Variant report

Variant	esv3409409
Chromosome Location	chr9:140407656-140410504
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	chr9:140408340-140408490	HepG2	liver:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
2	CTCF	chr9:140408241-140408480	T-47D	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
3	CTCF	chr9:140408359-140408458	Gliobla	brain:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
4	CTCF	chr9:140408335-140408470	MCF-7	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
5	CTCF	chr9:140408300-140408450	Hela-S3	cervix:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
6	CTCF	chr9:140408351-140408465	GM12892	blood:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
7	CTCF	chr9:140408361-140408469	Hela-S3	cervix:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
8	CTCF	chr9:140408329-140408474	MCF-7	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
9	CTCF	chr9:140408340-140408490	MCF-7	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
10	CTCF	chr9:140408348-140408468	MCF-7	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
11	CTCF	chr9:140408933-140408994	GM13977	blood:	n/a	n/a
12	CTCF	chr9:140408320-140408470	HMEC	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
13	CTCF	chr9:140408360-140408510	MCF-7	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
14	CTCF	chr9:140408320-140408470	Hela-S3	cervix:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
15	CTCF	chr9:140408202-140408586	MCF-7	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
16	CTCF	chr9:140408327-140408489	MCF-7	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
17	CTCF	chr9:140408325-140408510	MCF-7	breast:	n/a	chr9:140408388-140408406 chr9:140408391-140408404
18	E2F6	chr9:140409424-140409597	K562	blood:	n/a	chr9:140409523-140409535
19	E2F6	chr9:140409356-140409652	H1-hESC	embryonic stem cell:	n/a	chr9:140409523-140409535
20	E2F6	chr9:140409360-140409804	H1-hESC	embryonic stem cell:	n/a	chr9:140409523-140409535
21	EGR1	chr9:140409862-140410029	K562	blood:	n/a	n/a
22	EP300	chr9:140408217-140408597	MCF-7	breast:	n/a	n/a
23	ESR1	chr9:140408337-140408780	T-47D	breast:	n/a	n/a
24	ESR1	chr9:140408300-140409532	T-47D	breast:	n/a	n/a
25	ESR1	chr9:140408266-140409453	T-47D	breast:	n/a	n/a
26	ESR1	chr9:140408252-140409081	T-47D	breast:	n/a	n/a
27	ESR1	chr9:140408301-140408782	T-47D	breast:	n/a	n/a
28	GABPA	chr9:140408194-140408516	H1-hESC	embryonic stem cell:	n/a	n/a
29	GABPA	chr9:140409816-140410090	H1-hESC	embryonic stem cell:	n/a	n/a
30	GATA3	chr9:140408318-140408770	MCF-7	breast:	n/a	n/a
31	HA-E2F1	chr9:140408181-140408951	MCF-7	breast:	n/a	n/a
32	IKZF1	chr9:140407791-140408171	GM12878	blood:	n/a	n/a
33	IRF1	chr9:140408100-140408318	K562	blood:	n/a	n/a
34	IRF1	chr9:140408069-140408387	K562	blood:	n/a	n/a
35	MAX	chr9:140409322-140409821	MCF-7	breast:	n/a	chr9:140409704-140409713 chr9:140409702-140409711 chr9:140409703-140409710
36	MAX	chr9:140409370-140409667	K562	blood:	n/a	n/a
37	MAX	chr9:140409386-140409792	A549	lung:	n/a	chr9:140409704-140409713 chr9:140409702-140409711 chr9:140409703-140409710
38	MAX	chr9:140408288-140408552	Hela-S3	cervix:	n/a	n/a
39	MAX	chr9:140409403-140409700	H1-hESC	embryonic stem cell:	n/a	n/a
40	MAX	chr9:140409371-140409767	H1-hESC	embryonic stem cell:	n/a	chr9:140409704-140409713 chr9:140409702-140409711 chr9:140409703-140409710
41	MAZ	chr9:140408301-140408474	Hela-S3	cervix:	n/a	n/a
42	MEF2A	chr9:140407654-140408024	GM12878	blood:	n/a	n/a
43	MEF2A	chr9:140407618-140407980	GM12878	blood:	n/a	n/a
44	MEF2C	chr9:140407542-140407980	GM12878	blood:	n/a	chr9:140407775-140407790
45	MXI1	chr9:140408283-140408504	Hela-S3	cervix:	n/a	n/a
46	MYC	chr9:140408384-140408451	MCF-7	breast:	n/a	n/a
47	NFIC	chr9:140407631-140408106	GM12878	blood:	n/a	n/a
48	POLR2A	chr9:140408232-140408562	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr9:140408269-140408669	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr9:140408987-140409189	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140409915-140409965	GM12878	blood:	n/a
2	chr9:140408634-140408684	NHBE	bronchial:	n/a
3	chr9:140408634-140408684	HRE	kidney:	n/a
4	chr9:140408634-140408684	BJ	skin:	n/a
5	chr9:140408634-140408684	NHDF-neo	bronchial:	n/a
6	chr9:140408634-140408684	HL-60	blood:	n/a
7	chr9:140409915-140409965	HPAEpiC	pulmonary alveolar:	n/a
8	chr9:140408634-140408684	IMR90	lung:	fetal
9	chr9:140409915-140409965	T-47D	breast:	n/a
10	chr9:140409915-140409965	HRPEpiC	eye:	n/a
11	chr9:140409915-140409965	RPTEC	kidney:	n/a
12	chr9:140408634-140408684	GM12891	blood:	n/a
13	chr9:140408634-140408684	NT2-D1	testis:	n/a
14	chr9:140409915-140409965	BE2_C	brain:	n/a
15	chr9:140408634-140408684	HRPEpiC	eye:	n/a
16	chr9:140408634-140408684	HUVEC	blood vessel:	n/a
17	chr9:140409915-140409965	HNPCEpiC	eye:	n/a
18	chr9:140408634-140408684	HRCEpiC	kidney:	n/a
19	chr9:140408634-140408684	SK-N-SH	brain:	n/a
20	chr9:140408634-140408684	AoSMC	blood vessel:	n/a
21	chr9:140409915-140409965	MCF-7	breast:	n/a
22	chr9:140409915-140409965	A549	lung:	n/a
23	chr9:140409915-140409965	HUVEC	blood vessel:	n/a
24	chr9:140409915-140409965	GM12892	blood:	n/a
