Variant report

Variant	nsv1034707
Chromosome Location	chr7:106897237-106966215
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:345)
CpG islands
(count:0)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:106962487-106962772	K562	blood:	n/a	n/a
2	ARID3A	chr7:106949848-106950099	K562	blood:	n/a	n/a
3	ARID3A	chr7:106960386-106961048	K562	blood:	n/a	n/a
4	ARID3A	chr7:106958955-106959760	K562	blood:	n/a	n/a
5	ATF1	chr7:106962472-106962801	K562	blood:	n/a	n/a
6	ATF1	chr7:106958997-106959391	K562	blood:	n/a	n/a
7	ATF1	chr7:106960276-106960691	K562	blood:	n/a	n/a
8	ATF3	chr7:106958879-106959433	K562	blood:	n/a	n/a
9	BCL3	chr7:106914946-106915338	GM12878	blood:	n/a	n/a
10	BCL3	chr7:106914923-106915366	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:106960236-106960693	K562	blood:	n/a	n/a
12	BHLHE40	chr7:106962518-106962939	K562	blood:	n/a	n/a
13	BHLHE40	chr7:106926722-106926824	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:106958976-106959335	K562	blood:	n/a	n/a
15	CBX3	chr7:106945904-106946346	K562	blood:	n/a	n/a
16	CBX3	chr7:106962315-106963013	K562	blood:	n/a	n/a
17	CBX3	chr7:106958814-106959589	K562	blood:	n/a	n/a
18	CBX3	chr7:106960136-106960734	K562	blood:	n/a	n/a
19	CCNT2	chr7:106962546-106962844	K562	blood:	n/a	n/a
20	CCNT2	chr7:106961281-106961473	K562	blood:	n/a	n/a
21	CCNT2	chr7:106960178-106961024	K562	blood:	n/a	n/a
22	CCNT2	chr7:106959025-106959336	K562	blood:	n/a	n/a
23	CEBPB	chr7:106962079-106962860	K562	blood:	n/a	n/a
24	CEBPB	chr7:106958793-106959641	K562	blood:	n/a	n/a
25	CEBPB	chr7:106959885-106960161	K562	blood:	n/a	n/a
26	CEBPB	chr7:106943938-106944027	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:106917977-106918169	HepG2	liver:	n/a	chr7:106918089-106918100
28	CEBPB	chr7:106959048-106959287	K562	blood:	n/a	n/a
29	CEBPB	chr7:106962115-106962785	K562	blood:	n/a	n/a
30	CEBPB	chr7:106963145-106963176	K562	blood:	n/a	n/a
31	CEBPB	chr7:106960450-106960657	K562	blood:	n/a	n/a
32	CEBPB	chr7:106952849-106953212	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:106958979-106959321	IMR90	lung:	n/a	n/a
34	CEBPD	chr7:106960097-106961225	K562	blood:	n/a	n/a
35	CEBPD	chr7:106949785-106950048	K562	blood:	n/a	n/a
36	CEBPD	chr7:106960154-106961233	K562	blood:	n/a	n/a
37	CEBPD	chr7:106962318-106962884	K562	blood:	n/a	n/a
38	CEBPD	chr7:106962363-106962949	K562	blood:	n/a	n/a
39	CHD2	chr7:106899151-106899168	HepG2	liver:	n/a	n/a
40	CHD2	chr7:106958972-106959345	K562	blood:	n/a	n/a
41	CREB1	chr7:106958918-106959488	K562	blood:	n/a	n/a
42	CREB1	chr7:106958761-106959561	K562	blood:	n/a	n/a
43	CREB1	chr7:106962298-106963020	K562	blood:	n/a	n/a
44	CTCF	chr7:106931940-106932090	NHEK	skin:	n/a	n/a
45	CTCF	chr7:106958640-106958646	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr7:106905000-106905150	NB4	blood:	n/a	n/a
47	CTCF	chr7:106960313-106960336	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:106932500-106932650	GM12869	blood:	n/a	n/a
49	CTCF	chr7:106931952-106932068	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr7:106963913-106963933	MCF-7	breast:	n/a	n/a

