Variant report

Variant	esv1805506
Chromosome Location	chr12:120419963-120427915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:489)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:120426946-120426970	K562	blood:	n/a	n/a
2	ARID3A	chr12:120426272-120426439	K562	blood:	n/a	n/a
3	BACH1	chr12:120427640-120427818	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:120426133-120427103	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:120426289-120426464	K562	blood:	n/a	n/a
6	BCLAF1	chr12:120426645-120426999	GM12878	blood:	n/a	chr12:120426812-120426825 chr12:120426755-120426768 chr12:120426814-120426827
7	BHLHE40	chr12:120427649-120427835	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:120426388-120427256	K562	blood:	n/a	chr12:120426819-120426835 chr12:120426595-120426611 chr12:120426812-120426828 chr12:120426992-120427008 chr12:120426807-120426823
9	BHLHE40	chr12:120426527-120427257	GM12878	blood:	n/a	chr12:120426819-120426835 chr12:120426595-120426611 chr12:120426812-120426828 chr12:120426992-120427008 chr12:120426807-120426823
10	BRCA1	chr12:120426757-120426942	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr12:120427610-120427871	K562	blood:	n/a	n/a
12	CCNT2	chr12:120426485-120427334	K562	blood:	n/a	chr12:120426959-120426968 chr12:120426571-120426580
13	CCNT2	chr12:120427574-120427848	K562	blood:	n/a	n/a
14	CEBPB	chr12:120426536-120426634	K562	blood:	n/a	n/a
15	CEBPB	chr12:120426321-120426993	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:120426848-120426936	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:120422635-120422876	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:120422608-120422852	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:120422621-120422846	A549	lung:	n/a	n/a
20	CHD1	chr12:120427699-120427889	GM12878	blood:	n/a	n/a
21	CHD1	chr12:120427197-120427204	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr12:120427563-120428019	IMR90	lung:	n/a	n/a
23	CHD1	chr12:120427711-120427882	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr12:120426371-120427841	Hela-S3	cervix:	n/a	chr12:120426960-120426970 chr12:120426965-120426975 chr12:120426992-120427002 chr12:120427435-120427445
25	CHD2	chr12:120427635-120427848	GM12878	blood:	n/a	n/a
26	CHD2	chr12:120426789-120426904	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr12:120427300-120427421	HepG2	liver:	n/a	n/a
28	CREB1	chr12:120426373-120427938	HepG2	liver:	n/a	n/a
29	CREB1	chr12:120426488-120427436	A549	lung:	n/a	n/a
30	CREB1	chr12:120427577-120427805	A549	lung:	n/a	n/a
31	CTCF	chr12:120426400-120426550	SAEC	small airway:	n/a	n/a
32	CTCF	chr12:120427140-120427290	HMEC	breast:	n/a	n/a
33	CTCF	chr12:120426287-120426540	ProgFib	skin:	n/a	n/a
34	CTCF	chr12:120426360-120426510	GM12866	blood:	n/a	n/a
35	CTCF	chr12:120426360-120426510	GM12873	blood:	n/a	n/a
36	CTCF	chr12:120426638-120427039	K562	blood:	n/a	chr12:120427019-120427032
37	CTCF	chr12:120426280-120426430	AG10803	skin:	n/a	n/a
38	CTCF	chr12:120426758-120426935	GM13977	blood:	n/a	n/a
39	CTCF	chr12:120426320-120426470	AG04449	skin:	n/a	n/a
40	CTCF	chr12:120427207-120427311	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr12:120426433-120426530	GM20000	blood:	n/a	n/a
42	CTCF	chr12:120426720-120426870	GM12874	blood:	n/a	n/a
43	CTCF	chr12:120426380-120426530	GM12873	blood:	n/a	n/a
44	CTCF	chr12:120426320-120426470	GM12864	blood:	n/a	n/a
45	CTCF	chr12:120426320-120426470	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr12:120426326-120426511	GM12878	blood:	n/a	n/a
47	CTCF	chr12:120426400-120426550	HCT-116	colon:	n/a	n/a
48	CTCF	chr12:120426360-120426510	NHEK	skin:	n/a	n/a
49	CTCF	chr12:120426756-120426930	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:120426280-120426430	SAEC	small airway:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:120426784-120426834	HEEpiC	esophagus:	n/a
2	chr12:120426784-120426834	HEEpiC	esophagus:	n/a
3	chr12:120426784-120426834	HEK293	kidney:	embryo
4	chr12:120426784-120426834	NHDF-neo	bronchial:	n/a
5	chr12:120427182-120427232	PFSK-1	brain:	n/a
6	chr12:120426784-120426834	Hela-S3	cervix:	n/a
7	chr12:120426529-120426579	HCT-116	colon:	n/a
