Variant report

Variant	nsv10310
Chromosome Location	chr3:121311716-121313964
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	ATF2	chr3:121311674-121312713	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:121311633-121312689	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr3:121312116-121312453	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:121311672-121312712	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:121312115-121312384	HepG2	liver:	n/a	n/a
6	CEBPB	chr3:121312150-121312397	K562	blood:	n/a	n/a
7	CEBPB	chr3:121312057-121312606	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr3:121311645-121312717	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr3:121312073-121312587	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr3:121312160-121312310	GM12873	blood:	n/a	chr3:121312270-121312283
11	CTCF	chr3:121312218-121312350	GM12891	blood:	n/a	chr3:121312270-121312283
12	CTCF	chr3:121312200-121312350	GM12867	blood:	n/a	chr3:121312270-121312283
13	CTCF	chr3:121312231-121312339	K562	blood:	n/a	chr3:121312270-121312283
14	CTCF	chr3:121312229-121312357	Kidney_OC	kidney:	n/a	chr3:121312270-121312283
15	CTCF	chr3:121312120-121312270	GM12864	blood:	n/a	n/a
16	CTCF	chr3:121312260-121312410	NHEK	skin:	n/a	chr3:121312270-121312283
17	CTCF	chr3:121312220-121312370	GM12866	blood:	n/a	chr3:121312270-121312283
18	CTCF	chr3:121312237-121312348	GM19240	blood:	n/a	chr3:121312270-121312283
19	CTCF	chr3:121312141-121312423	K562	blood:	n/a	chr3:121312270-121312283
20	CTCF	chr3:121312220-121312370	RPTEC	kidney:	n/a	chr3:121312270-121312283
21	CTCF	chr3:121312200-121312350	GM12871	blood:	n/a	chr3:121312270-121312283
22	CTCF	chr3:121312200-121312350	HEEpiC	esophagus:	n/a	chr3:121312270-121312283
23	CTCF	chr3:121312220-121312370	GM12865	blood:	n/a	chr3:121312270-121312283
24	CTCF	chr3:121312192-121312371	H1-hESC	embryonic stem cell:	n/a	chr3:121312270-121312283
25	CTCF	chr3:121312240-121312390	RPTEC	kidney:	n/a	chr3:121312270-121312283
26	CTCF	chr3:121312160-121312310	GM12865	blood:	n/a	chr3:121312270-121312283
27	CTCF	chr3:121312140-121312290	GM06990	blood:	n/a	chr3:121312270-121312283
28	CTCF	chr3:121312160-121312310	GM12864	blood:	n/a	chr3:121312270-121312283
29	CTCF	chr3:121312246-121312293	NHEK	skin:	n/a	chr3:121312270-121312283
30	CTCF	chr3:121312200-121312350	WERI-Rb-1	eye:	n/a	chr3:121312270-121312283
31	CTCF	chr3:121312209-121312360	GM12892	blood:	n/a	chr3:121312270-121312283
32	CTCF	chr3:121312285-121312314	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr3:121312140-121312290	HEEpiC	esophagus:	n/a	chr3:121312270-121312283
34	CTCF	chr3:121312257-121312322	GM13977	blood:	n/a	chr3:121312270-121312283
35	E2F4	chr3:121313629-121313695	MCF10A-Er-Src	breast:	n/a	n/a
36	EP300	chr3:121312027-121312704	H1-hESC	embryonic stem cell:	n/a	chr3:121312528-121312542
37	FOXA1	chr3:121313746-121314114	HepG2	liver:	n/a	chr3:121313824-121313836
38	FOXA1	chr3:121313555-121314147	HepG2	liver:	n/a	chr3:121313824-121313836
39	FOXA1	chr3:121313581-121314144	HepG2	liver:	n/a	chr3:121313824-121313836
40	FOXA1	chr3:121313709-121314103	HepG2	liver:	n/a	chr3:121313824-121313836
41	FOXA2	chr3:121313441-121314370	HepG2	liver:	n/a	chr3:121313824-121313836
42	FOXA2	chr3:121313694-121314051	HepG2	liver:	n/a	chr3:121313824-121313836
43	GTF2F1	chr3:121312150-121312648	H1-hESC	embryonic stem cell:	n/a	n/a
44	GTF2F1	chr3:121311825-121311843	H1-hESC	embryonic stem cell:	n/a	n/a
45	HNF4A	chr3:121313675-121314076	HepG2	liver:	n/a	chr3:121313849-121313862 chr3:121313850-121313863 chr3:121313849-121313863 chr3:121313849-121313863 chr3:121313849-121313864 chr3:121313849-121313864 chr3:121313849-121313864 chr3:121313851-121313863 chr3:121313916-121313929 chr3:121313849-121313864 chr3:121313850-121313862 chr3:121313848-121313863 chr3:121313850-121313862 chr3:121313916-121313929 chr3:121313849-121313864 chr3:121313847-121313865 chr3:121313849-121313863 chr3:121313850-121313862
46	HNF4A	chr3:121313762-121314035	HepG2	liver:	n/a	chr3:121313849-121313862 chr3:121313850-121313863 chr3:121313849-121313863 chr3:121313849-121313863 chr3:121313849-121313864 chr3:121313849-121313864 chr3:121313849-121313864 chr3:121313851-121313863 chr3:121313916-121313929 chr3:121313849-121313864 chr3:121313850-121313862 chr3:121313848-121313863 chr3:121313850-121313862 chr3:121313916-121313929 chr3:121313849-121313864 chr3:121313847-121313865 chr3:121313849-121313863 chr3:121313850-121313862
47	JUN	chr3:121311893-121312671	H1-hESC	embryonic stem cell:	n/a	chr3:121312325-121312337 chr3:121312459-121312468 chr3:121312326-121312336
48	JUND	chr3:121313548-121313628	H1-hESC	embryonic stem cell:	n/a	n/a
49	JUND	chr3:121312147-121312416	H1-hESC	embryonic stem cell:	n/a	chr3:121312325-121312337 chr3:121312326-121312336
50	JUND	chr3:121311616-121312712	H1-hESC	embryonic stem cell:	n/a	chr3:121312325-121312337 chr3:121312459-121312468 chr3:121312326-121312336

