Variant report

Variant	nsv972306
Chromosome Location	chr9:33486353-33510883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:123)
Chromatin interactive
region (count:14)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:33498536-33498621	HepG2	liver:	n/a	n/a
2	ATF1	chr9:33506843-33506851	K562	blood:	n/a	n/a
3	BCL3	chr9:33510744-33511217	A549	lung:	n/a	chr9:33511190-33511203 chr9:33511193-33511202 chr9:33511190-33511199 chr9:33511200-33511209 chr9:33511191-33511204
4	BCL3	chr9:33506443-33507117	A549	lung:	n/a	chr9:33506842-33506851 chr9:33506843-33506852
5	BHLHE40	chr9:33506540-33506851	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:33510872-33511152	K562	blood:	n/a	n/a
7	BHLHE40	chr9:33493918-33494118	K562	blood:	n/a	chr9:33494026-33494035 chr9:33494026-33494035 chr9:33494024-33494037
8	BHLHE40	chr9:33506198-33506848	HepG2	liver:	n/a	n/a
9	BHLHE40	chr9:33506283-33506904	A549	lung:	n/a	n/a
10	BHLHE40	chr9:33506282-33506909	K562	blood:	n/a	n/a
11	BRCA1	chr9:33506711-33507243	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr9:33510862-33511278	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:33506554-33506944	A549	lung:	n/a	n/a
14	CEBPB	chr9:33506593-33507297	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:33510321-33510641	K562	blood:	n/a	n/a
16	CEBPB	chr9:33497035-33497155	HepG2	liver:	n/a	n/a
17	CEBPB	chr9:33510260-33510524	A549	lung:	n/a	n/a
18	CEBPB	chr9:33510357-33510612	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:33490169-33490224	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:33510360-33510613	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:33489173-33489436	IMR90	lung:	n/a	n/a
22	CEBPB	chr9:33506550-33506932	A549	lung:	n/a	n/a
23	CEBPB	chr9:33506528-33507255	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr9:33496971-33497083	IMR90	lung:	n/a	n/a
25	CEBPB	chr9:33510380-33510611	A549	lung:	n/a	n/a
26	CEBPB	chr9:33506544-33506862	A549	lung:	n/a	n/a
27	CEBPB	chr9:33506580-33506924	MCF-7	breast:	n/a	n/a
28	CEBPB	chr9:33487366-33487443	K562	blood:	n/a	n/a
29	CHD1	chr9:33510444-33511455	IMR90	lung:	n/a	n/a
30	CHD2	chr9:33510789-33511161	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr9:33510872-33511154	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr9:33506622-33506876	Hela-S3	cervix:	n/a	n/a
33	CREB1	chr9:33506499-33506899	A549	lung:	n/a	n/a
34	CREB1	chr9:33510857-33511420	A549	lung:	n/a	n/a
35	CTCF	chr9:33498541-33498609	GM13977	blood:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
36	CTCF	chr9:33498600-33498750	HRE	kidney:	n/a	n/a
37	CTCF	chr9:33498480-33498630	Caco-2	colon:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
38	CTCF	chr9:33498500-33498650	HCPEpiC	choroid plexus:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
39	CTCF	chr9:33498520-33498670	Caco-2	colon:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
40	CTCF	chr9:33497552-33497640	GM10266	blood:	n/a	n/a
41	CTCF	chr9:33498405-33498664	A549	lung:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
42	CTCF	chr9:33486427-33486557	GM10248	blood:	n/a	n/a
43	CTCF	chr9:33498500-33498650	HA-sp	spinal cord:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
44	CTCF	chr9:33498480-33498630	AoAF	blood vessel:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
45	CTCF	chr9:33498460-33498610	GM12878	blood:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
46	CTCF	chr9:33498480-33498630	SAEC	small airway:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
47	CTCF	chr9:33498480-33498630	HPAF	blood vessel:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
48	CTCF	chr9:33498520-33498670	AG09319	gingival:	n/a	chr9:33498588-33498606 chr9:33498583-33498604
49	CTCF	chr9:33498296-33498299	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr9:33498480-33498630	HCM	heart:	n/a	chr9:33498588-33498606 chr9:33498583-33498604

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:33510387-33510437	BE2_C	brain:	n/a
2	chr9:33510387-33510437	BE2_C	brain:	n/a
3	chr9:33510859-33510909	PANC-1	pancreas:	n/a
4	chr9:33510387-33510437	PrEC	prostate:	n/a
5	chr9:33510859-33510909	HAEpiC	amniotic membrane:	n/a
6	chr9:33510859-33510909	H1-hESC	embryonic stem cell:	embryo
7	chr9:33510387-33510437	Hepatocyte	liver:	n/a
8	chr9:33510859-33510909	T-47D	breast:	n/a
9	chr9:33510387-33510437	HMEC	breast:	n/a
10	chr9:33510859-33510909	K562	blood:	n/a
