Variant report

Variant	esv3345878
Chromosome Location	chr1:213714352-213841547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:625)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:625 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:213824064-213824299	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:213746227-213746755	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:213737635-213737997	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:213744874-213744949	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:213743764-213744217	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:213742445-213743469	HepG2	liver:	n/a	n/a
7	ATF1	chr1:213834810-213834982	K562	blood:	n/a	n/a
8	ATF1	chr1:213779101-213779412	K562	blood:	n/a	n/a
9	ATF1	chr1:213737692-213737815	K562	blood:	n/a	n/a
10	BACH1	chr1:213766501-213766507	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr1:213796044-213796367	GM12878	blood:	n/a	n/a
12	BATF	chr1:213732343-213732536	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:213786892-213787071	K562	blood:	n/a	chr1:213787035-213787048 chr1:213787038-213787047 chr1:213787031-213787052
14	BHLHE40	chr1:213786882-213787252	HepG2	liver:	n/a	chr1:213787035-213787048 chr1:213787038-213787047 chr1:213787031-213787052
15	BHLHE40	chr1:213786936-213787126	HepG2	liver:	n/a	chr1:213787035-213787048 chr1:213787038-213787047 chr1:213787031-213787052
16	BHLHE40	chr1:213779064-213779350	K562	blood:	n/a	n/a
17	BHLHE40	chr1:213746322-213746870	HepG2	liver:	n/a	n/a
18	BRCA1	chr1:213786367-213786368	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr1:213737413-213737835	K562	blood:	n/a	n/a
20	CBX3	chr1:213778920-213779424	K562	blood:	n/a	n/a
21	CCNT2	chr1:213792464-213792672	K562	blood:	n/a	n/a
22	CCNT2	chr1:213779116-213779493	K562	blood:	n/a	n/a
23	CEBPB	chr1:213742932-213743432	HCT-116	colon:	n/a	n/a
24	CEBPB	chr1:213830862-213831091	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:213746244-213746657	HepG2	liver:	n/a	chr1:213746630-213746641
26	CEBPB	chr1:213779044-213779537	K562	blood:	n/a	chr1:213779315-213779326
27	CEBPB	chr1:213742754-213743534	HCT-116	colon:	n/a	n/a
28	CEBPB	chr1:213830848-213831019	A549	lung:	n/a	n/a
29	CEBPB	chr1:213742532-213742904	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:213839561-213839837	K562	blood:	n/a	chr1:213839688-213839699
31	CEBPB	chr1:213746324-213746629	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:213742577-213742804	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:213839557-213839757	HepG2	liver:	n/a	chr1:213839688-213839699
34	CEBPB	chr1:213762905-213762967	HepG2	liver:	n/a	chr1:213762935-213762946
35	CEBPB	chr1:213779172-213779450	IMR90	lung:	n/a	chr1:213779315-213779326
36	CEBPB	chr1:213779113-213779457	K562	blood:	n/a	chr1:213779315-213779326
37	CEBPB	chr1:213839603-213839810	H1-hESC	embryonic stem cell:	n/a	chr1:213839688-213839699
38	CEBPB	chr1:213778983-213779561	K562	blood:	n/a	chr1:213779315-213779326
39	CEBPB	chr1:213821634-213821894	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:213779180-213779466	HepG2	liver:	n/a	chr1:213779315-213779326
41	CEBPB	chr1:213725418-213725769	HepG2	liver:	n/a	n/a
42	CEBPD	chr1:213778991-213779563	K562	blood:	n/a	chr1:213779316-213779327
43	CEBPD	chr1:213779005-213779559	K562	blood:	n/a	chr1:213779316-213779327
44	CHD2	chr1:213744786-213744801	HepG2	liver:	n/a	n/a
45	CTCF	chr1:213767110-213767173	Fibrobl	skin:	n/a	n/a
46	CTCF	chr1:213737677-213737782	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr1:213737620-213737770	K562	blood:	n/a	n/a
