Variant report

Variant	nsv899563
Chromosome Location	chr12:121543011-121600529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1291)
CpG islands
(count:671)
Chromatin interactive
region (count:63)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1291 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121554555-121555038	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:121548072-121548453	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:121566854-121567036	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:121562061-121562665	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:121566791-121567654	K562	blood:	n/a	n/a
6	ATF1	chr12:121562281-121562579	K562	blood:	n/a	n/a
7	ATF1	chr12:121554252-121554339	K562	blood:	n/a	n/a
8	ATF1	chr12:121566717-121567709	K562	blood:	n/a	n/a
9	ATF1	chr12:121569831-121570036	K562	blood:	n/a	n/a
10	ATF1	chr12:121551788-121552180	K562	blood:	n/a	n/a
11	ATF1	chr12:121582305-121582486	K562	blood:	n/a	n/a
12	ATF1	chr12:121558234-121558481	K562	blood:	n/a	n/a
13	ATF1	chr12:121548142-121548488	K562	blood:	n/a	n/a
14	ATF1	chr12:121570380-121570704	K562	blood:	n/a	n/a
15	ATF1	chr12:121581689-121582010	K562	blood:	n/a	n/a
16	ATF2	chr12:121548101-121548552	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr12:121581584-121582101	GM12878	blood:	n/a	n/a
18	ATF2	chr12:121566798-121567437	GM12878	blood:	n/a	n/a
19	ATF2	chr12:121566714-121567459	GM12878	blood:	n/a	n/a
20	ATF2	chr12:121547862-121548404	GM12878	blood:	n/a	n/a
21	ATF2	chr12:121597229-121597614	GM12878	blood:	n/a	n/a
22	ATF3	chr12:121562110-121562601	HCT-116	colon:	n/a	n/a
23	ATF3	chr12:121562132-121562469	A549	lung:	n/a	n/a
24	ATF3	chr12:121581608-121581979	K562	blood:	n/a	n/a
25	ATF3	chr12:121562226-121562539	K562	blood:	n/a	n/a
26	ATF3	chr12:121548098-121548416	K562	blood:	n/a	n/a
27	ATF3	chr12:121576172-121576432	K562	blood:	n/a	n/a
28	BATF	chr12:121582472-121582837	GM12878	blood:	n/a	chr12:121582639-121582650
29	BATF	chr12:121547894-121548437	GM12878	blood:	n/a	n/a
30	BATF	chr12:121581687-121581999	GM12878	blood:	n/a	n/a
31	BATF	chr12:121581691-121581953	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:121597274-121597579	GM12878	blood:	n/a	chr12:121597483-121597492
33	BCL11A	chr12:121547884-121548479	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:121581688-121581956	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:121581727-121581908	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:121547886-121548416	GM12878	blood:	n/a	n/a
37	BCL3	chr12:121562161-121562550	A549	lung:	n/a	chr12:121562488-121562497
38	BCLAF1	chr12:121566680-121567405	GM12878	blood:	n/a	n/a
39	BCLAF1	chr12:121547881-121548461	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:121576146-121576345	K562	blood:	n/a	n/a
41	BHLHE40	chr12:121581734-121581956	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:121597300-121597618	GM12878	blood:	n/a	n/a
43	BHLHE40	chr12:121566732-121567393	K562	blood:	n/a	n/a
44	BHLHE40	chr12:121566812-121567545	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:121561433-121561605	K562	blood:	n/a	chr12:121561504-121561525
46	BHLHE40	chr12:121566868-121567199	HepG2	liver:	n/a	n/a
47	BHLHE40	chr12:121558260-121558488	K562	blood:	n/a	n/a
48	BHLHE40	chr12:121570424-121571320	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:121551869-121552119	K562	blood:	n/a	n/a
50	BHLHE40	chr12:121581736-121581994	K562	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121593365-121593415	GM12892	blood:	n/a
2	chr12:121569969-121570019	GM19239	blood:	n/a
3	chr12:121570752-121570802	K562	blood:	n/a
4	chr12:121569969-121570019	HAEpiC	amniotic membrane:	n/a
5	chr12:121570677-121570727	H1-hESC	embryonic stem cell:	embryo
6	chr12:121570875-121570925	MCF-7	breast:	n/a
7	chr12:121569924-121569974	SAEC	small airway:	n/a
8	chr12:121570677-121570727	AG04449	skin:	fetal
9	chr12:121569969-121570019	HUVEC	blood vessel:	n/a
10	chr12:121570677-121570727	HPAEpiC	pulmonary alveolar:	n/a
11	chr12:121571068-121571118	GM12878	blood:	n/a
12	chr12:121569969-121570019	AG09319	gingival:	n/a
13	chr12:121569924-121569974	NT2-D1	testis:	n/a
14	chr12:121593365-121593415	HRPEpiC	eye:	n/a
15	chr12:121570677-121570727	ovcar-3	ovarian:	n/a
16	chr12:121570875-121570925	AG10803	skin:	n/a
17	chr12:121570571-121570621	LNCaP	prostate:	n/a
18	chr12:121582875-121582925	CMK	blood:	n/a
19	chr12:121569969-121570019	HL-60	blood:	n/a
20	chr12:121582875-121582925	LNCaP	prostate:	n/a
21	chr12:121570752-121570802	AG10803	skin:	n/a
22	chr12:121593365-121593415	NHDF-neo	bronchial:	n/a
23	chr12:121570677-121570727	HIPEpiC	eye:	n/a
24	chr12:121570616-121570666	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:121570752-121570802	SK-N-MC	brain:	n/a
