Variant report

Variant	nsv508552
Chromosome Location	chr9:78864913-78956326
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	chr9:78917903-78918226	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:78917918-78918291	K562	blood:	n/a	n/a
3	BHLHE40	chr9:78949419-78949420	K562	blood:	n/a	n/a
4	BHLHE40	chr9:78936121-78936302	K562	blood:	n/a	n/a
5	BHLHE40	chr9:78912579-78913109	K562	blood:	n/a	n/a
6	CEBPB	chr9:78870724-78871433	IMR90	lung:	n/a	chr9:78870968-78870979
7	CEBPB	chr9:78871067-78871285	HepG2	liver:	n/a	n/a
8	CEBPB	chr9:78871062-78871398	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:78930471-78930559	A549	lung:	n/a	n/a
10	CEBPB	chr9:78930585-78930655	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:78905560-78905800	A549	lung:	n/a	n/a
12	CEBPB	chr9:78915338-78915527	K562	blood:	n/a	chr9:78915383-78915394
13	CEBPB	chr9:78905577-78905753	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:78930511-78930727	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:78931086-78931360	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr9:78915270-78915517	HepG2	liver:	n/a	chr9:78915383-78915394
17	CEBPB	chr9:78944350-78944463	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:78905523-78905895	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:78905564-78905826	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:78928227-78928322	HepG2	liver:	n/a	chr9:78928265-78928276
21	CEBPB	chr9:78928294-78928301	A549	lung:	n/a	n/a
22	CEBPB	chr9:78937790-78937938	K562	blood:	n/a	n/a
23	CHD2	chr9:78953521-78953572	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr9:78936360-78936510	HAc	cerebellar:	n/a	n/a
25	CTCF	chr9:78917980-78918130	AG09319	gingival:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
26	CTCF	chr9:78917978-78918125	A549	lung:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
27	CTCF	chr9:78913820-78913970	RPTEC	kidney:	n/a	n/a
28	CTCF	chr9:78917960-78918110	GM12869	blood:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
29	CTCF	chr9:78917980-78918130	AG10803	skin:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
30	CTCF	chr9:78922100-78922250	AG04449	skin:	n/a	n/a
31	CTCF	chr9:78932420-78932570	HEK293	kidney:	n/a	n/a
32	CTCF	chr9:78922080-78922230	MCF-7	breast:	n/a	n/a
33	CTCF	chr9:78913784-78913956	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:78917971-78918114	SK-N-SH_RA	brain:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
35	CTCF	chr9:78915220-78915370	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr9:78917980-78918130	NHLF	lung:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
37	CTCF	chr9:78917475-78918508	A549	lung:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
38	CTCF	chr9:78897016-78897101	GM10248	blood:	n/a	n/a
39	CTCF	chr9:78915120-78915270	BE2_C	brain:	n/a	n/a
40	CTCF	chr9:78918020-78918170	NB4	blood:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
41	CTCF	chr9:78913820-78913970	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr9:78917980-78918130	AoAF	blood vessel:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
43	CTCF	chr9:78918020-78918170	HepG2	liver:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
44	CTCF	chr9:78918020-78918170	AG04450	lung:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
45	CTCF	chr9:78917966-78918175	Kidney_OC	kidney:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
46	CTCF	chr9:78913832-78913899	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr9:78922140-78922290	NHLF	lung:	n/a	n/a
48	CTCF	chr9:78922200-78922350	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr9:78917980-78918130	HCM	heart:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084
50	CTCF	chr9:78917960-78918110	BE2_C	brain:	n/a	chr9:78918074-78918083 chr9:78918068-78918086 chr9:78918063-78918084

