Variant report

Variant	nsv982643
Chromosome Location	chr9:21242163-21262125
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	CTCF	chr9:21253100-21253250	SAEC	small airway:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
2	CTCF	chr9:21253500-21253650	GM06990	blood:	n/a	n/a
3	CTCF	chr9:21253120-21253270	NHDF-neo	bronchial:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
4	CTCF	chr9:21253100-21253250	AG09319	gingival:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
5	CTCF	chr9:21253053-21253274	HepG2	liver:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
6	CTCF	chr9:21253100-21253250	HCT-116	colon:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
7	CTCF	chr9:21251284-21251428	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr9:21253040-21253190	RPTEC	kidney:	n/a	chr9:21253177-21253190
9	CTCF	chr9:21252772-21253516	A549	lung:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
10	CTCF	chr9:21251300-21251450	BE2_C	brain:	n/a	n/a
11	CTCF	chr9:21251255-21251529	GM12878	blood:	n/a	n/a
12	CTCF	chr9:21253111-21253251	GM20000	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
13	CTCF	chr9:21253142-21253225	A549	lung:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
14	CTCF	chr9:21252840-21252990	SAEC	small airway:	n/a	n/a
15	CTCF	chr9:21253065-21253306	Medullo	brain:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
16	CTCF	chr9:21253000-21253150	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr9:21253040-21253190	GM12864	blood:	n/a	chr9:21253177-21253190
18	CTCF	chr9:21253100-21253250	BJ	skin:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
19	CTCF	chr9:21251309-21251455	GM19238	blood:	n/a	n/a
20	CTCF	chr9:21251340-21251490	GM12865	blood:	n/a	n/a
21	CTCF	chr9:21253320-21253470	GM12865	blood:	n/a	n/a
22	CTCF	chr9:21251260-21251410	GM12873	blood:	n/a	n/a
23	CTCF	chr9:21253119-21253224	GM19239	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
24	CTCF	chr9:21253060-21253210	BJ	skin:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
25	CTCF	chr9:21253074-21253278	Gliobla	brain:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
26	CTCF	chr9:21253400-21253550	GM12878	blood:	n/a	n/a
27	CTCF	chr9:21253080-21253230	GM12874	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
28	CTCF	chr9:21253160-21253310	NHDF-neo	bronchial:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
29	CTCF	chr9:21252997-21253239	A549	lung:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
30	CTCF	chr9:21253060-21253210	GM12870	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
31	CTCF	chr9:21253080-21253230	GM12873	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
32	CTCF	chr9:21253080-21253230	GM12871	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
33	CTCF	chr9:21253080-21253230	GM12866	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
34	CTCF	chr9:21253070-21253390	MCF-7	breast:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
35	CTCF	chr9:21253080-21253230	HVMF	connective:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
36	CTCF	chr9:21253071-21253263	GM10248	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
37	CTCF	chr9:21253060-21253210	AoAF	blood vessel:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
38	CTCF	chr9:21253054-21253300	Hela-S3	cervix:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
39	CTCF	chr9:21253424-21253438	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr9:21251380-21251530	GM12864	blood:	n/a	n/a
41	CTCF	chr9:21252880-21253030	WI-38	lung:	n/a	n/a
42	CTCF	chr9:21253435-21253522	GM12892	blood:	n/a	n/a
43	CTCF	chr9:21253120-21253270	GM12801	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
44	CTCF	chr9:21252976-21253425	GM12878	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
45	CTCF	chr9:21251280-21251430	GM12878	blood:	n/a	n/a
46	CTCF	chr9:21253078-21253270	HepG2	liver:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
47	CTCF	chr9:21253240-21253390	HAc	cerebellar:	n/a	n/a
48	CTCF	chr9:21251260-21251410	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr9:21253120-21253270	AG04449	skin:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
50	CTCF	chr9:21251240-21251390	GM12866	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:21253305..21254010-chr9:21318409..21318973,2	MCF-7	breast:

Variant related genes	Relation type
IFNA14	TF binding region

Extended variants
information (count: 476 )
Associated
traits (count: 149 )

