Variant report

Variant	nsv917221
Chromosome Location	chr9:12074177-12424254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:618)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:12328968-12329168	HepG2	liver:	n/a	n/a
2	BACH1	chr9:12170667-12170713	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:12292536-12292567	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr9:12230772-12231081	GM12878	blood:	n/a	n/a
5	BATF	chr9:12329455-12329670	GM12878	blood:	n/a	n/a
6	BCLAF1	chr9:12329426-12329668	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:12328995-12329158	K562	blood:	n/a	n/a
8	BHLHE40	chr9:12328884-12329725	HepG2	liver:	n/a	n/a
9	BHLHE40	chr9:12414650-12414651	HepG2	liver:	n/a	n/a
10	BHLHE40	chr9:12329021-12329257	GM12878	blood:	n/a	n/a
11	BRCA1	chr9:12368889-12368916	GM12878	blood:	n/a	n/a
12	CEBPB	chr9:12129071-12129335	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:12195470-12195708	H1-hESC	embryonic stem cell:	n/a	chr9:12195611-12195622
14	CEBPB	chr9:12180768-12180970	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:12208833-12209071	HepG2	liver:	n/a	chr9:12208898-12208909 chr9:12208899-12208908 chr9:12208897-12208910
16	CEBPB	chr9:12195471-12195788	IMR90	lung:	n/a	chr9:12195611-12195622
17	CEBPB	chr9:12195488-12195695	K562	blood:	n/a	chr9:12195611-12195622
18	CEBPB	chr9:12193945-12194181	A549	lung:	n/a	chr9:12194071-12194082 chr9:12194071-12194084
19	CEBPB	chr9:12195456-12195797	HepG2	liver:	n/a	chr9:12195611-12195622
20	CEBPB	chr9:12288039-12288167	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:12367335-12367535	HepG2	liver:	n/a	chr9:12367443-12367454
22	CEBPB	chr9:12119993-12120079	A549	lung:	n/a	chr9:12120059-12120068 chr9:12120057-12120070 chr9:12120057-12120068
23	CHD1	chr9:12314638-12314797	GM12878	blood:	n/a	n/a
24	CHD2	chr9:12314733-12314838	GM12878	blood:	n/a	n/a
25	CHD2	chr9:12319226-12319370	GM12878	blood:	n/a	n/a
26	CTCF	chr9:12329500-12329650	AG04450	lung:	n/a	n/a
27	CTCF	chr9:12329460-12329610	BE2_C	brain:	n/a	n/a
28	CTCF	chr9:12329500-12329650	HepG2	liver:	n/a	n/a
29	CTCF	chr9:12329480-12329630	NB4	blood:	n/a	n/a
30	CTCF	chr9:12329442-12329697	Medullo	brain:	n/a	n/a
31	CTCF	chr9:12329390-12329697	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr9:12329500-12329650	K562	blood:	n/a	n/a
33	CTCF	chr9:12329480-12329630	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr9:12329425-12329701	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:12329460-12329610	HCT-116	colon:	n/a	n/a
36	CTCF	chr9:12215488-12215552	GM13977	blood:	n/a	n/a
37	CTCF	chr9:12329500-12329650	HL-60	blood:	n/a	n/a
38	CTCF	chr9:12329500-12329650	GM12864	blood:	n/a	n/a
39	CTCF	chr9:12329480-12329630	GM06990	blood:	n/a	n/a
40	CTCF	chr9:12329120-12329270	GM12866	blood:	n/a	n/a
41	CTCF	chr9:12329480-12329630	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr9:12329500-12329650	SAEC	small airway:	n/a	n/a
43	CTCF	chr9:12329520-12329670	GM12871	blood:	n/a	n/a
44	CTCF	chr9:12329371-12329713	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:12195600-12195750	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr9:12329480-12329630	RPTEC	kidney:	n/a	n/a
47	CTCF	chr9:12329440-12329590	AG09309	skin:	n/a	n/a
48	CTCF	chr9:12329436-12329697	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr9:12329520-12329670	GM12878	blood:	n/a	n/a
50	CTCF	chr9:12329322-12329716	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr18:21570976..21573123-chr9:12145530..12147030,2	MCF-7	breast:
2	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
3	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
4	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
5	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
6	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
7	chr6:116381055..116381867-chr9:12405688..12406208,2	Hela-S3	cervix:
8	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
9	chr16:89002000..89004763-chr9:12244429..12246932,2	MCF-7	breast:
10	chr9:10365979..10366914-chr9:12329143..12329893,2	MCF-7	breast:
11	chr9:10855828..10856443-chr9:12329128..12329639,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-2	chr9:12139007-12139044	XLOC_007648
2	lnc-MPDZ-2	chr9:12146273-12146401	XLOC_007648
3	lnc-MPDZ-9	chr9:12149117-12149147	NONHSAT130219
4	lnc-MPDZ-9	chr9:12136273-12136401	NONHSAT130219
5	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648
6	lnc-MPDZ-9	chr9:12088660-12089015	NONHSAT130219
7	lnc-MPDZ-2	chr9:12098660-12099015	XLOC_007648
8	lnc-MPDZ-2	chr9:12159117-12159147	XLOC_007648
9	lnc-TYRP1-4	chr9:12287320-12288238	NONHSAT130222
10	lnc-MPDZ-9	chr9:12106821-12106865	NONHSAT130219
11	lnc-MPDZ-2	chr9:12098714-12099015	XLOC_007648
12	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648