11	chr9:33510387-33510437	HCF	heart:	n/a
12	chr9:33510387-33510437	PFSK-1	brain:	n/a
13	chr9:33510387-33510437	NB4	blood:	n/a
14	chr9:33510859-33510909	HNPCEpiC	eye:	n/a
15	chr9:33510859-33510909	GM19239	blood:	n/a
16	chr9:33510859-33510909	AG10803	skin:	n/a
17	chr9:33510387-33510437	SK-N-SH_RA	brain:	n/a
18	chr9:33510387-33510437	GM12892	blood:	n/a
19	chr9:33510859-33510909	CMK	blood:	n/a
20	chr9:33510859-33510909	ProgFib	skin:	n/a
21	chr9:33510387-33510437	CMK	blood:	n/a
22	chr9:33510387-33510437	HL-60	blood:	n/a
23	chr9:33510859-33510909	AG04450	lung:	fetal
24	chr9:33510387-33510437	HCPEpiC	choroid plexus:	n/a
25	chr9:33510387-33510437	A549	lung:	n/a
26	chr9:33510859-33510909	MCF-7	breast:	n/a
27	chr9:33510859-33510909	NH-A	brain:	n/a
28	chr9:33510859-33510909	MCF10A-Er-Src	breast:	n/a
29	chr9:33510387-33510437	NHDF-neo	bronchial:	n/a
30	chr9:33510387-33510437	HRE	kidney:	n/a
31	chr9:33510387-33510437	HUVEC	blood vessel:	n/a
32	chr9:33510859-33510909	ECC-1	luminal epithelium:	n/a
33	chr9:33510859-33510909	LNCaP	prostate:	n/a
34	chr9:33510387-33510437	HepG2	liver:	n/a
35	chr9:33510859-33510909	HMEC	breast:	n/a
36	chr9:33510859-33510909	SKMC	muscle:	n/a
37	chr9:33510859-33510909	HRCEpiC	kidney:	n/a
38	chr9:33510859-33510909	IMR90	lung:	fetal
39	chr9:33510859-33510909	BJ	skin:	n/a
40	chr9:33510859-33510909	BE2_C	brain:	n/a
41	chr9:33510859-33510909	NHDF-neo	bronchial:	n/a
42	chr9:33510387-33510437	HEK293	kidney:	embryo
43	chr9:33510387-33510437	IMR90	lung:	fetal
44	chr9:33510387-33510437	AG09319	gingival:	n/a
45	chr9:33510387-33510437	GM12891	blood:	n/a
46	chr9:33510387-33510437	SKMC	muscle:	n/a
47	chr9:33510859-33510909	HRPEpiC	eye:	n/a
48	chr9:33510387-33510437	NH-A	brain:	n/a
49	chr9:33510859-33510909	A549	lung:	n/a
50	chr9:33510387-33510437	HPAEpiC	pulmonary alveolar:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:33500337..33502515-chr9:33504902..33506531,2	MCF-7	breast:
2	chr9:33506883..33509573-chr9:33522858..33524863,3	MCF-7	breast:
3	chr7:140624233..140624974-chr9:33510596..33511369,2	NB4	blood:
4	chr9:33464987..33466582-chr9:33491183..33494064,2	MCF-7	breast:
5	chr9:33493145..33495957-chr9:33815882..33818107,2	MCF-7	breast:
6	chr9:33233095..33235293-chr9:33495089..33497501,2	MCF-7	breast:
7	chr9:33167075..33168598-chr9:33506552..33508711,2	MCF-7	breast:
8	chr9:33230593..33233513-chr9:33497075..33498895,2	MCF-7	breast:
9	chr9:33508653..33511293-chr9:33522679..33524589,3	MCF-7	breast:
10	chr12:122710012..122710878-chr9:33510743..33511385,2	Hela-S3	cervix:
11	chr9:33496241..33497773-chr9:100020553..100022401,2	K562	blood:
12	chr9:33505343..33508128-chr9:33516249..33518237,2	MCF-7	breast:
13	chr9:33506278..33509110-chr9:33511393..33513037,2	MCF-7	breast:
14	chr9:33500337..33502515-chr9:33504902..33506531,2	MCF-7	breast:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOL6-4	chr9:33502957-33503090	NONHSAT130733
2	lnc-NOL6-1	chr9:33503653-33503841	NONHSAT130734
3	lnc-NOL6-1	chr9:33503824-33503841	XLOC_007668
4	lnc-NOL6-1	chr9:33509128-33509324	NONHSAT130740
5	lnc-NOL6-1	chr9:33509128-33509336	XLOC_007668
6	lnc-NOL6-4	chr9:33504213-33504323	NONHSAT130733
7	lnc-ANKRD18B-3	chr9:33486596-33487386	NONHSAT130728
8	lnc-NOL6-1	chr9:33510618-33510709	NONHSAT130734
9	lnc-NOL6-1	chr9:33509128-33509337	XLOC_007668
10	lnc-NOL6-1	chr9:33509128-33509334	NONHSAT130730
11	lnc-NOL6-1	chr9:33504536-33504589	NONHSAT130734
12	lnc-ANKRD18B-2	chr9:33502630-33502751	XLOC_007322
13	lnc-NOL6-1	chr9:33504536-33504589	XLOC_007668
14	lnc-NOL6-1	chr9:33504533-33504603	NONHSAT130740
15	lnc-NOL6-1	chr9:33508361-33508427	NONHSAT130740
16	lnc-ANKRD18B-2	chr9:33500945-33501244	NONHSAT130731
17	lnc-NOL6-1	chr9:33491094-33491203	NONHSAT130730
18	lnc-ANKRD18B-3	chr9:33487059-33487298	XLOC_007321
19	lnc-NOL6-1	chr9:33504546-33504589	XLOC_007668
20	lnc-NOL6-1	chr9:33503833-33503841	XLOC_007668
21	lnc-ANKRD18B-2	chr9:33502629-33502751	NONHSAT130731
22	lnc-NOL6-4	chr9:33504622-33504771	NONHSAT130733
23	lnc-NOL6-1	chr9:33508361-33508427	XLOC_007668
24	lnc-ANKRD18B-3	chr9:33489592-33489953	XLOC_007321
25	lnc-NOL6-1	chr9:33508357-33508427	NONHSAT130734
26	lnc-NOL6-1	chr9:33508361-33508427	XLOC_007668
27	lnc-NOL6-1	chr9:33508361-33508427	NONHSAT130730
28	lnc-NOL6-1	chr9:33504541-33504589	NONHSAT130730
29	lnc-ANKRD18B-3	chr9:33489591-33489953	NONHSAT130728
30	lnc-NOL6-1	chr9:33509128-33509197	NONHSAT130734
