Variant report

Variant	nsv541511
Chromosome Location	chr12:63562442-63879794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1284)
CpG islands
(count:61)
Chromatin interactive
region (count:32)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63687901-63688475	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:63813947-63814280	K562	blood:	n/a	n/a
3	ARID3A	chr12:63670554-63670812	HepG2	liver:	n/a	n/a
4	ATF1	chr12:63874624-63874684	K562	blood:	n/a	n/a
5	BACH1	chr12:63835477-63835549	K562	blood:	n/a	n/a
6	BATF	chr12:63812966-63813225	GM12878	blood:	n/a	chr12:63813058-63813069 chr12:63813086-63813097 chr12:63813114-63813125
7	BCL11A	chr12:63696177-63696349	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:63696066-63696525	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:63698603-63699162	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:63700346-63700760	GM12878	blood:	n/a	n/a
11	BRCA1	chr12:63600642-63601071	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr12:63813979-63814307	K562	blood:	n/a	n/a
13	CBX3	chr12:63812790-63813727	HCT-116	colon:	n/a	n/a
14	CBX3	chr12:63687968-63688473	HCT-116	colon:	n/a	n/a
15	CBX3	chr12:63812814-63813379	HCT-116	colon:	n/a	n/a
16	CBX3	chr12:63570065-63570332	K562	blood:	n/a	n/a
17	CBX3	chr12:63813973-63814373	K562	blood:	n/a	n/a
18	CEBPB	chr12:63787481-63787733	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:63569654-63569734	IMR90	lung:	n/a	chr12:63569707-63569718
20	CEBPB	chr12:63577350-63577566	HepG2	liver:	n/a	chr12:63577475-63577486
21	CEBPB	chr12:63839778-63840018	HepG2	liver:	n/a	chr12:63839911-63839922
22	CEBPB	chr12:63613516-63613778	IMR90	lung:	n/a	n/a
23	CEBPB	chr12:63625166-63625226	HepG2	liver:	n/a	chr12:63625189-63625200
24	CEBPB	chr12:63737276-63737551	K562	blood:	n/a	n/a
25	CEBPB	chr12:63607177-63607379	A549	lung:	n/a	n/a
26	CEBPB	chr12:63572966-63573073	K562	blood:	n/a	n/a
27	CEBPB	chr12:63572887-63573147	A549	lung:	n/a	n/a
28	CEBPB	chr12:63717194-63717420	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr12:63717188-63717473	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:63737279-63737586	MCF-7	breast:	n/a	n/a
31	CEBPB	chr12:63647886-63648072	A549	lung:	n/a	n/a
32	CEBPB	chr12:63600554-63601331	MCF-7	breast:	n/a	n/a
33	CEBPB	chr12:63577407-63577618	A549	lung:	n/a	chr12:63577475-63577486
34	CEBPB	chr12:63569649-63569765	A549	lung:	n/a	chr12:63569707-63569718
35	CEBPB	chr12:63572869-63573101	IMR90	lung:	n/a	n/a
36	CEBPB	chr12:63569647-63569844	HepG2	liver:	n/a	chr12:63569707-63569718
37	CEBPB	chr12:63613489-63613787	HepG2	liver:	n/a	n/a
38	CEBPB	chr12:63600679-63601182	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr12:63616923-63617223	HepG2	liver:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061
40	CEBPB	chr12:63748967-63749256	A549	lung:	n/a	chr12:63749160-63749171
41	CEBPB	chr12:63573010-63573086	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr12:63600785-63601096	A549	lung:	n/a	n/a
43	CEBPB	chr12:63600261-63601236	MCF-7	breast:	n/a	n/a
44	CEBPB	chr12:63616996-63617194	A549	lung:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061
45	CEBPB	chr12:63717272-63717478	A549	lung:	n/a	n/a
46	CEBPB	chr12:63749118-63749197	HepG2	liver:	n/a	chr12:63749160-63749171
47	CEBPB	chr12:63839788-63839947	H1-hESC	embryonic stem cell:	n/a	chr12:63839911-63839922
48	CEBPB	chr12:63717238-63717470	IMR90	lung:	n/a	n/a
49	CEBPB	chr12:63794562-63794848	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:63616909-63617221	IMR90	lung:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63754169-63754219	HAEpiC	amniotic membrane:	n/a
2	chr12:63754169-63754219	HUVEC	blood vessel:	n/a
3	chr12:63754169-63754219	AG04450	lung:	fetal
4	chr12:63754169-63754219	HCT-116	colon:	n/a
5	chr12:63754169-63754219	NHDF-neo	bronchial:	n/a
6	chr12:63754169-63754219	HEK293	kidney:	embryo
7	chr12:63754169-63754219	A549	lung:	n/a
8	chr12:63754169-63754219	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:63754169-63754219	HCF	heart:	n/a
10	chr12:63754169-63754219	AoSMC	blood vessel:	n/a
11	chr12:63754169-63754219	HNPCEpiC	eye:	n/a
12	chr12:63754169-63754219	Caco-2	colon:	n/a
13	chr12:63754169-63754219	PFSK-1	brain:	n/a
