Variant report

Variant	nsv900579
Chromosome Location	chr13:76244056-76307981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1523)
CpG islands
(count:429)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1523 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76248585-76248641	K562	blood:	n/a	n/a
2	ARID3A	chr13:76265424-76265447	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:76253645-76253903	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:76269963-76270226	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:76270038-76270210	K562	blood:	n/a	n/a
6	ATF2	chr13:76289741-76290147	GM12878	blood:	n/a	n/a
7	ATF3	chr13:76265207-76265684	A549	lung:	n/a	n/a
8	ATF3	chr13:76279484-76279861	A549	lung:	n/a	n/a
9	BATF	chr13:76259299-76259675	GM12878	blood:	n/a	chr13:76259494-76259505
10	BATF	chr13:76289754-76290041	GM12878	blood:	n/a	n/a
11	BATF	chr13:76259335-76259573	GM12878	blood:	n/a	chr13:76259494-76259505
12	BATF	chr13:76290324-76290664	GM12878	blood:	n/a	n/a
13	BCL11A	chr13:76289868-76290080	GM12878	blood:	n/a	n/a
14	BCL11A	chr13:76259338-76259577	GM12878	blood:	n/a	n/a
15	BCL3	chr13:76259281-76259673	GM12878	blood:	n/a	n/a
16	BCL3	chr13:76279396-76279953	A549	lung:	n/a	n/a
17	BCL3	chr13:76265186-76265752	A549	lung:	n/a	n/a
18	BDP1	chr13:76290983-76291615	Hela-S3	cervix:	n/a	n/a
19	BHLHE40	chr13:76270057-76270277	K562	blood:	n/a	n/a
20	BHLHE40	chr13:76273396-76273452	GM12878	blood:	n/a	n/a
21	BHLHE40	chr13:76253731-76253931	HepG2	liver:	n/a	n/a
22	BRCA1	chr13:76278828-76280200	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr13:76298981-76300594	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr13:76270132-76270225	HepG2	liver:	n/a	n/a
25	BRCA1	chr13:76289703-76291347	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr13:76273891-76274193	K562	blood:	n/a	n/a
27	CBX3	chr13:76278596-76280472	HCT-116	colon:	n/a	n/a
28	CBX3	chr13:76278969-76279965	HCT-116	colon:	n/a	n/a
29	CEBPB	chr13:76290708-76291323	HCT-116	colon:	n/a	chr13:76290923-76290935
30	CEBPB	chr13:76289620-76291376	Hela-S3	cervix:	n/a	chr13:76290923-76290935
31	CEBPB	chr13:76299278-76299650	ECC-1	luminal epithelium:	n/a	chr13:76299496-76299509
32	CEBPB	chr13:76297724-76297997	HepG2	liver:	n/a	chr13:76297846-76297857 chr13:76297847-76297856
33	CEBPB	chr13:76277933-76278286	Hela-S3	cervix:	n/a	chr13:76278104-76278115
34	CEBPB	chr13:76290923-76291289	A549	lung:	n/a	chr13:76290923-76290935
35	CEBPB	chr13:76268906-76269258	IMR90	lung:	n/a	n/a
36	CEBPB	chr13:76297713-76298015	IMR90	lung:	n/a	chr13:76297846-76297857 chr13:76297847-76297856
37	CEBPB	chr13:76265329-76265765	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr13:76248579-76248884	HepG2	liver:	n/a	chr13:76248822-76248834
39	CEBPB	chr13:76259337-76259906	IMR90	lung:	n/a	n/a
40	CEBPB	chr13:76277953-76278235	HepG2	liver:	n/a	chr13:76278104-76278115
41	CEBPB	chr13:76269038-76269257	K562	blood:	n/a	n/a
42	CEBPB	chr13:76282212-76282460	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr13:76248644-76248784	HepG2	liver:	n/a	n/a
44	CEBPB	chr13:76244413-76244659	HepG2	liver:	n/a	n/a
45	CEBPB	chr13:76277931-76278536	IMR90	lung:	n/a	chr13:76278104-76278115
46	CEBPB	chr13:76244365-76244945	IMR90	lung:	n/a	n/a
47	CEBPB	chr13:76299051-76299646	HCT-116	colon:	n/a	chr13:76299496-76299509
48	CEBPB	chr13:76270007-76270331	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr13:76278934-76280067	HCT-116	colon:	n/a	chr13:76279987-76280000 chr13:76279987-76280000 chr13:76279987-76279998
50	CEBPB	chr13:76278069-76278136	K562	blood:	n/a	chr13:76278104-76278115

