Variant report

Variant	esv3439156
Chromosome Location	chr12:21207396-21370189
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:561)
CpG islands
(count:184)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:21322799-21322999	K562	blood:	n/a	n/a
2	BACH1	chr12:21350777-21350898	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr12:21322801-21323167	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr12:21308670-21308879	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr12:21271000-21271136	HepG2	liver:	n/a	chr12:21271080-21271091
6	CEBPB	chr12:21358486-21358919	A549	lung:	n/a	n/a
7	CEBPB	chr12:21325090-21325330	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr12:21358479-21358755	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:21233354-21233510	A549	lung:	n/a	n/a
10	CEBPB	chr12:21356602-21356832	H1-hESC	embryonic stem cell:	n/a	chr12:21356695-21356706
11	CEBPB	chr12:21243014-21243312	A549	lung:	n/a	chr12:21243166-21243177
12	CEBPB	chr12:21234009-21234357	HepG2	liver:	n/a	chr12:21234179-21234190
13	CEBPB	chr12:21243024-21243307	HepG2	liver:	n/a	chr12:21243166-21243177
14	CEBPB	chr12:21260027-21260258	HepG2	liver:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
15	CEBPB	chr12:21356582-21356854	A549	lung:	n/a	chr12:21356695-21356706
16	CEBPB	chr12:21215636-21215960	A549	lung:	n/a	n/a
17	CEBPB	chr12:21359589-21359876	HepG2	liver:	n/a	chr12:21359721-21359734 chr12:21359721-21359732
18	CEBPB	chr12:21246783-21246933	HepG2	liver:	n/a	chr12:21246828-21246839
19	CEBPB	chr12:21297827-21298053	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:21234048-21234229	H1-hESC	embryonic stem cell:	n/a	chr12:21234179-21234190
21	CEBPB	chr12:21260029-21260209	A549	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
22	CEBPB	chr12:21260031-21260260	IMR90	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
23	CEBPB	chr12:21356579-21356809	HepG2	liver:	n/a	chr12:21356695-21356706
24	CEBPB	chr12:21356519-21356864	IMR90	lung:	n/a	chr12:21356695-21356706
25	CEBPB	chr12:21282343-21282678	HepG2	liver:	n/a	chr12:21282598-21282609 chr12:21282528-21282539
26	CEBPB	chr12:21234037-21234356	A549	lung:	n/a	chr12:21234179-21234190
27	CEBPB	chr12:21243036-21243304	IMR90	lung:	n/a	chr12:21243166-21243177
28	CHD2	chr12:21218752-21218883	GM12878	blood:	n/a	n/a
29	CTCF	chr12:21322818-21323169	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr12:21322884-21323129	GM19238	blood:	n/a	n/a
31	CTCF	chr12:21367304-21367342	GM10248	blood:	n/a	n/a
32	CTCF	chr12:21322900-21323050	GM12864	blood:	n/a	n/a
33	CTCF	chr12:21322895-21323096	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr12:21218900-21219050	HMEC	breast:	n/a	n/a
35	CTCF	chr12:21227140-21227290	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr12:21218860-21219010	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr12:21322940-21323090	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr12:21322793-21323180	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:21226320-21226470	HCT-116	colon:	n/a	n/a
40	CTCF	chr12:21302482-21302514	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:21322260-21322410	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr12:21227080-21227230	AG09309	skin:	n/a	n/a
43	CTCF	chr12:21218940-21219090	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr12:21322781-21323278	MCF-7	breast:	n/a	n/a
45	CTCF	chr12:21322881-21323123	ECC-1	luminal epithelium:	n/a	n/a
46	CTCF	chr12:21218680-21219310	HCT-116	colon:	n/a	n/a
47	CTCF	chr12:21218546-21219284	A549	lung:	n/a	n/a
48	CTCF	chr12:21323260-21323410	BJ	skin:	n/a	n/a
49	CTCF	chr12:21218880-21219030	HCT-116	colon:	n/a	n/a
