Variant report

Variant	esv3339338
Chromosome Location	chr3:52930462-52933260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:286)
CpG islands
(count:673)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:52931125-52931867	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr3:52931522-52931712	Hela-S3	cervix:	n/a	n/a
3	CCNT2	chr3:52931359-52931875	K562	blood:	n/a	n/a
4	CEBPB	chr3:52930680-52930771	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:52931539-52931683	Hela-S3	cervix:	n/a	n/a
6	CHD1	chr3:52931149-52931272	H1-hESC	embryonic stem cell:	n/a	chr3:52931188-52931198
7	CHD2	chr3:52931355-52931627	K562	blood:	n/a	n/a
8	CHD2	chr3:52931322-52931763	GM12878	blood:	n/a	n/a
9	CHD2	chr3:52931335-52931717	HepG2	liver:	n/a	n/a
10	CHD2	chr3:52931449-52931855	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr3:52931311-52931808	Hela-S3	cervix:	n/a	n/a
12	CREB1	chr3:52931463-52931667	A549	lung:	n/a	n/a
13	CREB1	chr3:52931328-52931868	A549	lung:	n/a	n/a
14	CREB1	chr3:52931252-52931876	HepG2	liver:	n/a	n/a
15	CREB1	chr3:52931153-52931807	GM12878	blood:	n/a	n/a
16	CTCF	chr3:52931320-52931470	GM12871	blood:	n/a	n/a
17	CTCF	chr3:52931400-52931550	HCM	heart:	n/a	n/a
18	CTCF	chr3:52931200-52931350	HMEC	breast:	n/a	n/a
19	CTCF	chr3:52931400-52931550	GM12868	blood:	n/a	n/a
20	CTCF	chr3:52931460-52931601	MCF-7	breast:	n/a	n/a
21	CTCF	chr3:52931460-52931610	GM12869	blood:	n/a	n/a
22	CTCF	chr3:52931260-52931410	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr3:52931180-52931330	GM12874	blood:	n/a	n/a
24	CTCF	chr3:52931200-52931450	GM12867	blood:	n/a	n/a
25	CTCF	chr3:52931327-52931366	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr3:52931588-52931589	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:52931220-52931370	GM12873	blood:	n/a	n/a
28	CTCF	chr3:52931329-52931517	Fibrobl	skin:	n/a	n/a
29	CTCF	chr3:52931280-52931430	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr3:52931240-52931390	GM12869	blood:	n/a	n/a
31	CTCF	chr3:52931498-52931513	IMR90	lung:	n/a	n/a
32	CTCF	chr3:52931240-52931390	Caco-2	colon:	n/a	n/a
33	CTCF	chr3:52931326-52931359	GM19239	blood:	n/a	n/a
34	CTCF	chr3:52931480-52931630	GM12870	blood:	n/a	n/a
35	CTCF	chr3:52931543-52931548	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:52931260-52931410	GM12873	blood:	n/a	n/a
37	CTCF	chr3:52931328-52931389	GM19238	blood:	n/a	n/a
38	CTCF	chr3:52931220-52931370	HAc	cerebellar:	n/a	n/a
39	CTCF	chr3:52931260-52931410	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr3:52931360-52931510	GM12865	blood:	n/a	n/a
41	CTCF	chr3:52931300-52931450	GM12866	blood:	n/a	n/a
42	CTCF	chr3:52931200-52931350	GM12872	blood:	n/a	n/a
43	CTCF	chr3:52931313-52931399	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:52931300-52931450	GM12875	blood:	n/a	n/a
45	CTCF	chr3:52931320-52931470	AG09319	gingival:	n/a	n/a
