Variant report

Variant	esv3326078
Chromosome Location	chr5:41710992-41743453
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:41738826-41739323	K562	blood:	n/a	n/a
2	ATF1	chr5:41738859-41739346	K562	blood:	n/a	n/a
3	ATF2	chr5:41740330-41741106	GM12878	blood:	n/a	n/a
4	ATF3	chr5:41738846-41739115	K562	blood:	n/a	n/a
5	CEBPB	chr5:41741341-41741660	HepG2	liver:	n/a	chr5:41741505-41741516 chr5:41741504-41741517
6	CEBPB	chr5:41736747-41737124	IMR90	lung:	n/a	n/a
7	CEBPD	chr5:41738758-41739171	K562	blood:	n/a	n/a
8	CREB1	chr5:41738703-41739240	K562	blood:	n/a	n/a
9	CTCF	chr5:41722440-41722590	BE2_C	brain:	n/a	n/a
10	CTCF	chr5:41722576-41722679	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr5:41722580-41722730	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr5:41722600-41722750	GM12872	blood:	n/a	n/a
13	CTCF	chr5:41722520-41722670	HVMF	connective:	n/a	n/a
14	CTCF	chr5:41722580-41722730	GM12869	blood:	n/a	n/a
15	CTCF	chr5:41722600-41722750	NHDF-neo	bronchial:	n/a	n/a
16	CTCF	chr5:41722664-41722722	GM19240	blood:	n/a	n/a
17	CTCF	chr5:41722520-41722670	GM12872	blood:	n/a	n/a
18	CTCF	chr5:41722500-41722650	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr5:41722539-41722716	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:41722560-41722710	AG04449	skin:	n/a	n/a
21	CTCF	chr5:41722580-41722730	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr5:41722580-41722730	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr5:41722520-41722670	GM12874	blood:	n/a	n/a
24	CTCF	chr5:41722520-41722670	HFF	foreskin:	n/a	n/a
25	CTCF	chr5:41722555-41722685	Medullo	brain:	n/a	n/a
26	CTCF	chr5:41722540-41722690	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr5:41735940-41736090	GM12865	blood:	n/a	n/a
28	CTCF	chr5:41739180-41739330	WERI-Rb-1	eye:	n/a	chr5:41739253-41739262 chr5:41739249-41739262
29	CTCF	chr5:41722520-41722670	RPTEC	kidney:	n/a	n/a
30	CTCF	chr5:41739227-41739310	K562	blood:	n/a	chr5:41739253-41739262 chr5:41739249-41739262
31	CTCF	chr5:41722560-41722710	RPTEC	kidney:	n/a	n/a
32	CTCF	chr5:41722600-41722750	BJ	skin:	n/a	n/a
33	CTCF	chr5:41722500-41722650	GM12864	blood:	n/a	n/a
34	CTCF	chr5:41722480-41722630	GM12865	blood:	n/a	n/a
35	CTCF	chr5:41722540-41722690	HMF	breast:	n/a	n/a
36	CTCF	chr5:41722520-41722670	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr5:41722580-41722730	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr5:41722560-41722710	BE2_C	brain:	n/a	n/a
39	CTCF	chr5:41722540-41722690	GM12870	blood:	n/a	n/a
40	CTCF	chr5:41722620-41722770	GM12875	blood:	n/a	n/a
41	CTCF	chr5:41722461-41722820	K562	blood:	n/a	n/a
42	CTCF	chr5:41722560-41722710	NHEK	skin:	n/a	n/a
43	CTCF	chr5:41722540-41722690	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:41722560-41722710	BJ	skin:	n/a	n/a
45	CTCF	chr5:41722480-41722630	HAc	cerebellar:	n/a	n/a
46	CTCF	chr5:41722518-41722718	Gliobla	brain:	n/a	n/a
47	CTCF	chr5:41719667-41719677	GM12878	blood:	n/a	n/a
48	CTCF	chr5:41722580-41722730	HCM	heart:	n/a	n/a
49	CTCF	chr5:41722500-41722650	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr5:41722500-41722650	HRE	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:41730687-41730737	HepG2	liver:	n/a
2	chr5:41730687-41730737	GM19239	blood:	n/a
3	chr5:41730687-41730737	ProgFib	skin:	n/a
4	chr5:41730687-41730737	PANC-1	pancreas:	n/a
5	chr5:41730687-41730737	SKMC	muscle:	n/a
6	chr5:41730687-41730737	RPTEC	kidney:	n/a
7	chr5:41730687-41730737	SAEC	small airway:	n/a
8	chr5:41730687-41730737	GM12891	blood:	n/a
9	chr5:41730687-41730737	HCF	heart:	n/a
10	chr5:41730687-41730737	SK-N-SH	brain:	n/a
11	chr5:41730687-41730737	NB4	blood:	n/a
12	chr5:41730687-41730737	LNCaP	prostate:	n/a
13	chr5:41730687-41730737	AG09309	skin:	n/a
14	chr5:41730687-41730737	T-47D	breast:	n/a
15	chr5:41730687-41730737	NH-A	brain:	n/a
16	chr5:41730687-41730737	ECC-1	luminal epithelium:	n/a
17	chr5:41730687-41730737	HRE	kidney:	n/a
18	chr5:41730687-41730737	HL-60	blood:	n/a
19	chr5:41730687-41730737	NHDF-neo	bronchial:	n/a
20	chr5:41730687-41730737	IMR90	lung:	fetal
21	chr5:41730687-41730737	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:41730687-41730737	Jurkat	blood:	n/a
23	chr5:41730687-41730737	K562	blood:	n/a
24	chr5:41730687-41730737	CMK	blood:	n/a
25	chr5:41730687-41730737	HCT-116	colon:	n/a
26	chr5:41730687-41730737	HRCEpiC	kidney:	n/a
27	chr5:41730687-41730737	HAEpiC	amniotic membrane:	n/a
28	chr5:41730687-41730737	HUVEC	blood vessel:	n/a
29	chr5:41730687-41730737	BE2_C	brain:	n/a
30	chr5:41730687-41730737	Hepatocyte	liver:	n/a
31	chr5:41730687-41730737	PFSK-1	brain:	n/a
32	chr5:41730687-41730737	AG09319	gingival:	n/a
33	chr5:41730687-41730737	AG10803	skin:	n/a
34	chr5:41730687-41730737	BJ	skin:	n/a
35	chr5:41730687-41730737	Hela-S3	cervix:	n/a
