Variant report

Variant	nsv825053
Chromosome Location	chr9:116150987-116158992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:62)
Chromatin interactive
region (count:13)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:116157562-116158054	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:116155929-116156064	HepG2	liver:	n/a	n/a
3	BHLHE40	chr9:116157616-116157913	HepG2	liver:	n/a	n/a
4	CEBPB	chr9:116157498-116157889	HepG2	liver:	n/a	n/a
5	CEBPB	chr9:116157493-116157906	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:116157481-116157928	HepG2	liver:	n/a	n/a
7	CEBPB	chr9:116157550-116157802	HepG2	liver:	n/a	n/a
8	CEBPB	chr9:116156181-116156400	HepG2	liver:	n/a	chr9:116156274-116156285
9	CEBPD	chr9:116157507-116158115	HepG2	liver:	n/a	n/a
10	CHD2	chr9:116157610-116158000	HepG2	liver:	n/a	n/a
11	EP300	chr9:116157556-116157827	HepG2	liver:	n/a	n/a
12	EP300	chr9:116157435-116157925	HepG2	liver:	n/a	n/a
13	EP300	chr9:116157437-116158026	HepG2	liver:	n/a	n/a
14	EP300	chr9:116156062-116156423	HepG2	liver:	n/a	n/a
15	FOSL2	chr9:116157501-116157894	HepG2	liver:	n/a	n/a
16	FOSL2	chr9:116157499-116158001	HepG2	liver:	n/a	n/a
17	FOXA1	chr9:116155932-116156384	HepG2	liver:	n/a	n/a
18	FOXA1	chr9:116157568-116157947	HepG2	liver:	n/a	n/a
19	FOXA1	chr9:116155990-116156341	HepG2	liver:	n/a	n/a
20	FOXA1	chr9:116157451-116158003	HepG2	liver:	n/a	n/a
21	FOXA1	chr9:116157448-116158082	HepG2	liver:	n/a	n/a
22	FOXA1	chr9:116157475-116158027	HepG2	liver:	n/a	n/a
23	FOXA2	chr9:116156061-116156317	HepG2	liver:	n/a	n/a
24	FOXA2	chr9:116157562-116157997	HepG2	liver:	n/a	n/a
25	HDAC2	chr9:116157515-116158033	HepG2	liver:	n/a	n/a
26	HDAC2	chr9:116157489-116158098	HepG2	liver:	n/a	n/a
27	HEY1	chr9:116157398-116157841	HepG2	liver:	n/a	n/a
28	HNF4A	chr9:116157482-116157930	HepG2	liver:	n/a	chr9:116157711-116157726
29	HNF4A	chr9:116157452-116157963	HepG2	liver:	n/a	chr9:116157711-116157726
30	HNF4A	chr9:116157464-116157951	HepG2	liver:	n/a	chr9:116157711-116157726
31	HNF4G	chr9:116157452-116157950	HepG2	liver:	n/a	chr9:116157710-116157725
32	HNF4G	chr9:116157483-116158030	HepG2	liver:	n/a	chr9:116157710-116157725
33	JUN	chr9:116157566-116157859	HepG2	liver:	n/a	n/a
34	JUND	chr9:116157606-116157806	HepG2	liver:	n/a	n/a
35	JUND	chr9:116157515-116157950	HepG2	liver:	n/a	n/a
36	JUND	chr9:116157551-116157871	HepG2	liver:	n/a	n/a
37	MAFF	chr9:116157571-116157839	HepG2	liver:	n/a	n/a
38	MAFK	chr9:116156966-116157016	HepG2	liver:	n/a	n/a
39	MAFK	chr9:116157630-116157982	HepG2	liver:	n/a	n/a
40	MAX	chr9:116157415-116158169	HepG2	liver:	n/a	n/a
41	MAX	chr9:116157599-116157899	HepG2	liver:	n/a	n/a
42	MAZ	chr9:116157452-116157611	HepG2	liver:	n/a	n/a
43	MBD4	chr9:116157469-116158027	HepG2	liver:	n/a	n/a
44	MXI1	chr9:116157498-116158012	HepG2	liver:	n/a	n/a
45	MYBL2	chr9:116157438-116158100	HepG2	liver:	n/a	n/a
46	MYBL2	chr9:116157376-116158018	HepG2	liver:	n/a	n/a
47	MYC	chr9:116157733-116157751	HepG2	liver:	n/a	n/a
48	MYC	chr9:116157699-116157731	HepG2	liver:	n/a	n/a
49	NFIC	chr9:116157497-116158007	HepG2	liver:	n/a	n/a
50	NFIC	chr9:116157429-116158013	HepG2	liver:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116151931-116151981	H1-hESC	embryonic stem cell:	embryo
2	chr9:116151931-116151981	H1-hESC	embryonic stem cell:	embryo
3	chr9:116151931-116151981	AoSMC	blood vessel:	n/a
4	chr9:116151931-116151981	SK-N-MC	brain:	n/a
5	chr9:116151931-116151981	NB4	blood:	n/a
6	chr9:116151931-116151981	MCF10A-Er-Src	breast:	n/a
7	chr9:116151931-116151981	HRCEpiC	kidney:	n/a
8	chr9:116151931-116151981	BJ	skin:	n/a
9	chr9:116151931-116151981	AG04450	lung:	fetal
10	chr9:116151931-116151981	AG10803	skin:	n/a
11	chr9:116151931-116151981	SKMC	muscle:	n/a
12	chr9:116151931-116151981	AG04449	skin:	fetal
13	chr9:116151931-116151981	GM06990	blood:	n/a
14	chr9:116151931-116151981	HUVEC	blood vessel:	n/a
15	chr9:116151931-116151981	HNPCEpiC	eye:	n/a
16	chr9:116151931-116151981	SK-N-SH_RA	brain:	n/a
17	chr9:116151931-116151981	NT2-D1	testis:	n/a
18	chr9:116151931-116151981	HIPEpiC	eye:	n/a
19	chr9:116151931-116151981	ProgFib	skin:	n/a
20	chr9:116151931-116151981	HMEC	breast:	n/a
21	chr9:116151931-116151981	HEK293	kidney:	embryo
22	chr9:116151931-116151981	HPAEpiC	pulmonary alveolar:	n/a
23	chr9:116151931-116151981	U87	brain:	n/a
24	chr9:116151931-116151981	HRPEpiC	eye:	n/a
25	chr9:116151931-116151981	RPTEC	kidney:	n/a
26	chr9:116151931-116151981	PFSK-1	brain:	n/a
27	chr9:116151931-116151981	SK-N-SH	brain:	n/a
28	chr9:116151931-116151981	AG09309	skin:	n/a
29	chr9:116151931-116151981	AG09319	gingival:	n/a
30	chr9:116151931-116151981	NHBE	bronchial:	n/a
31	chr9:116151931-116151981	Caco-2	colon:	n/a
32	chr9:116151931-116151981	LNCaP	prostate:	n/a
33	chr9:116151931-116151981	HCPEpiC	choroid plexus:	n/a
34	chr9:116151931-116151981	HEEpiC	esophagus:	n/a
35	chr9:116151931-116151981	MCF-7	breast:	n/a
36	chr9:116151931-116151981	Hela-S3	cervix:	n/a
37	chr9:116151931-116151981	BE2_C	brain:	n/a
38	chr9:116151931-116151981	GM12878	blood:	n/a
39	chr9:116151931-116151981	PrEC	prostate:	n/a
40	chr9:116151931-116151981	PANC-1	pancreas:	n/a
41	chr9:116151931-116151981	GM12891	blood:	n/a
