Variant report

Variant	nsv1031179
Chromosome Location	chr6:55237283-55372905
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	chr6:55298219-55298583	IMR90	lung:	n/a	chr6:55298389-55298400
2	CEBPB	chr6:55264114-55264494	IMR90	lung:	n/a	chr6:55264300-55264311 chr6:55264300-55264313 chr6:55264302-55264311
3	CEBPB	chr6:55257225-55257521	IMR90	lung:	n/a	chr6:55257384-55257395
4	CEBPB	chr6:55244717-55244983	HepG2	liver:	n/a	chr6:55244867-55244878
5	CEBPB	chr6:55366892-55367073	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:55299688-55299810	HepG2	liver:	n/a	n/a
7	CEBPB	chr6:55244739-55244990	ECC-1	luminal epithelium:	n/a	chr6:55244867-55244878
8	CEBPB	chr6:55257283-55257592	MCF-7	breast:	n/a	chr6:55257384-55257395
9	CEBPB	chr6:55264135-55264433	ECC-1	luminal epithelium:	n/a	chr6:55264300-55264311 chr6:55264300-55264313 chr6:55264302-55264311
10	CEBPB	chr6:55256365-55256560	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:55264142-55264470	HepG2	liver:	n/a	chr6:55264300-55264311 chr6:55264300-55264313 chr6:55264302-55264311
12	CEBPB	chr6:55244698-55245040	IMR90	lung:	n/a	chr6:55244867-55244878
13	CEBPB	chr6:55298214-55298564	Hela-S3	cervix:	n/a	chr6:55298389-55298400
14	CEBPB	chr6:55257207-55257541	HepG2	liver:	n/a	chr6:55257384-55257395
15	CEBPB	chr6:55262743-55263238	IMR90	lung:	n/a	n/a
16	CEBPB	chr6:55298259-55298598	ECC-1	luminal epithelium:	n/a	chr6:55298389-55298400
17	CEBPB	chr6:55298241-55298550	HepG2	liver:	n/a	chr6:55298389-55298400
18	CEBPB	chr6:55298290-55298525	A549	lung:	n/a	chr6:55298389-55298400
19	CEBPB	chr6:55298209-55298577	H1-hESC	embryonic stem cell:	n/a	chr6:55298389-55298400
20	CEBPB	chr6:55312755-55312946	A549	lung:	n/a	n/a
21	CEBPB	chr6:55244710-55244987	ECC-1	luminal epithelium:	n/a	chr6:55244867-55244878
22	CEBPB	chr6:55257235-55257548	H1-hESC	embryonic stem cell:	n/a	chr6:55257384-55257395
23	CEBPB	chr6:55264203-55264395	A549	lung:	n/a	chr6:55264300-55264311 chr6:55264300-55264313 chr6:55264302-55264311
24	CEBPB	chr6:55278882-55279059	H1-hESC	embryonic stem cell:	n/a	chr6:55279019-55279030 chr6:55279019-55279028 chr6:55279017-55279028 chr6:55279017-55279030
25	CEBPB	chr6:55298198-55298569	MCF-7	breast:	n/a	chr6:55298389-55298400
26	CEBPB	chr6:55278839-55279199	HepG2	liver:	n/a	chr6:55279019-55279030 chr6:55279019-55279028 chr6:55279017-55279028 chr6:55279017-55279030
27	CTCF	chr6:55310540-55310690	Caco-2	colon:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
28	CTCF	chr6:55310569-55310693	MCF-7	breast:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
29	CTCF	chr6:55310540-55310690	HFF	foreskin:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
30	CTCF	chr6:55310583-55310630	GM13976	blood:	n/a	chr6:55310608-55310626 chr6:55310609-55310625
31	CTCF	chr6:55314140-55314290	GM12865	blood:	n/a	n/a
32	CTCF	chr6:55310506-55310779	A549	lung:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
33	CTCF	chr6:55314140-55314290	AG09309	skin:	n/a	n/a
34	CTCF	chr6:55314140-55314290	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr6:55275960-55276110	HCT-116	colon:	n/a	n/a
36	CTCF	chr6:55310580-55310730	GM12868	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
37	CTCF	chr6:55314060-55314358	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:55310520-55310670	Hela-S3	cervix:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