14	chr12:63754169-63754219	BJ	skin:	n/a
15	chr12:63754169-63754219	SKMC	muscle:	n/a
16	chr12:63754169-63754219	NB4	blood:	n/a
17	chr12:63754169-63754219	HepG2	liver:	n/a
18	chr12:63754169-63754219	ProgFib	skin:	n/a
19	chr12:63754169-63754219	Hela-S3	cervix:	n/a
20	chr12:63754169-63754219	HIPEpiC	eye:	n/a
21	chr12:63754169-63754219	HEEpiC	esophagus:	n/a
22	chr12:63754169-63754219	BE2_C	brain:	n/a
23	chr12:63754169-63754219	NH-A	brain:	n/a
24	chr12:63754169-63754219	SK-N-MC	brain:	n/a
25	chr12:63754169-63754219	AG10803	skin:	n/a
26	chr12:63754169-63754219	RPTEC	kidney:	n/a
27	chr12:63754169-63754219	HRE	kidney:	n/a
28	chr12:63754169-63754219	T-47D	breast:	n/a
29	chr12:63754169-63754219	H1-hESC	embryonic stem cell:	embryo
30	chr12:63754169-63754219	SK-N-SH_RA	brain:	n/a
31	chr12:63754169-63754219	HL-60	blood:	n/a
32	chr12:63754169-63754219	CMK	blood:	n/a
33	chr12:63754169-63754219	PANC-1	pancreas:	n/a
34	chr12:63754169-63754219	SAEC	small airway:	n/a
35	chr12:63754169-63754219	SK-N-SH	brain:	n/a
36	chr12:63754169-63754219	GM12878	blood:	n/a
37	chr12:63754169-63754219	MCF10A-Er-Src	breast:	n/a
38	chr12:63754169-63754219	ECC-1	luminal epithelium:	n/a
39	chr12:63754169-63754219	Jurkat	blood:	n/a
40	chr12:63754169-63754219	MCF-7	breast:	n/a
41	chr12:63754169-63754219	NT2-D1	testis:	n/a
42	chr12:63754169-63754219	AG09319	gingival:	n/a
43	chr12:63754169-63754219	GM06990	blood:	n/a
44	chr12:63754169-63754219	IMR90	lung:	fetal
45	chr12:63754169-63754219	HCM	heart:	n/a
46	chr12:63754169-63754219	HMEC	breast:	n/a
47	chr12:63754169-63754219	NHBE	bronchial:	n/a
48	chr12:63754169-63754219	AG04449	skin:	fetal
49	chr12:63754169-63754219	Hepatocyte	liver:	n/a
50	chr12:63754169-63754219	HRPEpiC	eye:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63743207..63745868-chr12:63754623..63756737,2	K562	blood:
2	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
3	chr12:63743207..63745868-chr12:63754623..63756737,2	K562	blood:
4	chr12:63545448..63546470-chr12:63670124..63671316,6	MCF-7	breast:
5	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
6	chr12:63708417..63710682-chr12:63712108..63713769,2	K562	blood:
7	chr12:63793684..63795622-chr12:63796848..63799129,2	K562	blood:
8	chr12:63632053..63632963-chr5:177630919..177631572,2	Hela-S3	cervix:
9	chr12:63599815..63602634-chr12:63602685..63604731,2	MCF-7	breast:
10	chr12:63712966..63713795-chr12:64159977..64160513,2	MCF-7	breast:
11	chr12:63719488..63722157-chr12:63724086..63726677,2	K562	blood:
12	chr12:63599815..63602634-chr12:63602685..63604731,2	MCF-7	breast:
13	chr12:63544050..63546794-chr12:63669922..63672775,2	MCF-7	breast:
14	chr12:63768242..63768742-chr9:139887190..139887694,2	Hela-S3	cervix:
15	chr12:63678879..63681620-chr17:58469964..58471603,2	MCF-7	breast:
16	chr12:63799854..63801447-chr12:63805061..63807630,2	MCF-7	breast:
17	chr12:63545428..63546206-chr12:63674883..63675724,2	MCF-7	breast:
18	chr12:63545559..63546473-chr12:63669896..63671149,5	MCF-7	breast:
19	chr12:63497332..63498958-chr12:63670308..63671121,8	MCF-7	breast:
20	chr12:63708417..63710682-chr12:63712108..63713769,2	K562	blood:
21	chr12:63808447..63811341-chr3:64933107..64935525,2	MCF-7	breast:
22	chr12:63617360..63618250-chr8:143764719..143765546,2	MCF-7	breast:
23	chr12:63497053..63498247-chr12:63670255..63671252,4	K562	blood:
24	chr12:63813649..63814184-chr12:64195525..64196396,2	K562	blood:
25	chr12:63714796..63717603-chr12:63718432..63720998,3	K562	blood:
26	chr12:63799854..63801447-chr12:63805061..63807630,2	MCF-7	breast:
27	chr12:63719488..63722157-chr12:63724086..63726677,2	K562	blood:
28	chr12:63714796..63717603-chr12:63718432..63720998,3	K562	blood:
29	chr12:63779288..63781863-chr12:63785380..63788131,2	K562	blood:
30	chr12:63779288..63781863-chr12:63785380..63788131,2	K562	blood:
31	chr12:63793684..63795622-chr12:63796848..63799129,2	K562	blood:
32	chr12:63496969..63497998-chr12:63670271..63671167,8	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM5-5	chr12:63563605-63563746	l_664_chr12:63563604-63657550_brain
2	lnc-AVPR1A-1	chr12:63753656-63753817	ENSG00000258117
3	lnc-TMEM5-5	chr12:63580624-63580735	l_664_chr12:63563604-63657550_brain
