Variant report

Variant	nsv828551
Chromosome Location	chr19:41903176-41903656
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:546)
CpG islands
(count:430)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41903298-41903723	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41903379-41903850	K562	blood:	n/a	n/a
3	ATF2	chr19:41903381-41903829	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr19:41903355-41903781	GM12878	blood:	n/a	n/a
5	ATF2	chr19:41902883-41903769	GM12878	blood:	n/a	n/a
6	ATF3	chr19:41902883-41904008	A549	lung:	n/a	chr19:41903279-41903288
7	ATF3	chr19:41903095-41903454	K562	blood:	n/a	chr19:41903279-41903288
8	ATF3	chr19:41902767-41903959	A549	lung:	n/a	chr19:41903279-41903288
9	BCL3	chr19:41902714-41904265	A549	lung:	n/a	chr19:41903264-41903273 chr19:41903275-41903288
10	BCL3	chr19:41902776-41904253	A549	lung:	n/a	chr19:41903264-41903273 chr19:41903275-41903288
11	BHLHE40	chr19:41902885-41903710	A549	lung:	n/a	n/a
12	BHLHE40	chr19:41903053-41903518	HepG2	liver:	n/a	n/a
13	BHLHE40	chr19:41902970-41903850	K562	blood:	n/a	n/a
14	BHLHE40	chr19:41902941-41903937	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:41902924-41903818	HepG2	liver:	n/a	n/a
16	BRCA1	chr19:41903102-41903228	GM12878	blood:	n/a	n/a
17	BRCA1	chr19:41903479-41903773	HepG2	liver:	n/a	n/a
18	CBX3	chr19:41902988-41903869	K562	blood:	n/a	n/a
19	CCNT2	chr19:41903056-41903497	K562	blood:	n/a	n/a
20	CEBPB	chr19:41903129-41903688	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr19:41902958-41903777	K562	blood:	n/a	n/a
22	CEBPB	chr19:41903168-41903487	HepG2	liver:	n/a	n/a
23	CEBPB	chr19:41902990-41903791	A549	lung:	n/a	n/a
24	CEBPB	chr19:41903175-41903860	K562	blood:	n/a	n/a
25	CEBPB	chr19:41903154-41903842	IMR90	lung:	n/a	n/a
26	CEBPD	chr19:41903591-41903899	HepG2	liver:	n/a	n/a
27	CHD1	chr19:41903046-41904503	GM12878	blood:	n/a	n/a
28	CHD2	chr19:41903039-41903809	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr19:41903251-41903972	HepG2	liver:	n/a	n/a
30	CHD2	chr19:41903140-41903789	K562	blood:	n/a	n/a
31	CHD2	chr19:41902942-41903958	GM12878	blood:	n/a	n/a
32	CREB1	chr19:41902868-41903906	A549	lung:	n/a	n/a
33	CREB1	chr19:41903123-41903895	A549	lung:	n/a	n/a
34	CREB1	chr19:41902919-41903941	GM12878	blood:	n/a	n/a
35	CREB1	chr19:41902925-41903983	HepG2	liver:	n/a	n/a
36	CREB1	chr19:41902995-41903940	HepG2	liver:	n/a	n/a
37	CREB1	chr19:41903056-41903929	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr19:41903120-41903270	HAc	cerebellar:	n/a	n/a
39	CTCF	chr19:41903080-41903230	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr19:41903060-41903210	GM12867	blood:	n/a	n/a
41	CTCF	chr19:41903306-41903319	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr19:41903640-41903790	Caco-2	colon:	n/a	n/a
43	CTCF	chr19:41903520-41903670	SAEC	small airway:	n/a	n/a
44	CTCF	chr19:41903220-41903370	HEK293	kidney:	n/a	n/a
45	CTCF	chr19:41903140-41903290	BJ	skin:	n/a	n/a
46	CTCF	chr19:41903080-41903230	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr19:41903640-41903783	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr19:41903519-41903696	K562	blood:	n/a	n/a
49	CTCF	chr19:41903201-41903362	GM12878	blood:	n/a	n/a
50	CTCF	chr19:41903160-41903310	AG04449	skin:	n/a	n/a

