Variant report

Variant	esv2755862
Chromosome Location	chr6:49081541-49298041
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	ATF1	chr6:49159981-49160034	K562	blood:	n/a	n/a
2	BCL11A	chr6:49110095-49110336	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr6:49213138-49213155	GM12878	blood:	n/a	n/a
4	BRCA1	chr6:49083255-49083266	GM12878	blood:	n/a	n/a
5	CBX3	chr6:49293957-49294454	HCT-116	colon:	n/a	n/a
6	CBX3	chr6:49097673-49097874	K562	blood:	n/a	n/a
7	CCNT2	chr6:49132849-49132996	K562	blood:	n/a	n/a
8	CEBPB	chr6:49293563-49294501	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:49218988-49219318	A549	lung:	n/a	chr6:49219169-49219178 chr6:49219169-49219178 chr6:49219167-49219180 chr6:49219167-49219178 chr6:49219167-49219180 chr6:49219169-49219178
10	CEBPB	chr6:49214564-49214814	HepG2	liver:	n/a	chr6:49214712-49214723
11	CEBPB	chr6:49272778-49272862	HepG2	liver:	n/a	chr6:49272809-49272822 chr6:49272810-49272821
12	CEBPB	chr6:49294100-49294496	IMR90	lung:	n/a	n/a
13	CEBPB	chr6:49235106-49235311	A549	lung:	n/a	n/a
14	CEBPB	chr6:49235042-49235312	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:49211743-49211987	HepG2	liver:	n/a	chr6:49211765-49211776 chr6:49211826-49211837
16	CEBPB	chr6:49259699-49259825	K562	blood:	n/a	chr6:49259776-49259789 chr6:49259776-49259789 chr6:49259776-49259787
17	CEBPB	chr6:49218896-49219327	IMR90	lung:	n/a	chr6:49219169-49219178 chr6:49219169-49219178 chr6:49219167-49219180 chr6:49219167-49219178 chr6:49219167-49219180 chr6:49219169-49219178
18	CEBPB	chr6:49223828-49224021	HepG2	liver:	n/a	chr6:49223861-49223872
19	CEBPB	chr6:49169302-49169384	K562	blood:	n/a	chr6:49169330-49169343 chr6:49169330-49169341 chr6:49169330-49169343
20	CEBPB	chr6:49169725-49169812	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr6:49218853-49219322	HepG2	liver:	n/a	chr6:49219169-49219178 chr6:49219169-49219178 chr6:49219167-49219180 chr6:49219167-49219178 chr6:49219167-49219180 chr6:49219169-49219178
22	CEBPB	chr6:49218991-49219270	Hela-S3	cervix:	n/a	chr6:49219169-49219178 chr6:49219169-49219178 chr6:49219167-49219180 chr6:49219167-49219178 chr6:49219167-49219180 chr6:49219169-49219178
23	CEBPB	chr6:49223721-49223951	H1-hESC	embryonic stem cell:	n/a	chr6:49223861-49223872
24	CEBPB	chr6:49293961-49294536	HCT-116	colon:	n/a	n/a
25	CEBPB	chr6:49169169-49169491	HepG2	liver:	n/a	chr6:49169330-49169343 chr6:49169330-49169341 chr6:49169330-49169343
26	CEBPB	chr6:49169211-49169489	A549	lung:	n/a	chr6:49169330-49169343 chr6:49169330-49169341 chr6:49169330-49169343
27	CTCF	chr6:49235320-49235470	GM12875	blood:	n/a	n/a
28	CTCF	chr6:49285813-49285894	GM10266	blood:	n/a	n/a
29	CTCF	chr6:49232260-49232410	AG04449	skin:	n/a	n/a
30	CTCF	chr6:49235220-49235370	GM12864	blood:	n/a	n/a
31	CTCF	chr6:49235300-49235450	WI-38	lung:	n/a	n/a
32	CTCF	chr6:49235280-49235430	HepG2	liver:	n/a	n/a
33	CTCF	chr6:49232268-49232339	Fibrobl	skin:	n/a	n/a
34	CTCF	chr6:49232160-49232310	HepG2	liver:	n/a	n/a
35	CTCF	chr6:49202680-49202830	GM12865	blood:	n/a	n/a
36	CTCF	chr6:49235480-49235630	RPTEC	kidney:	n/a	n/a
37	CTCF	chr6:49235400-49235550	GM12864	blood:	n/a	n/a
38	CTCF	chr6:49165460-49165610	HPAF	blood vessel:	n/a	chr6:49165579-49165600 chr6:49165581-49165588
39	CTCF	chr6:49232264-49232323	NHEK	skin:	n/a	n/a
40	CTCF	chr6:49235340-49235490	HMF	breast:	n/a	n/a
41	CTCF	chr6:49235260-49235410	GM12874	blood:	n/a	n/a
42	CTCF	chr6:49267180-49267330	NHEK	skin:	n/a	n/a
43	CTCF	chr6:49170960-49171110	HMEC	breast:	n/a	n/a
44	CTCF	chr6:49235260-49235410	AG09309	skin:	n/a	n/a
45	CTCF	chr6:49235320-49235470	GM12878	blood:	n/a	n/a
46	CTCF	chr6:49126157-49126267	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr6:49267060-49267210	AoAF	blood vessel:	n/a	chr6:49267112-49267120
48	CTCF	chr6:49126660-49126810	Caco-2	colon:	n/a	n/a
49	CTCF	chr6:49235340-49235490	A549	lung:	n/a	n/a
50	CTCF	chr6:49165480-49165630	BE2_C	brain:	n/a	chr6:49165579-49165600 chr6:49165581-49165588

