Variant report

Variant	nsv1057949
Chromosome Location	chr19:43885058-43935170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr19:43917535-43917884	K562	blood:	n/a	n/a
2	CBX3	chr19:43917630-43917850	K562	blood:	n/a	n/a
3	CEBPB	chr19:43926815-43927157	K562	blood:	n/a	chr19:43926999-43927010
4	CEBPB	chr19:43896505-43896663	HepG2	liver:	n/a	n/a
5	CEBPB	chr19:43928942-43929136	K562	blood:	n/a	chr19:43929097-43929108
6	CEBPB	chr19:43928882-43929119	IMR90	lung:	n/a	chr19:43929097-43929108
7	CEBPB	chr19:43920752-43920932	K562	blood:	n/a	n/a
8	CEBPB	chr19:43896414-43896759	IMR90	lung:	n/a	n/a
9	CEBPB	chr19:43933642-43933750	A549	lung:	n/a	n/a
10	CEBPB	chr19:43926858-43927126	Hela-S3	cervix:	n/a	chr19:43926999-43927010
11	CEBPB	chr19:43933433-43933848	K562	blood:	n/a	n/a
12	CEBPB	chr19:43896574-43896768	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr19:43926853-43927151	HepG2	liver:	n/a	chr19:43926999-43927010
14	CEBPB	chr19:43896450-43896720	A549	lung:	n/a	n/a
15	CEBPB	chr19:43931758-43932062	HepG2	liver:	n/a	chr19:43931836-43931847 chr19:43931836-43931847
16	CEBPB	chr19:43926918-43927173	A549	lung:	n/a	chr19:43926999-43927010
17	CEBPB	chr19:43926854-43927175	IMR90	lung:	n/a	chr19:43926999-43927010
18	CEBPB	chr19:43928885-43929232	HepG2	liver:	n/a	chr19:43929097-43929108
19	CEBPB	chr19:43896514-43896714	K562	blood:	n/a	n/a
20	CEBPB	chr19:43928874-43929095	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr19:43928890-43929216	A549	lung:	n/a	chr19:43929097-43929108
22	CEBPB	chr19:43916687-43916887	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr19:43934260-43934410	Hela-S3	cervix:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
24	CTCF	chr19:43934300-43934450	AG10803	skin:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
25	CTCF	chr19:43929900-43930050	AG10803	skin:	n/a	n/a
26	CTCF	chr19:43929880-43930030	GM12867	blood:	n/a	n/a
27	CTCF	chr19:43934340-43934490	BJ	skin:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
28	CTCF	chr19:43934240-43934390	GM12878	blood:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
29	CTCF	chr19:43934284-43934422	GM12892	blood:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
30	CTCF	chr19:43929820-43929970	GM12801	blood:	n/a	n/a
31	CTCF	chr19:43934260-43934410	HEEpiC	esophagus:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
32	CTCF	chr19:43934220-43934370	HRPEpiC	eye:	n/a	chr19:43934357-43934370 chr19:43934361-43934370
33	CTCF	chr19:43892008-43892011	GM20000	blood:	n/a	n/a
34	CTCF	chr19:43929900-43930050	AG04449	skin:	n/a	n/a
35	CTCF	chr19:43919789-43919828	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr19:43929873-43930123	Gliobla	brain:	n/a	n/a
37	CTCF	chr19:43934240-43934390	WERI-Rb-1	eye:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
38	CTCF	chr19:43929920-43930070	AG04449	skin:	n/a	n/a
39	CTCF	chr19:43929900-43930050	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr19:43929889-43930087	HepG2	liver:	n/a	n/a
41	CTCF	chr19:43934280-43934430	GM12864	blood:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
42	CTCF	chr19:43929900-43930050	HRE	kidney:	n/a	n/a
43	CTCF	chr19:43934315-43934373	MCF-7	breast:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
44	CTCF	chr19:43929880-43930030	GM06990	blood:	n/a	n/a
45	CTCF	chr19:43929860-43930010	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr19:43929777-43930156	K562	blood:	n/a	n/a
47	CTCF	chr19:43929840-43929990	GM12866	blood:	n/a	n/a
48	CTCF	chr19:43934320-43934470	HPF	lung:	n/a	chr19:43934357-43934370 chr19:43934361-43934370 chr19:43934355-43934373
49	CTCF	chr19:43930215-43930291	Lung_OC	lung:	n/a	n/a
50	CTCF	chr19:43929900-43930050	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43911682-43911732	AG10803	skin:	n/a
2	chr19:43918465-43918515	Jurkat	blood:	n/a
3	chr19:43911682-43911732	AG10803	skin:	n/a
4	chr19:43918465-43918515	Jurkat	blood:	n/a
5	chr19:43913330-43913380	GM12892	blood:	n/a
6	chr19:43922723-43922773	NT2-D1	testis:	n/a
7	chr19:43918371-43918421	AoSMC	blood vessel:	n/a
8	chr19:43911682-43911732	HCM	heart:	n/a
9	chr19:43912492-43912542	CMK	blood:	n/a
10	chr19:43919536-43919586	SK-N-SH_RA	brain:	n/a
11	chr19:43912492-43912542	SKMC	muscle:	n/a
12	chr19:43891281-43891331	NHBE	bronchial:	n/a
13	chr19:43919028-43919078	T-47D	breast:	n/a
14	chr19:43922332-43922382	Hela-S3	cervix:	n/a
15	chr19:43918465-43918515	AG10803	skin:	n/a
16	chr19:43891866-43891916	AG10803	skin:	n/a
17	chr19:43918371-43918421	HL-60	blood:	n/a
18	chr19:43908315-43908365	Caco-2	colon:	n/a
19	chr19:43919536-43919586	U87	brain:	n/a
20	chr19:43918882-43918932	HEEpiC	esophagus:	n/a
21	chr19:43918882-43918932	BE2_C	brain:	n/a
22	chr19:43918868-43918918	GM06990	blood:	n/a
23	chr19:43918408-43918458	A549	lung:	n/a
24	chr19:43913330-43913380	HRPEpiC	eye:	n/a
25	chr19:43919028-43919078	LNCaP	prostate:	n/a
26	chr19:43913330-43913380	IMR90	lung:	fetal
27	chr19:43919039-43919089	GM12878	blood:	n/a
28	chr19:43918868-43918918	SAEC	small airway:	n/a
29	chr19:43919039-43919089	MCF-7	breast:	n/a
30	chr19:43912227-43912277	GM12892	blood:	n/a
31	chr19:43908315-43908365	PANC-1	pancreas:	n/a