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41903350-41903400	HIPEpiC	eye:	n/a
2	chr19:41903236-41903286	H1-hESC	embryonic stem cell:	embryo
3	chr19:41903236-41903286	HL-60	blood:	n/a
4	chr19:41903350-41903400	HIPEpiC	eye:	n/a
5	chr19:41903236-41903286	H1-hESC	embryonic stem cell:	embryo
6	chr19:41903236-41903286	HL-60	blood:	n/a
7	chr19:41903350-41903400	HEK293	kidney:	embryo
8	chr19:41903199-41903249	HNPCEpiC	eye:	n/a
9	chr19:41903350-41903400	MCF-7	breast:	n/a
10	chr19:41903199-41903249	HL-60	blood:	n/a
11	chr19:41903199-41903249	K562	blood:	n/a
12	chr19:41903199-41903249	ovcar-3	ovarian:	n/a
13	chr19:41903169-41903219	Jurkat	blood:	n/a
14	chr19:41903546-41903596	HCF	heart:	n/a
15	chr19:41903199-41903249	BE2_C	brain:	n/a
16	chr19:41903350-41903400	HAEpiC	amniotic membrane:	n/a
17	chr19:41903234-41903284	SK-N-SH_RA	brain:	n/a
18	chr19:41903455-41903505	A549	lung:	n/a
19	chr19:41903199-41903249	Hela-S3	cervix:	n/a
20	chr19:41903199-41903249	NHDF-neo	bronchial:	n/a
21	chr19:41903455-41903505	HCF	heart:	n/a
22	chr19:41903234-41903284	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:41903169-41903219	MCF10A-Er-Src	breast:	n/a
24	chr19:41903199-41903249	HCF	heart:	n/a
25	chr19:41903350-41903400	H1-hESC	embryonic stem cell:	embryo
26	chr19:41903350-41903400	BJ	skin:	n/a
27	chr19:41903169-41903219	CMK	blood:	n/a
28	chr19:41903234-41903284	Jurkat	blood:	n/a
29	chr19:41903350-41903400	SKMC	muscle:	n/a
30	chr19:41903234-41903284	HL-60	blood:	n/a
31	chr19:41903199-41903249	GM12891	blood:	n/a
32	chr19:41903236-41903286	SK-N-SH_RA	brain:	n/a
33	chr19:41903350-41903400	GM12878	blood:	n/a
34	chr19:41903169-41903219	BE2_C	brain:	n/a
35	chr19:41903234-41903284	NT2-D1	testis:	n/a
36	chr19:41903546-41903596	ovcar-3	ovarian:	n/a
37	chr19:41903455-41903505	T-47D	breast:	n/a
38	chr19:41903236-41903286	NT2-D1	testis:	n/a
39	chr19:41903169-41903219	GM12892	blood:	n/a
40	chr19:41903350-41903400	HCM	heart:	n/a
41	chr19:41903236-41903286	NB4	blood:	n/a
42	chr19:41903546-41903596	SK-N-MC	brain:	n/a
43	chr19:41903350-41903400	AoSMC	blood vessel:	n/a
44	chr19:41903236-41903286	IMR90	lung:	fetal
45	chr19:41903236-41903286	BE2_C	brain:	n/a
46	chr19:41903234-41903284	BE2_C	brain:	n/a
47	chr19:41903236-41903286	HUVEC	blood vessel:	n/a
48	chr19:41903455-41903505	GM12891	blood:	n/a
49	chr19:41903234-41903284	Caco-2	colon:	n/a
50	chr19:41903546-41903596	AG09309	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41855237..41861298-chr19:41901562..41905286,5	K562	blood:
2	chr19:41902654..41904815-chr19:41927221..41929015,2	K562	blood:
3	chr19:41899828..41905293-chr19:41906916..41917787,16	MCF-7	breast:
4	chr19:41815990..41817853-chr19:41901729..41903326,2	K562	blood:
5	chr19:41868161..41871707-chr19:41902716..41905358,4	MCF-7	breast:
6	chr19:41902636..41905103-chr19:41930716..41934044,4	MCF-7	breast:
7	chr19:41903201..41905318-chr19:41918567..41921516,2	MCF-7	breast:
8	chr19:41901991..41905119-chr19:41933008..41936084,3	MCF-7	breast:
9	chr19:41856174..41858570-chr19:41902142..41904818,3	MCF-7	breast:
10	chr19:41767651..41769904-chr19:41902855..41905283,2	K562	blood:
11	chr19:41856329..41860180-chr19:41901826..41904297,4	K562	blood:
12	chr19:41903342..41904945-chr19:41934241..41936024,2	MCF-7	breast:
13	chr19:41868160..41870059-chr19:41902135..41903854,4	K562	blood:
14	chr19:41868160..41871597-chr19:41899998..41904284,10	K562	blood:
15	chr19:41855447..41861218-chr19:41901143..41905435,7	MCF-7	breast:
16	chr19:41903473..41906087-chr19:41945278..41947256,2	MCF-7	breast:
17	chr19:41901938..41905441-chr19:41944047..41947443,5	K562	blood:

No data

Variant related genes	Relation type
EXOSC5	TF binding region
ENSG00000268987	TF binding region
BCKDHA	TF binding region
EXOSC5	CpG island
ENSG00000268987	CpG island
BCKDHA	CpG island
ENSG00000123810	chromatin interactions
ENSG00000142046	chromatin interactions
ENSG00000255730	chromatin interactions
ENSG00000105323	chromatin interactions
ENSG00000105329	chromatin interactions
ENSG00000177191	chromatin interactions
ENSG00000268475	chromatin interactions
ENSG00000105341	chromatin interactions
ENSG00000142039	chromatin interactions
ENSG00000248098	chromatin interactions

