Variant report

Variant	esv1803455
Chromosome Location	chr19:42768288-42788467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2482)
CpG islands
(count:1527)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2482 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:42784070-42784254	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:42772016-42773501	K562	blood:	n/a	n/a
3	ARID3A	chr19:42784604-42784632	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:42786054-42786370	K562	blood:	n/a	n/a
5	ARID3A	chr19:42772131-42772978	HepG2	liver:	n/a	n/a
6	ATF1	chr19:42771939-42773502	K562	blood:	n/a	n/a
7	ATF2	chr19:42787227-42787993	GM12878	blood:	n/a	n/a
8	ATF2	chr19:42771955-42773447	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr19:42784275-42784981	GM12878	blood:	n/a	n/a
10	ATF2	chr19:42771881-42773338	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr19:42787616-42787880	GM12878	blood:	n/a	n/a
12	ATF2	chr19:42772114-42773441	GM12878	blood:	n/a	n/a
13	ATF2	chr19:42784566-42784826	GM12878	blood:	n/a	n/a
14	ATF2	chr19:42774483-42775137	GM12878	blood:	n/a	n/a
15	ATF2	chr19:42772120-42773434	GM12878	blood:	n/a	n/a
16	ATF3	chr19:42783631-42784898	A549	lung:	n/a	chr19:42784295-42784304 chr19:42784547-42784556 chr19:42784588-42784597
17	ATF3	chr19:42783958-42784261	HepG2	liver:	n/a	n/a
18	ATF3	chr19:42787085-42787951	A549	lung:	n/a	n/a
19	ATF3	chr19:42772414-42773029	K562	blood:	n/a	chr19:42772602-42772615 chr19:42772828-42772836
20	ATF3	chr19:42771594-42773486	A549	lung:	n/a	chr19:42772602-42772615 chr19:42773461-42773470 chr19:42773235-42773244 chr19:42772828-42772836
21	ATF3	chr19:42783212-42785007	A549	lung:	n/a	chr19:42784295-42784304 chr19:42784977-42784986 chr19:42784547-42784556 chr19:42784588-42784597
22	ATF3	chr19:42784032-42784209	GM12878	blood:	n/a	n/a
23	ATF3	chr19:42771750-42773329	A549	lung:	n/a	chr19:42772602-42772615 chr19:42773235-42773244 chr19:42772828-42772836
24	ATF3	chr19:42772107-42772785	K562	blood:	n/a	chr19:42772602-42772615
25	ATF3	chr19:42788430-42788681	K562	blood:	n/a	n/a
26	ATF3	chr19:42785927-42786339	K562	blood:	n/a	n/a
27	ATF3	chr19:42783929-42784266	K562	blood:	n/a	n/a
28	ATF3	chr19:42786028-42786205	K562	blood:	n/a	n/a
29	ATF3	chr19:42783903-42784198	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr19:42772240-42772440	K562	blood:	n/a	n/a
31	BACH1	chr19:42772085-42772578	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr19:42787212-42787922	K562	blood:	n/a	n/a
33	BACH1	chr19:42785614-42785782	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr19:42784616-42784957	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr19:42786016-42786341	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr19:42787588-42788270	H1-hESC	embryonic stem cell:	n/a	n/a
37	BATF	chr19:42781008-42781295	GM12878	blood:	n/a	chr19:42781138-42781149
38	BATF	chr19:42774513-42775041	GM12878	blood:	n/a	n/a
39	BATF	chr19:42772347-42772644	GM12878	blood:	n/a	n/a
40	BCL11A	chr19:42772351-42772700	GM12878	blood:	n/a	n/a
41	BCL3	chr19:42774326-42775876	A549	lung:	n/a	chr19:42774782-42774795
42	BCL3	chr19:42771554-42773882	A549	lung:	n/a	chr19:42773504-42773513 chr19:42773235-42773248
43	BCL3	chr19:42783261-42788037	A549	lung:	n/a	chr19:42784292-42784305 chr19:42784099-42784112 chr19:42785738-42785746 chr19:42785147-42785160 chr19:42784294-42784303 chr19:42784104-42784113 chr19:42784556-42784569
44	BCL3	chr19:42771589-42773592	A549	lung:	n/a	chr19:42773504-42773513 chr19:42773235-42773248
45	BCL3	chr19:42787345-42788075	A549	lung:	n/a	n/a
46	BCL3	chr19:42783697-42784878	GM12878	blood:	n/a	chr19:42784292-42784305 chr19:42784099-42784112 chr19:42784294-42784303 chr19:42784104-42784113 chr19:42784556-42784569
47	BCL3	chr19:42783678-42785108	A549	lung:	n/a	chr19:42784292-42784305 chr19:42784099-42784112 chr19:42784294-42784303 chr19:42784104-42784113 chr19:42784556-42784569
48	BCLAF1	chr19:42772340-42773076	GM12878	blood:	n/a	n/a
49	BCLAF1	chr19:42774425-42775029	GM12878	blood:	n/a	chr19:42774782-42774795
50	BCLAF1	chr19:42783813-42785017	GM12878	blood:	n/a	chr19:42784292-42784305 chr19:42784099-42784112 chr19:42784294-42784303 chr19:42784104-42784113 chr19:42784556-42784569

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42788257-42788307	SKMC	muscle:	n/a
2	chr19:42785225-42785275	SK-N-MC	brain:	n/a
3	chr19:42788257-42788307	SKMC	muscle:	n/a
4	chr19:42785225-42785275	SK-N-MC	brain:	n/a
5	chr19:42782524-42782574	SKMC	muscle:	n/a
6	chr19:42788248-42788298	ovcar-3	ovarian:	n/a
7	chr19:42774803-42774853	AG10803	skin:	n/a
8	chr19:42772233-42772283	HRCEpiC	kidney:	n/a