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76279228-76279278	HPAEpiC	pulmonary alveolar:	n/a
2	chr13:76291075-76291125	GM19239	blood:	n/a
3	chr13:76279228-76279278	HPAEpiC	pulmonary alveolar:	n/a
4	chr13:76291075-76291125	GM19239	blood:	n/a
5	chr13:76259545-76259595	IMR90	lung:	fetal
6	chr13:76259545-76259595	ProgFib	skin:	n/a
7	chr13:76260314-76260364	HIPEpiC	eye:	n/a
8	chr13:76259545-76259595	AG10803	skin:	n/a
9	chr13:76279228-76279278	K562	blood:	n/a
10	chr13:76244804-76244854	Hela-S3	cervix:	n/a
11	chr13:76250138-76250188	GM19239	blood:	n/a
12	chr13:76259545-76259595	ECC-1	luminal epithelium:	n/a
13	chr13:76267059-76267109	GM06990	blood:	n/a
14	chr13:76291075-76291125	PANC-1	pancreas:	n/a
15	chr13:76259545-76259595	RPTEC	kidney:	n/a
16	chr13:76267059-76267109	BJ	skin:	n/a
17	chr13:76244804-76244854	HPAEpiC	pulmonary alveolar:	n/a
18	chr13:76244804-76244854	ProgFib	skin:	n/a
19	chr13:76250138-76250188	ovcar-3	ovarian:	n/a
20	chr13:76267059-76267109	PrEC	prostate:	n/a
21	chr13:76250138-76250188	NB4	blood:	n/a
22	chr13:76267059-76267109	LNCaP	prostate:	n/a
23	chr13:76259545-76259595	MCF10A-Er-Src	breast:	n/a
24	chr13:76267059-76267109	HMEC	breast:	n/a
25	chr13:76250138-76250188	HPAEpiC	pulmonary alveolar:	n/a
26	chr13:76259545-76259595	BE2_C	brain:	n/a
27	chr13:76267059-76267109	A549	lung:	n/a
28	chr13:76259545-76259595	GM12892	blood:	n/a
29	chr13:76250138-76250188	AG09319	gingival:	n/a
30	chr13:76291075-76291125	NB4	blood:	n/a
31	chr13:76279228-76279278	HepG2	liver:	n/a
32	chr13:76291075-76291125	GM12878	blood:	n/a
33	chr13:76259545-76259595	HMEC	breast:	n/a
34	chr13:76244804-76244854	Hepatocyte	liver:	n/a
35	chr13:76291075-76291125	MCF-7	breast:	n/a
36	chr13:76291075-76291125	HRE	kidney:	n/a
37	chr13:76244804-76244854	HCF	heart:	n/a
38	chr13:76260314-76260364	AG09319	gingival:	n/a
39	chr13:76260314-76260364	CMK	blood:	n/a
40	chr13:76244804-76244854	AG09309	skin:	n/a
41	chr13:76291075-76291125	H1-hESC	embryonic stem cell:	embryo
42	chr13:76244804-76244854	PANC-1	pancreas:	n/a
43	chr13:76259545-76259595	HEEpiC	esophagus:	n/a
44	chr13:76267059-76267109	AoSMC	blood vessel:	n/a
45	chr13:76260314-76260364	PANC-1	pancreas:	n/a
46	chr13:76267059-76267109	SK-N-SH_RA	brain:	n/a
47	chr13:76267059-76267109	SAEC	small airway:	n/a
48	chr13:76259545-76259595	HRPEpiC	eye:	n/a
49	chr13:76260314-76260364	HUVEC	blood vessel:	n/a
50	chr13:76250138-76250188	AG09309	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:76259690..76262311-chr13:77554320..77556191,2	MCF-7	breast:
2	chr13:76261020..76261898-chr13:76374424..76375313,3	MCF-7	breast:
3	chr13:76272265..76273781-chr13:76290115..76292337,2	MCF-7	breast:
4	chr13:76269693..76270610-chr13:76444514..76445100,2	MCF-7	breast:
5	chr13:76263691..76265417-chr13:76278168..76279745,2	MCF-7	breast:
6	chr13:76269710..76270622-chr13:76374395..76375242,4	MCF-7	breast:
7	chr13:76276545..76279107-chr13:76332973..76335084,2	MCF-7	breast:
8	chr13:76279169..76281047-chr13:76286022..76288231,2	MCF-7	breast:
9	chr13:76263691..76265417-chr13:76278168..76279745,2	MCF-7	breast:
10	chr13:76269577..76270548-chr13:77047371..77048675,5	K562	blood:
11	chr13:76276163..76278819-chr13:76286604..76288192,2	K562	blood:
12	chr13:76278980..76279662-chr13:76374280..76374967,2	MCF-7	breast:
13	chr13:76272265..76273781-chr13:76290115..76292337,2	MCF-7	breast:
14	chr13:76279169..76281047-chr13:76286022..76288231,2	MCF-7	breast:
15	chr13:76278744..76281053-chr13:76282794..76285725,2	K562	blood:
16	chr13:76123564..76125268-chr13:76253504..76256274,2	MCF-7	breast:
17	chr13:76278744..76281053-chr13:76282794..76285725,2	K562	blood:
18	chr13:76269711..76270627-chr13:77554340..77554905,3	K562	blood:
19	chr13:76276163..76278819-chr13:76286604..76288192,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD6-7	chr13:76262692-76263333	NONHSAT034370

