Variant report

Variant	esv3395568
Chromosome Location	chr3:67955462-68064660
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	chr3:68030854-68031193	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:68037035-68037272	A549	lung:	n/a	chr3:68037159-68037170
5	CEBPB	chr3:67997188-67997474	HepG2	liver:	n/a	chr3:67997344-67997355
6	CEBPB	chr3:67985164-67985454	IMR90	lung:	n/a	chr3:67985315-67985326
7	CEBPB	chr3:68037023-68037308	IMR90	lung:	n/a	chr3:68037159-68037170
8	CEBPB	chr3:68037096-68037312	K562	blood:	n/a	chr3:68037159-68037170
9	CEBPB	chr3:67980779-67981121	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr3:67974240-67974550	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:67964234-67964528	HepG2	liver:	n/a	chr3:67964358-67964369
12	CEBPB	chr3:68037007-68037284	H1-hESC	embryonic stem cell:	n/a	chr3:68037159-68037170
13	CEBPB	chr3:67985138-67985469	HepG2	liver:	n/a	chr3:67985315-67985326
14	CEBPB	chr3:68033366-68033687	HepG2	liver:	n/a	chr3:68033525-68033536 chr3:68033502-68033513
15	CEBPB	chr3:68030853-68031196	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:68055781-68055942	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:67974289-67974478	A549	lung:	n/a	n/a
18	CEBPB	chr3:67964275-67964462	H1-hESC	embryonic stem cell:	n/a	chr3:67964358-67964369
19	CEBPB	chr3:68037001-68037283	HepG2	liver:	n/a	chr3:68037159-68037170
20	CHD2	chr3:67998544-67998794	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr3:68056739-68057304	H1-hESC	embryonic stem cell:	n/a	chr3:68056886-68056896
22	CHD2	chr3:68047488-68047694	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr3:67998714-67998790	MCF-7	breast:	n/a	n/a
24	CTCF	chr3:68057300-68057450	GM12872	blood:	n/a	chr3:68057303-68057321
25	CTCF	chr3:68057171-68057418	H1-hESC	embryonic stem cell:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
26	CTCF	chr3:67991140-67991290	HRE	kidney:	n/a	n/a
27	CTCF	chr3:67991104-67991166	LNCaP	prostate:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
28	CTCF	chr3:68057220-68057370	HFF-Myc	foreskin:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
29	CTCF	chr3:68057267-68057312	Fibrobl	skin:	n/a	chr3:68057285-68057293
30	CTCF	chr3:68057180-68057330	HBMEC	blood vessel:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
31	CTCF	chr3:68057140-68057290	GM12874	blood:	n/a	n/a
32	CTCF	chr3:68057168-68057169	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr3:67998960-67999110	Caco-2	colon:	n/a	n/a
34	CTCF	chr3:68057180-68057330	RPTEC	kidney:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
35	CTCF	chr3:68057211-68057374	Gliobla	brain:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
36	CTCF	chr3:68057160-68057310	HBMEC	blood vessel:	n/a	chr3:68057285-68057293
37	CTCF	chr3:67991060-67991210	RPTEC	kidney:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
38	CTCF	chr3:67991040-67991190	HVMF	connective:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
39	CTCF	chr3:67991020-67991170	MCF-7	breast:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
40	CTCF	chr3:67991100-67991250	HCPEpiC	choroid plexus:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
41	CTCF	chr3:67998780-67998930	HepG2	liver:	n/a	n/a
42	CTCF	chr3:68057180-68057330	SK-N-SH_RA	brain:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
43	CTCF	chr3:68057076-68057406	H1-hESC	embryonic stem cell:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
44	CTCF	chr3:68063560-68063710	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:68057279-68057343	Kidney_OC	kidney:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
46	CTCF	chr3:68004720-68004870	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr3:68057182-68057417	Medullo	brain:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
48	CTCF	chr3:68057220-68057370	WERI-Rb-1	eye:	n/a	chr3:68057285-68057293 chr3:68057303-68057321
49	CTCF	chr3:67991000-67991150	HVMF	connective:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
50	CTCF	chr3:68057260-68057410	GM12874	blood:	n/a	chr3:68057285-68057293 chr3:68057303-68057321

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:68053949-68053999	NHDF-neo	bronchial:	n/a
2	chr3:68053949-68053999	NHDF-neo	bronchial:	n/a
3	chr3:68056976-68057026	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:68053484-68053534	NH-A	brain:	n/a
5	chr3:68057306-68057356	NT2-D1	testis:	n/a
6	chr3:68053273-68053323	NH-A	brain:	n/a
7	chr3:68056706-68056756	AG09309	skin:	n/a
8	chr3:68053371-68053421	Hela-S3	cervix:	n/a
9	chr3:68053949-68053999	GM12878	blood:	n/a
10	chr3:68057025-68057075	T-47D	breast:	n/a
11	chr3:68056706-68056756	PFSK-1	brain:	n/a
12	chr3:68057357-68057407	NB4	blood:	n/a
13	chr3:68056706-68056756	HUVEC	blood vessel:	n/a
14	chr3:68053949-68053999	T-47D	breast:	n/a
15	chr3:68057322-68057372	HRCEpiC	kidney:	n/a
16	chr3:68057322-68057372	HRPEpiC	eye:	n/a
17	chr3:68057025-68057075	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:68039483-68039533	HIPEpiC	eye:	n/a