9	chr19:42785225-42785275	AG04449	skin:	fetal
10	chr19:42785225-42785275	MCF10A-Er-Src	breast:	n/a
11	chr19:42777626-42777676	CMK	blood:	n/a
12	chr19:42773364-42773414	LNCaP	prostate:	n/a
13	chr19:42787762-42787812	AG10803	skin:	n/a
14	chr19:42777956-42778006	IMR90	lung:	fetal
15	chr19:42768724-42768774	HL-60	blood:	n/a
16	chr19:42768724-42768774	GM12892	blood:	n/a
17	chr19:42772446-42772496	HCM	heart:	n/a
18	chr19:42782524-42782574	PrEC	prostate:	n/a
19	chr19:42772831-42772881	PANC-1	pancreas:	n/a
20	chr19:42788248-42788298	SK-N-SH_RA	brain:	n/a
21	chr19:42777927-42777977	GM12891	blood:	n/a
22	chr19:42768724-42768774	HRE	kidney:	n/a
23	chr19:42787762-42787812	HCT-116	colon:	n/a
24	chr19:42776879-42776929	SKMC	muscle:	n/a
25	chr19:42785474-42785524	MCF-7	breast:	n/a
26	chr19:42777626-42777676	HRPEpiC	eye:	n/a
27	chr19:42785225-42785275	SKMC	muscle:	n/a
28	chr19:42777927-42777977	NT2-D1	testis:	n/a
29	chr19:42787762-42787812	GM12892	blood:	n/a
30	chr19:42784593-42784643	SAEC	small airway:	n/a
31	chr19:42787762-42787812	HCF	heart:	n/a
32	chr19:42785474-42785524	HUVEC	blood vessel:	n/a
33	chr19:42781334-42781384	GM19239	blood:	n/a
34	chr19:42777956-42778006	NB4	blood:	n/a
35	chr19:42776879-42776929	U87	brain:	n/a
36	chr19:42787762-42787812	HEK293	kidney:	embryo
37	chr19:42776879-42776929	AG04450	lung:	fetal
38	chr19:42785225-42785275	HCF	heart:	n/a
39	chr19:42772892-42772942	SAEC	small airway:	n/a
40	chr19:42788257-42788307	NHBE	bronchial:	n/a
41	chr19:42773364-42773414	K562	blood:	n/a
42	chr19:42777927-42777977	ProgFib	skin:	n/a
43	chr19:42774803-42774853	A549	lung:	n/a
44	chr19:42772831-42772881	HCM	heart:	n/a
45	chr19:42772446-42772496	GM19239	blood:	n/a
46	chr19:42785474-42785524	AoSMC	blood vessel:	n/a
47	chr19:42784593-42784643	U87	brain:	n/a
48	chr19:42772446-42772496	GM12891	blood:	n/a
49	chr19:42788257-42788307	GM12891	blood:	n/a
50	chr19:42772446-42772496	GM06990	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:42786293..42789026-chr19:42903312..42906811,3	MCF-7	breast:
2	chr19:42578746..42580250-chr19:42784655..42786734,2	K562	blood:
3	chr19:42783298..42787362-chr19:42802681..42808039,8	MCF-7	breast:
4	chr19:42720002..42723178-chr19:42782377..42785942,3	MCF-7	breast:
5	chr19:42747132..42763787-chr19:42768368..42776785,67	MCF-7	breast:
6	chr19:42598699..42600761-chr19:42786357..42787884,2	K562	blood:
7	chr19:42786948..42794333-chr19:42803465..42809501,23	K562	blood:
8	chr15:90808838..90809345-chr19:42785251..42785922,2	Hela-S3	cervix:
9	chr19:42579405..42581484-chr19:42787067..42789919,2	K562	blood:
10	chr19:42753011..42753994-chr19:42784711..42785693,2	K562	blood:
11	chr19:42774007..42775893-chr19:42829806..42832465,2	K562	blood:
12	chr19:42773801..42775756-chr19:42804416..42807088,2	K562	blood:
13	chr19:42788053..42790658-chr19:42828603..42831088,2	MCF-7	breast:
14	chr19:42637330..42637861-chr19:42783717..42784569,2	MCF-7	breast:
15	chr19:42720638..42724432-chr19:42771891..42775014,4	MCF-7	breast:
16	chr19:42787763..42791073-chr19:42804241..42808628,6	MCF-7	breast:
17	chr19:42771398..42774307-chr19:42804493..42807877,4	MCF-7	breast:
18	chr19:42768481..42770570-chr19:42770967..42773649,2	K562	blood:
19	chr19:42743599..42762610-chr19:42780302..42801550,102	MCF-7	breast:
20	chr19:42788208..42790691-chr19:42829217..42832174,3	K562	blood:
21	chr19:42785454..42788191-chr19:42828272..42829778,2	K562	blood:
22	chr19:42771105..42773106-chr19:42805155..42808634,5	K562	blood:
23	chr19:42783597..42784516-chr4:169552208..169552881,2	HCT-116	colon:
24	chr19:42597900..42600761-chr19:42786384..42788492,2	K562	blood:
25	chr19:42750067..42750945-chr19:42783006..42783636,2	K562	blood:
26	chr12:120729494..120731830-chr19:42774117..42775700,2	MCF-7	breast:
27	chr19:42786310..42789274-chr8:144099903..144101921,2	MCF-7	breast:
28	chr19:42784279..42785802-chr19:42816583..42819051,2	MCF-7	breast:
29	chr19:42775700..42778314-chr19:42814238..42816528,2	K562	blood:
30	chr19:42764600..42766454-chr19:42770815..42772327,3	MCF-7	breast:
31	chr19:42784464..42785059-chr19:42806215..42807066,2	HCT-116	colon:
32	chr19:42744297..42761073-chr19:42776978..42802286,113	MCF-7	breast:
33	chr19:42785237..42787439-chr19:42898347..42900741,2	K562	blood:
34	chr12:49524528..49525157-chr19:42787936..42788663,3	Hela-S3	cervix:
35	chr19:42785607..42786328-chr6:138149604..138150291,2	MCF-7	breast:
36	chr19:42719792..42722067-chr19:42782556..42784868,3	MCF-7	breast:
37	chr19:42784111..42786546-chr19:42805337..42807099,2	K562	blood:

No data

Variant related genes	Relation type