31	lnc-ANKRD18B-2	chr9:33500946-33501244	XLOC_007322

No data

Variant related genes	Relation type
ENSG00000226823	TF binding region
ENSG00000226823	CpG island
ENSG00000230453	chromatin interactions
ENSG00000184047	chromatin interactions
ENSG00000157764	chromatin interactions
ENSG00000107341	chromatin interactions
ENSG00000165271	chromatin interactions
ENSG00000086062	chromatin interactions
GREB1	miRNA target sites
GRB2	miRNA target sites

Extended variants
information (count: 822 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565818861	chr9:33486370-33486371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138183047	chr9:33486407-33486408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142770155	chr9:33486414-33486415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571549078	chr9:33486430-33486431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185764840	chr9:33486437-33486438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550548064	chr9:33486510-33486511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150784967	chr9:33486512-33486513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192487610	chr9:33486565-33486566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183329975	chr9:33486632-33486633	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs573358940	chr9:33486659-33486660	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs574393638	chr9:33486663-33486664	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs556110398	chr9:33486730-33486731	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs150837550	chr9:33486748-33486749	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs112438955	chr9:33486749-33486750	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs200838247	chr9:33486750-33486751	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs75722262	chr9:33486751-33486752	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs538964432	chr9:33486753-33486754	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs373165487	chr9:33486754-33486755	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs78329219	chr9:33486756-33486757	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs575512793	chr9:33486780-33486781	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs199807880	chr9:33486782-33486783	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs561292606	chr9:33486864-33486865	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs574837258	chr9:33486865-33486866	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs539725949	chr9:33486866-33486867	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs113670503	chr9:33486878-33486879	Weak transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
26	rs559298521	chr9:33486898-33486899	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs186220568	chr9:33486921-33486922	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs535446744	chr9:33486969-33486970	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs551579021	chr9:33486971-33486972	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs7022355	chr9:33487023-33487024	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs550213108	chr9:33487059-33487060	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs7038544	chr9:33487071-33487072	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs190543584	chr9:33487142-33487143	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs138085363	chr9:33487150-33487151	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs369337681	chr9:33487176-33487177	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs2992821	chr9:33487198-33487199	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs566216487	chr9:33487236-33487237	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs72709621	chr9:33487268-33487269	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs182920227	chr9:33487317-33487318	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs149547159	chr9:33487338-33487339	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs538099435	chr9:33487342-33487343	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs541648652	chr9:33487380-33487381	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs577844465	chr9:33487385-33487386	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs188309410	chr9:33487426-33487427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574739194	chr9:33487467-33487468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540247540	chr9:33487527-33487528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116517786	chr9:33487535-33487536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577412911	chr9:33487542-33487543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545263601	chr9:33487560-33487561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201607787	chr9:33487597-33487598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	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
