Variant report

Variant	nsv1000161
Chromosome Location	chr1:194918245-195340203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1243)
CpG islands
(count:61)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1243 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:195198697-195198705	K562	blood:	n/a	n/a
2	ATF1	chr1:194963175-194963179	K562	blood:	n/a	n/a
3	ATF1	chr1:194921272-194921554	K562	blood:	n/a	n/a
4	ATF1	chr1:194945122-194945347	K562	blood:	n/a	n/a
5	ATF1	chr1:195181877-195181932	K562	blood:	n/a	n/a
6	ATF1	chr1:194933783-194933793	K562	blood:	n/a	n/a
7	ATF1	chr1:194979275-194979408	K562	blood:	n/a	n/a
8	ATF1	chr1:194928895-194928956	K562	blood:	n/a	n/a
9	ATF2	chr1:195164308-195165083	GM12878	blood:	n/a	n/a
10	ATF2	chr1:195164239-195165053	GM12878	blood:	n/a	n/a
11	BACH1	chr1:195250537-195250544	K562	blood:	n/a	n/a
12	BACH1	chr1:195122356-195122540	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:195122285-195122583	K562	blood:	n/a	n/a
14	BATF	chr1:195164439-195165066	GM12878	blood:	n/a	n/a
15	BATF	chr1:195164462-195165019	GM12878	blood:	n/a	n/a
16	BATF	chr1:195301352-195301514	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:195164332-195165095	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:195164392-195165066	GM12878	blood:	n/a	n/a
19	BCL3	chr1:195164564-195164876	GM12878	blood:	n/a	n/a
20	BCL3	chr1:195164566-195164924	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:195164254-195165079	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:195164321-195165003	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:195164335-195165128	GM12878	blood:	n/a	n/a
24	BRCA1	chr1:195274225-195274324	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr1:195066119-195066969	HCT-116	colon:	n/a	n/a
26	CBX3	chr1:195066317-195066989	HCT-116	colon:	n/a	n/a
27	CBX3	chr1:194944969-194945511	HCT-116	colon:	n/a	n/a
28	CBX3	chr1:195314296-195314811	HCT-116	colon:	n/a	n/a
29	CCNT2	chr1:195082155-195082271	K562	blood:	n/a	n/a
30	CEBPB	chr1:194927941-194928159	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:195168244-195168617	IMR90	lung:	n/a	chr1:195168429-195168438 chr1:195168427-195168440 chr1:195168429-195168438 chr1:195168429-195168438
32	CEBPB	chr1:195319726-195320013	HepG2	liver:	n/a	chr1:195319852-195319863
33	CEBPB	chr1:195172090-195172493	HepG2	liver:	n/a	chr1:195172448-195172461
34	CEBPB	chr1:195261829-195262055	A549	lung:	n/a	n/a
35	CEBPB	chr1:194974428-194974799	MCF-7	breast:	n/a	n/a
36	CEBPB	chr1:195271930-195272163	A549	lung:	n/a	n/a
37	CEBPB	chr1:195271913-195272198	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:195220947-195221434	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr1:195172158-195172559	A549	lung:	n/a	chr1:195172448-195172461
40	CEBPB	chr1:194959643-194959906	K562	blood:	n/a	chr1:194959731-194959743
41	CEBPB	chr1:194959301-194959967	A549	lung:	n/a	chr1:194959731-194959743
42	CEBPB	chr1:194960299-194960553	A549	lung:	n/a	n/a
43	CEBPB	chr1:194959278-194959979	IMR90	lung:	n/a	chr1:194959731-194959743
44	CEBPB	chr1:195319784-195319990	A549	lung:	n/a	chr1:195319852-195319863
45	CEBPB	chr1:195321028-195321179	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:195168310-195168613	A549	lung:	n/a	chr1:195168429-195168438 chr1:195168427-195168440 chr1:195168429-195168438 chr1:195168429-195168438
47	CEBPB	chr1:195319715-195320030	IMR90	lung:	n/a	chr1:195319852-195319863
48	CEBPB	chr1:195168277-195168590	K562	blood:	n/a	chr1:195168429-195168438 chr1:195168427-195168440 chr1:195168429-195168438 chr1:195168429-195168438
49	CEBPB	chr1:195167728-195167959	H1-hESC	embryonic stem cell:	n/a	chr1:195167767-195167778
50	CEBPB	chr1:195128405-195128660	IMR90	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:195023534-195023584	HNPCEpiC	eye:	n/a
2	chr1:195023534-195023584	GM19239	blood:	n/a
3	chr1:195023534-195023584	K562	blood:	n/a
4	chr1:195023534-195023584	MCF10A-Er-Src	breast:	n/a
5	chr1:195023534-195023584	HMEC	breast:	n/a
6	chr1:195023534-195023584	HCPEpiC	choroid plexus:	n/a
7	chr1:195023534-195023584	A549	lung:	n/a
8	chr1:195023534-195023584	AG04450	lung:	fetal
9	chr1:195023534-195023584	ProgFib	skin:	n/a
10	chr1:195023534-195023584	ovcar-3	ovarian:	n/a
11	chr1:195023534-195023584	HEEpiC	esophagus:	n/a
12	chr1:195023534-195023584	PFSK-1	brain:	n/a
13	chr1:195023534-195023584	MCF-7	breast:	n/a
14	chr1:195023534-195023584	Hela-S3	cervix:	n/a
15	chr1:195023534-195023584	LNCaP	prostate:	n/a
16	chr1:195023534-195023584	HUVEC	blood vessel:	n/a
17	chr1:195023534-195023584	HCM	heart:	n/a
18	chr1:195023534-195023584	Jurkat	blood:	n/a
19	chr1:195023534-195023584	GM06990	blood:	n/a
20	chr1:195023534-195023584	HRE	kidney:	n/a
21	chr1:195023534-195023584	HAEpiC	amniotic membrane:	n/a
22	chr1:195023534-195023584	AG04449	skin:	fetal
23	chr1:195023534-195023584	U87	brain:	n/a
24	chr1:195023534-195023584	SK-N-MC	brain:	n/a
25	chr1:195023534-195023584	NHDF-neo	bronchial:	n/a
26	chr1:195023534-195023584	BJ	skin:	n/a
27	chr1:195023534-195023584	ECC-1	luminal epithelium:	n/a
28	chr1:195023534-195023584	HIPEpiC	eye:	n/a
29	chr1:195023534-195023584	SK-N-SH	brain:	n/a
30	chr1:195023534-195023584	NH-A	brain:	n/a
31	chr1:195023534-195023584	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:195023534-195023584	AoSMC	blood vessel:	n/a
33	chr1:195023534-195023584	HCT-116	colon:	n/a
34	chr1:195023534-195023584	AG09309	skin:	n/a
35	chr1:195023534-195023584	HCF	heart:	n/a
36	chr1:195023534-195023584	Caco-2	colon:	n/a
37	chr1:195023534-195023584	Hepatocyte	liver:	n/a
38	chr1:195023534-195023584	NT2-D1	testis:	n/a
39	chr1:195023534-195023584	HepG2	liver:	n/a
40	chr1:195023534-195023584	NHBE	bronchial:	n/a
41	chr1:195023534-195023584	HRCEpiC	kidney:	n/a
42	chr1:195023534-195023584	GM12892	blood:	n/a
43	chr1:195023534-195023584	BE2_C	brain:	n/a
