Variant report

Variant	nsv892068
Chromosome Location	chr9:2543888-2589739
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:340)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:340 , 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	chr9:2570935-2570937	HepG2	liver:	n/a	n/a
2	ATF1	chr9:2570654-2571097	K562	blood:	n/a	n/a
3	ATF2	chr9:2570575-2571089	GM12878	blood:	n/a	n/a
4	ATF2	chr9:2570491-2571088	GM12878	blood:	n/a	n/a
5	BACH1	chr9:2568840-2568890	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr9:2570593-2570937	GM12878	blood:	n/a	n/a
7	BATF	chr9:2570619-2571066	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:2570653-2571002	GM12878	blood:	n/a	n/a
9	BCL3	chr9:2570621-2571006	GM12878	blood:	n/a	n/a
10	BCLAF1	chr9:2570647-2571008	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:2570676-2571086	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:2570762-2571109	K562	blood:	n/a	n/a
13	BRCA1	chr9:2570638-2571415	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr9:2570525-2571114	HCT-116	colon:	n/a	n/a
15	CCNT2	chr9:2583456-2583656	K562	blood:	n/a	n/a
16	CEBPB	chr9:2570565-2571147	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr9:2559502-2559857	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:2570528-2571233	HCT-116	colon:	n/a	n/a
19	CEBPB	chr9:2570511-2571251	HCT-116	colon:	n/a	n/a
20	CEBPB	chr9:2570731-2570872	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:2570673-2570970	A549	lung:	n/a	n/a
22	CEBPB	chr9:2559300-2559816	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:2570757-2570957	K562	blood:	n/a	n/a
24	CEBPB	chr9:2557383-2557510	A549	lung:	n/a	n/a
25	CHD2	chr9:2570641-2571073	Hela-S3	cervix:	n/a	n/a
26	CREB1	chr9:2570586-2571126	GM12878	blood:	n/a	n/a
27	CREB1	chr9:2570620-2571078	GM12878	blood:	n/a	n/a
28	CTCF	chr9:2559540-2559690	AG10803	skin:	n/a	n/a
29	CTCF	chr9:2559680-2559830	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr9:2559300-2559450	AG04449	skin:	n/a	n/a
31	CTCF	chr9:2570608-2570811	GM12878	blood:	n/a	n/a
32	CTCF	chr9:2573980-2574130	HEK293	kidney:	n/a	chr9:2574071-2574078
33	CTCF	chr9:2570720-2570870	GM12873	blood:	n/a	n/a
34	CTCF	chr9:2559610-2559613	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr9:2556120-2556270	GM12866	blood:	n/a	n/a
36	CTCF	chr9:2570640-2570790	HEK293	kidney:	n/a	n/a
37	CTCF	chr9:2559600-2559750	AG04450	lung:	n/a	n/a
38	CTCF	chr9:2567332-2567367	GM10248	blood:	n/a	n/a
39	CTCF	chr9:2573985-2574145	Hela-S3	cervix:	n/a	chr9:2574071-2574078
40	CTCF	chr9:2559580-2559730	HPF	lung:	n/a	n/a
41	CTCF	chr9:2570620-2570770	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr9:2559640-2559790	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr9:2570660-2570810	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr9:2559680-2559830	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr9:2570669-2570802	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr9:2570700-2570850	BE2_C	brain:	n/a	n/a
