Variant report

Variant	nsv1032658
Chromosome Location	chr6:140928072-141051309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:556)
CpG islands
(count:63)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:141032327-141032490	K562	blood:	n/a	n/a
2	ATF2	chr6:140962459-140962964	GM12878	blood:	n/a	n/a
3	BACH1	chr6:140931711-140931747	K562	blood:	n/a	n/a
4	BATF	chr6:140962571-140962917	GM12878	blood:	n/a	n/a
5	BATF	chr6:140962532-140962960	GM12878	blood:	n/a	n/a
6	BATF	chr6:140957343-140957787	GM12878	blood:	n/a	n/a
7	BATF	chr6:140999274-140999525	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:140962597-140962976	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:140957373-140957725	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:140962665-140962965	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:140957284-140957740	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:140962545-140962966	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:141032530-141032747	GM12878	blood:	n/a	n/a
14	CBX3	chr6:140948115-140948497	K562	blood:	n/a	n/a
15	CCNT2	chr6:141006502-141006618	K562	blood:	n/a	n/a
16	CEBPB	chr6:140950730-140951057	IMR90	lung:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
17	CEBPB	chr6:140944554-140945005	IMR90	lung:	n/a	chr6:140944736-140944747
18	CEBPB	chr6:141006378-141006630	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:140944558-140944922	A549	lung:	n/a	chr6:140944736-140944747
20	CEBPB	chr6:140950521-140950534	K562	blood:	n/a	n/a
21	CEBPB	chr6:140978710-140979038	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:140944568-140944937	Hela-S3	cervix:	n/a	chr6:140944736-140944747
23	CEBPB	chr6:140978793-140979003	K562	blood:	n/a	n/a
24	CEBPB	chr6:140950761-140951042	K562	blood:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
25	CEBPB	chr6:141023864-141024001	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:140950735-140950999	A549	lung:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
27	CEBPB	chr6:140944453-140945069	HCT-116	colon:	n/a	chr6:140944736-140944747
28	CEBPB	chr6:140950874-140950971	Hela-S3	cervix:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
29	CEBPB	chr6:141046985-141047253	IMR90	lung:	n/a	chr6:141047121-141047132
30	CEBPB	chr6:141005694-141005708	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr6:140978749-140979032	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:140950786-140950984	H1-hESC	embryonic stem cell:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
33	CEBPB	chr6:140928375-140928391	K562	blood:	n/a	n/a
34	CEBPB	chr6:140944477-140945154	HCT-116	colon:	n/a	chr6:140944736-140944747
35	CEBPB	chr6:141019569-141019573	K562	blood:	n/a	n/a
36	CEBPB	chr6:140944593-140944912	A549	lung:	n/a	chr6:140944736-140944747
37	CEBPB	chr6:141046992-141047275	HepG2	liver:	n/a	chr6:141047121-141047132
38	CEBPB	chr6:141006465-141006576	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:140944651-140944864	HepG2	liver:	n/a	chr6:140944736-140944747
40	CEBPB	chr6:140992588-140992943	HepG2	liver:	n/a	chr6:140992865-140992876
41	CEBPB	chr6:140933530-140933696	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:140950718-140951059	HepG2	liver:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
43	CTCF	chr6:140993160-140993310	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr6:140993140-140993290	GM12865	blood:	n/a	n/a
45	CTCF	chr6:140993120-140993270	HMF	breast:	n/a	n/a
46	CTCF	chr6:140993120-140993270	NB4	blood:	n/a	n/a
47	CTCF	chr6:140993128-140993351	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:140971368-140971513	GM12878	blood:	n/a	n/a
49	CTCF	chr6:140993160-140993310	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr6:140993200-140993350	SAEC	small airway:	n/a	n/a

