Variant report

Variant	esv2762163
Chromosome Location	chr1:216982140-217015625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:126)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:126 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:216988803-216989184	ECC-1	luminal epithelium:	n/a	n/a
2	CEBPB	chr1:216995789-216996201	MCF-7	breast:	n/a	chr1:216995901-216995918
3	CEBPB	chr1:216988835-216989255	IMR90	lung:	n/a	n/a
4	CEBPB	chr1:216986256-216986610	IMR90	lung:	n/a	n/a
5	CEBPB	chr1:216988740-216989237	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr1:216995720-216996206	MCF-7	breast:	n/a	chr1:216995901-216995918
7	CEBPB	chr1:216988880-216989160	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:216988840-216989172	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr1:217005700-217005850	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr1:217005620-217005770	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr1:217005684-217005719	Pancreas_OC	pancreas:	n/a	n/a
12	CTCF	chr1:217005697-217005756	LNCaP	prostate:	n/a	n/a
13	CTCF	chr1:217005680-217005830	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr1:217005649-217005823	HepG2	liver:	n/a	n/a
15	CTCF	chr1:217004420-217004570	AG04450	lung:	n/a	n/a
16	CTCF	chr1:217005497-217005928	MCF-7	breast:	n/a	chr1:217005575-217005583
17	CTCF	chr1:217004320-217004470	NHEK	skin:	n/a	n/a
18	CTCF	chr1:216992079-216992111	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr1:217005640-217005790	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr1:217005660-217005810	HepG2	liver:	n/a	n/a
21	CTCF	chr1:217004340-217004490	NHEK	skin:	n/a	n/a
22	CTCF	chr1:217005640-217005790	MCF-7	breast:	n/a	n/a
23	CTCF	chr1:216991963-216992051	GM20000	blood:	n/a	n/a
24	CTCF	chr1:217004380-217004530	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr1:217005660-217005810	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr1:217005520-217005670	NHEK	skin:	n/a	chr1:217005575-217005583
27	CTCF	chr1:217014580-217014730	BE2_C	brain:	n/a	n/a
28	CTCF	chr1:217005620-217005851	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:217005627-217005830	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:217005671-217005803	HepG2	liver:	n/a	n/a
31	CTCF	chr1:216984920-216985070	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr1:217004380-217004530	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:217005660-217005810	Caco-2	colon:	n/a	n/a
34	CTCF	chr1:217004340-217004490	RPTEC	kidney:	n/a	n/a
35	CTCF	chr1:216983040-216983190	GM12872	blood:	n/a	n/a
36	CTCF	chr1:217005620-217005770	HMEC	breast:	n/a	n/a
37	CTCF	chr1:216983180-216983330	SAEC	small airway:	n/a	n/a
38	CTCF	chr1:217005580-217005730	A549	lung:	n/a	n/a
39	CTCF	chr1:217005600-217005750	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:216983092-216983104	GM13976	blood:	n/a	n/a
41	E2F4	chr1:217012570-217012583	MCF10A-Er-Src	breast:	n/a	n/a
42	EP300	chr1:217006627-217007529	SK-N-SH	brain:	n/a	n/a
43	EP300	chr1:217013799-217015354	SK-N-SH	brain:	n/a	chr1:217014552-217014565 chr1:217014695-217014705
44	EP300	chr1:217014455-217015018	SK-N-SH_RA	brain:	n/a	chr1:217014552-217014565 chr1:217014695-217014705
45	EP300	chr1:216993676-216993976	SK-N-SH_RA	brain:	n/a	chr1:216993818-216993825 chr1:216993703-216993717
