Variant report

Variant	nsv893642
Chromosome Location	chr9:104904454-105158032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:104949932-104950119	HepG2	liver:	n/a	n/a
2	ATF1	chr9:105157648-105157824	K562	blood:	n/a	n/a
3	CEBPB	chr9:105116836-105117075	A549	lung:	n/a	chr9:105117017-105117030 chr9:105117019-105117028 chr9:105117019-105117028 chr9:105117019-105117028 chr9:105117019-105117028 chr9:105117019-105117030 chr9:105116943-105116954
4	CEBPB	chr9:105053338-105053531	A549	lung:	n/a	chr9:105053392-105053403
5	CEBPB	chr9:105053288-105053488	HepG2	liver:	n/a	chr9:105053392-105053403
6	CEBPB	chr9:105045700-105045900	A549	lung:	n/a	n/a
7	CEBPB	chr9:104986298-104986457	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr9:105015369-105015524	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr9:105045628-105045943	HepG2	liver:	n/a	n/a
10	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
11	CEBPB	chr9:105123166-105123481	HepG2	liver:	n/a	chr9:105123302-105123313
12	CEBPB	chr9:104904806-104905159	HepG2	liver:	n/a	chr9:104904962-104904973 chr9:104904962-104904975
13	CEBPB	chr9:104931342-104931414	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:104904848-104905135	H1-hESC	embryonic stem cell:	n/a	chr9:104904962-104904973 chr9:104904962-104904975
15	CEBPB	chr9:104904788-104905091	IMR90	lung:	n/a	chr9:104904962-104904973 chr9:104904962-104904975
16	CEBPB	chr9:104999513-104999769	HepG2	liver:	n/a	chr9:104999628-104999639
17	CEBPB	chr9:104904860-104905106	A549	lung:	n/a	chr9:104904962-104904973 chr9:104904962-104904975
18	CEBPB	chr9:104904855-104905126	K562	blood:	n/a	chr9:104904962-104904973 chr9:104904962-104904975
19	CTCF	chr9:105118166-105118279	GM10266	blood:	n/a	n/a
20	CTCF	chr9:104915457-104915589	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr9:105118420-105118570	GM12875	blood:	n/a	n/a
22	CTCF	chr9:105007369-105007413	GM20000	blood:	n/a	n/a
23	CTCF	chr9:105134263-105134293	Gliobla	brain:	n/a	n/a
24	CTCF	chr9:104962715-104962785	K562	blood:	n/a	n/a
25	CTCF	chr9:105017180-105017330	GM12866	blood:	n/a	n/a
26	CTCF	chr9:104942181-104942208	LNCaP	prostate:	n/a	n/a
27	CTCF	chr9:105015506-105015634	MCF-7	breast:	n/a	chr9:105015565-105015573
28	CTCF	chr9:104948460-104948610	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr9:105015420-105015570	Caco-2	colon:	n/a	n/a
30	CTCF	chr9:105015408-105015699	H1-hESC	embryonic stem cell:	n/a	chr9:105015565-105015573
31	CTCF	chr9:104997625-104997683	Fibrobl	skin:	n/a	n/a
32	CTCF	chr9:105029673-105029679	GM10248	blood:	n/a	n/a
33	CTCF	chr9:105015420-105015729	H1-hESC	embryonic stem cell:	n/a	chr9:105015565-105015573
34	CTCF	chr9:105068383-105068442	GM20000	blood:	n/a	n/a
35	CTCF	chr9:105019456-105019525	GM13976	blood:	n/a	n/a
36	CTCF	chr9:104933044-104933076	GM20000	blood:	n/a	n/a
37	CTCF	chr9:105015460-105015610	HEK293	kidney:	n/a	chr9:105015565-105015573
38	CTCF	chr9:105074979-105075026	ProgFib	skin:	n/a	n/a
39	CTCF	chr9:105071620-105071770	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr9:104948440-104948590	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:105015560-105015710	WERI-Rb-1	eye:	n/a	chr9:105015565-105015573
42	CTCF	chr9:104982658-104982752	GM13976	blood:	n/a	n/a
43	CTCF	chr9:104973540-104973690	GM12871	blood:	n/a	n/a
44	CTCF	chr9:105015540-105015690	WERI-Rb-1	eye:	n/a	chr9:105015565-105015573
45	CTCF	chr9:104915361-104915580	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:105039793-105039858	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr9:105015517-105015635	MCF-7	breast:	n/a	chr9:105015565-105015573
48	CTCF	chr9:105071620-105071770	HEK293	kidney:	n/a	n/a
49	CTCF	chr9:105015460-105015610	MCF-7	breast:	n/a	chr9:105015565-105015573
50	CTCF	chr9:105065960-105066110	GM12869	blood:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:105142545..105144051-chr9:105153392..105154963,2	MCF-7	breast:
2	chr9:105142545..105144051-chr9:105153392..105154963,2	MCF-7	breast:
3	chr9:104996734..105000664-chr9:105001906..105004565,3	K562	blood:
4	chr9:104996734..105000664-chr9:105001906..105004565,3	K562	blood:
5	chr10:9229922..9230664-chr9:104997433..104997933,2	MCF-7	breast:
6	chr9:104973156..104974681-chr9:104986450..104988784,2	MCF-7	breast:
7	chr1:106538363..106538863-chr9:105123307..105123875,2	MCF-7	breast:
8	chr9:104998428..105001146-chr9:105002179..105004444,3	K562	blood:
9	chr9:104973156..104974681-chr9:104986450..104988784,2	MCF-7	breast:
10	chr9:104998428..105001146-chr9:105002179..105004444,3	K562	blood:

