Variant report

Variant	nsv898894
Chromosome Location	chr12:21545532-21583242
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:203)
CpG islands
(count:244)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:21571441-21572153	K562	blood:	n/a	n/a
2	ARID3A	chr12:21566604-21567125	K562	blood:	n/a	n/a
3	ARID3A	chr12:21566598-21566706	HepG2	liver:	n/a	n/a
4	ATF1	chr12:21566557-21567024	K562	blood:	n/a	n/a
5	BACH1	chr12:21566575-21566945	K562	blood:	n/a	chr12:21566726-21566740
6	BHLHE40	chr12:21572416-21572552	K562	blood:	n/a	n/a
7	BHLHE40	chr12:21566621-21567097	K562	blood:	n/a	n/a
8	CCNT2	chr12:21566714-21567203	K562	blood:	n/a	n/a
9	CEBPB	chr12:21546588-21546963	K562	blood:	n/a	chr12:21546784-21546795
10	CEBPB	chr12:21547658-21547858	K562	blood:	n/a	chr12:21547721-21547734
11	CEBPB	chr12:21566674-21566837	K562	blood:	n/a	n/a
12	CEBPB	chr12:21548420-21548434	K562	blood:	n/a	n/a
13	CEBPB	chr12:21546696-21546939	A549	lung:	n/a	chr12:21546784-21546795
14	CEBPB	chr12:21572424-21572551	K562	blood:	n/a	n/a
15	CEBPB	chr12:21546640-21546957	HepG2	liver:	n/a	chr12:21546784-21546795
16	CEBPB	chr12:21546630-21546943	IMR90	lung:	n/a	chr12:21546784-21546795
17	CEBPD	chr12:21566538-21567024	K562	blood:	n/a	n/a
18	CEBPD	chr12:21566573-21566995	K562	blood:	n/a	n/a
19	CHD2	chr12:21571389-21571679	K562	blood:	n/a	n/a
20	CHD2	chr12:21566706-21567183	K562	blood:	n/a	n/a
21	CHD2	chr12:21572376-21572670	K562	blood:	n/a	n/a
22	CTCF	chr12:21571737-21572173	K562	blood:	n/a	n/a
23	CTCF	chr12:21566660-21566810	Caco-2	colon:	n/a	n/a
24	CTCF	chr12:21557728-21557785	GM20000	blood:	n/a	n/a
25	CTCF	chr12:21566420-21566570	GM12869	blood:	n/a	n/a
26	CTCF	chr12:21578500-21578650	HMF	breast:	n/a	n/a
27	CUX1	chr12:21566670-21566961	K562	blood:	n/a	n/a
28	CUX1	chr12:21571314-21571473	K562	blood:	n/a	n/a
29	E2F4	chr12:21566724-21566895	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr12:21555197-21555397	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr12:21571384-21571661	GM12878	blood:	n/a	chr12:21571541-21571552
32	EGR1	chr12:21572407-21572602	K562	blood:	n/a	n/a
33	EP300	chr12:21566658-21566858	K562	blood:	n/a	chr12:21566728-21566737
34	EP300	chr12:21569501-21570013	A549	lung:	n/a	n/a
35	EP300	chr12:21547810-21547924	GM12878	blood:	n/a	n/a
36	EP300	chr12:21566578-21567043	K562	blood:	n/a	chr12:21566600-21566614 chr12:21566728-21566737
37	EP300	chr12:21569125-21569340	SK-N-SH_RA	brain:	n/a	n/a
38	FOS	chr12:21581268-21581536	HUVEC	blood vessel:	n/a	n/a
39	FOSL1	chr12:21566590-21566902	K562	blood:	n/a	chr12:21566728-21566737 chr12:21566727-21566738
40	FOSL1	chr12:21566450-21566942	K562	blood:	n/a	chr12:21566728-21566737 chr12:21566727-21566738
41	FOSL2	chr12:21566534-21566852	HepG2	liver:	n/a	chr12:21566728-21566737
42	FOSL2	chr12:21566449-21566976	A549	lung:	n/a	chr12:21566728-21566737
43	FOXA1	chr12:21572353-21572721	HepG2	liver:	n/a	n/a
44	FOXA1	chr12:21548221-21548560	HepG2	liver:	n/a	n/a
45	FOXA2	chr12:21572291-21572840	A549	lung:	n/a	n/a
46	FOXA2	chr12:21566426-21566936	A549	lung:	n/a	chr12:21566899-21566911 chr12:21566903-21566915
47	FOXA2	chr12:21572478-21572738	A549	lung:	n/a	n/a
48	FOXA2	chr12:21548266-21548651	A549	lung:	n/a	n/a
49	FOXA2	chr12:21548079-21548754	A549	lung:	n/a	n/a
50	GABPA	chr12:21566566-21566901	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21572311-21572361	HCT-116	colon:	n/a
2	chr12:21572425-21572475	SAEC	small airway:	n/a
3	chr12:21572311-21572361	ProgFib	skin:	n/a
4	chr12:21547892-21547942	ProgFib	skin:	n/a
5	chr12:21548228-21548278	HEEpiC	esophagus:	n/a
6	chr12:21572425-21572475	H1-hESC	embryonic stem cell:	embryo
7	chr12:21548228-21548278	LNCaP	prostate:	n/a
8	chr12:21572311-21572361	SK-N-SH_RA	brain:	n/a
9	chr12:21572425-21572475	SK-N-MC	brain:	n/a
10	chr12:21572425-21572475	MCF10A-Er-Src	breast:	n/a
11	chr12:21547892-21547942	HL-60	blood:	n/a
12	chr12:21548228-21548278	AG09319	gingival:	n/a
13	chr12:21572311-21572361	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:21572425-21572475	HRPEpiC	eye:	n/a
15	chr12:21547892-21547942	HCM	heart:	n/a
16	chr12:21548228-21548278	GM12878	blood:	n/a
17	chr12:21572311-21572361	AG04449	skin:	fetal
18	chr12:21547892-21547942	HEK293	kidney:	embryo
19	chr12:21548228-21548278	AG10803	skin:	n/a
20	chr12:21547892-21547942	ovcar-3	ovarian:	n/a
21	chr12:21547892-21547942	GM12892	blood:	n/a
22	chr12:21572425-21572475	HEEpiC	esophagus:	n/a
23	chr12:21572425-21572475	BJ	skin:	n/a
24	chr12:21548228-21548278	NHBE	bronchial:	n/a
25	chr12:21547892-21547942	AoSMC	blood vessel:	n/a
26	chr12:21547892-21547942	SK-N-MC	brain:	n/a
27	chr12:21572311-21572361	H1-hESC	embryonic stem cell:	embryo
28	chr12:21572311-21572361	Jurkat	blood:	n/a
29	chr12:21548228-21548278	A549	lung:	n/a
30	chr12:21547892-21547942	NHBE	bronchial:	n/a
31	chr12:21547892-21547942	K562	blood:	n/a
32	chr12:21572425-21572475	Hepatocyte	liver:	n/a
33	chr12:21547892-21547942	HUVEC	blood vessel:	n/a
34	chr12:21548228-21548278	AG04449	skin:	fetal
35	chr12:21547892-21547942	HCF	heart:	n/a
36	chr12:21548228-21548278	IMR90	lung:	fetal