No data

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:106959037..106960658-chr7:107219489..107223407,3	K562	blood:
2	chr7:106961525..106963597-chr7:106973933..106975827,2	K562	blood:
3	chr7:106926530..106928702-chr7:106956145..106958437,2	K562	blood:
4	chr7:106912900..106916299-chr7:106917013..106920101,3	K562	blood:
5	chr7:106926530..106928702-chr7:106956145..106958437,2	K562	blood:
6	chr7:106902439..106904593-chr7:106905205..106907557,2	K562	blood:
7	chr7:106943945..106946694-chr7:106956421..106959648,3	K562	blood:
8	chr7:106951124..106952783-chr7:106959596..106961656,2	MCF-7	breast:
9	chr7:106937175..106939993-chr7:106946887..106948924,2	K562	blood:
10	chr7:106923986..106926392-chr7:106929216..106932117,2	K562	blood:
11	chr7:106890607..106892740-chr7:106903344..106904868,2	K562	blood:
12	chr7:106909940..106911520-chr7:106918365..106920209,2	K562	blood:
13	chr7:106956489..106959227-chr7:106962952..106965707,2	K562	blood:
14	chr7:106943945..106946377-chr7:106956421..106958965,2	K562	blood:
15	chr7:106961529..106964322-chr7:106967286..106969231,2	K562	blood:
16	chr7:106909940..106911520-chr7:106918365..106920209,2	K562	blood:
17	chr7:106937175..106939993-chr7:106946887..106948924,2	K562	blood:
18	chr7:106923986..106926392-chr7:106929216..106932117,2	K562	blood:
19	chr7:106902439..106904593-chr7:106905205..106907557,2	K562	blood:
20	chr7:106951124..106952783-chr7:106959596..106961656,2	MCF-7	breast:
21	chr7:106923644..106925368-chr7:106925978..106927798,2	K562	blood:
22	chr7:106943945..106946694-chr7:106956421..106959648,3	K562	blood:
23	chr7:106910309..106913032-chr7:106924327..106926583,2	K562	blood:
24	chr7:106937807..106940017-chr7:106943156..106944916,2	MCF-7	breast:
25	chr7:106956489..106959227-chr7:106962952..106965707,2	K562	blood:
26	chr7:106934661..106938675-chr7:106946887..106950206,3	K562	blood:
27	chr7:106928239..106930553-chr7:106930960..106933126,2	MCF-7	breast:
28	chr7:106939523..106941482-chr7:106941827..106943489,2	K562	blood:
29	chr7:106939523..106941482-chr7:106941827..106943489,2	K562	blood:
30	chr7:106944112..106947438-chr7:106948348..106951754,4	K562	blood:
31	chr7:106897719..106899298-chr7:106902891..106905667,2	K562	blood:
32	chr7:106923644..106925368-chr7:106925978..106927798,2	K562	blood:
33	chr7:106910309..106913032-chr7:106924327..106926583,2	K562	blood:
34	chr7:106808462..106810785-chr7:106940399..106942038,2	MCF-7	breast:
35	chr7:106944112..106947438-chr7:106948348..106951754,4	K562	blood:
36	chr7:106928239..106930553-chr7:106930960..106933126,2	MCF-7	breast:
37	chr7:106808597..106811136-chr7:106920664..106923282,2	K562	blood:
38	chr7:106943945..106946377-chr7:106956421..106958965,2	K562	blood:
39	chr7:106937807..106940017-chr7:106943156..106944916,2	MCF-7	breast:
40	chr7:106912900..106916299-chr7:106917013..106920101,3	K562	blood:
41	chr7:106942508..106944552-chr7:106946505..106949146,2	MCF-7	breast:
42	chr7:106942508..106944552-chr7:106946505..106949146,2	MCF-7	breast:

No data

Variant related genes	Relation type
COG5	TF binding region
ENSG00000221356	TF binding region
ENSG00000105856	chromatin interactions
ENSG00000075790	chromatin interactions
ENSG00000221356	chromatin interactions
ENSG00000164597	chromatin interactions
ENSG00000272854	chromatin interactions

