Variant report

Variant	nsv873370
Chromosome Location	chr1:241566725-241608619
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:332)
CpG islands
(count:550)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:241587104-241587399	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr1:241586947-241587161	GM12878	blood:	n/a	n/a
3	BATF	chr1:241576725-241577065	GM12878	blood:	n/a	chr1:241576864-241576875 chr1:241576865-241576875
4	BATF	chr1:241576725-241577027	GM12878	blood:	n/a	chr1:241576864-241576875 chr1:241576865-241576875
5	CEBPB	chr1:241567786-241568103	IMR90	lung:	n/a	chr1:241567937-241567948 chr1:241567939-241567948 chr1:241567938-241567949
6	CEBPB	chr1:241567860-241567950	A549	lung:	n/a	chr1:241567937-241567948 chr1:241567939-241567948 chr1:241567938-241567949
7	CEBPB	chr1:241567764-241568114	HepG2	liver:	n/a	chr1:241567937-241567948 chr1:241567939-241567948 chr1:241567938-241567949
8	CEBPB	chr1:241573151-241573358	IMR90	lung:	n/a	n/a
9	CEBPB	chr1:241579740-241579812	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:241567828-241568028	K562	blood:	n/a	chr1:241567937-241567948 chr1:241567939-241567948 chr1:241567938-241567949
11	CHD2	chr1:241575289-241575610	K562	blood:	n/a	n/a
12	CHD2	chr1:241587112-241587410	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTBP2	chr1:241587051-241588231	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:241587600-241587750	Caco-2	colon:	n/a	n/a
15	CTCF	chr1:241571620-241571770	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr1:241571720-241571870	HFF	foreskin:	n/a	n/a
17	CTCF	chr1:241571660-241571810	HRE	kidney:	n/a	n/a
18	CTCF	chr1:241587700-241587850	AG04450	lung:	n/a	n/a
19	CTCF	chr1:241587123-241587255	GM10266	blood:	n/a	n/a
20	CTCF	chr1:241571580-241571730	Caco-2	colon:	n/a	n/a
21	CTCF	chr1:241587394-241587487	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr1:241586960-241587110	HAc	cerebellar:	n/a	n/a
23	CTCF	chr1:241571580-241571730	HMEC	breast:	n/a	n/a
24	CTCF	chr1:241601117-241601169	LNCaP	prostate:	n/a	n/a
25	CTCF	chr1:241587160-241587310	GM12864	blood:	n/a	n/a
26	CTCF	chr1:241587080-241587230	GM12868	blood:	n/a	n/a
27	CTCF	chr1:241587620-241587770	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr1:241587120-241587270	GM06990	blood:	n/a	n/a
29	CTCF	chr1:241587100-241587250	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr1:241590315-241590336	GM20000	blood:	n/a	n/a
31	CTCF	chr1:241571580-241571730	HRE	kidney:	n/a	n/a
32	CTCF	chr1:241587100-241587250	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr1:241571580-241571730	AG04450	lung:	n/a	n/a
34	CTCF	chr1:241571620-241571770	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr1:241587053-241587215	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr1:241587080-241587230	AG09309	skin:	n/a	n/a
37	CTCF	chr1:241571580-241571730	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr1:241590337-241590351	GM20000	blood:	n/a	n/a
39	CTCF	chr1:241571580-241571730	AG04449	skin:	n/a	n/a
40	CTCF	chr1:241585480-241585630	HMF	breast:	n/a	n/a
41	CTCF	chr1:241587065-241587303	Fibrobl	skin:	n/a	n/a
42	CTCF	chr1:241571600-241571750	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr1:241571640-241571790	RPTEC	kidney:	n/a	n/a
44	CTCF	chr1:241587140-241587290	HRE	kidney:	n/a	n/a
45	CTCF	chr1:241587000-241587150	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr1:241587360-241587510	HFF	foreskin:	n/a	n/a
47	CTCF	chr1:241571660-241571810	AG09309	skin:	n/a	n/a
48	CTCF	chr1:241571480-241571862	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:241587060-241587210	HMF	breast:	n/a	n/a
50	CTCF	chr1:241587100-241587250	SK-N-SH_RA	brain:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:241584653-241584703	AG09309	skin:	n/a
2	chr1:241584653-241584703	AG09309	skin:	n/a
3	chr1:241587234-241587284	H1-hESC	embryonic stem cell:	embryo
4	chr1:241587234-241587284	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:241587602-241587652	MCF10A-Er-Src	breast:	n/a
6	chr1:241587099-241587149	HNPCEpiC	eye:	n/a
7	chr1:241588176-241588226	SK-N-MC	brain:	n/a
8	chr1:241587099-241587149	GM12878	blood:	n/a
9	chr1:241587609-241587659	AG10803	skin:	n/a
10	chr1:241584653-241584703	HCT-116	colon:	n/a
11	chr1:241587602-241587652	SK-N-MC	brain:	n/a
12	chr1:241587602-241587652	ProgFib	skin:	n/a
13	chr1:241587126-241587176	HL-60	blood:	n/a
14	chr1:241587126-241587176	GM12878	blood:	n/a
15	chr1:241587126-241587176	HRCEpiC	kidney:	n/a
16	chr1:241587234-241587284	GM12878	blood:	n/a
17	chr1:241587609-241587659	NHBE	bronchial:	n/a
18	chr1:241587783-241587833	HNPCEpiC	eye:	n/a
19	chr1:241587602-241587652	GM19239	blood:	n/a
20	chr1:241587234-241587284	SK-N-SH_RA	brain:	n/a
21	chr1:241587126-241587176	RPTEC	kidney:	n/a
22	chr1:241587609-241587659	HCF	heart:	n/a
23	chr1:241584653-241584703	GM12878	blood:	n/a
24	chr1:241587126-241587176	PrEC	prostate:	n/a
25	chr1:241587234-241587284	BJ	skin:	n/a
26	chr1:241587602-241587652	Hela-S3	cervix:	n/a
27	chr1:241587234-241587284	HEK293	kidney:	embryo
28	chr1:241587783-241587833	HMEC	breast:	n/a
