Variant report

Variant	nsv877139
Chromosome Location	chr3:87600636-87766543
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:87614295-87614351	K562	blood:	n/a	n/a
2	ATF1	chr3:87661797-87661994	K562	blood:	n/a	n/a
3	ATF1	chr3:87676571-87676792	K562	blood:	n/a	n/a
4	ATF2	chr3:87723828-87724353	GM12878	blood:	n/a	n/a
5	ATF2	chr3:87723887-87724325	GM12878	blood:	n/a	n/a
6	BACH1	chr3:87611258-87611265	K562	blood:	n/a	n/a
7	BCL11A	chr3:87670905-87671200	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:87723898-87724281	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:87723571-87723850	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:87723845-87724273	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:87723553-87724426	GM12878	blood:	n/a	n/a
12	CBX3	chr3:87664665-87664997	K562	blood:	n/a	n/a
13	CBX3	chr3:87656209-87656523	K562	blood:	n/a	n/a
14	CBX3	chr3:87656185-87656439	K562	blood:	n/a	n/a
15	CBX3	chr3:87664686-87664965	K562	blood:	n/a	n/a
16	CEBPB	chr3:87751750-87752093	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:87665446-87665661	HepG2	liver:	n/a	chr3:87665588-87665599
18	CEBPB	chr3:87745312-87745604	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:87675289-87675572	HepG2	liver:	n/a	chr3:87675466-87675477
20	CEBPB	chr3:87600475-87600675	K562	blood:	n/a	n/a
21	CEBPB	chr3:87751861-87751982	A549	lung:	n/a	n/a
22	CEBPB	chr3:87674094-87674465	K562	blood:	n/a	n/a
23	CEBPB	chr3:87745305-87745603	K562	blood:	n/a	n/a
24	CEBPB	chr3:87733924-87734070	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr3:87751904-87751914	K562	blood:	n/a	n/a
26	CEBPB	chr3:87665485-87665674	A549	lung:	n/a	chr3:87665588-87665599
27	CEBPB	chr3:87745382-87745531	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:87674126-87674368	K562	blood:	n/a	n/a
29	CEBPB	chr3:87724235-87724530	K562	blood:	n/a	chr3:87724379-87724390 chr3:87724380-87724391 chr3:87724379-87724392
30	CEBPB	chr3:87733900-87734091	K562	blood:	n/a	n/a
31	CEBPB	chr3:87675358-87675558	K562	blood:	n/a	chr3:87675466-87675477
32	CEBPB	chr3:87724224-87724507	HepG2	liver:	n/a	chr3:87724379-87724390 chr3:87724380-87724391 chr3:87724379-87724392
33	CEBPB	chr3:87665503-87665712	K562	blood:	n/a	chr3:87665588-87665599
34	CHD1	chr3:87690489-87690513	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr3:87759864-87759865	GM12878	blood:	n/a	n/a
36	CHD2	chr3:87676545-87676752	K562	blood:	n/a	n/a
37	CHD2	chr3:87723628-87724380	GM12878	blood:	n/a	n/a
38	CREB1	chr3:87723856-87724260	GM12878	blood:	n/a	n/a
39	CTCF	chr3:87751472-87751493	GM10248	blood:	n/a	n/a
40	CTCF	chr3:87661942-87661977	LNCaP	prostate:	n/a	n/a
41	CTCF	chr3:87694100-87694250	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:87661861-87662057	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr3:87619507-87619562	Fibrobl	skin:	n/a	n/a
44	CTCF	chr3:87695346-87695411	K562	blood:	n/a	chr3:87695368-87695381 chr3:87695369-87695379
45	CTCF	chr3:87611500-87611650	HepG2	liver:	n/a	n/a
46	CTCF	chr3:87611522-87611624	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:87624827-87624902	GM20000	blood:	n/a	n/a
48	CTCF	chr3:87671288-87671310	Fibrobl	skin:	n/a	n/a
49	CTCF	chr3:87611506-87611643	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:87661901-87662000	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:87728433-87728483	NB4	blood:	n/a
2	chr3:87729320-87729370	HRPEpiC	eye:	n/a
3	chr3:87729320-87729370	AG10803	skin:	n/a
4	chr3:87729320-87729370	HAEpiC	amniotic membrane:	n/a
5	chr3:87728433-87728483	SKMC	muscle:	n/a
6	chr3:87729320-87729370	HIPEpiC	eye:	n/a
7	chr3:87729320-87729370	A549	lung:	n/a
8	chr3:87728433-87728483	HepG2	liver:	n/a
9	chr3:87729320-87729370	NHDF-neo	bronchial:	n/a
10	chr3:87729320-87729370	SK-N-SH_RA	brain:	n/a
11	chr3:87729320-87729370	ECC-1	luminal epithelium:	n/a
12	chr3:87728433-87728483	PrEC	prostate:	n/a
13	chr3:87729320-87729370	Hela-S3	cervix:	n/a
14	chr3:87728433-87728483	HRPEpiC	eye:	n/a
15	chr3:87729320-87729370	AoSMC	blood vessel:	n/a
16	chr3:87728433-87728483	MCF-7	breast:	n/a
17	chr3:87728433-87728483	K562	blood:	n/a
18	chr3:87728433-87728483	HAEpiC	amniotic membrane:	n/a
19	chr3:87728433-87728483	GM06990	blood:	n/a
20	chr3:87728433-87728483	BE2_C	brain:	n/a
21	chr3:87729320-87729370	GM12892	blood:	n/a
22	chr3:87729320-87729370	SK-N-MC	brain:	n/a
23	chr3:87729320-87729370	CMK	blood:	n/a
24	chr3:87729320-87729370	H1-hESC	embryonic stem cell:	embryo
25	chr3:87728433-87728483	NHDF-neo	bronchial:	n/a
26	chr3:87728433-87728483	GM12891	blood:	n/a
27	chr3:87729320-87729370	HRE	kidney:	n/a
28	chr3:87729320-87729370	LNCaP	prostate:	n/a
29	chr3:87729320-87729370	HEK293	kidney:	embryo
30	chr3:87729320-87729370	GM12878	blood:	n/a
31	chr3:87728433-87728483	HUVEC	blood vessel:	n/a
32	chr3:87729320-87729370	T-47D	breast:	n/a
33	chr3:87729320-87729370	Caco-2	colon:	n/a
