Variant report

Variant	nsv872860
Chromosome Location	chr1:194482304-194839289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1287)
CpG islands
(count:122)
Chromatin interactive
region (count:157)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:194831433-194831595	K562	blood:	n/a	n/a
2	ARID3A	chr1:194701547-194701671	K562	blood:	n/a	n/a
3	ARID3A	chr1:194819794-194819886	K562	blood:	n/a	n/a
4	ARID3A	chr1:194829614-194830491	K562	blood:	n/a	n/a
5	ARID3A	chr1:194828790-194829121	K562	blood:	n/a	n/a
6	ARID3A	chr1:194668067-194668506	K562	blood:	n/a	n/a
7	ARID3A	chr1:194823663-194823984	K562	blood:	n/a	n/a
8	ARID3A	chr1:194839283-194839285	K562	blood:	n/a	n/a
9	ARID3A	chr1:194667692-194667731	K562	blood:	n/a	n/a
10	ARID3A	chr1:194504737-194505069	K562	blood:	n/a	n/a
11	ATF1	chr1:194662702-194662856	K562	blood:	n/a	n/a
12	ATF1	chr1:194668119-194668497	K562	blood:	n/a	n/a
13	ATF1	chr1:194801183-194801389	K562	blood:	n/a	n/a
14	ATF1	chr1:194717188-194717242	K562	blood:	n/a	n/a
15	ATF1	chr1:194626403-194626731	K562	blood:	n/a	n/a
16	ATF1	chr1:194627281-194627586	K562	blood:	n/a	n/a
17	ATF1	chr1:194539567-194539748	K562	blood:	n/a	n/a
18	ATF1	chr1:194799503-194799511	K562	blood:	n/a	n/a
19	ATF2	chr1:194765001-194765435	GM12878	blood:	n/a	n/a
20	ATF2	chr1:194799428-194799830	GM12878	blood:	n/a	n/a
21	ATF2	chr1:194799350-194799932	GM12878	blood:	n/a	n/a
22	ATF3	chr1:194627281-194627622	K562	blood:	n/a	n/a
23	BACH1	chr1:194627157-194627629	K562	blood:	n/a	chr1:194627433-194627447
24	BACH1	chr1:194828928-194829127	K562	blood:	n/a	n/a
25	BATF	chr1:194765084-194765395	GM12878	blood:	n/a	chr1:194765234-194765245 chr1:194765266-194765277
26	BATF	chr1:194627337-194627489	GM12878	blood:	n/a	chr1:194627432-194627443 chr1:194627433-194627443
27	BCLAF1	chr1:194828925-194830232	K562	blood:	n/a	n/a
28	BHLHE40	chr1:194668203-194668522	K562	blood:	n/a	n/a
29	BHLHE40	chr1:194765128-194765404	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:194680352-194680402	K562	blood:	n/a	n/a
31	BHLHE40	chr1:194504591-194504863	K562	blood:	n/a	n/a
32	BHLHE40	chr1:194827856-194828137	K562	blood:	n/a	n/a
33	BHLHE40	chr1:194799496-194799924	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:194626323-194626770	K562	blood:	n/a	n/a
35	BRCA1	chr1:194710949-194711136	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr1:194626266-194626795	K562	blood:	n/a	n/a
37	CBX3	chr1:194831104-194831698	K562	blood:	n/a	n/a
38	CBX3	chr1:194827886-194829258	K562	blood:	n/a	n/a
39	CBX3	chr1:194626945-194627593	K562	blood:	n/a	n/a
40	CBX3	chr1:194627212-194627704	HCT-116	colon:	n/a	chr1:194627648-194627659
41	CBX3	chr1:194831199-194831717	K562	blood:	n/a	n/a
42	CBX3	chr1:194667984-194668547	K562	blood:	n/a	n/a
43	CCNT2	chr1:194827979-194828453	K562	blood:	n/a	n/a
44	CCNT2	chr1:194517300-194517500	K562	blood:	n/a	n/a
45	CCNT2	chr1:194664494-194664648	K562	blood:	n/a	n/a
46	CEBPB	chr1:194787841-194788146	H1-hESC	embryonic stem cell:	n/a	chr1:194788012-194788023 chr1:194788011-194788024
47	CEBPB	chr1:194574883-194575091	HepG2	liver:	n/a	chr1:194574939-194574950
48	CEBPB	chr1:194676232-194676520	K562	blood:	n/a	n/a
49	CEBPB	chr1:194787912-194788181	Hela-S3	cervix:	n/a	chr1:194788012-194788023 chr1:194788011-194788024
50	CEBPB	chr1:194757998-194758040	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:194828299-194828349	SAEC	small airway:	n/a
2	chr1:194828299-194828349	HRCEpiC	kidney:	n/a
3	chr1:194828299-194828349	HMEC	breast:	n/a
4	chr1:194828448-194828498	CMK	blood:	n/a
5	chr1:194828448-194828498	HMEC	breast:	n/a
6	chr1:194828448-194828498	HCM	heart:	n/a
7	chr1:194828448-194828498	NH-A	brain:	n/a
8	chr1:194828448-194828498	SK-N-SH	brain:	n/a
9	chr1:194828448-194828498	PANC-1	pancreas:	n/a
10	chr1:194828448-194828498	HNPCEpiC	eye:	n/a
11	chr1:194828448-194828498	GM12878	blood:	n/a
12	chr1:194828448-194828498	HAEpiC	amniotic membrane:	n/a
13	chr1:194828448-194828498	PrEC	prostate:	n/a
14	chr1:194828448-194828498	U87	brain:	n/a
15	chr1:194828299-194828349	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:194828299-194828349	HCT-116	colon:	n/a
17	chr1:194828299-194828349	HNPCEpiC	eye:	n/a
18	chr1:194828299-194828349	NH-A	brain:	n/a
19	chr1:194828448-194828498	HIPEpiC	eye:	n/a
20	chr1:194828299-194828349	Jurkat	blood:	n/a
21	chr1:194828448-194828498	HCPEpiC	choroid plexus:	n/a
22	chr1:194828299-194828349	SK-N-SH_RA	brain:	n/a
23	chr1:194828448-194828498	A549	lung:	n/a
