Variant report

Variant	esv3439048
Chromosome Location	chr6:27351973-27357171
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	chr6:27356543-27356879	K562	blood:	n/a	n/a
2	ARID3A	chr6:27356437-27356828	HepG2	liver:	n/a	n/a
3	ATF2	chr6:27356346-27356930	GM12878	blood:	n/a	n/a
4	ATF2	chr6:27356395-27356962	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:27356515-27356961	GM12878	blood:	n/a	n/a
6	ATF2	chr6:27356479-27356915	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr6:27356439-27356968	K562	blood:	n/a	n/a
8	ATF3	chr6:27356499-27356852	A549	lung:	n/a	n/a
9	ATF3	chr6:27356390-27356930	A549	lung:	n/a	n/a
10	BACH1	chr6:27356396-27357077	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr6:27356502-27356863	GM12878	blood:	n/a	n/a
12	BCL3	chr6:27356441-27356912	A549	lung:	n/a	n/a
13	BCLAF1	chr6:27356365-27356967	GM12878	blood:	n/a	n/a
14	BCLAF1	chr6:27356389-27357011	K562	blood:	n/a	n/a
15	BCLAF1	chr6:27356253-27357006	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:27356411-27357053	K562	blood:	n/a	n/a
17	BHLHE40	chr6:27356282-27356857	HepG2	liver:	n/a	n/a
18	BHLHE40	chr6:27356226-27357046	K562	blood:	n/a	n/a
19	BRCA1	chr6:27356606-27356910	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr6:27356528-27356880	HepG2	liver:	n/a	n/a
21	CBX3	chr6:27356350-27356928	K562	blood:	n/a	n/a
22	CBX3	chr6:27356238-27357706	K562	blood:	n/a	n/a
23	CCNT2	chr6:27356216-27357079	K562	blood:	n/a	chr6:27356422-27356431
24	CEBPB	chr6:27355966-27356808	Hela-S3	cervix:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
25	CEBPB	chr6:27355943-27356733	K562	blood:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
26	CEBPB	chr6:27355921-27357031	A549	lung:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
27	CEBPB	chr6:27356207-27357014	GM12878	blood:	n/a	chr6:27356433-27356444
28	CEBPB	chr6:27356328-27356883	MCF-7	breast:	n/a	chr6:27356433-27356444
29	CEBPB	chr6:27355860-27356747	IMR90	lung:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
30	CEBPB	chr6:27355931-27356309	MCF-7	breast:	n/a	chr6:27356124-27356135 chr6:27355981-27355990 chr6:27356126-27356135
31	CEBPB	chr6:27355968-27356744	A549	lung:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
32	CEBPB	chr6:27355805-27356909	ECC-1	luminal epithelium:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
33	CEBPB	chr6:27355927-27356905	K562	blood:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
34	CEBPB	chr6:27355900-27356769	HepG2	liver:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
35	CEBPB	chr6:27355827-27356877	H1-hESC	embryonic stem cell:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
36	CEBPB	chr6:27356370-27356785	HepG2	liver:	n/a	chr6:27356433-27356444
37	CEBPD	chr6:27356331-27356922	HepG2	liver:	n/a	n/a
38	CEBPD	chr6:27356444-27356847	HepG2	liver:	n/a	n/a
39	CHD2	chr6:27356376-27356888	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr6:27356325-27356815	HepG2	liver:	n/a	n/a
41	CHD2	chr6:27356460-27356919	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr6:27356418-27356847	K562	blood:	n/a	n/a
43	CHD2	chr6:27356506-27356937	GM12878	blood:	n/a	n/a
44	CREB1	chr6:27356313-27356935	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr6:27356195-27357021	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr6:27356413-27356898	A549	lung:	n/a	n/a
47	CTCF	chr6:27356675-27356691	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:27356520-27356670	BE2_C	brain:	n/a	n/a
49	CTCF	chr6:27356470-27356481	Fibrobl	skin:	n/a	n/a
50	CTCF	chr6:27356340-27356490	AG10803	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:27357008-27357058	SKMC	muscle:	n/a
2	chr6:27357008-27357058	SKMC	muscle:	n/a
