Variant report

Variant	nsv876924
Chromosome Location	chr3:67978367-68063259
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	BACH1	chr3:68017186-68017276	K562	blood:	n/a	n/a
2	CCNT2	chr3:68033067-68033322	K562	blood:	n/a	n/a
3	CEBPB	chr3:68055781-68055942	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:68037096-68037312	K562	blood:	n/a	chr3:68037159-68037170
5	CEBPB	chr3:68033366-68033687	HepG2	liver:	n/a	chr3:68033525-68033536 chr3:68033502-68033513
6	CEBPB	chr3:68037035-68037272	A549	lung:	n/a	chr3:68037159-68037170
7	CEBPB	chr3:67997188-67997474	HepG2	liver:	n/a	chr3:67997344-67997355
8	CEBPB	chr3:68030854-68031193	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:68037001-68037283	HepG2	liver:	n/a	chr3:68037159-68037170
10	CEBPB	chr3:68037023-68037308	IMR90	lung:	n/a	chr3:68037159-68037170
11	CEBPB	chr3:68037007-68037284	H1-hESC	embryonic stem cell:	n/a	chr3:68037159-68037170
12	CEBPB	chr3:68030853-68031196	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:67985164-67985454	IMR90	lung:	n/a	chr3:67985315-67985326
14	CEBPB	chr3:67985138-67985469	HepG2	liver:	n/a	chr3:67985315-67985326
15	CEBPB	chr3:67980779-67981121	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr3:68056739-68057304	H1-hESC	embryonic stem cell:	n/a	chr3:68056886-68056896
17	CHD2	chr3:67998544-67998794	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr3:68047488-68047694	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr3:68016637-68016692	Lung_OC	lung:	n/a	n/a
20	CTCF	chr3:68057260-68057410	HRE	kidney:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
21	CTCF	chr3:68057295-68057319	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr3:68057180-68057330	HBMEC	blood vessel:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
23	CTCF	chr3:68057267-68057312	Fibrobl	skin:	n/a	chr3:68057285-68057293
24	CTCF	chr3:68057279-68057343	Kidney_OC	kidney:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
25	CTCF	chr3:68015842-68015927	Lung_OC	lung:	n/a	n/a
26	CTCF	chr3:67991000-67991150	HVMF	connective:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
27	CTCF	chr3:68057260-68057410	GM12874	blood:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
28	CTCF	chr3:67998780-67998930	HepG2	liver:	n/a	n/a
29	CTCF	chr3:67991040-67991190	HVMF	connective:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
30	CTCF	chr3:68057180-68057330	WERI-Rb-1	eye:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
31	CTCF	chr3:67991040-67991190	HCPEpiC	choroid plexus:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
32	CTCF	chr3:68024200-68024350	Caco-2	colon:	n/a	n/a
33	CTCF	chr3:67991120-67991270	RPTEC	kidney:	n/a	chr3:67991123-67991141 chr3:67991128-67991136
34	CTCF	chr3:68057171-68057418	H1-hESC	embryonic stem cell:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
35	CTCF	chr3:67991060-67991210	RPTEC	kidney:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
36	CTCF	chr3:68057160-68057310	HBMEC	blood vessel:	n/a	chr3:68057285-68057293
37	CTCF	chr3:68057180-68057330	RPTEC	kidney:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
38	CTCF	chr3:67991180-67991330	HVMF	connective:	n/a	n/a
39	CTCF	chr3:68057200-68057350	HRPEpiC	eye:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
40	CTCF	chr3:68057140-68057290	GM12874	blood:	n/a	n/a
41	CTCF	chr3:68057200-68057350	HAc	cerebellar:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
42	CTCF	chr3:68057300-68057450	GM12872	blood:	n/a	chr3:68057303-68057321
43	CTCF	chr3:68057220-68057370	WERI-Rb-1	eye:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
44	CTCF	chr3:67998860-67999010	HVMF	connective:	n/a	n/a
45	CTCF	chr3:67991060-67991210	NHDF-neo	bronchial:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
46	CTCF	chr3:67998714-67998790	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:67991140-67991290	HRE	kidney:	n/a	n/a
48	CTCF	chr3:68057220-68057370	BE2_C	brain:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
49	CTCF	chr3:68057182-68057417	Medullo	brain:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
50	CTCF	chr3:67991100-67991250	HCPEpiC	choroid plexus:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:68060925-68060975	HNPCEpiC	eye:	n/a
2	chr3:68060925-68060975	HNPCEpiC	eye:	n/a
3	chr3:68053273-68053323	Hepatocyte	liver:	n/a
4	chr3:68053484-68053534	Hela-S3	cervix:	n/a
5	chr3:68056976-68057026	NHDF-neo	bronchial:	n/a
6	chr3:68057306-68057356	GM12891	blood:	n/a
7	chr3:68057322-68057372	ProgFib	skin:	n/a
8	chr3:68057357-68057407	NB4	blood:	n/a
9	chr3:68053273-68053323	HIPEpiC	eye:	n/a
10	chr3:68057322-68057372	GM12892	blood:	n/a
11	chr3:68047840-68047890	U87	brain:	n/a
12	chr3:68053484-68053534	Jurkat	blood:	n/a
13	chr3:68039483-68039533	SK-N-SH	brain:	n/a
14	chr3:68056706-68056756	AG09309	skin:	n/a
15	chr3:68057025-68057075	PrEC	prostate:	n/a
16	chr3:68047840-68047890	GM12878	blood:	n/a
17	chr3:68056706-68056756	GM12891	blood:	n/a
18	chr3:68060925-68060975	PrEC	prostate:	n/a
19	chr3:68047840-68047890	NB4	blood:	n/a
20	chr3:68056976-68057026	HUVEC	blood vessel:	n/a
