Variant report

Variant	nsv1012400
Chromosome Location	chr3:46801805-46872992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:235)
CpG islands
(count:733)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:235 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:46871161-46871655	GM12878	blood:	n/a	n/a
2	BACH1	chr3:46853993-46854163	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
4	BATF	chr3:46871182-46871599	GM12878	blood:	n/a	n/a
5	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:46871123-46871508	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
8	BCLAF1	chr3:46871037-46871634	GM12878	blood:	n/a	n/a
9	CBX3	chr3:46853564-46854307	K562	blood:	n/a	n/a
10	CBX3	chr3:46864817-46865093	K562	blood:	n/a	n/a
11	CBX3	chr3:46862333-46862734	K562	blood:	n/a	n/a
12	CBX3	chr3:46862397-46862721	K562	blood:	n/a	n/a
13	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
14	CCNT2	chr3:46853838-46854110	K562	blood:	n/a	chr3:46854080-46854089
15	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr3:46871277-46871496	GM12878	blood:	n/a	n/a
17	CHD2	chr3:46853890-46853892	GM12878	blood:	n/a	n/a
18	CHD2	chr3:46853361-46853740	H1-hESC	embryonic stem cell:	n/a	chr3:46853514-46853524
19	CREB1	chr3:46871225-46871696	GM12878	blood:	n/a	n/a
20	CREB1	chr3:46871143-46871711	GM12878	blood:	n/a	n/a
21	CTCF	chr3:46871020-46871170	GM12872	blood:	n/a	n/a
22	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
23	CTCF	chr3:46850120-46850270	GM12873	blood:	n/a	chr3:46850217-46850226
24	CTCF	chr3:46871040-46871190	GM12875	blood:	n/a	n/a
25	CTCF	chr3:46846140-46846290	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr3:46853580-46853730	SAEC	small airway:	n/a	n/a
27	CTCF	chr3:46871020-46871170	K562	blood:	n/a	n/a
28	CTCF	chr3:46871000-46871150	GM12866	blood:	n/a	n/a
29	CTCF	chr3:46850200-46850350	GM12864	blood:	n/a	chr3:46850217-46850226
30	CTCF	chr3:46854876-46854950	GM20000	blood:	n/a	n/a
31	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
34	CTCF	chr3:46819600-46819750	GM12873	blood:	n/a	n/a
35	CTCF	chr3:46871040-46871190	GM12873	blood:	n/a	n/a
36	CTCF	chr3:46871060-46871210	GM12864	blood:	n/a	n/a
37	CTCF	chr3:46871111-46871197	Lung_OC	lung:	n/a	n/a
38	CTCF	chr3:46871180-46871330	GM12870	blood:	n/a	n/a
39	CTCF	chr3:46801730-46801825	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr3:46865442-46865496	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr3:46871220-46871370	GM12864	blood:	n/a	n/a
42	CTCF	chr3:46871000-46871150	GM12864	blood:	n/a	n/a
43	CTCF	chr3:46850080-46850230	GM12873	blood:	n/a	chr3:46850217-46850226
44	CTCF	chr3:46871020-46871170	GM12865	blood:	n/a	n/a
45	CTCF	chr3:46854325-46854386	GM20000	blood:	n/a	n/a
46	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:46871060-46871210	GM12873	blood:	n/a	n/a
48	E2F6	chr3:46853813-46854245	A549	lung:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
49	E2F6	chr3:46852724-46853059	H1-hESC	embryonic stem cell:	n/a	n/a
50	E2F6	chr3:46853655-46854327	A549	lung:	n/a	chr3:46854080-46854089 chr3:46854114-46854124

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46853631-46853681	AG10803	skin:	n/a
2	chr3:46853631-46853681	AG10803	skin:	n/a
3	chr3:46854311-46854361	HEK293	kidney:	embryo
4	chr3:46850588-46850638	NB4	blood:	n/a
5	chr3:46854297-46854347	BE2_C	brain:	n/a
6	chr3:46872949-46872999	HL-60	blood:	n/a
7	chr3:46850588-46850638	U87	brain:	n/a
8	chr3:46854173-46854223	HL-60	blood:	n/a
9	chr3:46850588-46850638	Caco-2	colon:	n/a
10	chr3:46854231-46854281	U87	brain:	n/a
11	chr3:46853986-46854036	GM06990	blood:	n/a
12	chr3:46853850-46853900	GM19239	blood:	n/a
13	chr3:46853910-46853960	GM12891	blood:	n/a
14	chr3:46854297-46854347	A549	lung:	n/a
15	chr3:46872239-46872289	HPAEpiC	pulmonary alveolar:	n/a
16	chr3:46856803-46856853	MCF10A-Er-Src	breast:	n/a
17	chr3:46856803-46856853	T-47D	breast:	n/a
18	chr3:46853850-46853900	AG04449	skin:	fetal
19	chr3:46854173-46854223	NB4	blood:	n/a
20	chr3:46854231-46854281	HMEC	breast:	n/a
21	chr3:46856803-46856853	U87	brain:	n/a
22	chr3:46853850-46853900	HRPEpiC	eye:	n/a
23	chr3:46853631-46853681	U87	brain:	n/a
24	chr3:46872949-46872999	GM19239	blood:	n/a
25	chr3:46854173-46854223	T-47D	breast:	n/a
26	chr3:46853631-46853681	ECC-1	luminal epithelium:	n/a
27	chr3:46854297-46854347	Caco-2	colon:	n/a
28	chr3:46853631-46853681	T-47D	breast:	n/a
29	chr3:46853986-46854036	BE2_C	brain:	n/a
30	chr3:46856803-46856853	K562	blood:	n/a
31	chr3:46853910-46853960	HRCEpiC	kidney:	n/a
32	chr3:46854297-46854347	AG04450	lung:	fetal
33	chr3:46853910-46853960	Jurkat	blood:	n/a
34	chr3:46853631-46853681	NH-A	brain:	n/a
35	chr3:46854231-46854281	HNPCEpiC	eye:	n/a
36	chr3:46850588-46850638	NHBE	bronchial:	n/a
37	chr3:46853986-46854036	AoSMC	blood vessel:	n/a
38	chr3:46850588-46850638	AG10803	skin:	n/a
