Variant report

Variant	nsv1048951
Chromosome Location	chr12:73018354-73151893
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:285)
CpG islands
(count:185)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:73071729-73071865	K562	blood:	n/a	n/a
2	ATF2	chr12:73040903-73041319	GM12878	blood:	n/a	n/a
3	ATF2	chr12:73067526-73068137	GM12878	blood:	n/a	n/a
4	BACH1	chr12:73074983-73075111	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:73085107-73085586	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:73040940-73041214	GM12878	blood:	n/a	n/a
7	BCLAF1	chr12:73067501-73068061	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:73067799-73068001	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:73085142-73085302	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:73066581-73066626	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:73069299-73069320	GM12878	blood:	n/a	n/a
12	BRCA1	chr12:73036607-73036730	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:73121205-73121535	IMR90	lung:	n/a	chr12:73121373-73121386 chr12:73121375-73121386 chr12:73121373-73121386 chr12:73121373-73121386 chr12:73121375-73121386
14	CEBPB	chr12:73026095-73026405	IMR90	lung:	n/a	chr12:73026256-73026269
15	CEBPB	chr12:73063480-73063680	HepG2	liver:	n/a	chr12:73063547-73063560 chr12:73063601-73063618
16	CEBPB	chr12:73074666-73074866	A549	lung:	n/a	chr12:73074782-73074795 chr12:73074779-73074796
17	CEBPB	chr12:73020979-73021186	HepG2	liver:	n/a	chr12:73021076-73021087
18	CEBPB	chr12:73058184-73058384	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr12:73067777-73067994	GM12878	blood:	n/a	n/a
20	CTCF	chr12:73093460-73093610	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr12:73093220-73093370	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr12:73093260-73093410	HMEC	breast:	n/a	n/a
23	CTCF	chr12:73093240-73093390	NB4	blood:	n/a	n/a
24	CTCF	chr12:73093268-73093434	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:73093240-73093390	GM12872	blood:	n/a	n/a
26	CTCF	chr12:73093240-73093390	GM12870	blood:	n/a	n/a
27	CTCF	chr12:73091100-73091250	NHLF	lung:	n/a	n/a
28	CTCF	chr12:73093280-73093430	GM12873	blood:	n/a	n/a
29	CTCF	chr12:73093240-73093390	GM12869	blood:	n/a	n/a
30	CTCF	chr12:73093280-73093430	GM12878	blood:	n/a	n/a
31	CTCF	chr12:73093220-73093370	GM12873	blood:	n/a	n/a
32	CTCF	chr12:73093300-73093450	GM12872	blood:	n/a	n/a
33	CTCF	chr12:73031470-73031506	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr12:73093280-73093430	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr12:73093180-73093330	BJ	skin:	n/a	n/a
36	CTCF	chr12:73093292-73093294	A549	lung:	n/a	n/a
37	CTCF	chr12:73093280-73093430	HL-60	blood:	n/a	n/a
38	CTCF	chr12:73093280-73093430	HEK293	kidney:	n/a	n/a
39	CTCF	chr12:73093301-73093403	A549	lung:	n/a	n/a
40	CTCF	chr12:73093300-73093450	BE2_C	brain:	n/a	n/a
41	CTCF	chr12:73093260-73093410	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:73093260-73093423	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:73093220-73093370	GM12878	blood:	n/a	n/a
44	CTCF	chr12:73093280-73093430	AG04450	lung:	n/a	n/a
45	CTCF	chr12:73093316-73093376	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:73093180-73093330	AG04449	skin:	n/a	n/a
47	CTCF	chr12:73093260-73093410	Caco-2	colon:	n/a	n/a
48	CTCF	chr12:73093300-73093450	GM12864	blood:	n/a	n/a
49	CTCF	chr12:73093240-73093390	GM12867	blood:	n/a	n/a
50	CTCF	chr12:73090763-73090864	GM10248	blood:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:73057369-73057419	GM12878	blood:	n/a
2	chr12:73085225-73085275	GM19239	blood:	n/a
3	chr12:73057369-73057419	GM12878	blood:	n/a
4	chr12:73085225-73085275	GM19239	blood:	n/a
5	chr12:73057369-73057419	RPTEC	kidney:	n/a
6	chr12:73057369-73057419	NH-A	brain:	n/a
7	chr12:73057369-73057419	HL-60	blood:	n/a
8	chr12:73085225-73085275	NHBE	bronchial:	n/a
9	chr12:73034008-73034058	Hepatocyte	liver:	n/a
10	chr12:73034008-73034058	SKMC	muscle:	n/a
11	chr12:73085225-73085275	HL-60	blood:	n/a
12	chr12:73085225-73085275	Jurkat	blood:	n/a
13	chr12:73057369-73057419	NHBE	bronchial:	n/a
14	chr12:73034008-73034058	GM12891	blood:	n/a
15	chr12:73057369-73057419	SK-N-SH_RA	brain:	n/a
16	chr12:73085225-73085275	K562	blood:	n/a
17	chr12:73057369-73057419	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:73057369-73057419	BJ	skin:	n/a
19	chr12:73057369-73057419	HAEpiC	amniotic membrane:	n/a
20	chr12:73034008-73034058	HCM	heart:	n/a
21	chr12:73085225-73085275	AG10803	skin:	n/a
22	chr12:73085225-73085275	ECC-1	luminal epithelium:	n/a
23	chr12:73034008-73034058	CMK	blood:	n/a
24	chr12:73034008-73034058	NT2-D1	testis:	n/a
25	chr12:73034008-73034058	HAEpiC	amniotic membrane:	n/a
26	chr12:73085225-73085275	GM12892	blood:	n/a
27	chr12:73057369-73057419	HCF	heart:	n/a
28	chr12:73034008-73034058	AoSMC	blood vessel:	n/a
29	chr12:73085225-73085275	U87	brain:	n/a
30	chr12:73057369-73057419	HepG2	liver:	n/a
