Variant report

Variant	nsv898644
Chromosome Location	chr12:7873411-7993316
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:944)
CpG islands
(count:1834)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:944 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:7984728-7985022	K562	blood:	n/a	n/a
2	ARID3A	chr12:7959526-7959828	K562	blood:	n/a	n/a
3	ARID3A	chr12:7984707-7984990	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:7959548-7959804	HepG2	liver:	n/a	n/a
5	BACH1	chr12:7915505-7915636	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr12:7884222-7884269	HepG2	liver:	n/a	n/a
7	BHLHE40	chr12:7884232-7884425	K562	blood:	n/a	n/a
8	BHLHE40	chr12:7959591-7959830	K562	blood:	n/a	n/a
9	BHLHE40	chr12:7901429-7901788	K562	blood:	n/a	n/a
10	CEBPB	chr12:7987356-7987616	IMR90	lung:	n/a	n/a
11	CEBPB	chr12:7921585-7921831	A549	lung:	n/a	n/a
12	CEBPB	chr12:7901408-7901724	MCF-7	breast:	n/a	n/a
13	CEBPB	chr12:7946678-7946878	HepG2	liver:	n/a	chr12:7946725-7946736
14	CEBPB	chr12:7878906-7879146	IMR90	lung:	n/a	chr12:7879028-7879041 chr12:7879028-7879039 chr12:7879030-7879039
15	CEBPB	chr12:7987335-7987623	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:7987790-7988017	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:7878922-7879142	H1-hESC	embryonic stem cell:	n/a	chr12:7879028-7879041 chr12:7879028-7879039 chr12:7879030-7879039
18	CEBPB	chr12:7921535-7921866	A549	lung:	n/a	n/a
19	CEBPB	chr12:7939789-7939790	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr12:7926343-7926544	A549	lung:	n/a	n/a
21	CEBPB	chr12:7921547-7921880	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:7926356-7926423	K562	blood:	n/a	n/a
23	CEBPB	chr12:7901343-7901698	K562	blood:	n/a	n/a
24	CEBPB	chr12:7911498-7911677	HepG2	liver:	n/a	chr12:7911573-7911584
25	CEBPB	chr12:7921568-7921836	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr12:7979722-7979842	HepG2	liver:	n/a	chr12:7979762-7979773
27	CEBPB	chr12:7901379-7901673	K562	blood:	n/a	n/a
28	CEBPB	chr12:7987387-7987701	MCF-7	breast:	n/a	n/a
29	CEBPB	chr12:7926337-7926536	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:7878866-7879168	A549	lung:	n/a	chr12:7879028-7879041 chr12:7879028-7879039 chr12:7879030-7879039
31	CEBPB	chr12:7901364-7901690	K562	blood:	n/a	n/a
32	CEBPB	chr12:7878919-7879182	K562	blood:	n/a	chr12:7879028-7879041 chr12:7879028-7879039 chr12:7879030-7879039
33	CEBPB	chr12:7926333-7926522	HepG2	liver:	n/a	n/a
34	CEBPB	chr12:7921534-7921858	IMR90	lung:	n/a	n/a
35	CEBPB	chr12:7987437-7988030	A549	lung:	n/a	n/a
36	CEBPB	chr12:7949934-7950094	Hela-S3	cervix:	n/a	chr12:7950009-7950020
37	CEBPB	chr12:7949920-7950186	H1-hESC	embryonic stem cell:	n/a	chr12:7950009-7950020
38	CEBPB	chr12:7921573-7921834	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr12:7949971-7950161	K562	blood:	n/a	chr12:7950009-7950020
40	CEBPB	chr12:7911451-7911673	H1-hESC	embryonic stem cell:	n/a	chr12:7911573-7911584
41	CEBPB	chr12:7878902-7879179	Hela-S3	cervix:	n/a	chr12:7879028-7879041 chr12:7879028-7879039 chr12:7879030-7879039
42	CEBPB	chr12:7987400-7987531	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:7878756-7879256	A549	lung:	n/a	chr12:7879028-7879041 chr12:7879028-7879039 chr12:7879030-7879039
44	CEBPB	chr12:7949962-7950173	HepG2	liver:	n/a	chr12:7950009-7950020
45	CEBPB	chr12:7878822-7879220	MCF-7	breast:	n/a	chr12:7879028-7879041 chr12:7879028-7879039 chr12:7879030-7879039
46	CEBPB	chr12:7987334-7987689	MCF-7	breast:	n/a	n/a
47	CEBPB	chr12:7921546-7921810	MCF-7	breast:	n/a	n/a
48	CEBPB	chr12:7987839-7987992	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:7921480-7921806	MCF-7	breast:	n/a	n/a
50	CEBPB	chr12:7926262-7926549	IMR90	lung:	n/a	n/a

