Variant report

Variant	nsv1026690
Chromosome Location	chr6:150419115-150485583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:1466)
Chromatin interactive
region (count:60)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 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	ARID3A	chr6:150472015-150472823	K562	blood:	n/a	n/a
2	ARID3A	chr6:150466906-150467292	K562	blood:	n/a	n/a
3	ARID3A	chr6:150484739-150484759	K562	blood:	n/a	n/a
4	ARID3A	chr6:150439874-150440128	HepG2	liver:	n/a	n/a
5	ATF1	chr6:150472028-150472739	K562	blood:	n/a	n/a
6	ATF3	chr6:150471929-150472732	K562	blood:	n/a	n/a
7	BACH1	chr6:150466906-150467189	K562	blood:	n/a	n/a
8	BACH1	chr6:150464335-150464775	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:150463766-150464064	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:150478344-150478362	K562	blood:	n/a	n/a
11	BHLHE40	chr6:150471514-150472899	K562	blood:	n/a	n/a
12	BHLHE40	chr6:150465618-150465684	K562	blood:	n/a	n/a
13	BHLHE40	chr6:150465179-150465378	K562	blood:	n/a	n/a
14	BHLHE40	chr6:150439788-150440200	HepG2	liver:	n/a	n/a
15	BHLHE40	chr6:150463969-150464551	K562	blood:	n/a	n/a
16	CBX3	chr6:150459013-150459369	K562	blood:	n/a	n/a
17	CBX3	chr6:150463796-150464328	K562	blood:	n/a	n/a
18	CBX3	chr6:150433315-150433703	K562	blood:	n/a	n/a
19	CBX3	chr6:150471211-150473040	K562	blood:	n/a	chr6:150471228-150471239
20	CCNT2	chr6:150477879-150477890	K562	blood:	n/a	n/a
21	CCNT2	chr6:150466696-150466829	K562	blood:	n/a	n/a
22	CCNT2	chr6:150472046-150472779	K562	blood:	n/a	n/a
23	CCNT2	chr6:150463711-150465001	K562	blood:	n/a	chr6:150464656-150464665
24	CEBPB	chr6:150460620-150460967	K562	blood:	n/a	chr6:150460785-150460798 chr6:150460785-150460796 chr6:150460787-150460798 chr6:150460785-150460798
25	CEBPB	chr6:150465663-150465991	K562	blood:	n/a	chr6:150465959-150465972 chr6:150465824-150465837
26	CEBPB	chr6:150439799-150440242	MCF-7	breast:	n/a	n/a
27	CEBPB	chr6:150468544-150468955	MCF-7	breast:	n/a	chr6:150468747-150468758
28	CEBPB	chr6:150439866-150440067	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:150439838-150440181	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:150460612-150460936	K562	blood:	n/a	chr6:150460785-150460798 chr6:150460785-150460796 chr6:150460787-150460798 chr6:150460785-150460798
31	CEBPB	chr6:150468549-150469065	MCF-7	breast:	n/a	chr6:150468747-150468758
32	CEBPB	chr6:150434507-150434701	A549	lung:	n/a	n/a
33	CEBPB	chr6:150439880-150440115	A549	lung:	n/a	n/a
34	CEBPB	chr6:150439881-150440139	MCF-7	breast:	n/a	n/a
35	CEBPB	chr6:150459838-150460039	K562	blood:	n/a	n/a
36	CEBPB	chr6:150460568-150460988	MCF-7	breast:	n/a	chr6:150460785-150460798 chr6:150460785-150460796 chr6:150460787-150460798 chr6:150460785-150460798
37	CEBPB	chr6:150472028-150472915	K562	blood:	n/a	n/a
38	CEBPB	chr6:150421027-150421517	K562	blood:	n/a	n/a
39	CEBPB	chr6:150463483-150463720	A549	lung:	n/a	n/a
40	CEBPB	chr6:150468635-150468888	Hela-S3	cervix:	n/a	chr6:150468747-150468758
41	CEBPB	chr6:150421106-150421448	IMR90	lung:	n/a	n/a
42	CEBPB	chr6:150421273-150421316	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr6:150460635-150460894	HepG2	liver:	n/a	chr6:150460785-150460798 chr6:150460785-150460796 chr6:150460787-150460798 chr6:150460785-150460798
44	CEBPB	chr6:150421117-150421443	K562	blood:	n/a	n/a
45	CEBPB	chr6:150472006-150472937	K562	blood:	n/a	n/a
46	CEBPB	chr6:150427576-150427797	K562	blood:	n/a	n/a
47	CEBPB	chr6:150463488-150463753	K562	blood:	n/a	n/a
48	CEBPB	chr6:150421073-150421473	K562	blood:	n/a	n/a
49	CEBPB	chr6:150421188-150421401	A549	lung:	n/a	n/a
50	CEBPB	chr6:150470237-150470566	K562	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150463965-150464015	Caco-2	colon:	n/a
2	chr6:150463500-150463550	NHDF-neo	bronchial:	n/a
3	chr6:150463965-150464015	Caco-2	colon:	n/a
4	chr6:150463500-150463550	NHDF-neo	bronchial:	n/a
5	chr6:150464265-150464315	HRCEpiC	kidney:	n/a
6	chr6:150471163-150471213	Caco-2	colon:	n/a
7	chr6:150436654-150436704	HRE	kidney:	n/a
8	chr6:150471163-150471213	NHBE	bronchial:	n/a
9	chr6:150464644-150464694	HEEpiC	esophagus:	n/a
10	chr6:150437072-150437122	Caco-2	colon:	n/a
11	chr6:150464990-150465040	BE2_C	brain:	n/a
12	chr6:150464117-150464167	HCF	heart:	n/a
13	chr6:150464020-150464070	ovcar-3	ovarian:	n/a
14	chr6:150465049-150465099	Hela-S3	cervix:	n/a
15	chr6:150463990-150464040	HRPEpiC	eye:	n/a
16	chr6:150464265-150464315	NHDF-neo	bronchial:	n/a
17	chr6:150464124-150464174	Hela-S3	cervix:	n/a
