Variant report

Variant	nsv533923
Chromosome Location	chr12:85647133-85713608
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	chr12:85673925-85674351	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:85674234-85674859	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	chr12:85674051-85674416	A549	lung:	n/a	chr12:85674286-85674302
8	BHLHE40	chr12:85694864-85695174	GM12878	blood:	n/a	n/a
9	BRCA1	chr12:85673812-85674196	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr12:85673932-85674153	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr12:85674532-85675298	Hela-S3	cervix:	n/a	n/a
12	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
13	CEBPB	chr12:85652282-85652436	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:85688019-85688136	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:85674187-85674666	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr12:85657681-85657860	K562	blood:	n/a	n/a
17	CEBPB	chr12:85659173-85659496	IMR90	lung:	n/a	chr12:85659315-85659326
18	CEBPB	chr12:85653520-85653539	Hela-S3	cervix:	n/a	chr12:85653520-85653529
19	CEBPB	chr12:85659161-85659499	HepG2	liver:	n/a	chr12:85659315-85659326
20	CEBPB	chr12:85647607-85648083	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:85666449-85666664	HepG2	liver:	n/a	n/a
22	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
23	CEBPB	chr12:85659239-85659501	A549	lung:	n/a	chr12:85659315-85659326
24	CEBPB	chr12:85673583-85675940	Hela-S3	cervix:	n/a	n/a
25	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
26	CEBPB	chr12:85657771-85657832	A549	lung:	n/a	n/a
27	CEBPB	chr12:85659294-85659415	K562	blood:	n/a	chr12:85659315-85659326
28	CEBPB	chr12:85671689-85671797	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:85666453-85666732	H1-hESC	embryonic stem cell:	n/a	n/a
30	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
31	CHD1	chr12:85674004-85674385	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr12:85673361-85673574	H1-hESC	embryonic stem cell:	n/a	chr12:85673513-85673523
33	CHD2	chr12:85672170-85672308	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr12:85647638-85648104	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr12:85673372-85675289	Hela-S3	cervix:	n/a	chr12:85673513-85673523
36	CHD2	chr12:85673863-85674704	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr12:85673779-85674985	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr12:85674483-85674811	A549	lung:	n/a	n/a
39	CREB1	chr12:85673876-85674778	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr12:85674176-85674475	A549	lung:	n/a	n/a
41	CTBP2	chr12:85671727-85674564	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTBP2	chr12:85667099-85667756	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr12:85674240-85674328	Fibrobl	skin:	n/a	chr12:85674282-85674295
44	CTCF	chr12:85704700-85704850	GM12873	blood:	n/a	n/a
45	CTCF	chr12:85704360-85704510	HVMF	connective:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
46	CTCF	chr12:85704380-85704530	HCPEpiC	choroid plexus:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
47	CTCF	chr12:85704340-85704490	BJ	skin:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
48	CTCF	chr12:85674300-85674450	HAc	cerebellar:	n/a	n/a
49	CTCF	chr12:85704420-85704570	WERI-Rb-1	eye:	n/a	chr12:85704441-85704459 chr12:85704444-85704457 chr12:85704442-85704458 chr12:85704443-85704464
50	CTCF	chr12:85674210-85674365	H1-hESC	embryonic stem cell:	n/a	chr12:85674282-85674295