34	chr3:87729320-87729370	MCF-7	breast:	n/a
35	chr3:87729320-87729370	HCF	heart:	n/a
36	chr3:87729320-87729370	AG09319	gingival:	n/a
37	chr3:87729320-87729370	HCM	heart:	n/a
38	chr3:87728433-87728483	NHBE	bronchial:	n/a
39	chr3:87728433-87728483	GM12878	blood:	n/a
40	chr3:87728433-87728483	AG09319	gingival:	n/a
41	chr3:87729320-87729370	PFSK-1	brain:	n/a
42	chr3:87728433-87728483	HRE	kidney:	n/a
43	chr3:87728433-87728483	PFSK-1	brain:	n/a
44	chr3:87729320-87729370	GM12891	blood:	n/a
45	chr3:87728433-87728483	HNPCEpiC	eye:	n/a
46	chr3:87729320-87729370	IMR90	lung:	fetal
47	chr3:87728433-87728483	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:87729320-87729370	HRCEpiC	kidney:	n/a
49	chr3:87728433-87728483	T-47D	breast:	n/a
50	chr3:87728433-87728483	PANC-1	pancreas:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:87715509..87718110-chr3:87725077..87727832,2	MCF-7	breast:
2	chr3:87670698..87673462-chr3:87675838..87678506,3	K562	blood:
3	chr3:87752670..87754550-chr3:87776800..87779392,2	MCF-7	breast:
4	chr3:87715509..87718110-chr3:87725077..87727832,2	MCF-7	breast:
5	chr3:87670698..87673462-chr3:87676763..87678506,2	K562	blood:
6	chr3:87745181..87747327-chr3:87772407..87775801,3	K562	blood:
7	chr3:87670698..87673462-chr3:87676763..87678506,2	K562	blood:
8	chr3:87670698..87673462-chr3:87675838..87678506,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHMP2B-3	chr3:87643988-87644526	NONHSAT090690
2	lnc-POU1F1-1	chr3:87679451-87680769	NONHSAT090691

No data

Variant related genes	Relation type
PSMC1P6	TF binding region
APOOP2	TF binding region
PSMC1P6	CpG island
APOOP2	CpG island

Extended variants
information (count: 2382 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2382 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530660763	chr3:87600858-87600859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548766448	chr3:87600859-87600860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148322716	chr3:87600875-87600876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193195260	chr3:87600985-87600986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547490603	chr3:87600995-87600996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72923524	chr3:87601228-87601229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs555955211	chr3:87601231-87601232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76124912	chr3:87601241-87601242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9823029	chr3:87601254-87601255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs559772028	chr3:87601268-87601269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150825538	chr3:87601272-87601273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115828072	chr3:87601325-87601326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543474730	chr3:87601368-87601369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540770168	chr3:87601391-87601392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571936018	chr3:87601407-87601408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530479690	chr3:87601418-87601419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139841581	chr3:87601462-87601463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560716075	chr3:87601513-87601514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528397691	chr3:87601535-87601536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184596816	chr3:87601582-87601583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571436144	chr3:87601596-87601597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144112026	chr3:87601608-87601609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9865089	chr3:87601624-87601625	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs368115709	chr3:87601628-87601629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537507653	chr3:87601656-87601657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147321615	chr3:87601657-87601658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140948065	chr3:87601722-87601723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567873345	chr3:87601723-87601724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534888708	chr3:87601739-87601740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553667764	chr3:87601771-87601772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578186485	chr3:87601772-87601773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189867603	chr3:87601774-87601775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149823950	chr3:87601801-87601802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529214773	chr3:87601858-87601859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575013540	chr3:87601882-87601883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375581452	