Variant report

Variant	nsv1058505
Chromosome Location	chr19:23903764-24031324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1249)
CpG islands
(count:1465)
Chromatin interactive
region (count:18)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:23941611-23941919	K562	blood:	n/a	n/a
2	ARID3A	chr19:23946565-23946828	K562	blood:	n/a	n/a
3	ARID3A	chr19:23953533-23953728	K562	blood:	n/a	n/a
4	ATF1	chr19:23958138-23958329	K562	blood:	n/a	n/a
5	ATF1	chr19:24006791-24007164	K562	blood:	n/a	n/a
6	ATF1	chr19:23941540-23941902	K562	blood:	n/a	n/a
7	BACH1	chr19:23922436-23922552	K562	blood:	n/a	n/a
8	BACH1	chr19:24000521-24000697	K562	blood:	n/a	n/a
9	BATF	chr19:23955417-23955716	GM12878	blood:	n/a	n/a
10	BATF	chr19:23967036-23967332	GM12878	blood:	n/a	n/a
11	BATF	chr19:23967080-23967345	GM12878	blood:	n/a	n/a
12	BATF	chr19:23955472-23955714	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:23943218-23943418	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:23941310-23941885	K562	blood:	n/a	n/a
15	BHLHE40	chr19:24006925-24007160	K562	blood:	n/a	n/a
16	BHLHE40	chr19:23911603-23911632	GM12878	blood:	n/a	n/a
17	BHLHE40	chr19:23968376-23968383	K562	blood:	n/a	n/a
18	BHLHE40	chr19:23945754-23945986	K562	blood:	n/a	n/a
19	CBX3	chr19:24006670-24007006	K562	blood:	n/a	n/a
20	CBX3	chr19:23941229-23941835	K562	blood:	n/a	n/a
21	CBX3	chr19:24006626-24007181	K562	blood:	n/a	n/a
22	CBX3	chr19:23945432-23946054	K562	blood:	n/a	n/a
23	CCNT2	chr19:23945563-23946451	K562	blood:	n/a	n/a
24	CEBPB	chr19:23954211-23954496	A549	lung:	n/a	n/a
25	CEBPB	chr19:23952594-23952832	K562	blood:	n/a	n/a
26	CEBPB	chr19:23966086-23966642	K562	blood:	n/a	chr19:23966205-23966216 chr19:23966237-23966248
27	CEBPB	chr19:24000487-24000738	K562	blood:	n/a	n/a
28	CEBPB	chr19:23946654-23946904	K562	blood:	n/a	n/a
29	CEBPB	chr19:23965636-23965845	IMR90	lung:	n/a	chr19:23965729-23965740
30	CEBPB	chr19:23962419-23962766	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:23964661-23965311	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:23961586-23961803	K562	blood:	n/a	n/a
33	CEBPB	chr19:23965616-23965852	A549	lung:	n/a	chr19:23965729-23965740
34	CEBPB	chr19:23964755-23965279	K562	blood:	n/a	n/a
35	CEBPB	chr19:23969436-23970244	A549	lung:	n/a	n/a
36	CEBPB	chr19:23954779-23955040	A549	lung:	n/a	n/a
37	CEBPB	chr19:23964650-23965334	A549	lung:	n/a	n/a
38	CEBPB	chr19:23959198-23959416	IMR90	lung:	n/a	n/a
39	CEBPB	chr19:23970646-23970667	A549	lung:	n/a	n/a
40	CEBPB	chr19:23945691-23946218	MCF-7	breast:	n/a	n/a
41	CEBPB	chr19:23934829-23934838	K562	blood:	n/a	n/a
42	CEBPB	chr19:23971276-23971470	A549	lung:	n/a	chr19:23971380-23971391
43	CEBPB	chr19:23971312-23971526	HepG2	liver:	n/a	chr19:23971380-23971391
44	CEBPB	chr19:23965636-23965837	HepG2	liver:	n/a	chr19:23965729-23965740
45	CEBPB	chr19:23960182-23960665	K562	blood:	n/a	n/a
46	CEBPB	chr19:23965652-23965852	K562	blood:	n/a	chr19:23965729-23965740
47	CEBPB	chr19:23945549-23946148	K562	blood:	n/a	n/a
48	CEBPB	chr19:23903521-23903797	Hela-S3	cervix:	n/a	chr19:23903671-23903682
49	CEBPB	chr19:23957054-23957915	MCF-7	breast:	n/a	n/a
50	CEBPB	chr19:23959786-23960810	HepG2	liver:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:23942040-23942090	HPAEpiC	pulmonary alveolar:	n/a
2	chr19:23942040-23942090	HPAEpiC	pulmonary alveolar:	n/a
3	chr19:23945641-23945691	HAEpiC	amniotic membrane:	n/a
4	chr19:23945743-23945793	LNCaP	prostate:	n/a
5	chr19:23941575-23941625	MCF10A-Er-Src	breast:	n/a
6	chr19:23945996-23946046	HEEpiC	esophagus:	n/a
7	chr19:23945903-23945953	SK-N-SH	brain:	n/a
8	chr19:23941408-23941458	NT2-D1	testis:	n/a
9	chr19:23942040-23942090	HRE	kidney:	n/a
10	chr19:23945996-23946046	ovcar-3	ovarian:	n/a
11	chr19:23942126-23942176	HRCEpiC	kidney:	n/a
12	chr19:23945903-23945953	Jurkat	blood:	n/a
13	chr19:23941313-23941363	AG09309	skin:	n/a
14	chr19:23942040-23942090	Caco-2	colon:	n/a
15	chr19:23944615-23944665	HAEpiC	amniotic membrane:	n/a
16	chr19:23941575-23941625	GM12892	blood:	n/a
17	chr19:23945761-23945811	ECC-1	luminal epithelium:	n/a
18	chr19:23941859-23941909	NB4	blood:	n/a
19	chr19:23946205-23946255	BE2_C	brain:	n/a
