Variant report

Variant	nsv886807
Chromosome Location	chr6:160549080-160559234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:213)
CpG islands
(count:305)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:213 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:160558222-160558701	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:160558963-160559923	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:160556141-160556530	HepG2	liver:	n/a	n/a
4	BHLHE40	chr6:160558127-160558929	HepG2	liver:	n/a	chr6:160558646-160558662
5	BHLHE40	chr6:160559226-160559644	K562	blood:	n/a	n/a
6	BHLHE40	chr6:160548959-160549204	K562	blood:	n/a	n/a
7	BHLHE40	chr6:160559196-160559605	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:160558297-160558517	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:160558239-160558635	HepG2	liver:	n/a	chr6:160558575-160558587
10	CHD2	chr6:160558102-160558653	HepG2	liver:	n/a	n/a
11	CTCF	chr6:160558780-160558930	HPF	lung:	n/a	n/a
12	CTCF	chr6:160559110-160559160	GM13977	blood:	n/a	n/a
13	CTCF	chr6:160556518-160556602	HepG2	liver:	n/a	n/a
14	CTCF	chr6:160559204-160559604	A549	lung:	n/a	n/a
15	CTCF	chr6:160559195-160560172	K562	blood:	n/a	n/a
16	CTCF	chr6:160558980-160559130	HFF	foreskin:	n/a	n/a
17	CTCF	chr6:160558980-160559130	AG04449	skin:	n/a	n/a
18	CTCF	chr6:160559205-160559716	HepG2	liver:	n/a	n/a
19	CTCF	chr6:160559031-160559796	A549	lung:	n/a	n/a
20	CTCF	chr6:160559200-160559350	GM12868	blood:	n/a	n/a
21	CTCF	chr6:160559133-160559146	GM12891	blood:	n/a	n/a
22	CTCF	chr6:160556472-160556667	HepG2	liver:	n/a	n/a
23	CTCF	chr6:160558860-160559010	GM12870	blood:	n/a	n/a
24	CTCF	chr6:160559000-160559150	HVMF	connective:	n/a	n/a
25	CTCF	chr6:160559000-160559150	HMF	breast:	n/a	n/a
26	CTCF	chr6:160559222-160559602	K562	blood:	n/a	n/a
27	CTCF	chr6:160559151-160559695	HCT-116	colon:	n/a	n/a
28	CTCF	chr6:160559200-160559350	GM12870	blood:	n/a	n/a
29	CTCF	chr6:160559207-160560055	GM12878	blood:	n/a	n/a
30	CTCF	chr6:160559040-160559190	GM12873	blood:	n/a	n/a
31	CTCF	chr6:160557100-160557250	GM12874	blood:	n/a	n/a
32	CTCF	chr6:160559020-160559170	GM12865	blood:	n/a	n/a
33	CTCF	chr6:160559020-160559170	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr6:160559150-160559630	K562	blood:	n/a	n/a
35	CTCF	chr6:160558840-160558990	GM12874	blood:	n/a	n/a
36	CTCF	chr6:160558640-160558790	HepG2	liver:	n/a	n/a
37	CTCF	chr6:160559200-160559350	K562	blood:	n/a	n/a
38	CTCF	chr6:160558940-160559090	HCM	heart:	n/a	n/a
39	CTCF	chr6:160557460-160557610	SAEC	small airway:	n/a	n/a
40	CTCF	chr6:160559228-160559666	IMR90	lung:	n/a	n/a
41	CTCF	chr6:160559000-160559150	BE2_C	brain:	n/a	n/a
42	CTCF	chr6:160558660-160558810	GM12873	blood:	n/a	n/a
43	CTCF	chr6:160558818-160559783	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr6:160559080-160559230	NHEK	skin:	n/a	n/a
45	CTCF	chr6:160559080-160559230	GM12864	blood:	n/a	n/a
46	CTCF	chr6:160550020-160550170	GM12865	blood:	n/a	n/a
47	CTCF	chr6:160556440-160556590	Caco-2	colon:	n/a	n/a
48	CTCF	chr6:160559091-160559173	GM19240	blood:	n/a	n/a
49	CTCF	chr6:160559149-160559648	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:160559086-160559225	GM19238	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:160555312-160555362	SK-N-MC	brain:	n/a
2	chr6:160555573-160555623	PANC-1	pancreas:	n/a
3	chr6:160555573-160555623	BE2_C	brain:	n/a
4	chr6:160555086-160555136	GM12892	blood:	n/a
5	chr6:160554674-160554724	HIPEpiC	eye:	n/a
6	chr6:160555086-160555136	HRE	kidney:	n/a
7	chr6:160554674-160554724	HEEpiC	esophagus:	n/a
8	chr6:160555312-160555362	ECC-1	luminal epithelium:	n/a
9	chr6:160555573-160555623	NHDF-neo	bronchial:	n/a
10	chr6:160555086-160555136	PrEC	prostate:	n/a
11	chr6:160555573-160555623	SAEC	small airway:	n/a
12	chr6:160555312-160555362	HRE	kidney:	n/a
13	chr6:160554674-160554724	ovcar-3	ovarian:	n/a
14	chr6:160555573-160555623	HIPEpiC	eye:	n/a
15	chr6:160555312-160555362	GM19239	blood:	n/a
16	chr6:160554674-160554724	HUVEC	blood vessel:	n/a
17	chr6:160554674-160554724	NT2-D1	testis:	n/a
18	chr6:160555086-160555136	Hela-S3	cervix:	n/a
19	chr6:160554003-160554053	HCT-116	colon:	n/a
20	chr6:160554003-160554053	HEEpiC	esophagus:	n/a
21	chr6:160555573-160555623	Caco-2	colon:	n/a
22	chr6:160555573-160555623	AG09319	gingival:	n/a
23	chr6:160554003-160554053	RPTEC	kidney:	n/a
24	chr6:160554003-160554053	HMEC	breast:	n/a
25	chr6:160554003-160554053	BE2_C	brain:	n/a
26	chr6:160555086-160555136	GM19239	blood:	n/a
27	chr6:160554003-160554053	IMR90	lung:	fetal
28	chr6:160555086-160555136	BE2_C	brain:	n/a
29	chr6:160555312-160555362	BE2_C	brain:	n/a
30	chr6:160554674-160554724	MCF10A-Er-Src	breast:	n/a
31	chr6:160554003-160554053	Caco-2	colon:	n/a
32	chr6:160554003-160554053	ECC-1	luminal epithelium:	n/a
33	chr6:160555086-160555136	H1-hESC	embryonic stem cell:	embryo
34	chr6:160555573-160555623	PrEC	prostate:	n/a
35	chr6:160555312-160555362	HEEpiC	esophagus:	n/a
