Variant report

Variant	nsv535233
Chromosome Location	chr1:189092551-189214548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:556)
CpG islands
(count:61)
Chromatin interactive
region (count:47)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:189118670-189118888	K562	blood:	n/a	n/a
2	ATF1	chr1:189204451-189204466	K562	blood:	n/a	n/a
3	ATF1	chr1:189202401-189202585	K562	blood:	n/a	n/a
4	ATF1	chr1:189118704-189119125	K562	blood:	n/a	n/a
5	BATF	chr1:189206204-189206354	GM12878	blood:	n/a	chr1:189206300-189206311
6	BCLAF1	chr1:189118637-189119186	K562	blood:	n/a	n/a
7	BHLHE40	chr1:189118889-189119095	K562	blood:	n/a	n/a
8	CBX3	chr1:189118747-189119060	K562	blood:	n/a	n/a
9	CBX3	chr1:189094793-189095258	HCT-116	colon:	n/a	n/a
10	CBX3	chr1:189118641-189119561	K562	blood:	n/a	n/a
11	CEBPB	chr1:189166339-189166622	A549	lung:	n/a	n/a
12	CEBPB	chr1:189181835-189182167	K562	blood:	n/a	n/a
13	CEBPB	chr1:189175252-189175255	K562	blood:	n/a	n/a
14	CEBPB	chr1:189166348-189166590	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:189195940-189196280	HepG2	liver:	n/a	chr1:189196099-189196110
16	CEBPB	chr1:189149291-189149572	A549	lung:	n/a	chr1:189149525-189149536 chr1:189149432-189149443
17	CEBPB	chr1:189195932-189196282	K562	blood:	n/a	chr1:189196099-189196110
18	CEBPB	chr1:189166341-189166619	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:189195947-189196272	A549	lung:	n/a	chr1:189196099-189196110
20	CEBPB	chr1:189184524-189184748	A549	lung:	n/a	n/a
21	CEBPB	chr1:189184575-189184755	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:189118636-189118957	K562	blood:	n/a	n/a
23	CEBPB	chr1:189118695-189119077	K562	blood:	n/a	n/a
24	CEBPB	chr1:189183608-189183801	K562	blood:	n/a	n/a
25	CEBPB	chr1:189149375-189149525	K562	blood:	n/a	chr1:189149432-189149443
26	CEBPB	chr1:189195970-189196243	H1-hESC	embryonic stem cell:	n/a	chr1:189196099-189196110
27	CEBPB	chr1:189195939-189196276	IMR90	lung:	n/a	chr1:189196099-189196110
28	CEBPB	chr1:189149263-189149576	HepG2	liver:	n/a	chr1:189149525-189149536 chr1:189149432-189149443
29	CEBPB	chr1:189149272-189149581	IMR90	lung:	n/a	chr1:189149525-189149536 chr1:189149432-189149443
30	CEBPD	chr1:189181740-189182174	K562	blood:	n/a	n/a
31	CEBPD	chr1:189118669-189119222	K562	blood:	n/a	n/a
32	CHD2	chr1:189118857-189119073	K562	blood:	n/a	n/a
33	CHD2	chr1:189118851-189119132	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr1:189109985-189110031	K562	blood:	n/a	n/a
35	CREB1	chr1:189118777-189119112	A549	lung:	n/a	n/a
36	CTCF	chr1:189119020-189119170	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr1:189118940-189119090	GM12865	blood:	n/a	n/a
38	CTCF	chr1:189190000-189190150	HCT-116	colon:	n/a	n/a
39	CTCF	chr1:189119040-189119190	GM12875	blood:	n/a	n/a
40	CTCF	chr1:189189980-189190130	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr1:189190030-189190145	LNCaP	prostate:	n/a	n/a
42	CTCF	chr1:189190042-189190166	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:189118960-189119110	HepG2	liver:	n/a	n/a
44	CTCF	chr1:189189980-189190130	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr1:189190040-189190190	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr1:189118871-189119124	A549	lung:	n/a	n/a
47	CTCF	chr1:189190000-189190150	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:189119020-189119170	GM12878	blood:	n/a	n/a
49	CTCF	chr1:189190020-189190170	HCT-116	colon:	n/a	n/a
50	CTCF	chr1:189118799-189119173	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:189194949-189194999	Caco-2	colon:	n/a
2	chr1:189194949-189194999	HNPCEpiC	eye:	n/a
3	chr1:189194949-189194999	HCF	heart:	n/a
4	chr1:189194949-189194999	SK-N-MC	brain:	n/a
5	chr1:189194949-189194999	MCF-7	breast:	n/a
6	chr1:189194949-189194999	AG04450	lung:	fetal
7	chr1:189194949-189194999	MCF10A-Er-Src	breast:	n/a
8	chr1:189194949-189194999	GM06990	blood:	n/a
9	chr1:189194949-189194999	HRPEpiC	eye:	n/a
10	chr1:189194949-189194999	GM19239	blood:	n/a
11	chr1:189194949-189194999	GM12892	blood:	n/a
12	chr1:189194949-189194999	HEEpiC	esophagus:	n/a
13	chr1:189194949-189194999	NHBE	bronchial:	n/a
14	chr1:189194949-189194999	U87	brain:	n/a