46	EP300	chr1:216993607-216994155	SK-N-SH	brain:	n/a	chr1:216993818-216993825 chr1:216993703-216993717
47	EP300	chr1:217014540-217014913	SK-N-SH_RA	brain:	n/a	chr1:217014552-217014565 chr1:217014695-217014705
48	FOS	chr1:216997886-216998210	MCF10A-Er-Src	breast:	n/a	chr1:216998044-216998054 chr1:216998045-216998054 chr1:216998043-216998055 chr1:216998046-216998053 chr1:216998044-216998053 chr1:216998041-216998052
49	FOS	chr1:216997897-216998212	MCF10A-Er-Src	breast:	n/a	chr1:216998044-216998054 chr1:216998045-216998054 chr1:216998043-216998055 chr1:216998046-216998053 chr1:216998044-216998053 chr1:216998041-216998052
50	FOS	chr1:216986333-216986596	MCF10A-Er-Src	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:217004524-217004574	AG04449	skin:	fetal
2	chr1:217004524-217004574	AG04449	skin:	fetal
3	chr1:217010062-217010112	ECC-1	luminal epithelium:	n/a
4	chr1:217010062-217010112	HL-60	blood:	n/a
5	chr1:217004524-217004574	HCT-116	colon:	n/a
6	chr1:217004524-217004574	NB4	blood:	n/a
7	chr1:216988411-216988461	HCF	heart:	n/a
8	chr1:217004524-217004574	SAEC	small airway:	n/a
9	chr1:216988411-216988461	IMR90	lung:	fetal
10	chr1:217004524-217004574	HNPCEpiC	eye:	n/a
11	chr1:216988411-216988461	HNPCEpiC	eye:	n/a
12	chr1:216988411-216988461	K562	blood:	n/a
13	chr1:217004524-217004574	Hela-S3	cervix:	n/a
14	chr1:217010062-217010112	NHBE	bronchial:	n/a
15	chr1:217004524-217004574	SKMC	muscle:	n/a
16	chr1:216988411-216988461	AG04450	lung:	fetal
17	chr1:217010062-217010112	NT2-D1	testis:	n/a
18	chr1:216988411-216988461	Hela-S3	cervix:	n/a
19	chr1:216988411-216988461	PFSK-1	brain:	n/a
20	chr1:217004524-217004574	NH-A	brain:	n/a
21	chr1:216988411-216988461	ECC-1	luminal epithelium:	n/a
22	chr1:216988411-216988461	AG09319	gingival:	n/a
23	chr1:216988411-216988461	NH-A	brain:	n/a
24	chr1:216988411-216988461	HCM	heart:	n/a
25	chr1:217010062-217010112	HepG2	liver:	n/a
26	chr1:217010062-217010112	HNPCEpiC	eye:	n/a
27	chr1:216988411-216988461	HCT-116	colon:	n/a
28	chr1:217010062-217010112	U87	brain:	n/a
29	chr1:216988411-216988461	HL-60	blood:	n/a
30	chr1:217010062-217010112	HEK293	kidney:	embryo
31	chr1:216988411-216988461	AG10803	skin:	n/a
32	chr1:217004524-217004574	HEK293	kidney:	embryo
33	chr1:217004524-217004574	HUVEC	blood vessel:	n/a
34	chr1:216988411-216988461	NHBE	bronchial:	n/a
35	chr1:217004524-217004574	GM12878	blood:	n/a
36	chr1:217004524-217004574	AG10803	skin:	n/a
37	chr1:217004524-217004574	ECC-1	luminal epithelium:	n/a
38	chr1:217010062-217010112	HRPEpiC	eye:	n/a
39	chr1:216988411-216988461	PrEC	prostate:	n/a
40	chr1:217010062-217010112	AG04450	lung:	fetal
41	chr1:217004524-217004574	HRCEpiC	kidney:	n/a
42	chr1:217004524-217004574	GM12892	blood:	n/a
43	chr1:217010062-217010112	GM12891	blood:	n/a
44	chr1:217004524-217004574	BE2_C	brain:	n/a
45	chr1:217010062-217010112	HIPEpiC	eye:	n/a
46	chr1:216988411-216988461	CMK	blood:	n/a
47	chr1:217004524-217004574	HRPEpiC	eye:	n/a
48	chr1:216988411-216988461	NHDF-neo	bronchial:	n/a
49	chr1:217010062-217010112	HCF	heart:	n/a
50	chr1:217004524-217004574	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:217005236..217007424-chr12:14926627..14928347,2	MCF-7	breast:
2	chr1:216993429..216994300-chr20:49343611..49344266,2	MCF-7	breast:

