPB	chr19:40413769-40413876	A549	lung:	n/a	n/a
50	CEBPB	chr19:40450066-40450346	IMR90	lung:	n/a	chr19:40450188-40450199

(count:3176 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40398384-40398434	HIPEpiC	eye:	n/a
2	chr19:40376883-40376933	HL-60	blood:	n/a
3	chr19:40399454-40399504	H1-hESC	embryonic stem cell:	embryo
4	chr19:40368830-40368880	GM06990	blood:	n/a
5	chr19:40398384-40398434	HIPEpiC	eye:	n/a
6	chr19:40376883-40376933	HL-60	blood:	n/a
7	chr19:40399454-40399504	H1-hESC	embryonic stem cell:	embryo
8	chr19:40368830-40368880	GM06990	blood:	n/a
9	chr19:40396538-40396588	GM12892	blood:	n/a
10	chr19:40399454-40399504	Hela-S3	cervix:	n/a
11	chr19:40380853-40380903	HCPEpiC	choroid plexus:	n/a
12	chr19:40411970-40412020	IMR90	lung:	fetal
13	chr19:40392568-40392618	HAEpiC	amniotic membrane:	n/a
14	chr19:40375973-40376023	BE2_C	brain:	n/a
15	chr19:40375973-40376023	HUVEC	blood vessel:	n/a
16	chr19:40441469-40441519	SK-N-MC	brain:	n/a
17	chr19:40366607-40366657	GM12892	blood:	n/a
18	chr19:40380853-40380903	HAEpiC	amniotic membrane:	n/a
19	chr19:40398384-40398434	ECC-1	luminal epithelium:	n/a
20	chr19:40360856-40360906	HepG2	liver:	n/a
21	chr19:40429988-40430038	HMEC	breast:	n/a
22	chr19:40417583-40417633	NHDF-neo	bronchial:	n/a
23	chr19:40441647-40441697	RPTEC	kidney:	n/a
24	chr19:40421743-40421793	NT2-D1	testis:	n/a
25	chr19:40368830-40368880	ProgFib	skin:	n/a
26	chr19:40377434-40377484	GM19239	blood:	n/a
27	chr19:40440570-40440620	AoSMC	blood vessel:	n/a
28	chr19:40379680-40379730	HCT-116	colon:	n/a
29	chr19:40368363-40368413	BE2_C	brain:	n/a
30	chr19:40380853-40380903	HNPCEpiC	eye:	n/a
31	chr19:40440416-40440466	ProgFib	skin:	n/a
32	chr19:40368830-40368880	MCF10A-Er-Src	breast:	n/a
33	chr19:40421700-40421750	HepG2	liver:	n/a
34	chr19:40392568-40392618	HepG2	liver:	n/a
35	chr19:40422963-40423013	HRCEpiC	kidney:	n/a
36	chr19:40364151-40364201	NT2-D1	testis:	n/a
37	chr19:40441469-40441519	H1-hESC	embryonic stem cell:	embryo
38	chr19:40362773-40362823	IMR90	lung:	fetal
39	chr19:40363285-40363335	IMR90	lung:	fetal
40	chr19:40440416-40440466	HCPEpiC	choroid plexus:	n/a
41	chr19:40417583-40417633	HNPCEpiC	eye:	n/a
42	chr19:40392568-40392618	Jurkat	blood:	n/a
43	chr19:40368363-40368413	GM12892	blood:	n/a
44	chr19:40414986-40415036	HCT-116	colon:	n/a
45	chr19:40375973-40376023	AG10803	skin:	n/a
46	chr19:40440570-40440620	Jurkat	blood:	n/a
47	chr19:40363285-40363335	GM12891	blood:	n/a
48	chr19:40372977-40373027	HCT-116	colon:	n/a
49	chr19:40379680-40379730	HUVEC	blood vessel:	n/a
50	chr19:40368830-40368880	HCF	heart:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40371880..40372846-chr19:40476486..40477439,2	MCF-7	breast:
2	chr19:40343735..40346295-chr19:40347078..40349470,2	MCF-7	breast:
3	chr19:40446423..40448525-chr19:40595370..40597652,2	MCF-7	breast:
4	chr19:40414305..40416214-chr19:40418924..40420802,2	K562	blood:
5	chr19:40430563..40432420-chr19:40476488..40478585,2	K562	blood:
6	chr19:40449986..40451522-chr19:40453683..40455500,2	MCF-7	breast:
7	chr19:40337506..40339114-chr19:40356435..40358897,2	MCF-7	breast:
8	chr19:40424412..40427269-chr19:40428969..40431145,2	K562	blood:
9	chr19:40337126..40339206-chr19:40352976..40355937,2	K562	blood:
10	chr19:40440432..40442359-chr19:40443718..40445248,2	K562	blood:
11	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
12	chr19:40413091..40415843-chr19:40476143..40478695,2	K562	blood:
13	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:
14	chr19:40350892..40352430-chr19:40476216..40478037,2	K562	blood:
15	chr19:40335929..40339892-chr19:40340090..40345342,6	K562	blood:
16	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
17	chr19:40439263..40441192-chr19:40446766..40448427,2	K562	blood:
18	chr19:40345236..40348068-chr19:40350382..40353367,3	K562	blood:
19	chr19:40417302..40418803-chr19:40438310..40440290,2	K562	blood:
20	chr12:53840252..53841772-chr19:40447090..40448611,2	MCF-7	breast:
21	chr19:40445775..40448041-chr19:40449337..40452328,2	MCF-7	breast:
22	chr19:40345236..40348068-chr19:40350382..40353367,3	K562	blood:
23	chr19:40335334..40338693-chr19:40343842..40347781,4	K562	blood:
24	chr19:40438670..40441318-chr19:40451236..40453498,2	MCF-7	breast:
25	chr19:40417302..40418803-chr19:40438310..40440290,2	K562	blood:
26	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:
27	chr19:40338036..40340893-chr19:40348527..40351769,3	MCF-7	breast:
28	chr19:40322768..40325198-chr19:40344061..40345998,2	K562	blood:
29	chr19:40403844..40404724-chr19:40476336..40477181,3	MCF-7	breast:
30	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
31	chr19:40419026..40420915-chr19:40421238..40424178,2	K562	blood:
32	chr19:40424412..40427269-chr19:40428969..40431145,2	K562	blood:
33	chr19:40333922..40335627-chr19:40352940..40355252,2	K562	blood:
34	chr19:40432414..40434132-chr19:40502600..40505156,2	K562	blood:
35	chr19:40419026..40420915-chr19:40421238..40424178,2	K562	blood:
36	chr19:40335567..40338351-chr19:40347856..40350907,4	MCF-7	breast:
37	chr19:40441756..40443271-chr19:40480700..40482309,2	K562	blood:
38	chr19:40340776..40343743-chr19:40345587..40347160,2	K562	blood:
39	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
40	chr19:40343735..40346295-chr19:40347078..40349470,2	MCF-7	breast:
41	chr19:40414305..40416214-chr19:40418924..40420802,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FCGBP-1	chr19:40448563-40449473	NONHSAT066326
2	lnc-FCGBP-1	chr19:40449146-40449587	NONHSAT066327
3	lnc-FCGBP-1	chr19:40449570-40449634	NONHSAT066326

