Variant report

Variant	nsv1005323
Chromosome Location	chr3:112171990-112274613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1393)
CpG islands
(count:244)
Chromatin interactive
region (count:41)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1393 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:112250194-112250459	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:112250371-112250382	K562	blood:	n/a	n/a
3	ATF2	chr3:112174606-112175451	GM12878	blood:	n/a	n/a
4	ATF2	chr3:112233307-112233940	GM12878	blood:	n/a	n/a
5	ATF2	chr3:112201412-112201996	GM12878	blood:	n/a	n/a
6	ATF2	chr3:112233216-112233958	GM12878	blood:	n/a	n/a
7	ATF2	chr3:112237760-112238685	GM12878	blood:	n/a	n/a
8	ATF2	chr3:112181963-112182703	GM12878	blood:	n/a	n/a
9	ATF2	chr3:112191977-112192593	GM12878	blood:	n/a	n/a
10	ATF2	chr3:112258495-112259308	GM12878	blood:	n/a	n/a
11	ATF2	chr3:112208191-112210297	GM12878	blood:	n/a	n/a
12	ATF2	chr3:112258649-112259179	GM12878	blood:	n/a	n/a
13	ATF2	chr3:112217882-112218686	GM12878	blood:	n/a	n/a
14	ATF2	chr3:112208326-112210333	GM12878	blood:	n/a	n/a
15	ATF2	chr3:112217577-112218762	GM12878	blood:	n/a	n/a
16	ATF2	chr3:112178323-112180365	GM12878	blood:	n/a	n/a
17	ATF2	chr3:112174716-112175428	GM12878	blood:	n/a	n/a
18	ATF2	chr3:112182945-112183787	GM12878	blood:	n/a	n/a
19	ATF2	chr3:112181801-112183834	GM12878	blood:	n/a	n/a
20	ATF2	chr3:112202984-112203674	GM12878	blood:	n/a	n/a
21	ATF2	chr3:112178586-112180203	GM12878	blood:	n/a	n/a
22	BATF	chr3:112178649-112178996	GM12878	blood:	n/a	n/a
23	BATF	chr3:112179289-112179926	GM12878	blood:	n/a	chr3:112179889-112179899 chr3:112179585-112179594
24	BATF	chr3:112222377-112222753	GM12878	blood:	n/a	n/a
25	BATF	chr3:112183210-112183468	GM12878	blood:	n/a	n/a
26	BATF	chr3:112233387-112233955	GM12878	blood:	n/a	n/a
27	BATF	chr3:112208739-112209174	GM12878	blood:	n/a	n/a
28	BATF	chr3:112180623-112180947	GM12878	blood:	n/a	chr3:112180796-112180807
29	BATF	chr3:112233345-112233906	GM12878	blood:	n/a	n/a
30	BATF	chr3:112258695-112259018	GM12878	blood:	n/a	n/a
31	BATF	chr3:112208785-112209113	GM12878	blood:	n/a	n/a
32	BATF	chr3:112179396-112179832	GM12878	blood:	n/a	chr3:112179585-112179594
33	BATF	chr3:112183149-112183504	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:112179330-112179886	GM12878	blood:	n/a	chr3:112179524-112179533
35	BCL11A	chr3:112183088-112183485	GM12878	blood:	n/a	n/a
36	BCL11A	chr3:112233466-112233775	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:112233338-112233797	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:112208757-112209201	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:112192183-112192464	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:112179271-112179712	GM12878	blood:	n/a	chr3:112179524-112179533
41	BCL11A	chr3:112178672-112178956	GM12878	blood:	n/a	n/a
42	BCL3	chr3:112181977-112182583	GM12878	blood:	n/a	n/a
43	BCL3	chr3:112174642-112175427	GM12878	blood:	n/a	n/a
44	BCL3	chr3:112183082-112183515	GM12878	blood:	n/a	n/a
45	BCL3	chr3:112208660-112209498	GM12878	blood:	n/a	n/a
46	BCL3	chr3:112245548-112245831	GM12878	blood:	n/a	n/a
47	BCL3	chr3:112210835-112211375	GM12878	blood:	n/a	n/a
48	BCL3	chr3:112208669-112209195	GM12878	blood:	n/a	n/a
49	BCL3	chr3:112178509-112180324	GM12878	blood:	n/a	chr3:112179524-112179533
50	BCL3	chr3:112233334-112233931	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112184271-112184321	AG04449	skin:	fetal
2	chr3:112218510-112218560	RPTEC	kidney:	n/a
3	chr3:112218761-112218811	Hela-S3	cervix:	n/a
4	chr3:112217973-112218023	NH-A	brain:	n/a
5	chr3:112218510-112218560	H1-hESC	embryonic stem cell:	embryo
6	chr3:112184271-112184321	BJ	skin:	n/a
7	chr3:112218761-112218811	K562	blood:	n/a
8	chr3:112218510-112218560	Hepatocyte	liver:	n/a
9	chr3:112218510-112218560	PANC-1	pancreas:	n/a
10	chr3:112217973-112218023	H1-hESC	embryonic stem cell:	embryo
11	chr3:112217973-112218023	BE2_C	brain:	n/a
12	chr3:112184271-112184321	SKMC	muscle:	n/a
13	chr3:112217973-112218023	SAEC	small airway:	n/a
14	chr3:112184271-112184321	HRE	kidney:	n/a
15	chr3:112217973-112218023	GM12878	blood:	n/a
16	chr3:112184271-112184321	GM12891	blood:	n/a
17	chr3:112217973-112218023	NHBE	bronchial:	n/a
18	chr3:112218761-112218811	AoSMC	blood vessel:	n/a
19	chr3:112217973-112218023	MCF-7	breast:	n/a
20	chr3:112218510-112218560	NH-A	brain:	n/a
21	chr3:112217973-112218023	HRCEpiC	kidney:	n/a
22	chr3:112218510-112218560	NHBE	bronchial:	n/a
23	chr3:112218510-112218560	IMR90	lung:	fetal
24	chr3:112217973-112218023	HCPEpiC	choroid plexus:	n/a