36	chr5:41730687-41730737	GM06990	blood:	n/a
37	chr5:41730687-41730737	HRPEpiC	eye:	n/a
38	chr5:41730687-41730737	GM12878	blood:	n/a
39	chr5:41730687-41730737	HEK293	kidney:	embryo
40	chr5:41730687-41730737	AoSMC	blood vessel:	n/a
41	chr5:41730687-41730737	MCF10A-Er-Src	breast:	n/a
42	chr5:41730687-41730737	SK-N-MC	brain:	n/a
43	chr5:41730687-41730737	HMEC	breast:	n/a
44	chr5:41730687-41730737	MCF-7	breast:	n/a
45	chr5:41730687-41730737	HIPEpiC	eye:	n/a
46	chr5:41730687-41730737	NHBE	bronchial:	n/a
47	chr5:41730687-41730737	AG04450	lung:	fetal
48	chr5:41730687-41730737	U87	brain:	n/a
49	chr5:41730687-41730737	A549	lung:	n/a
50	chr5:41730687-41730737	HEEpiC	esophagus:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:41726795..41729567-chr5:41730109..41732618,2	K562	blood:
2	chr5:41725766..41729567-chr5:41730109..41733963,3	K562	blood:
3	chr5:41723873..41725703-chr5:41731043..41733042,2	K562	blood:
4	chr5:41725766..41729567-chr5:41730109..41733963,3	K562	blood:
5	chr5:41713901..41715819-chr5:41720276..41722337,2	K562	blood:
6	chr5:41707271..41710047-chr5:41712912..41714812,2	MCF-7	breast:
7	chr5:41726795..41729567-chr5:41730109..41732618,2	K562	blood:
8	chr5:41736012..41737687-chr5:41741619..41743667,2	K562	blood:
9	chr5:41715717..41717936-chr5:41762141..41764322,2	K562	blood:
10	chr5:41736012..41737687-chr5:41741619..41743667,2	K562	blood:
11	chr5:41713901..41715819-chr5:41720276..41722337,2	K562	blood:
12	chr5:41723873..41725703-chr5:41731043..41733042,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	OXCT1	hsa-miR-1	chr5:41730284-41730308

Variant related genes	Relation type
OXCT1	TF binding region
OXCT1	CpG island

Extended variants
information (count: 791 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114643163	chr5:41718233-41718234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572720281	chr5:41718314-41718315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546463360	chr5:41718329-41718330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145059735	chr5:41718386-41718387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146833556	chr5:41718390-41718391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187813937	chr5:41718426-41718427	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs192914874	chr5:41718487-41718488	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs529301508	chr5:41718501-41718502	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs547525367	chr5:41718515-41718516	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs370076400	chr5:41718533-41718534	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs183306988	chr5:41718582-41718583	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs79612760	chr5:41718636-41718637	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs551574265	chr5:41718712-41718713	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs56943343	chr5:41718756-41718757	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs316724	chr5:41718781-41718782	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs72317515	chr5:41718784-41718785	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs534986511	chr5:41721003-41721004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114902934	chr5:41721016-41721017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs578000073	chr5:41721094-41721095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545159651	chr5:41721095-41721096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs77909801	chr5:41721109-41721110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373325483	chr5:41721116-41721117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs57365158	chr5:41721144-41721145	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542812546	chr5:41721217-41721218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371219910	chr5:41721226-41721227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561073413	chr5:41721259-41721260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528349880	chr5:41721282-41721283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72746918	chr5:41721296-41721297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs72746919	chr5:41721301-41721302	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532160965	chr5:41721373-41721374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539099056	chr5:41721380-41721381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568899183	chr5:41721391-41721392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577843863	chr5:41721409-41721410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552704739	chr5:41721415-41721416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147166756	