Variant report

Variant	nsv885886
Chromosome Location	chr6:53956877-54009067
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	ARID3A	chr6:54000571-54001192	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:53962447-53962872	HepG2	liver:	n/a	n/a
3	BACH1	chr6:53968321-53968664	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:53968331-53968637	K562	blood:	n/a	n/a
5	BHLHE40	chr6:53972403-53972554	HepG2	liver:	n/a	chr6:53972454-53972463 chr6:53972454-53972463 chr6:53972455-53972464 chr6:53972448-53972469
6	BHLHE40	chr6:53962611-53962857	HepG2	liver:	n/a	n/a
7	CEBPB	chr6:54000686-54001217	HCT-116	colon:	n/a	chr6:54001140-54001152
8	CEBPB	chr6:53962535-53962901	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
9	CEBPB	chr6:53984491-53984712	HepG2	liver:	n/a	chr6:53984572-53984583
10	CEBPB	chr6:54000793-54001084	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr6:53962505-53962816	A549	lung:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
12	CEBPB	chr6:53999730-54000040	IMR90	lung:	n/a	chr6:53999861-53999874 chr6:53999861-53999874 chr6:53999863-53999874 chr6:53999863-53999874 chr6:53999861-53999872
13	CEBPB	chr6:53962546-53962803	Hela-S3	cervix:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
14	CEBPB	chr6:53962398-53962934	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
15	CEBPB	chr6:54000781-54001160	Hela-S3	cervix:	n/a	chr6:54001140-54001152
16	CEBPB	chr6:54000804-54001144	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:54000822-54001146	A549	lung:	n/a	n/a
18	CEBPB	chr6:54000889-54001075	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:54000830-54001154	MCF-7	breast:	n/a	chr6:54001140-54001152
20	CEBPB	chr6:54008035-54008201	HepG2	liver:	n/a	chr6:54008071-54008082
21	CEBPB	chr6:54000729-54001186	A549	lung:	n/a	chr6:54001140-54001152
22	CEBPB	chr6:53962593-53962858	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
23	CEBPB	chr6:53999774-54000050	HepG2	liver:	n/a	chr6:53999861-53999874 chr6:53999861-53999874 chr6:53999863-53999874 chr6:53999863-53999874 chr6:53999861-53999872
24	CEBPB	chr6:54000745-54001162	MCF-7	breast:	n/a	chr6:54001140-54001152
25	CEBPB	chr6:53962549-53962950	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
26	CEBPB	chr6:54000759-54001219	ECC-1	luminal epithelium:	n/a	chr6:54001140-54001152
27	CEBPD	chr6:53962610-53962878	HepG2	liver:	n/a	chr6:53962728-53962739
28	CTCF	chr6:53975180-53975247	Lung_OC	lung:	n/a	n/a
29	CTCF	chr6:54002340-54002490	GM12869	blood:	n/a	n/a
30	CTCF	chr6:54008783-54008849	Fibrobl	skin:	n/a	n/a
31	CTCF	chr6:53994580-53994730	HepG2	liver:	n/a	chr6:53994600-53994609 chr6:53994600-53994613
32	CUX1	chr6:53965712-53965730	GM12878	blood:	n/a	n/a
33	E2F4	chr6:53988468-53988758	MCF10A-Er-Src	breast:	n/a	n/a
34	EGR1	chr6:53996022-53996460	ECC-1	luminal epithelium:	n/a	n/a
35	ELF1	chr6:54000790-54001065	HepG2	liver:	n/a	n/a
36	ELK1	chr6:53967800-53967839	K562	blood:	n/a	n/a
37	EP300	chr6:54000727-54001171	ECC-1	luminal epithelium:	n/a	chr6:54000911-54000920
38	EP300	chr6:53965697-53965707	GM12878	blood:	n/a	n/a
39	EP300	chr6:54000730-54001080	HepG2	liver:	n/a	chr6:54000911-54000920
40	EP300	chr6:54000801-54001112	Hela-S3	cervix:	n/a	chr6:54000911-54000920
41	EP300	chr6:53962594-53962837	HepG2	liver:	n/a	n/a
42	EP300	chr6:53962455-53962911	HepG2	liver:	n/a	n/a
43	EP300	chr6:53963244-53963655	HepG2	liver:	n/a	chr6:53963460-53963474
44	EP300	chr6:53963198-53963651	HepG2	liver:	n/a	chr6:53963460-53963474
45	EP300	chr6:54000682-54001135	HepG2	liver:	n/a	chr6:54000911-54000920
46	EP300	chr6:53962516-53962977	HepG2	liver:	n/a	n/a
47	ESR1	chr6:54000760-54001071	ECC-1	luminal epithelium:	n/a	n/a
48	FAM48A	chr6:53995925-53996058	GM12878	blood:	n/a	n/a
49	FOS	chr6:53977047-53978383	HUVEC	blood vessel:	n/a	chr6:53978114-53978123
50	FOS	chr6:53978986-53979276	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:54001665-54001715	HUVEC	blood vessel:	n/a
2	chr6:54001895-54001945	HAEpiC	amniotic membrane:	n/a
3	chr6:54001895-54001945	HUVEC	blood vessel:	n/a
4	chr6:54001665-54001715	HMEC	breast:	n/a
5	chr6:54001868-54001918	HIPEpiC	eye:	n/a
6	chr6:54001665-54001715	AG04450	lung:	fetal
7	chr6:54001895-54001945	AG09309	skin:	n/a
8	chr6:54001665-54001715	LNCaP	prostate:	n/a
9	chr6:54001868-54001918	H1-hESC	embryonic stem cell:	embryo
10	chr6:54001895-54001945	RPTEC	kidney:	n/a
11	chr6:54001895-54001945	BE2_C	brain:	n/a
12	chr6:54001868-54001918	HepG2	liver:	n/a
13	chr6:54001665-54001715	PFSK-1	brain:	n/a
14	chr6:54001868-54001918	BE2_C	brain:	n/a
15	chr6:54001895-54001945	K562	blood:	n/a
16	chr6:54001868-54001918	NT2-D1	testis:	n/a
17	chr6:54001868-54001918	LNCaP	prostate:	n/a
18	chr6:54001868-54001918	AG10803	skin:	n/a
19	chr6:54001895-54001945	SK-N-MC	brain:	n/a
20	chr6:54001665-54001715	SAEC	small airway:	n/a
21	chr6:54001868-54001918	HCT-116	colon:	n/a
22	chr6:54001868-54001918	CMK	blood:	n/a
23	chr6:54001895-54001945	GM06990	blood:	n/a
24	chr6:54001665-54001715	HEK293	kidney:	embryo