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85667616-85667666	LNCaP	prostate:	n/a
2	chr12:85673879-85673929	SKMC	muscle:	n/a
3	chr12:85673270-85673320	BE2_C	brain:	n/a
4	chr12:85673918-85673968	PFSK-1	brain:	n/a
5	chr12:85667616-85667666	LNCaP	prostate:	n/a
6	chr12:85673879-85673929	SKMC	muscle:	n/a
7	chr12:85673270-85673320	BE2_C	brain:	n/a
8	chr12:85673918-85673968	PFSK-1	brain:	n/a
9	chr12:85673884-85673934	SK-N-SH_RA	brain:	n/a
10	chr12:85673221-85673271	SK-N-MC	brain:	n/a
11	chr12:85674140-85674190	HRCEpiC	kidney:	n/a
12	chr12:85671892-85671942	MCF-7	breast:	n/a
13	chr12:85673200-85673250	T-47D	breast:	n/a
14	chr12:85674296-85674346	AG04449	skin:	fetal
15	chr12:85673200-85673250	SK-N-SH_RA	brain:	n/a
16	chr12:85667616-85667666	HCPEpiC	choroid plexus:	n/a
17	chr12:85673884-85673934	HCT-116	colon:	n/a
18	chr12:85667353-85667403	HCT-116	colon:	n/a
19	chr12:85674022-85674072	Caco-2	colon:	n/a
20	chr12:85673270-85673320	HAEpiC	amniotic membrane:	n/a
21	chr12:85674140-85674190	GM12878	blood:	n/a
22	chr12:85671811-85671861	AG09309	skin:	n/a
23	chr12:85674022-85674072	Hepatocyte	liver:	n/a
24	chr12:85671976-85672026	Jurkat	blood:	n/a
25	chr12:85674458-85674508	HIPEpiC	eye:	n/a
26	chr12:85674694-85674744	GM12878	blood:	n/a
27	chr12:85673200-85673250	HRE	kidney:	n/a
28	chr12:85673879-85673929	SK-N-SH	brain:	n/a
29	chr12:85672285-85672335	AoSMC	blood vessel:	n/a
30	chr12:85673884-85673934	HRE	kidney:	n/a
31	chr12:85671811-85671861	PANC-1	pancreas:	n/a
32	chr12:85677430-85677480	ProgFib	skin:	n/a
33	chr12:85672285-85672335	HIPEpiC	eye:	n/a
34	chr12:85673879-85673929	T-47D	breast:	n/a
35	chr12:85674296-85674346	SAEC	small airway:	n/a
36	chr12:85677430-85677480	HRE	kidney:	n/a
37	chr12:85673221-85673271	HepG2	liver:	n/a
38	chr12:85673270-85673320	NHBE	bronchial:	n/a
39	chr12:85673270-85673320	NH-A	brain:	n/a
40	chr12:85673347-85673397	BJ	skin:	n/a
41	chr12:85673221-85673271	BE2_C	brain:	n/a
42	chr12:85673884-85673934	HCPEpiC	choroid plexus:	n/a
43	chr12:85671892-85671942	SK-N-MC	brain:	n/a
44	chr12:85667353-85667403	K562	blood:	n/a
45	chr12:85674458-85674508	K562	blood:	n/a
46	chr12:85673918-85673968	SKMC	muscle:	n/a
47	chr12:85674140-85674190	NHDF-neo	bronchial:	n/a
48	chr12:85673270-85673320	HUVEC	blood vessel:	n/a
49	chr12:85667451-85667501	SK-N-SH_RA	brain:	n/a
50	chr12:85672285-85672335	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85673978..85677049-chr12:85677580..85680082,3	MCF-7	breast:
2	chr12:85712831..85715377-chr12:85729265..85730997,2	MCF-7	breast:
3	chr12:85673846..85674381-chr15:59664602..59665102,2	Hela-S3	cervix:
4	chr1:11968120..11968947-chr12:85674873..85675678,2	Hela-S3	cervix:
5	chr12:85693571..85695610-chr12:85696379..85699321,2	MCF-7	breast:
6	chr12:85688551..85691285-chr12:85694636..85697474,2	MCF-7	breast:
7	chr12:85693571..85695610-chr12:85696379..85699321,2	MCF-7	breast:
8	chr12:85703964..85704769-chr12:85788512..85789218,4	MCF-7	breast:
9	chr12:85673978..85677049-chr12:85677580..85680082,3	MCF-7	breast:
10	chr12:85704213..85704892-chr12:85788326..85789139,2	MCF-7	breast:
11	chr12:85688551..85691285-chr12:85694636..85697474,2	MCF-7	breast:
12	chr12:85704116..85704872-chr12:85842034..85842872,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALX1-1	chr12:85712736-85712757	ENSG00000258815
2	lnc-LRRIQ1-3	chr12:85657322-85658235	ENSG00000269916.1
3	lnc-ALX1-1	chr12:85712733-85712757	NONHSAT029749
4	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: 1906 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1906 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7488598	chr12:85647810-85647811	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139884735	chr12:85647826-85647827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529591744	chr12:85647830-85647831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550516261	chr12:85647872-85647873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568920957	chr12:85647911-85647912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183507112	chr12:85647956-85647957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551873796	chr12:85647965-85647966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566880691	chr12:85647974-85647975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540991242	chr12:85649833-85649834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550043062	chr12:85649871-85649872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571565355	chr12:85649892-85649893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11612775	chr12:85649896-85649897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs36010388	chr12:85649901-85649902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538562778	chr12:85649910-85649911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538403716	chr12:85649932-85649933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs11116761	chr12:85649964-85649965	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs575298331	chr12:85649975-85649976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565556637	chr12:85649989-85649990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536318250	chr12:85650007-85650008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150337641	chr12:85650016-85650017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575767599	chr12:85650030-85650031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372854590	chr12:85650061-85650062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544390868	chr12:85650107-85650108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542398824	chr12:85650209-85650210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556385718	chr12:85650225-85650226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11834339	chr12:85650237-85650238	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545385809	chr12:85650238-85650239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190104188	chr12:85650240-85650241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374887989	chr12:85650256-85650257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181145957	chr12:85650257-85650258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145140939	chr12:85650262-85650263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572535400	chr12:85650265-85650266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79299881	chr12:85650363-85650364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561350378	chr12:85650378-85650379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531890218	chr12:85650384-85650385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113146003	chr12:85650401-85650402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549957402	chr12:85650421-85650422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185339168	chr12:85650454-85650455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142262836	chr12:85650515-85650516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9651975	chr12:85650539-85650540	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564796345	chr12:85650586-85650587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190198645	chr12:85650594-85650595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35609457	chr12:85650623-85650624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535856235	chr12:85650624-85650625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547822815	chr12:85650659-85650660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368345622	chr12:85650814-85650815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11837882	chr12:85650819-85650820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372685290	chr12:85650822-85650823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541495250	chr12:85650824-85650825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530643270	chr12:85650834-85650835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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

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