50	CTCF	chr12:21218896-21219073	MCF-7	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21324585-21324635	Jurkat	blood:	n/a
2	chr12:21324585-21324635	Jurkat	blood:	n/a
3	chr12:21287375-21287425	ECC-1	luminal epithelium:	n/a
4	chr12:21324585-21324635	T-47D	breast:	n/a
5	chr12:21283725-21283775	HIPEpiC	eye:	n/a
6	chr12:21283725-21283775	HAEpiC	amniotic membrane:	n/a
7	chr12:21283725-21283775	LNCaP	prostate:	n/a
8	chr12:21287375-21287425	HNPCEpiC	eye:	n/a
9	chr12:21324585-21324635	SAEC	small airway:	n/a
10	chr12:21287375-21287425	AG04449	skin:	fetal
11	chr12:21283725-21283775	HCT-116	colon:	n/a
12	chr12:21324585-21324635	U87	brain:	n/a
13	chr12:21287375-21287425	HepG2	liver:	n/a
14	chr12:21283725-21283775	SKMC	muscle:	n/a
15	chr12:21324585-21324635	HAEpiC	amniotic membrane:	n/a
16	chr12:21287375-21287425	IMR90	lung:	fetal
17	chr12:21283725-21283775	HNPCEpiC	eye:	n/a
18	chr12:21283725-21283775	IMR90	lung:	fetal
19	chr12:21324585-21324635	HCM	heart:	n/a
20	chr12:21324585-21324635	ovcar-3	ovarian:	n/a
21	chr12:21324585-21324635	NT2-D1	testis:	n/a
22	chr12:21324585-21324635	SK-N-SH_RA	brain:	n/a
23	chr12:21324585-21324635	ECC-1	luminal epithelium:	n/a
24	chr12:21283725-21283775	AoSMC	blood vessel:	n/a
25	chr12:21287375-21287425	NT2-D1	testis:	n/a
26	chr12:21287375-21287425	LNCaP	prostate:	n/a
27	chr12:21324585-21324635	NHBE	bronchial:	n/a
28	chr12:21287375-21287425	MCF10A-Er-Src	breast:	n/a
29	chr12:21324585-21324635	HUVEC	blood vessel:	n/a
30	chr12:21283725-21283775	HL-60	blood:	n/a
31	chr12:21324585-21324635	GM06990	blood:	n/a
32	chr12:21324585-21324635	AG09319	gingival:	n/a
33	chr12:21287375-21287425	NHBE	bronchial:	n/a
34	chr12:21283725-21283775	MCF10A-Er-Src	breast:	n/a
35	chr12:21287375-21287425	HL-60	blood:	n/a
36	chr12:21287375-21287425	AG10803	skin:	n/a
37	chr12:21287375-21287425	BJ	skin:	n/a
38	chr12:21283725-21283775	NH-A	brain:	n/a
39	chr12:21287375-21287425	GM12892	blood:	n/a
40	chr12:21283725-21283775	NHBE	bronchial:	n/a
41	chr12:21283725-21283775	HRPEpiC	eye:	n/a
42	chr12:21324585-21324635	AoSMC	blood vessel:	n/a
43	chr12:21283725-21283775	H1-hESC	embryonic stem cell:	embryo
44	chr12:21283725-21283775	SK-N-MC	brain:	n/a
45	chr12:21324585-21324635	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:21324585-21324635	HCPEpiC	choroid plexus:	n/a
47	chr12:21287375-21287425	AoSMC	blood vessel:	n/a
48	chr12:21287375-21287425	NB4	blood:	n/a
49	chr12:21324585-21324635	ProgFib	skin:	n/a
50	chr12:21287375-21287425	SK-N-SH	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
2	chr12:21368652..21370975-chr12:21374890..21377722,2	K562	blood:
3	chr12:21154478..21155199-chr12:21322720..21323314,2	MCF-7	breast:
4	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
5	chr12:21367379..21369612-chr12:21376922..21378821,2	K562	blood:
6	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
7	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
8	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
9	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
10	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
11	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
12	chr12:21268556..21269333-chr7:84915114..84915941,2	MCF-7	breast:
13	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
14	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
15	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:
16	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:
17	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1B1-1	chr12:21228194-21228718	NONHSAT027240
2	lnc-SLCO1B1-1	chr12:21220285-21220317	NONHSAT027240

