Variant report

Variant	nsv1065886
Chromosome Location	chr19:41339857-41397661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:732)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41378197-41378436	K562	blood:	n/a	n/a
2	ARID3A	chr19:41370633-41370945	K562	blood:	n/a	n/a
3	ATF1	chr19:41339642-41339915	K562	blood:	n/a	n/a
4	ATF1	chr19:41378237-41378485	K562	blood:	n/a	n/a
5	ATF1	chr19:41370536-41370948	K562	blood:	n/a	n/a
6	ATF3	chr19:41370620-41370877	K562	blood:	n/a	n/a
7	ATF3	chr19:41339727-41339986	K562	blood:	n/a	n/a
8	ATF3	chr19:41378141-41378430	K562	blood:	n/a	n/a
9	CBX3	chr19:41347938-41348304	K562	blood:	n/a	n/a
10	CBX3	chr19:41339143-41339980	K562	blood:	n/a	n/a
11	CBX3	chr19:41370123-41371107	K562	blood:	n/a	n/a
12	CBX3	chr19:41347915-41348277	K562	blood:	n/a	n/a
13	CBX3	chr19:41379821-41380148	K562	blood:	n/a	n/a
14	CBX3	chr19:41349182-41350047	K562	blood:	n/a	n/a
15	CBX3	chr19:41381255-41381833	K562	blood:	n/a	n/a
16	CBX3	chr19:41379769-41380227	K562	blood:	n/a	n/a
17	CCNT2	chr19:41370582-41370786	K562	blood:	n/a	n/a
18	CCNT2	chr19:41339675-41339875	K562	blood:	n/a	n/a
19	CEBPB	chr19:41368416-41368601	K562	blood:	n/a	n/a
20	CEBPB	chr19:41343058-41343265	A549	lung:	n/a	chr19:41343121-41343132
21	CEBPB	chr19:41343006-41343268	IMR90	lung:	n/a	chr19:41343121-41343132
22	CEBPB	chr19:41362024-41362201	K562	blood:	n/a	n/a
23	CEBPB	chr19:41342862-41343338	A549	lung:	n/a	chr19:41343121-41343132
24	CEBPB	chr19:41378139-41378466	K562	blood:	n/a	n/a
25	CEBPB	chr19:41378202-41378474	K562	blood:	n/a	n/a
26	CEBPB	chr19:41373920-41374208	K562	blood:	n/a	n/a
27	CEBPB	chr19:41370543-41370910	K562	blood:	n/a	n/a
28	CEBPB	chr19:41339647-41339931	K562	blood:	n/a	n/a
29	CEBPB	chr19:41339552-41339909	K562	blood:	n/a	n/a
30	CEBPB	chr19:41373834-41374300	A549	lung:	n/a	n/a
31	CEBPB	chr19:41343053-41343247	H1-hESC	embryonic stem cell:	n/a	chr19:41343121-41343132
32	CEBPB	chr19:41370305-41370801	K562	blood:	n/a	chr19:41370433-41370441
33	CEBPB	chr19:41368761-41369068	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr19:41343011-41343287	HepG2	liver:	n/a	chr19:41343121-41343132
35	CEBPB	chr19:41370209-41371189	K562	blood:	n/a	chr19:41370433-41370441
36	CEBPB	chr19:41368480-41368982	A549	lung:	n/a	n/a
37	CEBPB	chr19:41367289-41367476	A549	lung:	n/a	n/a
38	CEBPB	chr19:41342957-41343295	K562	blood:	n/a	chr19:41343121-41343132
39	CEBPB	chr19:41374056-41374100	A549	lung:	n/a	n/a
40	CEBPB	chr19:41339359-41340046	K562	blood:	n/a	chr19:41339540-41339548
41	CEBPD	chr19:41392214-41392550	K562	blood:	n/a	n/a
42	CEBPD	chr19:41339436-41340105	K562	blood:	n/a	n/a
43	CEBPD	chr19:41370661-41370862	K562	blood:	n/a	n/a
44	CEBPD	chr19:41370295-41371143	K562	blood:	n/a	n/a
45	CEBPZ	chr19:41395862-41395912	HepG2	liver:	n/a	n/a
46	CTCF	chr19:41367560-41367710	HEK293	kidney:	n/a	n/a
47	CTCF	chr19:41362907-41362927	GM20000	blood:	n/a	n/a