26	chr12:121570752-121570802	NB4	blood:	n/a
27	chr12:121570616-121570666	IMR90	lung:	fetal
28	chr12:121569969-121570019	Hela-S3	cervix:	n/a
29	chr12:121571068-121571118	RPTEC	kidney:	n/a
30	chr12:121569969-121570019	HCPEpiC	choroid plexus:	n/a
31	chr12:121570081-121570131	RPTEC	kidney:	n/a
32	chr12:121570677-121570727	Hepatocyte	liver:	n/a
33	chr12:121570752-121570802	ECC-1	luminal epithelium:	n/a
34	chr12:121570677-121570727	BE2_C	brain:	n/a
35	chr12:121570875-121570925	SKMC	muscle:	n/a
36	chr12:121570571-121570621	GM12891	blood:	n/a
37	chr12:121582875-121582925	GM12892	blood:	n/a
38	chr12:121582875-121582925	AG10803	skin:	n/a
39	chr12:121571068-121571118	PANC-1	pancreas:	n/a
40	chr12:121570677-121570727	SKMC	muscle:	n/a
41	chr12:121570616-121570666	HNPCEpiC	eye:	n/a
42	chr12:121569924-121569974	NH-A	brain:	n/a
43	chr12:121570875-121570925	GM12892	blood:	n/a
44	chr12:121569924-121569974	GM19239	blood:	n/a
45	chr12:121570081-121570131	ECC-1	luminal epithelium:	n/a
46	chr12:121571068-121571118	SK-N-SH	brain:	n/a
47	chr12:121593365-121593415	T-47D	breast:	n/a
48	chr12:121569924-121569974	MCF-7	breast:	n/a
49	chr12:121571068-121571118	HMEC	breast:	n/a
50	chr12:121570677-121570727	NHDF-neo	bronchial:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:121550087..121552294-chr12:121646919..121649909,2	MCF-7	breast:
2	chr12:121577786..121581315-chr12:121582515..121587821,6	K562	blood:
3	chr12:121498418..121499035-chr12:121547998..121548758,2	K562	blood:
4	chr12:121576075..121577787-chr12:121578961..121580944,2	K562	blood:
5	chr12:121569906..121572539-chr12:121647803..121649868,2	MCF-7	breast:
6	chr12:121550438..121552806-chr12:121556760..121558947,2	K562	blood:
7	chr12:121578629..121580685-chr12:121583466..121586479,3	K562	blood:
8	chr12:121442844..121443785-chr12:121547734..121548804,3	K562	blood:
9	chr12:121550877..121553101-chr12:121566808..121569789,2	MCF-7	breast:
10	chr12:121574197..121575819-chr12:121598623..121600574,2	MCF-7	breast:
11	chr12:121593680..121596400-chr12:121646406..121649307,2	K562	blood:
12	chr12:121562465..121564050-chr12:121566966..121568974,2	MCF-7	breast:
13	chr12:121548947..121551862-chr12:121555011..121556681,2	MCF-7	breast:
14	chr12:121499365..121500300-chr12:121547555..121548757,7	MCF-7	breast:
15	chr12:121566738..121568870-chr12:121570376..121572315,2	MCF-7	breast:
16	chr12:121581791..121584022-chr12:121646215..121648780,2	K562	blood:
17	chr12:121592630..121595667-chr12:121601270..121604261,3	K562	blood:
18	chr12:121409514..121410021-chr12:121548070..121548945,2	K562	blood:
19	chr12:121555909..121558170-chr12:121651475..121654023,2	K562	blood:
20	chr12:121575022..121577625-chr12:121581601..121583531,2	MCF-7	breast:
21	chr12:121552789..121554818-chr12:121661360..121664343,2	MCF-7	breast:
22	chr12:121590684..121593729-chr12:121595219..121598462,4	K562	blood:
23	chr12:121593895..121595665-chr12:121598530..121600220,2	K562	blood:
24	chr12:121563121..121566575-chr12:121568260..121572155,4	K562	blood:
25	chr12:121593895..121595665-chr12:121598530..121600220,2	K562	blood:
26	chr12:121547752..121548609-chr12:121647435..121648349,3	MCF-7	breast:
27	chr12:121566845..121568445-chr12:121570737..121572613,2	K562	blood:
28	chr12:121578629..121580685-chr12:121583466..121586479,3	K562	blood:
29	chr12:121574197..121575819-chr12:121598623..121600574,2	MCF-7	breast:
30	chr12:121550438..121552806-chr12:121556760..121558947,2	K562	blood:
31	chr12:121548947..121551862-chr12:121555011..121556681,2	MCF-7	breast:
32	chr12:121564281..121567226-chr12:121569639..121571152,2	MCF-7	breast:
33	chr12:121575022..121577625-chr12:121581601..121583531,2	MCF-7	breast:
34	chr12:121569572..121570160-chr12:121640475..121641223,2	MCF-7	breast:
35	chr12:121559257..121561994-chr12:121565943..121568175,2	K562	blood:
36	chr12:121547911..121548611-chr12:121647690..121648251,2	MCF-7	breast:
37	chr12:121561837..121563360-chr12:121583686..121585355,2	K562	blood:
38	chr12:121590684..121593729-chr12:121595219..121598462,4	K562	blood:
39	chr12:121547509..121549908-chr12:121645627..121647537,2	MCF-7	breast:
40	chr12:121569648..121570492-chr12:121613509..121614358,5	MCF-7	breast:
41	chr12:121565478..121567856-chr12:121646838..121650208,3	K562	blood:
42	chr12:121562465..121564050-chr12:121566966..121568974,2	MCF-7	breast:
43	chr12:121550877..121553101-chr12:121566808..121569789,2	MCF-7	breast:
44	chr12:121570400..121573469-chr12:121573505..121577665,4	K562	blood:
45	chr12:121561171..121566774-chr12:121646455..121649214,5	MCF-7	breast:
46	chr12:121531941..121534103-chr12:121555507..121557731,2	K562	blood:
47	chr12:121569636..121570366-chr12:121640682..121641273,2	MCF-7	breast:
48	chr12:121540942..121542575-chr12:121550109..121552835,2	K562	blood:
49	chr12:121447305..121448170-chr12:121547918..121548565,2	MCF-7	breast:
50	chr12:121582333..121584547-chr12:121587526..121589341,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAMKK2-6	chr12:121600009-121600220	NONHSAT031413
2	lnc-P2RX7-2	chr12:121557252-121557692	XLOC_009912
3	lnc-P2RX7-2	chr12:121555321-121555362	XLOC_009912
4	lnc-P2RX7-2	chr12:121556258-121556287	XLOC_009912
5	lnc-P2RX7-2	chr12:121557252-121558609	XLOC_009912

No data

Variant related genes	Relation type
ENSG00000223538	TF binding region
ENSG00000201945	TF binding region
P2RX7	TF binding region
ENSG00000257053	TF binding region
ENSG00000223538	CpG island
ENSG00000201945	CpG island
P2RX7	CpG island
ENSG00000257053	CpG island
ENSG00000257053	chromatin interactions
ENSG00000089041	chromatin interactions
ENSG00000135124	chromatin interactions
HIVEP2	miRNA target sites

Extended variants
information (count: 2447 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2447 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1796415	chr12:121543011-121543012	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34514885	chr12:121543028-121543029	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs560485881	chr12:121543031-121543032	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs537750512	chr12:121543146-121543147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527713501	chr12:121543156-121543157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1618331	chr12:121543166-121543167	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs373835783	chr12:121543191-121543192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567199388	chr12:121543217-121543218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536326550	chr12:121543225-121543226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147929982	chr12:121543235-121543236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538391045	chr12:121543280-121543281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376733298	chr12:121543290-121543291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550112249	chr12:121543326-121543327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568362797	chr12:121543375-121543376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535737609	chr12:121543394-121543395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs5801420	chr12:121543417-121543418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554079603	chr12:121543424-121543425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202114369	chr12:121543426-121543427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201376619	chr12:121543430-121543431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144097690	chr12:121543433-121543434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs202088389	chr12:121543434-121543435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142469340	chr12:121543436-121543437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72374208	chr12:121543444-121543445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566112622	chr12:121543540-121543541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533577536	chr12:121543559-121543560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558588881	chr12:121543570-121543571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115383227	chr12:121543608-121543609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544338663	chr12:121543632-121543633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs3861796	chr12:121543645-121543646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs113096974	chr12:121543658-121543659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113967439	chr12:121543678-121543679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs5801421	chr12:121543690-121543691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11322076	chr12:121543703-121543704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1794900	chr12:121543712-121543713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs575153678	chr12:121543715-121543716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373127910	chr12:121543718-121543719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527650903	chr12:121543746-121543747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188012764	chr12:121543754-121543755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377558766	chr12:121543757-121543758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564556466	chr12:121543760-121543761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531709797	