No data

Variant related genes	Relation type
ENSG00000257062	TF binding region
SLCO1B1	TF binding region
SLCO1B7	TF binding region
ENSG00000257062	CpG island
SLCO1B1	CpG island
SLCO1B7	CpG island

Extended variants
information (count: 5527 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5527 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200795485	chr12:21207429-21207430	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs535157302	chr12:21207437-21207438	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs574290856	chr12:21207444-21207445	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs200498218	chr12:21207472-21207473	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs183504858	chr12:21207479-21207480	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs370734418	chr12:21207494-21207495	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs201857305	chr12:21207810-21207811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs386761039	chr12:21207834-21207835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549950828	chr12:21207844-21207845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10841735	chr12:21207845-21207846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs371027193	chr12:21207849-21207850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11045701	chr12:21207883-21207884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs375251131	chr12:21207902-21207903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565714256	chr12:21207934-21207935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534591263	chr12:21207983-21207984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558535914	chr12:21208010-21208011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs578251059	chr12:21208041-21208042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537308161	chr12:21208071-21208072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557547076	chr12:21208102-21208103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183482169	chr12:21208115-21208116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543138642	chr12:21208145-21208146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559402525	chr12:21208183-21208184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535444396	chr12:21208195-21208196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572938884	chr12:21208206-21208207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188484809	chr12:21208222-21208223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564888467	chr12:21208255-21208256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377638020	chr12:21208302-21208303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200111485	chr12:21208312-21208313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72246350	chr12:21208314-21208315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367854388	chr12:21208316-21208317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199993539	chr12:21208317-21208318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61925271	chr12:21208318-21208319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533265251	chr12:21208321-21208322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112003931	chr12:21208323-21208324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78033717	chr12:21208324-21208325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543317270	chr12:21208359-21208360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11045702	chr12:21208388-21208389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191864077	chr12:21208401-21208402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546359845	chr12:21208414-21208415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113268283	chr12:21208455-21208456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375041460	chr12:21208461-21208462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368124419	chr12:21208495-21208496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1502496	chr12:21208501-21208502	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs557961764	chr12:21208521-21208522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551408256	chr12:21208542-21208543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578006457	chr12:21208549-21208550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537774197	chr12:21208609-21208610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564003657	chr12:21208611-21208612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576234702	chr12:21208641-21208642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557352168	chr12:21208688-21208689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	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
Non-syndromic sensorineural hearing loss	22037309	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
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21207800-21226600	Weak transcription	Liver	Liver
2	chr12:21226000-21226600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr12:21226200-21227000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:21226200-21227200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr12:21226200-21227600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr12:21226200-21227800	Enhancers	NH-A	brain
7	chr12:21226600-21227000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:21226600-21227200	Strong transcription	Liver	Liver
9	chr12:21227000-21231000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:21227200-21227400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr12:21227200-21241600	Weak transcription	Liver	Liver
12	chr12:21227400-21227600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:21227600-21227800	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr12:21257400-21258200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:21258000-21258600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:21262600-21262800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr12:21262600-21263000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:21263400-21263600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr12:21264400-21264600	Active TSS	Liver	Liver
20	chr12:21264600-21264800	Flanking Active TSS	Liver	Liver
21	chr12:21264800-21265000	Enhancers	Liver	Liver
22	chr12:21271000-21271600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr12:21271400-21272000	Active TSS	A549	lung
24	chr12:21271600-21272600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr12:21272000-21272600	Enhancers	A549	lung
26	chr12:21272200-21272600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr12:21272400-21272800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr12:21272400-21272800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:21272600-21272800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:21275400-21276200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr12:21281800-21282800	Enhancers	Liver	Liver
32	chr12:21282400-21283400	Enhancers	A549	lung
33	chr12:21282800-21283800	Flanking Active TSS	Liver	Liver
34	chr12:21283200-21283400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:21283800-21287600	Active TSS	Liver	Liver
36	chr12:21287600-21289400	Weak transcription	Liver	Liver
37	chr12:21289400-21289600	Flanking Active TSS	Liver	Liver
38	chr12:21289600-21290400	Enhancers	Liver	Liver
39	chr12:21290400-21291400	Flanking Active TSS	Liver	Liver
40	chr12:21291400-21292000	Enhancers	Liver	Liver
41	chr12:21291400-21294200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr12:21292000-21292400	Weak transcription	Liver	Liver
43	chr12:21292400-21293800	Enhancers	Liver	Liver
44	chr12:21293800-21296600	Genic enhancers	Liver	Liver
45	chr12:21296600-21297800	Strong transcription	Liver	Liver
46	chr12:21297800-21298200	Genic enhancers	Liver	Liver
47	chr12:21298200-21298400	Weak transcription	Liver	Liver
48	chr12:21298400-21298600	Enhancers	Liver	Liver
49	chr12:21298600-21299000	Weak transcription	Liver	Liver
50	chr12:21299000-21299600	Enhancers	Liver	Liver

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