39	CTCF	chr6:55314147-55314263	HepG2	liver:	n/a	n/a
40	CTCF	chr6:55310480-55310630	GM12875	blood:	n/a	chr6:55310608-55310626 chr6:55310609-55310625
41	CTCF	chr6:55313974-55314367	T-47D	breast:	n/a	n/a
42	CTCF	chr6:55310560-55310710	Hela-S3	cervix:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
43	CTCF	chr6:55310560-55310710	HCPEpiC	choroid plexus:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
44	CTCF	chr6:55310500-55310650	GM12867	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
45	CTCF	chr6:55310680-55310830	A549	lung:	n/a	n/a
46	CTCF	chr6:55310520-55310670	GM12865	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
47	CTCF	chr6:55276172-55276254	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr6:55310511-55310707	GM13977	blood:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
49	CTCF	chr6:55310500-55310650	HepG2	liver:	n/a	chr6:55310608-55310626 chr6:55310610-55310631 chr6:55310609-55310625
50	CTCF	chr6:55314127-55314289	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:55263110-55263160	GM12892	blood:	n/a
2	chr6:55314478-55314528	NHBE	bronchial:	n/a
3	chr6:55263110-55263160	T-47D	breast:	n/a
4	chr6:55298362-55298412	BE2_C	brain:	n/a
5	chr6:55314478-55314528	HPAEpiC	pulmonary alveolar:	n/a
6	chr6:55263110-55263160	PrEC	prostate:	n/a
7	chr6:55263110-55263160	HRCEpiC	kidney:	n/a
8	chr6:55263110-55263160	GM19239	blood:	n/a
9	chr6:55314478-55314528	AG10803	skin:	n/a
10	chr6:55298362-55298412	A549	lung:	n/a
11	chr6:55263110-55263160	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:55263110-55263160	MCF10A-Er-Src	breast:	n/a
13	chr6:55314478-55314528	AG09309	skin:	n/a
14	chr6:55314478-55314528	HCT-116	colon:	n/a
15	chr6:55314478-55314528	SK-N-SH	brain:	n/a
16	chr6:55298362-55298412	NH-A	brain:	n/a
17	chr6:55314478-55314528	T-47D	breast:	n/a
18	chr6:55298362-55298412	NHBE	bronchial:	n/a
19	chr6:55314478-55314528	LNCaP	prostate:	n/a
20	chr6:55267138-55267188	GM12891	blood:	n/a
21	chr6:55298362-55298412	PrEC	prostate:	n/a
22	chr6:55267138-55267188	MCF10A-Er-Src	breast:	n/a
23	chr6:55314478-55314528	HEK293	kidney:	embryo
24	chr6:55263110-55263160	HCPEpiC	choroid plexus:	n/a
25	chr6:55314478-55314528	IMR90	lung:	fetal
26	chr6:55263110-55263160	PANC-1	pancreas:	n/a
27	chr6:55263110-55263160	CMK	blood:	n/a
28	chr6:55263110-55263160	SAEC	small airway:	n/a
29	chr6:55298362-55298412	BJ	skin:	n/a
30	chr6:55267138-55267188	AG10803	skin:	n/a
31	chr6:55267138-55267188	HRPEpiC	eye:	n/a
32	chr6:55263110-55263160	HL-60	blood:	n/a
33	chr6:55263110-55263160	BJ	skin:	n/a
34	chr6:55314478-55314528	RPTEC	kidney:	n/a
35	chr6:55267138-55267188	HCPEpiC	choroid plexus:	n/a
36	chr6:55267138-55267188	HL-60	blood:	n/a
37	chr6:55314478-55314528	HepG2	liver:	n/a
38	chr6:55314478-55314528	PANC-1	pancreas:	n/a
39	chr6:55263110-55263160	GM12891	blood:	n/a
40	chr6:55298362-55298412	HCT-116	colon:	n/a
41	chr6:55298362-55298412	SK-N-SH	brain:	n/a
42	chr6:55263110-55263160	HEEpiC	esophagus:	n/a
43	chr6:55263110-55263160	SKMC	muscle:	n/a
44	chr6:55263110-55263160	ovcar-3	ovarian:	n/a
45	chr6:55314478-55314528	CMK	blood:	n/a
46	chr6:55267138-55267188	RPTEC	kidney:	n/a
47	chr6:55263110-55263160	ECC-1	luminal epithelium:	n/a
48	chr6:55298362-55298412	HRPEpiC	eye:	n/a
49	chr6:55298362-55298412	GM12878	blood:	n/a
50	chr6:55267138-55267188	NHBE	bronchial:	n/a