25	chr9:140408634-140408684	HMEC	breast:	n/a
26	chr9:140408634-140408684	ECC-1	luminal epithelium:	n/a
27	chr9:140409915-140409965	Caco-2	colon:	n/a
28	chr9:140409915-140409965	HEEpiC	esophagus:	n/a
29	chr9:140409915-140409965	HRE	kidney:	n/a
30	chr9:140409915-140409965	CMK	blood:	n/a
31	chr9:140409915-140409965	HRCEpiC	kidney:	n/a
32	chr9:140409915-140409965	HCT-116	colon:	n/a
33	chr9:140408634-140408684	A549	lung:	n/a
34	chr9:140408634-140408684	AG10803	skin:	n/a
35	chr9:140409915-140409965	GM12891	blood:	n/a
36	chr9:140409915-140409965	HL-60	blood:	n/a
37	chr9:140408634-140408684	GM12892	blood:	n/a
38	chr9:140409915-140409965	SK-N-MC	brain:	n/a
39	chr9:140409915-140409965	HepG2	liver:	n/a
40	chr9:140409915-140409965	AoSMC	blood vessel:	n/a
41	chr9:140409915-140409965	HEK293	kidney:	embryo
42	chr9:140408634-140408684	SK-N-MC	brain:	n/a
43	chr9:140409915-140409965	SAEC	small airway:	n/a
44	chr9:140408634-140408684	HCM	heart:	n/a
45	chr9:140408634-140408684	H1-hESC	embryonic stem cell:	embryo
46	chr9:140409915-140409965	NHDF-neo	bronchial:	n/a
47	chr9:140409915-140409965	Hepatocyte	liver:	n/a
48	chr9:140408634-140408684	Jurkat	blood:	n/a
49	chr9:140409915-140409965	NT2-D1	testis:	n/a
50	chr9:140408634-140408684	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:140402660..140405211-chr9:140405983..140408009,2	MCF-7	breast:
2	chr9:140406468..140408073-chr9:140409419..140412188,2	K562	blood:
3	chr9:140189647..140191629-chr9:140408835..140411014,2	MCF-7	breast:
4	chr9:140406492..140409440-chr9:140417122..140420049,2	MCF-7	breast:
5	chr9:140406477..140408426-chr9:140424774..140426363,2	K562	blood:
6	chr9:140352371..140354173-chr9:140410410..140412850,2	MCF-7	breast:
7	chr9:140352304..140355788-chr9:140405232..140410099,5	MCF-7	breast:
8	chr9:140406090..140408073-chr9:140408484..140412188,3	K562	blood:
9	chr9:140354790..140356755-chr9:140406317..140408071,2	K562	blood:
10	chr9:140195213..140197521-chr9:140405287..140408136,3	MCF-7	breast:

Variant related genes	Relation type
PNPLA7	TF binding region
PNPLA7	CpG island
ENSG00000165802	chromatin interactions
ENSG00000260996	chromatin interactions
ENSG00000198435	chromatin interactions
ENSG00000130653	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561104371	chr9:140407672-140407673	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs13440140	chr9:140407709-140407710	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs182124089	chr9:140407748-140407749	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs13440001	chr9:140407751-140407752	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs13439931	chr9:140407755-140407756	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs551435004	chr9:140407859-140407860	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs186227978	chr9:140407888-140407889	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs534675372	chr9:140407899-140407900	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs527261403	chr9:140407928-140407929	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs367774091	chr9:140407930-140407931	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs11422303	chr9:140407942-140407943	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs371950596	chr9:140408038-140408039	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs573746185	chr9:140408091-140408092	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs17065442	chr9:140408189-140408190	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs553412862	chr9:140408255-140408256	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573294318	chr9:140408319-140408320	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145758138	chr9:140408320-140408321	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs115576125	chr9:140408385-140408386	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs10780201	chr9:140408386-140408387	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs138402273	chr9:140408395-140408396	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536078215	chr9:140408412-140408413	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544467386	chr9:140408427-140408428	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572886745	chr9:140408437-140408438	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142882710	chr9:140408440-140408441	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542480604	chr9:140408450-140408451	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs146090206	chr9:140408477-140408478	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545104890	chr9:140408511-140408512	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528220426	chr9:140408516-140408517	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs551503759	chr9:140408531-140408532	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571223337	chr9:140408537-140408538	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376609880	chr9:140408549-140408550	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs530537507	chr9:140408561-140408562	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs550866149	chr9:140408570-140408571	