Variant report

Variant	nsv872862
Chromosome Location	chr1:194506982-194869500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1407)
CpG islands
(count:123)
Chromatin interactive
region (count:162)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:194819794-194819886	K562	blood:	n/a	n/a
2	ARID3A	chr1:194839283-194839285	K562	blood:	n/a	n/a
3	ARID3A	chr1:194668067-194668506	K562	blood:	n/a	n/a
4	ARID3A	chr1:194667692-194667731	K562	blood:	n/a	n/a
5	ARID3A	chr1:194828790-194829121	K562	blood:	n/a	n/a
6	ARID3A	chr1:194829614-194830491	K562	blood:	n/a	n/a
7	ARID3A	chr1:194701547-194701671	K562	blood:	n/a	n/a
8	ARID3A	chr1:194823663-194823984	K562	blood:	n/a	n/a
9	ARID3A	chr1:194842516-194842831	K562	blood:	n/a	n/a
10	ARID3A	chr1:194831433-194831595	K562	blood:	n/a	n/a
11	ATF1	chr1:194539567-194539748	K562	blood:	n/a	n/a
12	ATF1	chr1:194842202-194842859	K562	blood:	n/a	n/a
13	ATF1	chr1:194662702-194662856	K562	blood:	n/a	n/a
14	ATF1	chr1:194841972-194841974	K562	blood:	n/a	n/a
15	ATF1	chr1:194854272-194854396	K562	blood:	n/a	n/a
16	ATF1	chr1:194717188-194717242	K562	blood:	n/a	n/a
17	ATF1	chr1:194627281-194627586	K562	blood:	n/a	n/a
18	ATF1	chr1:194668119-194668497	K562	blood:	n/a	n/a
19	ATF1	chr1:194801183-194801389	K562	blood:	n/a	n/a
20	ATF1	chr1:194626403-194626731	K562	blood:	n/a	n/a
21	ATF1	chr1:194799503-194799511	K562	blood:	n/a	n/a
22	ATF2	chr1:194765001-194765435	GM12878	blood:	n/a	n/a
23	ATF2	chr1:194799428-194799830	GM12878	blood:	n/a	n/a
24	ATF2	chr1:194799350-194799932	GM12878	blood:	n/a	n/a
25	ATF3	chr1:194627281-194627622	K562	blood:	n/a	n/a
26	ATF3	chr1:194842509-194842860	HCT-116	colon:	n/a	n/a
27	ATF3	chr1:194842420-194842851	K562	blood:	n/a	n/a
28	ATF3	chr1:194842480-194842881	HCT-116	colon:	n/a	n/a
29	BACH1	chr1:194828928-194829127	K562	blood:	n/a	n/a
30	BACH1	chr1:194627157-194627629	K562	blood:	n/a	chr1:194627433-194627447
31	BATF	chr1:194765084-194765395	GM12878	blood:	n/a	chr1:194765234-194765245 chr1:194765266-194765277
32	BATF	chr1:194627337-194627489	GM12878	blood:	n/a	chr1:194627432-194627443 chr1:194627433-194627443
33	BCLAF1	chr1:194828925-194830232	K562	blood:	n/a	n/a
34	BHLHE40	chr1:194799496-194799924	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:194668203-194668522	K562	blood:	n/a	n/a
36	BHLHE40	chr1:194626323-194626770	K562	blood:	n/a	n/a
37	BHLHE40	chr1:194680352-194680402	K562	blood:	n/a	n/a
38	BHLHE40	chr1:194765128-194765404	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:194827856-194828137	K562	blood:	n/a	n/a
40	BRCA1	chr1:194710949-194711136	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr1:194842530-194842919	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr1:194831199-194831717	K562	blood:	n/a	n/a
43	CBX3	chr1:194627212-194627704	HCT-116	colon:	n/a	chr1:194627648-194627659
44	CBX3	chr1:194626945-194627593	K562	blood:	n/a	n/a
45	CBX3	chr1:194626266-194626795	K562	blood:	n/a	n/a
46	CBX3	chr1:194831104-194831698	K562	blood:	n/a	n/a
47	CBX3	chr1:194667984-194668547	K562	blood:	n/a	n/a
48	CBX3	chr1:194827886-194829258	K562	blood:	n/a	n/a
49	CBX3	chr1:194842486-194842764	K562	blood:	n/a	n/a
50	CCNT2	chr1:194664494-194664648	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:194828299-194828349	AoSMC	blood vessel:	n/a
2	chr1:194828299-194828349	AoSMC	blood vessel:	n/a
3	chr1:194828448-194828498	Caco-2	colon:	n/a
4	chr1:194828448-194828498	HUVEC	blood vessel:	n/a
5	chr1:194828299-194828349	LNCaP	prostate:	n/a
6	chr1:194828299-194828349	HRPEpiC	eye:	n/a
7	chr1:194828448-194828498	Hepatocyte	liver:	n/a
8	chr1:194828448-194828498	AG10803	skin:	n/a
9	chr1:194828448-194828498	SK-N-MC	brain:	n/a
10	chr1:194828299-194828349	HUVEC	blood vessel:	n/a
11	chr1:194828448-194828498	AG09319	gingival:	n/a
12	chr1:194828448-194828498	A549	lung:	n/a
13	chr1:194828448-194828498	GM12891	blood:	n/a
14	chr1:194828448-194828498	Hela-S3	cervix:	n/a
15	chr1:194828299-194828349	HCM	heart:	n/a
16	chr1:194828448-194828498	HCT-116	colon:	n/a
17	chr1:194828448-194828498	NHBE	bronchial:	n/a
18	chr1:194828299-194828349	Hela-S3	cervix:	n/a
19	chr1:194828299-194828349	Jurkat	blood:	n/a
20	chr1:194828299-194828349	K562	blood:	n/a
21	chr1:194828299-194828349	HNPCEpiC	eye:	n/a
22	chr1:194828299-194828349	SKMC	muscle:	n/a