(count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:140957775-140957825	PrEC	prostate:	n/a
2	chr6:140957775-140957825	NT2-D1	testis:	n/a
3	chr6:140957775-140957825	PrEC	prostate:	n/a
4	chr6:140957775-140957825	NT2-D1	testis:	n/a
5	chr6:140957775-140957825	GM12891	blood:	n/a
6	chr6:140957775-140957825	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:140957775-140957825	AG04449	skin:	fetal
8	chr6:140957775-140957825	HMEC	breast:	n/a
9	chr6:140957775-140957825	BJ	skin:	n/a
10	chr6:140957775-140957825	AG10803	skin:	n/a
11	chr6:140957775-140957825	NHBE	bronchial:	n/a
12	chr6:140957775-140957825	GM06990	blood:	n/a
13	chr6:140957775-140957825	RPTEC	kidney:	n/a
14	chr6:140957775-140957825	H1-hESC	embryonic stem cell:	embryo
15	chr6:140957775-140957825	HIPEpiC	eye:	n/a
16	chr6:140957775-140957825	GM19239	blood:	n/a
17	chr6:140957775-140957825	SK-N-SH	brain:	n/a
18	chr6:140957775-140957825	HRE	kidney:	n/a
19	chr6:140957775-140957825	SK-N-SH_RA	brain:	n/a
20	chr6:140957775-140957825	IMR90	lung:	fetal
21	chr6:140957775-140957825	SKMC	muscle:	n/a
22	chr6:140957775-140957825	MCF10A-Er-Src	breast:	n/a
23	chr6:140957775-140957825	HCT-116	colon:	n/a
24	chr6:140957775-140957825	BE2_C	brain:	n/a
25	chr6:140957775-140957825	SK-N-MC	brain:	n/a
26	chr6:140957775-140957825	HUVEC	blood vessel:	n/a
27	chr6:140957775-140957825	NHDF-neo	bronchial:	n/a
28	chr6:140957775-140957825	HAEpiC	amniotic membrane:	n/a
29	chr6:140957775-140957825	K562	blood:	n/a
30	chr6:140957775-140957825	HEK293	kidney:	embryo
31	chr6:140957775-140957825	AG09319	gingival:	n/a
32	chr6:140957775-140957825	SAEC	small airway:	n/a
33	chr6:140957775-140957825	PFSK-1	brain:	n/a
34	chr6:140957775-140957825	Jurkat	blood:	n/a
35	chr6:140957775-140957825	HCF	heart:	n/a
36	chr6:140957775-140957825	MCF-7	breast:	n/a
37	chr6:140957775-140957825	CMK	blood:	n/a
38	chr6:140957775-140957825	NB4	blood:	n/a
39	chr6:140957775-140957825	GM12878	blood:	n/a
40	chr6:140957775-140957825	ProgFib	skin:	n/a
41	chr6:140957775-140957825	AG09309	skin:	n/a
42	chr6:140957775-140957825	Hepatocyte	liver:	n/a
43	chr6:140957775-140957825	Caco-2	colon:	n/a
44	chr6:140957775-140957825	NH-A	brain:	n/a
45	chr6:140957775-140957825	AoSMC	blood vessel:	n/a
46	chr6:140957775-140957825	HCPEpiC	choroid plexus:	n/a
47	chr6:140957775-140957825	ECC-1	luminal epithelium:	n/a
48	chr6:140957775-140957825	HNPCEpiC	eye:	n/a
49	chr6:140957775-140957825	HepG2	liver:	n/a
50	chr6:140957775-140957825	T-47D	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
2	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
3	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
4	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
5	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
6	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
7	chr6:139691177..139693399-chr6:140971784..140974474,2	MCF-7	breast:
8	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
9	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
10	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
11	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
12	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
13	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
14	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
15	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
16	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HECA-10	chr6:140928455-140928491	l_3279_chr6:140928454-140973185_placenta
2	lnc-HECA-10	chr6:140972927-140973185	l_3279_chr6:140928454-140973185_placenta

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4465	chr6:141004992-141005013	MIMAT0018992

No data

Variant related genes	Relation type
ENSG00000221336	TF binding region
MIR4465	TF binding region
ENSG00000221336	CpG island
MIR4465	CpG island