Extended variants
information (count: 2533 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2533 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17349904	chr7:106897237-106897238	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185473214	chr7:106897271-106897272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190091716	chr7:106897273-106897274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181035971	chr7:106897277-106897278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541597023	chr7:106897362-106897363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546393036	chr7:106897407-106897408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115097070	chr7:106897434-106897435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530162996	chr7:106897469-106897470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186016521	chr7:106897475-106897476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2395868	chr7:106897500-106897501	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs576792181	chr7:106897514-106897515	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs543800015	chr7:106897533-106897534	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs532368844	chr7:106897599-106897600	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs575483696	chr7:106897612-106897613	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs552184049	chr7:106897629-106897630	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs145605444	chr7:106897692-106897693	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs192049995	chr7:106897743-106897744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6964152	chr7:106897784-106897785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148894594	chr7:106897793-106897794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112185370	chr7:106897818-106897819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73415431	chr7:106897868-106897869	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs547777250	chr7:106897869-106897870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184113184	chr7:106897892-106897893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187730819	chr7:106897900-106897901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs367787538	chr7:106897931-106897932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569811051	chr7:106897967-106897968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538616459	chr7:106897980-106897981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs578013774	chr7:106897987-106897988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs3801963	chr7:106898036-106898037	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs147016327	chr7:106898065-106898066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535027832	chr7:106898104-106898105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77761212	chr7:106898161-106898162	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs555105421	chr7:106898162-106898163	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs574926940	chr7:106898192-106898193	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs533272252	chr7:106898208-106898209	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs544041601	chr7:106898268-106898269	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs141971940	chr7:106898281-106898282	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs529486755	chr7:106898293-106898294	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs112884006	chr7:106898294-106898295	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs569557368	chr7:106898337-106898338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545760358	chr7:106898414-106898415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10487271	chr7:106898458-106898459	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs145862124	chr7:106898465-106898466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547382261	chr7:106898500-106898501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561274132	chr7:106898518-106898519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529844015	chr7:106898536-106898537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550028602	chr7:106898606-106898607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531955773	chr7:106898615-106898616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201247119	chr7:106898616-106898617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569752296	chr7:106898622-106898623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106846000-106925800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr7:106851000-106897600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr7:106851000-106946000	Weak transcription	Esophagus	oesophagus
4	chr7:106853400-106925600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr7:106866600-106909600	Weak transcription	Placenta	Placenta
6	chr7:106874000-106917800	Weak transcription	Osteobl	bone
7	chr7:106874000-106922600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:106874000-106929200	Weak transcription	NH-A	brain
9	chr7:106874000-106945600	Weak transcription	Pancreas	Pancrea
10	chr7:106875400-106908000	Weak transcription	HMEC	breast
11	chr7:106875600-106898400	Weak transcription	HUVEC	blood vessel
12	chr7:106883000-106918800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:106883400-106910200	Weak transcription	Lung	lung
14	chr7:106883400-106911400	Weak transcription	Right Ventricle	heart
15	chr7:106885000-106897800	Weak transcription	Fetal Thymus	thymus
16	chr7:106886400-106971400	Weak transcription	Fetal Muscle Trunk	muscle
17	chr7:106886800-106946000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:106887000-106935800	Weak transcription	Small Intestine	intestine
19	chr7:106887400-106898200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:106887600-106910200	Weak transcription	Adipose Nuclei	Adipose
21	chr7:106887600-106910400	Weak transcription	Psoas Muscle	Psoas
22	chr7:106887800-106903000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:106888400-106900600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr7:106888600-106899000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:106888600-106910000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr7:106888600-106926600	Weak transcription	Ovary	ovary
27	chr7:106888600-106930800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr7:106888600-106931600	Weak transcription	Dnd41	blood
29	chr7:106888800-106897600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:106888800-106910200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr7:106888800-106910200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:106888800-106910200	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr7:106888800-106911400	Weak transcription	Fetal Intestine Small	intestine
34	chr7:106888800-106913200	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr7:106888800-106917400	Weak transcription	HSMM	muscle
36	chr7:106888800-106930800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:106888800-106932000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:106888800-106933400	Weak transcription	Fetal Stomach	stomach
39	chr7:106888800-106946000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:106888800-106946200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr7:106888800-106999400	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr7:106889000-106900800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr7:106889000-106902600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:106889000-106910200	Weak transcription	Fetal Muscle Leg	muscle
45	chr7:106889000-106933400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:106889000-106934400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr7:106889200-106898800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr7:106889200-106910200	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr7:106889200-106914800	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr7:106889200-106922600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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