Variant report

Variant	nsv43
Chromosome Location	chr9:6651440-6672988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:450)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6664541-6665413	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6667619-6667991	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6667709-6667966	K562	blood:	n/a	n/a
4	ATF2	chr9:6654995-6655416	GM12878	blood:	n/a	n/a
5	ATF2	chr9:6654912-6655463	GM12878	blood:	n/a	n/a
6	ATF3	chr9:6664294-6664873	A549	lung:	n/a	n/a
7	ATF3	chr9:6664488-6664934	A549	lung:	n/a	n/a
8	BACH1	chr9:6667638-6667964	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:6656332-6656632	GM12878	blood:	n/a	n/a
10	BATF	chr9:6655058-6655371	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:6655034-6655412	GM12878	blood:	n/a	n/a
12	BCL3	chr9:6664480-6665034	A549	lung:	n/a	n/a
13	BCL3	chr9:6664426-6665297	A549	lung:	n/a	chr9:6665033-6665042
14	BCLAF1	chr9:6667616-6668061	GM12878	blood:	n/a	n/a
15	BCLAF1	chr9:6654844-6655458	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:6664329-6665171	HepG2	liver:	n/a	n/a
17	BHLHE40	chr9:6654915-6655315	GM12878	blood:	n/a	n/a
18	BRCA1	chr9:6664596-6664874	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr9:6664464-6664732	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:6664643-6664861	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:6664589-6665192	A549	lung:	n/a	n/a
22	CEBPB	chr9:6664551-6665250	A549	lung:	n/a	n/a
23	CEBPB	chr9:6658750-6659166	HepG2	liver:	n/a	chr9:6658871-6658882
24	CEBPB	chr9:6652027-6652178	A549	lung:	n/a	n/a
25	CEBPB	chr9:6664453-6665284	A549	lung:	n/a	n/a
26	CEBPB	chr9:6658601-6659127	A549	lung:	n/a	chr9:6658871-6658882
27	CEBPB	chr9:6664574-6665059	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr9:6658721-6659242	A549	lung:	n/a	chr9:6658871-6658882
29	CEBPB	chr9:6657074-6657184	K562	blood:	n/a	n/a
30	CEBPB	chr9:6664492-6665376	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:6672379-6672395	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr9:6664576-6665291	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:6658749-6659061	IMR90	lung:	n/a	chr9:6658871-6658882
34	CEBPB	chr9:6658728-6659036	K562	blood:	n/a	chr9:6658871-6658882
35	CEBPB	chr9:6662560-6662584	K562	blood:	n/a	n/a
36	CEBPB	chr9:6658722-6659320	MCF-7	breast:	n/a	chr9:6658871-6658882
37	CEBPB	chr9:6664875-6665208	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:6654850-6655851	GM12878	blood:	n/a	n/a
39	CEBPB	chr9:6664583-6664967	MCF-7	breast:	n/a	n/a
40	CEBPB	chr9:6664533-6665234	MCF-7	breast:	n/a	n/a
41	CEBPB	chr9:6662460-6662719	HepG2	liver:	n/a	chr9:6662551-6662562
42	CEBPB	chr9:6664587-6665287	HepG2	liver:	n/a	n/a
43	CEBPD	chr9:6664550-6665175	HepG2	liver:	n/a	n/a
44	CEBPD	chr9:6664675-6665149	HepG2	liver:	n/a	n/a
45	CEBPZ	chr9:6664872-6665103	HepG2	liver:	n/a	n/a
46	CHD2	chr9:6664463-6664849	HepG2	liver:	n/a	n/a
47	CHD2	chr9:6664515-6664915	Hela-S3	cervix:	n/a	n/a
48	CREB1	chr9:6664582-6664891	A549	lung:	n/a	n/a
49	CREB1	chr9:6654862-6655412	GM12878	blood:	n/a	n/a
50	CREB1	chr9:6664317-6665332	HepG2	liver:	n/a	n/a

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6652273..6654630-chr9:6673766..6675385,2	MCF-7	breast:
2	chr9:6654607..6656764-chr9:6663214..6664911,2	K562	blood:
3	chr9:6643546..6649129-chr9:6652921..6657149,5	MCF-7	breast:
4	chr9:6523722..6524445-chr9:6667595..6668159,2	K562	blood:
5	chr9:6585232..6587306-chr9:6664888..6666750,2	MCF-7	breast:
6	chr9:6654607..6656764-chr9:6663214..6664911,2	K562	blood:
7	chr9:6672368..6674682-chr9:6676645..6678823,3	MCF-7	breast:
8	chr9:6662765..6664429-chr9:6666367..6668579,2	MCF-7	breast:
9	chr9:6644301..6646741-chr9:6667847..6669482,2	MCF-7	breast:
10	chr9:6656639..6659482-chr9:6662780..6664665,3	MCF-7	breast:
11	chr9:6663663..6666675-chr9:6715678..6718421,3	MCF-7	breast:
12	chr9:6584834..6585802-chr9:6667386..6668426,5	MCF-7	breast:
13	chr9:6663029..6667664-chr9:6679639..6683357,9	MCF-7	breast:
14	chr9:6667615..6669315-chr9:6679006..6681464,2	K562	blood:
15	chr9:6641084..6643158-chr9:6652442..6654682,2	MCF-7	breast:
16	chr9:6662765..6664429-chr9:6666367..6668579,2	MCF-7	breast:
17	chr9:6656639..6659482-chr9:6662780..6664665,3	MCF-7	breast:
18	chr9:6665749..6668244-chr9:6673822..6675444,2	MCF-7	breast:
19	chr9:6354241..6354767-chr9:6667295..6668097,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-14	chr9:6661651-6661936	NONHSAT130147
2	lnc-KDM4C-5	chr9:6669544-6669728	NONHSAT130145
3	lnc-KDM4C-5	chr9:6669544-6669728	ENSG00000236924.1
4	lnc-KDM4C-14	chr9:6661291-6661345	NONHSAT130146
5	lnc-KDM4C-13	chr9:6663156-6663366	NONHSAT130148
6	lnc-KDM4C-5	chr9:6670425-6670690	NONHSAT130145
7	lnc-KDM4C-13	chr9:6663657-6663792	NONHSAT130148
8	lnc-KDM4C-13	chr9:6662424-6662810	NONHSAT130148
9	lnc-KDM4C-14	chr9:6660407-6661044	NONHSAT130146
10	lnc-KDM4C-5	chr9:6670425-6670635	ENSG00000236924.1
11	lnc-KDM4C-14	chr9:6661783-6661845	NONHSAT130146