42	chr9:116151931-116151981	HCM	heart:	n/a
43	chr9:116151931-116151981	ECC-1	luminal epithelium:	n/a
44	chr9:116151931-116151981	IMR90	lung:	fetal
45	chr9:116151931-116151981	HepG2	liver:	n/a
46	chr9:116151931-116151981	NH-A	brain:	n/a
47	chr9:116151931-116151981	ovcar-3	ovarian:	n/a
48	chr9:116151931-116151981	NHDF-neo	bronchial:	n/a
49	chr9:116151931-116151981	HAEpiC	amniotic membrane:	n/a
50	chr9:116151931-116151981	Jurkat	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116148030..116156107-chr9:116161914..116166950,9	MCF-7	breast:
2	chr9:116149664..116152667-chr9:116172993..116176331,3	K562	blood:
3	chr9:116149427..116152233-chr9:116182929..116184530,2	K562	blood:
4	chr9:116137615..116140170-chr9:116150544..116152687,3	MCF-7	breast:
5	chr9:116149635..116151577-chr9:116153234..116155559,2	MCF-7	breast:
6	chr9:116151263..116154918-chr9:116155923..116160670,6	K562	blood:
7	chr9:116156326..116158367-chr9:116163400..116165119,2	MCF-7	breast:
8	chr9:116156284..116160950-chr9:116161266..116165857,7	MCF-7	breast:
9	chr9:116150738..116153082-chr9:116153236..116155969,3	MCF-7	breast:
10	chr9:116149305..116153675-chr9:116170904..116174330,4	MCF-7	breast:
11	chr9:116156868..116159133-chr9:116160303..116163490,3	K562	blood:
12	chr9:116151263..116154918-chr9:116155923..116160670,6	K562	blood:
13	chr9:116127846..116129499-chr9:116156115..116158388,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLE3-3	chr9:116155441-116155914	NONHSAT134344
2	lnc-POLE3-3	chr9:116155727-116155910	NONHSAT134342
3	lnc-POLE3-3	chr9:116153186-116153213	NONHSAT134343
4	lnc-POLE3-3	chr9:116154399-116154835	NONHSAT134343
5	lnc-POLE3-3	chr9:116152908-116153213	NONHSAT134342
6	lnc-POLE3-3	chr9:116153807-116153903	NONHSAT134343

No data

Variant related genes	Relation type
ALAD	TF binding region
ALAD	CpG island
ENSG00000157653	chromatin interactions
ENSG00000119431	chromatin interactions
ENSG00000148229	chromatin interactions
ENSG00000148218	chromatin interactions

Extended variants
information (count: 383 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76259073	chr9:116150993-116150994	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs79681565	chr9:116150994-116150995	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs540576835	chr9:116151007-116151008	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs8177818	chr9:116151013-116151014	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs373499139	chr9:116151043-116151044	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs566527551	chr9:116151075-116151076	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs866564	chr9:116151088-116151089	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs188722626	chr9:116151100-116151101	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs376903755	chr9:116151133-116151134	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs371933814	chr9:116151140-116151141	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs531311653	chr9:116151179-116151180	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs548228812	chr9:116151180-116151181	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs148683351	chr9:116151184-116151185	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs1805313	chr9:116151191-116151192	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs8177817	chr9:116151223-116151224	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs546001979	chr9:116151229-116151230	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs550332573	chr9:116151236-116151237	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs372316464	chr9:116151237-116151238	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs4986829	chr9:116151240-116151241	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs539712107	chr9:116151253-116151254	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs556307080	chr9:116151266-116151267	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs36087664	chr9:116151277-116151278	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs370242589	chr9:116151291-116151292	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs201859063	chr9:116151301-116151302	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs373715261	chr9:116151311-116151312	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs150649205	chr9:116151312-116151313	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs200781693	chr9:116151314-116151315	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs200378521	chr9:116151315-116151316	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs367823672	chr9:116151325-116151326	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs61729493	chr9:116151335-116151336	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs202188395	chr9:116151344-116151345	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs553974879	chr9:116151348-116151349	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs144785407	chr9:116151356-116151357	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs121912981	chr9:116151365-116151366	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs371639473	chr9:116151366-116151367	