chr3:87601884-87601885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542287477	chr3:87601892-87601893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145533062	chr3:87601964-87601965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528324771	chr3:87601965-87601966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540046100	chr3:87601986-87601987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35069491	chr3:87602052-87602053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565187754	chr3:87602134-87602135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35410198	chr3:87602143-87602144	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs530588412	chr3:87602152-87602153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35887006	chr3:87602153-87602154	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs118183891	chr3:87602187-87602188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191177084	chr3:87602210-87602211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148431219	chr3:87602211-87602212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567644057	chr3:87602231-87602232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142537358	chr3:87602276-87602277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:87600800-87601000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr3:87601200-87602600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:87602200-87602800	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr3:87602400-87603000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:87602600-87603600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr3:87603000-87603200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:87603200-87608000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:87608000-87608600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:87612800-87613200	Active TSS	A549	lung
10	chr3:87613200-87613400	Weak transcription	A549	lung
11	chr3:87613400-87614000	Enhancers	A549	lung
12	chr3:87623600-87623800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:87624400-87624600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr3:87624600-87625000	Enhancers	Fetal Muscle Leg	muscle
15	chr3:87624800-87625200	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr3:87624800-87625400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr3:87636000-87636600	Active TSS	Fetal Heart	heart
18	chr3:87645400-87646200	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr3:87646000-87646400	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr3:87646200-87648000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr3:87648000-87648600	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr3:87649400-87650200	Enhancers	Hela-S3	cervix
23	chr3:87655600-87656600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr3:87657000-87657800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
25	chr3:87662000-87664400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:87664200-87664600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr3:87664400-87664800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr3:87664400-87665000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr3:87664600-87664800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr3:87664800-87665200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:87664800-87669800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr3:87666800-87667000	Bivalent Enhancer	Esophagus	oesophagus
33	chr3:87675000-87676000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr3:87675600-87676400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:87675600-87677200	Enhancers	K562	blood
36	chr3:87676400-87677000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr3:87676600-87677200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr3:87683000-87683200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
39	chr3:87683000-87683400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
40	chr3:87683200-87683400	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr3:87686600-87687600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr3:87686800-87687400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr3:87686800-87687400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr3:87686800-87687600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr3:87687000-87687400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr3:87687000-87687400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr3:87687000-87687400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:87687600-87694000	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr3:87693800-87694200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
50	chr3:87693800-87694200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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