8	chr12:120426784-120426834	HRCEpiC	kidney:	n/a
9	chr12:120426550-120426600	LNCaP	prostate:	n/a
10	chr12:120426550-120426600	ovcar-3	ovarian:	n/a
11	chr12:120426550-120426600	GM19239	blood:	n/a
12	chr12:120426550-120426600	HIPEpiC	eye:	n/a
13	chr12:120427182-120427232	HRE	kidney:	n/a
14	chr12:120426529-120426579	AG09319	gingival:	n/a
15	chr12:120426529-120426579	HEEpiC	esophagus:	n/a
16	chr12:120427178-120427228	SAEC	small airway:	n/a
17	chr12:120423883-120423933	SK-N-MC	brain:	n/a
18	chr12:120427182-120427232	NH-A	brain:	n/a
19	chr12:120426618-120426668	Caco-2	colon:	n/a
20	chr12:120426550-120426600	T-47D	breast:	n/a
21	chr12:120426550-120426600	AG09319	gingival:	n/a
22	chr12:120426784-120426834	AG04449	skin:	fetal
23	chr12:120423883-120423933	HCM	heart:	n/a
24	chr12:120426618-120426668	AoSMC	blood vessel:	n/a
25	chr12:120427178-120427228	H1-hESC	embryonic stem cell:	embryo
26	chr12:120426784-120426834	SAEC	small airway:	n/a
27	chr12:120426618-120426668	HL-60	blood:	n/a
28	chr12:120426529-120426579	PrEC	prostate:	n/a
29	chr12:120426784-120426834	HNPCEpiC	eye:	n/a
30	chr12:120427178-120427228	ECC-1	luminal epithelium:	n/a
31	chr12:120427178-120427228	HCM	heart:	n/a
32	chr12:120427667-120427717	HCPEpiC	choroid plexus:	n/a
33	chr12:120427182-120427232	HCM	heart:	n/a
34	chr12:120427178-120427228	AG10803	skin:	n/a
35	chr12:120426618-120426668	ProgFib	skin:	n/a
36	chr12:120426529-120426579	Hela-S3	cervix:	n/a
37	chr12:120426550-120426600	HMEC	breast:	n/a
38	chr12:120426618-120426668	Hepatocyte	liver:	n/a
39	chr12:120427667-120427717	MCF10A-Er-Src	breast:	n/a
40	chr12:120426784-120426834	BJ	skin:	n/a
41	chr12:120427667-120427717	Hela-S3	cervix:	n/a
42	chr12:120426618-120426668	AG04449	skin:	fetal
43	chr12:120426529-120426579	LNCaP	prostate:	n/a
44	chr12:120427182-120427232	PANC-1	pancreas:	n/a
45	chr12:120427667-120427717	PANC-1	pancreas:	n/a
46	chr12:120427667-120427717	GM12892	blood:	n/a
47	chr12:120427178-120427228	NHDF-neo	bronchial:	n/a
48	chr12:120426784-120426834	GM19239	blood:	n/a
49	chr12:120423883-120423933	HMEC	breast:	n/a
50	chr12:120426529-120426579	NH-A	brain:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:120420153..120423656-chr12:120424541..120427660,4	MCF-7	breast:
2	chr12:120426493..120428297-chr12:120534910..120538709,3	MCF-7	breast:
3	chr12:120313729..120318058-chr12:120425281..120428238,3	K562	blood:
4	chr12:120420153..120423656-chr12:120424541..120427660,4	MCF-7	breast:
5	chr12:120424652..120426403-chr12:120728776..120730834,2	MCF-7	breast:
6	chr12:120424699..120427677-chr12:120728453..120732318,6	K562	blood:
7	chr12:120426002..120427624-chr12:120517341..120518989,2	MCF-7	breast:
8	chr12:120419275..120421989-chr12:120429002..120431271,2	K562	blood:
9	chr12:120426746..120427474-chr12:133338037..133338792,2	HCT-116	colon:
10	chr12:120426261..120428229-chr12:120638078..120640091,2	MCF-7	breast:
11	chr12:120426982..120427577-chr19:56825701..56826223,2	Hela-S3	cervix:
12	chr12:120427745..120429727-chr12:120729725..120731576,2	MCF-7	breast:
13	chr12:120426620..120429059-chr12:120727400..120730169,3	MCF-7	breast:
14	chr12:120419269..120420900-chr12:120635417..120637963,2	MCF-7	breast:
15	chr12:120425209..120429306-chr12:120552934..120555400,5	MCF-7	breast:
16	chr12:120420772..120424084-chr12:120424860..120426963,3	MCF-7	breast:
17	chr12:120427086..120431307-chr12:120435070..120439124,5	MCF-7	breast:
18	chr12:120420772..120424084-chr12:120424860..120426963,3	MCF-7	breast:
19	chr12:120410929..120415600-chr12:120416913..120420697,4	MCF-7	breast:
20	chr12:120425840..120426796-chr20:19097523..19098151,2	MCF-7	breast:
21	chr12:120413777..120415664-chr12:120421623..120425591,4	MCF-7	breast:
22	chr12:120425546..120427435-chr12:120477512..120479258,2	MCF-7	breast:
23	chr12:120414941..120417051-chr12:120419035..120420939,2	MCF-7	breast:
24	chr12:120426492..120427432-chr12:120524501..120525382,2	K562	blood:
25	chr12:120425735..120427312-chr12:120553344..120556119,2	MCF-7	breast:
26	chr12:120425977..120426934-chr12:120517209..120518213,3	MCF-7	breast:
27	chr12:120424138..120428272-chr12:120728453..120731316,5	K562	blood:
28	chr12:120425404..120428200-chr12:120435927..120438924,2	K562	blood:

