Variant report

Variant	nsv1054132
Chromosome Location	chr12:21165101-21402544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:734)
CpG islands
(count:184)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:21387015-21387268	K562	blood:	n/a	n/a
2	ATF1	chr12:21392742-21392928	K562	blood:	n/a	n/a
3	BACH1	chr12:21350777-21350898	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:21380331-21380521	K562	blood:	n/a	n/a
5	BACH1	chr12:21322799-21322999	K562	blood:	n/a	n/a
6	BRCA1	chr12:21308670-21308879	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr12:21322801-21323167	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:21356602-21356832	H1-hESC	embryonic stem cell:	n/a	chr12:21356695-21356706
9	CEBPB	chr12:21260027-21260258	HepG2	liver:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
10	CEBPB	chr12:21234009-21234357	HepG2	liver:	n/a	chr12:21234179-21234190
11	CEBPB	chr12:21325090-21325330	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr12:21271000-21271136	HepG2	liver:	n/a	chr12:21271080-21271091
13	CEBPB	chr12:21168858-21169067	H1-hESC	embryonic stem cell:	n/a	chr12:21168919-21168930
14	CEBPB	chr12:21193602-21193866	HepG2	liver:	n/a	chr12:21193754-21193765
15	CEBPB	chr12:21394755-21395080	A549	lung:	n/a	chr12:21394924-21394935
16	CEBPB	chr12:21394753-21395095	HepG2	liver:	n/a	chr12:21394924-21394935
17	CEBPB	chr12:21175930-21176170	HepG2	liver:	n/a	chr12:21176036-21176047 chr12:21176037-21176048 chr12:21176036-21176049 chr12:21176038-21176047
18	CEBPB	chr12:21260031-21260260	IMR90	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
19	CEBPB	chr12:21193668-21193806	K562	blood:	n/a	chr12:21193754-21193765
20	CEBPB	chr12:21282343-21282678	HepG2	liver:	n/a	chr12:21282598-21282609 chr12:21282528-21282539
21	CEBPB	chr12:21193668-21193868	Hela-S3	cervix:	n/a	chr12:21193754-21193765
22	CEBPB	chr12:21260029-21260209	A549	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
23	CEBPB	chr12:21243014-21243312	A549	lung:	n/a	chr12:21243166-21243177
24	CEBPB	chr12:21359589-21359876	HepG2	liver:	n/a	chr12:21359721-21359734 chr12:21359721-21359732
25	CEBPB	chr12:21358486-21358919	A549	lung:	n/a	n/a
26	CEBPB	chr12:21358479-21358755	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:21193722-21193901	H1-hESC	embryonic stem cell:	n/a	chr12:21193754-21193765
28	CEBPB	chr12:21168774-21169104	HepG2	liver:	n/a	chr12:21168919-21168930
29	CEBPB	chr12:21246783-21246933	HepG2	liver:	n/a	chr12:21246828-21246839
30	CEBPB	chr12:21356579-21356809	HepG2	liver:	n/a	chr12:21356695-21356706
31	CEBPB	chr12:21215636-21215960	A549	lung:	n/a	n/a
32	CEBPB	chr12:21234048-21234229	H1-hESC	embryonic stem cell:	n/a	chr12:21234179-21234190
33	CEBPB	chr12:21168771-21169100	A549	lung:	n/a	chr12:21168919-21168930
34	CEBPB	chr12:21193579-21193868	A549	lung:	n/a	chr12:21193754-21193765
35	CEBPB	chr12:21243024-21243307	HepG2	liver:	n/a	chr12:21243166-21243177
36	CEBPB	chr12:21175943-21176096	H1-hESC	embryonic stem cell:	n/a	chr12:21176036-21176047 chr12:21176037-21176048 chr12:21176036-21176049 chr12:21176038-21176047
37	CEBPB	chr12:21356519-21356864	IMR90	lung:	n/a	chr12:21356695-21356706
38	CEBPB	chr12:21233354-21233510	A549	lung:	n/a	n/a
39	CEBPB	chr12:21234037-21234356	A549	lung:	n/a	chr12:21234179-21234190
40	CEBPB	chr12:21356582-21356854	A549	lung:	n/a	chr12:21356695-21356706
41	CEBPB	chr12:21297827-21298053	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:21243036-21243304	IMR90	lung:	n/a	chr12:21243166-21243177
43	CHD2	chr12:21218752-21218883	GM12878	blood:	n/a	n/a
44	CTCF	chr12:21227200-21227350	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr12:21401667-21401984	K562	blood:	n/a	chr12:21401818-21401839
46	CTCF	chr12:21401680-21401830	HMF	breast:	n/a	n/a
47	CTCF	chr12:21227081-21227331	Gliobla	brain:	n/a	n/a
48	CTCF	chr12:21322960-21323110	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr12:21322940-21323090	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr12:21322960-21323110	HA-sp	spinal cord:	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	GM12878	blood:	n/a
2	chr12:21324585-21324635	GM12878	blood:	n/a
3	chr12:21287375-21287425	NT2-D1	testis:	n/a
4	chr12:21283725-21283775	H1-hESC	embryonic stem cell:	embryo
5	chr12:21287375-21287425	AoSMC	blood vessel:	n/a
6	chr12:21324585-21324635	A549	lung:	n/a
7	chr12:21324585-21324635	SK-N-MC	brain:	n/a
8	chr12:21324585-21324635	HepG2	liver:	n/a
9	chr12:21324585-21324635	BJ	skin:	n/a
10	chr12:21287375-21287425	GM19239	blood:	n/a
11	chr12:21324585-21324635	MCF10A-Er-Src	breast:	n/a
12	chr12:21287375-21287425	LNCaP	prostate:	n/a
13	chr12:21283725-21283775	RPTEC	kidney:	n/a
14	chr12:21324585-21324635	PANC-1	pancreas:	n/a
15	chr12:21287375-21287425	H1-hESC	embryonic stem cell:	embryo
16	chr12:21287375-21287425	HEK293	kidney:	embryo
17	chr12:21287375-21287425	HepG2	liver:	n/a
18	chr12:21287375-21287425	HNPCEpiC	eye:	n/a
19	chr12:21283725-21283775	ovcar-3	ovarian:	n/a
20	chr12:21283725-21283775	IMR90	lung:	fetal
21	chr12:21283725-21283775	PANC-1	pancreas:	n/a
22	chr12:21324585-21324635	HAEpiC	amniotic membrane:	n/a
23	chr12:21324585-21324635	HCF	heart:	n/a
24	chr12:21324585-21324635	HUVEC	blood vessel:	n/a
25	chr12:21287375-21287425	BE2_C	brain:	n/a
26	chr12:21324585-21324635	AG09319	gingival:	n/a
27	chr12:21287375-21287425	HRE	kidney:	n/a