Extended variants
information (count: 3723 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3723 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79337930	chr6:140928089-140928090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181611047	chr6:140928128-140928129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148864667	chr6:140928149-140928150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146989740	chr6:140928178-140928179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568568306	chr6:140928190-140928191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536424547	chr6:140928230-140928231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147632510	chr6:140928257-140928258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73583544	chr6:140928287-140928288	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs543695652	chr6:140928318-140928319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367982479	chr6:140928381-140928382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7764230	chr6:140928384-140928385	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540657887	chr6:140928410-140928411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113650279	chr6:140928418-140928419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142258898	chr6:140928421-140928422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs207467473	chr6:140928422-140928423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146217624	chr6:140928427-140928428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541969771	chr6:140928469-140928470	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs563916388	chr6:140928484-140928485	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs531053013	chr6:140928504-140928505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552830943	chr6:140928513-140928514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76402069	chr6:140928519-140928520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528461056	chr6:140928526-140928527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547040622	chr6:140928534-140928535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571217349	chr6:140928553-140928554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371215252	chr6:140928562-140928563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556307766	chr6:140928577-140928578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373626300	chr6:140928605-140928606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568519848	chr6:140928617-140928618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527362699	chr6:140928642-140928643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535964109	chr6:140928644-140928645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150312428	chr6:140928732-140928733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs137983426	chr6:140928774-140928775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149395816	chr6:140928794-140928795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78240033	chr6:140928818-140928819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535886989	chr6:140928820-140928821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556001895	chr6:140928826-140928827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372211134	chr6:140928846-140928847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146368720	chr6:140928905-140928906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569621141	chr6:140928938-140928939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577795902	chr6:140928965-140928966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148413826	chr6:140928967-140928968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201868105	chr6:140928997-140928998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371157176	chr6:140929002-140929003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540593420	chr6:140929009-140929010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552550313	chr6:140929027-140929028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574153863	chr6:140929096-140929097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376747061	chr6:140929097-140929098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139722392	chr6:140929100-140929101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184739856	chr6:140929213-140929214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189218325	chr6:140929235-140929236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Autism	21448237	CNVD
Autism	22495311	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
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140924600-140929400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:140929400-140929800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:140930400-140931400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:140930400-140931600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:140930400-140947200	Weak transcription	Placenta	Placenta
6	chr6:140930600-140931600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:140930600-140931600	Enhancers	Fetal Heart	heart
8	chr6:140931200-140931600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:140931200-140931600	Enhancers	Ovary	ovary
10	chr6:140936800-140945000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:140941800-140942200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:140942200-140945400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:140944200-140945000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:140944400-140945200	Enhancers	NHEK	skin
15	chr6:140944400-140945400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:140944400-140945400	Enhancers	HSMM	muscle
17	chr6:140944600-140945600	Enhancers	Muscle Satellite Cultured Cells	--
18	chr6:140944800-140945000	Enhancers	NH-A	brain
19	chr6:140944800-140945400	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr6:140944800-140945400	Enhancers	Fetal Lung	lung
21	chr6:140944800-140945600	Enhancers	Ovary	ovary
22	chr6:140944800-140945600	Enhancers	HMEC	breast
23	chr6:140945000-140945600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr6:140945000-140946600	Weak transcription	NH-A	brain
25	chr6:140945400-140945600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:140945600-140946200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:140945600-140946600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:140946200-140946400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:140946600-140948600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:140947000-140948200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
31	chr6:140947200-140948400	ZNF genes & repeats	Placenta	Placenta
32	chr6:140947600-140948200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:140947600-140948400	ZNF genes & repeats	Aorta	Aorta
34	chr6:140948200-140948400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr6:140948600-140991200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:140949000-140957400	Weak transcription	Right Atrium	heart
37	chr6:140954200-140954800	Enhancers	Fetal Heart	heart
38	chr6:140954800-140956800	Weak transcription	Fetal Heart	heart
39	chr6:140956600-140957200	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr6:140956800-140958000	Enhancers	Fetal Heart	heart
41	chr6:140956800-140958400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr6:140957200-140957400	Enhancers	Brain Germinal Matrix	brain
43	chr6:140957200-140957400	Enhancers	Fetal Brain Female	brain
44	chr6:140957200-140957400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr6:140957200-140958200	Active TSS	Brain Anterior Caudate	brain
46	chr6:140957400-140957600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr6:140957400-140957600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:140957400-140957600	Active TSS	GM12878-XiMat	blood
49	chr6:140957400-140957800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:140957400-140957800	Enhancers	Primary B cells from peripheral blood	blood

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