37	chr12:21572311-21572361	BE2_C	brain:	n/a
38	chr12:21548228-21548278	U87	brain:	n/a
39	chr12:21572311-21572361	GM06990	blood:	n/a
40	chr12:21548228-21548278	HAEpiC	amniotic membrane:	n/a
41	chr12:21547892-21547942	Hepatocyte	liver:	n/a
42	chr12:21572425-21572475	Hela-S3	cervix:	n/a
43	chr12:21572311-21572361	ovcar-3	ovarian:	n/a
44	chr12:21548228-21548278	PrEC	prostate:	n/a
45	chr12:21548228-21548278	RPTEC	kidney:	n/a
46	chr12:21572311-21572361	NB4	blood:	n/a
47	chr12:21547892-21547942	U87	brain:	n/a
48	chr12:21572425-21572475	NHBE	bronchial:	n/a
49	chr12:21572425-21572475	LNCaP	prostate:	n/a
50	chr12:21547892-21547942	GM12878	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:21569338..21572113-chr12:21589171..21592854,4	K562	blood:
2	chr12:21556694..21559135-chr12:21561507..21563153,3	K562	blood:
3	chr12:21578534..21580531-chr12:21589180..21591050,2	K562	blood:
4	chr12:21561087..21564511-chr12:21564541..21567665,4	K562	blood:
5	chr12:21561087..21564511-chr12:21564541..21567665,4	K562	blood:
6	chr12:21570524..21573513-chr12:21578970..21581790,2	K562	blood:
7	chr12:21569338..21572113-chr12:21589171..21592483,4	K562	blood:
8	chr12:21476298..21478074-chr12:21570042..21572071,2	K562	blood:
9	chr12:21556694..21559135-chr12:21561507..21563153,3	K562	blood:
10	chr12:21558528..21560980-chr12:21590497..21592132,2	K562	blood:
11	chr12:21576479..21578232-chr12:21588416..21590955,2	K562	blood:
12	chr12:21527361..21529300-chr12:21544200..21546826,2	K562	blood:
13	chr12:21578861..21581322-chr12:21589967..21591700,2	MCF-7	breast:
14	chr12:21581278..21584655-chr12:21586014..21590785,5	K562	blood:

No data

Variant related genes	Relation type
SLCO1A2	TF binding region
SLCO1A2	CpG island
ENSG00000084453	chromatin interactions
ENSG00000121350	chromatin interactions

Extended variants
information (count: 1029 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11830214	chr12:21545532-21545533	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369792705	chr12:21545536-21545537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563096995	chr12:21545554-21545555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376648082	chr12:21545581-21545582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370976167	chr12:21545601-21545602	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs570700624	chr12:21545674-21545675	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs55820877	chr12:21545759-21545760	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs77174875	chr12:21545797-21545798	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs186169479	chr12:21545805-21545806	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs35419909	chr12:21545966-21545967	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs397948110	chr12:21545968-21545969	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs148184069	chr12:21545970-21545971	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs537915994	chr12:21545973-21545974	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs576208720	chr12:21545986-21545987	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs574958022	chr12:21546008-21546009	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs190444738	chr12:21546018-21546019	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs554437997	chr12:21546032-21546033	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs554110452	chr12:21546108-21546109	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs182703382	chr12:21546110-21546111	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs546523715	chr12:21546166-21546167	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs574414437	chr12:21546197-21546198	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs150077744	chr12:21546215-21546216	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs138392377	chr12:21546308-21546309	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs540093209	chr12:21546328-21546329	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs541927972	chr12:21546333-21546334	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs141608153	chr12:21546337-21546338	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs527478554	chr12:21546397-21546398	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs145325022	chr12:21546405-21546406	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs185660166	chr12:21546439-21546440	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533030280	chr12:21546464-21546465	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs371552033	chr12:21546466-21546467	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs568896751	chr12:21546467-21546468	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs191209031	chr12:21546510-21546511	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs548273379	chr12:21546531-21546532	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs553562664	chr12:21546542-21546543	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs568505616	chr12:21546621-21546622	