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs121912983	chr9:116151368-116151369	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs201745784	chr9:116151389-116151390	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs200713896	chr9:116151413-116151414	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs375023469	chr9:116151419-116151420	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs8177816	chr9:116151428-116151429	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs531328691	chr9:116151429-116151430	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs541607831	chr9:116151434-116151435	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs372582179	chr9:116151445-116151446	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs8177815	chr9:116151446-116151447	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs8177814	chr9:116151450-116151451	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs141159567	chr9:116151500-116151501	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs8177813	chr9:116151501-116151502	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs377249770	chr9:116151503-116151504	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs569995634	chr9:116151504-116151505	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs8177812	chr9:116151527-116151528	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD
Melanoma	20877625	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116127800-116160400	Weak transcription	Fetal Heart	heart
2	chr9:116139800-116151200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr9:116139800-116152600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:116139800-116159000	Weak transcription	HSMM	muscle
5	chr9:116139800-116159600	Weak transcription	NH-A	brain
6	chr9:116139800-116160400	Weak transcription	NHDF-Ad	bronchial
7	chr9:116139800-116161400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr9:116139800-116161400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr9:116139800-116162000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr9:116140000-116152400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr9:116140000-116160200	Weak transcription	HMEC	breast
12	chr9:116140000-116162000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr9:116140200-116152600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:116141400-116152800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr9:116143400-116151200	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr9:116143400-116160200	Weak transcription	Small Intestine	intestine
17	chr9:116144600-116162600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr9:116144800-116153200	Weak transcription	NHEK	skin
19	chr9:116144800-116158600	Weak transcription	K562	blood
20	chr9:116146600-116162800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr9:116147800-116159800	Strong transcription	Fetal Stomach	stomach
22	chr9:116148000-116155800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr9:116148000-116155800	Strong transcription	Brain Anterior Caudate	brain
24	chr9:116148000-116155800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr9:116148000-116156000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr9:116148000-116156200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:116148000-116156400	Strong transcription	Primary T cells from cord blood	blood
28	chr9:116148000-116156800	Strong transcription	Fetal Muscle Leg	muscle
29	chr9:116148000-116158000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:116148000-116159000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr9:116148000-116159400	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr9:116148200-116156400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr9:116148200-116158000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr9:116148400-116153400	Genic enhancers	Fetal Intestine Large	intestine
35	chr9:116148400-116155000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr9:116148400-116156000	Strong transcription	Stomach Smooth Muscle	stomach
37	chr9:116148600-116154800	Strong transcription	Fetal Brain Female	brain
38	chr9:116148600-116154800	Strong transcription	Left Ventricle	heart
39	chr9:116148600-116155600	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr9:116148600-116156200	Strong transcription	Brain Hippocampus Middle	brain
41	chr9:116148600-116156800	Strong transcription	Brain Germinal Matrix	brain
42	chr9:116148600-116159200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:116148800-116155800	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr9:116148800-116155800	Strong transcription	Placenta Amnion	Placenta Amnion
45	chr9:116148800-116156000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr9:116148800-116156200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr9:116148800-116156200	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr9:116149000-116153000	Strong transcription	GM12878-XiMat	blood
49	chr9:116149000-116154600	Strong transcription	Spleen	Spleen
50	chr9:116149000-116155200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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