29	chr1:241588176-241588226	AG09319	gingival:	n/a
30	chr1:241588176-241588226	H1-hESC	embryonic stem cell:	embryo
31	chr1:241587783-241587833	PFSK-1	brain:	n/a
32	chr1:241587602-241587652	Hepatocyte	liver:	n/a
33	chr1:241587493-241587543	HRCEpiC	kidney:	n/a
34	chr1:241584653-241584703	ovcar-3	ovarian:	n/a
35	chr1:241587099-241587149	SAEC	small airway:	n/a
36	chr1:241588176-241588226	Jurkat	blood:	n/a
37	chr1:241587609-241587659	HL-60	blood:	n/a
38	chr1:241587783-241587833	HepG2	liver:	n/a
39	chr1:241587099-241587149	GM12891	blood:	n/a
40	chr1:241587234-241587284	NHDF-neo	bronchial:	n/a
41	chr1:241584653-241584703	PrEC	prostate:	n/a
42	chr1:241587099-241587149	MCF10A-Er-Src	breast:	n/a
43	chr1:241587783-241587833	BJ	skin:	n/a
44	chr1:241587609-241587659	T-47D	breast:	n/a
45	chr1:241587099-241587149	NHBE	bronchial:	n/a
46	chr1:241587493-241587543	T-47D	breast:	n/a
47	chr1:241587602-241587652	HEEpiC	esophagus:	n/a
48	chr1:241587602-241587652	HL-60	blood:	n/a
49	chr1:241587234-241587284	MCF-7	breast:	n/a
50	chr1:241587126-241587176	ProgFib	skin:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:241576862..241577389-chr1:241648832..241649350,2	MCF-7	breast:
2	chr1:241051402..241051959-chr1:241571198..241571784,2	MCF-7	breast:
3	chr1:241130154..241131047-chr1:241571299..241572146,2	MCF-7	breast:
4	chr1:241605819..241607589-chr1:241612987..241614955,2	K562	blood:
5	chr1:241474375..241475396-chr1:241571431..241572468,4	MCF-7	breast:
6	chr1:241562543..241564148-chr1:241572299..241574103,2	K562	blood:
7	chr1:241536411..241539410-chr1:241565265..241567814,2	K562	blood:
8	chr1:241579712..241582046-chr1:241585096..241587822,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KMO-1	chr1:241581510-241582731	NONHSAT010538
2	lnc-KMO-1	chr1:241596469-241597028	NONHSAT010539
3	lnc-KMO-1	chr1:241577057-241577136	NONHSAT010539
4	lnc-KMO-1	chr1:241577057-241577136	NONHSAT010538

No data

Variant related genes	Relation type
ENSG00000225554	TF binding region
ENSG00000225554	CpG island
ENSG00000225554	chromatin interactions

Extended variants
information (count: 1735 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1735 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111605588	chr1:241569846-241569847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574296689	chr1:241569894-241569895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542918647	chr1:241569901-241569902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560074197	chr1:241570004-241570005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527310303	chr1:241570010-241570011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547412610	chr1:241570013-241570014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2341942	chr1:241570018-241570019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs111870246	chr1:241570057-241570058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139509854	chr1:241570060-241570061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549948895	chr1:241570101-241570102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551328563	chr1:241570160-241570161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546457036	chr1:241570247-241570248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561573150	chr1:241570271-241570272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181833996	chr1:241570276-241570277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535754885	chr1:241570326-241570327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184803515	chr1:241570330-241570331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115636285	chr1:241570341-241570342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540804401	chr1:241570369-241570370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568845827	chr1:241570439-241570440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369065327	chr1:241570456-241570457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557692202	chr1:241570483-241570484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190728280	chr1:241570629-241570630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537121869	chr1:241570638-241570639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557547034	chr1:241570670-241570671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574187656	chr1:241570674-241570675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149728111	chr1:241570689-241570690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373515529	chr1:241570721-241570722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72762451	chr1:241570736-241570737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573568655	chr1:241570764-241570765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572911854	chr1:241570878-241570879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564021334	chr1:241570909-241570910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148486860	chr1:241570971-241570972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543114709	chr1:241570998-241570999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377440256	