Variant report

Variant	esv2752014
Chromosome Location	chr3:68091879-68416989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:68175198-68175199	HepG2	liver:	n/a	n/a
2	BACH1	chr3:68251296-68251397	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr3:68339543-68339811	GM12878	blood:	n/a	n/a
4	BATF	chr3:68339560-68339738	GM12878	blood:	n/a	n/a
5	BCL11A	chr3:68339537-68339762	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:68137527-68137547	GM12878	blood:	n/a	n/a
7	BRCA1	chr3:68188828-68188830	H1-hESC	embryonic stem cell:	n/a	n/a
8	CCNT2	chr3:68415523-68415723	K562	blood:	n/a	n/a
9	CEBPB	chr3:68172422-68172736	ECC-1	luminal epithelium:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
10	CEBPB	chr3:68234269-68234337	A549	lung:	n/a	n/a
11	CEBPB	chr3:68250635-68250945	HepG2	liver:	n/a	chr3:68250768-68250779
12	CEBPB	chr3:68172397-68172761	IMR90	lung:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
13	CEBPB	chr3:68172477-68172721	MCF-7	breast:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
14	CEBPB	chr3:68172399-68172765	H1-hESC	embryonic stem cell:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
15	CEBPB	chr3:68172394-68172762	A549	lung:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
16	CEBPB	chr3:68172337-68172836	A549	lung:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
17	CEBPB	chr3:68123108-68123364	HepG2	liver:	n/a	chr3:68123273-68123284
18	CEBPB	chr3:68172432-68172733	K562	blood:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
19	CEBPB	chr3:68368582-68368815	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:68172398-68172763	Hela-S3	cervix:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
21	CEBPB	chr3:68107196-68107640	A549	lung:	n/a	chr3:68107519-68107530
22	CEBPB	chr3:68274869-68275082	HepG2	liver:	n/a	chr3:68274991-68275002
23	CEBPB	chr3:68235190-68235394	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr3:68107206-68107669	HepG2	liver:	n/a	chr3:68107519-68107530
25	CEBPB	chr3:68123103-68123471	H1-hESC	embryonic stem cell:	n/a	chr3:68123273-68123284
26	CEBPB	chr3:68107248-68107689	IMR90	lung:	n/a	chr3:68107519-68107530
27	CEBPB	chr3:68216840-68217068	HepG2	liver:	n/a	chr3:68216978-68216989
28	CEBPB	chr3:68172496-68172642	HepG2	liver:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
29	CEBPB	chr3:68172396-68172766	HepG2	liver:	n/a	chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172575-68172584 chr3:68172573-68172584 chr3:68172575-68172584 chr3:68172573-68172586
30	CEBPB	chr3:68221977-68222241	HepG2	liver:	n/a	chr3:68222102-68222113
31	CHD2	chr3:68137435-68137546	GM12878	blood:	n/a	n/a
32	CTCF	chr3:68305713-68306158	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:68305900-68306050	BE2_C	brain:	n/a	n/a
34	CTCF	chr3:68305900-68306050	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr3:68305906-68306077	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr3:68255789-68255955	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:68255700-68255850	Caco-2	colon:	n/a	n/a
38	CTCF	chr3:68305750-68306131	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr3:68305920-68306070	GM12866	blood:	n/a	n/a
40	CTCF	chr3:68305931-68306032	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr3:68255780-68255930	NB4	blood:	n/a	n/a
42	CTCF	chr3:68305920-68306070	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr3:68305920-68306070	RPTEC	kidney:	n/a	n/a
44	CTCF	chr3:68255720-68255870	BE2_C	brain:	n/a	n/a
45	CTCF	chr3:68255760-68255910	GM12874	blood:	n/a	n/a
46	CTCF	chr3:68255740-68255980	K562	blood:	n/a	n/a
47	CTCF	chr3:68255752-68256011	IMR90	lung:	n/a	n/a
48	CTCF	chr3:68305940-68306090	HMEC	breast:	n/a	n/a
49	CTCF	chr3:68159399-68159465	Medullo	brain:	n/a	n/a
50	CTCF	chr3:68305791-68306162	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:68316096-68316146	RPTEC	kidney:	n/a
2	chr3:68131323-68131373	SK-N-MC	brain:	n/a
3	chr3:68131323-68131373	AoSMC	blood vessel:	n/a
4	chr3:68131323-68131373	PFSK-1	brain:	n/a
5	chr3:68185630-68185680	HepG2	liver:	n/a
6	chr3:68131323-68131373	PANC-1	pancreas:	n/a
7	chr3:68316096-68316146	HAEpiC	amniotic membrane:	n/a
8	chr3:68185630-68185680	HAEpiC	amniotic membrane:	n/a
9	chr3:68185630-68185680	HRPEpiC	eye:	n/a
10	chr3:68131204-68131254	SK-N-SH	brain:	n/a
11	chr3:68131284-68131334	BE2_C	brain:	n/a
12	chr3:68131284-68131334	BJ	skin:	n/a
13	chr3:68185630-68185680	BE2_C	brain:	n/a
14	chr3:68316096-68316146	HIPEpiC	eye:	n/a
15	chr3:68131323-68131373	HUVEC	blood vessel:	n/a
16	chr3:68131323-68131373	MCF-7	breast:	n/a
17	chr3:68131204-68131254	Hepatocyte	liver:	n/a
18	chr3:68131284-68131334	HepG2	liver:	n/a
19	chr3:68185630-68185680	SK-N-SH	brain:	n/a
20	chr3:68131323-68131373	BE2_C	brain:	n/a
21	chr3:68131284-68131334	HAEpiC	amniotic membrane:	n/a
22	chr3:68131323-68131373	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:68131323-68131373	BJ	skin:	n/a
24	chr3:68131204-68131254	SK-N-SH_RA	brain:	n/a
25	chr3:68316096-68316146	A549	lung:	n/a
26	chr3:68316096-68316146	HNPCEpiC	eye:	n/a
27	chr3:68185630-68185680	BJ	skin:	n/a
28	chr3:68131323-68131373	NT2-D1	testis:	n/a
29	chr3:68131284-68131334	PANC-1	pancreas:	n/a