44	chr1:195023534-195023584	IMR90	lung:	fetal
45	chr1:195023534-195023584	GM12878	blood:	n/a
46	chr1:195023534-195023584	GM12891	blood:	n/a
47	chr1:195023534-195023584	SK-N-SH_RA	brain:	n/a
48	chr1:195023534-195023584	RPTEC	kidney:	n/a
49	chr1:195023534-195023584	CMK	blood:	n/a
50	chr1:195023534-195023584	PrEC	prostate:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:195270062..195272293-chr1:195296328..195299059,2	MCF-7	breast:
2	chr1:195076488..195078314-chr16:29816661..29818822,2	MCF-7	breast:
3	chr1:195308037..195310638-chr1:195312070..195313866,2	MCF-7	breast:
4	chr1:194976691..194979568-chr1:194983292..194986112,2	K562	blood:
5	chr1:195005563..195007915-chr1:195009562..195011162,2	K562	blood:
6	chr1:195270062..195272293-chr1:195296328..195299059,2	MCF-7	breast:
7	chr1:195236405..195237102-chr2:169335217..169335963,2	MCF-7	breast:
8	chr1:195022148..195022648-chr5:180672971..180673497,2	HCT-116	colon:
9	chr1:194956938..194959266-chr1:194974594..194976244,2	K562	blood:
10	chr1:195130839..195132878-chr1:195138252..195140071,2	K562	blood:
11	chr1:194940992..194943005-chr1:194943083..194945420,2	MCF-7	breast:
12	chr1:194976691..194979568-chr1:194983292..194986112,2	K562	blood:
13	chr1:195130839..195132878-chr1:195138252..195140071,2	K562	blood:
14	chr1:195233955..195235990-chr1:195238834..195240836,2	K562	blood:
15	chr1:194956938..194959266-chr1:194974594..194976244,2	K562	blood:
16	chr1:195314819..195316810-chr1:195319212..195320954,2	MCF-7	breast:
17	chr1:194940992..194943005-chr1:194943083..194945420,2	MCF-7	breast:
18	chr1:194975514..194978503-chr1:194979065..194981637,2	MCF-7	breast:
19	chr1:194927782..194929413-chr1:194932247..194935027,2	MCF-7	breast:
20	chr1:195262020..195263706-chr1:195272247..195274831,2	K562	blood:
21	chr1:194927782..194929413-chr1:194932247..194935027,2	MCF-7	breast:
22	chr1:195314819..195316810-chr1:195319212..195320954,2	MCF-7	breast:
23	chr1:194820017..194822446-chr1:194943208..194945267,2	K562	blood:
24	chr1:195180067..195181644-chr1:195189750..195192618,2	K562	blood:
25	chr1:195180067..195181644-chr1:195189750..195192618,2	K562	blood:
26	chr1:195233955..195235990-chr1:195238834..195240836,2	K562	blood:
27	chr1:195211970..195213512-chr1:195217966..195220235,2	K562	blood:
28	chr1:195308037..195310638-chr1:195312070..195313866,2	MCF-7	breast:
29	chr1:195311544..195312044-chr17:56756797..56757332,2	Hela-S3	cervix:
30	chr1:195211970..195213512-chr1:195217966..195220235,2	K562	blood:
31	chr1:195262020..195263706-chr1:195272247..195274831,2	K562	blood:
32	chr1:194975514..194978503-chr1:194979065..194981637,2	MCF-7	breast:
33	chr1:195005563..195007915-chr1:195009562..195011162,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000265108	TF binding region
ENSG00000265108	CpG island
ENSG00000103495	chromatin interactions
ENSG00000200997	chromatin interactions

Extended variants
information (count: 2423 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2423 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12562570	chr1:194921202-194921203	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532400499	chr1:194921207-194921208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182398391	chr1:194921267-194921268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566915706	chr1:194921272-194921273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527871812	chr1:194921301-194921302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs61817161	chr1:194921318-194921319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549625658	chr1:194921334-194921335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371365741	chr1:194921393-194921394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568153619	chr1:194921397-194921398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535554023	chr1:194921404-194921405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556638900	chr1:194921466-194921467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568858810	chr1:194921467-194921468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573766931	chr1:194921483-194921484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188711702	chr1:194921519-194921520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573086020	chr1:194921522-194921523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192501685	chr1:194921534-194921535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374683313	chr1:194921537-194921538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540037248	chr1:194921585-194921586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555180221	chr1:194921607-194921608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367635944	chr1:194921662-194921663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2221371	chr1:194921683-194921684	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs116440777	chr1:194921684-194921685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374727838	chr1:194921757-194921758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184006272	chr1:194934801-194934802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1328319	chr1:194934811-194934812	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs141567678	chr1:194934864-194934865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567797642	chr1:194934901-194934902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74218376	chr1:194934926-194934927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138411570	chr1:194934954-194934955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115557804	chr1:194934955-194934956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559897242	chr1:194934970-194934971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564404832	chr1:194934992-194934993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146080107	