Variant report

Variant	nsv885904
Chromosome Location	chr6:55156812-55344782
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	CEBPB	chr6:55158736-55159067	HepG2	liver:	n/a	chr6:55158883-55158894
2	CEBPB	chr6:55244717-55244983	HepG2	liver:	n/a	chr6:55244867-55244878
3	CEBPB	chr6:55158827-55159011	A549	lung:	n/a	chr6:55158883-55158894
4	CEBPB	chr6:55278839-55279199	HepG2	liver:	n/a	chr6:55279019-55279030 chr6:55279019-55279028 chr6:55279017-55279028 chr6:55279017-55279030
5	CEBPB	chr6:55158810-55158971	H1-hESC	embryonic stem cell:	n/a	chr6:55158883-55158894
6	CEBPB	chr6:55298219-55298583	IMR90	lung:	n/a	chr6:55298389-55298400
7	CEBPB	chr6:55262743-55263238	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:55256365-55256560	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:55264142-55264470	HepG2	liver:	n/a	chr6:55264300-55264311 chr6:55264300-55264313 chr6:55264302-55264311
10	CEBPB	chr6:55244698-55245040	IMR90	lung:	n/a	chr6:55244867-55244878
11	CEBPB	chr6:55158811-55158942	Hela-S3	cervix:	n/a	chr6:55158883-55158894
12	CEBPB	chr6:55264135-55264433	ECC-1	luminal epithelium:	n/a	chr6:55264300-55264311 chr6:55264300-55264313 chr6:55264302-55264311
13	CEBPB	chr6:55244739-55244990	ECC-1	luminal epithelium:	n/a	chr6:55244867-55244878
14	CEBPB	chr6:55257225-55257521	IMR90	lung:	n/a	chr6:55257384-55257395
15	CEBPB	chr6:55257207-55257541	HepG2	liver:	n/a	chr6:55257384-55257395
16	CEBPB	chr6:55278882-55279059	H1-hESC	embryonic stem cell:	n/a	chr6:55279019-55279030 chr6:55279019-55279028 chr6:55279017-55279028 chr6:55279017-55279030
17	CEBPB	chr6:55158743-55159059	IMR90	lung:	n/a	chr6:55158883-55158894
18	CEBPB	chr6:55298209-55298577	H1-hESC	embryonic stem cell:	n/a	chr6:55298389-55298400
19	CEBPB	chr6:55257235-55257548	H1-hESC	embryonic stem cell:	n/a	chr6:55257384-55257395
20	CEBPB	chr6:55244710-55244987	ECC-1	luminal epithelium:	n/a	chr6:55244867-55244878
21	CEBPB	chr6:55298198-55298569	MCF-7	breast:	n/a	chr6:55298389-55298400
22	CEBPB	chr6:55169601-55169886	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:55264203-55264395	A549	lung:	n/a	chr6:55264300-55264311 chr6:55264300-55264313 chr6:55264302-55264311
24	CEBPB	chr6:55298241-55298550	HepG2	liver:	n/a	chr6:55298389-55298400
25	CEBPB	chr6:55299688-55299810	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:55312755-55312946	A549	lung:	n/a	n/a
27	CEBPB	chr6:55169647-55169866	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr6:55201206-55201343	HepG2	liver:	n/a	chr6:55201247-55201258
29	CEBPB	chr6:55194726-55195070	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:55257283-55257592	MCF-7	breast:	n/a	chr6:55257384-55257395
31	CEBPB	chr6:55298259-55298598	ECC-1	luminal epithelium:	n/a	chr6:55298389-55298400
32	CEBPB	chr6:55264114-55264494	IMR90	lung:	n/a	chr6:55264300-55264311 chr6:55264300-55264313 chr6:55264302-55264311
33	CEBPB	chr6:55298214-55298564	Hela-S3	cervix:	n/a	chr6:55298389-55298400
34	CEBPB	chr6:55298290-55298525	A549	lung:	n/a	chr6:55298389-55298400
35	CTCF	chr6:55158080-55158230	AG04449	skin:	n/a	chr6:55158097-55158115 chr6:55158102-55158112 chr6:55158098-55158114 chr6:55158099-55158120
36	CTCF	chr6:55314200-55314350	BE2_C	brain:	n/a	n/a
37	CTCF	chr6:55158020-55158170	HPAF	blood vessel:	n/a	chr6:55158097-55158115 chr6:55158102-55158112 chr6:55158098-55158114 chr6:55158099-55158120
38	CTCF	chr6:55314200-55314350	HepG2	liver:	n/a	n/a
39	CTCF	chr6:55157940-55158090	WI-38	lung:	n/a	n/a
40	CTCF	chr6:55314140-55314290	GM12865	blood:	n/a	n/a
41	CTCF	chr6:55310520-55310670	GM12873	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
42	CTCF	chr6:55310540-55310690	GM12869	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
43	CTCF	chr6:55158000-55158150	GM12870	blood:	n/a	chr6:55158097-55158115 chr6:55158102-55158112 chr6:55158098-55158114 chr6:55158099-55158120
44	CTCF	chr6:55310520-55310670	GM12865	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
45	CTCF	chr6:55158040-55158190	HUVEC	blood vessel:	n/a	chr6:55158097-55158115 chr6:55158102-55158112 chr6:55158098-55158114 chr6:55158099-55158120