32	chr19:43908315-43908365	U87	brain:	n/a
33	chr19:43911682-43911732	MCF10A-Er-Src	breast:	n/a
34	chr19:43922723-43922773	ovcar-3	ovarian:	n/a
35	chr19:43892826-43892876	HepG2	liver:	n/a
36	chr19:43908315-43908365	GM19239	blood:	n/a
37	chr19:43918408-43918458	CMK	blood:	n/a
38	chr19:43916594-43916644	K562	blood:	n/a
39	chr19:43922332-43922382	PFSK-1	brain:	n/a
40	chr19:43911682-43911732	HCT-116	colon:	n/a
41	chr19:43918974-43919024	AG09309	skin:	n/a
42	chr19:43892826-43892876	SKMC	muscle:	n/a
43	chr19:43912227-43912277	GM12891	blood:	n/a
44	chr19:43919039-43919089	U87	brain:	n/a
45	chr19:43919003-43919053	SK-N-SH_RA	brain:	n/a
46	chr19:43918974-43919024	GM12892	blood:	n/a
47	chr19:43916594-43916644	ECC-1	luminal epithelium:	n/a
48	chr19:43918943-43918993	PFSK-1	brain:	n/a
49	chr19:43919039-43919089	PFSK-1	brain:	n/a
50	chr19:43922723-43922773	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:43820685..43821690-chr19:43929045..43930443,5	MCF-7	breast:
2	chr17:42852520..42853209-chr19:43915333..43915833,2	HCT-116	colon:
3	chr19:43928435..43931381-chr19:43932773..43935782,3	K562	blood:
4	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
5	chr19:43821071..43821590-chr19:43929652..43930334,2	MCF-7	breast:
6	chr19:43928535..43930747-chr19:43966422..43969412,2	MCF-7	breast:
7	chr19:43909136..43910754-chr19:43912460..43914552,2	MCF-7	breast:
8	chr19:43928435..43931381-chr19:43932773..43935782,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TEX101-1	chr19:43895826-43896306	expReg_chr19_6147_+
2	lnc-TEX101-2	chr19:43893587-43893979	expReg_chr19_6146_+

Variant related genes	Relation type
CD177P1	TF binding region
TEX101	TF binding region
CD177P1	CpG island
TEX101	CpG island
ENSG00000124466	chromatin interactions
ENSG00000131126	chromatin interactions
ENSG00000073670	chromatin interactions

Extended variants
information (count: 1787 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1787 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541782904	chr19:43885064-43885065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566397114	chr19:43885078-43885079	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs7259375	chr19:43885085-43885086	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs548666316	chr19:43885172-43885173	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs530226321	chr19:43885179-43885180	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs191774674	chr19:43885207-43885208	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs538168180	chr19:43885220-43885221	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs112806109	chr19:43885236-43885237	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs149213802	chr19:43885245-43885246	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs143406664	chr19:43885249-43885250	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs562324554	chr19:43885255-43885256	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs147973017	chr19:43885279-43885280	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs76607685	chr19:43885285-43885286	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs536673552	chr19:43885299-43885300	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs556311533	chr19:43885302-43885303	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs576369724	chr19:43885314-43885315	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545335021	chr19:43885464-43885465	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs113077026	chr19:43885484-43885485	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs374690108	chr19:43885485-43885486	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs202235330	chr19:43885486-43885487	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs565234097	chr19:43885489-43885490	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs572308502	chr19:43885502-43885503	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs78646400	chr19:43885519-43885520	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs541185797	chr19:43885526-43885527	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs560207991	chr19:43885533-43885534	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs12463154	chr19:43885579-43885580	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549038787	chr19:43885625-43885626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562375554	chr19:43885647-43885648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185486753	chr19:43885650-43885651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569177358	chr19:43885670-43885671	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs534595978	chr19:43885709-43885710	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs551707230	chr19:43885715-43885716	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571528972	chr19:43885752-43885753	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs533995063	chr19:43885770-43885771	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs144635069	chr19:43885797-43885798	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs373816365	