20	chr19:23941207-23941257	GM06990	blood:	n/a
21	chr19:23944615-23944665	AG09319	gingival:	n/a
22	chr19:23945743-23945793	AG09309	skin:	n/a
23	chr19:23941408-23941458	NB4	blood:	n/a
24	chr19:23945743-23945793	NB4	blood:	n/a
25	chr19:23945722-23945772	AG09319	gingival:	n/a
26	chr19:23941313-23941363	BJ	skin:	n/a
27	chr19:23944615-23944665	T-47D	breast:	n/a
28	chr19:23941438-23941488	AG04449	skin:	fetal
29	chr19:23941575-23941625	SK-N-MC	brain:	n/a
30	chr19:23941871-23941921	Hepatocyte	liver:	n/a
31	chr19:23941575-23941625	GM12891	blood:	n/a
32	chr19:23946205-23946255	HRE	kidney:	n/a
33	chr19:23945659-23945709	HCM	heart:	n/a
34	chr19:23945996-23946046	Hepatocyte	liver:	n/a
35	chr19:23942040-23942090	GM12892	blood:	n/a
36	chr19:23944615-23944665	U87	brain:	n/a
37	chr19:23941711-23941761	ProgFib	skin:	n/a
38	chr19:23941871-23941921	RPTEC	kidney:	n/a
39	chr19:23941718-23941768	GM12891	blood:	n/a
40	chr19:23945641-23945691	LNCaP	prostate:	n/a
41	chr19:23945472-23945522	HRCEpiC	kidney:	n/a
42	chr19:23941575-23941625	NH-A	brain:	n/a
43	chr19:23942073-23942123	GM19239	blood:	n/a
44	chr19:23941408-23941458	HRCEpiC	kidney:	n/a
45	chr19:23941313-23941363	SK-N-SH	brain:	n/a
46	chr19:23945996-23946046	MCF10A-Er-Src	breast:	n/a
47	chr19:23941313-23941363	SK-N-MC	brain:	n/a
48	chr19:23941718-23941768	AG04450	lung:	fetal
49	chr19:23942040-23942090	K562	blood:	n/a
50	chr19:23945903-23945953	RPTEC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:23956310..23957870-chr19:23960230..23962213,2	K562	blood:
2	chr19:23940633..23942866-chr19:23945047..23947463,3	K562	blood:
3	chr19:23990207..23992454-chr19:24002314..24004892,2	K562	blood:
4	chr16:10416054..10418828-chr19:23906524..23908025,2	MCF-7	breast:
5	chr19:23934332..23937161-chr19:23938726..23941711,2	K562	blood:
6	chr19:24000616..24002168-chr19:24002694..24005183,2	MCF-7	breast:
7	chr19:23935159..23938010-chr19:23940371..23942575,2	K562	blood:
8	chr19:23939020..23940771-chr19:23944929..23946876,2	K562	blood:
9	chr19:23946413..23950001-chr19:23953368..23955533,3	K562	blood:
10	chr19:23990207..23992454-chr19:24002314..24004892,2	K562	blood:
11	chr19:23947709..23949776-chr19:23958415..23961237,2	K562	blood:
12	chr19:23944623..23946640-chr19:23952768..23956450,3	MCF-7	breast:
13	chr19:23946413..23950001-chr19:23953368..23955533,3	K562	blood:
14	chr19:23947709..23949776-chr19:23958415..23961237,2	K562	blood:
15	chr19:23956310..23957870-chr19:23960230..23962213,2	K562	blood:
16	chr19:23940633..23942866-chr19:23945047..23947463,3	K562	blood:
17	chr19:24000616..24002168-chr19:24002694..24005183,2	MCF-7	breast:
18	chr19:23941209..23941866-chr7:64126456..64127217,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPSAP58-2	chr19:24014399-24014998	NONHSAT063934
2	lnc-RPSAP58-2	chr19:23990628-23990741	NONHSAT063933
3	lnc-RPSAP58-2	chr19:23945746-23945936	NONHSAT063933
4	lnc-ZNF726-1	chr19:23969947-23970608	ENSG00000250795
5	lnc-ZNF675-2	chr19:23922003-23923732	NONHSAT063932
6	lnc-ZNF726-1	chr19:23969576-23969850	ENSG00000250795
7	lnc-ZNF726-1	chr19:23968384-23969193	ENSG00000250795
8	lnc-RPSAP58-2	chr19:23991521-23992317	NONHSAT063935
9	lnc-RPSAP58-2	chr19:23990628-23990741	NONHSAT063935
10	lnc-RPSAP58-2	chr19:23964883-23965301	NONHSAT063935
11	lnc-RPSAP58-2	chr19:23991521-23991616	NONHSAT063933
12	lnc-ZNF675-3	chr19:23932373-23932637	l_1665_chr19:23924177-23932637_testes
13	lnc-RPSAP58-2	chr19:24014399-24014998	NONHSAT063933
14	lnc-ZNF681-3	chr19:23981726-23982279	NONHSAT063937
15	lnc-RPSAP58-2	chr19:23945814-23945936	NONHSAT063934
16	lnc-ZNF675-3	chr19:23924178-23924868	l_1665_chr19:23924177-23932637_testes
17	lnc-ZNF675-3	chr19:23926812-23927078	l_1665_chr19:23924177-23932637_testes

No data

Variant related genes	Relation type
RPSAP58	TF binding region
ENSG00000269662	TF binding region
ZNF681	TF binding region
ENSG00000233836	TF binding region
RPSAP58	CpG island
ENSG00000269662	CpG island
ZNF681	CpG island
ENSG00000233836	CpG island
ENSG00000196247	chromatin interactions
ENSG00000233836	chromatin interactions
ENSG00000196172	chromatin interactions
ENSG00000205246	chromatin interactions
TIAL1	miRNA target sites
GATA6	miRNA target sites
