Variant report

Variant	nsv1048227
Chromosome Location	chr9:104546761-105162810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1497)
CpG islands
(count:0)
Chromatin interactive
region (count:57)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1497 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:104656203-104656979	K562	blood:	n/a	n/a
2	ARID3A	chr9:104949932-104950119	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:104604440-104604568	K562	blood:	n/a	n/a
4	ARID3A	chr9:104689227-104689231	K562	blood:	n/a	n/a
5	ARID3A	chr9:104602870-104603634	K562	blood:	n/a	n/a
6	ARID3A	chr9:104603974-104604201	K562	blood:	n/a	n/a
7	ARID3A	chr9:104604790-104605089	K562	blood:	n/a	n/a
8	ARID3A	chr9:104868818-104868993	K562	blood:	n/a	n/a
9	ATF1	chr9:104602937-104603620	K562	blood:	n/a	n/a
10	ATF1	chr9:104692769-104692902	K562	blood:	n/a	n/a
11	ATF1	chr9:104667150-104667409	K562	blood:	n/a	n/a
12	ATF1	chr9:105157648-105157824	K562	blood:	n/a	n/a
13	ATF3	chr9:104602886-104603521	K562	blood:	n/a	n/a
14	BACH1	chr9:104666707-104666740	K562	blood:	n/a	n/a
15	BCL3	chr9:104603020-104603535	K562	blood:	n/a	n/a
16	BCLAF1	chr9:104602989-104603485	K562	blood:	n/a	n/a
17	BHLHE40	chr9:104629233-104629302	K562	blood:	n/a	n/a
18	BHLHE40	chr9:104656000-104656660	K562	blood:	n/a	n/a
19	BHLHE40	chr9:104602981-104603519	K562	blood:	n/a	n/a
20	BHLHE40	chr9:104693595-104693643	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:104603872-104603981	K562	blood:	n/a	n/a
22	BHLHE40	chr9:104641860-104641886	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:104808797-104808879	HepG2	liver:	n/a	n/a
24	CBX3	chr9:104601296-104601594	K562	blood:	n/a	n/a
25	CBX3	chr9:104602864-104603528	K562	blood:	n/a	n/a
26	CBX3	chr9:104656265-104656906	K562	blood:	n/a	n/a
27	CBX3	chr9:104602902-104603580	K562	blood:	n/a	n/a
28	CCNT2	chr9:104656253-104656608	K562	blood:	n/a	n/a
29	CCNT2	chr9:104602949-104603796	K562	blood:	n/a	n/a
30	CEBPB	chr9:104688976-104689041	K562	blood:	n/a	n/a
31	CEBPB	chr9:104804246-104804649	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr9:104757408-104758008	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr9:105053288-105053488	HepG2	liver:	n/a	chr9:105053392-105053403
34	CEBPB	chr9:104557461-104557739	H1-hESC	embryonic stem cell:	n/a	chr9:104557616-104557627
35	CEBPB	chr9:104557510-104557633	K562	blood:	n/a	chr9:104557616-104557627
36	CEBPB	chr9:104571492-104571600	HepG2	liver:	n/a	chr9:104571514-104571525
37	CEBPB	chr9:104695306-104695416	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:104603004-104603626	K562	blood:	n/a	n/a
39	CEBPB	chr9:104904860-104905106	A549	lung:	n/a	chr9:104904962-104904973 chr9:104904962-104904975
40	CEBPB	chr9:105116776-105117104	HepG2	liver:	n/a	chr9:105117017-105117030 chr9:105117019-105117028 chr9:105117019-105117028 chr9:105117019-105117028 chr9:105117019-105117028 chr9:105117019-105117030 chr9:105116943-105116954
41	CEBPB	chr9:104557424-104557737	A549	lung:	n/a	chr9:104557616-104557627
42	CEBPB	chr9:104904848-104905135	H1-hESC	embryonic stem cell:	n/a	chr9:104904962-104904973 chr9:104904962-104904975
43	CEBPB	chr9:104586855-104587085	K562	blood:	n/a	chr9:104587024-104587035 chr9:104587023-104587034 chr9:104587023-104587034
44	CEBPB	chr9:104557455-104557771	Hela-S3	cervix:	n/a	chr9:104557616-104557627
45	CEBPB	chr9:105045700-105045900	A549	lung:	n/a	n/a
46	CEBPB	chr9:104557453-104557803	HepG2	liver:	n/a	chr9:104557616-104557627
47	CEBPB	chr9:104820520-104820527	A549	lung:	n/a	n/a
48	CEBPB	chr9:104726861-104727114	A549	lung:	n/a	chr9:104726984-104726995 chr9:104727014-104727025
49	CEBPB	chr9:104832504-104832566	A549	lung:	n/a	n/a
50	CEBPB	chr9:104861803-104861860	HepG2	liver:	n/a	chr9:104861817-104861828 chr9:104861819-104861830 chr9:104861817-104861830