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121312164-121312214	AG09319	gingival:	n/a
2	chr3:121312164-121312214	PFSK-1	brain:	n/a
3	chr3:121312127-121312177	HNPCEpiC	eye:	n/a
4	chr3:121312127-121312177	AG04450	lung:	fetal
5	chr3:121312127-121312177	BE2_C	brain:	n/a
6	chr3:121312164-121312214	HCT-116	colon:	n/a
7	chr3:121312164-121312214	NT2-D1	testis:	n/a
8	chr3:121312127-121312177	Hela-S3	cervix:	n/a
9	chr3:121312127-121312177	MCF-7	breast:	n/a
10	chr3:121312164-121312214	HRE	kidney:	n/a
11	chr3:121312241-121312291	H1-hESC	embryonic stem cell:	embryo
12	chr3:121312127-121312177	GM12878	blood:	n/a
13	chr3:121312164-121312214	MCF-7	breast:	n/a
14	chr3:121312241-121312291	NHBE	bronchial:	n/a
15	chr3:121312127-121312177	Hepatocyte	liver:	n/a
16	chr3:121312127-121312177	HUVEC	blood vessel:	n/a
17	chr3:121312127-121312177	NHDF-neo	bronchial:	n/a
18	chr3:121312164-121312214	SK-N-SH	brain:	n/a
19	chr3:121312241-121312291	HRCEpiC	kidney:	n/a
20	chr3:121312164-121312214	PrEC	prostate:	n/a
21	chr3:121312127-121312177	SKMC	muscle:	n/a
22	chr3:121312127-121312177	GM19239	blood:	n/a
23	chr3:121312241-121312291	SK-N-MC	brain:	n/a
24	chr3:121312127-121312177	SK-N-MC	brain:	n/a
25	chr3:121312241-121312291	MCF-7	breast:	n/a
26	chr3:121312164-121312214	Hepatocyte	liver:	n/a
27	chr3:121312127-121312177	GM12892	blood:	n/a
28	chr3:121312241-121312291	AG09309	skin:	n/a
29	chr3:121312127-121312177	H1-hESC	embryonic stem cell:	embryo
30	chr3:121312127-121312177	ovcar-3	ovarian:	n/a
31	chr3:121312241-121312291	HNPCEpiC	eye:	n/a
32	chr3:121312164-121312214	ECC-1	luminal epithelium:	n/a
33	chr3:121312127-121312177	U87	brain:	n/a
34	chr3:121312241-121312291	SK-N-SH_RA	brain:	n/a
35	chr3:121312241-121312291	PANC-1	pancreas:	n/a
36	chr3:121312127-121312177	CMK	blood:	n/a
37	chr3:121312241-121312291	BJ	skin:	n/a
38	chr3:121312127-121312177	BJ	skin:	n/a
39	chr3:121312241-121312291	NH-A	brain:	n/a
40	chr3:121312127-121312177	HCPEpiC	choroid plexus:	n/a
41	chr3:121312164-121312214	NH-A	brain:	n/a
42	chr3:121312164-121312214	HMEC	breast:	n/a
43	chr3:121312164-121312214	GM12878	blood:	n/a
44	chr3:121312164-121312214	AG09309	skin:	n/a
45	chr3:121312164-121312214	SAEC	small airway:	n/a
46	chr3:121312241-121312291	HAEpiC	amniotic membrane:	n/a
47	chr3:121312241-121312291	ovcar-3	ovarian:	n/a
48	chr3:121312241-121312291	RPTEC	kidney:	n/a
49	chr3:121312127-121312177	HRCEpiC	kidney:	n/a
50	chr3:121312127-121312177	HIPEpiC	eye:	n/a

