Variant report

Variant	nsv885888
Chromosome Location	chr6:54132353-54266032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:705)
CpG islands
(count:427)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:54172209-54172486	HepG2	liver:	n/a	n/a
2	ATF3	chr6:54200535-54201147	HCT-116	colon:	n/a	n/a
3	BATF	chr6:54156610-54156773	GM12878	blood:	n/a	n/a
4	BATF	chr6:54155961-54156168	GM12878	blood:	n/a	chr6:54156063-54156074
5	BATF	chr6:54156506-54156868	GM12878	blood:	n/a	chr6:54156793-54156803
6	BATF	chr6:54155936-54156220	GM12878	blood:	n/a	chr6:54156063-54156074
7	BCL11A	chr6:54156528-54156850	GM12878	blood:	n/a	n/a
8	BRCA1	chr6:54200670-54201342	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr6:54200558-54201142	HCT-116	colon:	n/a	n/a
10	CBX3	chr6:54231293-54231939	HCT-116	colon:	n/a	n/a
11	CBX3	chr6:54231362-54231845	HCT-116	colon:	n/a	n/a
12	CEBPB	chr6:54200877-54201077	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:54147036-54147444	HCT-116	colon:	n/a	n/a
14	CEBPB	chr6:54146971-54147453	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:54168309-54168547	IMR90	lung:	n/a	chr6:54168414-54168427
16	CEBPB	chr6:54168233-54168605	Hela-S3	cervix:	n/a	chr6:54168414-54168427
17	CEBPB	chr6:54200403-54201409	HCT-116	colon:	n/a	n/a
18	CEBPB	chr6:54168276-54168476	H1-hESC	embryonic stem cell:	n/a	chr6:54168414-54168427
19	CEBPB	chr6:54202382-54202668	HepG2	liver:	n/a	chr6:54202510-54202521 chr6:54202509-54202520
20	CEBPB	chr6:54200569-54201180	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:54200453-54201181	HCT-116	colon:	n/a	n/a
22	CEBPB	chr6:54200654-54201120	A549	lung:	n/a	n/a
23	CEBPB	chr6:54209959-54210232	HepG2	liver:	n/a	chr6:54210104-54210115 chr6:54210104-54210117 chr6:54210106-54210117 chr6:54210104-54210117 chr6:54210104-54210117
24	CEBPB	chr6:54209998-54210164	K562	blood:	n/a	chr6:54210104-54210115 chr6:54210104-54210117 chr6:54210106-54210117 chr6:54210104-54210117 chr6:54210104-54210117
25	CEBPB	chr6:54164359-54164641	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:54200580-54201180	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:54166134-54166210	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:54200522-54201233	A549	lung:	n/a	n/a
29	CEBPB	chr6:54200661-54201108	A549	lung:	n/a	n/a
30	CHD2	chr6:54200645-54201113	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr6:54177600-54177750	AG10803	skin:	n/a	n/a
32	CTCF	chr6:54132679-54132856	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr6:54132611-54132970	IMR90	lung:	n/a	n/a
34	CTCF	chr6:54229020-54229170	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr6:54132700-54132850	GM06990	blood:	n/a	n/a
36	CTCF	chr6:54228960-54229110	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:54228980-54229130	HMF	breast:	n/a	n/a
38	CTCF	chr6:54132700-54132850	AG04450	lung:	n/a	n/a
39	CTCF	chr6:54132720-54132870	BJ	skin:	n/a	n/a
40	CTCF	chr6:54132720-54132870	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr6:54132700-54132850	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr6:54132740-54132890	HCT-116	colon:	n/a	n/a
43	CTCF	chr6:54132720-54132870	HAc	cerebellar:	n/a	n/a
44	CTCF	chr6:54132740-54132890	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr6:54132740-54132890	GM12874	blood:	n/a	n/a
46	CTCF	chr6:54132820-54132970	GM12869	blood:	n/a	n/a
47	CTCF	chr6:54132677-54132879	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:54132720-54132870	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr6:54176840-54176990	GM12872	blood:	n/a	n/a
50	CTCF	chr6:54132840-54132990	K562	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:54254826-54254876	BE2_C	brain:	n/a
2	chr6:54172378-54172428	SK-N-MC	brain:	n/a
3	chr6:54200888-54200938	H1-hESC	embryonic stem cell:	embryo
4	chr6:54254826-54254876	AG04450	lung:	fetal
5	chr6:54172997-54173047	CMK	blood:	n/a
6	chr6:54172997-54173047	NH-A	brain:	n/a
7	chr6:54172378-54172428	AG04449	skin:	fetal
8	chr6:54173316-54173366	SK-N-MC	brain:	n/a
9	chr6:54200888-54200938	MCF-7	breast:	n/a
10	chr6:54200888-54200938	SK-N-SH	brain:	n/a
11	chr6:54172378-54172428	BJ	skin:	n/a
12	chr6:54172378-54172428	SAEC	small airway:	n/a
13	chr6:54156824-54156874	IMR90	lung:	fetal
14	chr6:54172997-54173047	NHBE	bronchial:	n/a
15	chr6:54172183-54172233	PFSK-1	brain:	n/a
16	chr6:54172183-54172233	NH-A	brain:	n/a
17	chr6:54172378-54172428	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:54200888-54200938	HL-60	blood:	n/a
19	chr6:54156824-54156874	HRCEpiC	kidney:	n/a
20	chr6:54254826-54254876	HUVEC	blood vessel:	n/a
21	chr6:54254826-54254876	Hela-S3	cervix:	n/a
22	chr6:54172183-54172233	HEEpiC	esophagus:	n/a
23	chr6:54173316-54173366	HUVEC	blood vessel:	n/a
24	chr6:54200888-54200938	Caco-2	colon:	n/a
25	chr6:54172378-54172428	HCM	heart:	n/a
26	chr6:54200888-54200938	PrEC	prostate:	n/a
27	chr6:54172997-54173047	A549	lung:	n/a
28	chr6:54172183-54172233	HEK293	kidney:	embryo
29	chr6:54254826-54254876	MCF-7	breast:	n/a
30	chr6:54172997-54173047	NT2-D1	testis:	n/a
31	chr6:54200888-54200938	HCPEpiC	choroid plexus:	n/a
32	chr6:54156824-54156874	HRPEpiC	eye:	n/a
