Variant report

Variant	nsv998569
Chromosome Location	chr1:158317392-158443389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:207)
CpG islands
(count:977)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:158341119-158341416	GM12878	blood:	n/a	n/a
2	BATF	chr1:158340924-158341438	GM12878	blood:	n/a	chr1:158341094-158341104
3	BATF	chr1:158332810-158333051	GM12878	blood:	n/a	chr1:158332952-158332963 chr1:158332953-158332963
4	BCL11A	chr1:158341074-158341392	GM12878	blood:	n/a	chr1:158341143-158341152 chr1:158341096-158341105
5	BRCA1	chr1:158326248-158326297	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr1:158403201-158403528	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:158388471-158388678	A549	lung:	n/a	n/a
8	CEBPB	chr1:158388420-158388687	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:158373329-158373375	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:158388416-158388707	IMR90	lung:	n/a	n/a
11	CTCF	chr1:158370720-158370870	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr1:158324729-158324776	GM10248	blood:	n/a	n/a
13	CTCF	chr1:158425060-158425210	NHEK	skin:	n/a	n/a
14	CTCF	chr1:158346956-158347001	GM13977	blood:	n/a	n/a
15	CTCF	chr1:158394940-158395090	MCF-7	breast:	n/a	n/a
16	CTCF	chr1:158318999-158319042	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr1:158323619-158323651	GM12891	blood:	n/a	n/a
18	CTCF	chr1:158365560-158365710	BE2_C	brain:	n/a	n/a
19	CTCF	chr1:158394991-158395049	K562	blood:	n/a	n/a
20	CTCF	chr1:158396993-158397070	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr1:158344446-158344516	GM13976	blood:	n/a	n/a
22	CTCF	chr1:158323653-158323677	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr1:158370890-158370991	GM12878	blood:	n/a	n/a
24	CTCF	chr1:158400925-158401023	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr1:158318707-158318777	GM10248	blood:	n/a	n/a
26	CTCF	chr1:158370912-158370951	LNCaP	prostate:	n/a	n/a
27	CUX1	chr1:158421797-158421919	GM12878	blood:	n/a	n/a
28	E2F4	chr1:158354975-158355138	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr1:158429611-158429887	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr1:158387283-158387374	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr1:158415853-158416116	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr1:158412084-158412265	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr1:158339478-158339603	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr1:158349205-158349415	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr1:158374285-158374458	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr1:158341054-158341617	GM12878	blood:	n/a	n/a
37	EBF1	chr1:158340831-158341442	GM12878	blood:	n/a	n/a
38	EBF1	chr1:158341134-158341585	GM12878	blood:	n/a	n/a
39	ELK1	chr1:158385808-158385812	K562	blood:	n/a	n/a
40	EP300	chr1:158340887-158341400	GM12878	blood:	n/a	chr1:158341096-158341105
41	EP300	chr1:158393153-158393213	K562	blood:	n/a	n/a
42	EP300	chr1:158360112-158360193	GM12878	blood:	n/a	n/a
43	FAM48A	chr1:158426699-158426852	GM12878	blood:	n/a	n/a