46	CTCF	chr3:52931488-52931603	GM12878	blood:	n/a	n/a
47	CTCF	chr3:52931040-52931190	RPTEC	kidney:	n/a	n/a
48	CTCF	chr3:52931390-52931394	GM19238	blood:	n/a	n/a
49	CTCF	chr3:52931260-52931410	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr3:52931240-52931390	GM12874	blood:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:52931826-52931876	HRE	kidney:	n/a
2	chr3:52931527-52931577	HEK293	kidney:	embryo
3	chr3:52931826-52931876	HRE	kidney:	n/a
4	chr3:52931527-52931577	HEK293	kidney:	embryo
5	chr3:52931532-52931582	GM12878	blood:	n/a
6	chr3:52931306-52931356	HepG2	liver:	n/a
7	chr3:52931857-52931907	HepG2	liver:	n/a
8	chr3:52932208-52932258	HepG2	liver:	n/a
9	chr3:52931946-52931996	HRE	kidney:	n/a
10	chr3:52931532-52931582	SK-N-MC	brain:	n/a
11	chr3:52931857-52931907	A549	lung:	n/a
12	chr3:52931857-52931907	BJ	skin:	n/a
13	chr3:52931857-52931907	GM12892	blood:	n/a
14	chr3:52931664-52931714	MCF10A-Er-Src	breast:	n/a
15	chr3:52931664-52931714	SKMC	muscle:	n/a
16	chr3:52931857-52931907	MCF-7	breast:	n/a
17	chr3:52931664-52931714	HepG2	liver:	n/a
18	chr3:52931604-52931654	LNCaP	prostate:	n/a
19	chr3:52931946-52931996	HIPEpiC	eye:	n/a
20	chr3:52931826-52931876	HRPEpiC	eye:	n/a
21	chr3:52931946-52931996	HepG2	liver:	n/a
22	chr3:52931306-52931356	NB4	blood:	n/a
23	chr3:52931826-52931876	LNCaP	prostate:	n/a
24	chr3:52931604-52931654	GM12892	blood:	n/a
25	chr3:52931306-52931356	AG04449	skin:	fetal
26	chr3:52932208-52932258	H1-hESC	embryonic stem cell:	embryo
27	chr3:52931657-52931707	AG09319	gingival:	n/a
28	chr3:52931604-52931654	PFSK-1	brain:	n/a
29	chr3:52931657-52931707	PANC-1	pancreas:	n/a
30	chr3:52931664-52931714	K562	blood:	n/a
31	chr3:52932208-52932258	GM12892	blood:	n/a
32	chr3:52931527-52931577	GM12878	blood:	n/a
33	chr3:52931826-52931876	MCF10A-Er-Src	breast:	n/a
34	chr3:52931532-52931582	AG10803	skin:	n/a
35	chr3:52931527-52931577	HCT-116	colon:	n/a
36	chr3:52931857-52931907	GM06990	blood:	n/a
37	chr3:52931826-52931876	HAEpiC	amniotic membrane:	n/a
38	chr3:52931527-52931577	CMK	blood:	n/a
39	chr3:52931664-52931714	GM12891	blood:	n/a
40	chr3:52931664-52931714	GM06990	blood:	n/a
41	chr3:52931604-52931654	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:52931527-52931577	HCPEpiC	choroid plexus:	n/a
43	chr3:52931946-52931996	GM12878	blood:	n/a
44	chr3:52931604-52931654	T-47D	breast:	n/a
45	chr3:52931657-52931707	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:52931657-52931707	HL-60	blood:	n/a
47	chr3:52931664-52931714	PANC-1	pancreas:	n/a
48	chr3:52930628-52930678	HAEpiC	amniotic membrane:	n/a
49	chr3:52931532-52931582	HIPEpiC	eye:	n/a
50	chr3:52930628-52930678	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:52932221..52934839-chr3:53107486..53109426,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITIH3-4	chr3:52931793-52931843	NONHSAT089973

