Variant report

Variant	nsv970330
Chromosome Location	chr6:49921724-49940183
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	CEBPB	chr6:49934561-49934924	Hela-S3	cervix:	n/a	chr6:49934730-49934741
2	CEBPB	chr6:49934572-49934876	K562	blood:	n/a	chr6:49934730-49934741
3	CEBPB	chr6:49933245-49933270	K562	blood:	n/a	n/a
4	CEBPB	chr6:49934545-49934928	K562	blood:	n/a	chr6:49934730-49934741
5	CEBPB	chr6:49933202-49933427	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr6:49934640-49934807	HepG2	liver:	n/a	chr6:49934730-49934741
7	CEBPB	chr6:49934575-49934897	A549	lung:	n/a	chr6:49934730-49934741
8	CTCF	chr6:49932495-49932590	Hela-S3	cervix:	n/a	chr6:49932528-49932536
9	CTCF	chr6:49932471-49932601	K562	blood:	n/a	chr6:49932528-49932536
10	EP300	chr6:49936044-49936115	GM12878	blood:	n/a	n/a
11	FOS	chr6:49937338-49937665	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr6:49937393-49937629	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr6:49938000-49938264	MCF10A-Er-Src	breast:	n/a	chr6:49938128-49938138 chr6:49938129-49938137 chr6:49938129-49938137 chr6:49938129-49938136 chr6:49938128-49938138 chr6:49938128-49938138 chr6:49938128-49938138
14	FOS	chr6:49937419-49937669	MCF10A-Er-Src	breast:	n/a	n/a
15	FOXP2	chr6:49936336-49936572	SK-N-MC	brain:	n/a	n/a
16	FOXP2	chr6:49937281-49937646	SK-N-MC	brain:	n/a	chr6:49937613-49937625
17	GATA3	chr6:49933562-49933688	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr6:49926103-49926300	SH-SY5Y	brain:	n/a	n/a
19	GTF2F1	chr6:49934158-49934441	H1-hESC	embryonic stem cell:	n/a	n/a
20	HDAC2	chr6:49934074-49934401	H1-hESC	embryonic stem cell:	n/a	chr6:49934237-49934251
21	IKZF1	chr6:49921735-49921797	GM12878	blood:	n/a	n/a
22	JUN	chr6:49923694-49923894	HepG2	liver:	n/a	chr6:49923725-49923738
23	JUN	chr6:49933209-49933254	K562	blood:	n/a	n/a
24	JUND	chr6:49923645-49923870	HepG2	liver:	n/a	n/a
25	KAP1	chr6:49930705-49930989	K562	blood:	n/a	n/a
26	KAP1	chr6:49933967-49934120	K562	blood:	n/a	n/a
27	MAFF	chr6:49926050-49926165	K562	blood:	n/a	chr6:49926090-49926108
28	MAFF	chr6:49925989-49926234	HepG2	liver:	n/a	chr6:49926090-49926108
29	MAFK	chr6:49926058-49926091	Hela-S3	cervix:	n/a	n/a
30	MAFK	chr6:49924006-49924184	K562	blood:	n/a	n/a
31	MAFK	chr6:49925992-49926235	HepG2	liver:	n/a	chr6:49926091-49926106
32	MAFK	chr6:49925944-49926267	HepG2	liver:	n/a	chr6:49926091-49926106
33	NANOG	chr6:49934101-49934334	H1-hESC	embryonic stem cell:	n/a	chr6:49934226-49934235
34	POLR2A	chr6:49928013-49928035	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr6:49939086-49939171	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr6:49929868-49929896	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr6:49923479-49923493	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr6:49926644-49926713	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr6:49938743-49938852	GM12878	blood:	n/a	n/a
40	POLR2A	chr6:49926299-49926415	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr6:49936810-49936857	MCF10A-Er-Src	breast:	n/a	n/a
42	POU5F1	chr6:49934068-49934344	H1-hESC	embryonic stem cell:	n/a	chr6:49934224-49934238 chr6:49934259-49934273 chr6:49934224-49934238 chr6:49934224-49934238
43	POU5F1	chr6:49934087-49934396	H1-hESC	embryonic stem cell:	n/a	chr6:49934224-49934238 chr6:49934259-49934273 chr6:49934224-49934238 chr6:49934224-49934238
44	STAT3	chr6:49926140-49926276	MCF10A-Er-Src	breast:	n/a	n/a
45	TBP	chr6:49931566-49931601	H1-hESC	embryonic stem cell:	n/a	n/a
46	TCF12	chr6:49936366-49936589	H1-hESC	embryonic stem cell:	n/a	n/a
47	TEAD4	chr6:49934032-49934378	H1-hESC	embryonic stem cell:	n/a	n/a
48	TEAD4	chr6:49936400-49936599	H1-hESC	embryonic stem cell:	n/a	n/a
49	UBTF	chr6:49921766-49921884	K562	blood:	n/a	n/a
50	USF1	chr6:49934195-49934473	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:49928115-49928165	Hela-S3	cervix:	n/a
2	chr6:49928115-49928165	HCT-116	colon:	n/a
3	chr6:49928115-49928165	RPTEC	kidney:	n/a
4	chr6:49937814-49937864	HCM	heart:	n/a
5	chr6:49928115-49928165	Jurkat	blood:	n/a
6	chr6:49937814-49937864	Caco-2	colon:	n/a
7	chr6:49937814-49937864	HUVEC	blood vessel:	n/a
8	chr6:49937814-49937864	AG04449	skin:	fetal
9	chr6:49928115-49928165	K562	blood:	n/a
10	chr6:49928115-49928165	HepG2	liver:	n/a
11	chr6:49928115-49928165	IMR90	lung:	fetal
12	chr6:49928115-49928165	ProgFib	skin:	n/a
13	chr6:49928115-49928165	AG09319	gingival:	n/a
14	chr6:49937814-49937864	BE2_C	brain:	n/a
15	chr6:49928115-49928165	HRE	kidney:	n/a
16	chr6:49928115-49928165	NHDF-neo	bronchial:	n/a
17	chr6:49937814-49937864	AG10803	skin:	n/a
18	chr6:49937814-49937864	Hela-S3	cervix:	n/a
19	chr6:49937814-49937864	H1-hESC	embryonic stem cell:	embryo
20	chr6:49937814-49937864	SK-N-MC	brain:	n/a
21	chr6:49937814-49937864	HNPCEpiC	eye:	n/a