25	chr3:112218761-112218811	HepG2	liver:	n/a
26	chr3:112184271-112184321	HEEpiC	esophagus:	n/a
27	chr3:112218761-112218811	CMK	blood:	n/a
28	chr3:112217973-112218023	NHDF-neo	bronchial:	n/a
29	chr3:112184271-112184321	HL-60	blood:	n/a
30	chr3:112217973-112218023	HUVEC	blood vessel:	n/a
31	chr3:112217973-112218023	ProgFib	skin:	n/a
32	chr3:112184271-112184321	NHDF-neo	bronchial:	n/a
33	chr3:112218761-112218811	HEEpiC	esophagus:	n/a
34	chr3:112217973-112218023	NB4	blood:	n/a
35	chr3:112184271-112184321	HepG2	liver:	n/a
36	chr3:112218510-112218560	NT2-D1	testis:	n/a
37	chr3:112218761-112218811	HMEC	breast:	n/a
38	chr3:112218761-112218811	Jurkat	blood:	n/a
39	chr3:112217973-112218023	HIPEpiC	eye:	n/a
40	chr3:112218510-112218560	BJ	skin:	n/a
41	chr3:112217973-112218023	IMR90	lung:	fetal
42	chr3:112218761-112218811	LNCaP	prostate:	n/a
43	chr3:112218510-112218560	NB4	blood:	n/a
44	chr3:112218761-112218811	AG04450	lung:	fetal
45	chr3:112217973-112218023	A549	lung:	n/a
46	chr3:112218761-112218811	U87	brain:	n/a
47	chr3:112218761-112218811	ovcar-3	ovarian:	n/a
48	chr3:112184271-112184321	PrEC	prostate:	n/a
49	chr3:112218510-112218560	AG04449	skin:	fetal
50	chr3:112184271-112184321	Hela-S3	cervix:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:112215809..112217939-chr3:112219323..112221326,2	K562	blood:
2	chr3:112267679..112269481-chr3:112276502..112278431,2	MCF-7	breast:
3	chr3:111856051..111856906-chr3:112237978..112238501,2	MCF-7	breast:
4	chr11:65325880..65326380-chr3:112226218..112226735,2	Hela-S3	cervix:
5	chr3:112271839..112274196-chr3:112276069..112278465,2	K562	blood:
6	chr3:112255866..112257509-chr3:112258178..112260464,2	K562	blood:
7	chr3:112267834..112269856-chr3:112273355..112275580,2	MCF-7	breast:
8	chr3:112265348..112267048-chr3:112278268..112281074,2	K562	blood:
9	chr3:112189206..112190998-chr3:112191867..112193876,2	K562	blood:
10	chr3:112259312..112262688-chr3:112264103..112268109,5	MCF-7	breast:
11	chr3:112255414..112258114-chr3:112258815..112260452,2	MCF-7	breast:
12	chr3:112257894..112260182-chr3:112261876..112264065,2	K562	blood:
13	chr3:112268324..112269882-chr3:112359880..112361529,2	MCF-7	breast:
14	chr3:112267834..112269856-chr3:112273355..112275580,2	MCF-7	breast:
15	chr3:112257894..112260182-chr3:112261876..112264065,2	K562	blood:
16	chr3:112045925..112046858-chr3:112237972..112238492,2	K562	blood:
17	chr3:112263776..112266083-chr3:112359451..112361414,2	MCF-7	breast:
18	chr3:112030207..112032434-chr3:112262315..112264380,2	K562	blood:
19	chr3:112274013..112276880-chr3:112736926..112739647,2	MCF-7	breast:
20	chr3:112272255..112274870-chr3:112277581..112280165,3	K562	blood:
21	chr3:112257611..112259171-chr3:112300442..112301943,2	K562	blood:
22	chr3:112215809..112217939-chr3:112219323..112221326,2	K562	blood:
23	chr3:112046305..112046882-chr3:112237913..112238884,3	MCF-7	breast:
24	chr3:112045750..112047025-chr3:112237531..112238950,15	MCF-7	breast:
25	chr3:112253284..112253915-chr3:126107853..126108632,2	MCF-7	breast:
26	chr3:112270443..112273330-chr3:112277844..112281278,5	MCF-7	breast:
27	chr3:112011899..112013194-chr3:112237762..112239193,5	MCF-7	breast:
28	chr3:111830661..111831289-chr3:112238353..112238915,2	K562	blood:
29	chr3:112011976..112013367-chr3:112237943..112239384,10	MCF-7	breast:
30	chr3:112273986..112276332-chr3:112279376..112281873,3	MCF-7	breast:
31	chr3:112262046..112263985-chr3:112278635..112280484,2	K562	blood:
32	chr3:112250901..112252598-chr3:112279157..112281596,2	MCF-7	breast:
33	chr3:112257078..112259281-chr3:112279236..112282506,3	MCF-7	breast:
34	chr3:112253490..112256363-chr3:112279039..112281187,3	K562	blood:
35	chr17:58220578..58221151-chr3:112183496..112184268,2	MCF-7	breast:
36	chr3:111830383..111831315-chr3:112250332..112250864,2	K562	blood:
37	chr3:112270877..112274678-chr3:112278992..112281610,4	MCF-7	breast:
38	chr3:112265548..112268745-chr3:112278905..112281998,3	K562	blood:
39	chr3:112272044..112274714-chr3:112358450..112360286,2	MCF-7	breast:
40	chr3:112259312..112262688-chr3:112264103..112268109,5	MCF-7	breast:
41	chr3:111855697..111856656-chr3:112238008..112238836,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG3-3	chr3:112188819-112189300	NONHSAT091180
2	lnc-ATG3-1	chr3:112244395-112246989	NONHSAT091182
3	lnc-ATG3-3	chr3:112188603-112188651	NONHSAT091180
4	lnc-SLC35A5-2	chr3:112273149-112273439	expReg_chr3_7492_+
5	lnc-BTLA-4	chr3:112178630-112179297	NONHSAT091178
6	lnc-BTLA-4	chr3:112179309-112179627	NONHSAT091178