No data

Variant related genes	Relation type
ESRRG	TF binding region
ESRRG	CpG island
ENSG00000246705	chromatin interactions

Extended variants
information (count: 1397 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1397 , 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	rs2813673	chr1:216982140-216982141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144916640	chr1:216982165-216982166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147942182	chr1:216982178-216982179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141726403	chr1:216982184-216982185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561007071	chr1:216982226-216982227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574702622	chr1:216982231-216982232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150018075	chr1:216982239-216982240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543011037	chr1:216982253-216982254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111980187	chr1:216982260-216982261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528982901	chr1:216982279-216982280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184838567	chr1:216982304-216982305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188389268	chr1:216982358-216982359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145254802	chr1:216982376-216982377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534872985	chr1:216982399-216982400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558438362	chr1:216982407-216982408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181189141	chr1:216982452-216982453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537098070	chr1:216982472-216982473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115845222	chr1:216982488-216982489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573822248	chr1:216982502-216982503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543126729	chr1:216982585-216982586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143243852	chr1:216982639-216982640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553156385	chr1:216982661-216982662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376670218	chr1:216982666-216982667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572213294	chr1:216982668-216982669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77597864	chr1:216982670-216982671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs397862019	chr1:216982688-216982689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397810989	chr1:216982689-216982690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531795139	chr1:216982715-216982716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113150525	chr1:216982716-216982717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12097929	chr1:216982737-216982738	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs375502111	chr1:216982777-216982778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140456193	chr1:216982852-216982853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1030846	chr1:216982853-216982854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12145972	chr1:216982886-216982887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77823737	chr1:216982938-216982939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2789716	chr1:216982951-216982952	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12146000	chr1:216982966-216982967	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs565599428	chr1:216983023-216983024	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12760372	chr1:216983034-216983035	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs138065471	chr1:216983060-216983061	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs571651167	chr1:216983087-216983088	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs547999025	chr1:216983088-216983089	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567836846	chr1:216983103-216983104	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs141743764	chr1:216983144-216983145	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557199629	chr1:216983210-216983211	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185229437	chr1:216983215-216983216	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs150133191	chr1:216983217-216983218	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs553443424	chr1:216983225-216983226	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs573247996	chr1:216983242-216983243	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs541267145	chr1:216983254-216983255	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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	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
Basal cell lymphoma	17170743	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
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216979000-216986200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:216979400-216983000	Weak transcription	Psoas Muscle	Psoas
3	chr1:216979600-216983200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:216979800-216985000	Weak transcription	Fetal Heart	heart
5	chr1:216979800-216985200	Weak transcription	Brain Substantia Nigra	brain
6	chr1:216979800-216988800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:216979800-216989000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:216980000-216984800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr1:216980200-216986400	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:216980200-216987400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:216980400-216988000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr1:216981200-216986000	Weak transcription	HSMMtube	muscle
13	chr1:216982000-216983000	Weak transcription	Gastric	stomach
14	chr1:216983000-216983200	Genic enhancers	Gastric	stomach
15	chr1:216983000-216983200	Enhancers	Right Atrium	heart
16	chr1:216983000-216983600	Enhancers	Psoas Muscle	Psoas
17	chr1:216983200-216983400	Enhancers	Fetal Lung	lung
18	chr1:216983200-216983400	Weak transcription	Left Ventricle	heart
19	chr1:216983200-216983600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:216983200-216988600	Weak transcription	Right Atrium	heart
21	chr1:216983200-216989200	Weak transcription	Gastric	stomach
22	chr1:216983400-216983600	Enhancers	Left Ventricle	heart
23	chr1:216983600-216986200	Weak transcription	Psoas Muscle	Psoas
24	chr1:216983600-216986400	Weak transcription	Fetal Lung	lung
25	chr1:216983600-216988600	Weak transcription	Left Ventricle	heart
26	chr1:216983600-216988800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:216983800-216985000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:216984000-216985000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:216984800-216985000	Enhancers	Fetal Kidney	kidney
30	chr1:216984800-216985200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr1:216984800-216985200	Enhancers	Fetal Intestine Large	intestine
32	chr1:216985000-216985400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:216985000-216985400	Enhancers	Duodenum Mucosa	Duodenum
34	chr1:216985000-216985400	Enhancers	Fetal Intestine Small	intestine
35	chr1:216985000-216985600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:216985000-216986400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr1:216985000-216987600	Weak transcription	Fetal Kidney	kidney
38	chr1:216985000-216988600	Enhancers	Fetal Heart	heart
39	chr1:216985200-216985400	Enhancers	Brain Substantia Nigra	brain
40	chr1:216985200-216985600	Weak transcription	Fetal Intestine Large	intestine
41	chr1:216985200-216988400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr1:216985400-216986200	Weak transcription	Brain Substantia Nigra	brain
43	chr1:216985400-216988200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:216985400-216988400	Weak transcription	Fetal Intestine Small	intestine
45	chr1:216985400-216989000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr1:216985600-216985800	Enhancers	Fetal Intestine Large	intestine
47	chr1:216985600-216988400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:216985800-216989000	Weak transcription	Fetal Intestine Large	intestine
49	chr1:216986000-216986400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:216986000-216986400	Enhancers	Muscle Satellite Cultured Cells	--

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