Variant report

Variant	esv2761757
Chromosome Location	chr12:85626466-85741934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:85704287-85704562	HepG2	liver:	n/a	n/a
2	ATF2	chr12:85674234-85674859	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:85673925-85674351	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr12:85673890-85674445	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:85672070-85672089	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr12:85674086-85674392	HepG2	liver:	n/a	chr12:85674286-85674302
7	BHLHE40	chr12:85694864-85695174	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:85674051-85674416	A549	lung:	n/a	chr12:85674286-85674302
9	BRCA1	chr12:85673932-85674153	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr12:85674532-85675298	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr12:85725088-85725176	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:85673812-85674196	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:85674187-85674666	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:85659239-85659501	A549	lung:	n/a	chr12:85659315-85659326
15	CEBPB	chr12:85718358-85718597	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:85637235-85637436	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:85641358-85641697	Hela-S3	cervix:	n/a	chr12:85641501-85641513
18	CEBPB	chr12:85722443-85722800	IMR90	lung:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722735-85722752 chr12:85722610-85722619
19	CEBPB	chr12:85722457-85722786	A549	lung:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722735-85722752 chr12:85722610-85722619
20	CEBPB	chr12:85659173-85659496	IMR90	lung:	n/a	chr12:85659315-85659326
21	CEBPB	chr12:85666449-85666664	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:85686722-85687025	Hela-S3	cervix:	n/a	chr12:85686874-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686885 chr12:85686874-85686885 chr12:85686874-85686885 chr12:85686874-85686883
23	CEBPB	chr12:85722482-85722750	H1-hESC	embryonic stem cell:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722610-85722619
24	CEBPB	chr12:85652282-85652436	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr12:85686734-85687014	K562	blood:	n/a	chr12:85686874-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686885 chr12:85686874-85686885 chr12:85686874-85686885 chr12:85686874-85686883
26	CEBPB	chr12:85686698-85687011	HepG2	liver:	n/a	chr12:85686874-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686885 chr12:85686874-85686885 chr12:85686874-85686885 chr12:85686874-85686883
27	CEBPB	chr12:85722468-85722799	HepG2	liver:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722735-85722752 chr12:85722610-85722619
28	CEBPB	chr12:85657771-85657832	A549	lung:	n/a	n/a
29	CEBPB	chr12:85666453-85666732	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:85673583-85675940	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:85722452-85722751	K562	blood:	n/a	chr12:85722609-85722620 chr12:85722608-85722621 chr12:85722608-85722619 chr12:85722610-85722619
32	CEBPB	chr12:85688019-85688136	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:85671689-85671797	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr12:85659294-85659415	K562	blood:	n/a	chr12:85659315-85659326
35	CEBPB	chr12:85653520-85653539	Hela-S3	cervix:	n/a	chr12:85653520-85653529
36	CEBPB	chr12:85686742-85686942	A549	lung:	n/a	chr12:85686874-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686883 chr12:85686874-85686883 chr12:85686872-85686885 chr12:85686872-85686885 chr12:85686874-85686885 chr12:85686874-85686885 chr12:85686874-85686883
37	CEBPB	chr12:85657681-85657860	K562	blood:	n/a	n/a
38	CEBPB	chr12:85659161-85659499	HepG2	liver:	n/a	chr12:85659315-85659326
39	CEBPB	chr12:85647607-85648083	Hela-S3	cervix:	n/a	n/a
40	CHD1	chr12:85673361-85673574	H1-hESC	embryonic stem cell:	n/a	chr12:85673513-85673523
41	CHD1	chr12:85674004-85674385	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr12:85673863-85674704	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr12:85672170-85672308	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr12:85647638-85648104	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr12:85673372-85675289	Hela-S3	cervix:	n/a	chr12:85673513-85673523
46	CREB1	chr12:85674176-85674475	A549	lung:	n/a	n/a
47	CREB1	chr12:85674483-85674811	A549	lung:	n/a	n/a
48	CREB1	chr12:85673876-85674778	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr12:85673779-85674985	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTBP2	chr12:85671727-85674564	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85673879-85673929	MCF-7	breast:	n/a
2	chr12:85667616-85667666	NB4	blood:	n/a
3	chr12:85673918-85673968	AG04449	skin:	fetal
4	chr12:85673879-85673929	MCF-7	breast:	n/a
5	chr12:85667616-85667666	NB4	blood:	n/a
6	chr12:85673918-85673968	AG04449	skin:	fetal
7	chr12:85672285-85672335	NB4	blood:	n/a
8	chr12:85673879-85673929	Jurkat	blood:	n/a
9	chr12:85674458-85674508	HAEpiC	amniotic membrane:	n/a
10	chr12:85673270-85673320	RPTEC	kidney:	n/a
11	chr12:85672285-85672335	HEEpiC	esophagus:	n/a
12	chr12:85673915-85673965	GM12891	blood:	n/a
13	chr12:85673200-85673250	HEEpiC	esophagus:	n/a
14	chr12:85673860-85673910	HepG2	liver:	n/a
15	chr12:85673200-85673250	HRE	kidney:	n/a
16	chr12:85674458-85674508	HRPEpiC	eye:	n/a
17	chr12:85674458-85674508	ECC-1	luminal epithelium:	n/a
18	chr12:85673918-85673968	LNCaP	prostate:	n/a
19	chr12:85671976-85672026	Hela-S3	cervix:	n/a
20	chr12:85677430-85677480	NHDF-neo	bronchial:	n/a
21	chr12:85674531-85674581	HL-60	blood:	n/a
22	chr12:85673221-85673271	BJ	skin:	n/a
23	chr12:85673879-85673929	SK-N-MC	brain:	n/a
24	chr12:85674531-85674581	MCF-7	breast:	n/a