(count:39 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000222117	TF binding region
RNU6-329P	TF binding region

Extended variants
information (count: 1569 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1569 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146754557	chr9:104904647-104904648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529147994	chr9:104904648-104904649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140454187	chr9:104904665-104904666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533520104	chr9:104904683-104904684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547705072	chr9:104904687-104904688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143226478	chr9:104904698-104904699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560615740	chr9:104904706-104904707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528932547	chr9:104904789-104904790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548676685	chr9:104904823-104904824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs55781627	chr9:104904843-104904844	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs151257308	chr9:104904862-104904863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140454535	chr9:104904940-104904941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571111540	chr9:104904981-104904982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533707349	chr9:104904989-104904990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537111802	chr9:104915601-104915602	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs200873760	chr9:104915604-104915605	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs576920087	chr9:104915605-104915606	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs546089960	chr9:104915609-104915610	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs552982924	chr9:104915627-104915628	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs572156712	chr9:104915638-104915639	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs192931	chr9:104915669-104915670	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs188537822	chr9:104915672-104915673	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs181341247	chr9:104915687-104915688	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs567196295	chr9:104915694-104915695	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs58460494	chr9:104915695-104915696	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs192930	chr9:104915698-104915699	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs563916369	chr9:104915699-104915700	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs532585159	chr9:104915708-104915709	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs144087235	chr9:104915709-104915710	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs185120657	chr9:104915715-104915716	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs552817697	chr9:104915733-104915734	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs568034864	chr9:104915748-104915749	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs537156364	chr9:104915756-104915757	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs189872941	chr9:104915760-104915761	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs570928691	chr9:104915765-104915766	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs570667277	chr9:104915774-104915775	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs536930206	chr9:104915782-104915783	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs539253720	chr9:104915789-104915790	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs148684102	chr9:104915791-104915792	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs572787352	chr9:104915805-104915806	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs373944129	chr9:104915846-104915847	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113482372	chr9:104915863-104915864	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs144550154	chr9:104915879-104915880	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs368672125	chr9:104915889-104915890	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs556243886	chr9:104915890-104915891	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs574451761	chr9:104915899-104915900	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs543936775	chr9:104915904-104915905	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs370726115	chr9:104915914-104915915	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs563182239	chr9:104915917-104915918	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs556247223	chr9:104915946-104915947	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Schizophrenia	23813976	CNVD
Basal cell lymphoma	21115979	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104904600-104905000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr9:104915600-104916000	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr9:104940400-104941800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr9:104940600-104941400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:104947400-104950200	Enhancers	Fetal Heart	heart
6	chr9:104947800-104948000	Enhancers	Ovary	ovary
7	chr9:104947800-104948400	Enhancers	Stomach Smooth Muscle	stomach
8	chr9:104947800-104948800	Enhancers	Adipose Nuclei	Adipose
9	chr9:104948000-104948800	Enhancers	Fetal Kidney	kidney
10	chr9:104948200-104948800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:104948600-104949200	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr9:104948800-104949800	Weak transcription	Fetal Kidney	kidney
13	chr9:104949200-104949600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr9:104949600-104950400	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr9:104950000-104950200	Enhancers	Fetal Kidney	kidney
16	chr9:104950000-104950800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr9:104950000-104950800	Enhancers	Ovary	ovary
18	chr9:104971400-104971800	Active TSS	Aorta	Aorta
19	chr9:104985600-104986200	Active TSS	H1 Cell Line	embryonic stem cell
20	chr9:104985600-104986200	Active TSS	H9 Cell Line	embryonic stem cell
21	chr9:104985600-104986200	Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr9:104985600-104986200	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr9:104985600-104986200	Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr9:104985600-104986200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr9:104985600-104986200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:104985600-104986400	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr9:104985600-104986400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr9:104985600-104986600	Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr9:104985600-104986600	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr9:104985800-104986200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr9:104985800-104986200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr9:104985800-104986200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr9:104985800-104986400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr9:104985800-104986400	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr9:104985800-104986400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr9:104985800-104986400	Active TSS	Liver	Liver
37	chr9:104985800-104986400	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr9:104985800-104986400	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr9:104985800-104986600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr9:104986200-104986400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
41	chr9:104986200-104986400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr9:104986200-104986600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr9:104986200-104986600	Active TSS	K562	blood
44	chr9:104986200-104986800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
45	chr9:104986400-104986600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr9:104986400-104986600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr9:104986400-104986600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr9:104986600-104987000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr9:104986600-104988800	Weak transcription	K562	blood
50	chr9:104988000-104989000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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