NOTCH2	miRNA target sites

Extended variants
information (count: 5149 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:5149 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191982533	chr19:23903821-23903822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs71357988	chr19:23903879-23903880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4932917	chr19:23903888-23903889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs183358490	chr19:23903931-23903932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572755254	chr19:23903934-23903935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540882425	chr19:23903935-23903936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186842208	chr19:23903955-23903956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532713606	chr19:23904001-23904002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540427744	chr19:23904017-23904018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528270599	chr19:23904087-23904088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs55757733	chr19:23904088-23904089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199731768	chr19:23904092-23904093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551177299	chr19:23904104-23904105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11671055	chr19:23904329-23904330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs530205862	chr19:23904376-23904377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548745320	chr19:23904399-23904400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566808543	chr19:23904412-23904413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527693765	chr19:23904434-23904435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141546156	chr19:23904435-23904436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571472644	chr19:23904517-23904518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538952489	chr19:23904519-23904520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190986429	chr19:23904521-23904522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556729184	chr19:23904532-23904533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138195756	chr19:23904544-23904545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183082939	chr19:23904577-23904578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115544074	chr19:23904596-23904597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554255424	chr19:23904628-23904629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186696243	chr19:23904633-23904634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7253833	chr19:23904658-23904659	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571243322	chr19:23904663-23904664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558554901	chr19:23904740-23904741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577455046	chr19:23904823-23904824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544958183	chr19:23904837-23904838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139977907	chr19:23904839-23904840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373220274	chr19:23904840-23904841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7254105	chr19:23904865-23904866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541840602	chr19:23904892-23904893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530318492	chr19:23904949-23904950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542301308	chr19:23904961-23904962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375253344	chr19:23904980-23904981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143386847	chr19:23905018-23905019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372377592	chr19:23905044-23905045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7254506	chr19:23905083-23905084	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs561720933	chr19:23905086-23905087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531111022	chr19:23905102-23905103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7254756	chr19:23905126-23905127	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs570864815	chr19:23905137-23905138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532271750	chr19:23905189-23905190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139492303	chr19:23905191-23905192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189678908	chr19:23905296-23905297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:42)