44	FOS	chr1:158340959-158341268	MCF10A-Er-Src	breast:	n/a	chr1:158341095-158341107 chr1:158341097-158341106
45	FOS	chr1:158340967-158341219	MCF10A-Er-Src	breast:	n/a	chr1:158341095-158341107 chr1:158341097-158341106
46	FOS	chr1:158340972-158341267	MCF10A-Er-Src	breast:	n/a	chr1:158341095-158341107 chr1:158341097-158341106
47	FOS	chr1:158340997-158341219	MCF10A-Er-Src	breast:	n/a	chr1:158341095-158341107 chr1:158341097-158341106
48	GATA3	chr1:158376629-158376753	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr1:158391991-158392534	MCF-7	breast:	n/a	chr1:158392495-158392502 chr1:158392376-158392385
50	IKZF1	chr1:158340942-158341464	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158323482-158323532	U87	brain:	n/a
2	chr1:158323482-158323532	U87	brain:	n/a
3	chr1:158322841-158322891	A549	lung:	n/a
4	chr1:158322845-158322895	NH-A	brain:	n/a
5	chr1:158435277-158435327	HCF	heart:	n/a
6	chr1:158322845-158322895	Caco-2	colon:	n/a
7	chr1:158435277-158435327	HEEpiC	esophagus:	n/a
8	chr1:158391119-158391169	HUVEC	blood vessel:	n/a
9	chr1:158324331-158324381	NHDF-neo	bronchial:	n/a
10	chr1:158369112-158369162	HMEC	breast:	n/a
11	chr1:158324331-158324381	Hepatocyte	liver:	n/a
12	chr1:158369112-158369162	H1-hESC	embryonic stem cell:	embryo
13	chr1:158322845-158322895	H1-hESC	embryonic stem cell:	embryo
14	chr1:158319083-158319133	HIPEpiC	eye:	n/a
15	chr1:158369112-158369162	AG10803	skin:	n/a
16	chr1:158325254-158325304	Jurkat	blood:	n/a
17	chr1:158369112-158369162	Jurkat	blood:	n/a
18	chr1:158323482-158323532	T-47D	breast:	n/a
19	chr1:158435396-158435446	SK-N-SH	brain:	n/a
20	chr1:158368889-158368939	GM12892	blood:	n/a
21	chr1:158319083-158319133	CMK	blood:	n/a
22	chr1:158390649-158390699	ovcar-3	ovarian:	n/a
23	chr1:158435277-158435327	HCM	heart:	n/a
24	chr1:158390759-158390809	HRCEpiC	kidney:	n/a
25	chr1:158390759-158390809	HL-60	blood:	n/a
26	chr1:158390842-158390892	GM06990	blood:	n/a
27	chr1:158322841-158322891	HCM	heart:	n/a
28	chr1:158391119-158391169	HRPEpiC	eye:	n/a
29	chr1:158390759-158390809	U87	brain:	n/a
30	chr1:158390759-158390809	HIPEpiC	eye:	n/a
31	chr1:158435396-158435446	K562	blood:	n/a
32	chr1:158390759-158390809	GM06990	blood:	n/a
33	chr1:158322841-158322891	NT2-D1	testis:	n/a
34	chr1:158323482-158323532	HCM	heart:	n/a
35	chr1:158390842-158390892	AG09319	gingival:	n/a
36	chr1:158390842-158390892	Jurkat	blood:	n/a
37	chr1:158390759-158390809	SK-N-SH	brain:	n/a
38	chr1:158322841-158322891	GM12878	blood:	n/a
39	chr1:158319083-158319133	MCF-7	breast:	n/a
40	chr1:158322841-158322891	Caco-2	colon:	n/a
41	chr1:158327383-158327433	Hela-S3	cervix:	n/a
42	chr1:158327383-158327433	LNCaP	prostate:	n/a
43	chr1:158319083-158319133	SK-N-MC	brain:	n/a
44	chr1:158324331-158324381	ProgFib	skin:	n/a
45	chr1:158391119-158391169	AG09309	skin:	n/a
46	chr1:158325254-158325304	GM12892	blood:	n/a
47	chr1:158435277-158435327	AG04450	lung:	fetal
48	chr1:158324471-158324521	HRPEpiC	eye:	n/a
49	chr1:158323482-158323532	NHDF-neo	bronchial:	n/a
50	chr1:158435396-158435446	HRPEpiC	eye:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR10K1-1	chr1:158423988-158425063	NONHSAT006985