46	CTCF	chr6:55158080-55158230	HAc	cerebellar:	n/a	chr6:55158097-55158115 chr6:55158102-55158112 chr6:55158098-55158114 chr6:55158099-55158120
47	CTCF	chr6:55157980-55158130	HPF	lung:	n/a	chr6:55158097-55158115 chr6:55158102-55158112 chr6:55158098-55158114 chr6:55158099-55158120
48	CTCF	chr6:55314160-55314310	HAc	cerebellar:	n/a	n/a
49	CTCF	chr6:55310560-55310710	HPF	lung:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
50	CTCF	chr6:55313933-55314552	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:55190909-55190959	U87	brain:	n/a
2	chr6:55190909-55190959	U87	brain:	n/a
3	chr6:55234085-55234135	HCPEpiC	choroid plexus:	n/a
4	chr6:55190909-55190959	ovcar-3	ovarian:	n/a
5	chr6:55267138-55267188	IMR90	lung:	fetal
6	chr6:55267138-55267188	PrEC	prostate:	n/a
7	chr6:55234085-55234135	ovcar-3	ovarian:	n/a
8	chr6:55263110-55263160	T-47D	breast:	n/a
9	chr6:55192049-55192099	HNPCEpiC	eye:	n/a
10	chr6:55267138-55267188	HCT-116	colon:	n/a
11	chr6:55234172-55234222	H1-hESC	embryonic stem cell:	embryo
12	chr6:55314478-55314528	HCT-116	colon:	n/a
13	chr6:55234172-55234222	HEK293	kidney:	embryo
14	chr6:55190909-55190959	SK-N-SH	brain:	n/a
15	chr6:55190909-55190959	ProgFib	skin:	n/a
16	chr6:55192049-55192099	NH-A	brain:	n/a
17	chr6:55234085-55234135	GM12892	blood:	n/a
18	chr6:55263110-55263160	HRE	kidney:	n/a
19	chr6:55234085-55234135	AG09319	gingival:	n/a
20	chr6:55267138-55267188	Hepatocyte	liver:	n/a
21	chr6:55190909-55190959	IMR90	lung:	fetal
22	chr6:55234172-55234222	NB4	blood:	n/a
23	chr6:55192049-55192099	HCM	heart:	n/a
24	chr6:55267138-55267188	HUVEC	blood vessel:	n/a
25	chr6:55192049-55192099	AG09319	gingival:	n/a
26	chr6:55234085-55234135	Caco-2	colon:	n/a
27	chr6:55267138-55267188	HNPCEpiC	eye:	n/a
28	chr6:55314478-55314528	NT2-D1	testis:	n/a
29	chr6:55192049-55192099	HepG2	liver:	n/a
30	chr6:55263110-55263160	CMK	blood:	n/a
31	chr6:55314478-55314528	IMR90	lung:	fetal
32	chr6:55192049-55192099	PANC-1	pancreas:	n/a
33	chr6:55314478-55314528	HepG2	liver:	n/a
34	chr6:55314478-55314528	SK-N-SH_RA	brain:	n/a
35	chr6:55234085-55234135	HAEpiC	amniotic membrane:	n/a
36	chr6:55314478-55314528	Hepatocyte	liver:	n/a
37	chr6:55234085-55234135	MCF-7	breast:	n/a
38	chr6:55234172-55234222	HIPEpiC	eye:	n/a
39	chr6:55263110-55263160	HepG2	liver:	n/a
40	chr6:55314478-55314528	MCF10A-Er-Src	breast:	n/a
41	chr6:55298362-55298412	SK-N-SH_RA	brain:	n/a
42	chr6:55263110-55263160	AG04450	lung:	fetal
43	chr6:55298362-55298412	Hela-S3	cervix:	n/a
44	chr6:55234085-55234135	NH-A	brain:	n/a
45	chr6:55234085-55234135	NHDF-neo	bronchial:	n/a
46	chr6:55267138-55267188	GM12891	blood:	n/a
47	chr6:55267138-55267188	RPTEC	kidney:	n/a
48	chr6:55298362-55298412	LNCaP	prostate:	n/a
49	chr6:55314478-55314528	HCPEpiC	choroid plexus:	n/a
50	chr6:55267138-55267188	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:55313181..55315342-chr6:55800874..55802800,2	MCF-7	breast:
2	chr6:55313762..55314282-chr6:56157199..56157825,2	MCF-7	breast:
3	chr6:55313718..55314729-chr6:55817986..55818869,4	MCF-7	breast:
4	chr6:55313713..55314676-chr6:55750196..55751674,4	MCF-7	breast:
5	chr6:55328874..55330567-chr6:55343460..55346330,2	K562	blood:
6	chr6:55310131..55310914-chr6:55750826..55751625,3	MCF-7	breast:
7	chr6:55300666..55302654-chr6:55304305..55306294,2	MCF-7	breast:
8	chr6:55296640..55298261-chr6:55299680..55302209,2	K562	blood:
9	chr6:55328874..55330567-chr6:55343460..55346330,2	K562	blood:
10	chr6:55309906..55311058-chr6:55817976..55819297,5	MCF-7	breast:
11	chr6:55296640..55298261-chr6:55299680..55302209,2	K562	blood:
12	chr6:55310143..55310712-chr6:55818032..55818931,2	MCF-7	breast:
13	chr6:55310142..55311120-chr6:56157237..56158075,2	MCF-7	breast:
14	chr6:55314098..55314636-chr6:55750998..55751586,2	MCF-7	breast:
15	chr6:55313873..55314721-chr6:55806208..55806737,2	MCF-7	breast:
16	chr6:55310627..55311224-chr6:55806307..55806968,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMP5-4	chr6:55310232-55312709	NONHSAT113233