4	lnc-AVPR1A-1	chr12:63686409-63686716	ENSG00000258117
5	lnc-TMEM5-5	chr12:63563762-63563912	l_664_chr12:63563604-63657550_brain
6	lnc-TMEM5-5	chr12:63654629-63657550	l_664_chr12:63563604-63657550_brain

No data

Variant related genes	Relation type
HNRNPA1P69	TF binding region
ENSG00000258117	TF binding region
HNRNPA1P69	CpG island
ENSG00000258117	CpG island
ENSG00000148362	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000166148	chromatin interactions

Extended variants
information (count: 6164 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6164 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192003876	chr12:63563606-63563607	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs573670691	chr12:63563644-63563645	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs542780042	chr12:63563661-63563662	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs373055410	chr12:63563677-63563678	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs114622859	chr12:63563690-63563691	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs142383432	chr12:63563699-63563700	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs184464254	chr12:63563711-63563712	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs532769128	chr12:63563714-63563715	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs188514924	chr12:63563746-63563747	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs564938921	chr12:63563807-63563808	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs368013041	chr12:63563833-63563834	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs552813244	chr12:63563834-63563835	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs146541926	chr12:63563840-63563841	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs575655069	chr12:63564078-63564079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543433554	chr12:63564079-63564080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74097660	chr12:63564107-63564108	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184270919	chr12:63564121-63564122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145645611	chr12:63564163-63564164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546252867	chr12:63564209-63564210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559596877	chr12:63564216-63564217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189199390	chr12:63564219-63564220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548415247	chr12:63564245-63564246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568411871	chr12:63564265-63564266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182239047	chr12:63564367-63564368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370142984	chr12:63564375-63564376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551006248	chr12:63564387-63564388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187298074	chr12:63564389-63564390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367814903	chr12:63566410-63566411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555429769	chr12:63566411-63566412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370199506	chr12:63566440-63566441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544767341	chr12:63566457-63566458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564556747	chr12:63566494-63566495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs578137852	chr12:63566552-63566553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542616708	chr12:63566554-63566555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540902215	chr12:63566577-63566578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554328253	chr12:63566578-63566579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558227918	chr12:63566592-63566593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541006883	chr12:63566636-63566637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536316233	chr12:63566644-63566645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552694658	chr12:63566733-63566734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528855559	chr12:63566743-63566744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112771717	