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:78906644-78906694	NT2-D1	testis:	n/a
2	chr9:78912437-78912487	A549	lung:	n/a
3	chr9:78912437-78912487	H1-hESC	embryonic stem cell:	embryo
4	chr9:78912437-78912487	T-47D	breast:	n/a
5	chr9:78912437-78912487	SK-N-MC	brain:	n/a
6	chr9:78905335-78905385	HEK293	kidney:	embryo
7	chr9:78906644-78906694	AG04449	skin:	fetal
8	chr9:78912437-78912487	PrEC	prostate:	n/a
9	chr9:78912437-78912487	HCT-116	colon:	n/a
10	chr9:78912437-78912487	GM12878	blood:	n/a
11	chr9:78906644-78906694	K562	blood:	n/a
12	chr9:78912437-78912487	GM12892	blood:	n/a
13	chr9:78905335-78905385	GM12891	blood:	n/a
14	chr9:78912437-78912487	HEEpiC	esophagus:	n/a
15	chr9:78912437-78912487	Jurkat	blood:	n/a
16	chr9:78912437-78912487	NT2-D1	testis:	n/a
17	chr9:78906644-78906694	PANC-1	pancreas:	n/a
18	chr9:78906644-78906694	ECC-1	luminal epithelium:	n/a
19	chr9:78906644-78906694	HPAEpiC	pulmonary alveolar:	n/a
20	chr9:78906644-78906694	BJ	skin:	n/a
21	chr9:78906644-78906694	ProgFib	skin:	n/a
22	chr9:78906644-78906694	HAEpiC	amniotic membrane:	n/a
23	chr9:78906644-78906694	HCPEpiC	choroid plexus:	n/a
24	chr9:78906644-78906694	HCM	heart:	n/a
25	chr9:78905335-78905385	U87	brain:	n/a
26	chr9:78912437-78912487	HUVEC	blood vessel:	n/a
27	chr9:78912437-78912487	SKMC	muscle:	n/a
28	chr9:78912437-78912487	AG09319	gingival:	n/a
29	chr9:78906644-78906694	CMK	blood:	n/a
30	chr9:78912437-78912487	HRCEpiC	kidney:	n/a
31	chr9:78905335-78905385	MCF10A-Er-Src	breast:	n/a
32	chr9:78906644-78906694	GM19239	blood:	n/a
33	chr9:78905335-78905385	GM12878	blood:	n/a
34	chr9:78905335-78905385	IMR90	lung:	fetal
35	chr9:78905335-78905385	NHDF-neo	bronchial:	n/a
36	chr9:78905335-78905385	Caco-2	colon:	n/a
37	chr9:78905335-78905385	SK-N-MC	brain:	n/a
38	chr9:78905335-78905385	NT2-D1	testis:	n/a
39	chr9:78906644-78906694	ovcar-3	ovarian:	n/a
40	chr9:78906644-78906694	HL-60	blood:	n/a
41	chr9:78905335-78905385	HCM	heart:	n/a
42	chr9:78905335-78905385	T-47D	breast:	n/a
43	chr9:78906644-78906694	SKMC	muscle:	n/a
44	chr9:78905335-78905385	HepG2	liver:	n/a
45	chr9:78905335-78905385	SK-N-SH_RA	brain:	n/a
46	chr9:78906644-78906694	HCF	heart:	n/a
47	chr9:78906644-78906694	AoSMC	blood vessel:	n/a
48	chr9:78905335-78905385	HIPEpiC	eye:	n/a
49	chr9:78912437-78912487	HMEC	breast:	n/a
50	chr9:78906644-78906694	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:78879319..78882364-chr9:78884660..78887114,3	K562	blood:
2	chr9:78701639..78702246-chr9:78917623..78918458,2	MCF-7	breast:
3	chr9:78945479..78947333-chr9:79007569..79009424,2	MCF-7	breast:
4	chr9:78879319..78882364-chr9:78884660..78887114,3	K562	blood:
5	chr9:78936413..78937926-chr9:78939459..78941379,2	MCF-7	breast:
6	chr9:78936413..78937926-chr9:78939459..78941379,2	MCF-7	breast:
7	chr9:78834517..78835118-chr9:78917910..78918421,2	MCF-7	breast:
8	chr17:57918233..57920069-chr9:78928143..78930323,2	MCF-7	breast:
9	chr9:78593538..78594448-chr9:78917639..78918554,2	MCF-7	breast:
10	chr9:78917718..78920640-chr9:78922356..78925203,2	K562	blood:
11	chr9:78594386..78595229-chr9:78917510..78918589,3	MCF-7	breast:
12	chr9:78593987..78594566-chr9:78913006..78913887,2	MCF-7	breast:
13	chr9:78917718..78920640-chr9:78922356..78925203,2	K562	blood:
14	chr9:78624133..78625062-chr9:78913423..78914349,5	MCF-7	breast:
15	chr9:78937965..78939769-chr9:78983813..78985736,2	K562	blood:

Variant related genes	Relation type
RBM22P5	TF binding region
RBM22P5	CpG island
ENSG00000135002	chromatin interactions
ENSG00000199004	chromatin interactions