Variant related genes	Relation type
HMGCLL1	TF binding region
GFRAL	TF binding region
HMGCLL1	CpG island
GFRAL	CpG island
ENSG00000146151	chromatin interactions

Extended variants
information (count: 2544 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2544 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571294915	chr6:55157802-55157803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370188066	chr6:55157808-55157809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543780074	chr6:55157861-55157862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537020614	chr6:55157878-55157879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144040406	chr6:55157892-55157893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187129117	chr6:55157921-55157922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2653360	chr6:55158000-55158001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189919181	chr6:55158002-55158003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150245063	chr6:55158052-55158053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79145752	chr6:55158066-55158067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182488839	chr6:55158105-55158106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113454183	chr6:55158166-55158167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149406944	chr6:55158211-55158212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558007497	chr6:55158220-55158221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114536346	chr6:55158308-55158309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543443986	chr6:55158325-55158326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144649723	chr6:55158354-55158355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187063279	chr6:55158362-55158363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529322644	chr6:55158377-55158378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542829941	chr6:55158460-55158461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559554161	chr6:55158465-55158466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148655709	chr6:55158467-55158468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551724693	chr6:55158481-55158482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538371548	chr6:55158493-55158494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372969796	chr6:55158512-55158513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189897760	chr6:55158554-55158555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530560310	chr6:55158557-55158558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376199285	chr6:55158563-55158564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539488181	chr6:55158568-55158569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371319198	chr6:55158570-55158571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142883192	chr6:55158641-55158642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535936073	chr6:55158674-55158675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572557405	chr6:55158675-55158676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147701058	chr6:55158700-55158701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200044761	chr6:55158711-55158712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs386701359	chr6:55158712-55158713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2653362	chr6:55158713-55158714	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs558072620	chr6:55158720-55158721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377457368	chr6:55158729-55158730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371153462	chr6:55158738-55158739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541784486	chr6:55158742-55158743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555296071	chr6:55158749-55158750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528389450	chr6:55158789-55158790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577877037	