Variant report

Variant	nsv1036159
Chromosome Location	chr12:7924713-8040592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1527)
CpG islands
(count:1770)
Chromatin interactive
region (count:13)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:7959526-7959828	K562	blood:	n/a	n/a
2	ARID3A	chr12:7984707-7984990	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:8003917-8004749	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:7959548-7959804	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:7984728-7985022	K562	blood:	n/a	n/a
6	ATF1	chr12:8017264-8017507	K562	blood:	n/a	n/a
7	ATF1	chr12:7996816-7996880	K562	blood:	n/a	n/a
8	ATF1	chr12:8021845-8022067	K562	blood:	n/a	n/a
9	ATF2	chr12:8012580-8013428	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr12:8012535-8013325	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:8009353-8009400	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr12:8012531-8012835	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:8012546-8012846	GM12878	blood:	n/a	chr12:8012761-8012770
14	BHLHE40	chr12:8017224-8017578	K562	blood:	n/a	n/a
15	BHLHE40	chr12:7959591-7959830	K562	blood:	n/a	n/a
16	BHLHE40	chr12:8040472-8040534	K562	blood:	n/a	n/a
17	BHLHE40	chr12:8012724-8012773	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:8004272-8004591	HepG2	liver:	n/a	n/a
19	BHLHE40	chr12:8004230-8004592	HepG2	liver:	n/a	n/a
20	BRCA1	chr12:8013131-8013375	Hela-S3	cervix:	n/a	n/a
21	CCNT2	chr12:8021795-8022050	K562	blood:	n/a	n/a
22	CEBPB	chr12:8021808-8022088	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:7951401-7951531	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr12:7946678-7946878	HepG2	liver:	n/a	chr12:7946725-7946736
25	CEBPB	chr12:7996233-7996412	IMR90	lung:	n/a	n/a
26	CEBPB	chr12:7987356-7987616	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:7987437-7988030	A549	lung:	n/a	n/a
28	CEBPB	chr12:7926343-7926544	A549	lung:	n/a	n/a
29	CEBPB	chr12:7939789-7939790	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:8038614-8038897	K562	blood:	n/a	chr12:8038813-8038824
31	CEBPB	chr12:7987400-7987531	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:8021759-8022095	IMR90	lung:	n/a	n/a
33	CEBPB	chr12:8012161-8012797	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:7949971-7950161	K562	blood:	n/a	chr12:7950009-7950020
35	CEBPB	chr12:8021741-8022070	K562	blood:	n/a	n/a
36	CEBPB	chr12:8012586-8013610	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr12:8038778-8038931	H1-hESC	embryonic stem cell:	n/a	chr12:8038813-8038824
38	CEBPB	chr12:7987790-7988017	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr12:7926356-7926423	K562	blood:	n/a	n/a
40	CEBPB	chr12:8021776-8022087	K562	blood:	n/a	n/a
41	CEBPB	chr12:7987309-7987661	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:8013033-8013601	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr12:7987300-7987985	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:8021756-8022087	HepG2	liver:	n/a	n/a
45	CEBPB	chr12:7949962-7950173	HepG2	liver:	n/a	chr12:7950009-7950020
46	CEBPB	chr12:8013012-8013531	A549	lung:	n/a	n/a
47	CEBPB	chr12:7987334-7987689	MCF-7	breast:	n/a	n/a
48	CEBPB	chr12:7987778-7988037	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr12:7979722-7979842	HepG2	liver:	n/a	chr12:7979762-7979773
50	CEBPB	chr12:8021766-8022066	A549	lung:	n/a	n/a