Extended variants
information (count: 35 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75733136	chr19:41903177-41903178	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
2	rs538950148	chr19:41903179-41903180	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs147526684	chr19:41903199-41903200	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs547685483	chr19:41903210-41903211	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs376304827	chr19:41903214-41903215	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs139413206	chr19:41903218-41903219	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs10853751	chr19:41903220-41903221	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs145189417	chr19:41903222-41903223	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs200113563	chr19:41903226-41903227	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs576501387	chr19:41903255-41903256	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs112381655	chr19:41903261-41903262	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs369844444	chr19:41903272-41903273	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs141003824	chr19:41903290-41903291	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs577063014	chr19:41903309-41903310	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs541383622	chr19:41903320-41903321	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs111259136	chr19:41903342-41903343	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs574382037	chr19:41903354-41903355	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs545965404	chr19:41903386-41903387	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs188181303	chr19:41903397-41903398	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs12983789	chr19:41903421-41903422	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs530530492	chr19:41903439-41903440	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs201629762	chr19:41903467-41903468	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs576345541	chr19:41903469-41903470	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs545446463	chr19:41903470-41903471	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs565185072	chr19:41903476-41903477	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs532560988	chr19:41903519-41903520	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs531902668	chr19:41903527-41903528	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs367599467	chr19:41903533-41903534	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs114191970	chr19:41903540-41903541	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs191758599	chr19:41903559-41903560	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs562117355	chr19:41903561-41903562	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs386809358	chr19:41903572-41903573	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs530303012	chr19:41903574-41903575	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs77558911	chr19:41903582-41903583	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
35	rs553808220	chr19:41903633-41903634	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	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
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	21987784	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41901400-41903200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr19:41901600-41903200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
3	chr19:41901600-41904000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:41901600-41904200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr19:41901800-41903200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
6	chr19:41901800-41904400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr19:41902000-41904400	Active TSS	Hela-S3	cervix
8	chr19:41902000-41904600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr19:41902200-41904400	Active TSS	H1 Cell Line	embryonic stem cell
10	chr19:41902200-41904400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr19:41902200-41904400	Active TSS	HSMM	muscle
12	chr19:41902200-41904600	Active TSS	Pancreas	Pancrea
13	chr19:41902200-41904600	Active TSS	GM12878-XiMat	blood
14	chr19:41902200-41904600	Active TSS	K562	blood
15	chr19:41902200-41905200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr19:41902400-41903200	Flanking Active TSS	Primary B cells from cord blood	blood
17	chr19:41902400-41903200	Flanking Active TSS	Primary B cells from peripheral blood	blood
18	chr19:41902400-41903200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
19	chr19:41902400-41903200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr19:41902400-41903200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
21	chr19:41902400-41903200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr19:41902400-41903200	Flanking Active TSS	Liver	Liver
23	chr19:41902400-41903200	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr19:41902400-41903200	Flanking Active TSS	Fetal Muscle Leg	muscle
25	chr19:41902400-41903200	Flanking Active TSS	Fetal Thymus	thymus
26	chr19:41902400-41903200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
27	chr19:41902400-41903200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr19:41902400-41903200	Flanking Active TSS	Stomach Smooth Muscle	stomach
29	chr19:41902400-41903200	Flanking Active TSS	NH-A	brain
30	chr19:41902400-41903800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr19:41902400-41904200	Active TSS	Placenta Amnion	Placenta Amnion
32	chr19:41902400-41904400	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr19:41902400-41904400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr19:41902400-41904400	Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr19:41902400-41904400	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr19:41902400-41904400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr19:41902400-41904400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr19:41902400-41904400	Active TSS	Brain Cingulate Gyrus	brain
39	chr19:41902400-41904400	Active TSS	Brain Germinal Matrix	brain
40	chr19:41902400-41904400	Active TSS	Colonic Mucosa	Colon
41	chr19:41902400-41904400	Active TSS	Fetal Intestine Small	intestine
42	chr19:41902400-41904400	Active TSS	Fetal Kidney	kidney
43	chr19:41902400-41904400	Active TSS	Right Ventricle	heart
44	chr19:41902400-41904600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr19:41902400-41904600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
46	chr19:41902400-41904600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr19:41902400-41904600	Active TSS	Fetal Intestine Large	intestine
48	chr19:41902400-41904600	Active TSS	Psoas Muscle	Psoas
49	chr19:41902400-41904800	Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr19:41902400-41905000	Active TSS	HUES48 Cell Line	embryonic stem cell

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