7	lnc-ATG3-3	chr3:112188605-112188651	NONHSAT091179
8	lnc-ATG3-3	chr3:112188819-112188869	NONHSAT091179
9	lnc-ATG3-3	chr3:112184773-112185230	NONHSAT091179

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ATG3	hsa-miR-155-5p	chr3:112251414-112251436

Variant related genes	Relation type
ATG3	TF binding region
BTLA	TF binding region
OR7E100P	TF binding region
ATG3	CpG island
BTLA	CpG island
OR7E100P	CpG island
ENSG00000240057	chromatin interactions
ENSG00000091986	chromatin interactions
ENSG00000186265	chromatin interactions
ENSG00000144848	chromatin interactions
ENSG00000138459	chromatin interactions
ENSG00000163608	chromatin interactions
ENSG00000172139	chromatin interactions
CHUK	miRNA target sites

Extended variants
information (count: 3764 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3764 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539483992	chr3:112172028-112172029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552825192	chr3:112172038-112172039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572772348	chr3:112172053-112172054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72936290	chr3:112172106-112172107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs72936292	chr3:112172149-112172150	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs1488257	chr3:112172180-112172181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143371393	chr3:112172191-112172192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191048260	chr3:112172192-112172193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10609206	chr3:112172250-112172251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397876991	chr3:112172253-112172254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563506885	chr3:112172351-112172352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2683914	chr3:112172363-112172364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs183277266	chr3:112172367-112172368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187217139	chr3:112172368-112172369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563713673	chr3:112172375-112172376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192192209	chr3:112172383-112172384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74826295	chr3:112172393-112172394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149473583	chr3:112172437-112172438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562065374	chr3:112172475-112172476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2633565	chr3:112172569-112172570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550907249	chr3:112172594-112172595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2683915	chr3:112172622-112172623	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539281185	chr3:112172642-112172643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35349813	chr3:112172671-112172672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs530229884	chr3:112172675-112172676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs63501661	chr3:112172676-112172677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566407251	chr3:112172682-112172683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386664690	chr3:112172683-112172684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372370492	chr3:112172684-112172685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554917626	chr3:112172705-112172706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574911106	chr3:112172726-112172727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2633564	chr3:112172736-112172737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs557398686	chr3:112172768-112172769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141545295	chr3:112172773-112172774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188087934	chr3:112172782-112172783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192707273	chr3:112172807-112172808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184511255	chr3:112172836-112172837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577024891	chr3:112172849-112172850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374042543	chr3:112172850-112172851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201673241	chr3:112172852-112172853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199933531	chr3:112172870-112172871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71134834	chr3:112172891-112172892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs386397640	