28	chr12:21324585-21324635	BE2_C	brain:	n/a
29	chr12:21287375-21287425	HCF	heart:	n/a
30	chr12:21324585-21324635	Hepatocyte	liver:	n/a
31	chr12:21287375-21287425	NHDF-neo	bronchial:	n/a
32	chr12:21287375-21287425	HL-60	blood:	n/a
33	chr12:21283725-21283775	GM12878	blood:	n/a
34	chr12:21324585-21324635	Hela-S3	cervix:	n/a
35	chr12:21283725-21283775	HCF	heart:	n/a
36	chr12:21324585-21324635	GM12892	blood:	n/a
37	chr12:21324585-21324635	SAEC	small airway:	n/a
38	chr12:21324585-21324635	AG09309	skin:	n/a
39	chr12:21324585-21324635	HCT-116	colon:	n/a
40	chr12:21283725-21283775	HNPCEpiC	eye:	n/a
41	chr12:21283725-21283775	AoSMC	blood vessel:	n/a
42	chr12:21324585-21324635	AoSMC	blood vessel:	n/a
43	chr12:21283725-21283775	AG04450	lung:	fetal
44	chr12:21283725-21283775	NT2-D1	testis:	n/a
45	chr12:21287375-21287425	Caco-2	colon:	n/a
46	chr12:21283725-21283775	NB4	blood:	n/a
47	chr12:21324585-21324635	HEEpiC	esophagus:	n/a
48	chr12:21324585-21324635	Caco-2	colon:	n/a
49	chr12:21324585-21324635	U87	brain:	n/a
50	chr12:21283725-21283775	K562	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:21373190..21374871-chr12:21381396..21383038,2	K562	blood:
2	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:
3	chr12:21368652..21370975-chr12:21374890..21377722,2	K562	blood:
4	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
5	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
6	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
7	chr12:21193958..21195458-chr17:59872939..59874521,2	MCF-7	breast:
8	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
9	chr12:21154478..21155199-chr12:21322720..21323314,2	MCF-7	breast:
10	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:
11	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
12	chr12:21368652..21370975-chr12:21374890..21377722,2	K562	blood:
13	chr12:21373190..21374871-chr12:21381396..21383038,2	K562	blood:
14	chr12:21372629..21374270-chr12:21375812..21377730,2	K562	blood:
15	chr12:21367379..21369612-chr12:21376922..21378821,2	K562	blood:
16	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
17	chr12:21372629..21374270-chr12:21375812..21377730,2	K562	blood:
18	chr12:21268556..21269333-chr7:84915114..84915941,2	MCF-7	breast:
19	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
20	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
21	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
22	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
23	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:
24	chr12:21367379..21369612-chr12:21376922..21378821,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1B1-1	chr12:21220285-21220317	NONHSAT027240
2	lnc-SLCO1B1-1	chr12:21228194-21228718	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: 7283 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7283 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150970531	chr12:21171005-21171006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547598667	chr12:21171020-21171021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116851799	chr12:21171077-21171078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371912852	chr12:21171121-21171122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1910191	chr12:21171203-21171204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs11045655	chr12:21171216-21171217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs569382822	chr12:21171296-21171297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372098485	chr12:21171323-21171324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535094657	chr12:21171349-21171350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140826012	chr12:21171366-21171367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141370028	chr12:21171390-21171391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566057628	chr12:21171397-21171398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12307944	chr12:21171398-21171399	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs145983047	chr12:21171403-21171404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578117742	chr12:21171417-21171418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138883228	chr12:21171463-21171464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142913068	chr12:21171487-21171488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546303210	chr12:21171491-21171492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73066349	chr12:21171495-21171496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146302953	chr12:21171534-21171535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527624694	chr12:21171585-21171586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10841724	chr12:21171719-21171720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs528514660	chr12:21171722-21171723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138705823	chr12:21171735-21171736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531998379	chr12:21171751-21171752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552094014	chr12:21171785-21171786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569444628	chr12:21171792-21171793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528931736	chr12:21171797-21171798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565422251	