36	chr6:160555573-160555623	AG04449	skin:	fetal
37	chr6:160555312-160555362	HNPCEpiC	eye:	n/a
38	chr6:160555312-160555362	GM12891	blood:	n/a
39	chr6:160554003-160554053	NT2-D1	testis:	n/a
40	chr6:160555573-160555623	ovcar-3	ovarian:	n/a
41	chr6:160555086-160555136	NHBE	bronchial:	n/a
42	chr6:160554674-160554724	HNPCEpiC	eye:	n/a
43	chr6:160555573-160555623	PFSK-1	brain:	n/a
44	chr6:160555573-160555623	AG09309	skin:	n/a
45	chr6:160554003-160554053	HRE	kidney:	n/a
46	chr6:160555086-160555136	BJ	skin:	n/a
47	chr6:160555312-160555362	HepG2	liver:	n/a
48	chr6:160555573-160555623	K562	blood:	n/a
49	chr6:160555573-160555623	GM06990	blood:	n/a
50	chr6:160555086-160555136	AoSMC	blood vessel:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:160558114..160558643-chr6:160876721..160877596,2	MCF-7	breast:
2	chr6:160559166..160560422-chr6:160876706..160877623,9	K562	blood:
3	chr6:160519823..160522664-chr6:160558781..160560789,2	K562	blood:
4	chr6:160552829..160554455-chr6:160557488..160559667,2	K562	blood:
5	chr6:160559129..160560035-chr6:160876676..160877443,6	MCF-7	breast:
6	chr6:160558415..160560977-chr6:160562640..160565543,2	K562	blood:
7	chr6:160550752..160552280-chr6:160554452..160556406,2	K562	blood:
8	chr6:160559138..160559777-chr6:160954950..160955755,2	K562	blood:
9	chr6:160552829..160554455-chr6:160557488..160559667,2	K562	blood:
10	chr6:160559095..160559619-chr6:160789372..160789918,2	K562	blood:

No data

Variant related genes	Relation type
SLC22A1	TF binding region
SLC22A1	CpG island
ENSG00000175003	chromatin interactions

Extended variants
information (count: 478 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12526281	chr6:160549080-160549081	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs533953024	chr6:160549112-160549113	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs554105085	chr6:160549130-160549131	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571063684	chr6:160549142-160549143	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs547450499	chr6:160549233-160549234	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540088456	chr6:160549240-160549241	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs112288688	chr6:160549243-160549244	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs576227718	chr6:160549251-160549252	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs537578233	chr6:160549315-160549316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111695907	chr6:160549375-160549376	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs554228924	chr6:160549381-160549382	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs73025542	chr6:160549402-160549403	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs539850814	chr6:160549430-160549431	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs145209248	chr6:160549479-160549480	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs539990015	chr6:160549571-160549572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190220635	chr6:160549634-160549635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114509192	chr6:160549653-160549654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375920923	chr6:160549771-160549772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536236878	chr6:160549779-160549780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs80320193	chr6:160549797-160549798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562698065	chr6:160549820-160549821	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117910272	chr6:160549822-160549823	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369991627	chr6:160549844-160549845	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149160203	chr6:160549846-160549847	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143315281	chr6:160549910-160549911	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527740046	chr6:160549912-160549913	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561802143	chr6:160549927-160549928	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73025543	chr6:160549949-160549950	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs550586830	chr6:160549952-160549953	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs539794109	chr6:160549954-160549955	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs550041195	chr6:160550034-160550035	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs35346084	chr6:160550056-160550057	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs538109701	chr6:160550091-160550092	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs34285160	chr6:160550099-160550100	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs148022212	chr6:160550103-160550104	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs375584413	chr6:160550144-160550145	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs558046257	chr6:160550173-160550174	