3	chr6:27356624-27356674	GM12878	blood:	n/a
4	chr6:27356509-27356559	GM12878	blood:	n/a
5	chr6:27356234-27356284	H1-hESC	embryonic stem cell:	embryo
6	chr6:27356319-27356369	HCF	heart:	n/a
7	chr6:27356234-27356284	HIPEpiC	eye:	n/a
8	chr6:27356358-27356408	AG04450	lung:	fetal
9	chr6:27356509-27356559	HRPEpiC	eye:	n/a
10	chr6:27356509-27356559	CMK	blood:	n/a
11	chr6:27356513-27356563	Hepatocyte	liver:	n/a
12	chr6:27356624-27356674	AG09319	gingival:	n/a
13	chr6:27356234-27356284	SK-N-SH	brain:	n/a
14	chr6:27356499-27356549	AoSMC	blood vessel:	n/a
15	chr6:27356509-27356559	SAEC	small airway:	n/a
16	chr6:27356319-27356369	NHDF-neo	bronchial:	n/a
17	chr6:27356358-27356408	AG09309	skin:	n/a
18	chr6:27356624-27356674	NHBE	bronchial:	n/a
19	chr6:27357008-27357058	NHDF-neo	bronchial:	n/a
20	chr6:27356690-27356740	BJ	skin:	n/a
21	chr6:27356358-27356408	PANC-1	pancreas:	n/a
22	chr6:27356624-27356674	Hela-S3	cervix:	n/a
23	chr6:27356624-27356674	HEEpiC	esophagus:	n/a
24	chr6:27356513-27356563	HRPEpiC	eye:	n/a
25	chr6:27357008-27357058	SK-N-MC	brain:	n/a
26	chr6:27356414-27356464	HIPEpiC	eye:	n/a
27	chr6:27356414-27356464	NT2-D1	testis:	n/a
28	chr6:27356513-27356563	SKMC	muscle:	n/a
29	chr6:27356509-27356559	ovcar-3	ovarian:	n/a
30	chr6:27356319-27356369	HUVEC	blood vessel:	n/a
31	chr6:27356414-27356464	Hela-S3	cervix:	n/a
32	chr6:27356624-27356674	Caco-2	colon:	n/a
33	chr6:27357008-27357058	NB4	blood:	n/a
34	chr6:27356358-27356408	A549	lung:	n/a
35	chr6:27357040-27357090	SKMC	muscle:	n/a
36	chr6:27356319-27356369	PANC-1	pancreas:	n/a
37	chr6:27356690-27356740	HAEpiC	amniotic membrane:	n/a
38	chr6:27356319-27356369	SK-N-MC	brain:	n/a
39	chr6:27356358-27356408	HMEC	breast:	n/a
40	chr6:27356234-27356284	ovcar-3	ovarian:	n/a
41	chr6:27356624-27356674	SK-N-MC	brain:	n/a
42	chr6:27356624-27356674	NT2-D1	testis:	n/a
43	chr6:27357040-27357090	NB4	blood:	n/a
44	chr6:27356513-27356563	K562	blood:	n/a
45	chr6:27357008-27357058	HCPEpiC	choroid plexus:	n/a
46	chr6:27356624-27356674	GM06990	blood:	n/a
47	chr6:27357040-27357090	HUVEC	blood vessel:	n/a
48	chr6:27356499-27356549	H1-hESC	embryonic stem cell:	embryo
49	chr6:27356513-27356563	HRCEpiC	kidney:	n/a
50	chr6:27356513-27356563	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:27356362..27358956-chr6:27773296..27775539,3	K562	blood:
2	chr6:27350809..27354619-chr6:27354946..27358020,4	K562	blood:
3	chr6:27350962..27353140-chr6:27353482..27356207,2	MCF-7	breast:
4	chr6:27347361..27349811-chr6:27351442..27354112,2	K562	blood:
5	chr6:27291445..27294642-chr6:27355178..27358043,3	MCF-7	breast:
6	chr21:27542816..27543374-chr6:27355736..27356540,2	HCT-116	colon:
7	chr6:27350459..27352527-chr6:27353409..27355120,2	K562	blood:
8	chr6:27354651..27357206-chr6:27439212..27442131,3	K562	blood:
9	chr6:27342371..27343890-chr6:27355850..27358027,2	K562	blood:
10	chr6:27356907..27359078-chr6:27397692..27399728,2	K562	blood:
11	chr6:27114804..27117756-chr6:27356552..27360776,4	K562	blood:
12	chr6:27338163..27340340-chr6:27350329..27352907,2	MCF-7	breast:
13	chr6:27344880..27347098-chr6:27353310..27355092,2	K562	blood:
14	chr6:27356277..27359093-chr6:27439899..27443040,4	MCF-7	breast:
15	chr6:27350459..27352527-chr6:27353409..27355120,2	K562	blood:
16	chr6:27357105..27360959-chr6:27363374..27365305,4	K562	blood:
17	chr6:27350962..27353140-chr6:27353482..27356207,2	MCF-7	breast:
18	chr6:27113785..27116304-chr6:27356399..27358052,2	K562	blood:
19	chr6:27341304..27343058-chr6:27356076..27357820,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS16-3	chr6:27356683-27356854	NONHSAT108379
2	lnc-ZNF184-3	chr6:27356046-27357004	NONHSAT108378