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:7911603-7911653	LNCaP	prostate:	n/a
2	chr12:7948517-7948567	SK-N-SH_RA	brain:	n/a
3	chr12:7941959-7942009	NHBE	bronchial:	n/a
4	chr12:7948531-7948581	HCT-116	colon:	n/a
5	chr12:7911603-7911653	LNCaP	prostate:	n/a
6	chr12:7948517-7948567	SK-N-SH_RA	brain:	n/a
7	chr12:7941959-7942009	NHBE	bronchial:	n/a
8	chr12:7948531-7948581	HCT-116	colon:	n/a
9	chr12:7889195-7889245	SK-N-MC	brain:	n/a
10	chr12:7943244-7943294	RPTEC	kidney:	n/a
11	chr12:7943244-7943294	IMR90	lung:	fetal
12	chr12:7948531-7948581	HEEpiC	esophagus:	n/a
13	chr12:7902721-7902771	A549	lung:	n/a
14	chr12:7941120-7941170	HRCEpiC	kidney:	n/a
15	chr12:7918357-7918407	HNPCEpiC	eye:	n/a
16	chr12:7940546-7940596	GM12892	blood:	n/a
17	chr12:7902721-7902771	U87	brain:	n/a
18	chr12:7941959-7942009	NT2-D1	testis:	n/a
19	chr12:7943244-7943294	HEK293	kidney:	embryo
20	chr12:7904267-7904317	ProgFib	skin:	n/a
21	chr12:7904168-7904218	BJ	skin:	n/a
22	chr12:7939674-7939724	GM12878	blood:	n/a
23	chr12:7966784-7966834	HCPEpiC	choroid plexus:	n/a
24	chr12:7900651-7900701	NH-A	brain:	n/a
25	chr12:7946814-7946864	ECC-1	luminal epithelium:	n/a
26	chr12:7901661-7901711	HRPEpiC	eye:	n/a
27	chr12:7904168-7904218	HUVEC	blood vessel:	n/a
28	chr12:7900651-7900701	HMEC	breast:	n/a
29	chr12:7940852-7940902	GM12878	blood:	n/a
30	chr12:7948517-7948567	HCF	heart:	n/a
31	chr12:7941120-7941170	HIPEpiC	eye:	n/a
32	chr12:7903152-7903202	A549	lung:	n/a
33	chr12:7941120-7941170	HCM	heart:	n/a
34	chr12:7948517-7948567	Jurkat	blood:	n/a
35	chr12:7904168-7904218	HepG2	liver:	n/a
36	chr12:7917888-7917938	Caco-2	colon:	n/a
37	chr12:7966784-7966834	NHDF-neo	bronchial:	n/a
38	chr12:7940546-7940596	GM12891	blood:	n/a
39	chr12:7903170-7903220	AG04449	skin:	fetal
40	chr12:7926589-7926639	HCT-116	colon:	n/a
41	chr12:7904082-7904132	GM12891	blood:	n/a
42	chr12:7943244-7943294	HCT-116	colon:	n/a
43	chr12:7941043-7941093	NHDF-neo	bronchial:	n/a
44	chr12:7943244-7943294	NH-A	brain:	n/a
45	chr12:7902058-7902108	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:7916371-7916421	NHBE	bronchial:	n/a
47	chr12:7918357-7918407	BJ	skin:	n/a
48	chr12:7889195-7889245	MCF10A-Er-Src	breast:	n/a
49	chr12:7917828-7917878	SKMC	muscle:	n/a
50	chr12:7948517-7948567	T-47D	breast:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:7785661..7787296-chr12:7958245..7961143,2	K562	blood:
2	chr12:7830039..7830628-chr12:7959515..7960112,3	K562	blood:
3	chr12:7829622..7830601-chr12:7959144..7960112,6	MCF-7	breast:
4	chr12:7985856..7986361-chr12:8086765..8087460,2	Hela-S3	cervix:
5	chr12:7869134..7869702-chr12:7959145..7959716,2	MCF-7	breast:
6	chr12:7868671..7869617-chr12:7959225..7960025,4	MCF-7	breast:
7	chr12:7797730..7798285-chr12:7959327..7960129,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4C-1	chr12:7878128-7879277	NONHSAT026265