chr12:121543780-121543781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141686189	chr12:121543802-121543803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76334590	chr12:121543806-121543807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12320058	chr12:121543822-121543823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs529475738	chr12:121543899-121543900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545103762	chr12:121543917-121543918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547659201	chr12:121543927-121543928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12320178	chr12:121543979-121543980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs201157408	chr12:121543985-121543986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369987514	chr12:121544021-121544022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1242 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121534000-121545200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:121544200-121544400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:121544200-121544800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:121544400-121544600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:121544600-121544800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr12:121544800-121547200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:121545200-121546200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:121545400-121545800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:121545400-121545800	Enhancers	Placenta	Placenta
10	chr12:121545600-121545800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr12:121546000-121548600	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr12:121546200-121548200	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr12:121546600-121551800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr12:121547200-121548800	Enhancers	HepG2	liver
15	chr12:121547400-121548200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:121547400-121548400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr12:121547400-121548400	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr12:121547400-121548600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr12:121547800-121548000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr12:121548000-121548200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:121548000-121548200	Enhancers	Brain Anterior Caudate	brain
22	chr12:121548000-121548400	Enhancers	Primary B cells from peripheral blood	blood
23	chr12:121548000-121548400	Enhancers	Brain Substantia Nigra	brain
24	chr12:121548000-121548600	Enhancers	Brain Cingulate Gyrus	brain
25	chr12:121548000-121548600	Enhancers	Brain Hippocampus Middle	brain
26	chr12:121548000-121548600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr12:121548000-121548800	Enhancers	Fetal Intestine Small	intestine
28	chr12:121548200-121548400	Enhancers	Primary hematopoietic stem cells	blood
29	chr12:121548200-121548400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr12:121548200-121548600	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr12:121548200-121548600	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr12:121548200-121548800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr12:121548400-121548600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr12:121548400-121548800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr12:121548400-121549600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr12:121548600-121550200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr12:121548800-121550200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr12:121549600-121549800	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr12:121550200-121550400	Weak transcription	Primary hematopoietic stem cells	blood
40	chr12:121550200-121550800	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr12:121550200-121552400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:121550400-121551000	Enhancers	Primary hematopoietic stem cells	blood
43	chr12:121550400-121552200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr12:121550400-121552600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:121551000-121552000	Weak transcription	Primary hematopoietic stem cells	blood
46	chr12:121551000-121552000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr12:121551600-121552400	Enhancers	HMEC	breast
48	chr12:121551800-121552000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr12:121551800-121552400	Enhancers	K562	blood
50	chr12:121551800-121553200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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