Variant report

Variant	nsv886770
Chromosome Location	chr6:150395424-150499889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1277)
CpG islands
(count:1467)
Chromatin interactive
region (count:104)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150399954-150400171	K562	blood:	n/a	n/a
2	ARID3A	chr6:150466906-150467292	K562	blood:	n/a	n/a
3	ARID3A	chr6:150472015-150472823	K562	blood:	n/a	n/a
4	ARID3A	chr6:150439874-150440128	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:150490712-150491248	K562	blood:	n/a	n/a
6	ARID3A	chr6:150401828-150402053	K562	blood:	n/a	n/a
7	ARID3A	chr6:150484739-150484759	K562	blood:	n/a	n/a
8	ATF1	chr6:150472028-150472739	K562	blood:	n/a	n/a
9	ATF1	chr6:150399918-150400184	K562	blood:	n/a	n/a
10	ATF2	chr6:150489062-150489464	GM12878	blood:	n/a	n/a
11	ATF2	chr6:150489147-150489464	GM12878	blood:	n/a	n/a
12	ATF3	chr6:150471929-150472732	K562	blood:	n/a	n/a
13	ATF3	chr6:150401844-150402026	K562	blood:	n/a	n/a
14	BACH1	chr6:150401770-150402019	K562	blood:	n/a	n/a
15	BACH1	chr6:150478344-150478362	K562	blood:	n/a	n/a
16	BACH1	chr6:150466906-150467189	K562	blood:	n/a	n/a
17	BACH1	chr6:150463766-150464064	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:150401872-150402141	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:150464335-150464775	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr6:150490648-150491152	GM12878	blood:	n/a	n/a
21	BATF	chr6:150490744-150491127	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:150489133-150489363	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:150489107-150489337	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:150490787-150491092	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:150490682-150491161	GM12878	blood:	n/a	n/a
26	BCL3	chr6:150490759-150491135	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:150471514-150472899	K562	blood:	n/a	n/a
28	BHLHE40	chr6:150401754-150402119	K562	blood:	n/a	n/a
29	BHLHE40	chr6:150400020-150400054	K562	blood:	n/a	n/a
30	BHLHE40	chr6:150439788-150440200	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:150488762-150488813	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:150489137-150489524	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:150463969-150464551	K562	blood:	n/a	n/a
34	BHLHE40	chr6:150465179-150465378	K562	blood:	n/a	n/a
35	BHLHE40	chr6:150465618-150465684	K562	blood:	n/a	n/a
36	BHLHE40	chr6:150488791-150489413	K562	blood:	n/a	n/a
37	BHLHE40	chr6:150486994-150487355	K562	blood:	n/a	n/a
38	CBX3	chr6:150488584-150490189	K562	blood:	n/a	n/a
39	CBX3	chr6:150433315-150433703	K562	blood:	n/a	n/a
40	CBX3	chr6:150471211-150473040	K562	blood:	n/a	chr6:150471228-150471239
41	CBX3	chr6:150401737-150402259	K562	blood:	n/a	n/a
42	CBX3	chr6:150490672-150491300	HCT-116	colon:	n/a	n/a
43	CBX3	chr6:150489064-150489386	K562	blood:	n/a	n/a
44	CBX3	chr6:150459013-150459369	K562	blood:	n/a	n/a
45	CBX3	chr6:150486975-150487332	K562	blood:	n/a	n/a
46	CBX3	chr6:150463796-150464328	K562	blood:	n/a	n/a
47	CCNT2	chr6:150472046-150472779	K562	blood:	n/a	n/a
48	CCNT2	chr6:150488833-150489381	K562	blood:	n/a	n/a
49	CCNT2	chr6:150399968-150400225	K562	blood:	n/a	n/a
50	CCNT2	chr6:150463711-150465001	K562	blood:	n/a	chr6:150464656-150464665

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150437118-150437168	Jurkat	blood:	n/a
2	chr6:150464644-150464694	AG09309	skin:	n/a
3	chr6:150464124-150464174	Jurkat	blood:	n/a
4	chr6:150437118-150437168	Jurkat	blood:	n/a
5	chr6:150464644-150464694	AG09309	skin:	n/a
6	chr6:150464124-150464174	Jurkat	blood:	n/a
7	chr6:150465049-150465099	SAEC	small airway:	n/a
