Variant report

Variant	nsv892765
Chromosome Location	chr9:22705094-22847961
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	BHLHE40	chr9:22813725-22813875	GM12878	blood:	n/a	n/a
2	CEBPB	chr9:22845462-22845705	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr9:22776317-22776520	A549	lung:	n/a	chr9:22776409-22776418 chr9:22776407-22776418
4	CEBPB	chr9:22799083-22799268	A549	lung:	n/a	n/a
5	CEBPB	chr9:22766124-22766157	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr9:22709513-22709726	A549	lung:	n/a	n/a
7	CEBPB	chr9:22822556-22822741	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:22709428-22709726	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:22810956-22811124	HepG2	liver:	n/a	chr9:22811049-22811062 chr9:22811049-22811062 chr9:22811050-22811061 chr9:22811049-22811062 chr9:22811049-22811060
10	CEBPB	chr9:22776328-22776436	H1-hESC	embryonic stem cell:	n/a	chr9:22776409-22776418 chr9:22776407-22776418
11	CEBPB	chr9:22845556-22845648	IMR90	lung:	n/a	n/a
12	CEBPB	chr9:22776252-22776563	IMR90	lung:	n/a	chr9:22776409-22776418 chr9:22776407-22776418
13	CEBPB	chr9:22709485-22709771	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:22817159-22817473	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:22810946-22811142	IMR90	lung:	n/a	chr9:22811049-22811062 chr9:22811049-22811062 chr9:22811050-22811061 chr9:22811049-22811062 chr9:22811049-22811060
16	CEBPB	chr9:22776272-22776557	HepG2	liver:	n/a	chr9:22776409-22776418 chr9:22776407-22776418
17	CHD2	chr9:22813671-22813837	GM12878	blood:	n/a	n/a
18	CTCF	chr9:22719120-22719270	AG10803	skin:	n/a	n/a
19	CTCF	chr9:22718800-22718950	MCF-7	breast:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
20	CTCF	chr9:22718800-22718950	GM12872	blood:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
21	CTCF	chr9:22813701-22813769	ProgFib	skin:	n/a	chr9:22813711-22813729
22	CTCF	chr9:22717260-22717410	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr9:22813708-22813742	GM13976	blood:	n/a	chr9:22813711-22813729
24	CTCF	chr9:22718780-22718930	HRPEpiC	eye:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
25	CTCF	chr9:22813640-22813790	NHEK	skin:	n/a	chr9:22813711-22813729
26	CTCF	chr9:22717240-22717390	AG09319	gingival:	n/a	n/a
27	CTCF	chr9:22813660-22813810	GM12865	blood:	n/a	chr9:22813711-22813729
28	CTCF	chr9:22718700-22718850	HepG2	liver:	n/a	n/a
29	CTCF	chr9:22813560-22813710	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr9:22813539-22813934	GM12878	blood:	n/a	chr9:22813711-22813729
31	CTCF	chr9:22840640-22840790	GM12869	blood:	n/a	n/a
32	CTCF	chr9:22813627-22813833	LNCaP	prostate:	n/a	chr9:22813711-22813729
33	CTCF	chr9:22813660-22813810	HMEC	breast:	n/a	chr9:22813711-22813729
34	CTCF	chr9:22813640-22813790	MCF-7	breast:	n/a	chr9:22813711-22813729
35	CTCF	chr9:22717220-22717370	AG04450	lung:	n/a	n/a
36	CTCF	chr9:22813640-22813790	AG04449	skin:	n/a	chr9:22813711-22813729
37	CTCF	chr9:22813680-22813830	HPF	lung:	n/a	chr9:22813711-22813729
38	CTCF	chr9:22813664-22813793	HepG2	liver:	n/a	chr9:22813711-22813729
39	CTCF	chr9:22718780-22718930	HMEC	breast:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
40	CTCF	chr9:22813640-22813790	HPF	lung:	n/a	chr9:22813711-22813729
41	CTCF	chr9:22778405-22778427	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr9:22836360-22836510	GM12872	blood:	n/a	n/a
43	CTCF	chr9:22813564-22813573	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr9:22717330-22717462	LNCaP	prostate:	n/a	n/a
45	CTCF	chr9:22717355-22717400	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr9:22813760-22813910	BE2_C	brain:	n/a	n/a
47	CTCF	chr9:22718740-22718890	HPF	lung:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
48	CTCF	chr9:22813660-22813810	Hela-S3	cervix:	n/a	chr9:22813711-22813729
49	CTCF	chr9:22813664-22813801	Pancreas_OC	pancreas:	n/a	chr9:22813711-22813729
50	CTCF	chr9:22718700-22718850	HRE	kidney:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:65596780..65597412-chr9:22707344..22708364,4	MCF-7	breast:
2	chr11:73470070..73470855-chr9:22831107..22832031,2	MCF-7	breast:
3	chr15:65596803..65598452-chr9:22707864..22709364,2	K562	blood:
4	chr15:65596519..65598485-chr9:22707844..22709364,2	MCF-7	breast:
5	chr9:22813272..22814142-chr9:23088887..23089663,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMRTA1-1	chr9:22767961-22768315	ENSG00000224549
2	lnc-DMRTA1-12	chr9:22728286-22728585	NONHSAT130446
3	lnc-DMRTA1-15	chr9:22847494-22847573	NONHSAT130451
4	lnc-DMRTA1-15	chr9:22840524-22841967	NONHSAT130451
5	lnc-DMRTA1-11	chr9:22714322-22715083	NONHSAT130445
6	lnc-DMRTA1-1	chr9:22723308-22723429	NONHSAT130443
7	lnc-DMRTA1-15	chr9:22842077-22844127	NONHSAT130451
8	lnc-DMRTA1-2	chr9:22723308-22723429	ENSG00000234840.1
9	lnc-DMRTA1-1	chr9:22767106-22768486	NONHSAT130449
10	lnc-DMRTA1-1	chr9:22767174-22767265	ENSG00000224549
11	lnc-DMRTA1-2	chr9:22820737-22821597	ENSG00000234840.1
12	lnc-DMRTA1-1	chr9:22767174-22767298	NONHSAT130443
13	lnc-DMRTA1-14	chr9:22759737-22759837	NONHSAT130447
14	lnc-DMRTA1-11	chr9:22715216-22715757	NONHSAT130445
15	lnc-DMRTA1-14	chr9:22754997-22755223	NONHSAT130447
16	lnc-DMRTA1-2	chr9:22823251-22824212	ENSG00000234840.1
17	lnc-DMRTA1-12	chr9:22725718-22725880	NONHSAT130446
18	lnc-DMRTA1-14	chr9:22764211-22764434	NONHSAT130447
19	lnc-DMRTA1-10	chr9:22713308-22713435	l_3742_chr9:22664441-22713435_adipose
20	lnc-DMRTA1-13	chr9:22757174-22757265	NONHSAT130448
21	lnc-DMRTA1-11	chr9:22716040-22716456	NONHSAT130445
22	lnc-DMRTA1-13	chr9:22757961-22758315	NONHSAT130448