CIC	TF binding region
CIC	CpG island
ENSG00000105429	chromatin interactions
ENSG00000160570	chromatin interactions
ENSG00000105732	chromatin interactions
ENSG00000129116	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000268643	chromatin interactions
ENSG00000167625	chromatin interactions
ENSG00000167619	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000079432	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000188368	chromatin interactions
ENSG00000079462	chromatin interactions
ENSG00000160932	chromatin interactions
ENSG00000182768	chromatin interactions
ENSG00000266226	chromatin interactions
ENSG00000105722	chromatin interactions
ENSG00000105723	chromatin interactions
ENSG00000213904	chromatin interactions
ENSG00000028277	chromatin interactions
ENSG00000204957	chromatin interactions

Extended variants
information (count: 602 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:602 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34081629	chr19:42768288-42768289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559083563	chr19:42768289-42768290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528809820	chr19:42768291-42768292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184692900	chr19:42768323-42768324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375269539	chr19:42768335-42768336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145255764	chr19:42768397-42768398	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs542475270	chr19:42768453-42768454	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554347584	chr19:42768500-42768501	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs115957604	chr19:42768514-42768515	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs543536960	chr19:42768515-42768516	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs55678000	chr19:42768573-42768574	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs55973631	chr19:42768588-42768589	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs564807156	chr19:42768598-42768599	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557432901	chr19:42768614-42768615	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs369091312	chr19:42768701-42768702	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541041061	chr19:42768743-42768744	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs111816360	chr19:42768754-42768755	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs117359636	chr19:42768770-42768771	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs559293181	chr19:42768793-42768794	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs529443055	chr19:42768796-42768797	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs189360457	chr19:42768885-42768886	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs76406904	chr19:42768891-42768892	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs111523289	chr19:42768919-42768920	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs531799489	chr19:42768923-42768924	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs548585337	chr19:42768924-42768925	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs372902670	chr19:42768974-42768975	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs568016936	chr19:42768975-42768976	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs550279248	chr19:42768995-42768996	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs112668431	chr19:42769010-42769011	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs539089549	chr19:42769021-42769022	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs202101974	chr19:42769058-42769059	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs547397347	chr19:42769066-42769067	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs535534102	chr19:42769079-42769080	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs565690882	chr19:42769088-42769089	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs200420836	chr19:42769111-42769112	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs553628075	chr19:42769128-42769129	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs572055019	chr19:42769155-42769156	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs369841967	chr19:42769181-42769182	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs113379280	chr19:42769209-42769210	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs543375596	chr19:42769247-42769248	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs576871414	chr19:42769254-42769255	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs541078168	