47	CTCF	chr9:2570560-2570710	HCM	heart:	n/a	n/a
48	CTCF	chr9:2570720-2570870	HPF	lung:	n/a	n/a
49	CTCF	chr9:2559615-2559748	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr9:2559680-2559830	BJ	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2571396-2571446	NHBE	bronchial:	n/a
2	chr9:2571396-2571446	IMR90	lung:	fetal
3	chr9:2571396-2571446	AG04449	skin:	fetal
4	chr9:2571396-2571446	SK-N-MC	brain:	n/a
5	chr9:2571396-2571446	HUVEC	blood vessel:	n/a
6	chr9:2571396-2571446	HCPEpiC	choroid plexus:	n/a
7	chr9:2571396-2571446	NH-A	brain:	n/a
8	chr9:2571396-2571446	SAEC	small airway:	n/a
9	chr9:2571396-2571446	BE2_C	brain:	n/a
10	chr9:2571396-2571446	ECC-1	luminal epithelium:	n/a
11	chr9:2571396-2571446	HAEpiC	amniotic membrane:	n/a
12	chr9:2571396-2571446	PFSK-1	brain:	n/a
13	chr9:2571396-2571446	LNCaP	prostate:	n/a
14	chr9:2571396-2571446	ovcar-3	ovarian:	n/a
15	chr9:2571396-2571446	GM12892	blood:	n/a
16	chr9:2571396-2571446	HMEC	breast:	n/a
17	chr9:2571396-2571446	PANC-1	pancreas:	n/a
18	chr9:2571396-2571446	GM06990	blood:	n/a
19	chr9:2571396-2571446	Hepatocyte	liver:	n/a
20	chr9:2571396-2571446	NB4	blood:	n/a
21	chr9:2571396-2571446	HRCEpiC	kidney:	n/a
22	chr9:2571396-2571446	CMK	blood:	n/a
23	chr9:2571396-2571446	K562	blood:	n/a
24	chr9:2571396-2571446	A549	lung:	n/a
25	chr9:2571396-2571446	HPAEpiC	pulmonary alveolar:	n/a
26	chr9:2571396-2571446	HCM	heart:	n/a
27	chr9:2571396-2571446	SK-N-SH_RA	brain:	n/a
28	chr9:2571396-2571446	HepG2	liver:	n/a
29	chr9:2571396-2571446	BJ	skin:	n/a
30	chr9:2571396-2571446	AG09319	gingival:	n/a
31	chr9:2571396-2571446	HIPEpiC	eye:	n/a
32	chr9:2571396-2571446	RPTEC	kidney:	n/a
33	chr9:2571396-2571446	HRE	kidney:	n/a
34	chr9:2571396-2571446	Jurkat	blood:	n/a
35	chr9:2571396-2571446	T-47D	breast:	n/a
36	chr9:2571396-2571446	SK-N-SH	brain:	n/a
37	chr9:2571396-2571446	H1-hESC	embryonic stem cell:	embryo
38	chr9:2571396-2571446	AG04450	lung:	fetal
39	chr9:2571396-2571446	GM19239	blood:	n/a
40	chr9:2571396-2571446	HNPCEpiC	eye:	n/a
41	chr9:2571396-2571446	GM12891	blood:	n/a
42	chr9:2571396-2571446	HCF	heart:	n/a
43	chr9:2571396-2571446	MCF10A-Er-Src	breast:	n/a
44	chr9:2571396-2571446	HRPEpiC	eye:	n/a
45	chr9:2571396-2571446	HEEpiC	esophagus:	n/a
46	chr9:2571396-2571446	HCT-116	colon:	n/a
47	chr9:2571396-2571446	MCF-7	breast:	n/a
48	chr9:2571396-2571446	AG09309	skin:	n/a
49	chr9:2571396-2571446	Caco-2	colon:	n/a
50	chr9:2571396-2571446	SKMC	muscle:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2567610..2570420-chr9:2620713..2623138,2	MCF-7	breast:
2	chr9:2549233..2551309-chr9:2562434..2565091,2	K562	blood:
3	chr9:2549233..2551309-chr9:2562434..2565091,2	K562	blood:
4	chr9:2573981..2575628-chr9:2620967..2623639,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-1	chr9:2570622-2570754	ENSG00000236404
2	lnc-KIAA0020-1	chr9:2560622-2560842	l_3727_chr9:2411588-2611526_ovary