21	chr3:68039483-68039533	HL-60	blood:	n/a
22	chr3:68057025-68057075	Jurkat	blood:	n/a
23	chr3:68053273-68053323	HCM	heart:	n/a
24	chr3:68057306-68057356	U87	brain:	n/a
25	chr3:68053949-68053999	HNPCEpiC	eye:	n/a
26	chr3:68057322-68057372	PFSK-1	brain:	n/a
27	chr3:68060925-68060975	GM19239	blood:	n/a
28	chr3:68057306-68057356	PANC-1	pancreas:	n/a
29	chr3:68039483-68039533	HRCEpiC	kidney:	n/a
30	chr3:68053273-68053323	HepG2	liver:	n/a
31	chr3:68053949-68053999	U87	brain:	n/a
32	chr3:68057306-68057356	SK-N-SH_RA	brain:	n/a
33	chr3:68047840-68047890	NH-A	brain:	n/a
34	chr3:68053273-68053323	U87	brain:	n/a
35	chr3:68056706-68056756	Caco-2	colon:	n/a
36	chr3:68060925-68060975	CMK	blood:	n/a
37	chr3:68039483-68039533	HMEC	breast:	n/a
38	chr3:68039483-68039533	HEEpiC	esophagus:	n/a
39	chr3:68057357-68057407	BE2_C	brain:	n/a
40	chr3:68039483-68039533	AG10803	skin:	n/a
41	chr3:68053484-68053534	HCT-116	colon:	n/a
42	chr3:68056706-68056756	HEEpiC	esophagus:	n/a
43	chr3:68039483-68039533	K562	blood:	n/a
44	chr3:68053371-68053421	SK-N-MC	brain:	n/a
45	chr3:68047840-68047890	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:68056976-68057026	HCF	heart:	n/a
47	chr3:68053949-68053999	A549	lung:	n/a
48	chr3:68053273-68053323	ovcar-3	ovarian:	n/a
49	chr3:68060925-68060975	HRPEpiC	eye:	n/a
50	chr3:68057322-68057372	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:67991529..67993327-chr3:67994469..67996433,2	MCF-7	breast:
2	chr3:68045575..68047988-chr3:68059342..68060872,2	MCF-7	breast:
3	chr3:68058440..68060357-chr3:68076381..68078551,2	K562	blood:
4	chr3:67991094..67994023-chr3:67995213..67998211,2	MCF-7	breast:
5	chr3:68045575..68047988-chr3:68059342..68060872,2	MCF-7	breast:
6	chr3:67991529..67993327-chr3:67994469..67996433,2	MCF-7	breast:
7	chr3:67991094..67994023-chr3:67995213..67998211,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM19A1-1	chr3:67997565-67998137	ENSG00000241316
2	lnc-FAM19A1-1	chr3:67997565-67998136	NR_109992

Variant related genes	Relation type
FAM19A1	TF binding region
FAM19A1	CpG island

Extended variants
information (count: 1363 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1363 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567385248	chr3:67980807-67980808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188791164	chr3:67980815-67980816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529656510	chr3:67980831-67980832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540489154	chr3:67980857-67980858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1839042	chr3:67980858-67980859	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs576750160	chr3:67980865-67980866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545528492	chr3:67980898-67980899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562594474	chr3:67980918-67980919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191742943	chr3:67980920-67980921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147908375	chr3:67980993-67980994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371899356	chr3:67981016-67981017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4856916	chr3:67981043-67981044	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs547656091	chr3:67981044-67981045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570686562	chr3:67981051-67981052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532537882	chr3:67981059-67981060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142858680	chr3:67981060-67981061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568911173	chr3:67981145-67981146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541672423	chr3:67987811-67987812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75682905	chr3:67987877-67987878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556153459	chr3:67987878-67987879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569682892	chr3:67987896-67987897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535512924	chr3:67987914-67987915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1564870	chr3:67987930-67987931	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs148066328	chr3:67987976-67987977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6789718	chr3:67987977-67987978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557674055	chr3:67987987-67987988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150164471	chr3:67987992-67987993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374096611	chr3:67988058-67988059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532735222	chr3:67988062-67988063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562516035	chr3:67988108-67988109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs55833577	chr3:67988142-67988143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531625460	chr3:67988160-67988161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190491103	chr3:67988171-67988172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138615220	