18	chr6:150422010-150422060	SK-N-MC	brain:	n/a
19	chr6:150437118-150437168	BJ	skin:	n/a
20	chr6:150463417-150463467	GM12892	blood:	n/a
21	chr6:150462309-150462359	GM19239	blood:	n/a
22	chr6:150465049-150465099	GM19239	blood:	n/a
23	chr6:150468008-150468058	ProgFib	skin:	n/a
24	chr6:150437072-150437122	AG04450	lung:	fetal
25	chr6:150464124-150464174	AoSMC	blood vessel:	n/a
26	chr6:150463500-150463550	GM12891	blood:	n/a
27	chr6:150464124-150464174	HRE	kidney:	n/a
28	chr6:150436619-150436669	HIPEpiC	eye:	n/a
29	chr6:150464020-150464070	SKMC	muscle:	n/a
30	chr6:150464644-150464694	LNCaP	prostate:	n/a
31	chr6:150463965-150464015	NHDF-neo	bronchial:	n/a
32	chr6:150468008-150468058	SK-N-SH_RA	brain:	n/a
33	chr6:150437138-150437188	HCPEpiC	choroid plexus:	n/a
34	chr6:150462309-150462359	MCF10A-Er-Src	breast:	n/a
35	chr6:150437138-150437188	BE2_C	brain:	n/a
36	chr6:150464117-150464167	HEEpiC	esophagus:	n/a
37	chr6:150464265-150464315	HCPEpiC	choroid plexus:	n/a
38	chr6:150471163-150471213	PANC-1	pancreas:	n/a
39	chr6:150463417-150463467	MCF-7	breast:	n/a
40	chr6:150437118-150437168	PANC-1	pancreas:	n/a
41	chr6:150464117-150464167	T-47D	breast:	n/a
42	chr6:150461119-150461169	AG09309	skin:	n/a
43	chr6:150464124-150464174	HAEpiC	amniotic membrane:	n/a
44	chr6:150437118-150437168	HEK293	kidney:	embryo
45	chr6:150437072-150437122	T-47D	breast:	n/a
46	chr6:150465049-150465099	K562	blood:	n/a
47	chr6:150422010-150422060	AG09309	skin:	n/a
48	chr6:150437072-150437122	NH-A	brain:	n/a
49	chr6:150463990-150464040	AG10803	skin:	n/a
50	chr6:150437118-150437168	SK-N-MC	brain:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:150471157..150474765-chr6:150475895..150479622,5	K562	blood:
2	chr6:150448969..150450613-chr6:150472579..150475543,2	K562	blood:
3	chr6:150469308..150480268-chr6:150484066..150492629,15	K562	blood:
4	chr6:150447572..150449678-chr6:150453933..150456873,2	K562	blood:
5	chr6:150464023..150466191-chr6:150484823..150488710,3	K562	blood:
6	chr6:150429467..150431615-chr6:150433322..150437434,3	K562	blood:
7	chr6:150401453..150402381-chr6:150464218..150464794,3	MCF-7	breast:
8	chr6:150418965..150420517-chr6:150430533..150432429,2	K562	blood:
9	chr6:150469487..150471945-chr6:150477081..150478644,2	K562	blood:
10	chr6:150465090..150467055-chr6:150662955..150664731,2	K562	blood:
11	chr6:150417796..150419721-chr6:150422461..150424493,2	K562	blood:
12	chr6:150472442..150474765-chr6:150475018..150477880,4	K562	blood:
13	chr6:150448057..150450613-chr6:150472579..150475543,3	K562	blood:
14	chr6:150421701..150424614-chr6:150433615..150435705,2	K562	blood:
15	chr6:150419610..150420185-chr6:150610668..150611430,2	K562	blood:
16	chr6:150426417..150429410-chr6:150487738..150490654,2	K562	blood:
17	chr6:150418965..150420517-chr6:150430533..150432429,2	K562	blood:
18	chr17:78233901..78236190-chr6:150464382..150465882,2	MCF-7	breast:
19	chr6:150431155..150433658-chr6:150438075..150440832,2	K562	blood:
20	chr6:150430115..150432623-chr6:150435184..150437434,2	K562	blood:
21	chr6:150410116..150412744-chr6:150428842..150431815,2	K562	blood:
22	chr6:150450031..150451577-chr6:150457314..150459716,2	MCF-7	breast:
23	chr6:150475010..150477072-chr6:150477573..150480562,2	K562	blood:
24	chr6:150432794..150435145-chr6:150436084..150437701,2	K562	blood:
25	chr6:150432794..150435145-chr6:150436084..150437701,2	K562	blood:
26	chr6:150450031..150451577-chr6:150457314..150459716,2	MCF-7	breast:
27	chr6:150428307..150430967-chr6:150432896..150435130,3	K562	blood:
28	chr6:150448969..150450613-chr6:150472579..150475543,2	K562	blood:
29	chr6:150462370..150464017-chr6:150474588..150477355,2	K562	blood:
30	chr6:150420929..150422703-chr6:150428326..150430256,2	K562	blood:
31	chr6:150462370..150464017-chr6:150474588..150477355,2	K562	blood:
32	chr6:150449726..150451352-chr6:150464010..150466686,2	K562	blood:
33	chr6:150429467..150431615-chr6:150433322..150437434,3	K562	blood:
34	chr6:150427042..150429216-chr6:150430762..150432440,2	K562	blood:
35	chr6:150447572..150449678-chr6:150453933..150456873,2	K562	blood:
36	chr6:150430115..150432623-chr6:150435184..150437434,2	K562	blood:
37	chr6:150449407..150453183-chr6:150455080..150457364,4	K562	blood:
38	chr6:150451217..150453033-chr6:150459059..150461141,2	MCF-7	breast:
39	chr6:150427042..150429216-chr6:150430762..150432440,2	K562	blood:
40	chr6:150417796..150419721-chr6:150422461..150424493,2	K562	blood:
41	chr6:150461000..150463300-chr6:150463460..150465278,2	MCF-7	breast:
42	chr6:150472260..150480045-chr6:150481720..150491899,15	K562	blood:
43	chr6:150449726..150452663-chr6:150462298..150465510,3	K562	blood:
44	chr6:150428307..150430967-chr6:150432896..150435130,3	K562	blood:
45	chr6:150450612..150452742-chr6:150455452..150457364,2	K562	blood:
46	chr6:150469487..150471945-chr6:150477081..150478644,2	K562	blood:
47	chr6:150420929..150422703-chr6:150428326..150430256,2	K562	blood:
48	chr6:150450612..150452742-chr6:150455452..150457364,2	K562	blood:
49	chr6:150421701..150424614-chr6:150433615..150435705,2	K562	blood:
50	chr6:150431155..150433658-chr6:150438075..150440832,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000238594	TF binding region
PPP1R14C	TF binding region
ENSG00000238594	CpG island
PPP1R14C	CpG island
ENSG00000238594	chromatin interactions
ENSG00000198729	chromatin interactions
ENSG00000173821	chromatin interactions

Extended variants
information (count: 2761 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2761 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7452369	chr6:150419115-150419116	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573533573	chr6:150419139-150419140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372248576	chr6:150419175-150419176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555900377	chr6:150419289-150419290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116588861	chr6:150419311-150419312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544902386	chr6:150419320-150419321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573847969	chr6:150419433-150419434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193239959	chr6:150419455-150419456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77020169	chr6:150419456-150419457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374641027	chr6:150419498-150419499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs199970976	chr6:150419507-150419508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560665686	chr6:150419551-150419552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143335072	chr6:150419553-150419554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2184453	chr6:150419594-150419595	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs569555457	chr6:150419599-150419600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531996055	chr6:150419604-150419605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573043339	chr6:150419628-150419629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541951501	chr6:150419647-150419648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529050529	chr6:150419648-150419649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534421235	chr6:150419667-150419668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9371712	chr6:150419731-150419732	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567317930	chr6:150419733-150419734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148843158	chr6:150419740-150419741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556075276	chr6:150419780-150419781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184073182	chr6:150419807-150419808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11759308	chr6:150419808-150419809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs117401075	chr6:150419816-150419817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377726475	chr6:150419844-150419845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553861670	chr6:150419861-150419862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186649115	chr6:150419862-150419863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117702012	chr6:150419869-150419870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560942166	chr6:150419878-150419879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574040050	chr6:150419959-150419960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73004094	chr6:150419984-150419985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562899418	chr6:150419986-150419987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531772828	chr6:150420031-150420032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9371294	chr6:150420044-150420045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs112661686	chr6:150420068-150420069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565548379	chr6:150420086-150420087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528005734	chr6:150420106-150420107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547927515	