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs535668538	chr6:160550286-160550287	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs75442170	chr6:160550391-160550392	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146091457	chr6:160550408-160550409	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533877336	chr6:160550411-160550412	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553533052	chr6:160550422-160550423	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576750311	chr6:160550439-160550440	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192979070	chr6:160550473-160550474	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562784844	chr6:160550505-160550506	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576373441	chr6:160550514-160550515	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs184559776	chr6:160550519-160550520	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561827183	chr6:160550549-160550550	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs118116045	chr6:160550557-160550558	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs372962509	chr6:160550567-160550568	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	19459884	CNVD
Hearing loss	19459884	CNVD
Microcephaly	19459884	CNVD
Coronary artery disease	17160897	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:160527400-160549200	Weak transcription	Colonic Mucosa	Colon
2	chr6:160527400-160550000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr6:160529400-160559200	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr6:160530800-160553400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:160533400-160552800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:160538800-160557600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr6:160539000-160553000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:160539400-160554200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:160539400-160554800	Weak transcription	Spleen	Spleen
10	chr6:160539400-160558000	Weak transcription	Gastric	stomach
11	chr6:160539400-160559400	Weak transcription	Brain Angular Gyrus	brain
12	chr6:160539400-160559400	Weak transcription	HSMMtube	muscle
13	chr6:160539400-160559600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:160539400-160580400	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr6:160539600-160553400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:160539600-160574600	Weak transcription	Adipose Nuclei	Adipose
17	chr6:160539800-160553400	Weak transcription	Ovary	ovary
18	chr6:160540200-160576200	Weak transcription	Right Ventricle	heart
19	chr6:160540400-160568800	Weak transcription	Esophagus	oesophagus
20	chr6:160541600-160553200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr6:160543200-160561400	Weak transcription	Right Atrium	heart
22	chr6:160543400-160558600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:160543800-160551200	Weak transcription	Fetal Stomach	stomach
24	chr6:160544200-160552200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:160544200-160553000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr6:160545000-160555200	Weak transcription	Fetal Muscle Leg	muscle
27	chr6:160545000-160559000	Weak transcription	Stomach Smooth Muscle	stomach
28	chr6:160545200-160552200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:160545200-160553000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:160546000-160557000	Weak transcription	Pancreas	Pancrea
31	chr6:160546000-160559200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr6:160546400-160560200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:160546800-160550200	Weak transcription	Fetal Intestine Large	intestine
34	chr6:160547200-160549800	Enhancers	Liver	Liver
35	chr6:160548200-160550600	Enhancers	HepG2	liver
36	chr6:160548200-160560000	Weak transcription	Aorta	Aorta
37	chr6:160548600-160549400	Enhancers	K562	blood
38	chr6:160548800-160549200	Weak transcription	Fetal Intestine Small	intestine
39	chr6:160549200-160550600	Enhancers	Fetal Intestine Small	intestine
40	chr6:160549600-160559600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:160549800-160558400	Genic enhancers	Liver	Liver
42	chr6:160550200-160551000	Enhancers	Fetal Intestine Large	intestine
43	chr6:160550600-160553000	Weak transcription	Fetal Intestine Small	intestine
44	chr6:160550600-160555600	Weak transcription	HepG2	liver
45	chr6:160551600-160558200	Weak transcription	Stomach Mucosa	stomach
46	chr6:160552200-160555400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:160552200-160555600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:160552400-160552800	Enhancers	H1 Cell Line	embryonic stem cell
49	chr6:160552800-160553400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr6:160552800-160554200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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