No data

Variant related genes	Relation type
CCDC64	TF binding region
CCDC64	CpG island
ENSG00000255857	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000267549	chromatin interactions
ENSG00000131848	chromatin interactions
ENSG00000135127	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000176915	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000122966	chromatin interactions
ENSG00000111737	chromatin interactions

Extended variants
information (count: 171 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:171 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2893812	chr12:120419963-120419964	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373652711	chr12:120419985-120419986	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs75027987	chr12:120419988-120419989	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs570914588	chr12:120420009-120420010	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368061711	chr12:120420067-120420068	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533504609	chr12:120420068-120420069	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs113809301	chr12:120420132-120420133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs10660995	chr12:120420178-120420179	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs373967556	chr12:120420179-120420180	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs199917128	chr12:120420185-120420186	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200907267	chr12:120420188-120420189	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562805357	chr12:120420191-120420192	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs72321926	chr12:120420194-120420195	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200749241	chr12:120420197-120420198	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201876376	chr12:120420200-120420201	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558380770	chr12:120420221-120420222	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs80076600	chr12:120420271-120420272	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144491035	chr12:120420279-120420280	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535783922	chr12:120420283-120420284	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376488543	chr12:120420333-120420334	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555693396	chr12:120420412-120420413	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543091647	chr12:120420414-120420415	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562589466	chr12:120420443-120420444	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531487381	chr12:120420447-120420448	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551396566	chr12:120420461-120420462	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs111300221	chr12:120420479-120420480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369215232	chr12:120420482-120420483	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564806524	chr12:120420492-120420493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs527314139	chr12:120420493-120420494	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs146615706	chr12:120420501-120420502	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566909592	chr12:120420523-120420524	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536002053	chr12:120420535-120420536	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368177955	chr12:120420539-120420540	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs187032479	chr12:120420572-120420573	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141336687	chr12:120420642-120420643	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572318853	chr12:120420648-120420649	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7302874	chr12:120420670-120420671	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs35161344	chr12:120420671-120420672	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558502618	chr12:120420703-120420704	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs189211497	chr12:120420714-120420715	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143714735	chr12:120420771-120420772	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187053363	chr12:120422700-120422701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs543335430	chr12:120422707-120422708	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs192546979	chr12:120422726-120422727	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs528719428	chr12:120422801-120422802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs34826069	chr12:120422808-120422809	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs532008177	chr12:120422821-120422822	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs545923930	chr12:120422825-120422826	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs559456595	chr12:120422876-120422877	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs573010966	chr12:120423919-120423920	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Sudden cardiac death	19188705	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	21509527	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120424000-120425800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr12:120424600-120426200	Enhancers	H9 Cell Line	embryonic stem cell
3	chr12:120425200-120425800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
4	chr12:120425400-120426000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
5	chr12:120425600-120425800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr12:120425600-120425800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
7	chr12:120425600-120425800	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr12:120425600-120425800	Bivalent Enhancer	HepG2	liver
9	chr12:120425600-120426000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
10	chr12:120425600-120426000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr12:120425600-120426000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:120425600-120426200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr12:120425600-120426200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr12:120425800-120426000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
15	chr12:120425800-120426000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
16	chr12:120425800-120426000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
17	chr12:120425800-120426000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
18	chr12:120425800-120426000	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr12:120425800-120426000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:120425800-120426000	Enhancers	Brain Cingulate Gyrus	brain
21	chr12:120425800-120426000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
22	chr12:120425800-120426000	Bivalent Enhancer	Fetal Brain Female	brain
23	chr12:120425800-120426000	Bivalent Enhancer	A549	lung
24	chr12:120425800-120426200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
25	chr12:120425800-120426200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr12:120425800-120426200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
27	chr12:120425800-120426200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:120425800-120426200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr12:120425800-120426200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:120425800-120426200	Enhancers	Primary B cells from peripheral blood	blood
31	chr12:120425800-120426200	Enhancers	Primary T cells fromperipheralblood	blood
32	chr12:120425800-120426200	Enhancers	Primary hematopoietic stem cells	blood
33	chr12:120425800-120426200	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr12:120425800-120426200	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr12:120425800-120426200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:120425800-120426200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:120425800-120426200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr12:120425800-120426200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr12:120425800-120426200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr12:120425800-120426200	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr12:120425800-120426200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
42	chr12:120425800-120426200	Bivalent Enhancer	Dnd41	blood
43	chr12:120425800-120426200	Enhancers	Hela-S3	cervix
44	chr12:120425800-120426200	Enhancers	HepG2	liver
45	chr12:120425800-120426200	Enhancers	HMEC	breast
46	chr12:120425800-120426200	Enhancers	K562	blood
47	chr12:120425800-120426400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr12:120425800-120426400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
49	chr12:120425800-120426400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr12:120426000-120426200	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell

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