chr19:42769258-42769259	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs559435986	chr19:42769265-42769266	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs574478735	chr19:42769284-42769285	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs543379307	chr19:42769296-42769297	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs191379591	chr19:42769299-42769300	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs532005848	chr19:42769311-42769312	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs550122864	chr19:42769315-42769316	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556885647	chr19:42769316-42769317	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs373998719	chr19:42769336-42769337	Weak transcription	Chromatin interactive region	3 gene(s)	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
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2117 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42760400-42771800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:42761400-42771800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr19:42761800-42771800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr19:42762800-42771800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:42763400-42771600	Weak transcription	K562	blood
6	chr19:42763400-42771800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:42764600-42771800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr19:42766400-42771800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr19:42766800-42771800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr19:42767000-42769800	Weak transcription	A549	lung
11	chr19:42767800-42771600	Weak transcription	Brain Angular Gyrus	brain
12	chr19:42769800-42770000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr19:42769800-42770200	Enhancers	A549	lung
14	chr19:42770000-42770200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr19:42770000-42770200	Enhancers	Brain Substantia Nigra	brain
16	chr19:42770000-42771600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr19:42770200-42770400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr19:42770200-42770400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr19:42770200-42771400	Weak transcription	A549	lung
20	chr19:42770200-42771800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr19:42770200-42771800	Weak transcription	Brain Substantia Nigra	brain
22	chr19:42770400-42771600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr19:42770400-42771800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:42771400-42771600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr19:42771400-42771600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr19:42771400-42771600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr19:42771400-42771600	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr19:42771400-42771600	Weak transcription	Fetal Muscle Trunk	muscle
29	chr19:42771400-42771600	Enhancers	Dnd41	blood
30	chr19:42771400-42771800	Enhancers	Fetal Muscle Leg	muscle
31	chr19:42771400-42771800	Enhancers	A549	lung
32	chr19:42771600-42771800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr19:42771600-42771800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr19:42771600-42771800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr19:42771600-42771800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr19:42771600-42771800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr19:42771600-42771800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr19:42771600-42771800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr19:42771600-42771800	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr19:42771600-42771800	Enhancers	Primary B cells from cord blood	blood
41	chr19:42771600-42771800	Enhancers	Primary T cells from cord blood	blood
42	chr19:42771600-42771800	Enhancers	Primary hematopoietic stem cells	blood
43	chr19:42771600-42771800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr19:42771600-42771800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr19:42771600-42771800	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr19:42771600-42771800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr19:42771600-42771800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr19:42771600-42771800	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr19:42771600-42771800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr19:42771600-42771800	Enhancers	Primary T helper cells fromperipheralblood	blood

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