No data

Variant related genes	Relation type
FAM204CP	TF binding region
FAM204CP	CpG island
ENSG00000261553	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000188243	chromatin interactions
ENSG00000136153	chromatin interactions
ENSG00000233873	chromatin interactions

Extended variants
information (count: 2450 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2450 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2147006	chr13:76244056-76244057	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs544170322	chr13:76244126-76244127	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538141220	chr13:76244134-76244135	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114677510	chr13:76244193-76244194	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12583362	chr13:76244199-76244200	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532384030	chr13:76244208-76244209	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs57554394	chr13:76244231-76244232	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116563905	chr13:76244281-76244282	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545301671	chr13:76244296-76244297	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7337929	chr13:76244318-76244319	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs374863653	chr13:76244362-76244363	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527928166	chr13:76244371-76244372	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79832423	chr13:76244410-76244411	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561067493	chr13:76244412-76244413	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535270900	chr13:76244447-76244448	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531329399	chr13:76244462-76244463	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184691805	chr13:76244502-76244503	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571266215	chr13:76244523-76244524	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9600523	chr13:76244601-76244602	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs141097019	chr13:76244604-76244605	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150255992	chr13:76244606-76244607	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189431932	chr13:76244686-76244687	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145819237	chr13:76244708-76244709	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574048049	chr13:76244717-76244718	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537961451	chr13:76244804-76244805	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556093255	chr13:76244805-76244806	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77045408	chr13:76244833-76244834	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140640441	chr13:76244863-76244864	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539102928	chr13:76244902-76244903	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145373542	chr13:76244906-76244907	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572525979	chr13:76245046-76245047	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7322210	chr13:76245090-76245091	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs552236505	chr13:76245102-76245103	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201943179	chr13:76245120-76245121	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs118022095	chr13:76245132-76245133	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372522405	chr13:76245211-76245212	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531388197	chr13:76245213-76245214	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35724045	chr13:76245216-76245217	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs67810171	chr13:76245239-76245240	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs181484705	chr13:76245273-76245274	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532177617	chr13:76245279-76245280	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547691216	chr13:76245307-76245308	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs71127570	chr13:76245345-76245346	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570728224	chr13:76245346-76245347	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531466631	chr13:76245349-76245350	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565933601	chr13:76245353-76245354	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs202201485	chr13:76245358-76245359	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529958887	chr13:76245363-76245364	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs75235803	chr13:76245378-76245379	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79337529	chr13:76245380-76245381	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76213400-76267800	Weak transcription	Primary T cells from cord blood	blood
2	chr13:76215400-76258200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:76235800-76249200	Weak transcription	Aorta	Aorta
4	chr13:76236000-76249200	Weak transcription	Ovary	ovary
5	chr13:76236800-76267600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr13:76237200-76248800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr13:76240600-76244600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr13:76241200-76255600	Weak transcription	HSMMtube	muscle
9	chr13:76242200-76244400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr13:76242400-76247800	Genic enhancers	Muscle Satellite Cultured Cells	--
11	chr13:76242600-76244800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr13:76242600-76244800	Enhancers	NHDF-Ad	bronchial
13	chr13:76242800-76244800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr13:76242800-76248800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr13:76243000-76244600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr13:76243000-76244600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr13:76243000-76244800	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr13:76243000-76244800	Enhancers	Osteobl	bone
19	chr13:76243000-76245200	Enhancers	NH-A	brain
20	chr13:76243000-76246800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr13:76243200-76245400	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr13:76243600-76244200	Enhancers	Psoas Muscle	Psoas
23	chr13:76243800-76244200	Enhancers	Fetal Muscle Leg	muscle
24	chr13:76243800-76244200	Weak transcription	HSMM	muscle
25	chr13:76243800-76244800	Enhancers	NHLF	lung
26	chr13:76243800-76245400	Enhancers	HUVEC	blood vessel
27	chr13:76244000-76244600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr13:76244000-76245400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr13:76244200-76244800	Enhancers	HSMM	muscle
30	chr13:76244200-76245600	Weak transcription	Psoas Muscle	Psoas
31	chr13:76244400-76245000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr13:76244600-76246800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr13:76244600-76249600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr13:76244600-76253000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr13:76244800-76245200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr13:76244800-76245200	Weak transcription	NHLF	lung
37	chr13:76244800-76245200	Weak transcription	Osteobl	bone
38	chr13:76244800-76245400	Weak transcription	HSMM	muscle
39	chr13:76244800-76245400	Weak transcription	NHDF-Ad	bronchial
40	chr13:76244800-76246600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr13:76244800-76248800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr13:76245000-76248400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr13:76245200-76245400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr13:76245200-76247800	Genic enhancers	NHLF	lung
45	chr13:76245200-76248800	Weak transcription	NH-A	brain
46	chr13:76245200-76251600	Genic enhancers	Osteobl	bone
47	chr13:76245400-76245800	Strong transcription	NHDF-Ad	bronchial
48	chr13:76245400-76247200	Strong transcription	HSMM	muscle
49	chr13:76245400-76247400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr13:76245400-76247800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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