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:49110730-49110780	ProgFib	skin:	n/a
2	chr6:49110730-49110780	GM06990	blood:	n/a
3	chr6:49110730-49110780	HEEpiC	esophagus:	n/a
4	chr6:49123030-49123080	ProgFib	skin:	n/a
5	chr6:49110730-49110780	HNPCEpiC	eye:	n/a
6	chr6:49123030-49123080	HAEpiC	amniotic membrane:	n/a
7	chr6:49123030-49123080	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:49123030-49123080	HRCEpiC	kidney:	n/a
9	chr6:49123030-49123080	NHBE	bronchial:	n/a
10	chr6:49110730-49110780	NH-A	brain:	n/a
11	chr6:49123030-49123080	AG09319	gingival:	n/a
12	chr6:49110730-49110780	NT2-D1	testis:	n/a
13	chr6:49123030-49123080	ovcar-3	ovarian:	n/a
14	chr6:49110730-49110780	NB4	blood:	n/a
15	chr6:49123030-49123080	AG04450	lung:	fetal
16	chr6:49110730-49110780	NHBE	bronchial:	n/a
17	chr6:49110730-49110780	PFSK-1	brain:	n/a
18	chr6:49110730-49110780	NHDF-neo	bronchial:	n/a
19	chr6:49110730-49110780	GM12891	blood:	n/a
20	chr6:49123030-49123080	AoSMC	blood vessel:	n/a
21	chr6:49123030-49123080	SKMC	muscle:	n/a
22	chr6:49123030-49123080	SK-N-MC	brain:	n/a
23	chr6:49123030-49123080	NT2-D1	testis:	n/a
24	chr6:49110730-49110780	AG04449	skin:	fetal
25	chr6:49123030-49123080	Hepatocyte	liver:	n/a
26	chr6:49123030-49123080	SK-N-SH_RA	brain:	n/a
27	chr6:49110730-49110780	IMR90	lung:	fetal
28	chr6:49110730-49110780	CMK	blood:	n/a
29	chr6:49123030-49123080	AG10803	skin:	n/a
30	chr6:49110730-49110780	HRPEpiC	eye:	n/a
31	chr6:49110730-49110780	PrEC	prostate:	n/a
32	chr6:49110730-49110780	Jurkat	blood:	n/a
33	chr6:49110730-49110780	K562	blood:	n/a
34	chr6:49123030-49123080	GM19239	blood:	n/a
35	chr6:49123030-49123080	LNCaP	prostate:	n/a
36	chr6:49110730-49110780	BE2_C	brain:	n/a
37	chr6:49110730-49110780	AG09309	skin:	n/a
38	chr6:49123030-49123080	Jurkat	blood:	n/a
39	chr6:49110730-49110780	Caco-2	colon:	n/a
40	chr6:49110730-49110780	MCF10A-Er-Src	breast:	n/a
41	chr6:49110730-49110780	HCT-116	colon:	n/a
42	chr6:49110730-49110780	SK-N-SH	brain:	n/a
43	chr6:49123030-49123080	BE2_C	brain:	n/a
44	chr6:49110730-49110780	GM12892	blood:	n/a
45	chr6:49110730-49110780	A549	lung:	n/a
46	chr6:49123030-49123080	Caco-2	colon:	n/a
47	chr6:49110730-49110780	HCF	heart:	n/a
48	chr6:49110730-49110780	PANC-1	pancreas:	n/a
49	chr6:49123030-49123080	PFSK-1	brain:	n/a
50	chr6:49123030-49123080	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:28770203..28772237-chr6:49079734..49082291,2	MCF-7	breast:
2	chr19:3975477..3976200-chr6:49132848..49133652,2	MCF-7	breast:
3	chr6:49165091..49165837-chr6:49377428..49378325,3	MCF-7	breast:
4	chr6:49297248..49299308-chr6:49299565..49302261,2	K562	blood:
5	chr6:49160449..49163379-chr6:49168376..49170816,2	K562	blood:
6	chr1:37939002..37941734-chr6:49098087..49100973,2	MCF-7	breast:
7	chr6:49068560..49071402-chr6:49178600..49180630,2	K562	blood:
8	chr6:49100268..49102612-chr6:49105903..49108889,2	K562	blood:
9	chr6:49160449..49163379-chr6:49168376..49170816,2	K562	blood:
10	chr6:49100268..49102612-chr6:49105903..49108889,2	K562	blood:

Variant related genes	Relation type
ENSG00000217631	TF binding region
ENSG00000217631	CpG island
ENSG00000163874	chromatin interactions
ENSG00000233621	chromatin interactions

Extended variants
information (count: 5839 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5839 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181532693	chr6:49081545-49081546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12212993	chr6:49081548-49081549	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111232151	chr6:49081558-49081559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540424317	chr6:49081641-49081642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565114595	chr6:49081687-49081688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576850454	chr6:49081729-49081730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532723547	chr6:49081776-49081777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371072489	chr6:49081781-49081782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185984417	chr6:49081785-49081786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190675011	chr6:49081815-49081816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182503561	chr6:49081847-49081848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561239830	chr6:49081848-49081849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528807523	chr6:49081857-49081858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs80153628	chr6:49081905-49081906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151199177	chr6:49081914-49081915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538728222	chr6:49081967-49081968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551054544	chr6:49082077-49082078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569113933	chr6:49082086-49082087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186749000	chr6:49082094-49082095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149964421	chr6:49082104-49082105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116539870	chr6:49082171-49082172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562625623	chr6:49082199-49082200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75424232	chr6:49082275-49082276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76638547	chr6:49082287-49082288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576991820	chr6:49082308-49082309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145700753	chr6:49082327-49082328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190739665	chr6:49082329-49082330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35050494	chr6:49082414-49082415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182981192	chr6:49082445-49082446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541424754	chr6:49082448-49082449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559747611	chr6:49082463-49082464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114827982	chr6:49082496-49082497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570810417	chr6:49082510-49082511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188681100	chr6:49082579-49082580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539947138	chr6:49082598-49082599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111708534	chr6:49082627-49082628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183284774	chr6:49082667-49082668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569331009	chr6:49082700-49082701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187246409	chr6:49082716-49082717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548585163	chr6:49082721-49082722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192118434	chr6:49082737-49082738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566889453	chr6:49082826-49082827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534053189	chr6:49083005-49083006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558817841	chr6:49083045-49083046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183983765	chr6:49083065-49083066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140553220	chr6:49083102-49083103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116369591	chr6:49083104-49083105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77614362	chr6:49083165-49083166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190010559	chr6:49083176-49083177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192257982	chr6:49083177-49083178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
abnormal development	18461090	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

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49040400-49089600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:49084600-49085000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr6:49084800-49085400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:49085600-49086400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:49086400-49089400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:49089400-49089600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:49089400-49090600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:49089600-49090000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:49089600-49090400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:49089800-49090800	Enhancers	NHEK	skin
11	chr6:49090000-49091200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:49090400-49103600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:49095800-49098400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:49107800-49108000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr6:49108000-49109600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr6:49108400-49111800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr6:49108600-49109200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:49108600-49109800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr6:49108600-49110200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr6:49108600-49112000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr6:49108800-49109600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr6:49108800-49111600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:49109000-49109200	Enhancers	H9 Cell Line	embryonic stem cell
24	chr6:49109000-49112000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr6:49109200-49111000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:49109400-49110600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr6:49109600-49110600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr6:49109600-49112200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr6:49109800-49110000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:49109800-49110000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr6:49109800-49110800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:49110000-49110400	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr6:49110000-49110600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr6:49110000-49110800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:49110200-49110600	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr6:49110400-49111200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr6:49110400-49111400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr6:49110600-49111000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr6:49110600-49111000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr6:49110600-49111400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr6:49110600-49111800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr6:49111000-49112000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr6:49111000-49112000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:49111200-49111800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr6:49111400-49111800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:49111800-49112000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:49112000-49122600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr6:49117600-49118600	Enhancers	Placenta	Placenta
49	chr6:49118200-49119000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:49122200-49123600	Enhancers	HUES48 Cell Line	embryonic stem cell

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