Variant report

Variant	nsv892557
Chromosome Location	chr9:12168247-12663561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	chr9:12567176-12567212	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:12653013-12653212	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:12469180-12469392	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:12465730-12465736	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:12497880-12498136	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:12292536-12292567	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:12170667-12170713	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:12604207-12604421	H1-hESC	embryonic stem cell:	n/a	chr9:12604278-12604292
10	BATF	chr9:12329455-12329670	GM12878	blood:	n/a	n/a
11	BATF	chr9:12230772-12231081	GM12878	blood:	n/a	n/a
12	BCLAF1	chr9:12329426-12329668	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:12414650-12414651	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:12329021-12329257	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:12612186-12612202	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:12328884-12329725	HepG2	liver:	n/a	n/a
17	BHLHE40	chr9:12328995-12329158	K562	blood:	n/a	n/a
18	BRCA1	chr9:12368889-12368916	GM12878	blood:	n/a	n/a
19	CEBPB	chr9:12503775-12504054	MCF-7	breast:	n/a	chr9:12503986-12503998
20	CEBPB	chr9:12180768-12180970	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:12539775-12539867	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:12447534-12447781	A549	lung:	n/a	chr9:12447635-12447646
23	CEBPB	chr9:12503780-12504174	MCF-7	breast:	n/a	chr9:12503986-12503998
24	CEBPB	chr9:12491079-12491286	A549	lung:	n/a	n/a
25	CEBPB	chr9:12537944-12538164	HepG2	liver:	n/a	chr9:12538015-12538032 chr9:12537992-12538003 chr9:12538016-12538029
26	CEBPB	chr9:12208833-12209071	HepG2	liver:	n/a	chr9:12208898-12208909 chr9:12208899-12208908 chr9:12208897-12208910
27	CEBPB	chr9:12607448-12607767	HepG2	liver:	n/a	chr9:12607616-12607627 chr9:12607571-12607582
28	CEBPB	chr9:12607483-12607778	IMR90	lung:	n/a	chr9:12607616-12607627 chr9:12607571-12607582
29	CEBPB	chr9:12447570-12447769	H1-hESC	embryonic stem cell:	n/a	chr9:12447635-12447646
30	CEBPB	chr9:12195456-12195797	HepG2	liver:	n/a	chr9:12195611-12195622
31	CEBPB	chr9:12473238-12473507	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:12537932-12538011	K562	blood:	n/a	chr9:12537992-12538003
33	CEBPB	chr9:12656839-12657163	K562	blood:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
34	CEBPB	chr9:12473244-12473438	A549	lung:	n/a	n/a
35	CEBPB	chr9:12656816-12657170	A549	lung:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
36	CEBPB	chr9:12450499-12450835	HepG2	liver:	n/a	chr9:12450652-12450663
37	CEBPB	chr9:12553870-12554030	IMR90	lung:	n/a	chr9:12553921-12553932 chr9:12553919-12553930
38	CEBPB	chr9:12553807-12553971	HepG2	liver:	n/a	chr9:12553921-12553932 chr9:12553919-12553930
39	CEBPB	chr9:12656840-12657079	H1-hESC	embryonic stem cell:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
40	CEBPB	chr9:12195471-12195788	IMR90	lung:	n/a	chr9:12195611-12195622
41	CEBPB	chr9:12447528-12447785	HepG2	liver:	n/a	chr9:12447635-12447646
42	CEBPB	chr9:12656859-12657130	Hela-S3	cervix:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
43	CEBPB	chr9:12447532-12447761	IMR90	lung:	n/a	chr9:12447635-12447646
44	CEBPB	chr9:12288039-12288167	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:12195470-12195708	H1-hESC	embryonic stem cell:	n/a	chr9:12195611-12195622
46	CEBPB	chr9:12367335-12367535	HepG2	liver:	n/a	chr9:12367443-12367454
47	CEBPB	chr9:12643730-12643980	IMR90	lung:	n/a	n/a
48	CEBPB	chr9:12656603-12657162	IMR90	lung:	n/a	chr9:12656979-12656988 chr9:12656681-12656694 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656681-12656692 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988 chr9:12656681-12656694
49	CEBPB	chr9:12195488-12195695	K562	blood:	n/a	chr9:12195611-12195622
50	CEBPB	chr9:12193945-12194181	A549	lung:	n/a	chr9:12194071-12194082 chr9:12194071-12194084