15	chr1:189194949-189194999	AG09319	gingival:	n/a
16	chr1:189194949-189194999	A549	lung:	n/a
17	chr1:189194949-189194999	HCPEpiC	choroid plexus:	n/a
18	chr1:189194949-189194999	NH-A	brain:	n/a
19	chr1:189194949-189194999	HMEC	breast:	n/a
20	chr1:189194949-189194999	IMR90	lung:	fetal
21	chr1:189194949-189194999	Hepatocyte	liver:	n/a
22	chr1:189194949-189194999	NB4	blood:	n/a
23	chr1:189194949-189194999	GM12891	blood:	n/a
24	chr1:189194949-189194999	HL-60	blood:	n/a
25	chr1:189194949-189194999	HCT-116	colon:	n/a
26	chr1:189194949-189194999	HUVEC	blood vessel:	n/a
27	chr1:189194949-189194999	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:189194949-189194999	BJ	skin:	n/a
29	chr1:189194949-189194999	HepG2	liver:	n/a
30	chr1:189194949-189194999	SKMC	muscle:	n/a
31	chr1:189194949-189194999	RPTEC	kidney:	n/a
32	chr1:189194949-189194999	HRE	kidney:	n/a
33	chr1:189194949-189194999	SK-N-SH	brain:	n/a
34	chr1:189194949-189194999	AG09309	skin:	n/a
35	chr1:189194949-189194999	HEK293	kidney:	embryo
36	chr1:189194949-189194999	PANC-1	pancreas:	n/a
37	chr1:189194949-189194999	ECC-1	luminal epithelium:	n/a
38	chr1:189194949-189194999	PFSK-1	brain:	n/a
39	chr1:189194949-189194999	ovcar-3	ovarian:	n/a
40	chr1:189194949-189194999	NT2-D1	testis:	n/a
41	chr1:189194949-189194999	HAEpiC	amniotic membrane:	n/a
42	chr1:189194949-189194999	AG04449	skin:	fetal
43	chr1:189194949-189194999	K562	blood:	n/a
44	chr1:189194949-189194999	HCM	heart:	n/a
45	chr1:189194949-189194999	AG10803	skin:	n/a
46	chr1:189194949-189194999	GM12878	blood:	n/a
47	chr1:189194949-189194999	T-47D	breast:	n/a
48	chr1:189194949-189194999	H1-hESC	embryonic stem cell:	embryo
49	chr1:189194949-189194999	ProgFib	skin:	n/a
50	chr1:189194949-189194999	Hela-S3	cervix:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:189170367..189172924-chr1:189189578..189192081,2	K562	blood:
2	chr1:189148880..189151522-chr1:189151849..189154466,3	K562	blood:
3	chr1:189116028..189120237-chr1:189160506..189163276,3	K562	blood:
4	chr1:189117456..189122192-chr1:189126377..189132093,10	K562	blood:
5	chr1:188432976..188433772-chr1:189118543..189119245,2	MCF-7	breast:
6	chr1:189145733..189147839-chr1:189155751..189158462,2	K562	blood:
7	chr1:189118692..189120237-chr1:189161776..189163535,2	K562	blood:
8	chr1:188902220..188904596-chr1:189118871..189120838,2	K562	blood:
9	chr1:189112586..189116347-chr1:189117211..189120686,6	K562	blood:
10	chr1:189112586..189116347-chr1:189117211..189120686,6	K562	blood:
11	chr1:189110161..189112248-chr17:56736351..56738349,2	MCF-7	breast:
12	chr1:189129002..189131397-chr1:189134322..189136351,2	K562	blood:
13	chr1:189118996..189121109-chr1:189287929..189290792,2	K562	blood:
14	chr1:189205219..189208075-chr1:189212130..189213812,2	K562	blood:
15	chr1:189117472..189119445-chr1:189184383..189186495,2	K562	blood:
16	chr1:189167872..189169675-chr1:189171676..189174219,2	K562	blood:
17	chr1:189148880..189151522-chr1:189151849..189154466,3	K562	blood:
18	chr1:189118758..189120623-chr1:189121928..189123602,2	MCF-7	breast:
19	chr1:189116028..189120237-chr1:189160506..189163276,3	K562	blood:
20	chr1:189109069..189111895-chr1:189118017..189120459,2	K562	blood:
21	chr1:189166300..189168058-chr1:189173903..189175630,2	MCF-7	breast:
22	chr1:189119463..189122039-chr1:189394507..189396400,2	K562	blood:
23	chr1:189118692..189120237-chr1:189161776..189163535,2	K562	blood:
24	chr1:189145733..189147839-chr1:189155751..189158462,2	K562	blood:
25	chr1:189117897..189121261-chr1:189121594..189126238,14	K562	blood:
26	chr1:189055283..189057511-chr1:189118631..189120197,2	K562	blood:
27	chr1:189174928..189177287-chr1:189180109..189182692,2	K562	blood:
28	chr1:189205219..189208075-chr1:189212130..189213812,2	K562	blood:
29	chr1:189103992..189106373-chr1:189109756..189111271,2	MCF-7	breast:
30	chr1:189051136..189054044-chr1:189118022..189120373,2	K562	blood:
31	chr1:189118758..189120623-chr1:189121928..189123602,2	MCF-7	breast:
32	chr1:189109069..189111895-chr1:189118017..189120459,2	K562	blood:
33	chr1:189129002..189131397-chr1:189134322..189136351,2	K562	blood:
34	chr1:189170367..189172924-chr1:189189578..189192081,2	K562	blood:
35	chr1:189167872..189169675-chr1:189171676..189174219,2	K562	blood:
36	chr1:189103992..189106373-chr1:189109756..189111271,2	MCF-7	breast:
37	chr1:189189341..189190044-chr1:189398354..189398974,2	MCF-7	breast:
38	chr1:189117472..189119445-chr1:189184383..189186495,2	K562	blood:
39	chr1:189121464..189123287-chr1:189388904..189390413,2	K562	blood:
40	chr1:189174928..189177287-chr1:189180109..189182692,2	K562	blood:
41	chr1:188751072..188751772-chr1:189118548..189119200,2	MCF-7	breast:
42	chr1:189117897..189121261-chr1:189121594..189126238,14	K562	blood:
43	chr1:189166300..189168058-chr1:189173903..189175630,2	MCF-7	breast:
44	chr1:189117659..189120234-chr6:30584654..30587422,2	K562	blood:
45	chr1:189032912..189034690-chr1:189118689..189120245,2	K562	blood:
46	chr1:189117678..189120245-chr1:189847842..189850269,2	K562	blood:
47	chr1:189117456..189122192-chr1:189126377..189132093,10	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA2G4A-7	chr1:189119674-189119918	NONHSAT008484
2	lnc-PLA2G4A-7	chr1:189118917-189119007	XLOC_000502
3	lnc-PLA2G4A-7	chr1:189119673-189119860	XLOC_000502

No data

Variant related genes	Relation type
ENSG00000226196	TF binding region
ENSG00000226196	CpG island
ENSG00000204568	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000204569	chromatin interactions

Extended variants
information (count: 1176 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1176 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141528827	chr1:189098000-189098001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143725351	chr1:189098051-189098052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs193154536	chr1:189098057-189098058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547463794	chr1:189098058-189098059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201335677	chr1:189098076-189098077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552075302	chr1:189098079-189098080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571612143	chr1:189098139-189098140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537387150	chr1:189098143-189098144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs59296151	chr1:189098174-189098175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556931883	chr1:189098189-189098190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1912900	chr1:189098195-189098196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs542736647	chr1:189098199-189098200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548530469	chr1:189098203-189098204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553447718	chr1:189098232-189098233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201898349	chr1:189098234-189098235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371521234	chr1:189098294-189098295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541222693	chr1:189098303-189098304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564331387	chr1:189098324-189098325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142946962	chr1:189098330-189098331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35600971	chr1:189098331-189098332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151062595	chr1:189098342-189098343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543787321	chr1:189098351-189098352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs80289215	chr1:189098368-189098369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147486693	chr1:189098391-189098392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570457489	chr1:189098393-189098394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147411574	chr1:189098394-189098395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149033658	chr1:189098397-189098398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534572041	chr1:189098401-189098402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551569820	chr1:189098468-189098469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79404876	chr1:189098474-189098475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111813197	