19	chr3:68056976-68057026	SAEC	small airway:	n/a
20	chr3:68057025-68057075	HAEpiC	amniotic membrane:	n/a
21	chr3:68039483-68039533	H1-hESC	embryonic stem cell:	embryo
22	chr3:68053273-68053323	SK-N-MC	brain:	n/a
23	chr3:68047840-68047890	HEK293	kidney:	embryo
24	chr3:68053371-68053421	HMEC	breast:	n/a
25	chr3:68057306-68057356	SKMC	muscle:	n/a
26	chr3:68060925-68060975	NH-A	brain:	n/a
27	chr3:68053949-68053999	LNCaP	prostate:	n/a
28	chr3:68057322-68057372	K562	blood:	n/a
29	chr3:68056976-68057026	T-47D	breast:	n/a
30	chr3:68053484-68053534	SK-N-SH_RA	brain:	n/a
31	chr3:68057357-68057407	AG04449	skin:	fetal
32	chr3:68053484-68053534	HEK293	kidney:	embryo
33	chr3:68057306-68057356	SK-N-SH_RA	brain:	n/a
34	chr3:68057322-68057372	NB4	blood:	n/a
35	chr3:68057025-68057075	HRCEpiC	kidney:	n/a
36	chr3:68057306-68057356	PrEC	prostate:	n/a
37	chr3:68053949-68053999	HAEpiC	amniotic membrane:	n/a
38	chr3:68053371-68053421	GM12878	blood:	n/a
39	chr3:68053949-68053999	HEEpiC	esophagus:	n/a
40	chr3:68056706-68056756	SAEC	small airway:	n/a
41	chr3:68057322-68057372	MCF-7	breast:	n/a
42	chr3:68060925-68060975	HAEpiC	amniotic membrane:	n/a
43	chr3:68053484-68053534	BJ	skin:	n/a
44	chr3:68047840-68047890	HRPEpiC	eye:	n/a
45	chr3:68057357-68057407	RPTEC	kidney:	n/a
46	chr3:68057025-68057075	HepG2	liver:	n/a
47	chr3:68053949-68053999	AoSMC	blood vessel:	n/a
48	chr3:68060925-68060975	AG09309	skin:	n/a
49	chr3:68056976-68057026	HNPCEpiC	eye:	n/a
50	chr3:68056976-68057026	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:67991094..67994023-chr3:67995213..67998211,2	MCF-7	breast:
2	chr3:67991094..67994023-chr3:67995213..67998211,2	MCF-7	breast:
3	chr3:67991529..67993327-chr3:67994469..67996433,2	MCF-7	breast:
4	chr3:67991529..67993327-chr3:67994469..67996433,2	MCF-7	breast:
5	chr3:68045575..68047988-chr3:68059342..68060872,2	MCF-7	breast:
6	chr3:68058440..68060357-chr3:68076381..68078551,2	K562	blood:
7	chr3:68045575..68047988-chr3:68059342..68060872,2	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: 1767 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1767 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184596898	chr3:67956403-67956404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373779683	chr3:67956441-67956442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145512513	chr3:67956442-67956443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201583350	chr3:67956464-67956465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74589767	chr3:67956465-67956466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112028685	chr3:67956466-67956467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143425565	chr3:67956478-67956479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547365371	chr3:67956489-67956490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570312378	chr3:67956511-67956512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532944502	chr3:67956513-67956514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7609730	chr3:67956536-67956537	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs554484610	chr3:67956558-67956559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141771058	chr3:67956565-67956566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535631784	chr3:67956710-67956711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144857576	chr3:67956736-67956737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565979907	chr3:67956743-67956744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1550915	chr3:67956751-67956752	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs371111247	chr3:67956776-67956777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111524980	chr3:67956786-67956787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201029899	chr3:67956788-67956789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558039164	chr3:67956792-67956793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561382925	chr3:67956795-67956796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577114207	chr3:67956856-67956857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546198222	chr3:67956888-67956889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556346228	chr3:67956897-67956898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576162141	chr3:67956901-67956902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541996210	chr3:67956915-67956916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141735310	chr3:67956917-67956918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527968889	chr3:67956924-67956925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541315713	chr3:67956952-67956953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564824453	chr3:67956962-67956963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374425545	chr3:67956975-67956976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146346272	chr3:67956986-67956987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370600548	