25	chr12:85674531-85674581	PFSK-1	brain:	n/a
26	chr12:85673918-85673968	PFSK-1	brain:	n/a
27	chr12:85673918-85673968	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:85673200-85673250	HCM	heart:	n/a
29	chr12:85671976-85672026	NHBE	bronchial:	n/a
30	chr12:85674296-85674346	HUVEC	blood vessel:	n/a
31	chr12:85667616-85667666	HRPEpiC	eye:	n/a
32	chr12:85667451-85667501	HIPEpiC	eye:	n/a
33	chr12:85673270-85673320	Hepatocyte	liver:	n/a
34	chr12:85673884-85673934	SKMC	muscle:	n/a
35	chr12:85674458-85674508	MCF10A-Er-Src	breast:	n/a
36	chr12:85674458-85674508	HepG2	liver:	n/a
37	chr12:85673918-85673968	K562	blood:	n/a
38	chr12:85677430-85677480	ProgFib	skin:	n/a
39	chr12:85673918-85673968	HMEC	breast:	n/a
40	chr12:85673918-85673968	SK-N-MC	brain:	n/a
41	chr12:85673884-85673934	GM12878	blood:	n/a
42	chr12:85677430-85677480	SKMC	muscle:	n/a
43	chr12:85671892-85671942	SK-N-SH	brain:	n/a
44	chr12:85671811-85671861	MCF10A-Er-Src	breast:	n/a
45	chr12:85674140-85674190	AoSMC	blood vessel:	n/a
46	chr12:85673221-85673271	HRPEpiC	eye:	n/a
47	chr12:85671811-85671861	SKMC	muscle:	n/a
48	chr12:85673270-85673320	AG09309	skin:	n/a
49	chr12:85673270-85673320	HAEpiC	amniotic membrane:	n/a
50	chr12:85672285-85672335	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85703964..85704769-chr12:85788512..85789218,4	MCF-7	breast:
2	chr12:85712831..85715377-chr12:85729265..85730997,2	MCF-7	breast:
3	chr12:85693571..85695610-chr12:85696379..85699321,2	MCF-7	breast:
4	chr12:85693571..85695610-chr12:85696379..85699321,2	MCF-7	breast:
5	chr12:85688551..85691285-chr12:85694636..85697474,2	MCF-7	breast:
6	chr12:85704116..85704872-chr12:85842034..85842872,2	MCF-7	breast:
7	chr1:11968120..11968947-chr12:85674873..85675678,2	Hela-S3	cervix:
8	chr12:85712831..85715377-chr12:85729265..85730997,2	MCF-7	breast:
9	chr12:85673846..85674381-chr15:59664602..59665102,2	Hela-S3	cervix:
10	chr12:85673978..85677049-chr12:85677580..85680082,3	MCF-7	breast:
11	chr12:85713980..85716222-chr12:85718443..85721765,3	MCF-7	breast:
12	chr12:85673978..85677049-chr12:85677580..85680082,3	MCF-7	breast:
13	chr12:85735992..85737956-chr12:85742669..85744404,2	MCF-7	breast:
14	chr12:85713980..85716222-chr12:85718443..85721765,3	MCF-7	breast:
15	chr12:85625880..85629090-chr12:85630770..85633051,3	K562	blood:
16	chr12:85704213..85704892-chr12:85788326..85789139,2	MCF-7	breast:
17	chr12:85625880..85629090-chr12:85630770..85633051,3	K562	blood:
18	chr12:85688551..85691285-chr12:85694636..85697474,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRIQ1-3	chr12:85657322-85658235	ENSG00000269916.1
2	lnc-ALX1-1	chr12:85736216-85736970	NONHSAT029749
3	lnc-ALX1-1	chr12:85736250-85736690	ENSG00000258815
4	lnc-ALX1-1	chr12:85712736-85712757	ENSG00000258815
5	lnc-ALX1-1	chr12:85712733-85712757	NONHSAT029749
6	lnc-ALX1-1	chr12:85733174-85733276	NONHSAT029749
7	lnc-ALX1-1	chr12:85711838-85711893	ENSG00000258815

Variant related genes	Relation type
ALX1	TF binding region
ENSG00000269916	TF binding region
ENSG00000258815	TF binding region
ALX1	CpG island
ENSG00000269916	CpG island
ENSG00000258815	CpG island
ENSG00000199347	chromatin interactions
ENSG00000157483	chromatin interactions
ENSG00000157470	chromatin interactions

Extended variants
information (count: 2170 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2170 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185879714	chr12:85637604-85637605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141341065	chr12:85637641-85637642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564014643	chr12:85637699-85637700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377638009	chr12:85637720-85637721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs75754297	chr12:85637785-85637786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546176736	chr12:85637818-85637819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567726840	chr12:85637828-85637829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535484688	chr12:85637864-85637865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550424795	chr12:85637905-85637906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138160468	chr12:85637924-85637925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12298581	chr12:85637933-85637934	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs111492649	chr12:85638019-85638020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs57228595	chr12:85638029-85638030	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs188389477	chr12:85638034-85638035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12311669	chr12:85638089-85638090	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs553364877	chr12:85638107-85638108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574746558	chr12:85638115-85638116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537144518	chr12:85638122-85638123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181328468	chr12:85638138-85638139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185947635	chr12:85638147-85638148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575719425	chr12:85638173-85638174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7485144	chr12:85638210-85638211	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs563978077	chr12:85638223-85638224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370529981	chr12:85638239-85638240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143259295	chr12:85638246-85638247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546492397	chr12:85638318-85638319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561695746	chr12:85638323-85638324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376542327	