Variant report

Variant	nsv899136
Chromosome Location	chr12:60373244-60483607
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 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	chr12:60471816-60472199	K562	blood:	n/a	n/a
2	BHLHE40	chr12:60471887-60471910	GM12878	blood:	n/a	n/a
3	CEBPB	chr12:60428205-60428348	A549	lung:	n/a	chr12:60428277-60428288
4	CEBPB	chr12:60394344-60394410	A549	lung:	n/a	n/a
5	CEBPB	chr12:60428211-60428406	HepG2	liver:	n/a	chr12:60428277-60428288
6	CEBPB	chr12:60399603-60399803	A549	lung:	n/a	n/a
7	CEBPB	chr12:60464408-60464802	MCF-7	breast:	n/a	n/a
8	CTCF	chr12:60453040-60453190	NHEK	skin:	n/a	n/a
9	CTCF	chr12:60431540-60431690	HCT-116	colon:	n/a	n/a
10	CTCF	chr12:60415191-60415194	MCF-7	breast:	n/a	n/a
11	CTCF	chr12:60415195-60415245	MCF-7	breast:	n/a	n/a
12	CTCF	chr12:60470260-60470410	A549	lung:	n/a	n/a
13	CTCF	chr12:60453060-60453210	HCFaa	heart:	n/a	n/a
14	CTCF	chr12:60463523-60463609	Lung_OC	lung:	n/a	n/a
15	CTCF	chr12:60394112-60394149	GM10248	blood:	n/a	n/a
16	CTCF	chr12:60431569-60431633	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr12:60415080-60415230	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:60453060-60453210	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr12:60453060-60453210	SAEC	small airway:	n/a	n/a
20	CTCF	chr12:60394160-60394187	GM13976	blood:	n/a	n/a
21	CTCF	chr12:60453000-60453150	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:60453040-60453190	AG04450	lung:	n/a	n/a
23	CTCF	chr12:60452980-60453130	AG04450	lung:	n/a	n/a
24	CTCF	chr12:60453060-60453210	HMF	breast:	n/a	n/a
25	CTCF	chr12:60415160-60415310	AG09309	skin:	n/a	n/a
26	CTCF	chr12:60452960-60453110	HCT-116	colon:	n/a	n/a
27	CTCF	chr12:60453040-60453190	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr12:60452940-60453090	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:60453000-60453150	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr12:60399040-60399190	GM06990	blood:	n/a	n/a
31	CTCF	chr12:60453060-60453210	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr12:60431533-60431672	GM12878	blood:	n/a	n/a
33	CTCF	chr12:60453100-60453250	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr12:60477446-60477528	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:60453040-60453190	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr12:60393364-60393506	GM12878	blood:	n/a	n/a
37	CTCF	chr12:60471701-60471732	GM13976	blood:	n/a	n/a
38	CTCF	chr12:60453060-60453210	HMEC	breast:	n/a	n/a
39	E2F4	chr12:60459063-60459331	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr12:60399741-60399899	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr12:60438565-60438706	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr12:60459734-60459892	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr12:60464284-60464649	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr12:60408741-60408749	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr12:60429046-60429069	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr12:60470080-60470120	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr12:60381430-60381766	GM12878	blood:	n/a	chr12:60381591-60381602
48	EBF1	chr12:60465450-60465794	GM12878	blood:	n/a	n/a
49	ELF1	chr12:60435873-60436243	K562	blood:	n/a	chr12:60436015-60436028
50	EP300	chr12:60465597-60466133	MCF-7	breast:	n/a	n/a

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:60481263..60483527-chr12:60485827..60488653,2	K562	blood:
2	chr12:60471895..60473733-chr12:60474074..60477071,2	MCF-7	breast:
3	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
4	chr12:60466814..60469463-chr12:60479017..60481348,2	MCF-7	breast:
5	chr12:60473802..60475803-chr12:60480234..60482937,2	MCF-7	breast:
6	chr12:60468174..60469728-chr12:60471025..60473459,2	MCF-7	breast:
7	chr12:60471895..60473733-chr12:60474074..60477071,2	MCF-7	breast:
8	chr12:60466814..60469463-chr12:60479017..60481348,2	MCF-7	breast:
9	chr12:60472741..60475079-chr12:60479250..60481071,2	K562	blood:
10	chr12:60459856..60461380-chr12:60466711..60469397,2	MCF-7	breast:
11	chr12:60478315..60480971-chr12:60488037..60490719,3	MCF-7	breast:
12	chr12:60472741..60475079-chr12:60479250..60481071,2	K562	blood:
13	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
14	chr12:60419898..60420453-chr14:61344505..61345184,2	MCF-7	breast:
15	chr12:60459856..60461380-chr12:60466711..60469397,2	MCF-7	breast:
16	chr12:60437721..60438429-chr8:43096750..43097250,2	MCF-7	breast:
17	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
18	chr12:60424657..60427143-chr12:60427851..60429693,2	MCF-7	breast:
19	chr12:60461970..60464211-chr12:60465232..60466795,2	MCF-7	breast:
20	chr12:60460447..60462196-chr12:60466989..60469396,2	K562	blood:
21	chr12:60439937..60442180-chr12:60446699..60448272,2	MCF-7	breast:
22	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
23	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
24	chr12:60424657..60427143-chr12:60427851..60429693,2	MCF-7	breast:
25	chr12:60463450..60465824-chr12:60478986..60481258,2	MCF-7	breast:
26	chr12:60468174..60469728-chr12:60471025..60473459,2	MCF-7	breast:
27	chr12:60465097..60467873-chr12:60470417..60472937,3	MCF-7	breast:
28	chr12:60465097..60467873-chr12:60470417..60472937,3	MCF-7	breast:
29	chr12:60464696..60468583-chr12:60490353..60494821,4	MCF-7	breast:
30	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
31	chr12:60366694..60369623-chr12:60371578..60373431,2	MCF-7	breast:
32	chr12:60461970..60464211-chr12:60465232..60466795,2	MCF-7	breast:
33	chr12:60460447..60462196-chr12:60466989..60469396,2	K562	blood:
34	chr12:60466885..60469119-chr12:60493136..60496064,3	MCF-7	breast:
35	chr12:60463450..60465824-chr12:60478986..60481258,2	MCF-7	breast:
36	chr1:107703503..107704327-chr12:60399253..60400075,2	MCF-7	breast:
37	chr12:60439937..60442180-chr12:60446699..60448272,2	MCF-7	breast:
38	chr12:60473802..60475803-chr12:60480234..60482937,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000257294	TF binding region
ENSG00000264437	TF binding region
ENSG00000257294	chromatin interactions