33	chr6:54200888-54200938	SK-N-SH_RA	brain:	n/a
34	chr6:54172183-54172233	NHBE	bronchial:	n/a
35	chr6:54173316-54173366	NT2-D1	testis:	n/a
36	chr6:54156824-54156874	HEK293	kidney:	embryo
37	chr6:54254826-54254876	SK-N-MC	brain:	n/a
38	chr6:54172378-54172428	HMEC	breast:	n/a
39	chr6:54254826-54254876	NHDF-neo	bronchial:	n/a
40	chr6:54172378-54172428	GM12878	blood:	n/a
41	chr6:54156824-54156874	SAEC	small airway:	n/a
42	chr6:54173316-54173366	HIPEpiC	eye:	n/a
43	chr6:54254826-54254876	HRPEpiC	eye:	n/a
44	chr6:54173316-54173366	HEK293	kidney:	embryo
45	chr6:54172997-54173047	LNCaP	prostate:	n/a
46	chr6:54200888-54200938	NB4	blood:	n/a
47	chr6:54172183-54172233	GM12892	blood:	n/a
48	chr6:54172997-54173047	AoSMC	blood vessel:	n/a
49	chr6:54173316-54173366	NHDF-neo	bronchial:	n/a
50	chr6:54200888-54200938	A549	lung:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:54221394..54223737-chr6:54226905..54229813,2	MCF-7	breast:
2	chr6:54143853..54145479-chr6:54145535..54148075,2	K562	blood:
3	chr6:54138591..54140623-chr6:54150378..54152513,2	MCF-7	breast:
4	chr6:54177292..54179184-chr6:54200767..54202415,2	MCF-7	breast:
5	chr6:53844122..53844911-chr6:54132533..54133159,2	MCF-7	breast:
6	chr6:54239793..54241712-chr6:54244311..54245976,2	MCF-7	breast:
7	chr6:54164489..54166885-chr6:54172521..54174692,2	MCF-7	breast:
8	chr6:54138591..54140623-chr6:54150378..54152513,2	MCF-7	breast:
9	chr6:54221394..54223737-chr6:54226905..54229813,2	MCF-7	breast:
10	chr6:54239793..54241712-chr6:54244311..54245976,2	MCF-7	breast:
11	chr6:54250978..54253931-chr6:54256831..54259813,2	MCF-7	breast:
12	chr6:54177292..54179184-chr6:54200767..54202415,2	MCF-7	breast:
13	chr6:54250978..54253931-chr6:54256831..54259813,2	MCF-7	breast:
14	chr6:54143853..54145479-chr6:54145535..54148075,2	K562	blood:
15	chr6:54108891..54109489-chr6:54132720..54133570,3	MCF-7	breast:
16	chr6:54108947..54109656-chr6:54132424..54133064,2	MCF-7	breast:
17	chr6:53850715..53851537-chr6:54132516..54133234,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL31-4	chr6:54234709-54234769	ENSG00000228231.2
2	lnc-KLHL31-4	chr6:54230133-54230317	ENSG00000228231.2
3	lnc-KLHL31-4	chr6:54231803-54231976	ENSG00000228231.2

No data

Variant related genes	Relation type
ENSG00000228231	TF binding region
TINAG	TF binding region
ENSG00000228231	CpG island
TINAG	CpG island
ENSG00000137251	chromatin interactions

Extended variants
information (count: 4627 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:4627 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10484646	chr6:54132353-54132354	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551403994	chr6:54132385-54132386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9296745	chr6:54132391-54132392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs192375706	chr6:54132438-54132439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550490131	chr6:54132458-54132459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567486881	chr6:54132473-54132474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150217232	chr6:54132516-54132517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555802512	chr6:54132518-54132519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138858064	chr6:54132541-54132542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537300474	chr6:54132594-54132595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71792694	chr6:54132595-54132596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534660546	chr6:54132604-54132605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184765660	chr6:54132607-54132608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115051961	chr6:54132657-54132658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544136916	chr6:54132664-54132665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12201826	chr6:54132679-54132680	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs570440532	chr6:54132688-54132689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189018925	chr6:54132690-54132691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542877526	chr6:54132723-54132724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6915864	chr6:54132730-54132731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534645617	chr6:54132805-54132806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528467717	chr6:54132831-54132832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533081494	chr6:54132844-54132845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528195105	chr6:54132857-54132858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551389998	chr6:54132898-54132899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564911713	chr6:54132946-54132947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546683196	chr6:54132977-54132978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550878943	chr6:54133002-54133003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180925587	chr6:54133007-54133008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536412819	chr6:54133030-54133031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546398452	