48	CTCF	chr19:41354540-41354690	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr19:41354540-41354690	AG04450	lung:	n/a	n/a
50	CTCF	chr19:41354540-41354690	HCM	heart:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41354553-41354603	Jurkat	blood:	n/a
2	chr19:41385865-41385915	SKMC	muscle:	n/a
3	chr19:41351924-41351974	HRPEpiC	eye:	n/a
4	chr19:41388384-41388434	Caco-2	colon:	n/a
5	chr19:41388384-41388434	GM12892	blood:	n/a
6	chr19:41389684-41389734	HRCEpiC	kidney:	n/a
7	chr19:41351924-41351974	GM19239	blood:	n/a
8	chr19:41386441-41386491	HL-60	blood:	n/a
9	chr19:41388384-41388434	GM12891	blood:	n/a
10	chr19:41385865-41385915	AG10803	skin:	n/a
11	chr19:41354682-41354732	HPAEpiC	pulmonary alveolar:	n/a
12	chr19:41354682-41354732	HUVEC	blood vessel:	n/a
13	chr19:41355973-41356023	GM12878	blood:	n/a
14	chr19:41388384-41388434	NHBE	bronchial:	n/a
15	chr19:41354142-41354192	NB4	blood:	n/a
16	chr19:41355973-41356023	HEEpiC	esophagus:	n/a
17	chr19:41355973-41356023	HCT-116	colon:	n/a
18	chr19:41354553-41354603	HCF	heart:	n/a
19	chr19:41351924-41351974	RPTEC	kidney:	n/a
20	chr19:41385865-41385915	Hepatocyte	liver:	n/a
21	chr19:41354142-41354192	HMEC	breast:	n/a
22	chr19:41389684-41389734	AG04450	lung:	fetal
23	chr19:41354142-41354192	SK-N-SH	brain:	n/a
24	chr19:41385865-41385915	GM12892	blood:	n/a
25	chr19:41388232-41388282	SKMC	muscle:	n/a
26	chr19:41388384-41388434	BJ	skin:	n/a
27	chr19:41354553-41354603	HEEpiC	esophagus:	n/a
28	chr19:41354682-41354732	RPTEC	kidney:	n/a
29	chr19:41383654-41383704	HPAEpiC	pulmonary alveolar:	n/a
30	chr19:41386507-41386557	ECC-1	luminal epithelium:	n/a
31	chr19:41388232-41388282	HRE	kidney:	n/a
32	chr19:41386441-41386491	CMK	blood:	n/a
33	chr19:41383654-41383704	NHBE	bronchial:	n/a
34	chr19:41386507-41386557	U87	brain:	n/a
35	chr19:41385865-41385915	RPTEC	kidney:	n/a
36	chr19:41351924-41351974	HepG2	liver:	n/a
37	chr19:41355973-41356023	HL-60	blood:	n/a
38	chr19:41354682-41354732	HCT-116	colon:	n/a
39	chr19:41389684-41389734	HL-60	blood:	n/a
40	chr19:41385865-41385915	HCPEpiC	choroid plexus:	n/a
41	chr19:41386507-41386557	PFSK-1	brain:	n/a
42	chr19:41383654-41383704	HRPEpiC	eye:	n/a
43	chr19:41388384-41388434	HRE	kidney:	n/a
44	chr19:41386507-41386557	LNCaP	prostate:	n/a
45	chr19:41354682-41354732	AG04449	skin:	fetal
46	chr19:41354553-41354603	HEK293	kidney:	embryo
47	chr19:41386507-41386557	Jurkat	blood:	n/a
48	chr19:41388232-41388282	A549	lung:	n/a
49	chr19:41355973-41356023	AG04449	skin:	fetal
50	chr19:41383654-41383704	HL-60	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41168873..41171001-chr19:41337568..41339858,2	MCF-7	breast:
2	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
3	chr19:41195484..41197379-chr19:41368669..41371255,2	K562	blood:
4	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
5	chr16:4474827..4477394-chr19:41351022..41353007,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2A6-1	chr19:41342991-41343115	ENSG00000269843.1