chr1:241571030-241571031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547967434	chr1:241571037-241571038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529124780	chr1:241571040-241571041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548759004	chr1:241571081-241571082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs67270617	chr1:241571106-241571107	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs180738783	chr1:241571112-241571113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551383481	chr1:241571150-241571151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533701193	chr1:241571189-241571190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558350792	chr1:241571215-241571216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537439140	chr1:241571234-241571235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557202759	chr1:241571274-241571275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12034169	chr1:241571318-241571319	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs145277741	chr1:241571335-241571336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553563336	chr1:241571453-241571454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530427598	chr1:241571464-241571465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186124703	chr1:241571465-241571466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573580962	chr1:241571484-241571485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	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
Breast cancer	17603634	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
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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	17989066	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241569800-241570000	Enhancers	NHDF-Ad	bronchial
2	chr1:241569800-241570000	Enhancers	NHLF	lung
3	chr1:241570000-241572800	Weak transcription	NHDF-Ad	bronchial
4	chr1:241570000-241574000	Weak transcription	NHLF	lung
5	chr1:241571000-241571600	Enhancers	Osteobl	bone
6	chr1:241571600-241572200	Active TSS	K562	blood
7	chr1:241571600-241574200	Weak transcription	Osteobl	bone
8	chr1:241572800-241577000	Enhancers	NHDF-Ad	bronchial
9	chr1:241573600-241577000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:241573800-241574200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:241573800-241574200	Enhancers	Gastric	stomach
12	chr1:241573800-241575800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:241574000-241574400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:241574000-241575200	Enhancers	NHLF	lung
15	chr1:241574200-241574400	Enhancers	Osteobl	bone
16	chr1:241574200-241575200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:241574200-241587000	Weak transcription	Gastric	stomach
18	chr1:241574400-241574800	Weak transcription	Osteobl	bone
19	chr1:241574400-241575000	Enhancers	Stomach Mucosa	stomach
20	chr1:241574400-241576000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr1:241574600-241575000	Enhancers	HUVEC	blood vessel
22	chr1:241574800-241575000	Enhancers	Osteobl	bone
23	chr1:241575000-241576600	Weak transcription	Osteobl	bone
24	chr1:241575200-241576200	Weak transcription	NHLF	lung
25	chr1:241575200-241576600	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr1:241575800-241576800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:241576000-241577200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:241576200-241576600	Enhancers	NHLF	lung
29	chr1:241576600-241576800	Weak transcription	NHLF	lung
30	chr1:241576600-241577400	Enhancers	Osteobl	bone
31	chr1:241576600-241577600	Enhancers	Muscle Satellite Cultured Cells	--
32	chr1:241576800-241577000	Enhancers	NHLF	lung
33	chr1:241576800-241577600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:241576800-241577600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:241576800-241577600	Enhancers	HMEC	breast
36	chr1:241576800-241577800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr1:241577000-241577600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:241577000-241577800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:241577000-241578000	Flanking Active TSS	NHDF-Ad	bronchial
40	chr1:241577000-241578000	Flanking Active TSS	NHLF	lung
41	chr1:241577200-241577600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr1:241577200-241577600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr1:241577200-241577800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:241577400-241577800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:241577600-241578000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:241577600-241582800	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr1:241577600-241586600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:241577800-241578000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr1:241577800-241579000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:241577800-241580000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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