No data

Variant related genes	Relation type
FCGBP	TF binding region
ENSG00000187534	TF binding region
FCGBP	CpG island
ENSG00000187534	CpG island
ENSG00000105202	chromatin interactions
ENSG00000090920	chromatin interactions
ENSG00000105204	chromatin interactions
ENSG00000197782	chromatin interactions
ENSG00000187534	chromatin interactions
ENSG00000269296	chromatin interactions
ENSG00000269749	chromatin interactions
ENSG00000013275	chromatin interactions
ENSG00000187187	chromatin interactions

Extended variants
information (count: 4643 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4643 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112728066	chr19:40344366-40344367	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs181794370	chr19:40344382-40344383	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs574116229	chr19:40344422-40344423	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs186298347	chr19:40344431-40344432	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs55651210	chr19:40344503-40344504	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs577573922	chr19:40344514-40344515	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs545436190	chr19:40344519-40344520	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557633434	chr19:40344537-40344538	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545009013	chr19:40344567-40344568	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs200555826	chr19:40344576-40344577	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557809279	chr19:40344583-40344584	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs80323226	chr19:40344605-40344606	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs572159317	chr19:40344614-40344615	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs12609590	chr19:40344648-40344649	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs35172262	chr19:40344657-40344658	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs189602975	chr19:40344664-40344665	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs141247387	chr19:40344708-40344709	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs150780960	chr19:40344805-40344806	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs34398724	chr19:40344920-40344921	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs376579771	chr19:40344941-40344942	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541743520	chr19:40344969-40344970	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs533201391	chr19:40345006-40345007	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs551340347	chr19:40345067-40345068	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200300488	chr19:40345077-40345078	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs566658895	chr19:40345087-40345088	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs560128230	chr19:40345108-40345109	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs114182757	chr19:40345150-40345151	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs111327504	chr19:40345153-40345154	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs201253552	chr19:40345173-40345174	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs199792997	chr19:40345175-40345176	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs398101214	chr19:40345181-40345182	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs116982106	chr19:40345223-40345224	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs538011963	chr19:40345227-40345228	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201427285	chr19:40345271-40345272	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs113178501	chr19:40345295-40345296	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562431602	chr19:40345297-40345298	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs375360089	chr19:40345298-40345299	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs180844712	chr19:40345324-40345325	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs60487236	chr19:40345355-40345356	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs12986085	chr19:40345365-40345366	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs185246824	chr19:40345367-40345368	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs190803593	chr19:40345368-40345369	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs60370012	chr19:40345408-40345409	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs370370082	chr19:40345419-40345420	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs375379225	chr19:40345424-40345425	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs538675093	chr19:40345432-40345433	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs139074486	chr19:40345473-40345474	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183402899	chr19:40345493-40345494	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs530876150	chr19:40345519-40345520	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542749287	chr19:40345572-40345573	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21390271	CNVD

Chromatin state (count:1059 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40348600-40348800	Enhancers	Primary T cells from cord blood	blood
2	chr19:40348600-40348800	Enhancers	Dnd41	blood
3	chr19:40348800-40349000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr19:40348800-40349200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr19:40348800-40349200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr19:40348800-40349200	Flanking Active TSS	Primary T cells from cord blood	blood
7	chr19:40348800-40349800	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr19:40348800-40349800	Flanking Active TSS	Dnd41	blood
9	chr19:40348800-40349800	Active TSS	K562	blood
10	chr19:40349000-40349200	Active TSS	Brain Angular Gyrus	brain
11	chr19:40349000-40349400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr19:40349000-40349400	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
13	chr19:40349000-40349400	Active TSS	Right Atrium	heart
14	chr19:40349000-40349800	Active TSS	H9 Cell Line	embryonic stem cell
15	chr19:40349000-40349800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
16	chr19:40349000-40349800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr19:40349000-40349800	Active TSS	Brain Anterior Caudate	brain
18	chr19:40349200-40349400	Flanking Active TSS	Brain Angular Gyrus	brain
19	chr19:40349200-40349400	Active TSS	Colonic Mucosa	Colon
20	chr19:40349200-40349400	Enhancers	Placenta	Placenta
21	chr19:40349200-40349800	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr19:40349200-40349800	Enhancers	Primary T cells from cord blood	blood
23	chr19:40349400-40349800	Active TSS	Primary T cells fromperipheralblood	blood
24	chr19:40349400-40350000	Weak transcription	Placenta	Placenta
25	chr19:40349400-40354400	Weak transcription	Colonic Mucosa	Colon
26	chr19:40349800-40350400	Enhancers	Dnd41	blood
27	chr19:40349800-40353600	Weak transcription	Primary T cells from cord blood	blood
28	chr19:40349800-40356000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr19:40349800-40357400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr19:40349800-40369000	Weak transcription	Brain Anterior Caudate	brain
31	chr19:40350000-40350600	Enhancers	Placenta	Placenta
32	chr19:40350200-40353400	Weak transcription	Fetal Intestine Small	intestine
33	chr19:40350400-40372200	Weak transcription	Dnd41	blood
34	chr19:40350600-40365200	Weak transcription	Placenta	Placenta
35	chr19:40350800-40351000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
36	chr19:40350800-40353400	Weak transcription	Fetal Stomach	stomach
37	chr19:40351000-40361000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr19:40351200-40353600	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr19:40351400-40353400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr19:40351600-40353400	Weak transcription	Stomach Mucosa	stomach
41	chr19:40351600-40353800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr19:40351600-40357200	Weak transcription	Primary B cells from cord blood	blood
43	chr19:40352000-40357000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr19:40352000-40357200	Weak transcription	Fetal Muscle Leg	muscle
45	chr19:40352000-40363200	Weak transcription	Duodenum Mucosa	Duodenum
46	chr19:40352000-40364200	Weak transcription	Fetal Muscle Trunk	muscle
47	chr19:40352000-40372600	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr19:40352200-40356400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr19:40352400-40372400	Weak transcription	Fetal Intestine Large	intestine
50	chr19:40352600-40364000	Weak transcription	Rectal Smooth Muscle	rectum

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