22	chr6:49928115-49928165	T-47D	breast:	n/a
23	chr6:49937814-49937864	NHDF-neo	bronchial:	n/a
24	chr6:49928115-49928165	BE2_C	brain:	n/a
25	chr6:49928115-49928165	HEEpiC	esophagus:	n/a
26	chr6:49937814-49937864	HCPEpiC	choroid plexus:	n/a
27	chr6:49928115-49928165	ovcar-3	ovarian:	n/a
28	chr6:49928115-49928165	HEK293	kidney:	embryo
29	chr6:49928115-49928165	U87	brain:	n/a
30	chr6:49937814-49937864	HIPEpiC	eye:	n/a
31	chr6:49937814-49937864	ProgFib	skin:	n/a
32	chr6:49928115-49928165	LNCaP	prostate:	n/a
33	chr6:49937814-49937864	AG04450	lung:	fetal
34	chr6:49928115-49928165	HAEpiC	amniotic membrane:	n/a
35	chr6:49937814-49937864	GM12892	blood:	n/a
36	chr6:49937814-49937864	Jurkat	blood:	n/a
37	chr6:49928115-49928165	BJ	skin:	n/a
38	chr6:49928115-49928165	NB4	blood:	n/a
39	chr6:49928115-49928165	CMK	blood:	n/a
40	chr6:49928115-49928165	HUVEC	blood vessel:	n/a
41	chr6:49937814-49937864	HRPEpiC	eye:	n/a
42	chr6:49937814-49937864	SKMC	muscle:	n/a
43	chr6:49937814-49937864	AG09309	skin:	n/a
44	chr6:49928115-49928165	GM12891	blood:	n/a
45	chr6:49928115-49928165	MCF-7	breast:	n/a
46	chr6:49937814-49937864	GM12891	blood:	n/a
47	chr6:49928115-49928165	HMEC	breast:	n/a
48	chr6:49937814-49937864	GM06990	blood:	n/a
49	chr6:49928115-49928165	A549	lung:	n/a
50	chr6:49937814-49937864	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:49917812..49920215-chr6:49938804..49940384,2	K562	blood:
2	chr6:49939274..49941275-chr6:49942084..49943998,2	K562	blood:
3	chr6:49922102..49925301-chr6:49927046..49930079,3	K562	blood:
4	chr6:49920570..49922665-chr6:49946320..49948617,2	K562	blood:
5	chr6:49916297..49920485-chr6:49927814..49931575,4	K562	blood:
6	chr6:49918423..49920298-chr6:49924382..49926655,2	K562	blood:
7	chr6:49922102..49925301-chr6:49927046..49930079,3	K562	blood:
8	chr6:49917125..49919923-chr6:49925155..49927283,3	K562	blood:
9	chr6:49918496..49920485-chr6:49927814..49930518,2	K562	blood:
10	chr6:49930677..49932249-chr6:49932732..49935281,2	K562	blood:
11	chr6:49936013..49938927-chr6:49939519..49941883,2	K562	blood:

Variant related genes	Relation type
DEFB133	TF binding region
DEFB113	TF binding region
DEFB114	TF binding region
DEFB133	CpG island
DEFB113	CpG island
DEFB114	CpG island
ENSG00000177684	chromatin interactions
ENSG00000214643	chromatin interactions
ENSG00000214642	chromatin interactions

Extended variants
information (count: 525 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185640095	chr6:49921800-49921801	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs546384013	chr6:49921837-49921838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs548100882	chr6:49921851-49921852	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374715811	chr6:49921859-49921860	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs116834777	chr6:49921873-49921874	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs139598061	chr6:49921879-49921880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs190404239	chr6:49921884-49921885	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs573883666	chr6:49925159-49925160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs181692747	chr6:49925206-49925207	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs148368374	chr6:49925219-49925220	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573222853	chr6:49925257-49925258	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559932801	chr6:49925297-49925298	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540634365	chr6:49925301-49925302	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574172449	chr6:49925302-49925303	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs78662426	chr6:49925320-49925321	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs4715163	chr6:49925329-49925330	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372962897	chr6:49925353-49925354	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186274899	chr6:49925359-49925360	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs111326094	chr6:49925413-49925414	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572819207	chr6:49925431-49925432	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7754156	chr6:49925522-49925523	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190649933	chr6:49925548-49925549	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565954149	chr6:49925552-49925553	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528404924	chr6:49925557-49925558	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1337822	chr6:49925636-49925637	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs141569437	chr6:49925637-49925638	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537089148	chr6:49925653-49925654	