Variant report

Variant	esv3332670
Chromosome Location	chr19:40181720-40297955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1492)
CpG islands
(count:1039)
Chromatin interactive
region (count:40)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1492 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40264545-40264659	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40186329-40186749	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40256286-40256392	HepG2	liver:	n/a	n/a
4	ATF2	chr19:40182800-40183815	GM12878	blood:	n/a	n/a
5	ATF2	chr19:40191755-40192297	GM12878	blood:	n/a	n/a
6	ATF2	chr19:40194765-40195855	GM12878	blood:	n/a	n/a
7	ATF2	chr19:40250271-40250873	GM12878	blood:	n/a	n/a
8	ATF2	chr19:40196400-40196987	GM12878	blood:	n/a	n/a
9	ATF2	chr19:40182851-40183369	GM12878	blood:	n/a	n/a
10	ATF2	chr19:40285607-40286082	GM12878	blood:	n/a	n/a
11	ATF2	chr19:40217452-40218159	GM12878	blood:	n/a	n/a
12	ATF2	chr19:40196409-40196856	GM12878	blood:	n/a	n/a
13	ATF2	chr19:40191735-40192471	GM12878	blood:	n/a	n/a
14	ATF2	chr19:40250299-40250937	GM12878	blood:	n/a	n/a
15	ATF3	chr19:40283522-40283995	A549	lung:	n/a	n/a
16	BACH1	chr19:40220520-40220648	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr19:40181595-40181848	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr19:40243844-40243856	K562	blood:	n/a	n/a
19	BACH1	chr19:40293667-40294041	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr19:40256223-40256423	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr19:40243042-40243374	GM12878	blood:	n/a	n/a
22	BATF	chr19:40285717-40285968	GM12878	blood:	n/a	n/a
23	BATF	chr19:40269416-40269699	GM12878	blood:	n/a	n/a
24	BATF	chr19:40250525-40250763	GM12878	blood:	n/a	n/a
25	BATF	chr19:40189256-40189554	GM12878	blood:	n/a	n/a
26	BATF	chr19:40189261-40189535	GM12878	blood:	n/a	n/a
27	BATF	chr19:40269361-40269668	GM12878	blood:	n/a	n/a
28	BATF	chr19:40182871-40183555	GM12878	blood:	n/a	chr19:40183116-40183126
29	BCL11A	chr19:40199281-40199588	GM12878	blood:	n/a	chr19:40199450-40199459
30	BCL11A	chr19:40285720-40285955	GM12878	blood:	n/a	n/a
31	BCL11A	chr19:40250426-40250814	GM12878	blood:	n/a	n/a
32	BCL11A	chr19:40195179-40195439	GM12878	blood:	n/a	n/a
33	BCL3	chr19:40195147-40195808	GM12878	blood:	n/a	n/a
34	BCL3	chr19:40283604-40284194	A549	lung:	n/a	n/a
35	BCL3	chr19:40182720-40183232	GM12878	blood:	n/a	chr19:40183115-40183124 chr19:40183114-40183123
36	BCL3	chr19:40222311-40222662	GM12878	blood:	n/a	n/a
37	BCL3	chr19:40196414-40196839	GM12878	blood:	n/a	chr19:40196768-40196777
38	BCL3	chr19:40222329-40222619	GM12878	blood:	n/a	n/a
39	BCL3	chr19:40182662-40183301	GM12878	blood:	n/a	chr19:40183115-40183124 chr19:40183114-40183123
40	BCL3	chr19:40227965-40228346	GM12878	blood:	n/a	n/a
41	BCL3	chr19:40191856-40192273	GM12878	blood:	n/a	n/a
42	BCLAF1	chr19:40217620-40218132	GM12878	blood:	n/a	n/a
43	BCLAF1	chr19:40191657-40192395	GM12878	blood:	n/a	n/a
44	BCLAF1	chr19:40196448-40196899	GM12878	blood:	n/a	chr19:40196768-40196777
45	BCLAF1	chr19:40199155-40199615	GM12878	blood:	n/a	chr19:40199450-40199459
46	BCLAF1	chr19:40194839-40195814	GM12878	blood:	n/a	n/a
47	BCLAF1	chr19:40283583-40284007	GM12878	blood:	n/a	n/a
48	BCLAF1	chr19:40250441-40250954	GM12878	blood:	n/a	n/a
49	BCLAF1	chr19:40285542-40286061	GM12878	blood:	n/a	n/a
50	BHLHE40	chr19:40196585-40196856	GM12878	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40276380-40276430	HEK293	kidney:	embryo
2	chr19:40267283-40267333	Jurkat	blood:	n/a
3	chr19:40276380-40276430	HEK293	kidney:	embryo
4	chr19:40267283-40267333	Jurkat	blood:	n/a
5	chr19:40229366-40229416	SK-N-MC	brain:	n/a
6	chr19:40195028-40195078	HCT-116	colon:	n/a
7	chr19:40266791-40266841	PANC-1	pancreas:	n/a
8	chr19:40229215-40229265	Caco-2	colon:	n/a
9	chr19:40267283-40267333	NH-A	brain:	n/a
10	chr19:40267283-40267333	HCT-116	colon:	n/a
11	chr19:40269534-40269584	Jurkat	blood:	n/a
12	chr19:40227949-40227999	BJ	skin:	n/a
13	chr19:40195028-40195078	HAEpiC	amniotic membrane:	n/a
14	chr19:40229366-40229416	NT2-D1	testis:	n/a
15	chr19:40266546-40266596	SK-N-SH_RA	brain:	n/a
16	chr19:40195028-40195078	NH-A	brain:	n/a
17	chr19:40229266-40229316	Caco-2	colon:	n/a
18	chr19:40229266-40229316	AG09319	gingival:	n/a
19	chr19:40199676-40199726	RPTEC	kidney:	n/a
20	chr19:40276380-40276430	MCF-7	breast:	n/a