chr12:85638328-85638329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550585021	chr12:85638375-85638376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568837146	chr12:85638427-85638428	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs539589764	chr12:85638432-85638433	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs552795297	chr12:85638460-85638461	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs372636696	chr12:85638470-85638471	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs535290354	chr12:85638479-85638480	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs553727511	chr12:85638481-85638482	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs574744927	chr12:85638506-85638507	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs201185864	chr12:85638549-85638550	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs202126520	chr12:85638567-85638568	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs376086109	chr12:85638592-85638593	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs370803858	chr12:85638625-85638626	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs373537907	chr12:85638627-85638628	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs200114402	chr12:85638634-85638635	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs377651960	chr12:85638636-85638637	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs5799725	chr12:85638646-85638647	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs575637599	chr12:85638655-85638656	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs565483896	chr12:85638691-85638692	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs545899972	chr12:85638757-85638758	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs563890888	chr12:85638778-85638779	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs191146328	chr12:85638796-85638797	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs7488598	chr12:85647810-85647811	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Wilms tumour	21544195	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
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
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85637600-85637800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:85637600-85638600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:85638400-85638800	Active TSS	Hela-S3	cervix
4	chr12:85647800-85648000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:85649800-85650000	Enhancers	A549	lung
6	chr12:85650000-85651200	Weak transcription	A549	lung
7	chr12:85651200-85651400	Enhancers	A549	lung
8	chr12:85659600-85660000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:85659800-85660000	Enhancers	Adipose Nuclei	Adipose
10	chr12:85659800-85660800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:85660000-85660400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr12:85660000-85660600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:85660200-85660400	Enhancers	HUVEC	blood vessel
14	chr12:85660400-85660600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr12:85660400-85660600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr12:85660400-85660800	Enhancers	Primary hematopoietic stem cells	blood
17	chr12:85660600-85661000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:85666000-85666200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:85666600-85666800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
20	chr12:85666600-85666800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:85666800-85667000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
22	chr12:85666800-85667000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
23	chr12:85666800-85667200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
24	chr12:85666800-85667800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
25	chr12:85666800-85667800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:85666800-85668000	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
27	chr12:85666800-85668200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
28	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
29	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
30	chr12:85667000-85667200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr12:85667000-85667200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:85667000-85667200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr12:85667000-85667200	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
36	chr12:85667000-85667400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
37	chr12:85667000-85667400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
38	chr12:85667000-85667400	Bivalent Enhancer	Liver	Liver
39	chr12:85667000-85667400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
40	chr12:85667000-85667400	Bivalent Enhancer	Fetal Heart	heart
41	chr12:85667000-85667400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
42	chr12:85667000-85667400	Bivalent/Poised TSS	NH-A	brain
43	chr12:85667000-85667800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr12:85667000-85667800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
45	chr12:85667000-85667800	Bivalent/Poised TSS	NHDF-Ad	bronchial
46	chr12:85667000-85668000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
47	chr12:85667000-85668000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr12:85667000-85668200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
49	chr12:85667000-85668200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr12:85667200-85667400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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