31	chr12:73057369-73057419	K562	blood:	n/a
32	chr12:73057369-73057419	CMK	blood:	n/a
33	chr12:73034008-73034058	A549	lung:	n/a
34	chr12:73085225-73085275	Hepatocyte	liver:	n/a
35	chr12:73034008-73034058	K562	blood:	n/a
36	chr12:73057369-73057419	PFSK-1	brain:	n/a
37	chr12:73085225-73085275	HAEpiC	amniotic membrane:	n/a
38	chr12:73034008-73034058	ProgFib	skin:	n/a
39	chr12:73034008-73034058	RPTEC	kidney:	n/a
40	chr12:73085225-73085275	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:73034008-73034058	HNPCEpiC	eye:	n/a
42	chr12:73085225-73085275	SAEC	small airway:	n/a
43	chr12:73085225-73085275	LNCaP	prostate:	n/a
44	chr12:73034008-73034058	MCF10A-Er-Src	breast:	n/a
45	chr12:73057369-73057419	GM12891	blood:	n/a
46	chr12:73085225-73085275	MCF-7	breast:	n/a
47	chr12:73034008-73034058	AG09309	skin:	n/a
48	chr12:73085225-73085275	AoSMC	blood vessel:	n/a
49	chr12:73034008-73034058	PANC-1	pancreas:	n/a
50	chr12:73034008-73034058	GM19239	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:73066407..73068991-chr12:73070185..73072919,2	K562	blood:
2	chr12:73050089..73050693-chr4:90478139..90478639,2	MCF-7	breast:
3	chr12:73066407..73068991-chr12:73070185..73072919,2	K562	blood:
4	chr1:110863042..110863616-chr12:73109953..73110460,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFC3H1-14	chr12:73061098-73061371	NONHSAT029474
2	lnc-ZFC3H1-7	chr12:73122565-73122624	ENSG00000258235.1
3	lnc-ZFC3H1-7	chr12:73121703-73122023	ENSG00000258235.1
4	lnc-ZFC3H1-15	chr12:73065223-73065430	NONHSAT029475

No data

Variant related genes	Relation type
ENSG00000258235	TF binding region
ENSG00000258235	CpG island

Extended variants
information (count: 3799 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3799 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145351794	chr12:73018391-73018392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142598050	chr12:73018394-73018395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs71752741	chr12:73018418-73018419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560450261	chr12:73018427-73018428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572281903	chr12:73018429-73018430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34436749	chr12:73018452-73018453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11179288	chr12:73018453-73018454	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs531696551	chr12:73018490-73018491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549868758	chr12:73018508-73018509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562129728	chr12:73018513-73018514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181706100	chr12:73018561-73018562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547647975	chr12:73018617-73018618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566014026	chr12:73018631-73018632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186010792	chr12:73018633-73018634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146917068	chr12:73018679-73018680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs67915101	chr12:73018714-73018715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs398038886	chr12:73018724-73018725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533499707	chr12:73018763-73018764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191216010	chr12:73018766-73018767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs66495167	chr12:73018774-73018775	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs183341720	chr12:73018807-73018808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555026827	chr12:73018827-73018828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188896096	chr12:73018973-73018974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139014004	chr12:73018977-73018978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35546768	chr12:73018981-73018982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566844588	chr12:73018993-73018994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554036952	chr12:73018995-73018996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572456202	chr12:73019011-73019012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190801697	chr12:73019034-73019035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182711125	chr12:73019053-73019054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564352236	chr12:73019110-73019111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576094382	chr12:73019118-73019119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200930973	chr12:73019242-73019243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543919212	chr12:73019261-73019262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537006220	chr12:73019314-73019315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562069739	chr12:73019348-73019349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11179289	