No data

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:104828978..104830886-chr9:104836828..104839477,2	K562	blood:
2	chr9:104736126..104738310-chr9:104738745..104740994,2	K562	blood:
3	chr9:104628351..104631183-chr9:104634996..104637004,2	K562	blood:
4	chr9:104752145..104755127-chr9:104756633..104759561,2	MCF-7	breast:
5	chr1:106538363..106538863-chr9:105123307..105123875,2	MCF-7	breast:
6	chr9:105142545..105144051-chr9:105153392..105154963,2	MCF-7	breast:
7	chr9:104996734..105000664-chr9:105001906..105004565,3	K562	blood:
8	chr9:104554304..104554879-chr9:107148429..107149219,2	MCF-7	breast:
9	chr9:104973156..104974681-chr9:104986450..104988784,2	MCF-7	breast:
10	chr9:104712078..104714404-chr9:104717443..104718985,2	K562	blood:
11	chr9:104703090..104705673-chr9:104707089..104708983,2	MCF-7	breast:
12	chr9:104719927..104722291-chr9:104723715..104725489,2	K562	blood:
13	chr10:86116689..86117545-chr9:104638316..104638864,2	MCF-7	breast:
14	chr9:104712078..104714404-chr9:104717443..104718985,2	K562	blood:
15	chr10:9229922..9230664-chr9:104997433..104997933,2	MCF-7	breast:
16	chr11:118868629..118869144-chr9:104880609..104881109,2	MCF-7	breast:
17	chr9:104618154..104619898-chr9:104623303..104626288,2	K562	blood:
18	chr9:104996734..105000664-chr9:105001906..105004565,3	K562	blood:
19	chr9:104602976..104605098-chr9:104654861..104656583,2	K562	blood:
20	chr9:104846252..104847873-chr9:104851668..104854284,2	K562	blood:
21	chr9:104600370..104602657-chr9:104607856..104609607,2	K562	blood:
22	chr10:26587616..26588136-chr9:104616741..104617261,2	MCF-7	breast:
23	chr9:104628351..104631183-chr9:104634996..104637004,2	K562	blood:
24	chr9:104998428..105001146-chr9:105002179..105004444,3	K562	blood:
25	chr9:104736126..104738310-chr9:104738745..104740994,2	K562	blood:
26	chr9:104600370..104602657-chr9:104607856..104609607,2	K562	blood:
27	chr9:104973156..104974681-chr9:104986450..104988784,2	MCF-7	breast:
28	chr9:104733654..104735932-chr9:104741852..104744249,2	K562	blood:
29	chr9:104656494..104659292-chr9:104659378..104660947,2	K562	blood:
30	chr9:104998428..105001146-chr9:105002179..105004444,3	K562	blood:
31	chr9:105142545..105144051-chr9:105153392..105154963,2	MCF-7	breast:
32	chr9:104651692..104653674-chr9:104654831..104656536,3	K562	blood:
33	chr9:104707981..104710743-chr9:104711149..104712879,2	K562	blood:
34	chr9:104662236..104665131-chr9:104665548..104668439,2	K562	blood:
35	chr9:104554048..104554859-chr9:104734774..104735456,4	MCF-7	breast:
36	chr9:104752145..104755127-chr9:104756633..104759561,2	MCF-7	breast:
37	chr9:104790240..104792584-chr9:104811133..104813780,2	K562	blood:
38	chr9:104707981..104710743-chr9:104711149..104712879,2	K562	blood:
39	chr9:104828978..104830886-chr9:104836828..104839477,2	K562	blood:
40	chr9:104594444..104596154-chr9:104597009..104599073,2	MCF-7	breast:
41	chr9:104626627..104628605-chr9:104630406..104631919,2	K562	blood:
42	chr8:142134647..142136266-chr9:104766043..104767800,2	MCF-7	breast:
43	chr9:104846252..104847873-chr9:104851668..104854284,2	K562	blood:
44	chr9:104662236..104665131-chr9:104665548..104668439,2	K562	blood:
45	chr9:104658581..104661092-chr9:104661771..104663841,2	K562	blood:
46	chr9:104658581..104661092-chr9:104661771..104663841,2	K562	blood:
47	chr9:104618154..104619898-chr9:104623303..104626288,2	K562	blood:
48	chr9:104703090..104705673-chr9:104707089..104708983,2	MCF-7	breast:
49	chr9:104733654..104735932-chr9:104741852..104744249,2	K562	blood:
50	chr9:104651692..104653674-chr9:104654831..104656536,3	K562	blood:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf107-6	chr9:105022063-105022447	NONHSAT133760
2	lnc-RNF20-4	chr9:104567769-104567808	NONHSAT133752
3	lnc-GRIN3A-3	chr9:105078134-105078251	ucscGeneNc_uc004bbt_2
4	lnc-GRIN3A-3	chr9:105066627-105066753	NONHSAT133756
5	lnc-RNF20-2	chr9:104652669-104652689	XLOC_007493
6	lnc-GRIN3A-3	chr9:105029817-105029914	ucscGeneNc_uc004bbt_2
7	lnc-GRIN3A-3	chr9:105079433-105079602	ucscGeneNc_uc004bbt_2
8	lnc-GRIN3A-3	chr9:105122117-105122289	ucscGeneNc_uc004bbt_2
9	lnc-GRIN3A-3	chr9:105079433-105079602	NONHSAT133756
10	lnc-C9orf107-6	chr9:105022063-105022447	FPKM1_group_33627_transcript_2
11	lnc-GRIN3A-3	chr9:104990149-104990219	ucscGeneNc_uc004bbt_2
12	lnc-C9orf107-5	chr9:105045829-105045892	NONHSAT133761
13	lnc-C9orf107-1	chr9:105053028-105053194	XLOC_007495
14	lnc-GRIN3A-3	chr9:105078134-105078251	NONHSAT133764
15	lnc-GRIN3A-3	chr9:105126760-105126881	NONHSAT133764
16	lnc-RNF20-2	chr9:104654473-104654712	XLOC_007493
17	lnc-C9orf107-6	chr9:105022537-105022537	FPKM1_group_33627_transcript_2
18	lnc-GRIN3A-3	chr9:105122117-105122289	NONHSAT133756
19	lnc-C9orf107-2	chr9:104997351-104999003	NONHSAT133757
20	lnc-C9orf107-2	chr9:104997647-104997890	FPKM1_group_33624_transcript_3
21	lnc-GRIN3A-3	chr9:104946414-104946469	NONHSAT133756
22	lnc-C9orf107-2	chr9:104998737-104998845	XLOC_007494
23	lnc-C9orf107-7	chr9:104810504-104810756	NONHSAT133754
24	lnc-GRIN3A-3	chr9:105127094-105127137	NONHSAT133756
25	lnc-GRIN3A-3	chr9:104990149-104990219	NONHSAT133756
26	lnc-GRIN3A-3	chr9:105066714-105066751	NONHSAT133764
27	lnc-C9orf107-5	chr9:105055136-105055273	NONHSAT133761
28	lnc-GRIN3A-3	chr9:104942626-104945366	NONHSAT133756
29	lnc-C9orf107-2	chr9:104997351-104999003	FPKM1_group_33624_transcript_3
30	lnc-GRIN3A-3	chr9:105078134-105078251	NONHSAT133756
31	lnc-C9orf107-1	chr9:105052402-105052947	XLOC_007495
32	lnc-GRIN3A-3	chr9:105117245-105117384	NONHSAT133756
33	lnc-C9orf107-2	chr9:105000311-105000554	NONHSAT133757
34	lnc-GRIN3A-3	chr9:105117245-105117384	ucscGeneNc_uc004bbt_2
35	lnc-GRIN3A-3	chr9:104946414-104946469	ucscGeneNc_uc004bbt_2
36	lnc-RNF20-4	chr9:104567913-104568131	NONHSAT133752
37	lnc-GRIN3A-2	chr9:104817534-104818023	NONHSAT133755
38	lnc-GRIN3A-3	chr9:105079433-105079602	NONHSAT133764
39	lnc-C9orf107-7	chr9:104811295-104811420	NONHSAT133754
40	lnc-GRIN3A-3	chr9:105117245-105117384	NONHSAT133764
41	lnc-GRIN3A-3	chr9:104942631-104945366	ucscGeneNc_uc004bbt_2
42	lnc-C9orf107-6	chr9:105022537-105022636	NONHSAT133760
43	lnc-GRIN3A-3	chr9:105029817-105029914	NONHSAT133756
44	lnc-GRIN3A-3	chr9:105127094-105127133	ucscGeneNc_uc004bbt_2
45	lnc-C9orf107-2	chr9:105000314-105000407	XLOC_007494
46	lnc-GRIN3A-3	chr9:105066627-105066753	ucscGeneNc_uc004bbt_2

