Variant report

Variant	nsv948358
Chromosome Location	chr6:55351282-55477277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:636)
CpG islands
(count:735)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr6:55393389-55393856	HCT-116	colon:	n/a	n/a
2	CEBPB	chr6:55443265-55443629	A549	lung:	n/a	chr6:55443437-55443454
3	CEBPB	chr6:55385781-55385844	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:55443286-55443640	ECC-1	luminal epithelium:	n/a	chr6:55443437-55443454
5	CEBPB	chr6:55445995-55446021	H1-hESC	embryonic stem cell:	n/a	chr6:55446001-55446012
6	CEBPB	chr6:55445912-55446112	HepG2	liver:	n/a	chr6:55446001-55446012
7	CEBPB	chr6:55443262-55443616	IMR90	lung:	n/a	chr6:55443437-55443454
8	CEBPB	chr6:55408503-55408840	MCF-7	breast:	n/a	chr6:55408647-55408658
9	CEBPB	chr6:55443283-55443610	ECC-1	luminal epithelium:	n/a	chr6:55443437-55443454
10	CEBPB	chr6:55408489-55408766	Hela-S3	cervix:	n/a	chr6:55408647-55408658
11	CEBPB	chr6:55408555-55408697	HepG2	liver:	n/a	chr6:55408647-55408658
12	CEBPB	chr6:55383682-55383825	H1-hESC	embryonic stem cell:	n/a	chr6:55383795-55383804 chr6:55383795-55383804 chr6:55383795-55383804
13	CEBPB	chr6:55408510-55408778	ECC-1	luminal epithelium:	n/a	chr6:55408647-55408658
14	CEBPB	chr6:55383636-55383938	HepG2	liver:	n/a	chr6:55383795-55383804 chr6:55383795-55383804 chr6:55383795-55383804
15	CEBPB	chr6:55366892-55367073	IMR90	lung:	n/a	n/a
16	CEBPB	chr6:55408479-55408866	H1-hESC	embryonic stem cell:	n/a	chr6:55408647-55408658
17	CEBPB	chr6:55408521-55408781	A549	lung:	n/a	chr6:55408647-55408658
18	CEBPB	chr6:55443188-55443733	MCF-7	breast:	n/a	chr6:55443437-55443454
19	CEBPB	chr6:55401216-55401482	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:55450814-55451108	IMR90	lung:	n/a	chr6:55450936-55450949
21	CEBPB	chr6:55443279-55443962	H1-hESC	embryonic stem cell:	n/a	chr6:55443437-55443454
22	CEBPB	chr6:55373305-55373548	HepG2	liver:	n/a	chr6:55373422-55373431 chr6:55373420-55373433 chr6:55373420-55373431 chr6:55373422-55373433
23	CEBPB	chr6:55443277-55443623	HepG2	liver:	n/a	chr6:55443437-55443454
24	CEBPB	chr6:55429297-55429554	HepG2	liver:	n/a	chr6:55429427-55429440 chr6:55429429-55429438 chr6:55429429-55429440
25	CEBPB	chr6:55410571-55411034	MCF-7	breast:	n/a	n/a
26	CEBPB	chr6:55408455-55408858	MCF-7	breast:	n/a	chr6:55408647-55408658
27	CEBPB	chr6:55450783-55451015	HepG2	liver:	n/a	chr6:55450936-55450949
28	CEBPB	chr6:55383630-55383889	A549	lung:	n/a	chr6:55383795-55383804 chr6:55383795-55383804 chr6:55383795-55383804
29	CEBPB	chr6:55410535-55410988	MCF-7	breast:	n/a	n/a
30	CEBPB	chr6:55408464-55408799	HepG2	liver:	n/a	chr6:55408647-55408658
31	CHD2	chr6:55443888-55444121	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr6:55443468-55444221	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr6:55393580-55393730	BJ	skin:	n/a	n/a
34	CTCF	chr6:55377820-55377970	AG04449	skin:	n/a	n/a
35	CTCF	chr6:55393520-55393670	GM12875	blood:	n/a	n/a
36	CTCF	chr6:55393466-55393919	HCT-116	colon:	n/a	n/a
37	CTCF	chr6:55395900-55396050	HepG2	liver:	n/a	chr6:55395967-55395975
38	CTCF	chr6:55393580-55393730	GM12872	blood:	n/a	n/a
39	CTCF	chr6:55386494-55386553	GM13976	blood:	n/a	n/a
40	CTCF	chr6:55393520-55393670	SAEC	small airway:	n/a	n/a
41	CTCF	chr6:55393525-55393698	LNCaP	prostate:	n/a	n/a
42	CTCF	chr6:55408760-55408910	NHEK	skin:	n/a	n/a
43	CTCF	chr6:55393540-55393690	GM12866	blood:	n/a	n/a
44	CTCF	chr6:55443814-55444080	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:55393360-55393510	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr6:55377720-55377870	HCFaa	heart:	n/a	n/a
47	CTCF	chr6:55393520-55393670	RPTEC	kidney:	n/a	n/a
48	CTCF	chr6:55362640-55362790	Caco-2	colon:	n/a	n/a
49	CTCF	chr6:55393520-55393670	HCT-116	colon:	n/a	n/a
50	CTCF	chr6:55393580-55393730	HFF-Myc	foreskin:	n/a	n/a