No data

Variant related genes	Relation type
OR10T2	TF binding region
EI24P2	TF binding region
OR10T1P	TF binding region
CD1E	TF binding region
OR10K2	TF binding region
OR10K1	TF binding region
OR10T2	CpG island
EI24P2	CpG island
OR10T1P	CpG island
CD1E	CpG island
OR10K2	CpG island
OR10K1	CpG island

Extended variants
information (count: 4849 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:4849 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567852301	chr1:158317397-158317398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181032825	chr1:158317406-158317407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145005739	chr1:158317434-158317435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149073733	chr1:158317472-158317473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559726699	chr1:158317481-158317482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533879519	chr1:158317497-158317498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11588320	chr1:158317553-158317554	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs545336904	chr1:158317572-158317573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142232741	chr1:158317586-158317587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73027898	chr1:158317599-158317600	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs557203419	chr1:158317614-158317615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553536994	chr1:158317615-158317616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549136144	chr1:158317661-158317662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183902835	chr1:158317676-158317677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377462986	chr1:158317699-158317700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542303161	chr1:158317704-158317705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151213513	chr1:158317705-158317706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571266805	chr1:158317712-158317713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188436690	chr1:158317715-158317716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557302172	chr1:158317716-158317717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569125364	chr1:158317729-158317730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536466373	chr1:158317735-158317736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562214818	chr1:158317783-158317784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554839436	chr1:158317789-158317790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544895776	chr1:158317797-158317798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572932124	chr1:158317811-158317812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141254003	chr1:158317813-158317814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73027900	chr1:158317818-158317819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs370245980	chr1:158317826-158317827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577978478	chr1:158317834-158317835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111634340	chr1:158317870-158317871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs386635886	chr1:158317878-158317879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112430141	chr1:158317881-158317882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547785489	chr1:158317901-158317902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564610963	chr1:158317907-158317908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533473964	chr1:158317916-158317917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542896848	chr1:158317919-158317920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561556095	chr1:158317964-158317965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150417645	chr1:158317966-158317967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374380253	chr1:158317975-158317976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564786940	chr1:158318001-158318002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138273125	chr1:158318041-158318042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181257656	chr1:158318064-158318065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149606853	chr1:158318076-158318077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201776282	chr1:158318096-158318097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185716466	chr1:158318106-158318107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557970773	chr1:158318150-158318151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191893894	chr1:158318151-158318152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367917808	chr1:158318173-158318174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553437641	chr1:158318177-158318178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21045282	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ewing''s sarcoma	17952124	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158317000-158317600	Enhancers	Dnd41	blood
2	chr1:158317600-158319600	Weak transcription	Dnd41	blood
3	chr1:158318800-158319000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:158319000-158319200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:158319200-158319400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:158319400-158319800	Weak transcription	Fetal Thymus	thymus
7	chr1:158319600-158321600	Enhancers	Dnd41	blood
8	chr1:158319800-158321400	Enhancers	Fetal Thymus	thymus
9	chr1:158321400-158322600	Weak transcription	Fetal Thymus	thymus
10	chr1:158321600-158322000	Weak transcription	Dnd41	blood
11	chr1:158322000-158322800	Enhancers	Dnd41	blood
12	chr1:158322600-158324000	Flanking Active TSS	Fetal Thymus	thymus
13	chr1:158322800-158324600	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr1:158322800-158326600	Flanking Active TSS	Dnd41	blood
15	chr1:158322800-158328400	Active TSS	Thymus	Thymus
16	chr1:158323000-158323600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr1:158323000-158324600	Enhancers	Primary T cells from cord blood	blood
18	chr1:158323200-158324200	Enhancers	Primary hematopoietic stem cells	blood
19	chr1:158323200-158324800	Enhancers	Primary B cells from peripheral blood	blood
20	chr1:158323400-158323800	Enhancers	GM12878-XiMat	blood
21	chr1:158323400-158324200	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr1:158323600-158323800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr1:158323600-158324000	Enhancers	Adipose Nuclei	Adipose
24	chr1:158323600-158324000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr1:158323600-158324200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:158323600-158324600	Enhancers	Primary B cells from cord blood	blood
27	chr1:158324000-158324600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr1:158324000-158326800	Active TSS	Fetal Thymus	thymus
29	chr1:158324600-158325200	Weak transcription	Primary T cells from cord blood	blood
30	chr1:158325200-158326000	Active TSS	Primary T cells from cord blood	blood
31	chr1:158326600-158327600	Transcr. at gene 5' and 3'	Dnd41	blood
32	chr1:158326800-158329400	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
33	chr1:158327000-158327400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr1:158327000-158327600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr1:158327200-158327600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr1:158327200-158327800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr1:158327600-158327800	Active TSS	Dnd41	blood
38	chr1:158327800-158328400	Weak transcription	Dnd41	blood
39	chr1:158328400-158329000	Flanking Active TSS	Thymus	Thymus
40	chr1:158328400-158329600	Enhancers	Dnd41	blood
41	chr1:158329000-158329200	Active TSS	Thymus	Thymus
42	chr1:158329200-158329400	Flanking Active TSS	Thymus	Thymus
43	chr1:158329400-158329600	Active TSS	Thymus	Thymus
44	chr1:158329400-158330600	Genic enhancers	Fetal Thymus	thymus
45	chr1:158329600-158329800	Flanking Active TSS	Thymus	Thymus
46	chr1:158329600-158330200	Weak transcription	Dnd41	blood
47	chr1:158329800-158330600	Enhancers	Thymus	Thymus
48	chr1:158330200-158330600	Enhancers	Dnd41	blood
49	chr1:158330600-158331800	Weak transcription	Fetal Thymus	thymus
50	chr1:158330600-158331800	Weak transcription	Dnd41	blood

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