Variant report

Variant	nsv427905
Chromosome Location	chr12:20942215-21117820
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	ARID3A	chr12:20983563-20983814	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:20961418-20961995	HepG2	liver:	n/a	n/a
3	BATF	chr12:21021928-21022137	GM12878	blood:	n/a	chr12:21022019-21022030
4	BATF	chr12:21090344-21090547	GM12878	blood:	n/a	n/a
5	BCL3	chr12:20983287-20983862	A549	lung:	n/a	n/a
6	BHLHE40	chr12:21017099-21017177	GM12878	blood:	n/a	n/a
7	BRCA1	chr12:20975364-20975513	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr12:20946993-20947034	HepG2	liver:	n/a	n/a
9	BRCA1	chr12:21103222-21103500	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:21114301-21114316	A549	lung:	n/a	n/a
11	CEBPB	chr12:21037942-21038507	A549	lung:	n/a	n/a
12	CEBPB	chr12:20983601-20983801	Hela-S3	cervix:	n/a	chr12:20983711-20983722
13	CEBPB	chr12:21036286-21036659	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
14	CEBPB	chr12:20983561-20984147	A549	lung:	n/a	chr12:20983711-20983722
15	CEBPB	chr12:21056070-21056238	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:20982312-20982493	IMR90	lung:	n/a	chr12:20982413-20982424
17	CEBPB	chr12:21038089-21038427	A549	lung:	n/a	n/a
18	CEBPB	chr12:20975368-20976107	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:21065012-21065124	HepG2	liver:	n/a	chr12:21065034-21065045
20	CEBPB	chr12:21036323-21036549	HepG2	liver:	n/a	chr12:21036463-21036474
21	CEBPB	chr12:21015510-21015751	A549	lung:	n/a	n/a
22	CEBPB	chr12:20982284-20982555	A549	lung:	n/a	chr12:20982413-20982424
23	CEBPB	chr12:20961578-20961819	HepG2	liver:	n/a	chr12:20961744-20961757
24	CEBPB	chr12:20961440-20961862	HepG2	liver:	n/a	chr12:20961744-20961757
25	CEBPB	chr12:21036282-21036646	Hela-S3	cervix:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
26	CEBPB	chr12:20983497-20983867	A549	lung:	n/a	chr12:20983711-20983722
27	CEBPB	chr12:20991943-20992076	A549	lung:	n/a	chr12:20992038-20992049
28	CEBPB	chr12:21036268-21036667	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
29	CEBPB	chr12:20961462-20961896	HepG2	liver:	n/a	chr12:20961744-20961757
30	CEBPB	chr12:20983420-20984015	A549	lung:	n/a	chr12:20983711-20983722
31	CEBPB	chr12:20983564-20983877	HepG2	liver:	n/a	chr12:20983711-20983722
32	CEBPB	chr12:21071557-21071721	A549	lung:	n/a	n/a
33	CEBPB	chr12:20975351-20976142	A549	lung:	n/a	n/a
34	CEBPB	chr12:21038060-21038439	A549	lung:	n/a	n/a
35	CEBPB	chr12:20991877-20992081	HepG2	liver:	n/a	chr12:20992038-20992049
36	CEBPB	chr12:21036155-21036832	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
37	CEBPB	chr12:20982280-20982503	HepG2	liver:	n/a	chr12:20982413-20982424
38	CHD2	chr12:20975360-20975559	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr12:21022154-21022253	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:21103300-21103450	HMF	breast:	n/a	n/a
41	CTCF	chr12:21057658-21057757	GM10248	blood:	n/a	n/a
42	CTCF	chr12:21102860-21103010	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr12:20951600-20951750	NHLF	lung:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
44	CTCF	chr12:21009590-21009613	GM20000	blood:	n/a	n/a
45	CTCF	chr12:21099800-21099950	AG10803	skin:	n/a	chr12:21099862-21099883 chr12:21099861-21099877 chr12:21099860-21099878 chr12:21099863-21099872
46	CTCF	chr12:20951680-20951830	RPTEC	kidney:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
47	CTCF	chr12:21099747-21099980	MCF-7	breast:	n/a	chr12:21099862-21099883 chr12:21099861-21099877 chr12:21099860-21099878 chr12:21099863-21099872
48	CTCF	chr12:21102960-21103110	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr12:21009487-21009574	LNCaP	prostate:	n/a	n/a
50	CTCF	chr12:21022153-21022245	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:20966524-20966574	Jurkat	blood:	n/a
2	chr12:20960446-20960496	NHDF-neo	bronchial:	n/a
3	chr12:20966524-20966574	Jurkat	blood:	n/a
4	chr12:20960446-20960496	NHDF-neo	bronchial:	n/a
5	chr12:20960409-20960459	HL-60	blood:	n/a
6	chr12:21014317-21014367	HepG2	liver:	n/a
7	chr12:20966439-20966489	HepG2	liver:	n/a
8	chr12:20960409-20960459	NT2-D1	testis:	n/a
9	chr12:20960409-20960459	CMK	blood:	n/a
10	chr12:20966439-20966489	SKMC	muscle:	n/a
11	chr12:20983111-20983161	GM06990	blood:	n/a
12	chr12:21015340-21015390	MCF10A-Er-Src	breast:	n/a
13	chr12:20962423-20962473	RPTEC	kidney:	n/a
14	chr12:20966524-20966574	ovcar-3	ovarian:	n/a
15	chr12:20966439-20966489	HIPEpiC	eye:	n/a
16	chr12:20962423-20962473	GM19239	blood:	n/a
17	chr12:20966439-20966489	ECC-1	luminal epithelium:	n/a
18	chr12:20960446-20960496	AG04450	lung:	fetal
19	chr12:20966524-20966574	RPTEC	kidney:	n/a
20	chr12:20966524-20966574	GM12892	blood:	n/a
21	chr12:20966439-20966489	RPTEC	kidney:	n/a
22	chr12:20966524-20966574	ECC-1	luminal epithelium:	n/a
23	chr12:20983111-20983161	Hela-S3	cervix:	n/a
24	chr12:20966439-20966489	Caco-2	colon:	n/a
25	chr12:20962423-20962473	NHDF-neo	bronchial:	n/a
26	chr12:21014317-21014367	GM12878	blood:	n/a
