Variant report

Variant	esv2751975
Chromosome Location	chr3:115766285-115902901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:794)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:115812320-115812531	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:115778358-115778910	K562	blood:	n/a	n/a
3	ARID3A	chr3:115858959-115859269	K562	blood:	n/a	n/a
4	ATF2	chr3:115776189-115776779	GM12878	blood:	n/a	n/a
5	BATF	chr3:115858482-115858848	GM12878	blood:	n/a	chr3:115858669-115858679 chr3:115858668-115858679
6	BATF	chr3:115858497-115858790	GM12878	blood:	n/a	chr3:115858669-115858679 chr3:115858668-115858679
7	BHLHE40	chr3:115778549-115778848	K562	blood:	n/a	n/a
8	BHLHE40	chr3:115851656-115851780	K562	blood:	n/a	n/a
9	BRCA1	chr3:115866616-115866634	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr3:115778303-115779068	HCT-116	colon:	n/a	n/a
11	CBX3	chr3:115778404-115779035	HCT-116	colon:	n/a	n/a
12	CCNT2	chr3:115773192-115773494	K562	blood:	n/a	n/a
13	CEBPB	chr3:115804343-115804676	K562	blood:	n/a	chr3:115804485-115804496
14	CEBPB	chr3:115795928-115796270	K562	blood:	n/a	n/a
15	CEBPB	chr3:115867734-115867991	H1-hESC	embryonic stem cell:	n/a	chr3:115867847-115867858 chr3:115867845-115867856
16	CEBPB	chr3:115811429-115811740	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:115812354-115812601	HepG2	liver:	n/a	chr3:115812474-115812487
18	CEBPB	chr3:115811470-115811702	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:115795935-115796266	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:115798741-115799033	K562	blood:	n/a	chr3:115798908-115798921 chr3:115798908-115798921
21	CEBPB	chr3:115812343-115812567	Hela-S3	cervix:	n/a	chr3:115812474-115812487
22	CEBPB	chr3:115795936-115796265	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:115879392-115879617	A549	lung:	n/a	chr3:115879543-115879554
24	CEBPB	chr3:115795967-115796241	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:115778406-115779022	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr3:115867659-115868047	IMR90	lung:	n/a	chr3:115867847-115867858 chr3:115867845-115867856
27	CEBPB	chr3:115804419-115804677	A549	lung:	n/a	chr3:115804485-115804496
28	CEBPB	chr3:115900351-115900528	A549	lung:	n/a	chr3:115900418-115900431
29	CEBPB	chr3:115805718-115805719	K562	blood:	n/a	n/a
30	CEBPB	chr3:115778520-115778951	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:115811566-115811576	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr3:115798793-115799019	A549	lung:	n/a	chr3:115798908-115798921 chr3:115798908-115798921
33	CEBPB	chr3:115882867-115883325	IMR90	lung:	n/a	chr3:115883152-115883163 chr3:115883154-115883163 chr3:115883152-115883165
34	CEBPB	chr3:115899284-115899547	HepG2	liver:	n/a	chr3:115899409-115899420
35	CEBPB	chr3:115848613-115848639	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr3:115867670-115868027	HepG2	liver:	n/a	chr3:115867847-115867858 chr3:115867845-115867856
37	CEBPB	chr3:115804320-115804640	HepG2	liver:	n/a	chr3:115804485-115804496
38	CEBPB	chr3:115817274-115817421	K562	blood:	n/a	n/a
39	CEBPB	chr3:115804343-115804640	Hela-S3	cervix:	n/a	chr3:115804485-115804496
40	CEBPB	chr3:115867754-115867919	HepG2	liver:	n/a	chr3:115867847-115867858 chr3:115867845-115867856
41	CEBPB	chr3:115804340-115804625	H1-hESC	embryonic stem cell:	n/a	chr3:115804485-115804496
42	CEBPB	chr3:115884726-115884867	HepG2	liver:	n/a	chr3:115884769-115884780
43	CEBPB	chr3:115778544-115778733	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:115804301-115804635	K562	blood:	n/a	chr3:115804485-115804496
45	CEBPB	chr3:115811429-115811712	K562	blood:	n/a	n/a
46	CEBPB	chr3:115778480-115778906	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr3:115900319-115900556	IMR90	lung:	n/a	chr3:115900418-115900431
48	CEBPB	chr3:115795978-115796269	A549	lung:	n/a	n/a
49	CEBPB	chr3:115831619-115831938	IMR90	lung:	n/a	chr3:115831759-115831770 chr3:115831757-115831770 chr3:115831759-115831770 chr3:115831757-115831770
50	CEBPB	chr3:115883011-115883257	K562	blood:	n/a	chr3:115883152-115883163 chr3:115883154-115883163 chr3:115883152-115883165

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:115837501-115837551	ECC-1	luminal epithelium:	n/a
2	chr3:115837501-115837551	HepG2	liver:	n/a
3	chr3:115837501-115837551	MCF10A-Er-Src	breast:	n/a
4	chr3:115837501-115837551	CMK	blood:	n/a