24	chr1:194828299-194828349	HUVEC	blood vessel:	n/a
25	chr1:194828448-194828498	T-47D	breast:	n/a
26	chr1:194828448-194828498	NT2-D1	testis:	n/a
27	chr1:194828299-194828349	GM12891	blood:	n/a
28	chr1:194828448-194828498	K562	blood:	n/a
29	chr1:194828448-194828498	GM06990	blood:	n/a
30	chr1:194828299-194828349	AG09309	skin:	n/a
31	chr1:194828299-194828349	K562	blood:	n/a
32	chr1:194828448-194828498	AG04449	skin:	fetal
33	chr1:194828299-194828349	HCPEpiC	choroid plexus:	n/a
34	chr1:194828448-194828498	GM12891	blood:	n/a
35	chr1:194828448-194828498	Jurkat	blood:	n/a
36	chr1:194828448-194828498	NB4	blood:	n/a
37	chr1:194828299-194828349	HIPEpiC	eye:	n/a
38	chr1:194828299-194828349	Hepatocyte	liver:	n/a
39	chr1:194828448-194828498	BJ	skin:	n/a
40	chr1:194828299-194828349	NB4	blood:	n/a
41	chr1:194828299-194828349	HCF	heart:	n/a
42	chr1:194828299-194828349	AG04449	skin:	fetal
43	chr1:194828299-194828349	NT2-D1	testis:	n/a
44	chr1:194828448-194828498	AG09309	skin:	n/a
45	chr1:194828448-194828498	HRCEpiC	kidney:	n/a
46	chr1:194828299-194828349	T-47D	breast:	n/a
47	chr1:194828299-194828349	GM12878	blood:	n/a
48	chr1:194828299-194828349	CMK	blood:	n/a
49	chr1:194828448-194828498	MCF-7	breast:	n/a
50	chr1:194828448-194828498	AG10803	skin:	n/a

(count:157 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:194808956..194810740-chr1:194810823..194813359,2	K562	blood:
2	chr1:194627100..194628913-chr1:194635785..194637890,2	K562	blood:
3	chr1:194624614..194627443-chr1:194667316..194668924,2	K562	blood:
4	chr1:194666221..194668363-chr1:194676352..194679287,2	K562	blood:
5	chr1:194755852..194758022-chr1:194772512..194774166,2	K562	blood:
6	chr1:194674960..194679319-chr1:194679735..194682692,3	K562	blood:
7	chr1:194583954..194584474-chr11:21332888..21333408,2	MCF-7	breast:
8	chr1:194813574..194815333-chr1:194827926..194830696,3	K562	blood:
9	chr1:194603761..194606610-chr1:194613732..194616583,2	K562	blood:
10	chr1:194812845..194814562-chr1:194816106..194820089,3	K562	blood:
11	chr1:194722558..194724150-chr1:194725621..194727394,2	K562	blood:
12	chr1:194519474..194521221-chr1:194527873..194530649,2	K562	blood:
13	chr1:192862078..192864210-chr1:194807394..194809070,2	K562	blood:
14	chr1:194833686..194836577-chr1:194840293..194843252,2	K562	blood:
15	chr1:194681302..194685188-chr1:194688470..194690417,3	K562	blood:
16	chr1:194490383..194492848-chr1:194494979..194497910,2	K562	blood:
17	chr1:194647996..194650865-chr1:194651432..194653062,2	K562	blood:
18	chr1:194756457..194758169-chr1:194762213..194765024,2	K562	blood:
19	chr1:194624819..194626729-chr1:194711630..194714055,2	K562	blood:
20	chr1:194624819..194626729-chr1:194711630..194714055,2	K562	blood:
21	chr1:194827832..194830563-chr1:195590853..195593142,2	K562	blood:
22	chr1:194614011..194616413-chr1:194837683..194840680,2	K562	blood:
23	chr1:194761910..194763801-chr1:194771015..194773565,2	K562	blood:
24	chr1:194812847..194815308-chr1:194828726..194830936,3	K562	blood:
25	chr1:194761910..194763801-chr1:194771015..194773565,2	K562	blood:
26	chr1:194810751..194812791-chr1:194825406..194827084,2	K562	blood:
27	chr1:194760364..194761866-chr13:92000592..92002297,2	K562	blood:
28	chr1:194583954..194584474-chr4:116457976..116458496,2	MCF-7	breast:
29	chr1:194557101..194559742-chr1:194559800..194562767,2	K562	blood:
30	chr1:194803086..194804803-chr1:194807093..194810112,3	K562	blood:
31	chr1:194614073..194616914-chr1:194621058..194622953,2	K562	blood:
32	chr1:194758845..194760365-chr13:92006262..92008831,2	K562	blood:
33	chr1:194665790..194668787-chr1:194669663..194672481,2	K562	blood:
34	chr1:193074740..193076567-chr1:194827728..194830182,2	K562	blood:
35	chr1:194796974..194798913-chr1:194802192..194803906,2	K562	blood:
36	chr1:194627447..194629512-chr1:194630177..194631698,2	K562	blood:
37	chr1:194819540..194821176-chr1:194824149..194827039,2	K562	blood:
38	chr1:194599074..194600731-chr1:194604037..194606753,2	K562	blood:
39	chr1:194732100..194734092-chr1:194744925..194747815,2	K562	blood:
40	chr1:194720032..194722356-chr1:194806450..194808875,2	K562	blood:
41	chr1:194606466..194608189-chr1:194645387..194647364,2	K562	blood:
42	chr1:194786889..194788566-chr1:194794370..194797168,2	MCF-7	breast:
43	chr1:194645953..194649314-chr1:194649785..194652576,3	K562	blood:
44	chr1:194617591..194619813-chr1:194622946..194624693,2	K562	blood:
45	chr1:194553579..194555823-chr1:194557889..194560513,2	K562	blood:
46	chr1:194625999..194627526-chr1:194632822..194634735,2	K562	blood:
47	chr1:194738666..194741262-chr1:194743918..194745585,2	K562	blood:
48	chr1:194565462..194567193-chr1:194826327..194828767,2	K562	blood:
49	chr1:194810607..194812791-chr1:194825406..194826910,2	K562	blood:
50	chr1:194758841..194760344-chr13:92007287..92009017,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNT2-5	chr1:194750316-194750373	NONHSAT008587
2	lnc-KCNT2-5	chr1:194748907-194749629	NONHSAT008587
3	lnc-CDC73-13	chr1:194687925-194688366	NONHSAT008586

No data

Variant related genes	Relation type
ENSG00000228167	TF binding region
ENSG00000228167	CpG island
ENSG00000023572	chromatin interactions

Extended variants
information (count: 5626 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5626 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2494129	chr1:194482304-194482305	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539683364	chr1:194482332-194482333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557925882	chr1:194482333-194482334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs386638138	chr1:194482350-194482351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80097190	chr1:194482352-194482353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184503998	chr1:194482362-194482363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76678038	chr1:194482366-194482367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186935112	chr1:194482370-194482371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563333485	chr1:194482411-194482412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191836424	chr1:194482431-194482432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184054310	chr1:194482432-194482433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142041525	chr1:194482434-194482435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113087466	chr1:194482435-194482436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35719019	chr1:194482458-194482459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs199771275	chr1:194482523-194482524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112240111	chr1:194482528-194482529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6672773	chr1:194482529-194482530	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs114742735	chr1:194482545-194482546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550940469	chr1:194482572-194482573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75392950	chr1:194482575-194482576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180928962	chr1:194482590-194482591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79120811	chr1:194482600-194482601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139530468	chr1:194482678-194482679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2494128	chr1:194482687-194482688	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185511570	chr1:194482713-194482714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527482721	chr1:194482720-194482721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548873575	chr1:194482722-194482723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574384714	chr1:194482735-194482736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144223604	chr1:194482741-194482742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567575322	chr1:194482768-194482769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570370780	chr1:194482796-194482797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113899581	chr1:194482838-194482839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149105045	chr1:194482848-194482849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545878857	chr1:194482879-194482880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190811674	chr1:194482880-194482881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181522959	chr1:194482881-194482882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186225555	chr1:194482911-194482912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561871978	chr1:194482917-194482918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190696897	chr1:194482924-194482925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146540408	chr1:194482968-194482969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551031682	chr1:194483074-194483075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111683311	