27	chr12:20960446-20960496	H1-hESC	embryonic stem cell:	embryo
28	chr12:20966439-20966489	NT2-D1	testis:	n/a
29	chr12:20983111-20983161	HCF	heart:	n/a
30	chr12:20962423-20962473	SAEC	small airway:	n/a
31	chr12:21015340-21015390	GM12892	blood:	n/a
32	chr12:20966524-20966574	GM12891	blood:	n/a
33	chr12:20960446-20960496	HCPEpiC	choroid plexus:	n/a
34	chr12:20966439-20966489	HEEpiC	esophagus:	n/a
35	chr12:21014317-21014367	BE2_C	brain:	n/a
36	chr12:20960409-20960459	NHBE	bronchial:	n/a
37	chr12:20960409-20960459	BE2_C	brain:	n/a
38	chr12:20983111-20983161	T-47D	breast:	n/a
39	chr12:20960409-20960459	HCM	heart:	n/a
40	chr12:20983111-20983161	AG09319	gingival:	n/a
41	chr12:21015340-21015390	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:20983111-20983161	ovcar-3	ovarian:	n/a
43	chr12:20960409-20960459	SK-N-SH	brain:	n/a
44	chr12:20960409-20960459	PANC-1	pancreas:	n/a
45	chr12:20960409-20960459	T-47D	breast:	n/a
46	chr12:20960446-20960496	HNPCEpiC	eye:	n/a
47	chr12:20962423-20962473	H1-hESC	embryonic stem cell:	embryo
48	chr12:20966439-20966489	BE2_C	brain:	n/a
49	chr12:20960446-20960496	AG10803	skin:	n/a
50	chr12:20960446-20960496	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:20798864..20799798-chr12:20951213..20952118,4	MCF-7	breast:
2	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
3	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
4	chr12:20639028..20639571-chr12:20951385..20952022,2	MCF-7	breast:
5	chr12:20798899..20799416-chr12:20951641..20952181,2	MCF-7	breast:
6	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:
7	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:
8	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1A2-5	chr12:21083248-21084757	NONHSAT027238

Variant related genes	Relation type
ENSG00000256157	TF binding region
SLCO1B7	TF binding region
SLCO1B3	TF binding region
ENSG00000257046	TF binding region
ENSG00000256157	CpG island
SLCO1B7	CpG island
SLCO1B3	CpG island
ENSG00000257046	CpG island

Extended variants
information (count: 7462 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:7462 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148652613	chr12:20942613-20942614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542925402	chr12:20942632-20942633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144421745	chr12:20942651-20942652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147835086	chr12:20942681-20942682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569066236	chr12:20942682-20942683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564199835	chr12:20942689-20942690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139765656	chr12:20942696-20942697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530619197	chr12:20942697-20942698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112632599	chr12:20942767-20942768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191094327	chr12:20942775-20942776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115306878	chr12:20942778-20942779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530343552	chr12:20942803-20942804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546862114	chr12:20942823-20942824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567060081	chr12:20942903-20942904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112747978	chr12:20942933-20942934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369196359	chr12:20942934-20942935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145312110	chr12:20942943-20942944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555036167	chr12:20942976-20942977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551138215	chr12:20942993-20942994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4762784	chr12:20943011-20943012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs542964093	chr12:20943074-20943075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs151244003	chr12:20943092-20943093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2082524	chr12:20943095-20943096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12821015	chr12:20943096-20943097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140456886	chr12:20943111-20943112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565069071	chr12:20943118-20943119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564683338	chr12:20943119-20943120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530553867	chr12:20943137-20943138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553304675	chr12:20943173-20943174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543870223	chr12:20943203-20943204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560573536	chr12:20943233-20943234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529597949	chr12:20943255-20943256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74067212	chr12:20943258-20943259	