25	chr6:54001868-54001918	HRE	kidney:	n/a
26	chr6:54001895-54001945	GM12891	blood:	n/a
27	chr6:54001665-54001715	AG04449	skin:	fetal
28	chr6:54001665-54001715	H1-hESC	embryonic stem cell:	embryo
29	chr6:54001868-54001918	ProgFib	skin:	n/a
30	chr6:54001895-54001945	HepG2	liver:	n/a
31	chr6:54001868-54001918	U87	brain:	n/a
32	chr6:54001665-54001715	SK-N-SH_RA	brain:	n/a
33	chr6:54001665-54001715	BE2_C	brain:	n/a
34	chr6:54001895-54001945	HCM	heart:	n/a
35	chr6:54001665-54001715	MCF-7	breast:	n/a
36	chr6:54001895-54001945	AG09319	gingival:	n/a
37	chr6:54001895-54001945	GM19239	blood:	n/a
38	chr6:54001665-54001715	SKMC	muscle:	n/a
39	chr6:54001665-54001715	HIPEpiC	eye:	n/a
40	chr6:54001665-54001715	HRCEpiC	kidney:	n/a
41	chr6:54001665-54001715	HRPEpiC	eye:	n/a
42	chr6:54001665-54001715	HCT-116	colon:	n/a
43	chr6:54001665-54001715	NHBE	bronchial:	n/a
44	chr6:54001895-54001945	MCF10A-Er-Src	breast:	n/a
45	chr6:54001665-54001715	GM12878	blood:	n/a
46	chr6:54001868-54001918	ovcar-3	ovarian:	n/a
47	chr6:54001665-54001715	Jurkat	blood:	n/a
48	chr6:54001895-54001945	AG10803	skin:	n/a
49	chr6:54001895-54001945	ProgFib	skin:	n/a
50	chr6:54001895-54001945	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:53992281..53994885-chr6:54000066..54003038,2	MCF-7	breast:
2	chr6:53990110..53992835-chr6:54232926..54235323,2	K562	blood:
3	chr6:53992281..53994885-chr6:54000066..54003038,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC1-8	chr6:53967721-53970422	ucscGeneNc_uc003pce_2
2	lnc-LRRC1-9	chr6:53971647-53971816	NONHSAT113221
3	lnc-LRRC1-9	chr6:53979728-53979909	NONHSAT113221
4	lnc-LRRC1-8	chr6:53967547-53967621	NONHSAT113215
5	lnc-LRRC1-8	chr6:53967721-53970052	NONHSAT113215
6	lnc-LRRC1-9	chr6:53973667-53973851	NONHSAT113221
7	lnc-LRRC1-8	chr6:53967547-53967621	ucscGeneNc_uc003pce_2
8	lnc-LRRC1-9	chr6:53975371-53975476	NONHSAT113221

Variant related genes	Relation type
MLIP	TF binding region
MLIP	CpG island
ENSG00000228231	chromatin interactions

Extended variants
information (count: 1986 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1986 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557018	chr6:53956877-53956878	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62397373	chr6:53956884-53956885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571062525	chr6:53956886-53956887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79420907	chr6:53957002-53957003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186970246	chr6:53957058-53957059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570111991	chr6:53957086-53957087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535608955	chr6:53957097-53957098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192249254	chr6:53957185-53957186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148374820	chr6:53957210-53957211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183404978	chr6:53957286-53957287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs36055119	chr6:53957302-53957303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541696519	chr6:53957331-53957332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140653312	chr6:53957357-53957358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544927681	chr6:53957512-53957513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115748092	chr6:53957514-53957515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186577085	chr6:53957519-53957520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545063535	chr6:53957558-53957559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544030022	chr6:53957572-53957573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs625899	chr6:53957588-53957589	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs372943678	chr6:53957605-53957606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375089613	chr6:53957616-53957617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527685652	chr6:53957628-53957629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542374315	chr6:53957660-53957661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559274673	chr6:53957693-53957694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369178910	chr6:53957706-53957707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528079484	chr6:53957737-53957738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189601263	chr6:53957751-53957752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369199109	chr6:53957753-53957754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571204439	chr6:53957781-53957782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112707589	chr6:53957794-53957795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530741442	chr6:53957803-53957804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150483277	chr6:53957807-53957808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567364166	chr6:53957845-53957846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535913356	