chr12:21171817-21171818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548612201	chr12:21171826-21171827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565329608	chr12:21171828-21171829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534574286	chr12:21171849-21171850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1995409	chr12:21171864-21171865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs571884440	chr12:21171895-21171896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10505870	chr12:21171896-21171897	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs557575068	chr12:21171900-21171901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184993124	chr12:21171948-21171949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188630220	chr12:21171975-21171976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10505871	chr12:21172053-21172054	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs181063882	chr12:21172091-21172092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536428167	chr12:21172103-21172104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545357033	chr12:21172128-21172129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116068272	chr12:21172130-21172131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370918813	chr12:21172155-21172156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201210879	chr12:21172157-21172158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149357474	chr12:21172160-21172161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563137778	chr12:21172180-21172181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199946694	chr12:21172199-21172200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183641131	chr12:21172235-21172236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200269745	chr12:21172236-21172237	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
Non-syndromic sensorineural hearing loss	22037309	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
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:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21171000-21172800	Weak transcription	Liver	Liver
2	chr12:21172800-21173600	Strong transcription	Liver	Liver
3	chr12:21173600-21176000	Weak transcription	Liver	Liver
4	chr12:21176000-21178200	Strong transcription	Liver	Liver
5	chr12:21178200-21178400	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr12:21178200-21179800	Weak transcription	Liver	Liver
7	chr12:21179400-21179600	Enhancers	A549	lung
8	chr12:21179800-21180000	Strong transcription	Liver	Liver
9	chr12:21180000-21180200	ZNF genes & repeats	Liver	Liver
10	chr12:21180200-21180600	Weak transcription	Liver	Liver
11	chr12:21187400-21187800	Active TSS	Psoas Muscle	Psoas
12	chr12:21207800-21226600	Weak transcription	Liver	Liver
13	chr12:21226000-21226600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr12:21226200-21227000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:21226200-21227200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr12:21226200-21227600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr12:21226200-21227800	Enhancers	NH-A	brain
18	chr12:21226600-21227000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:21226600-21227200	Strong transcription	Liver	Liver
20	chr12:21227000-21231000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:21227200-21227400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr12:21227200-21241600	Weak transcription	Liver	Liver
23	chr12:21227400-21227600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:21227600-21227800	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr12:21257400-21258200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:21258000-21258600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr12:21262600-21262800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:21262600-21263000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:21263400-21263600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:21264400-21264600	Active TSS	Liver	Liver
31	chr12:21264600-21264800	Flanking Active TSS	Liver	Liver
32	chr12:21264800-21265000	Enhancers	Liver	Liver
33	chr12:21271000-21271600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:21271400-21272000	Active TSS	A549	lung
35	chr12:21271600-21272600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:21272000-21272600	Enhancers	A549	lung
37	chr12:21272200-21272600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr12:21272400-21272800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr12:21272400-21272800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr12:21272600-21272800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr12:21275400-21276200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr12:21281800-21282800	Enhancers	Liver	Liver
43	chr12:21282400-21283400	Enhancers	A549	lung
44	chr12:21282800-21283800	Flanking Active TSS	Liver	Liver
45	chr12:21283200-21283400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:21283800-21287600	Active TSS	Liver	Liver
47	chr12:21287600-21289400	Weak transcription	Liver	Liver
48	chr12:21289400-21289600	Flanking Active TSS	Liver	Liver
49	chr12:21289600-21290400	Enhancers	Liver	Liver
50	chr12:21290400-21291400	Flanking Active TSS	Liver	Liver

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