No data

Variant related genes	Relation type
NANOGNB	TF binding region
NANOG	TF binding region
ENSG00000201549	TF binding region
SLC2A14	TF binding region
ENSG00000199912	TF binding region
CLEC4C	TF binding region
NANOGNB	CpG island
NANOG	CpG island
ENSG00000201549	CpG island
SLC2A14	CpG island
ENSG00000199912	CpG island
CLEC4C	CpG island

Extended variants
information (count: 3715 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3715 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11609608	chr12:7873411-7873412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs141539746	chr12:7873495-7873496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201118448	chr12:7873496-7873497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532984421	chr12:7873498-7873499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541506146	chr12:7873560-7873561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141546512	chr12:7873660-7873661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146260938	chr12:7873677-7873678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148757603	chr12:7873686-7873687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10744026	chr12:7873701-7873702	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543827120	chr12:7873707-7873708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563578126	chr12:7873745-7873746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529540757	chr12:7873751-7873752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199889607	chr12:7873760-7873761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139730536	chr12:7873819-7873820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376787944	chr12:7873820-7873821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202234199	chr12:7873845-7873846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542959236	chr12:7873898-7873899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182016866	chr12:7873916-7873917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186172827	chr12:7873974-7873975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7957561	chr12:7874077-7874078	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs12306681	chr12:7874103-7874104	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs371798398	chr12:7874125-7874126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570196259	chr12:7874131-7874132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7980417	chr12:7874190-7874191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549365157	chr12:7874281-7874282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188633838	chr12:7874316-7874317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568074409	chr12:7874382-7874383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368414262	chr12:7874387-7874388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11055417	chr12:7874399-7874400	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs372277594	chr12:7874440-7874441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374272254	chr12:7874466-7874467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201181335	chr12:7874469-7874470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565843364	chr12:7874470-7874471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180724510	chr12:7874478-7874479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185018641	chr12:7874485-7874486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150622792	chr12:7874509-7874510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558022983	chr12:7874518-7874519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144081126	chr12:7874665-7874666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12579309	chr12:7874682-7874683	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs12578363	chr12:7874700-7874701	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs573966270	chr12:7874875-7874876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189826036	chr12:7874884-7874885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576465995	chr12:7874889-7874890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183850242	chr12:7874902-7874903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148740404	chr12:7875049-7875050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117713152	chr12:7875096-7875097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368693568	chr12:7875190-7875191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187643038	chr12:7875216-7875217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543277132	chr12:7875254-7875255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4883438	chr12:7875300-7875301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Nasopharyngeal cancer	20548289	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495309	CNVD
Bipolar disorder	19214233	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Autism	19492091	CNVD

Chromatin state (count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7871200-7873800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:7872000-7876200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr12:7872000-7876200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:7872000-7878600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:7873200-7875000	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr12:7873200-7876400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr12:7873400-7873600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr12:7875000-7876800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr12:7876200-7876600	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr12:7876200-7876600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:7876400-7876600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:7876400-7876800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr12:7876600-7878800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:7876600-7883400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr12:7876800-7882000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr12:7876800-7882200	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr12:7878600-7879200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:7878800-7879200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:7879200-7881800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:7879200-7882000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:7881800-7885600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:7882000-7882600	Enhancers	Primary hematopoietic stem cells	blood
23	chr12:7882000-7882800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr12:7882000-7885400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:7882200-7882800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr12:7882200-7882800	Enhancers	HepG2	liver
27	chr12:7882600-7883400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr12:7883400-7883600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr12:7883400-7884400	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr12:7883400-7884600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:7883400-7887200	Enhancers	Primary hematopoietic stem cells	blood
32	chr12:7883600-7884200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr12:7883600-7884400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:7883600-7884400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr12:7883600-7884400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr12:7883600-7884400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr12:7883600-7884400	Enhancers	K562	blood
38	chr12:7883600-7884600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr12:7883600-7884600	Enhancers	H9 Cell Line	embryonic stem cell
40	chr12:7883600-7884800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:7883800-7884600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr12:7884200-7884400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr12:7884200-7884600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr12:7884400-7885600	Weak transcription	K562	blood
45	chr12:7884400-7889600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr12:7885400-7886000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr12:7885600-7885800	Enhancers	K562	blood
48	chr12:7885600-7886000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr12:7886000-7887200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:7886000-7887600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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