chr6:55158827-55158828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543802390	chr6:55158854-55158855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190415110	chr6:55158882-55158883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557043642	chr6:55158898-55158899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550445166	chr6:55164200-55164201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560441851	chr6:55164216-55164217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535656705	chr6:55164221-55164222	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	22581003	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55157800-55159000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:55164200-55164800	Enhancers	Fetal Heart	heart
3	chr6:55164200-55165000	Enhancers	Fetal Lung	lung
4	chr6:55164400-55164800	Enhancers	Gastric	stomach
5	chr6:55164800-55165600	Enhancers	Fetal Brain Male	brain
6	chr6:55164800-55167400	Weak transcription	Fetal Heart	heart
7	chr6:55184800-55185400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:55184800-55185600	Enhancers	Fetal Heart	heart
9	chr6:55184800-55185800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr6:55185000-55185200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:55185200-55185600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:55185600-55186000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:55192000-55192400	Active TSS	Adipose Nuclei	Adipose
14	chr6:55205400-55206200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:55217800-55218200	Enhancers	Fetal Heart	heart
16	chr6:55233800-55234400	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr6:55234000-55234200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:55234000-55234400	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr6:55234000-55234400	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr6:55234600-55235000	Enhancers	Spleen	Spleen
21	chr6:55235000-55235400	Weak transcription	Spleen	Spleen
22	chr6:55235400-55235800	Enhancers	Spleen	Spleen
23	chr6:55248400-55248600	Enhancers	Fetal Lung	lung
24	chr6:55248600-55249600	Weak transcription	Fetal Lung	lung
25	chr6:55249600-55250200	Enhancers	Fetal Lung	lung
26	chr6:55252800-55253200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:55253600-55254000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr6:55254000-55254400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:55254400-55255000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr6:55254400-55255000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr6:55260600-55261000	Enhancers	Colon Smooth Muscle	Colon
32	chr6:55260600-55261000	Enhancers	Fetal Heart	heart
33	chr6:55260600-55261000	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr6:55260600-55261200	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr6:55261000-55262400	Weak transcription	Fetal Heart	heart
36	chr6:55262400-55263000	Enhancers	Fetal Heart	heart
37	chr6:55262400-55263200	Enhancers	Fetal Stomach	stomach
38	chr6:55263200-55269800	Weak transcription	Fetal Stomach	stomach
39	chr6:55263400-55263600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:55264400-55264600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:55268200-55268400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:55268400-55268800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:55269800-55270000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr6:55269800-55270800	Enhancers	Fetal Stomach	stomach
45	chr6:55270200-55271000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:55270200-55271200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr6:55270400-55271400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:55279600-55280400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr6:55279800-55280200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr6:55279800-55280200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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