48	CTCF	chr1:213795940-213796090	HMEC	breast:	n/a	n/a
49	CTCF	chr1:213737710-213737801	GM19239	blood:	n/a	n/a
50	CTCF	chr1:213737620-213737770	RPTEC	kidney:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:213831368-213831418	HUVEC	blood vessel:	n/a
2	chr1:213831368-213831418	Caco-2	colon:	n/a
3	chr1:213831368-213831418	IMR90	lung:	fetal
4	chr1:213831368-213831418	HAEpiC	amniotic membrane:	n/a
5	chr1:213823255-213823305	NB4	blood:	n/a
6	chr1:213831368-213831418	H1-hESC	embryonic stem cell:	embryo
7	chr1:213823255-213823305	NHDF-neo	bronchial:	n/a
8	chr1:213831368-213831418	HL-60	blood:	n/a
9	chr1:213831368-213831418	PFSK-1	brain:	n/a
10	chr1:213823255-213823305	HCF	heart:	n/a
11	chr1:213831368-213831418	LNCaP	prostate:	n/a
12	chr1:213831368-213831418	HepG2	liver:	n/a
13	chr1:213831368-213831418	AoSMC	blood vessel:	n/a
14	chr1:213831368-213831418	GM12892	blood:	n/a
15	chr1:213823255-213823305	A549	lung:	n/a
16	chr1:213823255-213823305	GM06990	blood:	n/a
17	chr1:213831368-213831418	RPTEC	kidney:	n/a
18	chr1:213831368-213831418	NHDF-neo	bronchial:	n/a
19	chr1:213831368-213831418	GM19239	blood:	n/a
20	chr1:213823255-213823305	HUVEC	blood vessel:	n/a
21	chr1:213823255-213823305	RPTEC	kidney:	n/a
22	chr1:213823255-213823305	HCPEpiC	choroid plexus:	n/a
23	chr1:213831368-213831418	ProgFib	skin:	n/a
24	chr1:213823255-213823305	LNCaP	prostate:	n/a
25	chr1:213823255-213823305	AG04450	lung:	fetal
26	chr1:213831368-213831418	A549	lung:	n/a
27	chr1:213823255-213823305	PFSK-1	brain:	n/a
28	chr1:213831368-213831418	HCM	heart:	n/a
29	chr1:213831368-213831418	SK-N-SH	brain:	n/a
30	chr1:213823255-213823305	Hepatocyte	liver:	n/a
31	chr1:213823255-213823305	AoSMC	blood vessel:	n/a
32	chr1:213831368-213831418	HRE	kidney:	n/a
33	chr1:213831368-213831418	SKMC	muscle:	n/a
34	chr1:213823255-213823305	HL-60	blood:	n/a
35	chr1:213823255-213823305	MCF10A-Er-Src	breast:	n/a
36	chr1:213823255-213823305	GM12878	blood:	n/a
37	chr1:213823255-213823305	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:213831368-213831418	HCPEpiC	choroid plexus:	n/a
39	chr1:213831368-213831418	NHBE	bronchial:	n/a
40	chr1:213823255-213823305	HCT-116	colon:	n/a
41	chr1:213823255-213823305	SK-N-MC	brain:	n/a
42	chr1:213831368-213831418	HEEpiC	esophagus:	n/a
43	chr1:213831368-213831418	HRCEpiC	kidney:	n/a
44	chr1:213831368-213831418	SK-N-MC	brain:	n/a
45	chr1:213831368-213831418	HMEC	breast:	n/a
46	chr1:213831368-213831418	AG04449	skin:	fetal
47	chr1:213823255-213823305	HRCEpiC	kidney:	n/a
48	chr1:213823255-213823305	HNPCEpiC	eye:	n/a
49	chr1:213823255-213823305	PANC-1	pancreas:	n/a
50	chr1:213831368-213831418	HRPEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:213826308..213828886-chr1:213831315..213833720,2	K562	blood:
2	chr1:213729520..213732362-chr1:213732486..213735394,2	K562	blood:
3	chr1:213776790..213779476-chr1:213780273..213782420,2	K562	blood:
4	chr1:213753502..213756205-chr1:213769622..213772542,2	K562	blood:
5	chr1:213764921..213766646-chr1:213766759..213768762,2	K562	blood:
6	chr1:213776790..213779476-chr1:213780273..213782420,2	K562	blood:
7	chr1:213764921..213766646-chr1:213766759..213768762,2	K562	blood:
8	chr1:213729520..213732362-chr1:213732486..213735394,2	K562	blood:
9	chr1:213729027..213731700-chr1:214452978..214455881,2	MCF-7	breast:
10	chr1:213753502..213756205-chr1:213769622..213772542,2	K562	blood:
11	chr1:213826308..213828886-chr1:213831315..213833720,2	K562	blood:
12	chr1:213737208..213738218-chr1:214296276..214297135,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPS6KC1-1	chr1:213719626-213719790	XLOC_000557