chr6:54133046-54133047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565790687	chr6:54133052-54133053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534837274	chr6:54133115-54133116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369247765	chr6:54133133-54133134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557722675	chr6:54133162-54133163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577651151	chr6:54133191-54133192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566151558	chr6:54133217-54133218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9464048	chr6:54133218-54133219	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs557607076	chr6:54133220-54133221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144658291	chr6:54133232-54133233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543156825	chr6:54133252-54133253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200739941	chr6:54133270-54133271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553646219	chr6:54133368-54133369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184758431	chr6:54133400-54133401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545157095	chr6:54133431-54133432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190006550	chr6:54133433-54133434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111590971	chr6:54133460-54133461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376663513	chr6:54133470-54133471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9382312	chr6:54133486-54133487	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs530495880	chr6:54133498-54133499	Weak transcription	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
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54131400-54132400	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr6:54131800-54137400	Weak transcription	Left Ventricle	heart
3	chr6:54135800-54136400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:54137400-54137600	Enhancers	Left Ventricle	heart
5	chr6:54145800-54146200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:54146000-54149600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr6:54146000-54151600	Enhancers	NHDF-Ad	bronchial
8	chr6:54146200-54146600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:54146400-54147600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:54146400-54147600	Enhancers	NHEK	skin
11	chr6:54146400-54148600	Enhancers	NHLF	lung
12	chr6:54146400-54152200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:54146600-54146800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:54146600-54146800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr6:54146600-54147000	Enhancers	HUVEC	blood vessel
16	chr6:54146600-54147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:54146600-54147400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:54146600-54147400	Enhancers	NH-A	brain
19	chr6:54146600-54147800	Enhancers	HMEC	breast
20	chr6:54146600-54148200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:54146600-54148400	Enhancers	HSMM	muscle
22	chr6:54146600-54149000	Enhancers	Osteobl	bone
23	chr6:54146800-54147400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:54146800-54147400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:54146800-54148200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:54147000-54147400	Enhancers	A549	lung
27	chr6:54147200-54147600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr6:54147400-54150400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:54147400-54150400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:54147400-54150600	Weak transcription	NH-A	brain
31	chr6:54147400-54151000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:54147400-54151400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:54147600-54148600	Enhancers	Fetal Intestine Small	intestine
34	chr6:54147600-54149000	Enhancers	Fetal Intestine Large	intestine
35	chr6:54147600-54150200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:54147600-54150200	Weak transcription	NHEK	skin
37	chr6:54147600-54150800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:54147800-54148200	Weak transcription	HMEC	breast
39	chr6:54148200-54148400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr6:54148200-54148400	Enhancers	HMEC	breast
41	chr6:54148200-54148600	Enhancers	Psoas Muscle	Psoas
42	chr6:54148200-54148800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr6:54148200-54150400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:54148400-54148800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr6:54148400-54148800	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr6:54148400-54150400	Weak transcription	HMEC	breast
47	chr6:54148400-54150800	Weak transcription	HSMM	muscle
48	chr6:54148600-54149000	Weak transcription	NHLF	lung
49	chr6:54148600-54150200	Weak transcription	Fetal Intestine Small	intestine
50	chr6:54148800-54149200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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