(count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8025593-8025643	PrEC	prostate:	n/a
2	chr12:8025593-8025643	PrEC	prostate:	n/a
3	chr12:8012926-8012976	ovcar-3	ovarian:	n/a
4	chr12:8025567-8025617	SK-N-SH_RA	brain:	n/a
5	chr12:7941043-7941093	HUVEC	blood vessel:	n/a
6	chr12:7940546-7940596	MCF10A-Er-Src	breast:	n/a
7	chr12:7946814-7946864	PFSK-1	brain:	n/a
8	chr12:7941120-7941170	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:8012926-8012976	PrEC	prostate:	n/a
10	chr12:7940852-7940902	NH-A	brain:	n/a
11	chr12:8015103-8015153	ovcar-3	ovarian:	n/a
12	chr12:7966784-7966834	BJ	skin:	n/a
13	chr12:8025394-8025444	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:7939674-7939724	HIPEpiC	eye:	n/a
15	chr12:7941043-7941093	SK-N-SH	brain:	n/a
16	chr12:7942817-7942867	MCF10A-Er-Src	breast:	n/a
17	chr12:7946814-7946864	GM19239	blood:	n/a
18	chr12:8012926-8012976	AG04449	skin:	fetal
19	chr12:8025861-8025911	NH-A	brain:	n/a
20	chr12:8025861-8025911	H1-hESC	embryonic stem cell:	embryo
21	chr12:8025567-8025617	K562	blood:	n/a
22	chr12:7926589-7926639	K562	blood:	n/a
23	chr12:8025517-8025567	AoSMC	blood vessel:	n/a
24	chr12:8025646-8025696	MCF10A-Er-Src	breast:	n/a
25	chr12:8012926-8012976	HCPEpiC	choroid plexus:	n/a
26	chr12:8015903-8015953	BJ	skin:	n/a
27	chr12:8022108-8022158	HMEC	breast:	n/a
28	chr12:7926589-7926639	SK-N-SH	brain:	n/a
29	chr12:8025567-8025617	NB4	blood:	n/a
30	chr12:7946814-7946864	HMEC	breast:	n/a
31	chr12:7926589-7926639	HRE	kidney:	n/a
32	chr12:8028945-8028995	GM12878	blood:	n/a
33	chr12:8025646-8025696	PANC-1	pancreas:	n/a
34	chr12:8025861-8025911	U87	brain:	n/a
35	chr12:8025517-8025567	HIPEpiC	eye:	n/a
36	chr12:8025567-8025617	ProgFib	skin:	n/a
37	chr12:8028945-8028995	Jurkat	blood:	n/a
38	chr12:7940546-7940596	GM12878	blood:	n/a
39	chr12:8012926-8012976	SK-N-SH	brain:	n/a
40	chr12:8025567-8025617	GM19239	blood:	n/a
41	chr12:8015903-8015953	Hepatocyte	liver:	n/a
42	chr12:7926589-7926639	PFSK-1	brain:	n/a
43	chr12:7939674-7939724	PrEC	prostate:	n/a
44	chr12:8015103-8015153	Jurkat	blood:	n/a
45	chr12:7941959-7942009	HMEC	breast:	n/a
46	chr12:8012926-8012976	LNCaP	prostate:	n/a
47	chr12:7940852-7940902	HRPEpiC	eye:	n/a
48	chr12:7948517-7948567	PANC-1	pancreas:	n/a
49	chr12:8025640-8025690	AG10803	skin:	n/a
50	chr12:8015103-8015153	Hela-S3	cervix:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:7830039..7830628-chr12:7959515..7960112,3	K562	blood:
2	chr12:7785661..7787296-chr12:7958245..7961143,2	K562	blood:
3	chr12:8010803..8012757-chr12:8088381..8089897,2	K562	blood:
4	chr12:8012482..8013075-chr12:8147622..8148284,2	MCF-7	breast:
5	chr12:8012297..8013140-chr12:8147611..8148236,3	K562	blood:
6	chr12:8036991..8037615-chr12:8067883..8068385,2	MCF-7	breast:
7	chr12:7829622..7830601-chr12:7959144..7960112,6	MCF-7	breast:
8	chr12:8037350..8037880-chr12:8072256..8073016,2	MCF-7	breast:
9	chr12:7869134..7869702-chr12:7959145..7959716,2	MCF-7	breast:
10	chr12:7985856..7986361-chr12:8086765..8087460,2	Hela-S3	cervix:
11	chr12:8021089..8023625-chr12:8037749..8040054,2	MCF-7	breast:
12	chr12:7868671..7869617-chr12:7959225..7960025,4	MCF-7	breast:
13	chr12:7797730..7798285-chr12:7959327..7960129,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A3-2	chr12:8023775-8023879	NONHSAT026272
2	lnc-SLC2A3-2	chr12:8025403-8025460	NONHSAT026272
3	lnc-SLC2A3-2	chr12:8024469-8024544	NONHSAT026272
4	lnc-NANOGP1-2	chr12:8013033-8013360	NONHSAT026271
5	lnc-SLC2A3-2	chr12:8023446-8023658	NONHSAT026272