Breast cancer	17133270	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21785460	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Melanoma	22183965	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Oral cancer	21386901	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Kartagener syndrome	16639409	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Malignant mesothelioma	18160781	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	17712417	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:33474800-33496000	Weak transcription	HUVEC	blood vessel
2	chr9:33474800-33498200	Weak transcription	HSMMtube	muscle
3	chr9:33475000-33488800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:33475000-33488800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:33475000-33492400	Weak transcription	Adipose Nuclei	Adipose
6	chr9:33475000-33494400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:33475000-33510400	Weak transcription	Fetal Lung	lung
8	chr9:33475000-33510600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr9:33475200-33488800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:33477000-33496000	Weak transcription	Brain Angular Gyrus	brain
11	chr9:33478800-33510600	Weak transcription	Fetal Muscle Leg	muscle
12	chr9:33485600-33486400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr9:33486400-33488600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr9:33488600-33489800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:33488800-33489200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:33488800-33489600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:33488800-33489600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:33488800-33489600	Enhancers	Osteobl	bone
19	chr9:33488800-33490000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr9:33488800-33490000	Enhancers	NHDF-Ad	bronchial
21	chr9:33489000-33489800	Enhancers	A549	lung
22	chr9:33489200-33489800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:33489400-33489800	Enhancers	HSMM	muscle
24	chr9:33489600-33494000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr9:33489800-33493800	Weak transcription	A549	lung
26	chr9:33489800-33494000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr9:33489800-33496000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:33490600-33493800	Weak transcription	K562	blood
29	chr9:33493800-33494200	Enhancers	NH-A	brain
30	chr9:33493800-33494400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr9:33493800-33494600	Flanking Active TSS	K562	blood
32	chr9:33493800-33494800	Enhancers	A549	lung
33	chr9:33493800-33495000	Enhancers	Stomach Mucosa	stomach
34	chr9:33493800-33495000	Enhancers	Hela-S3	cervix
35	chr9:33494000-33494400	Enhancers	Fetal Heart	heart
36	chr9:33494000-33494600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr9:33494000-33495200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:33494400-33505800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr9:33494600-33495600	Enhancers	K562	blood
40	chr9:33494800-33506000	Weak transcription	A549	lung
41	chr9:33495000-33506000	Weak transcription	Hela-S3	cervix
42	chr9:33495600-33496200	Enhancers	NHDF-Ad	bronchial
43	chr9:33495600-33510200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr9:33496000-33496800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr9:33496000-33497000	Enhancers	HUVEC	blood vessel
46	chr9:33497000-33505800	Weak transcription	HUVEC	blood vessel
47	chr9:33498200-33498400	Enhancers	HSMMtube	muscle
48	chr9:33498200-33510400	Weak transcription	Fetal Stomach	stomach
49	chr9:33500000-33510600	Weak transcription	Fetal Muscle Trunk	muscle
50	chr9:33500600-33500800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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