No data

Variant related genes	Relation type
TMEM110	TF binding region
TMEM110-MUSTN1	TF binding region
TMEM110	CpG island
TMEM110-MUSTN1	CpG island

Extended variants
information (count: 81 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11379141	chr3:52930477-52930478	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs563195922	chr3:52930483-52930484	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs530806949	chr3:52930484-52930485	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs398038706	chr3:52930486-52930487	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs375234625	chr3:52930508-52930509	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs189169065	chr3:52930591-52930592	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs181007099	chr3:52930662-52930663	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546786040	chr3:52930700-52930701	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566579221	chr3:52930762-52930763	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139924336	chr3:52930782-52930783	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149827784	chr3:52930803-52930804	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370803731	chr3:52930830-52930831	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183940691	chr3:52930846-52930847	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188668777	chr3:52930906-52930907	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558405370	chr3:52930973-52930974	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181258667	chr3:52931007-52931008	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs545745026	chr3:52931012-52931013	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs368476636	chr3:52931079-52931080	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs541636023	chr3:52931106-52931107	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs559228112	chr3:52931143-52931144	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs572964196	chr3:52931207-52931208	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561841346	chr3:52931219-52931220	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553148193	chr3:52931233-52931234	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530694654	chr3:52931275-52931276	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550616631	chr3:52931289-52931290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376857317	chr3:52931294-52931295	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200458743	chr3:52931299-52931300	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372649372	chr3:52931300-52931301	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533174899	chr3:52931443-52931444	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111561856	chr3:52931456-52931457	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546971111	chr3:52931494-52931495	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113908723	chr3:52931543-52931544	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566666536	chr3:52931570-52931571	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs535539150	chr3:52931582-52931583	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
35	rs549193739	chr3:52931613-52931614	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
36	rs569132894	chr3:52931682-52931683	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
37	rs559777814	chr3:52931688-52931689	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
38	rs377110320	chr3:52931709-52931710	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
39	rs185720229	chr3:52931758-52931759	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs533697037	chr3:52931778-52931779	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs538403040	chr3:52931820-52931821	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs558179390	chr3:52931843-52931844	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs190268321	chr3:52931896-52931897	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
44	rs377345855	chr3:52931946-52931947	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
45	rs539100361	chr3:52931954-52931955	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs570122935	chr3:52931958-52931959	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs552987325	chr3:52931962-52931963	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
48	rs9844736	chr3:52931971-52931972	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs541966391	chr3:52932033-52932034	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs561731548	chr3:52932034-52932035	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a

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:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52908400-52930600	Weak transcription	A549	lung
2	chr3:52916400-52930600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:52920400-52930600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:52920400-52930600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:52920400-52930600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr3:52921600-52930600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:52925600-52930600	Weak transcription	Esophagus	oesophagus
8	chr3:52927400-52930600	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr3:52927600-52930600	Enhancers	Gastric	stomach
10	chr3:52927600-52930600	Enhancers	Pancreas	Pancrea
11	chr3:52927800-52930600	Weak transcription	HSMMtube	muscle
12	chr3:52928200-52930600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr3:52928200-52930800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr3:52928400-52930600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr3:52928400-52931000	Weak transcription	Small Intestine	intestine
16	chr3:52928800-52930600	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr3:52929200-52930600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
18	chr3:52929200-52930600	Enhancers	Lung	lung
19	chr3:52929400-52930600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr3:52929400-52930600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr3:52929400-52930600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr3:52929400-52930600	Enhancers	Fetal Brain Male	brain
23	chr3:52929400-52930600	Weak transcription	Fetal Muscle Trunk	muscle
24	chr3:52929600-52930600	Weak transcription	Left Ventricle	heart
25	chr3:52929600-52931200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
26	chr3:52929600-52931200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr3:52929600-52931200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr3:52929800-52930600	Enhancers	Adipose Nuclei	Adipose
29	chr3:52929800-52930600	Enhancers	Fetal Lung	lung
30	chr3:52929800-52930600	Enhancers	Fetal Stomach	stomach
31	chr3:52929800-52931000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
32	chr3:52929800-52931000	Flanking Active TSS	Brain Angular Gyrus	brain
33	chr3:52929800-52931000	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr3:52929800-52931000	Flanking Active TSS	Thymus	Thymus
35	chr3:52929800-52931200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr3:52929800-52931200	Flanking Active TSS	Fetal Thymus	thymus
37	chr3:52929800-52931200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr3:52929800-52931400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr3:52929800-52932200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:52929800-52932200	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr3:52930000-52930600	Enhancers	Primary B cells from cord blood	blood
42	chr3:52930000-52930600	Enhancers	Primary T cells from cord blood	blood
43	chr3:52930000-52930600	Active TSS	Rectal Mucosa Donor 29	rectum
44	chr3:52930000-52930600	Enhancers	HUVEC	blood vessel
45	chr3:52930000-52930800	Enhancers	Fetal Heart	heart
46	chr3:52930000-52930800	Flanking Active TSS	HMEC	breast
47	chr3:52930000-52931000	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr3:52930000-52931000	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr3:52930000-52931200	Flanking Active TSS	Brain Substantia Nigra	brain
50	chr3:52930000-52931400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood

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