No data

Variant related genes	Relation type
ENSG00000201663	TF binding region
NANOG	TF binding region
ENSG00000201549	TF binding region
SLC2A14	TF binding region
ENSG00000222978	TF binding region
ENSG00000255885	TF binding region
ENSG00000241828	TF binding region
NANOGP1	TF binding region
ENSG00000199912	TF binding region
ENSG00000201663	CpG island
NANOG	CpG island
ENSG00000201549	CpG island
SLC2A14	CpG island
ENSG00000222978	CpG island
ENSG00000255885	CpG island
ENSG00000241828	CpG island
NANOGP1	CpG island
ENSG00000199912	CpG island
ENSG00000240739	chromatin interactions
ENSG00000255885	chromatin interactions
ENSG00000059804	chromatin interactions

Extended variants
information (count: 3634 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3634 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562914380	chr12:7924769-7924770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144018241	chr12:7924815-7924816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576794181	chr12:7924893-7924894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112922523	chr12:7924905-7924906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188874971	chr12:7924943-7924944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146457149	chr12:7925014-7925015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs193047277	chr12:7925022-7925023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562391511	chr12:7925153-7925154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs367672694	chr12:7925172-7925173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71038747	chr12:7925173-7925174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs398018315	chr12:7925192-7925193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371745823	chr12:7925216-7925217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527849105	chr12:7925267-7925268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547978304	chr12:7925555-7925556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140698157	chr12:7925584-7925585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376242993	chr12:7925587-7925588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79250975	chr12:7925678-7925679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs5796288	chr12:7925716-7925717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78501393	chr12:7925732-7925733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs397776682	chr12:7925733-7925734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559944193	chr12:7925753-7925754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185115985	chr12:7925763-7925764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532280954	chr12:7925764-7925765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551745757	chr12:7925786-7925787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568544985	chr12:7925851-7925852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190358299	chr12:7925883-7925884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117508279	chr12:7925928-7925929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112605271	chr12:7926049-7926050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373113302	chr12:7926140-7926141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs28457667	chr12:7926141-7926142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12813092	chr12:7926142-7926143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368301633	chr12:7926211-7926212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181258155	chr12:7926216-7926217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145606542	chr12:7926282-7926283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34488527	chr12:7926291-7926292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115063182	chr12:7926334-7926335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34408824	chr12:7926369-7926370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184126538	chr12:7926427-7926428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538087276	chr12:7926428-7926429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs58053555	chr12:7926509-7926510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187979580	chr12:7926611-7926612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs180838803	chr12:7926663-7926664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148911844	chr12:7926675-7926676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147013986	chr12:7926684-7926685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533703331	chr12:7926699-7926700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371494215	chr12:7926710-7926711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117275614	chr12:7926720-7926721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138084732	chr12:7926735-7926736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186144814	chr12:7926796-7926797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553981796	chr12:7926858-7926859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Nasopharyngeal cancer	20548289	CNVD
Type 2 diabetes	21526130	CNVD
Autism	22495309	CNVD
Bipolar disorder	19214233	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1053 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7918000-7929000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:7920200-7936800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr12:7923000-7925600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:7924600-7924800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr12:7924600-7925800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr12:7924800-7925200	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr12:7925200-7926000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr12:7925600-7926000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:7925600-7926000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:7929000-7929200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:7936800-7937800	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr12:7936800-7938400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:7937000-7937200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr12:7937000-7937400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:7937000-7937600	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr12:7937000-7937800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr12:7937000-7938200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:7937000-7938600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr12:7937200-7937400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:7937200-7937600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr12:7937200-7937600	Enhancers	Stomach Mucosa	stomach
22	chr12:7937200-7937800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr12:7937200-7938600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr12:7937200-7939200	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr12:7937200-7940000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr12:7937400-7937600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr12:7937400-7939000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:7937400-7940200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr12:7937600-7939800	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr12:7937600-7940200	Weak transcription	Stomach Mucosa	stomach
31	chr12:7937800-7938200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr12:7937800-7938200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr12:7937800-7939600	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr12:7938200-7938400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr12:7938200-7938400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr12:7938200-7939600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr12:7938400-7939200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr12:7938400-7939600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr12:7938400-7939600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr12:7938600-7939000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr12:7938600-7939000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr12:7939000-7940000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr12:7939000-7940000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr12:7939000-7941800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:7939200-7939400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr12:7939200-7940000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr12:7939400-7939800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr12:7939600-7939800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr12:7939600-7940000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr12:7939600-7940400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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