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:55444153-55444203	BJ	skin:	n/a
2	chr6:55443757-55443807	AG04450	lung:	fetal
3	chr6:55444335-55444385	GM12892	blood:	n/a
4	chr6:55444153-55444203	BJ	skin:	n/a
5	chr6:55443757-55443807	AG04450	lung:	fetal
6	chr6:55444335-55444385	GM12892	blood:	n/a
7	chr6:55444072-55444122	ProgFib	skin:	n/a
8	chr6:55443757-55443807	BJ	skin:	n/a
9	chr6:55441704-55441754	HNPCEpiC	eye:	n/a
10	chr6:55444488-55444538	ovcar-3	ovarian:	n/a
11	chr6:55444079-55444129	PrEC	prostate:	n/a
12	chr6:55444488-55444538	PrEC	prostate:	n/a
13	chr6:55444061-55444111	LNCaP	prostate:	n/a
14	chr6:55441704-55441754	ProgFib	skin:	n/a
15	chr6:55444079-55444129	SK-N-SH	brain:	n/a
16	chr6:55444821-55444871	HCT-116	colon:	n/a
17	chr6:55444072-55444122	AG10803	skin:	n/a
18	chr6:55444153-55444203	AG04449	skin:	fetal
19	chr6:55444335-55444385	HRE	kidney:	n/a
20	chr6:55444061-55444111	HepG2	liver:	n/a
21	chr6:55444079-55444129	HPAEpiC	pulmonary alveolar:	n/a
22	chr6:55444488-55444538	Jurkat	blood:	n/a
23	chr6:55441704-55441754	SK-N-MC	brain:	n/a
24	chr6:55444821-55444871	SK-N-MC	brain:	n/a
25	chr6:55444091-55444141	HCF	heart:	n/a
26	chr6:55444061-55444111	H1-hESC	embryonic stem cell:	embryo
27	chr6:55444091-55444141	SKMC	muscle:	n/a
28	chr6:55444488-55444538	ECC-1	luminal epithelium:	n/a
29	chr6:55444821-55444871	NT2-D1	testis:	n/a
30	chr6:55444335-55444385	PANC-1	pancreas:	n/a
31	chr6:55443757-55443807	NH-A	brain:	n/a
32	chr6:55444091-55444141	SK-N-SH	brain:	n/a
33	chr6:55444335-55444385	Caco-2	colon:	n/a
34	chr6:55443868-55443918	RPTEC	kidney:	n/a
35	chr6:55444153-55444203	H1-hESC	embryonic stem cell:	embryo
36	chr6:55444335-55444385	GM12878	blood:	n/a
37	chr6:55443868-55443918	PrEC	prostate:	n/a
38	chr6:55441704-55441754	RPTEC	kidney:	n/a
39	chr6:55443757-55443807	ovcar-3	ovarian:	n/a
40	chr6:55444488-55444538	AG04449	skin:	fetal
41	chr6:55443868-55443918	NB4	blood:	n/a
42	chr6:55444091-55444141	ECC-1	luminal epithelium:	n/a
43	chr6:55444061-55444111	HCF	heart:	n/a
44	chr6:55444335-55444385	NB4	blood:	n/a
45	chr6:55444488-55444538	HRE	kidney:	n/a
46	chr6:55444488-55444538	AG04450	lung:	fetal
47	chr6:55443868-55443918	ECC-1	luminal epithelium:	n/a
48	chr6:55443833-55443883	HIPEpiC	eye:	n/a
49	chr6:55444153-55444203	CMK	blood:	n/a
50	chr6:55444061-55444111	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr6:55378223..55380878-chr6:55387259..55389962,2	MCF-7	breast:
2	chr6:55447631..55450427-chr6:55457989..55460440,2	K562	blood:
3	chr18:68082649..68083606-chr6:55385827..55386468,2	MCF-7	breast:
4	chr6:55390675..55392661-chr6:55393968..55396967,2	K562	blood:
5	chr6:55447631..55450427-chr6:55457989..55460440,2	K562	blood:
6	chr6:55419764..55422161-chr6:55427119..55429857,2	MCF-7	breast:
7	chr6:55377485..55380117-chr6:55381946..55384931,2	MCF-7	breast:
8	chr6:55412158..55414482-chr6:55747955..55749467,2	MCF-7	breast:
9	chr6:55378223..55380878-chr6:55387259..55389962,2	MCF-7	breast:
10	chr6:55444071..55446451-chr6:55467125..55469280,2	K562	blood:
11	chr6:55377485..55380117-chr6:55381946..55384931,2	MCF-7	breast:
12	chr6:55456841..55459297-chr6:55463309..55465758,2	K562	blood:
13	chr6:55390675..55392661-chr6:55393968..55396967,2	K562	blood:
14	chr6:55419764..55422161-chr6:55427119..55429857,2	MCF-7	breast:
15	chr6:55408291..55411136-chr6:55443086..55445470,2	MCF-7	breast:
16	chr6:55435736..55437796-chr6:55442771..55444842,2	K562	blood:
17	chr6:55456841..55459297-chr6:55463309..55465758,2	K562	blood:
18	chr6:55444071..55446451-chr6:55467125..55469280,2	K562	blood:
19	chr6:55377472..55378318-chr6:55806611..55807235,2	MCF-7	breast:

No data

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

Extended variants
information (count: 3667 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3667 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532123713	chr6:55352406-55352407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558405179	chr6:55352419-55352420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551847712	chr6:55352566-55352567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6459081	chr6:55352586-55352587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs372528366	chr6:55352595-55352596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531924977	chr6:55352625-55352626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550253693	chr6:55352630-55352631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558583289	chr6:55352644-55352645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187494113	chr6:55352660-55352661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567966861	chr6:55352674-55352675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536527774	chr6:55352695-55352696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192934530	chr6:55352714-55352715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184572596	chr6:55352755-55352756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370544838	chr6:55352758-55352759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74916287	chr6:55352783-55352784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546378927	chr6:55352814-55352815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76891393	chr6:55352859-55352860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575600784	chr6:55352891-55352892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544417647	chr6:55352912-55352913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554453167	chr6:55352940-55352941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116426588	chr6:55352947-55352948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111329460	chr6:55352960-55352961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7756150	chr6:55353017-55353018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7756162	chr6:55353039-55353040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs545349204	chr6:55353057-55353058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9475313	chr6:55353069-55353070	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531276837	chr6:55353076-55353077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188260373	chr6:55353115-55353116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7756201	chr6:55353136-55353137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs10456714	chr6:55353154-55353155	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs144842031	chr6:55353170-55353171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9296784	chr6:55353233-55353234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147936840	chr6:55353242-55353243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192263191	chr6:55353244-55353245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569348969	chr6:55353268-55353269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537932495	chr6:55353293-55353294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554795821	chr6:55353299-55353300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574539101	chr6:55353313-55353314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61420782	chr6:55353316-55353317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9475314	chr6:55353353-55353354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs75451364	chr6:55353375-55353376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141732043	chr6:55353385-55353386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562332271	chr6:55353442-55353443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567224855	chr6:55353454-55353455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575250525	chr6:55353475-55353476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184282278	chr6:55353540-55353541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189439372	chr6:55353565-55353566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371862428	chr6:55353576-55353577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62407071	chr6:55353585-55353586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs547168804	chr6:55353597-55353598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55352400-55355200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr6:55358000-55358200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:55358000-55358200	Enhancers	NHEK	skin
4	chr6:55358200-55359200	Weak transcription	NHEK	skin
5	chr6:55358800-55359000	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
6	chr6:55359000-55359400	Enhancers	Colon Smooth Muscle	Colon
7	chr6:55359000-55360400	Enhancers	Fetal Lung	lung
8	chr6:55359200-55361400	Enhancers	NHEK	skin
9	chr6:55359200-55361600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:55359800-55361600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:55359800-55361600	Enhancers	HMEC	breast
12	chr6:55360000-55360400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:55360400-55361400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:55360600-55361800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr6:55361200-55361600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr6:55362400-55363000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:55362400-55363000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr6:55362400-55363000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr6:55362400-55363000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr6:55376400-55399200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr6:55376800-55396400	Weak transcription	Left Ventricle	heart
22	chr6:55384200-55384400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr6:55384400-55410200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr6:55385800-55386200	Enhancers	Fetal Lung	lung
25	chr6:55387400-55388200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:55389200-55390400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:55389400-55390400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr6:55389400-55390600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr6:55393600-55393800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:55394000-55407200	Weak transcription	Fetal Muscle Leg	muscle
31	chr6:55395800-55396200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:55396400-55396600	Enhancers	Left Ventricle	heart
33	chr6:55396600-55396800	Weak transcription	Left Ventricle	heart
34	chr6:55399200-55400400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr6:55399200-55402400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:55400400-55418600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr6:55400600-55404000	Weak transcription	Fetal Lung	lung
38	chr6:55402400-55402600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:55402400-55402600	Enhancers	Esophagus	oesophagus
40	chr6:55404000-55404200	Strong transcription	Fetal Lung	lung
41	chr6:55404200-55404400	ZNF genes & repeats	Fetal Lung	lung
42	chr6:55404400-55407600	Weak transcription	Fetal Lung	lung
43	chr6:55408400-55408800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr6:55410200-55411000	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr6:55411000-55411400	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr6:55411400-55412400	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr6:55412400-55412600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr6:55412600-55413000	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr6:55413000-55413200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr6:55413200-55413400	Enhancers	Pancreatic Islets	Pancreatic Islet

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