chr3:112172892-112172893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs398071927	chr3:112172900-112172901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188310819	chr3:112172947-112172948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530960706	chr3:112172998-112172999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550870147	chr3:112173010-112173011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs117963493	chr3:112173103-112173104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533269401	chr3:112173111-112173112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546434137	chr3:112173132-112173133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1873 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112165800-112173400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr3:112168400-112177800	Weak transcription	Primary T cells from cord blood	blood
3	chr3:112169400-112176600	Weak transcription	Primary B cells from cord blood	blood
4	chr3:112173000-112174200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:112173200-112173400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:112173200-112174000	Enhancers	Adipose Nuclei	Adipose
7	chr3:112173400-112173800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr3:112173400-112174000	Enhancers	Ovary	ovary
9	chr3:112173400-112174200	Enhancers	Fetal Lung	lung
10	chr3:112173400-112175400	Enhancers	Primary B cells from peripheral blood	blood
11	chr3:112173400-112182200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr3:112173800-112174000	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr3:112174000-112175000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr3:112174400-112178200	ZNF genes & repeats	GM12878-XiMat	blood
15	chr3:112175000-112175200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr3:112175000-112175200	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr3:112175200-112178000	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr3:112175200-112178800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:112175400-112176600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr3:112176400-112180200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr3:112176400-112180800	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr3:112176600-112177000	ZNF genes & repeats	Primary B cells from cord blood	blood
23	chr3:112176600-112178000	Enhancers	Primary B cells from peripheral blood	blood
24	chr3:112177000-112177200	Genic enhancers	Primary B cells from cord blood	blood
25	chr3:112177000-112181000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr3:112177200-112177800	Enhancers	Primary B cells from cord blood	blood
27	chr3:112177200-112180200	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr3:112177400-112180200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr3:112177800-112179600	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr3:112177800-112182200	Enhancers	Primary T cells from cord blood	blood
31	chr3:112178000-112178600	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr3:112178000-112178800	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr3:112178000-112180600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr3:112178200-112179000	Enhancers	Primary T cells fromperipheralblood	blood
35	chr3:112178200-112179200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr3:112178200-112179400	Flanking Active TSS	GM12878-XiMat	blood
37	chr3:112178200-112179800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:112178200-112180000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
39	chr3:112178200-112180000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr3:112178200-112180600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr3:112178400-112179200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr3:112178400-112179200	Enhancers	Fetal Thymus	thymus
43	chr3:112178400-112179400	Enhancers	Primary hematopoietic stem cells	blood
44	chr3:112178400-112180000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr3:112178400-112180200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr3:112178400-112180200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr3:112178400-112180200	Enhancers	Thymus	Thymus
48	chr3:112178600-112179000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr3:112178800-112179800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr3:112178800-112180400	Enhancers	Primary B cells from peripheral blood	blood

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