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182552521	chr6:49925660-49925661	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543848238	chr6:49925674-49925675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567422862	chr6:49925704-49925705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536419651	chr6:49925714-49925715	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150726909	chr6:49925715-49925716	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373890529	chr6:49925741-49925742	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185789807	chr6:49925762-49925763	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539296250	chr6:49925765-49925766	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190699715	chr6:49925825-49925826	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139451995	chr6:49925906-49925907	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543290246	chr6:49925959-49925960	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531771292	chr6:49925994-49925995	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564014901	chr6:49925997-49925998	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76724180	chr6:49925999-49926000	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs573804517	chr6:49926014-49926015	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182981193	chr6:49926052-49926053	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542812755	chr6:49926060-49926061	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs9367379	chr6:49926061-49926062	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs9473702	chr6:49926086-49926087	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs551642281	chr6:49926129-49926130	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565039809	chr6:49926130-49926131	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs9369927	chr6:49926147-49926148	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs147156154	chr6:49926178-49926179	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Melanoma	18172304	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
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD
Olfactory neuroblastoma	18408657	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
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49931000-49934800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:49932200-49932400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr6:49932400-49933000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr6:49932800-49934000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr6:49932800-49934000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr6:49933000-49934000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr6:49933000-49934000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr6:49933400-49934000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr6:49933600-49935200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr6:49933600-49935400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr6:49934000-49934400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr6:49934000-49934400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr6:49934000-49934600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr6:49934000-49935000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr6:49934000-49935000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr6:49934400-49936800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr6:49934400-49937600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr6:49934600-49935200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr6:49934800-49935200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:49935000-49936400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr6:49935000-49937800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:49935200-49935800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr6:49935200-49936400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr6:49935200-49937800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:49935400-49936400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr6:49935800-49936600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr6:49936400-49936800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr6:49936400-49936800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr6:49936800-49937000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr6:49936800-49937200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr6:49936800-49937600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr6:49937200-49937800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr6:49937800-49938000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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