chr12:73019354-73019355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs541107381	chr12:73019374-73019375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11179290	chr12:73019405-73019406	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs569490747	chr12:73019522-73019523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61933808	chr12:73019563-73019564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533266950	chr12:73019567-73019568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141582249	chr12:73019607-73019608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569879132	chr12:73019652-73019653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148111073	chr12:73019693-73019694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557960172	chr12:73019696-73019697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567281160	chr12:73019697-73019698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188053785	chr12:73019698-73019699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562734450	chr12:73019744-73019745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552556309	chr12:73019765-73019766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Autism	20685689	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:73005000-73051600	Weak transcription	Fetal Intestine Large	intestine
2	chr12:73005200-73038000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr12:73005200-73053200	Weak transcription	Ovary	ovary
4	chr12:73011400-73059000	Weak transcription	Pancreas	Pancrea
5	chr12:73014400-73042000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:73014800-73055800	Weak transcription	Adipose Nuclei	Adipose
7	chr12:73015200-73019000	Weak transcription	Fetal Intestine Small	intestine
8	chr12:73017600-73018400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr12:73017800-73018600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr12:73018400-73018600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr12:73020400-73022800	Weak transcription	NH-A	brain
12	chr12:73024000-73024200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr12:73024400-73025600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr12:73025600-73026800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr12:73026200-73026600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr12:73026200-73026800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr12:73026600-73027400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr12:73035600-73036000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr12:73035600-73037200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:73038000-73038800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr12:73038400-73038800	ZNF genes & repeats	Fetal Intestine Small	intestine
22	chr12:73038800-73053600	Weak transcription	Fetal Intestine Small	intestine
23	chr12:73038800-73053800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:73048200-73055200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:73051600-73052000	Strong transcription	Fetal Intestine Large	intestine
26	chr12:73052000-73060800	Weak transcription	Fetal Intestine Large	intestine
27	chr12:73053600-73054800	Strong transcription	Fetal Intestine Small	intestine
28	chr12:73053800-73054200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr12:73054200-73058400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr12:73054800-73056400	Weak transcription	Fetal Intestine Small	intestine
31	chr12:73058000-73058600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr12:73058000-73058600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr12:73058000-73058800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr12:73066200-73067200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr12:73066200-73067200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:73066200-73067200	Enhancers	Primary B cells from cord blood	blood
37	chr12:73066800-73069000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr12:73067000-73067600	Enhancers	GM12878-XiMat	blood
39	chr12:73067200-73067600	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr12:73067200-73071000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:73067400-73071400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr12:73067600-73068000	Active TSS	GM12878-XiMat	blood
43	chr12:73067600-73069800	Enhancers	Primary B cells from cord blood	blood
44	chr12:73068000-73068600	Flanking Active TSS	GM12878-XiMat	blood
45	chr12:73068600-73068800	Enhancers	GM12878-XiMat	blood
46	chr12:73069000-73070800	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr12:73069400-73069600	Enhancers	Liver	Liver
48	chr12:73069600-73070600	Weak transcription	Liver	Liver
49	chr12:73069800-73071200	Weak transcription	Primary B cells from cord blood	blood
50	chr12:73070400-73071400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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