Disease	PMID	Source
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2040 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:23902400-23903800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:23902600-23905400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr19:23902600-23905600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr19:23902600-23906200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr19:23902600-23906200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr19:23902800-23904400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr19:23902800-23905600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr19:23903000-23905400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr19:23903200-23906400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr19:23904400-23904800	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr19:23904800-23906200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr19:23905400-23905600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr19:23905400-23905600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr19:23905400-23905800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr19:23905400-23906200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr19:23905600-23905800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr19:23905600-23906000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr19:23905600-23906000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr19:23905600-23907800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr19:23905800-23906200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr19:23905800-23906200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr19:23906000-23906400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr19:23906000-23908000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr19:23906200-23906400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr19:23906200-23906400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr19:23906200-23907400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr19:23906200-23907600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr19:23906200-23908200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr19:23906400-23906600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr19:23906400-23906600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr19:23906400-23906600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr19:23906400-23906800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr19:23906400-23906800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:23906400-23906800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr19:23906400-23906800	Enhancers	Placenta	Placenta
36	chr19:23906400-23907600	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr19:23906400-23908000	Enhancers	K562	blood
38	chr19:23906600-23906800	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr19:23906600-23906800	Enhancers	Placenta Amnion	Placenta Amnion
40	chr19:23906600-23907000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr19:23906800-23907200	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr19:23906800-23907200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr19:23906800-23907200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr19:23906800-23907200	Weak transcription	Placenta	Placenta
45	chr19:23907000-23907400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr19:23907000-23907600	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr19:23907200-23907800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr19:23907200-23907800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr19:23907200-23907800	Enhancers	Placenta	Placenta
50	chr19:23907400-23907600	Enhancers	Placenta Amnion	Placenta Amnion

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