30	chr3:68131323-68131373	HMEC	breast:	n/a
31	chr3:68131204-68131254	A549	lung:	n/a
32	chr3:68131284-68131334	AG09319	gingival:	n/a
33	chr3:68316096-68316146	GM12878	blood:	n/a
34	chr3:68131284-68131334	GM12891	blood:	n/a
35	chr3:68131204-68131254	HRE	kidney:	n/a
36	chr3:68316096-68316146	HRCEpiC	kidney:	n/a
37	chr3:68316096-68316146	H1-hESC	embryonic stem cell:	embryo
38	chr3:68131323-68131373	ovcar-3	ovarian:	n/a
39	chr3:68316096-68316146	AG04450	lung:	fetal
40	chr3:68316096-68316146	HepG2	liver:	n/a
41	chr3:68131204-68131254	HCM	heart:	n/a
42	chr3:68131204-68131254	GM12891	blood:	n/a
43	chr3:68316096-68316146	Hela-S3	cervix:	n/a
44	chr3:68316096-68316146	PrEC	prostate:	n/a
45	chr3:68316096-68316146	IMR90	lung:	fetal
46	chr3:68131204-68131254	HepG2	liver:	n/a
47	chr3:68316096-68316146	BE2_C	brain:	n/a
48	chr3:68131284-68131334	GM06990	blood:	n/a
49	chr3:68131323-68131373	HEK293	kidney:	embryo
50	chr3:68316096-68316146	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:68260944..68263531-chr3:68263776..68266354,2	K562	blood:
2	chr3:67951881..67952772-chr3:68305559..68306337,2	MCF-7	breast:
3	chr3:68260944..68263531-chr3:68263776..68266354,2	K562	blood:
4	chr3:68228464..68231437-chr3:68234826..68237803,2	K562	blood:
5	chr3:68344569..68347557-chr3:68353420..68355980,2	K562	blood:
6	chr1:221790481..221791096-chr3:68162539..68163265,2	MCF-7	breast:
7	chr3:68207392..68209217-chr3:68210533..68213462,2	K562	blood:
8	chr3:67951814..67952581-chr3:68255379..68256164,2	MCF-7	breast:
9	chr3:68228464..68231437-chr3:68234826..68237803,2	K562	blood:
10	chr3:68207392..68209217-chr3:68210533..68213462,2	K562	blood:
11	chr3:68362451..68362951-chr7:120590619..120591187,2	MCF-7	breast:
12	chr3:68344569..68347557-chr3:68353420..68355980,2	K562	blood:

Variant related genes	Relation type
FAM19A1	TF binding region
ENSG00000240568	TF binding region
COPS8P2	TF binding region
FAM19A1	CpG island
ENSG00000240568	CpG island
COPS8P2	CpG island
ENSG00000071243	chromatin interactions

Extended variants
information (count: 5672 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:5672 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548188887	chr3:68094218-68094219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185775108	chr3:68094234-68094235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373935432	chr3:68094237-68094238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34798966	chr3:68094256-68094257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191076091	chr3:68094259-68094260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547634727	chr3:68094308-68094309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570580202	chr3:68094341-68094342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112983854	chr3:68094373-68094374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79816754	chr3:68094433-68094434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369950886	chr3:68094470-68094471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569847851	chr3:68094473-68094474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537876921	chr3:68094500-68094501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554527495	chr3:68094531-68094532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183129491	chr3:68094600-68094601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377643085	chr3:68094632-68094633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540298384	chr3:68094664-68094665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553947262	chr3:68094667-68094668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577325765	chr3:68094676-68094677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546079244	chr3:68094677-68094678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563226827	chr3:68094725-68094726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531899200	chr3:68094781-68094782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116578111	chr3:68094782-68094783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527821315	chr3:68094799-68094800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373068890	chr3:68094821-68094822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6548943	chr3:68094829-68094830	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs532673186	chr3:68094952-68094953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527386600	chr3:68095028-68095029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547475743	chr3:68095050-68095051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570443053	chr3:68095059-68095060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552881341	chr3:68095070-68095071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533199775	chr3:68095130-68095131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7430276	chr3:68095146-68095147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs569967385	chr3:68095150-68095151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535328512	chr3:68095153-68095154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538395428	chr3:68095159-68095160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555206250	