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs576956335	chr12:21546622-21546623	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs7316461	chr12:21546627-21546628	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs376227931	chr12:21546665-21546666	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182475938	chr12:21546677-21546678	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs137955707	chr12:21546723-21546724	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs565217107	chr12:21546745-21546746	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs114961616	chr12:21546768-21546769	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs11830952	chr12:21546770-21546771	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs189190847	chr12:21546789-21546790	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs112822139	chr12:21546791-21546792	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs541890917	chr12:21546841-21546842	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs561812259	chr12:21546842-21546843	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs572005051	chr12:21546860-21546861	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs142554708	chr12:21546862-21546863	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
Basal cell lymphoma	17053054	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
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
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	22237106	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
Multiple myeloma	17550852	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21537400-21547200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:21544600-21547000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr12:21545200-21547000	Weak transcription	K562	blood
4	chr12:21545400-21545600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr12:21545600-21546800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr12:21545600-21548400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:21546800-21548400	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr12:21546800-21548400	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr12:21546800-21548400	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr12:21546800-21548400	Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr12:21546800-21548800	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr12:21547000-21547200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr12:21547000-21547400	Enhancers	K562	blood
14	chr12:21547000-21548400	Active TSS	H1 Cell Line	embryonic stem cell
15	chr12:21547000-21548400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr12:21547200-21547400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:21547200-21547600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr12:21547200-21548400	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr12:21547200-21548400	Active TSS	H9 Cell Line	embryonic stem cell
20	chr12:21547400-21547600	Flanking Active TSS	K562	blood
21	chr12:21547400-21548200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:21547600-21548200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr12:21547600-21548200	Active TSS	K562	blood
24	chr12:21547600-21548400	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr12:21547800-21548400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr12:21560000-21560400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:21564600-21564800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:21564800-21572200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:21565200-21571000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr12:21566200-21566800	Enhancers	K562	blood
31	chr12:21566400-21566600	Enhancers	A549	lung
32	chr12:21566600-21566800	Flanking Active TSS	A549	lung
33	chr12:21566600-21567200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:21566800-21567200	Active TSS	A549	lung
35	chr12:21566800-21567200	Flanking Active TSS	K562	blood
36	chr12:21567000-21567200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:21567000-21567600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr12:21567200-21568000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:21567200-21568200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:21567200-21568200	Weak transcription	K562	blood
41	chr12:21567200-21569400	Weak transcription	A549	lung
42	chr12:21567600-21569200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr12:21568000-21570000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr12:21568200-21569000	Enhancers	K562	blood
45	chr12:21568200-21570200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr12:21568800-21571800	Enhancers	HUVEC	blood vessel
47	chr12:21569000-21570800	Weak transcription	K562	blood
48	chr12:21569200-21569800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:21569200-21569800	Enhancers	Osteobl	bone
50	chr12:21569200-21570200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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