chr3:67956989-67956990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374059162	chr3:67956990-67956991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs367911203	chr3:67956991-67956992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs56378027	chr3:67957067-67957068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543223276	chr3:67957104-67957105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189918329	chr3:67957121-67957122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139280911	chr3:67957123-67957124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375298834	chr3:67957125-67957126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543608448	chr3:67957134-67957135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549193056	chr3:67957147-67957148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191325123	chr3:67957160-67957161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534818059	chr3:67957306-67957307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557738052	chr3:67957320-67957321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546704162	chr3:67957329-67957330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34872070	chr3:67957349-67957350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77369976	chr3:67957357-67957358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571531638	chr3:67957377-67957378	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67956400-67957400	Enhancers	Primary T killer memory cells from peripheral blood	blood
2	chr3:67956400-67958200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr3:67956600-67957200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr3:67956600-67957400	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr3:67956600-67957600	Enhancers	Primary hematopoietic stem cells	blood
6	chr3:67956600-67958000	Enhancers	Primary T cells from cord blood	blood
7	chr3:67956600-67958000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr3:67956800-67957200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr3:67956800-67957200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr3:67956800-67957600	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr3:67956800-67957800	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr3:67957400-67957600	Enhancers	Primary T cells fromperipheralblood	blood
13	chr3:67958000-67958400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr3:67958000-67958400	Enhancers	Brain Substantia Nigra	brain
15	chr3:67966000-67966800	Enhancers	Colon Smooth Muscle	Colon
16	chr3:67966800-67967200	Enhancers	Stomach Smooth Muscle	stomach
17	chr3:67969800-67972600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr3:67971200-67971800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr3:67971400-67971600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:67971600-67975600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr3:67972200-67972600	Enhancers	Fetal Lung	lung
22	chr3:67975600-67975800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:67977600-67978200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr3:67980800-67981200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr3:67987800-67988600	Enhancers	Liver	Liver
26	chr3:67988600-67990200	Weak transcription	Liver	Liver
27	chr3:67990200-67990800	Enhancers	Liver	Liver
28	chr3:67990400-67998800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr3:67990600-67993000	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr3:67990800-67991800	Flanking Active TSS	Liver	Liver
31	chr3:67990800-67992800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr3:67991000-67992800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr3:67991000-67993200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr3:67991200-67991800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr3:67991200-67992200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr3:67991400-67991800	Enhancers	Right Atrium	heart
37	chr3:67991600-67992200	Enhancers	Brain Anterior Caudate	brain
38	chr3:67991600-67992400	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr3:67991800-67992200	Enhancers	Liver	Liver
40	chr3:67992200-67992800	Enhancers	Brain Germinal Matrix	brain
41	chr3:67992200-67996800	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr3:67992400-67997000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr3:67992800-67997000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr3:67993000-67997000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr3:67993200-67997000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr3:67994000-67994200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr3:67994200-67998200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr3:67995800-67996200	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr3:67996600-67998200	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr3:67996800-67997000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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