chr1:189098489-189098490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79626437	chr1:189098508-189098509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550894196	chr1:189098521-189098522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185196858	chr1:189098551-189098552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188908270	chr1:189098578-189098579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377079820	chr1:189098600-189098601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73057013	chr1:189098605-189098606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs140341641	chr1:189098624-189098625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574270559	chr1:189098638-189098639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150339724	chr1:189098664-189098665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538798768	chr1:189098667-189098668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115981897	chr1:189098675-189098676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577941432	chr1:189098690-189098691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370199015	chr1:189098692-189098693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145649064	chr1:189098696-189098697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138132728	chr1:189098707-189098708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563593607	chr1:189098732-189098733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73057015	chr1:189098795-189098796	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs1912901	chr1:189098833-189098834	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs146085201	chr1:189098850-189098851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17899364	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
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:189098000-189102000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:189106200-189110600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:189110400-189111000	ZNF genes & repeats	Pancreas	Pancrea
4	chr1:189110600-189111000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:189111000-189118800	Weak transcription	Pancreas	Pancrea
6	chr1:189115600-189116600	Enhancers	Brain Germinal Matrix	brain
7	chr1:189118400-189120000	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr1:189118800-189119200	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr1:189118800-189119200	Active TSS	Liver	Liver
10	chr1:189118800-189119200	Active TSS	Gastric	stomach
11	chr1:189118800-189119400	Active TSS	Duodenum Mucosa	Duodenum
12	chr1:189118800-189119400	Active TSS	Fetal Intestine Large	intestine
13	chr1:189118800-189119400	ZNF genes & repeats	Pancreas	Pancrea
14	chr1:189118800-189119400	Active TSS	Rectal Mucosa Donor 29	rectum
15	chr1:189118800-189120200	Active TSS	A549	lung
16	chr1:189118800-189121800	Active TSS	K562	blood
17	chr1:189127200-189127600	Active TSS	K562	blood
18	chr1:189152000-189152400	Enhancers	Fetal Heart	heart
19	chr1:189154000-189154600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:189154000-189154800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:189154000-189155000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr1:189154200-189154800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:189154200-189155200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:189154400-189155000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr1:189165000-189165200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr1:189165600-189167200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:189174200-189174800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr1:189175000-189175400	Enhancers	A549	lung
29	chr1:189181800-189182600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:189182000-189182800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:189194000-189194800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:189194600-189194800	ZNF genes & repeats	Gastric	stomach
33	chr1:189196000-189196400	Active TSS	Primary T killer memory cells from peripheral blood	blood

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