No data

Variant related genes	Relation type
ENSG00000236404	TF binding region
ENSG00000236404	CpG island
ENSG00000147852	chromatin interactions
ENSG00000236404	chromatin interactions
ZBTB34	miRNA target sites

Extended variants
information (count: 2242 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2242 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs496896	chr9:2543888-2543889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573940357	chr9:2543893-2543894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543040663	chr9:2543995-2543996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs55755264	chr9:2544000-2544001	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs13284385	chr9:2544001-2544002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs184963483	chr9:2544056-2544057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373450781	chr9:2544060-2544061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188117247	chr9:2544062-2544063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77289359	chr9:2544079-2544080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7048541	chr9:2544091-2544092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs542900372	chr9:2544125-2544126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs180886294	chr9:2544171-2544172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531921900	chr9:2544176-2544177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544557485	chr9:2544249-2544250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs118159373	chr9:2544275-2544276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527351685	chr9:2544298-2544299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547067389	chr9:2544383-2544384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145980992	chr9:2544416-2544417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529889546	chr9:2544417-2544418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147073587	chr9:2544431-2544432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550097444	chr9:2544440-2544441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185685252	chr9:2544442-2544443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74562045	chr9:2544463-2544464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146080950	chr9:2544464-2544465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551763523	chr9:2544484-2544485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116655642	chr9:2544488-2544489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539849175	chr9:2544527-2544528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534215490	chr9:2544531-2544532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561108849	chr9:2544561-2544562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1512709	chr9:2544566-2544567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1512710	chr9:2544583-2544584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs1512711	chr9:2544587-2544588	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs114297935	chr9:2544593-2544594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139810144	chr9:2544602-2544603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1512712	chr9:2544610-2544611	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181674476	chr9:2544621-2544622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560998178	chr9:2544694-2544695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529754708	chr9:2544703-2544704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4740692	chr9:2544707-2544708	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs143166138	chr9:2544773-2544774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557892511	chr9:2544778-2544779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146866143	chr9:2544789-2544790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs601170	chr9:2544794-2544795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187081135	chr9:2544821-2544822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560199857	chr9:2544824-2544825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs118007733	chr9:2544830-2544831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139418043	chr9:2544831-2544832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113760641	chr9:2544851-2544852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117760163	chr9:2544873-2544874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552312329	chr9:2544878-2544879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Schizophrenia	23813976	CNVD
Ovarian cancer	22355333	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2506600-2559200	Weak transcription	Adipose Nuclei	Adipose
2	chr9:2529200-2549800	Weak transcription	Aorta	Aorta
3	chr9:2537200-2556000	Weak transcription	Left Ventricle	heart
4	chr9:2538600-2549800	Weak transcription	Ovary	ovary
5	chr9:2542400-2559200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:2542800-2549200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:2545800-2546600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:2545800-2546600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:2545800-2546600	Enhancers	Brain Anterior Caudate	brain
10	chr9:2545800-2546800	Enhancers	Brain Substantia Nigra	brain
11	chr9:2546000-2546200	Enhancers	Psoas Muscle	Psoas
12	chr9:2546000-2546200	Enhancers	Stomach Mucosa	stomach
13	chr9:2546000-2546600	Enhancers	Brain Hippocampus Middle	brain
14	chr9:2546200-2546400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:2546200-2546800	Enhancers	Brain Angular Gyrus	brain
16	chr9:2546200-2551800	Weak transcription	Psoas Muscle	Psoas
17	chr9:2546400-2547000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:2546600-2550800	Weak transcription	Brain Hippocampus Middle	brain
19	chr9:2547000-2547600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:2549000-2559400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr9:2549200-2549400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr9:2549200-2549600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr9:2549800-2550400	Enhancers	Ovary	ovary
24	chr9:2550400-2556000	Weak transcription	Ovary	ovary
25	chr9:2551800-2552000	Enhancers	Psoas Muscle	Psoas
26	chr9:2556000-2556400	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr9:2556000-2556400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr9:2556000-2556400	Enhancers	Fetal Heart	heart
29	chr9:2556000-2556400	Enhancers	Left Ventricle	heart
30	chr9:2556000-2556400	Enhancers	Ovary	ovary
31	chr9:2556000-2556400	Enhancers	HMEC	breast
32	chr9:2556200-2556600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:2556400-2558400	Weak transcription	Fetal Heart	heart
34	chr9:2556400-2559000	Weak transcription	HMEC	breast
35	chr9:2556400-2559200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr9:2556400-2559200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:2556400-2559200	Weak transcription	Left Ventricle	heart
38	chr9:2556400-2559200	Weak transcription	Ovary	ovary
39	chr9:2556600-2558800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr9:2558200-2559000	Enhancers	A549	lung
41	chr9:2558400-2559200	Enhancers	HSMM	muscle
42	chr9:2558400-2560000	Enhancers	Fetal Heart	heart
43	chr9:2558400-2561200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr9:2558600-2559200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr9:2558600-2559400	Enhancers	NH-A	brain
46	chr9:2558800-2560800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:2558800-2561000	Enhancers	Fetal Lung	lung
48	chr9:2559000-2559200	Enhancers	Brain Substantia Nigra	brain
49	chr9:2559000-2559200	Enhancers	Stomach Smooth Muscle	stomach
50	chr9:2559000-2559200	Enhancers	Osteobl	bone

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