Variant report

Variant	nsv967253
Chromosome Location	chr3:52871714-52877079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:22)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr3:52875936-52876210	HepG2	liver:	n/a	n/a
2	CEBPB	chr3:52876001-52876125	A549	lung:	n/a	n/a
3	CTCF	chr3:52872929-52873005	GM19239	blood:	n/a	n/a
4	CTCF	chr3:52873009-52873010	GM19239	blood:	n/a	n/a
5	CTCF	chr3:52871600-52871750	HAc	cerebellar:	n/a	n/a
6	EBF1	chr3:52873110-52873121	GM12878	blood:	n/a	n/a
7	GATA3	chr3:52873382-52873721	T-47D	breast:	n/a	n/a
8	MAX	chr3:52876007-52876183	NB4	blood:	n/a	chr3:52876128-52876138
9	PAX5	chr3:52875259-52875468	GM12878	blood:	n/a	chr3:52875340-52875349 chr3:52875268-52875277
10	PML	chr3:52875108-52875541	GM12878	blood:	n/a	chr3:52875343-52875351
11	POLR2A	chr3:52875384-52875445	GM12878	blood:	n/a	n/a
12	POLR2A	chr3:52874172-52874181	MCF-7	breast:	n/a	n/a
13	POLR2A	chr3:52875472-52875507	GM12878	blood:	n/a	n/a
14	POLR2A	chr3:52876493-52876525	GM12878	blood:	n/a	n/a
15	POLR2A	chr3:52876534-52876583	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr3:52872677-52872729	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr3:52876701-52876715	GM12878	blood:	n/a	n/a
18	POLR2A	chr3:52873042-52873217	GM12878	blood:	n/a	n/a
19	RUNX3	chr3:52875209-52875521	GM12878	blood:	n/a	n/a
20	RUNX3	chr3:52875142-52875651	GM12878	blood:	n/a	n/a
21	SPI1	chr3:52876265-52877053	HL-60	blood:	n/a	n/a
22	TCF12	chr3:52875285-52875552	GM12878	blood:	n/a	chr3:52875440-52875448