39	chr3:46850588-46850638	HAEpiC	amniotic membrane:	n/a
40	chr3:46854231-46854281	AG09319	gingival:	n/a
41	chr3:46854311-46854361	BJ	skin:	n/a
42	chr3:46854297-46854347	PrEC	prostate:	n/a
43	chr3:46853986-46854036	T-47D	breast:	n/a
44	chr3:46850588-46850638	SAEC	small airway:	n/a
45	chr3:46854231-46854281	HRE	kidney:	n/a
46	chr3:46853850-46853900	Jurkat	blood:	n/a
47	chr3:46856803-46856853	NH-A	brain:	n/a
48	chr3:46853986-46854036	SK-N-MC	brain:	n/a
49	chr3:46872239-46872289	NB4	blood:	n/a
50	chr3:46853631-46853681	HCPEpiC	choroid plexus:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
2	chr3:46858188..46860125-chr3:46939783..46942119,2	K562	blood:
3	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
4	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
5	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
6	chr3:46864966..46867284-chr3:46873787..46876389,2	K562	blood:
7	chr3:46853522..46855564-chr3:46864841..46866780,2	K562	blood:
8	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
9	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
10	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS42-2	chr3:46869999-46870324	NONHSAT089461
2	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458
3	lnc-PRSS50-1	chr3:46853712-46854064	NONHSAT089457
4	lnc-PRSS42-3	chr3:46869645-46869919	NONHSAT089460

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS50	TF binding region
PRSS44	TF binding region
PRSS45	TF binding region
ENSG00000238013	CpG island
PRSS50	CpG island
PRSS44	CpG island
PRSS45	CpG island
ENSG00000188086	chromatin interactions
ENSG00000206549	chromatin interactions
ENSG00000178055	chromatin interactions

Extended variants
information (count: 1146 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1146 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575215348	chr3:46801897-46801898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114899802	chr3:46801906-46801907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112388080	chr3:46801920-46801921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370692858	chr3:46802015-46802016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74608692	chr3:46802039-46802040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563088979	chr3:46802094-46802095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546013007	chr3:46802267-46802268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564725691	chr3:46802393-46802394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532220721	chr3:46802397-46802398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116315921	chr3:46802416-46802417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6442028	chr3:46802435-46802436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs529959269	chr3:46802486-46802487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548142086	chr3:46802492-46802493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569579169	chr3:46802629-46802630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537135948	chr3:46802683-46802684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148759599	chr3:46802692-46802693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571055410	chr3:46802703-46802704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535183143	chr3:46802713-46802714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200900737	chr3:46802751-46802752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553616356	chr3:46802945-46802946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs180997623	chr3:46802970-46802971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532596930	chr3:46802977-46802978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535797793	chr3:46803016-46803017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557306682	chr3:46803078-46803079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374589663	chr3:46803154-46803155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185379469	chr3:46803158-46803159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190930819	chr3:46803164-46803165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564193788	chr3:46803180-46803181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573011105	chr3:46803200-46803201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540793178	chr3:46803203-46803204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368586323	chr3:46803245-46803246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141733338	chr3:46803275-46803276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559144478	chr3:46803276-46803277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563878059	chr3:46803291-46803292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548224045	chr3:46803299-46803300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147900645	