Variant related genes	Relation type
ZNF391	TF binding region
ZNF391	CpG island
ENSG00000184825	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000204789	chromatin interactions
ENSG00000220758	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000124613	chromatin interactions
ENSG00000217862	chromatin interactions
ENSG00000096654	chromatin interactions
ENSG00000142192	chromatin interactions
ENSG00000273492	chromatin interactions

Extended variants
information (count: 179 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12530073	chr6:27351995-27351996	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs367581417	chr6:27352002-27352003	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546886459	chr6:27352038-27352039	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2393930	chr6:27352040-27352041	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs192519875	chr6:27352051-27352052	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs562692677	chr6:27352107-27352108	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs139818701	chr6:27352129-27352130	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs548244697	chr6:27352147-27352148	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs377657665	chr6:27352179-27352180	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs113753446	chr6:27352250-27352251	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs200809735	chr6:27352259-27352260	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs376973768	chr6:27352260-27352261	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs61268861	chr6:27352261-27352262	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs199584956	chr6:27352263-27352264	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs200428401	chr6:27352265-27352266	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201778741	chr6:27352267-27352268	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527304626	chr6:27352323-27352324	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs73392669	chr6:27352366-27352367	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576584055	chr6:27352371-27352372	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs116470496	chr6:27352461-27352462	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs145286162	chr6:27352468-27352469	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550149443	chr6:27352555-27352556	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs370558270	chr6:27352563-27352564	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs575317941	chr6:27352569-27352570	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535605307	chr6:27352626-27352627	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs9461375	chr6:27352680-27352681	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs190438466	chr6:27352727-27352728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs386698286	chr6:27352750-27352751	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566827833	chr6:27352751-27352752	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs386698287	chr6:27352752-27352753	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs9468100	chr6:27352757-27352758	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs199742403	chr6:27352785-27352786	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs546061328	chr6:27352824-27352825	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs9468101	chr6:27352938-27352939	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs576206762	chr6:27352967-27352968	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs527647748	chr6:27352996-27352997	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs35004273	chr6:27353007-27353008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs397937374	chr6:27353012-27353013	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541590366	chr6:27353067-27353068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201631808	chr6:27353071-27353072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs35501833	chr6:27353101-27353102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2393931	chr6:27353114-27353115	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs527339356	chr6:27353191-27353192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs2393932	chr6:27353197-27353198	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs192030160	chr6:27353206-27353207	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563730271	chr6:27353226-27353227	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184621754	chr6:27353244-27353245	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570228304	chr6:27353248-27353249	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529508463	chr6:27353302-27353303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189183535	chr6:27353330-27353331	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
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
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD

Chromatin state (count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27343200-27356200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:27346800-27356200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:27353600-27353800	Enhancers	Adipose Nuclei	Adipose
4	chr6:27355000-27357400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:27355400-27355600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:27355400-27355800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:27355400-27355800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:27355600-27355800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr6:27355600-27355800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr6:27355600-27355800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:27355600-27355800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:27355600-27355800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:27355600-27355800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:27355600-27355800	Enhancers	Brain Anterior Caudate	brain
15	chr6:27355600-27355800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr6:27355600-27355800	Enhancers	Brain Substantia Nigra	brain
17	chr6:27355600-27355800	Enhancers	Colon Smooth Muscle	Colon
18	chr6:27355600-27355800	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr6:27355600-27355800	Enhancers	Fetal Brain Female	brain
20	chr6:27355600-27355800	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr6:27355600-27355800	Enhancers	Dnd41	blood
22	chr6:27355600-27355800	Enhancers	Osteobl	bone
23	chr6:27355600-27356000	Flanking Active TSS	Brain Germinal Matrix	brain
24	chr6:27355600-27356000	Active TSS	HepG2	liver
25	chr6:27355600-27356200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:27355600-27357600	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr6:27355600-27358400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:27355800-27356000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr6:27355800-27356000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr6:27355800-27356000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:27355800-27356000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:27355800-27356000	Enhancers	Primary B cells from peripheral blood	blood
33	chr6:27355800-27356000	Enhancers	Primary hematopoietic stem cells	blood
34	chr6:27355800-27356000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr6:27355800-27356000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr6:27355800-27356000	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr6:27355800-27356000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr6:27355800-27356000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr6:27355800-27356000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr6:27355800-27356000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:27355800-27356000	Enhancers	Adipose Nuclei	Adipose
42	chr6:27355800-27356000	Enhancers	Liver	Liver
43	chr6:27355800-27356000	Enhancers	Duodenum Mucosa	Duodenum
44	chr6:27355800-27356000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr6:27355800-27356000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr6:27355800-27356000	Enhancers	Fetal Heart	heart
47	chr6:27355800-27356000	Enhancers	Fetal Kidney	kidney
48	chr6:27355800-27356000	Flanking Active TSS	Fetal Lung	lung
49	chr6:27355800-27356000	Enhancers	Placenta	Placenta
50	chr6:27355800-27356000	Enhancers	Fetal Stomach	stomach

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