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:52874325-52874375	Caco-2	colon:	n/a
2	chr3:52874468-52874518	HCF	heart:	n/a
3	chr3:52874468-52874518	BJ	skin:	n/a
4	chr3:52874325-52874375	ECC-1	luminal epithelium:	n/a
5	chr3:52874325-52874375	AG09309	skin:	n/a
6	chr3:52874325-52874375	HAEpiC	amniotic membrane:	n/a
7	chr3:52874468-52874518	BE2_C	brain:	n/a
8	chr3:52874468-52874518	Caco-2	colon:	n/a
9	chr3:52874325-52874375	NH-A	brain:	n/a
10	chr3:52874325-52874375	NHDF-neo	bronchial:	n/a
11	chr3:52874468-52874518	HRCEpiC	kidney:	n/a
12	chr3:52874468-52874518	HAEpiC	amniotic membrane:	n/a
13	chr3:52874468-52874518	GM06990	blood:	n/a
14	chr3:52874325-52874375	HMEC	breast:	n/a
15	chr3:52874468-52874518	GM19239	blood:	n/a
16	chr3:52874325-52874375	GM12892	blood:	n/a
17	chr3:52874325-52874375	AoSMC	blood vessel:	n/a
18	chr3:52874468-52874518	GM12892	blood:	n/a
19	chr3:52874325-52874375	ovcar-3	ovarian:	n/a
20	chr3:52874468-52874518	HEK293	kidney:	embryo
21	chr3:52874468-52874518	HCM	heart:	n/a
22	chr3:52874468-52874518	HCPEpiC	choroid plexus:	n/a
23	chr3:52874325-52874375	AG10803	skin:	n/a
24	chr3:52874468-52874518	HNPCEpiC	eye:	n/a
25	chr3:52874468-52874518	HepG2	liver:	n/a
26	chr3:52874468-52874518	CMK	blood:	n/a
27	chr3:52874468-52874518	MCF10A-Er-Src	breast:	n/a
28	chr3:52874468-52874518	HCT-116	colon:	n/a
29	chr3:52874468-52874518	PFSK-1	brain:	n/a
30	chr3:52874468-52874518	AG09309	skin:	n/a
31	chr3:52874325-52874375	BJ	skin:	n/a
32	chr3:52874325-52874375	Jurkat	blood:	n/a
33	chr3:52874325-52874375	U87	brain:	n/a
34	chr3:52874325-52874375	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:52874325-52874375	NT2-D1	testis:	n/a
36	chr3:52874468-52874518	PrEC	prostate:	n/a
37	chr3:52874468-52874518	LNCaP	prostate:	n/a
38	chr3:52874325-52874375	ProgFib	skin:	n/a
39	chr3:52874468-52874518	HUVEC	blood vessel:	n/a
40	chr3:52874325-52874375	GM06990	blood:	n/a
41	chr3:52874325-52874375	A549	lung:	n/a
42	chr3:52874325-52874375	T-47D	breast:	n/a
43	chr3:52874468-52874518	K562	blood:	n/a
44	chr3:52874468-52874518	SK-N-SH	brain:	n/a
45	chr3:52874468-52874518	HMEC	breast:	n/a
46	chr3:52874325-52874375	SKMC	muscle:	n/a
47	chr3:52874325-52874375	BE2_C	brain:	n/a
48	chr3:52874325-52874375	HRE	kidney:	n/a
49	chr3:52874325-52874375	GM12878	blood:	n/a
50	chr3:52874468-52874518	PANC-1	pancreas:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:52865265..52868196-chr3:52870244..52872785,3	K562	blood:
2	chr3:52803715..52805902-chr3:52874029..52875964,2	MCF-7	breast:
3	chr3:52867798..52869834-chr3:52876401..52878497,2	MCF-7	breast:
4	chr3:52864085..52867017-chr3:52872869..52875445,2	MCF-7	breast:
5	chr3:52866935..52869268-chr3:52870360..52872444,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM110-MUSTN1-1	chr3:52872020-52873766	NONHSAT089970

No data

Variant related genes	Relation type
TMEM110	TF binding region
ENSG00000243696	TF binding region
MUSTN1	TF binding region
TMEM110-MUSTN1	TF binding region
TMEM110	CpG island
ENSG00000243696	CpG island
MUSTN1	CpG island
TMEM110-MUSTN1	CpG island
ENSG00000243696	chromatin interactions
ENSG00000055955	chromatin interactions
ENSG00000114904	chromatin interactions
ENSG00000272573	chromatin interactions