21	chr19:40267103-40267153	MCF-7	breast:	n/a
22	chr19:40266791-40266841	H1-hESC	embryonic stem cell:	embryo
23	chr19:40266546-40266596	HPAEpiC	pulmonary alveolar:	n/a
24	chr19:40267283-40267333	GM12891	blood:	n/a
25	chr19:40199676-40199726	SAEC	small airway:	n/a
26	chr19:40228820-40228870	HL-60	blood:	n/a
27	chr19:40269534-40269584	HEEpiC	esophagus:	n/a
28	chr19:40267283-40267333	BJ	skin:	n/a
29	chr19:40267103-40267153	HCF	heart:	n/a
30	chr19:40266791-40266841	SK-N-SH_RA	brain:	n/a
31	chr19:40267103-40267153	SAEC	small airway:	n/a
32	chr19:40266546-40266596	NH-A	brain:	n/a
33	chr19:40229266-40229316	HRPEpiC	eye:	n/a
34	chr19:40266791-40266841	NHBE	bronchial:	n/a
35	chr19:40195028-40195078	AoSMC	blood vessel:	n/a
36	chr19:40193890-40193940	SKMC	muscle:	n/a
37	chr19:40229215-40229265	ovcar-3	ovarian:	n/a
38	chr19:40266546-40266596	ovcar-3	ovarian:	n/a
39	chr19:40266791-40266841	IMR90	lung:	fetal
40	chr19:40227949-40227999	HCF	heart:	n/a
41	chr19:40229215-40229265	HCT-116	colon:	n/a
42	chr19:40227949-40227999	H1-hESC	embryonic stem cell:	embryo
43	chr19:40267283-40267333	PANC-1	pancreas:	n/a
44	chr19:40229215-40229265	AG04449	skin:	fetal
45	chr19:40229766-40229816	LNCaP	prostate:	n/a
46	chr19:40195028-40195078	BJ	skin:	n/a
47	chr19:40276380-40276430	SAEC	small airway:	n/a
48	chr19:40199676-40199726	HMEC	breast:	n/a
49	chr19:40276380-40276430	PFSK-1	brain:	n/a
50	chr19:40266546-40266596	AG04449	skin:	fetal

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40219606..40222689-chr19:40225665..40231232,5	K562	blood:
2	chr19:40245917..40247942-chr19:40249485..40251835,2	K562	blood:
3	chr19:40256350..40257493-chr19:40334257..40335289,4	MCF-7	breast:
4	chr19:40276822..40278831-chr19:40283845..40285832,2	K562	blood:
5	chr19:40295840..40298272-chr19:40322727..40325020,2	MCF-7	breast:
6	chr19:40294943..40296744-chr19:40337305..40340033,2	MCF-7	breast:
7	chr19:40191402..40192980-chr19:40193546..40196170,2	K562	blood:
8	chr19:40172219..40174410-chr19:40181019..40183380,2	MCF-7	breast:
9	chr19:40288934..40290936-chr19:40322818..40324514,2	K562	blood:
10	chr19:40166260..40168931-chr19:40253973..40255544,2	MCF-7	breast:
11	chr19:40187755..40190590-chr19:40198556..40200389,2	MCF-7	breast:
12	chr19:40283744..40284259-chr19:40332977..40333727,2	K562	blood:
13	chr19:40245917..40247942-chr19:40249485..40251835,2	K562	blood:
14	chr19:40163659..40164641-chr19:40256992..40257878,2	MCF-7	breast:
15	chr19:40264679..40266808-chr19:40276400..40277975,2	K562	blood:
16	chr19:40285675..40287389-chr19:40329469..40332136,2	MCF-7	breast:
17	chr19:40291125..40292741-chr19:40294358..40296178,2	K562	blood:
18	chr19:40264679..40266808-chr19:40276400..40277975,2	K562	blood:
19	chr19:40245917..40248026-chr19:40248937..40251835,4	K562	blood:
20	chr19:40282440..40284866-chr19:40332192..40334772,3	K562	blood:
21	chr19:40041769..40042752-chr19:40257039..40257543,2	K562	blood:
22	chr19:40276822..40278831-chr19:40283845..40285832,2	K562	blood:
23	chr19:40293371..40296306-chr19:40300428..40302557,2	K562	blood:
24	chr19:40285779..40290617-chr19:40292504..40296139,5	K562	blood:
25	chr19:40164188..40165085-chr19:40256246..40256847,2	MCF-7	breast:
26	chr19:40245917..40248026-chr19:40248937..40251835,4	K562	blood:
27	chr19:40255355..40257924-chr19:40332588..40334816,2	MCF-7	breast:
28	chr19:40283040..40287164-chr19:40335990..40338148,3	MCF-7	breast:
29	chr19:40283625..40284290-chr19:40332717..40333386,3	MCF-7	breast:
30	chr19:40245612..40247298-chr19:40255835..40257856,2	MCF-7	breast:
31	chr19:40296262..40298626-chr19:40313380..40316915,4	MCF-7	breast:
32	chr19:40255527..40257517-chr19:40266720..40268234,2	K562	blood:
33	chr19:40283298..40284231-chr19:40334333..40335337,5	MCF-7	breast:
34	chr19:40291125..40292741-chr19:40294358..40296178,2	K562	blood:
35	chr19:40245612..40247298-chr19:40255835..40257856,2	MCF-7	breast:
36	chr19:40285779..40290617-chr19:40292504..40296139,5	K562	blood:
37	chr19:40245446..40248757-chr19:40332343..40336010,3	MCF-7	breast:
38	chr19:40095220..40098051-chr19:40194257..40195861,2	K562	blood:
39	chr19:40283432..40284233-chr19:40334291..40335341,3	MCF-7	breast:
40	chr19:40218825..40222024-chr19:40225949..40228732,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS14-1	chr19:40185104-40185217	ENSG00000226025

No data

Variant related genes	Relation type
