Variant report

Variant	nsv427909
Chromosome Location	chr12:41054306-41322257
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	ATF1	chr12:41091506-41091600	K562	blood:	n/a	n/a
2	ATF2	chr12:41074934-41075291	GM12878	blood:	n/a	n/a
3	ATF2	chr12:41213368-41213748	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:41095553-41095922	GM12878	blood:	n/a	n/a
5	ATF2	chr12:41095495-41095972	GM12878	blood:	n/a	n/a
6	ATF2	chr12:41300798-41301289	GM12878	blood:	n/a	n/a
7	ATF3	chr12:41112137-41112996	A549	lung:	n/a	n/a
8	ATF3	chr12:41112133-41113026	A549	lung:	n/a	n/a
9	ATF3	chr12:41300763-41301489	HCT-116	colon:	n/a	n/a
10	ATF3	chr12:41300812-41301420	HCT-116	colon:	n/a	n/a
11	BACH1	chr12:41112882-41112949	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr12:41223460-41223758	H1-hESC	embryonic stem cell:	n/a	chr12:41223582-41223596
13	BATF	chr12:41095547-41095917	GM12878	blood:	n/a	n/a
14	BATF	chr12:41300851-41301164	GM12878	blood:	n/a	n/a
15	BATF	chr12:41095607-41095850	GM12878	blood:	n/a	n/a
16	BATF	chr12:41300829-41301349	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:41095533-41095952	GM12878	blood:	n/a	n/a
18	BCL3	chr12:41112152-41113088	A549	lung:	n/a	n/a
19	BCL3	chr12:41300832-41301111	GM12878	blood:	n/a	n/a
20	BCL3	chr12:41112128-41113731	A549	lung:	n/a	n/a
21	BHLHE40	chr12:41112220-41112589	A549	lung:	n/a	n/a
22	BHLHE40	chr12:41061948-41062165	A549	lung:	n/a	n/a
23	BHLHE40	chr12:41075076-41075141	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:41145933-41146140	HepG2	liver:	n/a	n/a
25	CBX3	chr12:41300680-41301419	HCT-116	colon:	n/a	n/a
26	CBX3	chr12:41300743-41301398	HCT-116	colon:	n/a	n/a
27	CEBPB	chr12:41136111-41136121	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr12:41292125-41292356	K562	blood:	n/a	chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292261-41292272 chr12:41292261-41292274 chr12:41292263-41292274 chr12:41292263-41292272
29	CEBPB	chr12:41111882-41113025	A549	lung:	n/a	chr12:41112729-41112741
30	CEBPB	chr12:41258094-41258328	HepG2	liver:	n/a	chr12:41258213-41258224
31	CEBPB	chr12:41292120-41292628	A549	lung:	n/a	chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292261-41292272 chr12:41292261-41292274 chr12:41292263-41292274 chr12:41292263-41292272
32	CEBPB	chr12:41164468-41164721	HepG2	liver:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
33	CEBPB	chr12:41164416-41164736	A549	lung:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
34	CEBPB	chr12:41084232-41084531	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr12:41084053-41084569	A549	lung:	n/a	n/a
36	CEBPB	chr12:41164478-41164649	H1-hESC	embryonic stem cell:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
37	CEBPB	chr12:41091457-41091956	A549	lung:	n/a	chr12:41091719-41091732 chr12:41091721-41091732 chr12:41091721-41091732
38	CEBPB	chr12:41301195-41301363	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:41240244-41240257	K562	blood:	n/a	n/a
40	CEBPB	chr12:41135344-41135544	HepG2	liver:	n/a	chr12:41135458-41135471
41	CEBPB	chr12:41084151-41084563	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr12:41300709-41301627	HCT-116	colon:	n/a	n/a
43	CEBPB	chr12:41316813-41317030	HepG2	liver:	n/a	chr12:41316885-41316896
44	CEBPB	chr12:41112135-41113710	A549	lung:	n/a	chr12:41112729-41112741
45	CEBPB	chr12:41164425-41164735	IMR90	lung:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
46	CEBPB	chr12:41292092-41292612	HepG2	liver:	n/a	chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292261-41292272 chr12:41292261-41292274 chr12:41292263-41292274 chr12:41292263-41292272
47	CEBPB	chr12:41276729-41276868	H1-hESC	embryonic stem cell:	n/a	chr12:41276831-41276848 chr12:41276836-41276847 chr12:41276834-41276845
48	CEBPB	chr12:41061695-41062153	A549	lung:	n/a	n/a
49	CEBPB	chr12:41084252-41084501	MCF-7	breast:	n/a	n/a
50	CEBPB	chr12:41098585-41098918	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:41087101-41087151	SAEC	small airway:	n/a
2	chr12:41289297-41289347	HAEpiC	amniotic membrane:	n/a
3	chr12:41087101-41087151	SAEC	small airway:	n/a
4	chr12:41289297-41289347	HAEpiC	amniotic membrane:	n/a
5	chr12:41289297-41289347	AG04450	lung:	fetal
6	chr12:41083590-41083640	RPTEC	kidney:	n/a
7	chr12:41087252-41087302	HRPEpiC	eye:	n/a
8	chr12:41086277-41086327	HCT-116	colon:	n/a
9	chr12:41087101-41087151	NHBE	bronchial:	n/a
10	chr12:41086680-41086730	AoSMC	blood vessel:	n/a
11	chr12:41086800-41086850	AG10803	skin:	n/a
12	chr12:41221689-41221739	GM12878	blood:	n/a
13	chr12:41086050-41086100	HRE	kidney:	n/a
14	chr12:41086198-41086248	Hepatocyte	liver:	n/a
15	chr12:41087092-41087142	HL-60	blood:	n/a
16	chr12:41087459-41087509	GM19239	blood:	n/a
17	chr12:41086800-41086850	ECC-1	luminal epithelium:	n/a
18	chr12:41086365-41086415	HL-60	blood:	n/a
19	chr12:41086050-41086100	LNCaP	prostate:	n/a
20	chr12:41221689-41221739	Jurkat	blood:	n/a
21	chr12:41086282-41086332	HUVEC	blood vessel:	n/a
22	chr12:41083590-41083640	Hepatocyte	liver:	n/a
23	chr12:41087252-41087302	HNPCEpiC	eye:	n/a
24	chr12:41087092-41087142	SAEC	small airway:	n/a
25	chr12:41221855-41221905	AG09319	gingival:	n/a
26	chr12:41087092-41087142	SK-N-MC	brain:	n/a
27	chr12:41221639-41221689	PrEC	prostate:	n/a
28	chr12:41086227-41086277	GM19239	blood:	n/a
29	chr12:41086680-41086730	BE2_C	brain:	n/a
30	chr12:41087101-41087151	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:41087520-41087570	AG04450	lung:	fetal