chr3:68095164-68095165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568065197	chr3:68095173-68095174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143327510	chr3:68095225-68095226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs137943823	chr3:68095274-68095275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186368618	chr3:68095315-68095316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs118126103	chr3:68095316-68095317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536372442	chr3:68095318-68095319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191013742	chr3:68095319-68095320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576830596	chr3:68095348-68095349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182846991	chr3:68095380-68095381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561678874	chr3:68095393-68095394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572919996	chr3:68095398-68095399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569059440	chr3:68095399-68095400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367580466	chr3:68095406-68095407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188835567	chr3:68095419-68095420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	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
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	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
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	17142309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68094200-68094800	Enhancers	Fetal Intestine Small	intestine
2	chr3:68094800-68098800	Weak transcription	Fetal Intestine Small	intestine
3	chr3:68097800-68098000	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr3:68098000-68105000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr3:68098600-68099800	Enhancers	Duodenum Mucosa	Duodenum
6	chr3:68098800-68099600	Enhancers	Sigmoid Colon	Sigmoid Colon
7	chr3:68098800-68099800	Enhancers	Fetal Intestine Large	intestine
8	chr3:68098800-68101800	Enhancers	Fetal Intestine Small	intestine
9	chr3:68099000-68099600	Enhancers	Aorta	Aorta
10	chr3:68099200-68099600	Enhancers	Small Intestine	intestine
11	chr3:68099400-68100200	Enhancers	Fetal Muscle Leg	muscle
12	chr3:68099600-68105800	Weak transcription	Small Intestine	intestine
13	chr3:68099800-68103600	Weak transcription	Fetal Intestine Large	intestine
14	chr3:68099800-68105000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr3:68101800-68103800	Weak transcription	Fetal Intestine Small	intestine
16	chr3:68103600-68105400	Enhancers	Fetal Intestine Large	intestine
17	chr3:68103800-68106200	Enhancers	Fetal Intestine Small	intestine
18	chr3:68104200-68106600	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr3:68104800-68106200	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr3:68105000-68106200	Enhancers	Primary T cells from cord blood	blood
21	chr3:68105000-68106200	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr3:68105000-68106200	Enhancers	Duodenum Mucosa	Duodenum
23	chr3:68105000-68106600	Enhancers	Primary T cells fromperipheralblood	blood
24	chr3:68105000-68106600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr3:68105000-68106600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr3:68105000-68109000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr3:68105200-68107000	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr3:68105400-68106000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr3:68105400-68106800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr3:68105400-68107000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr3:68105400-68108400	Weak transcription	Fetal Intestine Large	intestine
32	chr3:68105600-68106200	Enhancers	Aorta	Aorta
33	chr3:68105800-68106000	Enhancers	Small Intestine	intestine
34	chr3:68105800-68106800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr3:68106000-68106800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr3:68106000-68108200	Weak transcription	Small Intestine	intestine
37	chr3:68106200-68106600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr3:68106200-68106800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
39	chr3:68106200-68106800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr3:68106200-68108000	Flanking Active TSS	Primary T cells from cord blood	blood
41	chr3:68106200-68108200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr3:68106200-68108600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr3:68106200-68108600	Weak transcription	Fetal Intestine Small	intestine
44	chr3:68106400-68106600	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr3:68106600-68106800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr3:68106600-68107000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr3:68106600-68107800	Active TSS	Primary T cells fromperipheralblood	blood
48	chr3:68106600-68107800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr3:68106600-68108400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr3:68106600-68108600	Weak transcription	Sigmoid Colon	Sigmoid Colon

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