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

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

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

Extended variants
information (count: 2363 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2363 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11753608	chr6:55248402-55248403	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372682536	chr6:55248462-55248463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556264624	chr6:55248474-55248475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576149575	chr6:55248493-55248494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541885913	chr6:55248499-55248500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561555020	chr6:55248507-55248508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146986278	chr6:55248518-55248519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572908221	chr6:55248596-55248597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541809685	chr6:55248611-55248612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564210062	chr6:55248630-55248631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532972086	chr6:55248651-55248652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549824677	chr6:55248660-55248661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115016012	chr6:55248688-55248689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138080344	chr6:55248741-55248742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116683297	chr6:55248782-55248783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191117212	chr6:55248784-55248785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534119763	chr6:55248810-55248811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201081492	chr6:55248811-55248812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548102155	chr6:55248851-55248852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77858413	chr6:55248852-55248853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540094850	chr6:55248862-55248863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141669952	chr6:55248864-55248865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143727643	chr6:55248901-55248902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535555195	chr6:55248907-55248908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182527384	chr6:55248912-55248913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187175893	chr6:55248915-55248916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148110733	chr6:55248929-55248930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557905869	chr6:55248962-55248963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566732267	chr6:55248978-55248979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535436595	chr6:55249029-55249030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577878499	chr6:55249038-55249039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548674586	chr6:55249068-55249069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs578023093	chr6:55249069-55249070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374788881	chr6:55249076-55249077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs386701366	chr6:55249101-55249102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146448386	chr6:55249103-55249104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528893837	chr6:55249120-55249121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537520491	chr6:55249140-55249141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542782336	chr6:55249143-55249144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559165932	chr6:55249168-55249169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377182202	chr6:55249267-55249268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116573550	chr6:55249268-55249269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185424321	chr6:55249279-55249280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577013019	chr6:55249280-55249281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142604081	chr6:55249282-55249283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570991109	chr6:55249292-55249293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141864203	chr6:55249342-55249343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189896039	chr6:55249373-55249374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs193274131	chr6:55249402-55249403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539601237	chr6:55249404-55249405	Weak transcription	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55248400-55248600	Enhancers	Fetal Lung	lung
2	chr6:55248600-55249600	Weak transcription	Fetal Lung	lung
3	chr6:55249600-55250200	Enhancers	Fetal Lung	lung
4	chr6:55252800-55253200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:55253600-55254000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:55254000-55254400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:55254400-55255000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr6:55254400-55255000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr6:55260600-55261000	Enhancers	Colon Smooth Muscle	Colon
10	chr6:55260600-55261000	Enhancers	Fetal Heart	heart
11	chr6:55260600-55261000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr6:55260600-55261200	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr6:55261000-55262400	Weak transcription	Fetal Heart	heart
14	chr6:55262400-55263000	Enhancers	Fetal Heart	heart
15	chr6:55262400-55263200	Enhancers	Fetal Stomach	stomach
16	chr6:55263200-55269800	Weak transcription	Fetal Stomach	stomach
17	chr6:55263400-55263600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:55264400-55264600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:55268200-55268400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:55268400-55268800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:55269800-55270000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:55269800-55270800	Enhancers	Fetal Stomach	stomach
23	chr6:55270200-55271000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:55270200-55271200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:55270400-55271400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:55279600-55280400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:55279800-55280200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr6:55279800-55280200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr6:55288600-55289200	Enhancers	Fetal Lung	lung
30	chr6:55296000-55298400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr6:55297800-55299000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr6:55298000-55298600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:55298200-55298600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr6:55298200-55298800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr6:55298200-55298800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr6:55298200-55298800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr6:55298200-55298800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr6:55298200-55299000	Enhancers	H1 Cell Line	embryonic stem cell
39	chr6:55298200-55299000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr6:55298200-55299000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr6:55298200-55299000	Enhancers	HMEC	breast
42	chr6:55298200-55299200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr6:55298200-55299200	Enhancers	NHLF	lung
44	chr6:55298400-55298800	Enhancers	H9 Cell Line	embryonic stem cell
45	chr6:55298400-55299000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:55298400-55299000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr6:55298400-55299000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:55298400-55299000	Enhancers	NHDF-Ad	bronchial
49	chr6:55298400-55299000	Enhancers	Osteobl	bone
50	chr6:55298400-55299200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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