5	chr3:115837501-115837551	NHBE	bronchial:	n/a
6	chr3:115837501-115837551	GM12878	blood:	n/a
7	chr3:115837501-115837551	Hepatocyte	liver:	n/a
8	chr3:115837501-115837551	T-47D	breast:	n/a
9	chr3:115837501-115837551	SAEC	small airway:	n/a
10	chr3:115837501-115837551	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:115837501-115837551	HCPEpiC	choroid plexus:	n/a
12	chr3:115837501-115837551	PANC-1	pancreas:	n/a
13	chr3:115837501-115837551	NT2-D1	testis:	n/a
14	chr3:115837501-115837551	GM12892	blood:	n/a
15	chr3:115837501-115837551	BJ	skin:	n/a
16	chr3:115837501-115837551	SK-N-SH	brain:	n/a
17	chr3:115837501-115837551	HUVEC	blood vessel:	n/a
18	chr3:115837501-115837551	BE2_C	brain:	n/a
19	chr3:115837501-115837551	HMEC	breast:	n/a
20	chr3:115837501-115837551	NHDF-neo	bronchial:	n/a
21	chr3:115837501-115837551	GM19239	blood:	n/a
22	chr3:115837501-115837551	IMR90	lung:	fetal
23	chr3:115837501-115837551	A549	lung:	n/a
24	chr3:115837501-115837551	HCM	heart:	n/a
25	chr3:115837501-115837551	NH-A	brain:	n/a
26	chr3:115837501-115837551	MCF-7	breast:	n/a
27	chr3:115837501-115837551	HCF	heart:	n/a
28	chr3:115837501-115837551	GM12891	blood:	n/a
29	chr3:115837501-115837551	ProgFib	skin:	n/a
30	chr3:115837501-115837551	U87	brain:	n/a
31	chr3:115837501-115837551	Caco-2	colon:	n/a
32	chr3:115837501-115837551	Hela-S3	cervix:	n/a
33	chr3:115837501-115837551	RPTEC	kidney:	n/a
34	chr3:115837501-115837551	Jurkat	blood:	n/a
35	chr3:115837501-115837551	HRPEpiC	eye:	n/a
36	chr3:115837501-115837551	K562	blood:	n/a
37	chr3:115837501-115837551	SK-N-MC	brain:	n/a
38	chr3:115837501-115837551	PrEC	prostate:	n/a
39	chr3:115837501-115837551	AG04449	skin:	fetal
40	chr3:115837501-115837551	HEEpiC	esophagus:	n/a
41	chr3:115837501-115837551	HIPEpiC	eye:	n/a
42	chr3:115837501-115837551	HL-60	blood:	n/a
43	chr3:115837501-115837551	GM06990	blood:	n/a
44	chr3:115837501-115837551	HAEpiC	amniotic membrane:	n/a
45	chr3:115837501-115837551	AG09309	skin:	n/a
46	chr3:115837501-115837551	HRCEpiC	kidney:	n/a
47	chr3:115837501-115837551	H1-hESC	embryonic stem cell:	embryo
48	chr3:115837501-115837551	AG09319	gingival:	n/a
49	chr3:115837501-115837551	AoSMC	blood vessel:	n/a
50	chr3:115837501-115837551	AG10803	skin:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:115782312..115784390-chr3:115787119..115790072,2	K562	blood:
2	chr3:115844845..115847305-chr3:115848813..115850468,2	K562	blood:
3	chr3:115858909..115859556-chr3:116235958..116236759,2	MCF-7	breast:
4	chr3:115838925..115841642-chr3:115843217..115845978,2	MCF-7	breast:
5	chr11:62608624..62609620-chr3:115772145..115772665,2	NB4	blood:
6	chr3:115862450..115863088-chr7:54350364..54350864,2	MCF-7	breast:
7	chr3:115779019..115780579-chr3:115783540..115785831,2	K562	blood:
8	chr3:115844845..115847305-chr3:115848813..115850468,2	K562	blood:
9	chr3:115770645..115772165-chr6:142364804..142366315,2	MCF-7	breast:
10	chr17:41464664..41466373-chr3:115770665..115773645,2	MCF-7	breast:
11	chr3:115779019..115780579-chr3:115783540..115785831,2	K562	blood:
12	chr3:115811955..115814777-chr3:115816047..115817763,3	K562	blood:
13	chr3:73160073..73160628-chr3:115771645..115772645,4	HCT-116	colon:
14	chr3:115858694..115859203-chr3:116105156..116105712,2	MCF-7	breast:
15	chr3:73159068..73161464-chr3:115770665..115773645,3	MCF-7	breast:
16	chr3:115782312..115784390-chr3:115787119..115790072,2	K562	blood:
17	chr3:115892441..115895134-chr9:128466129..128468903,2	MCF-7	breast:
18	chr3:115890950..115893420-chr3:115897517..115899878,2	K562	blood:
19	chr3:115784918..115786597-chr3:115787841..115790560,2	K562	blood:
20	chr11:62608648..62609195-chr3:115772145..115772665,2	MCF-7	breast:
21	chr3:115784918..115786597-chr3:115787841..115790560,2	K562	blood:
22	chr10:103124108..103124631-chr3:115772145..115772665,2	HCT-116	colon:
23	chr11:62607723..62610629-chr3:115772165..115773665,2	K562	blood:
24	chr3:115811935..115813455-chr3:115816189..115817763,2	K562	blood:
25	chr17:41464397..41466181-chr3:115772145..115773645,2	MCF-7	breast:
26	chr3:115858744..115859345-chr3:117437910..117438488,2	MCF-7	breast:
27	chr11:18416876..18417614-chr3:115771645..115772165,2	Hela-S3	cervix:
28	chr17:41399462..41401706-chr3:115772145..115773645,2	MCF-7	breast:
29	chr3:115838925..115841642-chr3:115843217..115845978,2	MCF-7	breast:
30	chr17:41463814..41467387-chr3:115770645..115773645,5	K562	blood:
31	chr11:62608633..62609155-chr3:115772145..115772665,2	Hela-S3	cervix:
32	chr3:115811935..115813455-chr3:115816189..115817763,2	K562	blood:
33	chr11:62607697..62610629-chr3:115772145..115773665,2	K562	blood:
34	chr3:115890950..115893420-chr3:115897517..115899878,2	K562	blood:
35	chr3:115811955..115814777-chr3:115816047..115817763,3	K562	blood:
36	chr11:62608645..62609195-chr3:115772145..115772665,4	HCT-116	colon:
37	chr16:28081161..28081756-chr3:115784349..115785248,2	MCF-7	breast:

No data

Variant related genes	Relation type
LSAMP	TF binding region
LSAMP	CpG island
ENSG00000133316	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions

Extended variants
information (count: 5080 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5080 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17630430	chr3:115766285-115766286	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528463833	chr3:115766286-115766287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187846049	chr3:115766342-115766343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565947371	chr3:115766386-115766387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35878133	chr3:115766404-115766405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539378387	chr3:115766417-115766418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62271285	chr3:115766419-115766420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139173461	chr3:115766434-115766435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569833629	chr3:115766452-115766453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192476141	chr3:115766461-115766462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373388349	chr3:115766475-115766476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555457611	chr3:115766492-115766493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115955067	chr3:115766589-115766590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534604180	chr3:115766601-115766602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552731146	chr3:115766604-115766605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577613263	chr3:115766647-115766648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545164559	chr3:115766657-115766658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115767996	chr3:115766658-115766659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114193231	chr3:115766707-115766708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183916390	chr3:115766715-115766716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143109349	chr3:115766753-115766754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528596224	chr3:115766793-115766794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188652552	chr3:115766836-115766837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75602827	chr3:115766846-115766847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546434608	chr3:115766907-115766908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551345698	chr3:115767012-115767013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146037197	chr3:115767014-115767015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530724159	chr3:115767044-115767045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549242243	chr3:115767096-115767097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs118072299	chr3:115767097-115767098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191967759	chr3:115767118-115767119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9832312	chr3:115767145-115767146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs184390906	chr3:115767279-115767280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571114458	chr3:115767286-115767287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538629029	chr3:115767609-115767610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577965703	chr3:115767617-115767618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75573256	chr3:115767620-115767621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77346811	chr3:115767645-115767646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190199676	chr3:115767666-115767667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138837856	chr3:115767673-115767674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182389916	chr3:115767700-115767701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372414141	