No data

Variant related genes	Relation type
RNU6-329P	TF binding region
MTND3P4	TF binding region
ARL2BPP7	TF binding region
ENSG00000222117	TF binding region
ENSG00000255121	chromatin interactions
ENSG00000186166	chromatin interactions

Extended variants
information (count: 6668 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6668 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559754246	chr9:104550023-104550024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182398961	chr9:104550071-104550072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541915726	chr9:104550074-104550075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562250585	chr9:104550163-104550164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531008187	chr9:104550228-104550229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143917482	chr9:104550234-104550235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148640981	chr9:104550285-104550286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142149218	chr9:104550300-104550301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533413158	chr9:104550319-104550320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543484414	chr9:104550381-104550382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187900139	chr9:104552831-104552832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572073897	chr9:104552856-104552857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564299727	chr9:104552864-104552865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376721042	chr9:104552873-104552874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139228475	chr9:104552936-104552937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560860339	chr9:104552937-104552938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529895933	chr9:104552938-104552939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549740080	chr9:104552951-104552952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563229385	chr9:104553013-104553014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532241378	chr9:104553027-104553028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372769778	chr9:104553032-104553033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375483614	chr9:104553059-104553060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549865666	chr9:104553104-104553105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552078091	chr9:104553108-104553109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147535657	chr9:104553144-104553145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532099712	chr9:104553178-104553179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533969615	chr9:104553190-104553191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553608714	chr9:104553194-104553195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547394226	chr9:104553648-104553649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs559304063	chr9:104553653-104553654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572063245	chr9:104553729-104553730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139476315	chr9:104553758-104553759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs16920763	chr9:104553765-104553766	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533037299	chr9:104553769-104553770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551734260	chr9:104553783-104553784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144098305	chr9:104554258-104554259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539282044	chr9:104554306-104554307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559290617	chr9:104554322-104554323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1337702	chr9:104554346-104554347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187053754	chr9:104554361-104554362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534598755	chr9:104554368-104554369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554236615	chr9:104554390-104554391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201843900	chr9:104554397-104554398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146504021	chr9:104554398-104554399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543106481	chr9:104554409-104554410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556676383	chr9:104554425-104554426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539122349	chr9:104554439-104554440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557129068	chr9:104554454-104554455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545619109	chr9:104554531-104554532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559203764	chr9:104554540-104554541	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Neuroblastoma	20406844	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Basal cell lymphoma	21115979	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104550000-104550400	Enhancers	Fetal Brain Male	brain
2	chr9:104552800-104553200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:104553600-104553800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:104554200-104554800	Enhancers	Ovary	ovary
5	chr9:104558400-104558800	Enhancers	A549	lung
6	chr9:104565200-104565400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:104576000-104576200	Enhancers	Gastric	stomach
8	chr9:104586200-104586600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr9:104591800-104598800	Weak transcription	Liver	Liver
10	chr9:104594400-104596000	Enhancers	Fetal Intestine Large	intestine
11	chr9:104594400-104596000	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr9:104595000-104596000	Enhancers	Duodenum Mucosa	Duodenum
13	chr9:104595000-104596000	Enhancers	Fetal Intestine Small	intestine
14	chr9:104595200-104595400	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr9:104595400-104598000	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr9:104596000-104598000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr9:104596000-104598200	Weak transcription	Fetal Intestine Small	intestine
18	chr9:104597200-104599000	Enhancers	K562	blood
19	chr9:104598000-104598400	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr9:104598000-104598400	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr9:104598200-104598800	Enhancers	Fetal Intestine Small	intestine
22	chr9:104598800-104599000	ZNF genes & repeats	Liver	Liver
23	chr9:104599000-104599400	Weak transcription	Liver	Liver
24	chr9:104599000-104602000	Weak transcription	K562	blood
25	chr9:104602000-104603400	Enhancers	K562	blood
26	chr9:104603200-104604200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:104603400-104604000	Flanking Active TSS	K562	blood
28	chr9:104603400-104604200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr9:104604000-104604200	Enhancers	K562	blood
30	chr9:104604200-104610200	Weak transcription	K562	blood
31	chr9:104606600-104607200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:104606800-104607400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:104607600-104608200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr9:104610000-104610600	Enhancers	Duodenum Mucosa	Duodenum
35	chr9:104610000-104612400	Enhancers	Fetal Intestine Large	intestine
36	chr9:104610000-104612400	Enhancers	Fetal Intestine Small	intestine
37	chr9:104610200-104610600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr9:104610200-104610600	Enhancers	K562	blood
39	chr9:104610400-104610600	Enhancers	Colonic Mucosa	Colon
40	chr9:104610400-104610600	Enhancers	Colon Smooth Muscle	Colon
41	chr9:104610400-104610800	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr9:104610400-104610800	Enhancers	Small Intestine	intestine
43	chr9:104610400-104611000	Enhancers	Fetal Muscle Trunk	muscle
44	chr9:104610400-104611200	Enhancers	Adipose Nuclei	Adipose
45	chr9:104610600-104610800	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr9:104610600-104610800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
47	chr9:104610600-104610800	Active TSS	Rectal Smooth Muscle	rectum
48	chr9:104610600-104611000	Flanking Active TSS	Colonic Mucosa	Colon
49	chr9:104610600-104611000	Flanking Active TSS	Colon Smooth Muscle	Colon
50	chr9:104610600-104611200	Flanking Active TSS	K562	blood

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