No.	Distal block	Cell Line	Cell type
1	chr1:149223798..149224416-chr9:12526808..12527328,4	MCF-7	breast:
2	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
3	chr9:12554435..12555308-chr9:12639713..12640600,2	MCF-7	breast:
4	chr9:12631997..12633907-chr9:12634270..12637039,2	MCF-7	breast:
5	chr9:12494239..12495105-chr9:12503977..12504835,2	MCF-7	breast:
6	chr9:12631997..12633907-chr9:12634270..12637039,2	MCF-7	breast:
7	chr9:12495478..12497603-chr9:12499554..12502350,2	MCF-7	breast:
8	chr9:12615022..12617476-chr9:12617492..12619010,2	MCF-7	breast:
9	chr6:116381055..116381867-chr9:12405688..12406208,2	Hela-S3	cervix:
10	chr9:10365979..10366914-chr9:12329143..12329893,2	MCF-7	breast:
11	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
12	chr9:12526692..12528486-chr9:12531576..12533111,2	MCF-7	breast:
13	chr9:12494239..12495105-chr9:12503977..12504835,2	MCF-7	breast:
14	chr16:89002000..89004763-chr9:12244429..12246932,2	MCF-7	breast:
15	chr9:10855600..10856394-chr9:12425953..12426703,2	MCF-7	breast:
16	chr9:10855828..10856443-chr9:12329128..12329639,2	MCF-7	breast:
17	chr1:186649939..186650766-chr9:12429991..12430491,2	Hela-S3	cervix:
18	chr9:12554435..12555308-chr9:12639713..12640600,2	MCF-7	breast:
19	chr9:12526692..12528486-chr9:12531576..12533111,2	MCF-7	breast:
20	chr8:43095234..43095797-chr9:12480274..12480774,2	MCF-7	breast:
21	chr9:12425929..12426463-chr9:12464660..12465379,2	MCF-7	breast:
22	chr9:12607055..12609983-chr9:12671838..12674027,2	K562	blood:
23	chr9:12495478..12497603-chr9:12499554..12502350,2	MCF-7	breast:
24	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
25	chr9:12425929..12426463-chr9:12464660..12465379,2	MCF-7	breast:
26	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
27	chr9:12615022..12617476-chr9:12617492..12619010,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TYRP1-4	chr9:12287320-12288238	NONHSAT130222

Variant related genes	Relation type
ENSG00000231491	TF binding region
RNU2-47P	TF binding region
ENSG00000206737	chromatin interactions
ENSG00000261226	chromatin interactions

Extended variants
information (count: 8198 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:8198 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530723352	chr9:12191627-12191628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370654167	chr9:12191668-12191669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76868631	chr9:12191669-12191670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149255233	chr9:12191689-12191690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535507791	chr9:12191721-12191722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548035227	chr9:12191770-12191771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566055045	chr9:12191800-12191801	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs148390320	chr9:12191814-12191815	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs79925374	chr9:12191823-12191824	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs200386355	chr9:12191867-12191868	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs373178099	chr9:12191914-12191915	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs192674764	chr9:12191966-12191967	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs117067593	chr9:12191987-12191988	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs141797904	chr9:12192031-12192032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371310818	chr9:12192090-12192091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73645899	chr9:12192101-12192102	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs559367448	chr9:12192155-12192156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528175009	chr9:12192166-12192167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184751750	chr9:12192180-12192181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544762957	chr9:12192216-12192217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564727689	chr9:12192219-12192220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529086001	chr9:12192235-12192236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572491120	chr9:12192254-12192255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377750425	chr9:12192268-12192269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550827715	chr9:12192281-12192282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189151999	chr9:12192282-12192283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529251232	chr9:12192284-12192285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112609742	chr9:12192294-12192295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549128911	chr9:12192306-12192307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566134288	chr9:12192319-12192320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368697629	chr9:12192386-12192387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191376838	chr9:12192400-12192401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10809716	chr9:12192428-12192429	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs559509612	chr9:12192443-12192444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34362505	chr9:12192447-12192448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571867494	chr9:12192472-12192473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539046965	chr9:12192501-12192502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549789236	chr9:12192514-12192515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1339271	chr9:12192576-12192577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs557619672	chr9:12192616-12192617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10121149	chr9:12192641-12192642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs536196340	chr9:12192663-12192664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183499378	chr9:12192672-12192673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552702424	chr9:12192686-12192687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572543318	chr9:12192691-12192692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140540041	chr9:12192695-12192696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10115100	chr9:12192697-12192698	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs189975436	chr9:12192712-12192713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144384384	chr9:12192715-12192716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200875772	chr9:12192719-12192720	Weak transcription	n/a	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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12191600-12192000	Enhancers	H1 Cell Line	embryonic stem cell
2	chr9:12191600-12192000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:12191800-12192000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:12192000-12200800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:12200400-12200600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:12200400-12200800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr9:12200400-12202000	Enhancers	Placenta Amnion	Placenta Amnion
8	chr9:12200600-12201000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr9:12200800-12201200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:12201200-12204400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:12204400-12204800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr9:12212600-12213000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr9:12212600-12213600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:12212800-12214000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr9:12213000-12213400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:12213000-12213800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr9:12213400-12214200	Enhancers	Brain Germinal Matrix	brain
18	chr9:12213400-12214400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:12213800-12214200	Enhancers	Brain Hippocampus Middle	brain
20	chr9:12221800-12222000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr9:12222000-12224400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:12224200-12224600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr9:12224200-12225000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr9:12224200-12225000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr9:12224400-12224800	Enhancers	H9 Cell Line	embryonic stem cell
26	chr9:12224400-12224800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:12231000-12231400	Enhancers	Liver	Liver
28	chr9:12231200-12231600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr9:12231400-12233400	Weak transcription	Liver	Liver
30	chr9:12231600-12232000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr9:12233400-12233800	Enhancers	Liver	Liver
32	chr9:12235200-12235600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:12241200-12242000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr9:12241400-12243200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr9:12241600-12242000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr9:12241600-12242000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr9:12241600-12242000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr9:12241600-12242000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr9:12241600-12242000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr9:12242600-12242800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
41	chr9:12260800-12261200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr9:12271200-12271600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr9:12271200-12274800	Enhancers	Rectal Smooth Muscle	rectum
44	chr9:12271200-12275200	Enhancers	Fetal Brain Male	brain
45	chr9:12271400-12271600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr9:12271400-12272000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:12271400-12273400	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr9:12271600-12272000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr9:12271600-12272000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr9:12271600-12272600	Enhancers	Duodenum Smooth Muscle	Duodenum

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