Extended variants
information (count: 3711 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3711 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181016094	chr9:78864923-78864924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145569928	chr9:78864944-78864945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201675509	chr9:78864956-78864957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186304519	chr9:78865046-78865047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7469950	chr9:78865085-78865086	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs374367108	chr9:78865088-78865089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567338132	chr9:78865141-78865142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570222701	chr9:78865143-78865144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142658977	chr9:78865166-78865167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1587104	chr9:78865185-78865186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs150267135	chr9:78865195-78865196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529820005	chr9:78865198-78865199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145730304	chr9:78865243-78865244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148928929	chr9:78865247-78865248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7032580	chr9:78865248-78865249	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs1587103	chr9:78865300-78865301	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs190257986	chr9:78865319-78865320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562880265	chr9:78865341-78865342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576496270	chr9:78865342-78865343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78801616	chr9:78865500-78865501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565551450	chr9:78865501-78865502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527913414	chr9:78865508-78865509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143632163	chr9:78865528-78865529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181543813	chr9:78865555-78865556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569401856	chr9:78865561-78865562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62564575	chr9:78865565-78865566	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138331299	chr9:78865580-78865581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185670863	chr9:78865585-78865586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569351322	chr9:78865586-78865587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190528383	chr9:78865665-78865666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375311846	chr9:78865723-78865724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552089923	chr9:78865725-78865726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10781352	chr9:78865740-78865741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs142829784	chr9:78865783-78865784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183698241	chr9:78865826-78865827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs118065303	chr9:78865903-78865904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536784817	chr9:78865923-78865924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556693524	chr9:78865940-78865941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144805312	chr9:78865947-78865948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545404455	chr9:78865957-78865958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558644140	chr9:78865981-78865982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117741382	chr9:78866046-78866047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187506347	chr9:78866048-78866049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138655965	chr9:78866054-78866055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530219242	chr9:78866091-78866092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543158185	chr9:78866101-78866102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563020666	chr9:78866105-78866106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532046861	chr9:78866110-78866111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552174190	chr9:78866121-78866122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540706627	chr9:78866139-78866140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intellectual disability	22102821	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:625 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:78855800-78881800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr9:78856600-78870400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr9:78862000-78871800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr9:78862400-78872400	Weak transcription	Esophagus	oesophagus
5	chr9:78864200-78865800	Weak transcription	Fetal Intestine Small	intestine
6	chr9:78864400-78867400	Weak transcription	Aorta	Aorta
7	chr9:78864600-78874600	Weak transcription	Fetal Intestine Large	intestine
8	chr9:78865800-78866200	Strong transcription	Fetal Intestine Small	intestine
9	chr9:78866200-78872000	Weak transcription	Fetal Intestine Small	intestine
10	chr9:78866600-78866800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:78866800-78870200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:78867400-78867600	Enhancers	Aorta	Aorta
13	chr9:78867600-78870400	Weak transcription	Aorta	Aorta
14	chr9:78868800-78870600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr9:78870000-78871000	Enhancers	Placenta	Placenta
16	chr9:78870200-78870400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:78870200-78870400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:78870200-78872400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr9:78870400-78870600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr9:78870400-78870600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:78870400-78870600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr9:78870400-78870600	Enhancers	Adipose Nuclei	Adipose
23	chr9:78870400-78870600	Enhancers	Aorta	Aorta
24	chr9:78870400-78870600	Enhancers	Colon Smooth Muscle	Colon
25	chr9:78870400-78870600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr9:78870400-78870600	Enhancers	HSMMtube	muscle
27	chr9:78870400-78870600	Enhancers	Osteobl	bone
28	chr9:78870400-78870800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:78870400-78870800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr9:78870400-78870800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr9:78870400-78870800	Enhancers	Liver	Liver
32	chr9:78870400-78870800	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr9:78870400-78870800	Enhancers	NHLF	lung
34	chr9:78870400-78871000	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr9:78870400-78871200	Enhancers	Ovary	ovary
36	chr9:78870400-78872800	Enhancers	Fetal Muscle Leg	muscle
37	chr9:78870600-78870800	Flanking Active TSS	Colon Smooth Muscle	Colon
38	chr9:78870600-78870800	Enhancers	Fetal Lung	lung
39	chr9:78870600-78870800	Enhancers	Psoas Muscle	Psoas
40	chr9:78870600-78870800	Flanking Active TSS	Rectal Smooth Muscle	rectum
41	chr9:78870600-78870800	Flanking Active TSS	Osteobl	bone
42	chr9:78870600-78871000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr9:78870600-78871000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr9:78870600-78871000	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr9:78870600-78871000	Enhancers	Right Atrium	heart
46	chr9:78870600-78871200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr9:78870600-78871200	Active TSS	Stomach Smooth Muscle	stomach
48	chr9:78870600-78871200	Flanking Active TSS	HSMMtube	muscle
49	chr9:78870600-78871400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr9:78870600-78871400	Enhancers	Fetal Muscle Trunk	muscle

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