chr5:41721429-41721430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116254683	chr5:41721450-41721451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531692436	chr5:41721479-41721480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567566440	chr5:41721492-41721493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572764084	chr5:41721494-41721495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs67715253	chr5:41721503-41721504	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs571531998	chr5:41721504-41721505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368097578	chr5:41721547-41721548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538997485	chr5:41721673-41721674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555223930	chr5:41721682-41721683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs557094380	chr5:41721725-41721726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575768765	chr5:41721744-41721745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186492744	chr5:41721761-41721762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549720613	chr5:41721769-41721770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573116135	chr5:41721798-41721799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74678466	chr5:41721828-41721829	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41718200-41718400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:41718400-41718800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:41721000-41722000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:41721200-41722200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr5:41721800-41722000	Enhancers	HSMMtube	muscle
6	chr5:41722000-41736800	Weak transcription	HSMMtube	muscle
7	chr5:41722600-41722800	Enhancers	Right Atrium	heart
8	chr5:41722600-41723000	Enhancers	Fetal Muscle Leg	muscle
9	chr5:41722600-41723000	Enhancers	Ovary	ovary
10	chr5:41722800-41723000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:41722800-41723000	ZNF genes & repeats	Aorta	Aorta
12	chr5:41722800-41723000	Enhancers	GM12878-XiMat	blood
13	chr5:41723000-41724800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:41723000-41735800	Weak transcription	GM12878-XiMat	blood
15	chr5:41723000-41739200	Weak transcription	Aorta	Aorta
16	chr5:41725200-41725400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:41725200-41725400	Enhancers	Right Ventricle	heart
18	chr5:41725400-41725600	Enhancers	Fetal Kidney	kidney
19	chr5:41725400-41728400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr5:41725400-41739200	Weak transcription	Right Ventricle	heart
21	chr5:41725600-41747400	Weak transcription	Fetal Kidney	kidney
22	chr5:41726000-41726600	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr5:41726600-41736000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr5:41726600-41736000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:41726800-41728400	Weak transcription	Primary T cells from cord blood	blood
26	chr5:41727000-41730600	Weak transcription	Left Ventricle	heart
27	chr5:41727200-41727400	Enhancers	Fetal Brain Female	brain
28	chr5:41727200-41728800	Weak transcription	Fetal Thymus	thymus
29	chr5:41727200-41730600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr5:41727200-41735200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr5:41727200-41735800	Weak transcription	Lung	lung
32	chr5:41727200-41738400	Weak transcription	Thymus	Thymus
33	chr5:41727400-41729000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr5:41727400-41729000	Weak transcription	Dnd41	blood
35	chr5:41727400-41730400	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr5:41727400-41730400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr5:41727400-41735400	Weak transcription	Hela-S3	cervix
38	chr5:41727400-41751400	Weak transcription	Fetal Brain Female	brain
39	chr5:41727600-41730400	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr5:41727600-41735400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:41727600-41735400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr5:41727600-41738400	Weak transcription	Gastric	stomach
43	chr5:41727600-41738400	Weak transcription	Rectal Smooth Muscle	rectum
44	chr5:41727800-41738400	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr5:41727800-41747200	Weak transcription	NH-A	brain
46	chr5:41727800-41758200	Weak transcription	Esophagus	oesophagus
47	chr5:41728000-41739200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr5:41728200-41728600	Weak transcription	Primary B cells from cord blood	blood
49	chr5:41728200-41738400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr5:41728400-41729000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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