chr19:43885833-43885834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546537321	chr19:43885835-43885836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377482494	chr19:43885867-43885868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112412921	chr19:43885878-43885879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574304797	chr19:43885879-43885880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567434298	chr19:43885906-43885907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571214601	chr19:43885942-43885943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141683289	chr19:43885946-43885947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556611510	chr19:43885950-43885951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561920373	chr19:43885963-43885964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150767813	chr19:43885964-43885965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78813111	chr19:43885987-43885988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558833200	chr19:43885998-43885999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372896520	chr19:43886005-43886006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572369364	chr19:43886006-43886007	Weak transcription	n/a	n/a	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
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21240255	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43883200-43889200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr19:43884200-43885400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr19:43884400-43885400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr19:43884400-43885400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr19:43884400-43885400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr19:43884400-43885400	Enhancers	Stomach Mucosa	stomach
7	chr19:43884600-43885400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr19:43884600-43885400	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr19:43884600-43885600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr19:43884800-43885400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr19:43884800-43885400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr19:43884800-43885400	Enhancers	Duodenum Mucosa	Duodenum
13	chr19:43884800-43885400	Enhancers	Esophagus	oesophagus
14	chr19:43884800-43885600	Enhancers	HepG2	liver
15	chr19:43884800-43885600	Enhancers	NHEK	skin
16	chr19:43885000-43885400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr19:43885000-43885400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr19:43885400-43886400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr19:43885400-43886800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr19:43885400-43887000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr19:43885400-43887400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:43885600-43888000	Weak transcription	NHEK	skin
23	chr19:43886400-43886600	Enhancers	Duodenum Mucosa	Duodenum
24	chr19:43886600-43886800	Enhancers	Primary hematopoietic stem cells	blood
25	chr19:43886800-43887200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr19:43886800-43887600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr19:43886800-43889000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr19:43887000-43887200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr19:43887000-43887200	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr19:43887000-43889800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr19:43887200-43888000	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr19:43887200-43889800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:43887400-43887600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr19:43887400-43888200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:43888000-43888200	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr19:43888000-43888200	Enhancers	NHEK	skin
37	chr19:43888800-43889800	Enhancers	Primary B cells from cord blood	blood
38	chr19:43889000-43889600	Enhancers	Primary B cells from peripheral blood	blood
39	chr19:43889000-43889600	Enhancers	Primary hematopoietic stem cells	blood
40	chr19:43889200-43893000	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr19:43889400-43889600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr19:43889600-43890600	Weak transcription	Primary B cells from peripheral blood	blood
43	chr19:43889600-43891200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr19:43889800-43890800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr19:43889800-43891000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:43890600-43891200	Enhancers	Primary B cells from peripheral blood	blood
47	chr19:43890800-43893600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr19:43891000-43893600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr19:43891200-43892000	Enhancers	Primary hematopoietic stem cells	blood
50	chr19:43894000-43896400	Enhancers	Cortex derived primary cultured neurospheres	brain

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