32	chr12:41221855-41221905	HepG2	liver:	n/a
33	chr12:41086308-41086358	BE2_C	brain:	n/a
34	chr12:41087092-41087142	AG10803	skin:	n/a
35	chr12:41087252-41087302	AG10803	skin:	n/a
36	chr12:41221689-41221739	ECC-1	luminal epithelium:	n/a
37	chr12:41086879-41086929	HRPEpiC	eye:	n/a
38	chr12:41086274-41086324	NB4	blood:	n/a
39	chr12:41087252-41087302	NHBE	bronchial:	n/a
40	chr12:41086198-41086248	PANC-1	pancreas:	n/a
41	chr12:41086365-41086415	GM19239	blood:	n/a
42	chr12:41087520-41087570	MCF10A-Er-Src	breast:	n/a
43	chr12:41085901-41085951	A549	lung:	n/a
44	chr12:41087101-41087151	AG10803	skin:	n/a
45	chr12:41086308-41086358	HRPEpiC	eye:	n/a
46	chr12:41086800-41086850	HRPEpiC	eye:	n/a
47	chr12:41087092-41087142	MCF10A-Er-Src	breast:	n/a
48	chr12:41289297-41289347	HepG2	liver:	n/a
49	chr12:41086800-41086850	AG04450	lung:	fetal
50	chr12:41087520-41087570	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:41154089..41156351-chr12:41156663..41158742,2	K562	blood:
2	chr12:41266646..41269338-chr13:42807949..42810576,2	MCF-7	breast:
3	chr12:41298926..41301018-chr12:41302618..41305586,2	K562	blood:
4	chr12:41249860..41251480-chr12:41252962..41255382,2	K562	blood:
5	chr12:41058052..41059920-chr12:41067347..41069015,2	K562	blood:
6	chr12:41015843..41016729-chr12:41315089..41315598,2	K562	blood:
7	chr12:41058052..41059920-chr12:41067347..41069015,2	K562	blood:
8	chr12:41298926..41301018-chr12:41302618..41305586,2	K562	blood:
9	chr12:41106289..41108607-chr12:41111961..41113819,2	K562	blood:
10	chr12:41311476..41312055-chr19:35811147..35811765,2	MCF-7	breast:
11	chr12:41222882..41225557-chr7:143112465..143114503,2	MCF-7	breast:
12	chr12:41151197..41153698-chr12:41160986..41163331,2	K562	blood:
13	chr12:41162174..41163889-chr12:41167656..41170084,3	K562	blood:
14	chr12:41162174..41163889-chr12:41167656..41170084,3	K562	blood:
15	chr12:41249860..41251480-chr12:41252962..41255382,2	K562	blood:
16	chr12:41061679..41063997-chr12:41066307..41068227,2	K562	blood:
17	chr12:41227812..41228332-chr8:90860181..90861388,5	MCF-7	breast:
18	chr12:41154089..41156351-chr12:41156663..41158742,2	K562	blood:
19	chr12:41061679..41063997-chr12:41066307..41068227,2	K562	blood:
20	chr12:41015662..41016670-chr12:41314832..41315906,5	MCF-7	breast:
21	chr12:41106289..41108607-chr12:41111961..41113819,2	K562	blood:
22	chr12:41015832..41017042-chr12:41315031..41316480,11	MCF-7	breast:
23	chr12:41151197..41153698-chr12:41160986..41163331,2	K562	blood:
24	chr12:40719199..40719744-chr12:41315365..41315912,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC19-5	chr12:41221897-41222103	NONHSAT027744
2	lnc-MUC19-3	chr12:41122613-41123699	NONHSAT027743

Variant related genes	Relation type
ENSG00000257680	TF binding region
CNTN1	TF binding region
ENSG00000257680	CpG island
CNTN1	CpG island

Extended variants
information (count: 8962 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:8962 , 50 per page) page: 1 2 3 4 5 6 7 ... 180

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543390079	chr12:41056414-41056415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs565468828	chr12:41056418-41056419	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs577118053	chr12:41056419-41056420	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs117501555	chr12:41056427-41056428	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs34413303	chr12:41056429-41056430	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs528384093	chr12:41056457-41056458	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs192245406	chr12:41056459-41056460	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs568523358	chr12:41056465-41056466	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs532491993	chr12:41056466-41056467	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs550688651	chr12:41056503-41056504	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs568994119	chr12:41056562-41056563	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs144555349	chr12:41056570-41056571	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs530139378	chr12:41056576-41056577	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs373506669	chr12:41056596-41056597	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs567052902	chr12:41056604-41056605	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs534462777	chr12:41056611-41056612	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs373766548	chr12:41056623-41056624	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs117826669	chr12:41056624-41056625	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs376816303	chr12:41056647-41056648	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs146662109	chr12:41056687-41056688	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs2083957	chr12:41056743-41056744	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs575402341	chr12:41056748-41056749	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs3940638	chr12:41056749-41056750	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs560894140	chr12:41056753-41056754	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs532208468	chr12:41057001-41057002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142537681	chr12:41057010-41057011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374108294	chr12:41057015-41057016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562686163	