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111331293	chr9:140408613-140408614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs36067663	chr9:140408615-140408616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536433609	chr9:140408620-140408621	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369818384	chr9:140408632-140408633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs564801339	chr9:140408683-140408684	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566954969	chr9:140408712-140408713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191939888	chr9:140408733-140408734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558639174	chr9:140408756-140408757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533570719	chr9:140408781-140408782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575205002	chr9:140408782-140408783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs373545717	chr9:140408788-140408789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375647480	chr9:140408794-140408795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555227915	chr9:140408795-140408796	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370215574	chr9:140408822-140408823	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375092373	chr9:140408825-140408826	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373260019	chr9:140408830-140408831	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184239231	chr9:140408862-140408863	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140376800-140444000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:140377000-140437000	Weak transcription	Left Ventricle	heart
3	chr9:140377200-140420200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr9:140388400-140425200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr9:140392000-140425800	Weak transcription	Primary T cells from cord blood	blood
6	chr9:140393000-140417800	Weak transcription	Fetal Brain Female	brain
7	chr9:140393000-140429400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr9:140394000-140419800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr9:140394000-140429200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr9:140394800-140415600	Weak transcription	Brain Angular Gyrus	brain
11	chr9:140395000-140414000	Weak transcription	Brain Substantia Nigra	brain
12	chr9:140395200-140409400	Weak transcription	Spleen	Spleen
13	chr9:140396200-140409200	Weak transcription	Right Ventricle	heart
14	chr9:140396400-140429200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr9:140401400-140413600	Weak transcription	Gastric	stomach
16	chr9:140402000-140409400	Weak transcription	Fetal Stomach	stomach
17	chr9:140404000-140408200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:140404000-140413400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr9:140404200-140413800	Weak transcription	Primary B cells from cord blood	blood
20	chr9:140404200-140414000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr9:140404200-140414000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr9:140404200-140415000	Weak transcription	HSMMtube	muscle
23	chr9:140404200-140415600	Weak transcription	Brain Hippocampus Middle	brain
24	chr9:140404200-140420000	Weak transcription	Brain Anterior Caudate	brain
25	chr9:140404200-140429200	Weak transcription	Aorta	Aorta
26	chr9:140404400-140415600	Weak transcription	Lung	lung
27	chr9:140405600-140408200	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr9:140406000-140413800	Weak transcription	Fetal Intestine Small	intestine
29	chr9:140406800-140420000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr9:140407000-140408000	Weak transcription	Hela-S3	cervix
31	chr9:140407000-140408600	Enhancers	GM12878-XiMat	blood
32	chr9:140407000-140409200	Weak transcription	Stomach Mucosa	stomach
33	chr9:140407000-140413600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr9:140407000-140414000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr9:140407200-140408200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr9:140407200-140409400	Weak transcription	Adipose Nuclei	Adipose
37	chr9:140407200-140409400	Weak transcription	Pancreas	Pancrea
38	chr9:140407200-140413400	Weak transcription	K562	blood
39	chr9:140407200-140414000	Weak transcription	Liver	Liver
40	chr9:140407200-140414000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr9:140407400-140409400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr9:140407600-140409200	Weak transcription	Ovary	ovary
43	chr9:140407600-140409400	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr9:140408000-140408200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr9:140408000-140408200	Enhancers	HMEC	breast
46	chr9:140408000-140408600	Flanking Active TSS	Hela-S3	cervix
47	chr9:140408200-140408400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr9:140408200-140408400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr9:140408200-140408400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr9:140408200-140408400	Active TSS	Colonic Mucosa	Colon

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