chr1:194935035-194935036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs5779765	chr1:194935050-194935051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527545406	chr1:194935071-194935072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572525672	chr1:194935122-194935123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140033498	chr1:194935161-194935162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561618665	chr1:194935181-194935182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573686497	chr1:194935185-194935186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543756886	chr1:194935205-194935206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs339585	chr1:194935235-194935236	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs533022353	chr1:194935295-194935296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551248329	chr1:194935299-194935300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567614589	chr1:194935312-194935313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560426630	chr1:194935317-194935318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78051859	chr1:194935349-194935350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549203064	chr1:194935389-194935390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149343790	chr1:194935403-194935404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538346481	chr1:194935450-194935451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184630	chr1:194935461-194935462	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	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
Hepatocellular carcinoma	18803288	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Maculopathy	22022419	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Maculopathy	22355348	CNVD
Schizophrenia	21346763	CNVD
early-passage human iPS cells	21368824	CNVD
Recurrent pregnancy loss	19789632	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Maculopathy	21850184	CNVD
Schizophrenia	20967226	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Asthma	20841430	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194921200-194921800	Enhancers	Brain Germinal Matrix	brain
2	chr1:194934800-194936400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:194937400-194937800	Enhancers	Brain Germinal Matrix	brain
4	chr1:194951400-194951600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:194976800-194977800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr1:194976800-194977800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr1:194977800-194980000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:194977800-194980200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:194980000-194980800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:194980200-194980600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr1:194980200-194980800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:194988600-194989000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:194988600-194989000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr1:194988800-194989200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr1:194999600-195000200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:195005000-195005400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:195022600-195023000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
18	chr1:195045000-195045200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:195045200-195045600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:195045600-195046800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:195045600-195046800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:195046800-195047400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:195046800-195047600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:195047400-195050800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:195047600-195050200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:195050200-195051800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:195050800-195051200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:195054200-195054800	Enhancers	Fetal Lung	lung
29	chr1:195063000-195065400	Weak transcription	Right Atrium	heart
30	chr1:195063600-195064000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:195064000-195066200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:195065200-195065600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:195065200-195065600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:195065400-195065600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr1:195065400-195065600	ZNF genes & repeats	Right Atrium	heart
36	chr1:195066200-195067200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:195066200-195067200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:195066200-195067600	Enhancers	HMEC	breast
39	chr1:195066400-195066800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:195066400-195067000	Enhancers	NHEK	skin
41	chr1:195066400-195067200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:195128600-195129200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr1:195128800-195130200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr1:195128800-195130400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr1:195129200-195129600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr1:195129200-195130200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr1:195129600-195130400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:195130000-195130400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:195130000-195130400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr1:195130200-195130600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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