chr12:41057027-41057028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565335653	chr12:41057037-41057038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs180699100	chr12:41057045-41057046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377379757	chr12:41057048-41057049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548299067	chr12:41057064-41057065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566822457	chr12:41057101-41057102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114568076	chr12:41057109-41057110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571489314	chr12:41057116-41057117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185906907	chr12:41057138-41057139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150963000	chr12:41057197-41057198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1816857	chr12:41057231-41057232	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575415283	chr12:41057241-41057242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536313393	chr12:41057261-41057262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554289676	chr12:41057268-41057269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35469400	chr12:41057270-41057271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572822827	chr12:41057275-41057276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145925563	chr12:41057299-41057300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547615387	chr12:41057307-41057308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147831428	chr12:41057320-41057321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374284761	chr12:41057346-41057347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576720316	chr12:41057380-41057381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141429904	chr12:41057403-41057404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562299894	chr12:41057438-41057439	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ewing''s sarcoma	19144156	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41056400-41056800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:41057000-41058200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr12:41057200-41058200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:41057600-41058000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:41057600-41058000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:41057600-41058200	Enhancers	HMEC	breast
7	chr12:41057600-41058200	Enhancers	NHEK	skin
8	chr12:41057600-41061600	Weak transcription	A549	lung
9	chr12:41061400-41064200	Enhancers	Fetal Lung	lung
10	chr12:41061600-41062600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:41061600-41063200	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr12:41061600-41063200	Enhancers	A549	lung
13	chr12:41062000-41062600	Enhancers	Adipose Nuclei	Adipose
14	chr12:41062000-41062600	Enhancers	Fetal Stomach	stomach
15	chr12:41062000-41063000	Enhancers	Liver	Liver
16	chr12:41062400-41062800	Enhancers	Fetal Kidney	kidney
17	chr12:41062600-41066600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr12:41062800-41066600	Weak transcription	Fetal Kidney	kidney
19	chr12:41063000-41063200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr12:41063200-41064400	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr12:41063400-41063600	Bivalent Enhancer	Liver	Liver
22	chr12:41064200-41066000	Weak transcription	Fetal Lung	lung
23	chr12:41064600-41064800	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr12:41065800-41067400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr12:41066000-41066600	Enhancers	Fetal Lung	lung
26	chr12:41066600-41066800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:41066600-41066800	Enhancers	Colon Smooth Muscle	Colon
28	chr12:41066600-41067000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr12:41066600-41067000	Flanking Active TSS	Fetal Kidney	kidney
30	chr12:41066600-41067000	Flanking Active TSS	Fetal Lung	lung
31	chr12:41066600-41067200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:41066600-41067200	Active TSS	Ovary	ovary
33	chr12:41066800-41067000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr12:41067000-41067200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:41067000-41072600	Weak transcription	Fetal Kidney	kidney
36	chr12:41067200-41067400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr12:41080400-41081000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:41081000-41085800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:41081800-41082000	Enhancers	A549	lung
40	chr12:41082000-41082200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr12:41082000-41082200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:41082000-41082200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr12:41082000-41082400	Enhancers	Ovary	ovary
44	chr12:41082000-41082600	Enhancers	Brain Anterior Caudate	brain
45	chr12:41082000-41082600	Flanking Active TSS	A549	lung
46	chr12:41082200-41083200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:41082200-41085600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr12:41082400-41082600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr12:41082400-41082600	Enhancers	Fetal Kidney	kidney
50	chr12:41082400-41084000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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