chr3:46803300-46803301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567002186	chr3:46803572-46803573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534935938	chr3:46803588-46803589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73065582	chr3:46803617-46803618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs183905559	chr3:46803624-46803625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372771289	chr3:46803841-46803842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532149723	chr3:46803845-46803846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs57059994	chr3:46803895-46803896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552207347	chr3:46803914-46803915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570524382	chr3:46803938-46803939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11291099	chr3:46803947-46803948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534725420	chr3:46803999-46804000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370651771	chr3:46804000-46804001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568591430	chr3:46804007-46804008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188511454	chr3:46804120-46804121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46801000-46802000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:46801000-46802000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:46801000-46802000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr3:46801200-46802000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:46801400-46802000	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr3:46801600-46803400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr3:46802000-46804400	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr3:46804600-46805200	Enhancers	HMEC	breast
9	chr3:46804600-46805400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:46804800-46805000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:46804800-46805200	Enhancers	NHEK	skin
12	chr3:46805000-46809200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:46806000-46806200	Weak transcription	Pancreas	Pancrea
14	chr3:46806200-46806400	ZNF genes & repeats	Pancreas	Pancrea
15	chr3:46809600-46810000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr3:46819200-46820200	Enhancers	Primary B cells from cord blood	blood
17	chr3:46819600-46820000	Enhancers	Primary B cells from peripheral blood	blood
18	chr3:46829800-46831000	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr3:46830400-46831000	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr3:46830800-46831200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr3:46844000-46844400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr3:46844000-46844400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr3:46844400-46847400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:46845600-46846400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:46846400-46851400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:46847800-46849600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr3:46848400-46852800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr3:46848600-46849200	Enhancers	Fetal Intestine Large	intestine
29	chr3:46849000-46852600	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr3:46849200-46851800	Weak transcription	Fetal Intestine Large	intestine
31	chr3:46849600-46849800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr3:46849800-46850000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr3:46850000-46850400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr3:46850000-46850600	Enhancers	GM12878-XiMat	blood
35	chr3:46850000-46852600	Weak transcription	Right Ventricle	heart
36	chr3:46850200-46850400	Enhancers	Fetal Thymus	thymus
37	chr3:46850400-46850600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr3:46850400-46851400	Weak transcription	Fetal Thymus	thymus
39	chr3:46850400-46853200	Weak transcription	Fetal Intestine Small	intestine
40	chr3:46850600-46850800	Enhancers	Lung	lung
41	chr3:46850600-46851800	Weak transcription	GM12878-XiMat	blood
42	chr3:46850600-46852000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:46851000-46852200	Weak transcription	Lung	lung
44	chr3:46851000-46853600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr3:46851400-46852000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:46851400-46852200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr3:46851400-46852200	Enhancers	Thymus	Thymus
48	chr3:46851400-46853200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:46851400-46853200	Enhancers	Fetal Thymus	thymus
50	chr3:46851800-46852000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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