23	chr1:194828299-194828349	T-47D	breast:	n/a
24	chr1:194828448-194828498	NT2-D1	testis:	n/a
25	chr1:194828448-194828498	GM12878	blood:	n/a
26	chr1:194828299-194828349	HL-60	blood:	n/a
27	chr1:194828299-194828349	HRE	kidney:	n/a
28	chr1:194828299-194828349	NB4	blood:	n/a
29	chr1:194828299-194828349	GM12891	blood:	n/a
30	chr1:194828448-194828498	T-47D	breast:	n/a
31	chr1:194828448-194828498	PFSK-1	brain:	n/a
32	chr1:194828299-194828349	A549	lung:	n/a
33	chr1:194828448-194828498	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:194828299-194828349	H1-hESC	embryonic stem cell:	embryo
35	chr1:194828448-194828498	SK-N-SH	brain:	n/a
36	chr1:194828299-194828349	GM12878	blood:	n/a
37	chr1:194828448-194828498	AG09309	skin:	n/a
38	chr1:194828448-194828498	MCF-7	breast:	n/a
39	chr1:194828448-194828498	HIPEpiC	eye:	n/a
40	chr1:194828299-194828349	NHDF-neo	bronchial:	n/a
41	chr1:194828448-194828498	AG04449	skin:	fetal
42	chr1:194828299-194828349	HCPEpiC	choroid plexus:	n/a
43	chr1:194828299-194828349	NT2-D1	testis:	n/a
44	chr1:194828299-194828349	AG04449	skin:	fetal
45	chr1:194828448-194828498	BE2_C	brain:	n/a
46	chr1:194828448-194828498	IMR90	lung:	fetal
47	chr1:194828448-194828498	GM19239	blood:	n/a
48	chr1:194828448-194828498	HAEpiC	amniotic membrane:	n/a
49	chr1:194828299-194828349	NHBE	bronchial:	n/a
50	chr1:194828299-194828349	BE2_C	brain:	n/a

(count:162 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:194804501..194806498-chr1:194816896..194818919,2	K562	blood:
2	chr1:194679059..194680742-chr1:194682290..194685138,2	K562	blood:
3	chr1:194681302..194685188-chr1:194688470..194690417,3	K562	blood:
4	chr1:194765896..194768506-chr1:194770244..194772765,3	K562	blood:
5	chr1:194630620..194633320-chr1:194634573..194637306,2	K562	blood:
6	chr1:194715893..194719551-chr1:194826480..194829868,3	K562	blood:
7	chr1:194839665..194841497-chr1:194856335..194858376,2	K562	blood:
8	chr1:194833686..194836577-chr1:194840293..194843252,2	K562	blood:
9	chr1:194830894..194836206-chr1:194840671..194844167,5	K562	blood:
10	chr1:194645953..194649314-chr1:194649785..194652576,3	K562	blood:
11	chr1:194750527..194754803-chr1:194755317..194759083,5	K562	blood:
12	chr1:194736657..194739277-chr1:194743434..194745468,2	K562	blood:
13	chr1:194811883..194813573-chr1:194831877..194834030,2	K562	blood:
14	chr1:194729999..194731616-chr1:194739799..194741340,2	K562	blood:
15	chr1:194666221..194668363-chr1:194676352..194679287,2	K562	blood:
16	chr1:194740229..194742934-chr1:194768540..194770092,2	K562	blood:
17	chr1:194812845..194814562-chr1:194816106..194820089,3	K562	blood:
18	chr1:194583954..194584474-chr11:21332888..21333408,2	MCF-7	breast:
19	chr1:194614073..194616914-chr1:194621058..194622953,2	K562	blood:
20	chr1:194603761..194606610-chr1:194613732..194616583,2	K562	blood:
21	chr1:194612527..194614953-chr1:194616786..194619309,3	K562	blood:
22	chr1:194732100..194734092-chr1:194744925..194747815,2	K562	blood:
23	chr1:194617867..194623924-chr1:194625130..194627689,6	K562	blood:
24	chr1:194532647..194534539-chr1:194535882..194538033,2	K562	blood:
25	chr1:194804501..194806498-chr1:194816896..194818919,2	K562	blood:
26	chr1:194626043..194628671-chr1:194827977..194829972,2	K562	blood:
27	chr1:194532647..194534539-chr1:194535882..194538033,2	K562	blood:
28	chr1:194803086..194804803-chr1:194807093..194810112,3	K562	blood:
29	chr1:194674960..194679319-chr1:194679735..194682692,3	K562	blood:
30	chr1:194742165..194743890-chr1:194745588..194747378,2	K562	blood:
31	chr1:194786889..194788566-chr1:194794370..194797168,2	MCF-7	breast:
32	chr1:194761910..194763801-chr1:194771015..194773565,2	K562	blood:
33	chr1:194557101..194559742-chr1:194559800..194562767,2	K562	blood:
34	chr1:194796974..194798913-chr1:194802192..194803906,2	K562	blood:
35	chr1:194583954..194584474-chr4:116457976..116458496,2	MCF-7	breast:
36	chr1:194519474..194521221-chr1:194527873..194530649,2	K562	blood:
37	chr1:194565462..194567193-chr1:194826327..194828767,2	K562	blood:
38	chr1:194720032..194722356-chr1:194806450..194808875,2	K562	blood:
39	chr1:194812847..194815308-chr1:194828726..194830936,3	K562	blood:
40	chr1:194819540..194821176-chr1:194824149..194827039,2	K562	blood:
41	chr1:194625999..194627526-chr1:194632822..194634735,2	K562	blood:
42	chr1:194647996..194650865-chr1:194651432..194653062,2	K562	blood:
43	chr1:194819060..194821727-chr1:194842540..194844189,2	K562	blood:
44	chr1:194553579..194555823-chr1:194557889..194560513,2	K562	blood:
45	chr1:194603761..194606610-chr1:194613732..194616583,2	K562	blood:
46	chr1:194819540..194821176-chr1:194824149..194827039,2	K562	blood:
47	chr1:194813574..194815333-chr1:194827926..194830696,3	K562	blood:
48	chr1:194765896..194768506-chr1:194770244..194772765,3	K562	blood:
49	chr1:194617591..194619813-chr1:194622946..194624693,2	K562	blood:
50	chr1:194624819..194626729-chr1:194711630..194714055,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 5619 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5619 , 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	rs2494164	chr1:194506982-194506983	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536287660	chr1:194507013-194507014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547688207	chr1:194507024-194507025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562255521	chr1:194507053-194507054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547839000	chr1:194507118-194507119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569773904	chr1:194507136-194507137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537116068	chr1:194507158-194507159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532834679	chr1:194507162-194507163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577145216	chr1:194507207-194507208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139436419	chr1:194507263-194507264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553278035	chr1:194507268-194507269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574635080	chr1:194507280-194507281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542215542	chr1:194507283-194507284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563295357	chr1:194507291-194507292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115942478	chr1:194507292-194507293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545856572	chr1:194507300-194507301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564223487	chr1:194507355-194507356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528709919	chr1:194507359-194507360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546871448	chr1:194507424-194507425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562416006	chr1:194507465-194507466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77886313	chr1:194507483-194507484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190997791	chr1:194507503-194507504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548192298	chr1:194507509-194507510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569636656	chr1:194507545-194507546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181486376	chr1:194507563-194507564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186602832	chr1:194507572-194507573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191971379	chr1:194507580-194507581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569304149	chr1:194507588-194507589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534857684	chr1:194507595-194507596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139200109	chr1:194507604-194507605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552851764	chr1:194507651-194507652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574680051	chr1:194507674-194507675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535355927	chr1:194507689-194507690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556949937	chr1:194507697-194507698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527622915	chr1:194507710-194507711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575267453	chr1:194507803-194507804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545768515	chr1:194507806-194507807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557873753	chr1:194507844-194507845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549012505	chr1:194507891-194507892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573219095	