No data

Variant related genes	Relation type
ENSG00000269843	TF binding region
CYP2G1P	TF binding region
CYP2A6	TF binding region
CYP2A7	TF binding region
ENSG00000269843	CpG island
CYP2G1P	CpG island
CYP2A6	CpG island
CYP2A7	CpG island
ENSG00000105245	chromatin interactions
ENSG00000262246	chromatin interactions
ENSG00000103423	chromatin interactions

Extended variants
information (count: 3060 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3060 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186037008	chr19:41339871-41339872	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs12459249	chr19:41339896-41339897	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs548827996	chr19:41339913-41339914	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs145934699	chr19:41339936-41339937	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs190365632	chr19:41339977-41339978	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs558687680	chr19:41340027-41340028	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs576970663	chr19:41340030-41340031	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs373566223	chr19:41340057-41340058	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs577551847	chr19:41340059-41340060	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs368407258	chr19:41340076-41340077	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs141552778	chr19:41340097-41340098	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs144371570	chr19:41340101-41340102	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs542088777	chr19:41340109-41340110	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148799714	chr19:41340129-41340130	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs575089821	chr19:41340140-41340141	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs545105103	chr19:41340163-41340164	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs142379023	chr19:41340176-41340177	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs531143401	chr19:41340218-41340219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139968700	chr19:41340223-41340224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561143153	chr19:41340230-41340231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34904343	chr19:41340284-41340285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532606719	chr19:41340296-41340297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs398034643	chr19:41340302-41340303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs59179277	chr19:41340303-41340304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11083569	chr19:41340321-41340322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs56007948	chr19:41340323-41340324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142328850	chr19:41340360-41340361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113188526	chr19:41340366-41340367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548890777	chr19:41340399-41340400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150197843	chr19:41340403-41340404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531136468	chr19:41340404-41340405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552768558	chr19:41340446-41340447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571321364	chr19:41340483-41340484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534692407	chr19:41340557-41340558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538625668	chr19:41340558-41340559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10853742	chr19:41340573-41340574	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs12327581	chr19:41340579-41340580	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs376788431	chr19:41340629-41340630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182579069	chr19:41340634-41340635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536743512	chr19:41340635-41340636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369746826	chr19:41340645-41340646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374128775	chr19:41340696-41340697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563145311	chr19:41340705-41340706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187942643	chr19:41340711-41340712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192179809	chr19:41340714-41340715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557504626	chr19:41340717-41340718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577296785	chr19:41340748-41340749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541500790	chr19:41340749-41340750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567449195	chr19:41340814-41340815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534950663	chr19:41340836-41340837	Weak transcription Enhancers	n/a	n/a	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41330200-41349400	Weak transcription	Right Ventricle	heart
2	chr19:41333600-41349400	Weak transcription	Left Ventricle	heart
3	chr19:41336400-41340200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr19:41336400-41340800	Enhancers	Fetal Intestine Large	intestine
5	chr19:41336600-41340800	Enhancers	Fetal Intestine Small	intestine
6	chr19:41337200-41340000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr19:41337200-41340000	Enhancers	Adipose Nuclei	Adipose
8	chr19:41337200-41340000	Enhancers	Liver	Liver
9	chr19:41337200-41340000	Enhancers	Osteobl	bone
10	chr19:41337200-41340200	Enhancers	Placenta	Placenta
11	chr19:41337400-41340200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr19:41337400-41340200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr19:41337400-41340200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr19:41337600-41340000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr19:41338600-41344000	Weak transcription	A549	lung
16	chr19:41338800-41341000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr19:41339200-41340000	Enhancers	Primary hematopoietic stem cells	blood
18	chr19:41339200-41340000	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr19:41339200-41340000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr19:41339200-41340000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr19:41339200-41340000	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr19:41339200-41340000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr19:41339200-41340000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr19:41339200-41340000	Enhancers	Brain Substantia Nigra	brain
25	chr19:41339600-41349400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr19:41339800-41340000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr19:41339800-41340000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr19:41339800-41340000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr19:41339800-41340000	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr19:41339800-41340000	Enhancers	Fetal Lung	lung
31	chr19:41339800-41340000	Enhancers	HepG2	liver
32	chr19:41339800-41340200	Flanking Active TSS	K562	blood
33	chr19:41340000-41340800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:41340200-41341800	Enhancers	K562	blood
35	chr19:41341800-41349400	Weak transcription	K562	blood
36	chr19:41344000-41344400	Enhancers	A549	lung
37	chr19:41347600-41347800	Enhancers	Lung	lung
38	chr19:41347800-41349000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr19:41347800-41349800	Weak transcription	Lung	lung
40	chr19:41348800-41349000	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr19:41348800-41349000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr19:41349000-41349200	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr19:41349000-41349200	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr19:41349000-41349200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr19:41349000-41349200	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr19:41349000-41349200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr19:41349000-41349200	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr19:41349000-41349200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr19:41349000-41349200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr19:41349000-41349200	Enhancers	Duodenum Mucosa	Duodenum

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