No data

Variant related genes	Relation type
ENSG00000221026	TF binding region
ENSG00000221026	CpG island
ENSG00000143499	chromatin interactions

Extended variants
information (count: 3460 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3460 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536473967	chr1:213717202-213717203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190885337	chr1:213717203-213717204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543061806	chr1:213717232-213717233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556076204	chr1:213717235-213717236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs578099219	chr1:213717248-213717249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs180873158	chr1:213717298-213717299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12737358	chr1:213717326-213717327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573421070	chr1:213717336-213717337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545604030	chr1:213717357-213717358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370047722	chr1:213717359-213717360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78556829	chr1:213717362-213717363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560347095	chr1:213717396-213717397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186507872	chr1:213717430-213717431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150154020	chr1:213717454-213717455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373783871	chr1:213717465-213717466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564615138	chr1:213717476-213717477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17020949	chr1:213717492-213717493	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs549929900	chr1:213717508-213717509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191446629	chr1:213717570-213717571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535988927	chr1:213717578-213717579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73090817	chr1:213717583-213717584	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1532535	chr1:213717600-213717601	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs548768576	chr1:213719634-213719635	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs17020954	chr1:213719643-213719644	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs35775719	chr1:213719731-213719732	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs532690485	chr1:213719734-213719735	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs561942449	chr1:213722440-213722441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545924621	chr1:213722447-213722448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185097045	chr1:213722492-213722493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531388888	chr1:213722531-213722532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145564984	chr1:213722595-213722596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148878176	chr1:213722629-213722630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550813774	chr1:213722630-213722631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548447811	chr1:213722644-213722645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143477448	chr1:213722693-213722694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148011383	chr1:213722702-213722703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79503589	chr1:213722742-213722743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375788263	chr1:213722759-213722760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12730824	chr1:213722764-213722765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538315863	chr1:213722771-213722772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556409941	chr1:213722893-213722894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs61649181	chr1:213722909-213722910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375403051	chr1:213722921-213722922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200687419	chr1:213722922-213722923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541243965	chr1:213722931-213722932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377053899	chr1:213722945-213722946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200217558	chr1:213722949-213722950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201503413	chr1:213722954-213722955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546408018	chr1:213722956-213722957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574900439	chr1:213722973-213722974	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213717200-213717600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr1:213722400-213723600	Enhancers	HepG2	liver
3	chr1:213723400-213723800	Enhancers	Fetal Heart	heart
4	chr1:213723600-213725400	Weak transcription	HepG2	liver
5	chr1:213725400-213725600	Enhancers	HepG2	liver
6	chr1:213732800-213744200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:213737200-213737800	Weak transcription	Pancreas	Pancrea
8	chr1:213737600-213738000	Enhancers	Liver	Liver
9	chr1:213737600-213738200	Enhancers	Fetal Intestine Large	intestine
10	chr1:213737800-213738000	Enhancers	Pancreas	Pancrea
11	chr1:213737800-213738200	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr1:213737800-213738200	Enhancers	HepG2	liver
13	chr1:213738000-213738200	Enhancers	Fetal Intestine Small	intestine
14	chr1:213738000-213742200	Weak transcription	Pancreas	Pancrea
15	chr1:213738200-213741000	Weak transcription	HepG2	liver
16	chr1:213738200-213742000	Weak transcription	Fetal Intestine Large	intestine
17	chr1:213738200-213743000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr1:213741000-213748200	Enhancers	HepG2	liver
19	chr1:213741400-213742200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr1:213741400-213744200	Enhancers	Fetal Intestine Small	intestine
21	chr1:213742000-213743400	Enhancers	Fetal Intestine Large	intestine
22	chr1:213742200-213742600	ZNF genes & repeats	Aorta	Aorta
23	chr1:213742200-213742600	Enhancers	Pancreas	Pancrea
24	chr1:213742200-213746000	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr1:213742400-213743600	Enhancers	Duodenum Mucosa	Duodenum
26	chr1:213742600-213746400	Weak transcription	Pancreas	Pancrea
27	chr1:213743000-213743800	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr1:213743200-213744200	Enhancers	Small Intestine	intestine
29	chr1:213743200-213744400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:213743400-213744600	Weak transcription	Fetal Intestine Large	intestine
31	chr1:213743600-213744400	Enhancers	HSMM	muscle
32	chr1:213743600-213746800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr1:213743800-213746000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr1:213744200-213745400	Weak transcription	Fetal Intestine Small	intestine
35	chr1:213744200-213747200	Weak transcription	Small Intestine	intestine
36	chr1:213744600-213748400	Enhancers	Fetal Intestine Large	intestine
37	chr1:213745400-213748200	Enhancers	Fetal Intestine Small	intestine
38	chr1:213746000-213747200	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr1:213746000-213747200	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr1:213746000-213747400	Enhancers	Brain Germinal Matrix	brain
41	chr1:213746200-213747400	Enhancers	Fetal Lung	lung
42	chr1:213746400-213747000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr1:213746400-213747200	Enhancers	Brain Cingulate Gyrus	brain
44	chr1:213746400-213747400	Enhancers	Brain Substantia Nigra	brain
45	chr1:213746400-213747600	Enhancers	Pancreas	Pancrea
46	chr1:213746600-213747000	Enhancers	Adipose Nuclei	Adipose
47	chr1:213746600-213747200	Enhancers	Brain Anterior Caudate	brain
48	chr1:213746600-213747400	Enhancers	Brain Angular Gyrus	brain
49	chr1:213746800-213747400	Enhancers	Duodenum Mucosa	Duodenum
50	chr1:213747200-213747400	Enhancers	Small Intestine	intestine

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