No data

Variant related genes	Relation type
ENSG00000231491	TF binding region
ENSG00000224935	TF binding region
RNU2-47P	TF binding region
ENSG00000168234	chromatin interactions
ENSG00000261226	chromatin interactions

Extended variants
information (count: 5553 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:5553 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370688565	chr9:12076416-12076417	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs571072043	chr9:12076453-12076454	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs571911988	chr9:12076468-12076469	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs540706148	chr9:12076479-12076480	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs536848472	chr9:12076486-12076487	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs12380894	chr9:12076490-12076491	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs7863896	chr9:12076500-12076501	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs7863909	chr9:12076517-12076518	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs374423502	chr9:12076522-12076523	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs9694981	chr9:12076542-12076543	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs556806856	chr9:12076548-12076549	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs28542029	chr9:12076552-12076553	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs28709961	chr9:12076558-12076559	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs537651727	chr9:12076592-12076593	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs557542520	chr9:12076609-12076610	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs536316990	chr9:12076618-12076619	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs553368235	chr9:12076621-12076622	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs573135125	chr9:12076645-12076646	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs541355738	chr9:12076648-12076649	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs529655897	chr9:12076750-12076751	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs566094983	chr9:12076758-12076759	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs202169114	chr9:12076762-12076763	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs557637094	chr9:12076766-12076767	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs577465823	chr9:12076781-12076782	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs542545077	chr9:12076783-12076784	Flanking Bivalent TSS/Enh Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs114142463	chr9:12088660-12088661	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs75252818	chr9:12088680-12088681	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs571778127	chr9:12088684-12088685	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs150099711	chr9:12088688-12088689	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs377410314	chr9:12088693-12088694	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs138375921	chr9:12088715-12088716	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs116441762	chr9:12088744-12088745	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs544100635	chr9:12088758-12088759	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs563933328	chr9:12088785-12088786	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs529529498	chr9:12088804-12088805	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs190645305	chr9:12088822-12088823	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs80029364	chr9:12088831-12088832	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs117532771	chr9:12088856-12088857	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs551527126	chr9:12088859-12088860	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs201964788	chr9:12088865-12088866	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs200007104	chr9:12088867-12088868	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs200952415	chr9:12088868-12088869	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs181744627	chr9:12088877-12088878	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs527252020	chr9:12088886-12088887	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs571613716	chr9:12088894-12088895	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs536998082	chr9:12088901-12088902	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs149233908	chr9:12088922-12088923	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs554348196	chr9:12088932-12088933	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs569579994	chr9:12088962-12088963	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs375525840	chr9:12088978-12088979	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Disorders of sex development	21048976	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
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Chordoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12076400-12076600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
2	chr9:12076400-12076800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:12076600-12076800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
4	chr9:12091200-12096400	Enhancers	Placenta Amnion	Placenta Amnion
5	chr9:12091600-12092600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:12091800-12092200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr9:12092600-12096200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:12096200-12096400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr9:12096400-12101600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:12101600-12102200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:12101600-12102400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr9:12101800-12102800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:12102400-12104200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr9:12104200-12104400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr9:12135800-12137400	Enhancers	Fetal Heart	heart
16	chr9:12137600-12138400	Enhancers	Placenta Amnion	Placenta Amnion
17	chr9:12137800-12138200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr9:12139800-12142600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr9:12142400-12144000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:12155400-12156200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr9:12156200-12161400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr9:12161400-12167200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr9:12161600-12164800	Enhancers	Brain Germinal Matrix	brain
24	chr9:12162200-12162400	Active TSS	Brain Anterior Caudate	brain
25	chr9:12162200-12162600	Active TSS	Brain Angular Gyrus	brain
26	chr9:12162200-12162800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr9:12162200-12163200	Enhancers	Fetal Brain Female	brain
28	chr9:12162400-12162600	Flanking Active TSS	Brain Anterior Caudate	brain
29	chr9:12162400-12162600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr9:12162400-12162800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr9:12162400-12163000	Enhancers	Brain Hippocampus Middle	brain
32	chr9:12162600-12162800	Enhancers	Brain Anterior Caudate	brain
33	chr9:12162600-12163000	Enhancers	Brain Angular Gyrus	brain
34	chr9:12162600-12163400	Enhancers	Fetal Brain Male	brain
35	chr9:12162800-12166400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr9:12162800-12166600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:12163200-12164000	Weak transcription	Fetal Brain Female	brain
38	chr9:12164000-12164200	Enhancers	Fetal Brain Female	brain
39	chr9:12164200-12166200	Weak transcription	Fetal Brain Female	brain
40	chr9:12165800-12166400	Enhancers	Brain Substantia Nigra	brain
41	chr9:12166200-12166400	Enhancers	Fetal Brain Female	brain
42	chr9:12166400-12167000	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr9:12166600-12167000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr9:12191600-12192000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr9:12191600-12192000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr9:12191800-12192000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr9:12192000-12200800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:12200400-12200600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:12200400-12200800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr9:12200400-12202000	Enhancers	Placenta Amnion	Placenta Amnion

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