Extended variants
information (count: 235 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:235 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138521612	chr3:52871761-52871762	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs571118488	chr3:52871774-52871775	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs144112088	chr3:52871783-52871784	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs552172530	chr3:52871789-52871790	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs565515315	chr3:52871790-52871791	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs188505243	chr3:52871843-52871844	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs547983900	chr3:52871886-52871887	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs147241319	chr3:52871910-52871911	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs192910564	chr3:52871928-52871929	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs3733047	chr3:52871929-52871930	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs556849857	chr3:52871941-52871942	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs533964175	chr3:52871942-52871943	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs113892040	chr3:52872001-52872002	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs59363675	chr3:52872003-52872004	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs2336150	chr3:52872009-52872010	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs2336151	chr3:52872010-52872011	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs2336152	chr3:52872011-52872012	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs2336153	chr3:52872015-52872016	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs2336154	chr3:52872018-52872019	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552978050	chr3:52872035-52872036	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs552445600	chr3:52872040-52872041	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs573141164	chr3:52872063-52872064	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs542351300	chr3:52872101-52872102	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs561993594	chr3:52872118-52872119	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs570736630	chr3:52872218-52872219	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs544782588	chr3:52872233-52872234	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs184697325	chr3:52872237-52872238	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs2878633	chr3:52872264-52872265	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs2878634	chr3:52872311-52872312	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs559337743	chr3:52872312-52872313	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs575555544	chr3:52872325-52872326	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs376742317	chr3:52872383-52872384	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs187928892	chr3:52872429-52872430	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs548271444	chr3:52872439-52872440	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs568026798	chr3:52872478-52872479	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs60438672	chr3:52872484-52872485	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs370429899	chr3:52872521-52872522	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs140740227	chr3:52872536-52872537	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs115610367	chr3:52872660-52872661	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs9856485	chr3:52872691-52872692	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs191229349	chr3:52872702-52872703	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs368918243	chr3:52872718-52872719	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs573193033	chr3:52872725-52872726	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs554757224	chr3:52872736-52872737	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs555845680	chr3:52872789-52872790	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs11373519	chr3:52872823-52872824	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
47	rs35066143	chr3:52872824-52872825	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
48	rs141466069	chr3:52872855-52872856	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
49	rs544693576	chr3:52872868-52872869	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
50	rs2336155	chr3:52872874-52872875	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:92)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Lung cancer	16618734	CNVD
Neuroblastoma	19686582	CNVD
Renal cell carcinoma	18765545	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52854200-52874200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:52854800-52888400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:52856000-52875000	Weak transcription	Fetal Intestine Large	intestine
4	chr3:52862000-52882600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr3:52863200-52872600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr3:52864400-52875800	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr3:52865600-52874200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:52865600-52875200	Weak transcription	Dnd41	blood
9	chr3:52865800-52878600	Weak transcription	Small Intestine	intestine
10	chr3:52866000-52884800	Weak transcription	HMEC	breast
11	chr3:52866200-52872600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr3:52866200-52872600	Weak transcription	Esophagus	oesophagus
13	chr3:52866200-52885200	Weak transcription	NHEK	skin
14	chr3:52866400-52871800	Strong transcription	Primary T cells from cord blood	blood
15	chr3:52866400-52872400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr3:52866600-52873600	Weak transcription	Hela-S3	cervix
17	chr3:52866600-52879200	Weak transcription	Osteobl	bone
18	chr3:52866800-52872000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr3:52866800-52876400	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr3:52866800-52878200	Strong transcription	Fetal Brain Female	brain
21	chr3:52866800-52879600	Genic enhancers	Fetal Thymus	thymus
22	chr3:52867000-52876400	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr3:52867000-52881600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr3:52867000-52881800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr3:52867200-52875200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr3:52867600-52871800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr3:52868000-52878800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr3:52868000-52883200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr3:52868400-52877800	Strong transcription	Brain Germinal Matrix	brain
30	chr3:52868600-52872000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
31	chr3:52868600-52875200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr3:52868800-52873000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr3:52868800-52876800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr3:52869000-52873400	Strong transcription	Brain Anterior Caudate	brain
35	chr3:52869000-52878800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:52869000-52879400	Strong transcription	Fetal Intestine Small	intestine
37	chr3:52869000-52881800	Weak transcription	Fetal Kidney	kidney
38	chr3:52869200-52871800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr3:52869200-52871800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
40	chr3:52869200-52873000	Strong transcription	Primary B cells from cord blood	blood
41	chr3:52869400-52872800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr3:52869400-52874200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:52869400-52875200	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr3:52869400-52875600	Weak transcription	Colonic Mucosa	Colon
45	chr3:52869600-52872400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:52869600-52872600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:52869600-52873000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr3:52869600-52873400	Enhancers	Psoas Muscle	Psoas
49	chr3:52869600-52875000	Strong transcription	Brain Angular Gyrus	brain
50	chr3:52869600-52875200	Strong transcription	Brain Inferior Temporal Lobe	brain

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