chr1:194483076-194483077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17641332	chr1:194483139-194483140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs551436336	chr1:194483153-194483154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13375448	chr1:194483171-194483172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534092551	chr1:194483175-194483176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112280857	chr1:194483219-194483220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190626939	chr1:194483269-194483270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538514540	chr1:194483349-194483350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539985588	chr1:194483387-194483388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194480200-194484200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:194482200-194482800	Enhancers	Rectal Smooth Muscle	rectum
3	chr1:194484200-194484400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:194485000-194485600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:194486400-194487400	Enhancers	Primary B cells from cord blood	blood
6	chr1:194486600-194487200	Enhancers	Primary B cells from peripheral blood	blood
7	chr1:194487000-194487400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr1:194487400-194488400	Weak transcription	Primary B cells from cord blood	blood
9	chr1:194488400-194488600	Enhancers	Primary B cells from cord blood	blood
10	chr1:194490400-194490600	Enhancers	Primary B cells from cord blood	blood
11	chr1:194502400-194503400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:194503000-194503400	Enhancers	A549	lung
13	chr1:194503000-194504800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:194503000-194505000	Enhancers	HMEC	breast
15	chr1:194503200-194504600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:194503200-194504800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:194503200-194504800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:194503200-194505200	Enhancers	NHEK	skin
19	chr1:194503400-194503800	Enhancers	Placenta	Placenta
20	chr1:194503600-194504600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:194503600-194504600	Enhancers	Placenta Amnion	Placenta Amnion
22	chr1:194503600-194504800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:194503800-194504000	Enhancers	Adipose Nuclei	Adipose
24	chr1:194503800-194504200	Flanking Active TSS	Placenta	Placenta
25	chr1:194503800-194504800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:194504000-194504800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:194504000-194504800	Enhancers	Primary hematopoietic stem cells	blood
28	chr1:194504000-194505000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr1:194504200-194504400	Active TSS	Placenta	Placenta
30	chr1:194504200-194504800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:194504200-194504800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:194504200-194505000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:194504400-194504600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr1:194504400-194504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr1:194504400-194504600	Flanking Active TSS	Placenta	Placenta
36	chr1:194504400-194504800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:194504400-194504800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr1:194504400-194504800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:194504400-194505000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr1:194504600-194504800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr1:194504600-194504800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr1:194504600-194505000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr1:194504600-194508600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:194504800-194506400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:194505000-194507400	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr1:194506200-194506600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr1:194506400-194507800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr1:194506600-194507600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr1:194506600-194507800	Enhancers	H1 Cell Line	embryonic stem cell
50	chr1:194506600-194507800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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