Variant related genes	Relation type
ENSG00000236739	TF binding region
ENSG00000224549	TF binding region
ENSG00000200156	chromatin interactions

Extended variants
information (count: 6160 )
Associated
traits (count: 155 )

Variant overlapped rSNPs/rCNVs (count:6160 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533533833	chr9:22705688-22705689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192074700	chr9:22705699-22705700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183197227	chr9:22705701-22705702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553114384	chr9:22705708-22705709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111459094	chr9:22705712-22705713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535170733	chr9:22705747-22705748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555007235	chr9:22705782-22705783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140410195	chr9:22705784-22705785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543779720	chr9:22705785-22705786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142727210	chr9:22705813-22705814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578185738	chr9:22705834-22705835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75687101	chr9:22705853-22705854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560735105	chr9:22705857-22705858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529448404	chr9:22705860-22705861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549506877	chr9:22705862-22705863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575667897	chr9:22705892-22705893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544568574	chr9:22705927-22705928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557872734	chr9:22705947-22705948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200035089	chr9:22705950-22705951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531759473	chr9:22705951-22705952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551715301	chr9:22705954-22705955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570686660	chr9:22705959-22705960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533231554	chr9:22706032-22706033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546522238	chr9:22706061-22706062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566341221	chr9:22706082-22706083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535227963	chr9:22706094-22706095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376654647	chr9:22706128-22706129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113342834	chr9:22706139-22706140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1375290	chr9:22706144-22706145	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs537477637	chr9:22706151-22706152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576220837	chr9:22706161-22706162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112778583	chr9:22706178-22706179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557715474	chr9:22706179-22706180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576715884	chr9:22706182-22706183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139168897	chr9:22706193-22706194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549814868	chr9:22707344-22707345	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145771830	chr9:22707370-22707371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534784463	chr9:22707372-22707373	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554603301	chr9:22707379-22707380	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574494652	chr9:22707388-22707389	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs377668530	chr9:22707403-22707404	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371207667	chr9:22707419-22707420	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376296788	chr9:22707426-22707427	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138694379	chr9:22707472-22707473	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576240546	chr9:22707474-22707475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376612896	chr9:22707476-22707477	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs142693211	chr9:22707482-22707483	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541637557	chr9:22707502-22707503	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556166098	chr9:22707533-22707534	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs367854104	chr9:22707544-22707545	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:155)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Cancer	20581869	CNVD
Oral cancer	22144094	CNVD
Barrett''s syndrome	19417022	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	17237825	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22705600-22706200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:22712800-22713200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:22716800-22717600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr9:22721000-22722600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:22722000-22722800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:22722200-22724200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr9:22722400-22723000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr9:22722600-22722800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:22722800-22723800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:22722800-22724000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr9:22723000-22724000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:22723800-22725800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr9:22724000-22724200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr9:22724000-22724800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr9:22724800-22725400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:22725400-22725800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:22725800-22739800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:22725800-22801600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:22731200-22732200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr9:22731600-22732000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:22738800-22778800	Weak transcription	Liver	Liver
22	chr9:22739800-22740200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr9:22739800-22740600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:22740600-22742600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr9:22742600-22742800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr9:22749200-22749400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr9:22755000-22755400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr9:22763800-22803600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:22767600-22770200	Weak transcription	Adipose Nuclei	Adipose
30	chr9:22770400-22770800	Enhancers	Fetal Brain Male	brain
31	chr9:22770600-22771000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr9:22770800-22771000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:22770800-22771200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr9:22771000-22773400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr9:22771200-22773200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr9:22772800-22773000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr9:22773000-22774200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr9:22773200-22774200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr9:22773400-22774200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr9:22773400-22774400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr9:22773600-22774200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr9:22773800-22774200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr9:22791800-22792600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr9:22792200-22792600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr9:22792200-22792600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr9:22792200-22792800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr9:22792200-22793400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr9:22794400-22794600	Bivalent Enhancer	Left Ventricle	heart
49	chr9:22797600-22803800	Weak transcription	Liver	Liver
50	chr9:22803600-22805000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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