ENSG00000268088	TF binding region
LGALS14	TF binding region
LEUTX	TF binding region
CLC	TF binding region
ENSG00000240320	TF binding region
ENSG00000268088	CpG island
LGALS14	CpG island
LEUTX	CpG island
CLC	CpG island
ENSG00000240320	CpG island
ENSG00000240320	chromatin interactions
ENSG00000105202	chromatin interactions
ENSG00000213921	chromatin interactions
ENSG00000105204	chromatin interactions
ENSG00000105205	chromatin interactions
ENSG00000105198	chromatin interactions
ENSG00000006659	chromatin interactions

Extended variants
information (count: 4109 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4109 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550058942	chr19:40181734-40181735	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs571753819	chr19:40181742-40181743	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200428869	chr19:40181780-40181781	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs141923392	chr19:40181782-40181783	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373176690	chr19:40181783-40181784	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs60991573	chr19:40181784-40181785	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs200706338	chr19:40181785-40181786	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs60086280	chr19:40181788-40181789	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs554276208	chr19:40181791-40181792	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs142392325	chr19:40181805-40181806	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs575695766	chr19:40181841-40181842	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs543622581	chr19:40181842-40181843	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs17709242	chr19:40181873-40181874	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs2159169	chr19:40181922-40181923	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs541011356	chr19:40181925-40181926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2159170	chr19:40181926-40181927	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs16973570	chr19:40182115-40182116	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551764609	chr19:40182134-40182135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs16973571	chr19:40182135-40182136	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs78068534	chr19:40182142-40182143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79629795	chr19:40182151-40182152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185974288	chr19:40182154-40182155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145279000	chr19:40182162-40182163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73035636	chr19:40182179-40182180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs151015469	chr19:40182187-40182188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs16973572	chr19:40182193-40182194	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs192123557	chr19:40182207-40182208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575732907	chr19:40182230-40182231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56960663	chr19:40182242-40182243	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184069339	chr19:40182261-40182262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577014045	chr19:40182356-40182357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574721701	chr19:40182401-40182402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374934362	chr19:40182413-40182414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541200885	chr19:40182444-40182445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140804166	chr19:40182446-40182447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574751826	chr19:40182447-40182448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376502674	chr19:40182460-40182461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112418773	chr19:40182482-40182483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368338479	chr19:40182484-40182485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34805230	chr19:40182492-40182493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531721164	chr19:40182544-40182545	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs6508902	chr19:40182595-40182596	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs565356651	