chr3:115767726-115767727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs72959730	chr3:115767841-115767842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565389394	chr3:115767924-115767925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9289039	chr3:115767937-115767938	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs544665099	chr3:115768001-115768002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1920384	chr3:115768062-115768063	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs530862994	chr3:115768154-115768155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141233736	chr3:115768178-115768179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567432593	chr3:115768187-115768188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Ovarian cancer	22174824	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115753800-115767400	Weak transcription	Fetal Lung	lung
2	chr3:115754000-115770400	Weak transcription	Brain Substantia Nigra	brain
3	chr3:115758000-115772800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:115758800-115769800	Weak transcription	NHEK	skin
5	chr3:115759000-115778200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:115762000-115769000	Weak transcription	Colon Smooth Muscle	Colon
7	chr3:115765200-115766400	Enhancers	Brain Germinal Matrix	brain
8	chr3:115765400-115768000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr3:115765800-115768000	Weak transcription	Fetal Muscle Leg	muscle
10	chr3:115765800-115768800	Weak transcription	K562	blood
11	chr3:115765800-115769600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr3:115765800-115770000	Weak transcription	Brain Cingulate Gyrus	brain
13	chr3:115765800-115770200	Weak transcription	Brain Anterior Caudate	brain
14	chr3:115765800-115770400	Weak transcription	Brain Hippocampus Middle	brain
15	chr3:115766000-115774000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr3:115766000-115775800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr3:115766200-115770000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:115766200-115770000	Weak transcription	Brain Angular Gyrus	brain
19	chr3:115766200-115770200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr3:115766200-115794200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr3:115767400-115768200	Enhancers	Fetal Lung	lung
22	chr3:115767600-115769000	Enhancers	Rectal Smooth Muscle	rectum
23	chr3:115767800-115768400	Enhancers	Fetal Stomach	stomach
24	chr3:115768000-115768200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr3:115768000-115768200	Enhancers	Fetal Muscle Leg	muscle
26	chr3:115768200-115768600	Weak transcription	Fetal Lung	lung
27	chr3:115768200-115768800	Weak transcription	Fetal Muscle Leg	muscle
28	chr3:115768200-115770000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr3:115768400-115768800	Weak transcription	Fetal Stomach	stomach
30	chr3:115768600-115770200	Enhancers	Fetal Lung	lung
31	chr3:115768600-115770600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr3:115768800-115769600	Enhancers	Fetal Stomach	stomach
33	chr3:115768800-115770400	Enhancers	K562	blood
34	chr3:115768800-115770800	Enhancers	Fetal Muscle Leg	muscle
35	chr3:115769000-115770200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr3:115769000-115770400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr3:115769000-115770400	Enhancers	Colon Smooth Muscle	Colon
38	chr3:115769400-115770000	Enhancers	Stomach Smooth Muscle	stomach
39	chr3:115769600-115770400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr3:115769600-115770400	Enhancers	HMEC	breast
41	chr3:115769600-115770600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr3:115769600-115770600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr3:115769600-115771000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr3:115769800-115770000	Enhancers	GM12878-XiMat	blood
45	chr3:115769800-115770200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr3:115769800-115770200	Enhancers	NHEK	skin
47	chr3:115769800-115770600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr3:115770000-115770400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr3:115770000-115770400	Flanking Active TSS	GM12878-XiMat	blood
50	chr3:115770000-115770600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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