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs187330175	chr12:20943262-20943263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115525436	chr12:20943292-20943293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112823597	chr12:20943299-20943300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59465808	chr12:20943305-20943306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs2099368	chr12:20943318-20943319	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs150416584	chr12:20943325-20943326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555071023	chr12:20943343-20943344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558965438	chr12:20943439-20943440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11045497	chr12:20943463-20943464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs534141907	chr12:20943496-20943497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145252069	chr12:20943500-20943501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573100497	chr12:20943501-20943502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545272836	chr12:20943507-20943508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558489502	chr12:20943514-20943515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149175368	chr12:20943552-20943553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191754857	chr12:20943556-20943557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12823467	chr12:20943576-20943577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:74)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20942600-20961200	Weak transcription	A549	lung
2	chr12:20949400-20949600	Enhancers	Brain Anterior Caudate	brain
3	chr12:20951200-20951600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr12:20951200-20951600	Enhancers	Liver	Liver
5	chr12:20951200-20952000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:20951200-20953000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:20951400-20951600	Enhancers	Adipose Nuclei	Adipose
8	chr12:20951600-20952800	Weak transcription	Adipose Nuclei	Adipose
9	chr12:20951600-20953200	Weak transcription	Liver	Liver
10	chr12:20951800-20952200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:20952000-20953000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:20952800-20953400	Enhancers	Adipose Nuclei	Adipose
13	chr12:20953000-20953200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr12:20953000-20953600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:20953000-20954600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr12:20953200-20953600	Enhancers	Liver	Liver
17	chr12:20953200-20958000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr12:20953600-20954600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:20954600-20957800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:20954600-20957800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:20957000-20957200	Enhancers	Primary hematopoietic stem cells	blood
22	chr12:20957200-20957800	Weak transcription	Primary hematopoietic stem cells	blood
23	chr12:20957800-20959800	Enhancers	Primary hematopoietic stem cells	blood
24	chr12:20957800-20961200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:20957800-20962400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:20958000-20960000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr12:20959600-20959800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:20959800-20960800	Weak transcription	Primary hematopoietic stem cells	blood
29	chr12:20960000-20960800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr12:20960200-20961000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr12:20960800-20961000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:20960800-20961800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr12:20960800-20962400	Enhancers	Primary hematopoietic stem cells	blood
34	chr12:20961000-20961400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr12:20961000-20961400	Enhancers	Liver	Liver
36	chr12:20961200-20962000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:20961200-20962000	Strong transcription	A549	lung
38	chr12:20961400-20961800	Enhancers	Fetal Kidney	kidney
39	chr12:20961400-20962200	Flanking Active TSS	Liver	Liver
40	chr12:20961400-20962400	Enhancers	HepG2	liver
41	chr12:20962000-20963000	Weak transcription	A549	lung
42	chr12:20962000-20965000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:20962200-20963000	Enhancers	Liver	Liver
44	chr12:20962400-20962800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr12:20962400-20964000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:20963000-20963200	Flanking Active TSS	Liver	Liver
47	chr12:20963000-20964200	Enhancers	A549	lung
48	chr12:20963200-20964600	Active TSS	Liver	Liver
49	chr12:20964000-20964800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:20964200-20964600	Flanking Active TSS	A549	lung

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