chr19:40182640-40182641	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs532629219	chr19:40182641-40182642	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs547549502	chr19:40182679-40182680	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566051734	chr19:40182691-40182692	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs112945061	chr19:40182693-40182694	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs118039923	chr19:40182699-40182700	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs149721567	chr19:40182774-40182775	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs34426444	chr19:40182799-40182800	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Pleomorphic liposarcoma	18784837	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
Disorders of sex development	21048976	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
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40170000-40184600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:40171200-40189000	Weak transcription	Psoas Muscle	Psoas
3	chr19:40181200-40182400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr19:40181400-40182000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr19:40181800-40182000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr19:40182000-40184600	Enhancers	GM12878-XiMat	blood
7	chr19:40182200-40182800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr19:40182200-40183200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr19:40182400-40184000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr19:40182800-40183400	Enhancers	Pancreas	Pancrea
11	chr19:40182800-40184000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr19:40182800-40184600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr19:40183200-40184600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr19:40184400-40188000	Enhancers	HepG2	liver
15	chr19:40184600-40185000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr19:40184600-40185200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr19:40184600-40185200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:40184600-40185200	Enhancers	Placenta	Placenta
19	chr19:40184600-40186400	Weak transcription	GM12878-XiMat	blood
20	chr19:40185200-40186400	Weak transcription	Placenta	Placenta
21	chr19:40186400-40186800	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr19:40186400-40187400	Enhancers	GM12878-XiMat	blood
23	chr19:40186400-40188400	Enhancers	Placenta	Placenta
24	chr19:40186800-40187200	Bivalent Enhancer	A549	lung
25	chr19:40187200-40187600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr19:40187400-40187800	Weak transcription	GM12878-XiMat	blood
27	chr19:40187800-40189000	Enhancers	GM12878-XiMat	blood
28	chr19:40188400-40192800	Weak transcription	Placenta	Placenta
29	chr19:40189000-40189200	Enhancers	Psoas Muscle	Psoas
30	chr19:40189000-40189400	Flanking Active TSS	GM12878-XiMat	blood
31	chr19:40189400-40190000	Enhancers	GM12878-XiMat	blood
32	chr19:40190000-40191000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr19:40190000-40191000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:40190000-40191400	Flanking Active TSS	GM12878-XiMat	blood
35	chr19:40190600-40190800	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr19:40191400-40191600	Active TSS	GM12878-XiMat	blood
37	chr19:40191600-40192800	Flanking Active TSS	GM12878-XiMat	blood
38	chr19:40192400-40193200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr19:40192800-40193400	Enhancers	Placenta	Placenta
40	chr19:40192800-40193800	Enhancers	GM12878-XiMat	blood
41	chr19:40193200-40193400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr19:40193400-40195000	Weak transcription	Placenta	Placenta
43	chr19:40193400-40195600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:40193800-40194000	Flanking Active TSS	GM12878-XiMat	blood
45	chr19:40194000-40194400	Enhancers	GM12878-XiMat	blood
46	chr19:40194400-40198000	Flanking Active TSS	GM12878-XiMat	blood
47	chr19:40195000-40196800	Active TSS	Placenta	Placenta
48	chr19:40195000-40198000	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr19:40195200-40195400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr19:40195200-40195400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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