chr1:194507918-194507919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78087480	chr1:194507931-194507932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535867096	chr1:194507967-194507968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562116483	chr1:194507982-194507983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149858440	chr1:194508014-194508015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544955970	chr1:194508040-194508041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144823042	chr1:194508062-194508063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148582359	chr1:194508066-194508067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552191202	chr1:194508100-194508101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570535510	chr1:194508203-194508204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10754109	chr1:194508235-194508236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194504600-194508600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:194505000-194507400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr1:194506400-194507800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:194506600-194507600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr1:194506600-194507800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr1:194506600-194507800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr1:194506600-194507800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr1:194507000-194507400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr1:194507400-194507800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr1:194517200-194518400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:194533200-194533600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr1:194544800-194546200	Enhancers	Dnd41	blood
13	chr1:194552800-194553400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr1:194553400-194553600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
15	chr1:194567400-194567600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:194569400-194570000	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr1:194575200-194576400	Enhancers	Dnd41	blood
18	chr1:194579600-194580000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:194585000-194585200	Enhancers	Dnd41	blood
20	chr1:194585200-194585600	Flanking Active TSS	Dnd41	blood
21	chr1:194585600-194586400	Active TSS	Dnd41	blood
22	chr1:194594200-194594400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:194626200-194626400	Active TSS	K562	blood
24	chr1:194626400-194626800	Flanking Active TSS	K562	blood
25	chr1:194626600-194627200	Active TSS	Placenta	Placenta
26	chr1:194626600-194627400	Enhancers	HepG2	liver
27	chr1:194626800-194627800	Active TSS	K562	blood
28	chr1:194627000-194627600	Enhancers	HMEC	breast
29	chr1:194627800-194628200	Enhancers	K562	blood
30	chr1:194637200-194644800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr1:194643000-194643400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:194644800-194645000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:194648000-194649200	Enhancers	Fetal Lung	lung
34	chr1:194648800-194649200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:194667800-194668200	Enhancers	Ovary	ovary
36	chr1:194668000-194668800	Active TSS	K562	blood
37	chr1:194668200-194668600	Active TSS	Ovary	ovary
38	chr1:194668200-194668800	Enhancers	Fetal Heart	heart
39	chr1:194668800-194669600	Weak transcription	K562	blood
40	chr1:194669400-194670000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:194669600-194670000	Enhancers	K562	blood
42	chr1:194670000-194671000	Weak transcription	K562	blood
43	chr1:194670000-194674400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:194671000-194671200	Enhancers	K562	blood
45	chr1:194674000-194675000	Enhancers	Fetal Lung	lung
46	chr1:194674200-194674600	Enhancers	Brain Hippocampus Middle	brain
47	chr1:194674200-194674800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:194674200-194674800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:194674200-194675000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr1:194674400-194675000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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