chr6:53957918-53957919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555580516	chr6:53957926-53957927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182249186	chr6:53957929-53957930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543832644	chr6:53957955-53957956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138249058	chr6:53957960-53957961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571761323	chr6:53957966-53957967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558233666	chr6:53957975-53957976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs578245067	chr6:53957978-53957979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529885982	chr6:53958087-53958088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377029001	chr6:53958127-53958128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371373279	chr6:53958128-53958129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9474733	chr6:53958132-53958133	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557497222	chr6:53958133-53958134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149888089	chr6:53958146-53958147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574175451	chr6:53958167-53958168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542660619	chr6:53958181-53958182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs70980891	chr6:53958192-53958193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Hodgkin''s lymphoma	17606441	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
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
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53945000-53970800	Weak transcription	Right Atrium	heart
2	chr6:53950800-53958200	Weak transcription	HSMMtube	muscle
3	chr6:53951000-53958200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:53951000-53958200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:53952400-53959000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:53952800-53957800	Weak transcription	Left Ventricle	heart
7	chr6:53953200-53957800	Weak transcription	Fetal Muscle Leg	muscle
8	chr6:53954600-53957200	Enhancers	Fetal Heart	heart
9	chr6:53955600-53958400	Weak transcription	Right Ventricle	heart
10	chr6:53956000-53957800	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr6:53956200-53958400	Weak transcription	HSMM	muscle
12	chr6:53956600-53957600	Weak transcription	Psoas Muscle	Psoas
13	chr6:53956800-53957200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr6:53957200-53958400	Weak transcription	Fetal Heart	heart
15	chr6:53957200-53958400	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr6:53957600-53958800	Enhancers	Psoas Muscle	Psoas
17	chr6:53957800-53958800	Enhancers	Left Ventricle	heart
18	chr6:53957800-53959400	Enhancers	Fetal Muscle Leg	muscle
19	chr6:53957800-53960600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr6:53958200-53958800	Enhancers	HSMMtube	muscle
21	chr6:53958200-53960000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:53958200-53960000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:53958200-53960200	Enhancers	Fetal Lung	lung
24	chr6:53958400-53958600	Enhancers	HSMM	muscle
25	chr6:53958400-53958800	Enhancers	Right Ventricle	heart
26	chr6:53958400-53959200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr6:53958400-53959200	Enhancers	Fetal Stomach	stomach
28	chr6:53958400-53959800	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr6:53958400-53960000	Enhancers	Fetal Heart	heart
30	chr6:53958400-53961000	Enhancers	Fetal Brain Male	brain
31	chr6:53958800-53961200	Weak transcription	Left Ventricle	heart
32	chr6:53958800-53961200	Weak transcription	Psoas Muscle	Psoas
33	chr6:53958800-53961200	Weak transcription	Right Ventricle	heart
34	chr6:53959000-53960200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr6:53959200-53959400	Enhancers	Fetal Brain Female	brain
36	chr6:53959400-53959600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr6:53959400-53959800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:53959400-53960600	Weak transcription	Fetal Brain Female	brain
39	chr6:53959400-53975800	Weak transcription	Fetal Muscle Leg	muscle
40	chr6:53959800-53967000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr6:53960000-53965400	Weak transcription	Fetal Heart	heart
42	chr6:53960200-53964200	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr6:53960600-53961400	Enhancers	Fetal Brain Female	brain
44	chr6:53960600-53962600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr6:53960600-53963600	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr6:53961000-53964400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr6:53961000-53966800	Weak transcription	Fetal Brain Male	brain
48	chr6:53961200-53961600	Genic enhancers	Left Ventricle	heart
49	chr6:53961200-53961600	Enhancers	Psoas Muscle	Psoas
50	chr6:53961200-53961600	Enhancers	Right Ventricle	heart

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