Variant related genes	Relation type
FBXO40	TF binding region
FBXO40	CpG island

Extended variants
information (count: 99 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370570588	chr3:121311726-121311727	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs190381724	chr3:121311761-121311762	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs193282098	chr3:121311769-121311770	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs554649187	chr3:121311775-121311776	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs575043385	chr3:121311793-121311794	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs574804336	chr3:121311890-121311891	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs368352627	chr3:121311967-121311968	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs199578793	chr3:121311969-121311970	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs536498762	chr3:121311999-121312000	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs185112358	chr3:121312013-121312014	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs537267936	chr3:121312051-121312052	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs572658623	chr3:121312056-121312057	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs369591262	chr3:121312078-121312079	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs564782379	chr3:121312087-121312088	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs557558434	chr3:121312095-121312096	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs111926308	chr3:121312116-121312117	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs190301189	chr3:121312138-121312139	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs374588621	chr3:121312205-121312206	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs529717041	chr3:121312224-121312225	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs539919417	chr3:121312242-121312243	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs544751868	chr3:121312252-121312253	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs116666533	chr3:121312282-121312283	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs532706761	chr3:121312283-121312284	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs181179710	chr3:121312304-121312305	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs367739954	chr3:121312383-121312384	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs552803089	chr3:121312393-121312394	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs569514101	chr3:121312407-121312408	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs114538772	chr3:121312423-121312424	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs548883664	chr3:121312507-121312508	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs568328157	chr3:121312519-121312520	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs77137628	chr3:121312569-121312570	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs553927226	chr3:121312574-121312575	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs185735543	chr3:121312609-121312610	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs79444863	chr3:121312612-121312613	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs558313767	chr3:121312626-121312627	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs71621662	chr3:121312673-121312674	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575126714	chr3:121312778-121312779	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs544153135	chr3:121312782-121312783	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs554867237	chr3:121312790-121312791	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs188834677	chr3:121312873-121312874	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs540226761	chr3:121312874-121312875	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs560237937	chr3:121312900-121312901	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs532237901	chr3:121312926-121312927	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs10934553	chr3:121312951-121312952	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs368740112	chr3:121312952-121312953	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs543333693	chr3:121312979-121312980	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs531947915	chr3:121312980-121312981	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs563513850	chr3:121312990-121312991	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs532342299	chr3:121313000-121313001	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs180863579	chr3:121313015-121313016	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121293600-121311800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:121309200-121311800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:121311000-121313200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr3:121311400-121315000	Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr3:121311600-121311800	Flanking Active TSS	H9 Cell Line	embryonic stem cell
6	chr3:121311600-121311800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:121311600-121311800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr3:121311600-121312000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:121311600-121312000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr3:121311600-121312000	Flanking Active TSS	Fetal Heart	heart
11	chr3:121311600-121312000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr3:121311600-121312000	Enhancers	Stomach Smooth Muscle	stomach
13	chr3:121311600-121312200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr3:121311600-121312200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr3:121311600-121312200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr3:121311600-121312200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr3:121311600-121312200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr3:121311600-121312200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:121311600-121312600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:121311600-121312600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr3:121311600-121312600	Enhancers	Ovary	ovary
22	chr3:121311600-121312600	Enhancers	HSMMtube	muscle
23	chr3:121311600-121313000	Active TSS	Right Ventricle	heart
24	chr3:121311800-121312000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr3:121311800-121312000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr3:121311800-121312000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:121311800-121312000	Enhancers	Spleen	Spleen
28	chr3:121311800-121312200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr3:121311800-121312200	Enhancers	Adipose Nuclei	Adipose
30	chr3:121311800-121312200	Enhancers	Right Atrium	heart
31	chr3:121311800-121312400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr3:121311800-121312400	Enhancers	Fetal Muscle Trunk	muscle
33	chr3:121311800-121312400	Enhancers	Lung	lung
34	chr3:121311800-121312400	Enhancers	Pancreas	Pancrea
35	chr3:121311800-121312400	Enhancers	K562	blood
36	chr3:121311800-121312800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr3:121311800-121315200	Enhancers	Liver	Liver
38	chr3:121311800-121315200	Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr3:121312000-121312200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
40	chr3:121312000-121312200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr3:121312000-121312200	Enhancers	Fetal Intestine Small	intestine
42	chr3:121312000-121312200	Enhancers	HepG2	liver
43	chr3:121312000-121312400	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr3:121312000-121312400	Active TSS	Stomach Smooth Muscle	stomach
45	chr3:121312000-121312600	Active TSS	Psoas Muscle	Psoas
46	chr3:121312000-121312600	Enhancers	GM12878-XiMat	blood
47	chr3:121312000-121313400	Active TSS	Fetal Heart	heart
48	chr3:121312000-121317600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr3:121312000-121320000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr3:121312200-121312400	Enhancers	H9 Cell Line	embryonic stem cell

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