chr3:67988229-67988230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527876853	chr3:67988260-67988261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7615755	chr3:67988426-67988427	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs146335260	chr3:67988435-67988436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139582997	chr3:67988471-67988472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561864599	chr3:67988478-67988479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113850247	chr3:67988497-67988498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554826268	chr3:67988523-67988524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144247369	chr3:67988572-67988573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183103826	chr3:67988654-67988655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547733492	chr3:67988667-67988668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369145740	chr3:67988678-67988679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547232726	chr3:67988679-67988680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565725774	chr3:67988697-67988698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148712331	chr3:67988760-67988761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111464423	chr3:67988787-67988788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186193332	chr3:67988837-67988838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67980800-67981200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr3:67987800-67988600	Enhancers	Liver	Liver
3	chr3:67988600-67990200	Weak transcription	Liver	Liver
4	chr3:67990200-67990800	Enhancers	Liver	Liver
5	chr3:67990400-67998800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:67990600-67993000	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr3:67990800-67991800	Flanking Active TSS	Liver	Liver
8	chr3:67990800-67992800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr3:67991000-67992800	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr3:67991000-67993200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr3:67991200-67991800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr3:67991200-67992200	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr3:67991400-67991800	Enhancers	Right Atrium	heart
14	chr3:67991600-67992200	Enhancers	Brain Anterior Caudate	brain
15	chr3:67991600-67992400	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr3:67991800-67992200	Enhancers	Liver	Liver
17	chr3:67992200-67992800	Enhancers	Brain Germinal Matrix	brain
18	chr3:67992200-67996800	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr3:67992400-67997000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr3:67992800-67997000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr3:67993000-67997000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr3:67993200-67997000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr3:67994000-67994200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr3:67994200-67998200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr3:67995800-67996200	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr3:67996600-67998200	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr3:67996800-67997000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr3:67996800-67998400	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr3:67997000-67997800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr3:67997000-67998000	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr3:67997000-67998200	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr3:67997000-67998200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr3:67997000-67998400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr3:67997000-67998400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr3:67997000-67998400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr3:67997800-67998200	Enhancers	Primary T cells fromperipheralblood	blood
37	chr3:67997800-67998200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr3:67998000-67998200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:67998000-67998200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr3:67998000-67998200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr3:67998000-67998400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:67998000-67998400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr3:67998000-67998800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr3:67998000-67999200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
45	chr3:67998200-67998400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:67998200-67998400	Enhancers	HepG2	liver
47	chr3:67998200-67998600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr3:67998200-67998600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr3:67998200-67998600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr3:67998200-67998600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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