chr12:63566852-63566853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572755719	chr12:63566892-63566893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149922928	chr12:63566902-63566903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368087588	chr12:63566906-63566907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144156481	chr12:63566912-63566913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576017477	chr12:63566926-63566927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190868625	chr12:63566936-63566937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551538333	chr12:63566979-63566980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571325840	chr12:63566991-63566992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63564000-63564400	Enhancers	Liver	Liver
2	chr12:63566400-63570000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr12:63586200-63586400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:63586200-63586600	Enhancers	Gastric	stomach
5	chr12:63586400-63586800	Enhancers	Liver	Liver
6	chr12:63586600-63587200	Enhancers	Stomach Mucosa	stomach
7	chr12:63586600-63590000	Weak transcription	Gastric	stomach
8	chr12:63587200-63589800	Weak transcription	Stomach Mucosa	stomach
9	chr12:63589800-63590800	Enhancers	Stomach Mucosa	stomach
10	chr12:63590000-63590400	Enhancers	Gastric	stomach
11	chr12:63599200-63600400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr12:63599400-63601200	Enhancers	Hela-S3	cervix
13	chr12:63599600-63603000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr12:63599800-63600400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:63599800-63601400	Enhancers	Adipose Nuclei	Adipose
16	chr12:63599800-63602600	Enhancers	Liver	Liver
17	chr12:63600000-63601000	Enhancers	Fetal Intestine Large	intestine
18	chr12:63600200-63600800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:63600400-63600800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:63600400-63601000	Enhancers	Stomach Mucosa	stomach
21	chr12:63600400-63601200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:63600800-63601000	Enhancers	Pancreas	Pancrea
23	chr12:63600800-63601200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:63600800-63603800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:63601000-63602000	Weak transcription	Fetal Intestine Large	intestine
26	chr12:63601200-63602600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr12:63602000-63602200	Enhancers	Fetal Intestine Large	intestine
28	chr12:63602000-63602800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:63602600-63603600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:63603600-63603800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:63612800-63613000	Enhancers	Fetal Kidney	kidney
32	chr12:63613400-63614600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr12:63614000-63615200	Enhancers	HMEC	breast
34	chr12:63614200-63620200	Enhancers	Liver	Liver
35	chr12:63614400-63615000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:63614600-63614800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr12:63614600-63615200	Enhancers	Adipose Nuclei	Adipose
38	chr12:63614800-63615000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr12:63615000-63615200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:63615200-63616200	Weak transcription	Adipose Nuclei	Adipose
41	chr12:63615200-63616600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr12:63616400-63616600	Enhancers	Adipose Nuclei	Adipose
43	chr12:63616600-63617000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr12:63617000-63617800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr12:63617000-63617800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr12:63617000-63618000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr12:63617000-63618400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:63617400-63617800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr12:63618000-63621400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr12:63620200-63621000	Flanking Active TSS	Liver	Liver

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