chr6:150420160-150420161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567759465	chr6:150420197-150420198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191111249	chr6:150420235-150420236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532507249	chr6:150420305-150420306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549649213	chr6:150420337-150420338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374051093	chr6:150420376-150420377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552291682	chr6:150420385-150420386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538277474	chr6:150420419-150420420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183659861	chr6:150420499-150420500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143460527	chr6:150420500-150420501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Gastric cancer	17908304	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
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150410400-150421800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:150416000-150420800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:150418400-150419600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr6:150419000-150419400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:150419000-150419800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr6:150419200-150419400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:150420800-150421000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:150420800-150421800	Bivalent Enhancer	K562	blood
9	chr6:150421800-150422400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:150422400-150436800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:150428200-150428800	Bivalent Enhancer	K562	blood
12	chr6:150432400-150433600	Bivalent Enhancer	K562	blood
13	chr6:150434400-150434800	Bivalent Enhancer	K562	blood
14	chr6:150436800-150437600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:150436800-150437800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr6:150436800-150438200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:150437000-150437800	Enhancers	Esophagus	oesophagus
18	chr6:150437000-150438000	Enhancers	HMEC	breast
19	chr6:150437200-150438000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:150437200-150438000	Enhancers	NHEK	skin
21	chr6:150437200-150438200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr6:150437200-150438200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:150437200-150438200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:150437200-150440000	Weak transcription	Fetal Intestine Small	intestine
25	chr6:150437400-150438000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr6:150437400-150438000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr6:150437400-150439800	Weak transcription	Right Atrium	heart
28	chr6:150437600-150437800	Enhancers	Brain Cingulate Gyrus	brain
29	chr6:150437600-150437800	Enhancers	Pancreas	Pancrea
30	chr6:150437600-150438000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:150437800-150438000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:150437800-150438000	Enhancers	Brain Substantia Nigra	brain
33	chr6:150437800-150439600	Weak transcription	Esophagus	oesophagus
34	chr6:150437800-150440000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:150438000-150439400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:150438000-150439400	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr6:150438000-150439400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:150438000-150440200	Weak transcription	Brain Cingulate Gyrus	brain
39	chr6:150438200-150439400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr6:150438200-150439800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:150438200-150440200	Weak transcription	Brain Substantia Nigra	brain
42	chr6:150438400-150441000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr6:150438600-150439800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:150439200-150440400	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr6:150439200-150441000	Enhancers	Fetal Kidney	kidney
46	chr6:150439200-150441200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:150439200-150441200	Enhancers	Fetal Brain Male	brain
48	chr6:150439400-150440200	Enhancers	Fetal Heart	heart
49	chr6:150439400-150440600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr6:150439400-150440600	Enhancers	Fetal Stomach	stomach

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