Extended variants
information (count: 3470 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3470 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4432063	chr12:60373244-60373245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141562517	chr12:60373316-60373317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528077310	chr12:60373317-60373318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557453874	chr12:60373333-60373334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs578057406	chr12:60373357-60373358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534234764	chr12:60373374-60373375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556649636	chr12:60373375-60373376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187781704	chr12:60373412-60373413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147523339	chr12:60373413-60373414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554213849	chr12:60373460-60373461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7970962	chr12:60373514-60373515	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs543324072	chr12:60373548-60373549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573409128	chr12:60373563-60373564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542377524	chr12:60373582-60373583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190243739	chr12:60373599-60373600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571200198	chr12:60373602-60373603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374382212	chr12:60373629-60373630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182420356	chr12:60373753-60373754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79267979	chr12:60373771-60373772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187458585	chr12:60373822-60373823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138471101	chr12:60373824-60373825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs17574734	chr12:60373831-60373832	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs567730267	chr12:60373916-60373917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191882200	chr12:60374050-60374051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116940015	chr12:60374051-60374052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368365910	chr12:60374130-60374131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570299827	chr12:60374131-60374132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538955168	chr12:60374153-60374154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543957677	chr12:60374215-60374216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12319889	chr12:60374231-60374232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143952863	chr12:60374285-60374286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184733822	chr12:60374295-60374296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188928220	chr12:60374304-60374305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193247416	chr12:60374328-60374329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11173261	chr12:60374358-60374359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200215869	chr12:60374373-60374374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116026769	chr12:60374391-60374392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573372617	chr12:60374413-60374414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542340820	chr12:60374443-60374444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12320017	chr12:60374472-60374473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs207472963	chr12:60374475-60374476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562327012	chr12:60374499-60374500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184462028	chr12:60374504-60374505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147273903	chr12:60374589-60374590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565137916	chr12:60374610-60374611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527598296	chr12:60374643-60374644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372320681	chr12:60374660-60374661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532762357	chr12:60374671-60374672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139749339	chr12:60374688-60374689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561297452	chr12:60374712-60374713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60368200-60373600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr12:60368400-60376600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:60373600-60375600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:60374400-60375400	Enhancers	NHDF-Ad	bronchial
5	chr12:60375400-60375600	Bivalent Enhancer	Aorta	Aorta
6	chr12:60376600-60377400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:60377400-60403800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:60382800-60383600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:60387000-60387400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:60391000-60392600	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr12:60391200-60392600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:60391200-60392800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr12:60391400-60392800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:60391600-60392000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr12:60391800-60392600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr12:60392600-60395200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:60395200-60395400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:60401200-60401600	Enhancers	Fetal Brain Female	brain
19	chr12:60404000-60405000	Enhancers	Fetal Intestine Small	intestine
20	chr12:60404000-60405200	Enhancers	Fetal Intestine Large	intestine
21	chr12:60404200-60404800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:60404400-60404800	Enhancers	Stomach Mucosa	stomach
23	chr12:60404800-60408000	Weak transcription	Stomach Mucosa	stomach
24	chr12:60405000-60407400	Weak transcription	Fetal Intestine Small	intestine
25	chr12:60405200-60408200	Weak transcription	Fetal Intestine Large	intestine
26	chr12:60407400-60408800	Enhancers	Fetal Intestine Small	intestine
27	chr12:60408000-60408800	Enhancers	Stomach Mucosa	stomach
28	chr12:60408200-60408800	Enhancers	Duodenum Mucosa	Duodenum
29	chr12:60408200-60409000	Enhancers	Fetal Intestine Large	intestine
30	chr12:60408800-60420600	Weak transcription	Fetal Intestine Small	intestine
31	chr12:60413200-60414200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:60414200-60418400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:60418400-60422000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:60419600-60427000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:60420600-60421600	Enhancers	Fetal Intestine Small	intestine
36	chr12:60426800-60428200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:60427000-60428200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:60427400-60427800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:60427400-60428200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr12:60428200-60429800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:60428800-60430800	Enhancers	HUVEC	blood vessel
42	chr12:60429400-60430200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:60429400-60430400	Enhancers	NHEK	skin
44	chr12:60429400-60430600	Enhancers	HMEC	breast
45	chr12:60429800-60430400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr12:60429800-60430600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:60429800-60430600	Enhancers	NHDF-Ad	bronchial
48	chr12:60436600-60437000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:60436800-60437000	Enhancers	HUVEC	blood vessel
50	chr12:60437000-60437400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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