Variant overlapped rSNPs/rCNVs (count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190290786	chr9:21242176-21242177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539670681	chr9:21242182-21242183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1411437	chr9:21242249-21242250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs192550028	chr9:21242263-21242264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78361878	chr9:21242292-21242293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555883883	chr9:21242346-21242347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575776970	chr9:21242371-21242372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184895580	chr9:21242438-21242439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558974749	chr9:21242443-21242444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564460767	chr9:21242445-21242446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533467204	chr9:21242447-21242448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144249956	chr9:21242456-21242457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146630620	chr9:21242466-21242467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs57727728	chr9:21242467-21242468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560361603	chr9:21242475-21242476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34993015	chr9:21242490-21242491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs397975904	chr9:21242491-21242492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35775488	chr9:21242492-21242493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34654162	chr9:21242521-21242522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34859431	chr9:21242526-21242527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547916020	chr9:21242575-21242576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567830045	chr9:21242585-21242586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189780722	chr9:21242596-21242597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550308076	chr9:21242599-21242600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180841857	chr9:21242628-21242629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57122438	chr9:21242645-21242646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs57146220	chr9:21242651-21242652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs566699261	chr9:21242657-21242658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138909389	chr9:21242679-21242680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1831390	chr9:21242685-21242686	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs563271328	chr9:21242748-21242749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575813596	chr9:21242757-21242758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544654664	chr9:21242758-21242759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs72691931	chr9:21242779-21242780	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs116116747	chr9:21242827-21242828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1411436	chr9:21242863-21242864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs560398341	chr9:21242866-21242867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529509442	chr9:21242875-21242876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149004498	chr9:21242879-21242880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562695218	chr9:21242891-21242892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530563367	chr9:21242893-21242894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530527471	chr9:21242928-21242929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530525868	chr9:21242941-21242942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367725318	chr9:21242961-21242962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566549183	chr9:21242966-21242967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75020543	chr9:21242972-21242973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374104045	chr9:21242991-21242992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185445467	chr9:21243016-21243017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550348877	chr9:21243018-21243019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546587201	chr9:21243048-21243049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:149)

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
Oral cancer	21386901	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
Breast cancer	21858162	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	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21236200-21244600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:21236400-21244600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:21240200-21244600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:21240400-21245000	Weak transcription	GM12878-XiMat	blood
5	chr9:21240600-21245000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr9:21243200-21243600	Enhancers	Hela-S3	cervix
7	chr9:21244600-21245400	Enhancers	Primary hematopoietic stem cells	blood
8	chr9:21244600-21245400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr9:21244600-21245600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:21244600-21245800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr9:21244600-21245800	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr9:21244600-21246000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
13	chr9:21245000-21245200	Enhancers	GM12878-XiMat	blood
14	chr9:21245000-21245400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr9:21245400-21246000	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr9:21251000-21251200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:21251000-21251200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr9:21251000-21251400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr9:21251000-21251600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr9:21251000-21252000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr9:21251000-21254400	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr9:21251200-21251600	Enhancers	H9 Cell Line	embryonic stem cell
23	chr9:21251200-21251600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr9:21251200-21251600	Enhancers	HepG2	liver
25	chr9:21251200-21251800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr9:21251200-21251800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr9:21251200-21252000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr9:21251200-21252400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr9:21251400-21252800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:21251600-21251800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
31	chr9:21251600-21252800	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr9:21251600-21252800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr9:21251600-21253000	Enhancers	Primary hematopoietic stem cells	blood
34	chr9:21251600-21253200	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr9:21251800-21252000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr9:21251800-21253600	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr9:21251800-21254200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr9:21252000-21252800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr9:21252200-21254000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr9:21252400-21253400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr9:21252600-21253200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr9:21252600-21253600	Enhancers	Adipose Nuclei	Adipose
43	chr9:21252600-21253600	Enhancers	Dnd41	blood
44	chr9:21252800-21253000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr9:21252800-21253000	Bivalent Enhancer	NHLF	lung
46	chr9:21252800-21253200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:21252800-21253200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:21252800-21253600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:21252800-21253600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr9:21252800-21253600	Enhancers	Primary B cells from cord blood	blood

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