No data

Variant related genes	Relation type
RNF2P1	TF binding region
RN7SL123P	TF binding region
ENSG00000232946	TF binding region
ENSG00000229057	TF binding region
ENSG00000178445	chromatin interactions
ENSG00000232946	chromatin interactions
ENSG00000236924	chromatin interactions
ENSG00000225489	chromatin interactions

Extended variants
information (count: 1221 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1138718	chr9:6651474-6651475	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs4742235	chr9:6651494-6651495	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs543910053	chr9:6651500-6651501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185621111	chr9:6651521-6651522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113669927	chr9:6651527-6651528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547146278	chr9:6651550-6651551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2578284	chr9:6651552-6651553	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs10975713	chr9:6651564-6651565	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs527589658	chr9:6651577-6651578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182479866	chr9:6651579-6651580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570445904	chr9:6651583-6651584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199999725	chr9:6651643-6651644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571203625	chr9:6651644-6651645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544335499	chr9:6651645-6651646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373645597	chr9:6651646-6651647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552780929	chr9:6651663-6651664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565786279	chr9:6651679-6651680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35892889	chr9:6651684-6651685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs28626232	chr9:6651722-6651723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535526723	chr9:6651731-6651732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553990113	chr9:6651788-6651789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112377251	chr9:6651813-6651814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7853600	chr9:6651814-6651815	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs186548283	chr9:6651857-6651858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75522518	chr9:6651860-6651861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576403881	chr9:6651865-6651866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35119187	chr9:6651878-6651879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs2438412	chr9:6651947-6651948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs574100646	chr9:6651959-6651960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541493827	chr9:6651960-6651961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2438411	chr9:6651979-6651980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs527450543	chr9:6651997-6651998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552522728	chr9:6652070-6652071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs60308809	chr9:6652085-6652086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112678973	chr9:6652086-6652087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547345714	chr9:6652093-6652094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397957535	chr9:6652097-6652098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564253185	chr9:6652100-6652101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116347590	chr9:6652122-6652123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375931389	chr9:6652139-6652140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189110216	chr9:6652184-6652185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555267962	chr9:6652197-6652198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150920058	chr9:6652220-6652221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535179761	chr9:6652244-6652245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181255574	chr9:6652245-6652246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113472782	chr9:6652252-6652253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539613639	chr9:6652276-6652277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560764045	chr9:6652279-6652280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs35387949	chr9:6652335-6652336	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs552453677	chr9:6652336-6652337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	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
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6646600-6656800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:6646800-6657000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:6647000-6656600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:6647600-6654600	Weak transcription	GM12878-XiMat	blood
5	chr9:6648000-6656600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr9:6648200-6653800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr9:6648200-6670400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr9:6648400-6658200	Weak transcription	A549	lung
9	chr9:6648400-6669400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr9:6648400-6680400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr9:6648600-6652800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr9:6648600-6653600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr9:6648600-6656600	Weak transcription	Liver	Liver
14	chr9:6648600-6677600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr9:6648600-6680400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr9:6648800-6680400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr9:6649600-6651600	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:6649800-6652600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr9:6649800-6656600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:6649800-6664200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:6650000-6657000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr9:6650000-6658400	Weak transcription	HepG2	liver
23	chr9:6651600-6652800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr9:6652600-6654200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
25	chr9:6652800-6653200	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr9:6652800-6654000	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr9:6653200-6656800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr9:6653600-6654000	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr9:6654000-6656600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr9:6654000-6669400	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr9:6654200-6656600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr9:6654600-6654800	Enhancers	GM12878-XiMat	blood
33	chr9:6654800-6655200	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr9:6654800-6655400	Enhancers	Primary B cells from peripheral blood	blood
35	chr9:6654800-6655600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr9:6654800-6655600	Enhancers	Fetal Thymus	thymus
37	chr9:6654800-6655800	Enhancers	Dnd41	blood
38	chr9:6654800-6656000	Flanking Active TSS	GM12878-XiMat	blood
39	chr9:6655000-6655200	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr9:6655000-6655200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr9:6655000-6655200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr9:6655000-6655200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr9:6655000-6655800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
44	chr9:6656000-6656400	Enhancers	GM12878-XiMat	blood
45	chr9:6656400-6656600	Flanking Active TSS	GM12878-XiMat	blood
46	chr9:6656600-6656800	Genic enhancers	HUES6 Cell Line	embryonic stem cell
47	chr9:6656600-6656800	Enhancers	GM12878-XiMat	blood
48	chr9:6656600-6657200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr9:6656600-6657200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:6656600-6657400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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