8	chr6:150436619-150436669	HEEpiC	esophagus:	n/a
9	chr6:150464265-150464315	ECC-1	luminal epithelium:	n/a
10	chr6:150471163-150471213	Caco-2	colon:	n/a
11	chr6:150463500-150463550	HCPEpiC	choroid plexus:	n/a
12	chr6:150464020-150464070	PrEC	prostate:	n/a
13	chr6:150461119-150461169	NT2-D1	testis:	n/a
14	chr6:150471163-150471213	CMK	blood:	n/a
15	chr6:150464020-150464070	HAEpiC	amniotic membrane:	n/a
16	chr6:150422093-150422143	GM12892	blood:	n/a
17	chr6:150464644-150464694	T-47D	breast:	n/a
18	chr6:150462309-150462359	H1-hESC	embryonic stem cell:	embryo
19	chr6:150436654-150436704	PrEC	prostate:	n/a
20	chr6:150463775-150463825	AG04450	lung:	fetal
21	chr6:150465049-150465099	SK-N-SH	brain:	n/a
22	chr6:150461119-150461169	NH-A	brain:	n/a
23	chr6:150422010-150422060	U87	brain:	n/a
24	chr6:150463417-150463467	Hepatocyte	liver:	n/a
25	chr6:150461119-150461169	HCF	heart:	n/a
26	chr6:150464265-150464315	Caco-2	colon:	n/a
27	chr6:150463417-150463467	ovcar-3	ovarian:	n/a
28	chr6:150464124-150464174	GM12891	blood:	n/a
29	chr6:150464000-150464050	PANC-1	pancreas:	n/a
30	chr6:150463417-150463467	HRE	kidney:	n/a
31	chr6:150464265-150464315	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:150422010-150422060	ovcar-3	ovarian:	n/a
33	chr6:150464124-150464174	HRCEpiC	kidney:	n/a
34	chr6:150436654-150436704	CMK	blood:	n/a
35	chr6:150464020-150464070	K562	blood:	n/a
36	chr6:150422010-150422060	AG09309	skin:	n/a
37	chr6:150463417-150463467	HL-60	blood:	n/a
38	chr6:150464990-150465040	PrEC	prostate:	n/a
39	chr6:150471163-150471213	GM12891	blood:	n/a
40	chr6:150422010-150422060	ProgFib	skin:	n/a
41	chr6:150462309-150462359	Hepatocyte	liver:	n/a
42	chr6:150461119-150461169	HCT-116	colon:	n/a
43	chr6:150422093-150422143	PANC-1	pancreas:	n/a
44	chr6:150464020-150464070	H1-hESC	embryonic stem cell:	embryo
45	chr6:150464265-150464315	NHDF-neo	bronchial:	n/a
46	chr6:150437138-150437188	HRCEpiC	kidney:	n/a
47	chr6:150436654-150436704	GM19239	blood:	n/a
48	chr6:150464117-150464167	AG10803	skin:	n/a
49	chr6:150464644-150464694	LNCaP	prostate:	n/a
50	chr6:150436654-150436704	SKMC	muscle:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:150409275..150411139-chr6:150425128..150427756,2	K562	blood:
2	chr6:150449407..150453183-chr6:150455080..150457364,4	K562	blood:
3	chr6:150464023..150466191-chr6:150484823..150488710,3	K562	blood:
4	chr6:150417796..150419721-chr6:150422461..150424493,2	K562	blood:
5	chr6:150426417..150429410-chr6:150487738..150490654,2	K562	blood:
6	chr6:150409275..150411139-chr6:150425128..150427756,2	K562	blood:
7	chr6:150400674..150403275-chr6:150407304..150409849,2	K562	blood:
8	chr6:150388542..150390431-chr6:150401978..150404443,2	MCF-7	breast:
9	chr6:150491837..150493416-chr6:150504605..150507001,2	K562	blood:
10	chr6:150399642..150402199-chr6:150464178..150465810,2	MCF-7	breast:
11	chr6:150489381..150492154-chr6:150493380..150496594,3	K562	blood:
12	chr6:150396641..150398617-chr6:150664104..150666636,2	K562	blood:
13	chr6:150464023..150466191-chr6:150484823..150488710,3	K562	blood:
14	chr6:150487685..150490900-chrX:41144153..41147153,5	K562	blood:
15	chr6:150430115..150432623-chr6:150435184..150437434,2	K562	blood:
16	chr6:150421701..150424614-chr6:150433615..150435705,2	K562	blood:
17	chr6:150401082..150403253-chr6:150656281..150658165,2	MCF-7	breast:
18	chr6:150401452..150402235-chr6:150654477..150655029,2	MCF-7	breast:
19	chr6:150417796..150419721-chr6:150422461..150424493,2	K562	blood:
20	chr6:150429467..150431615-chr6:150433322..150437434,3	K562	blood:
21	chr6:150450612..150452742-chr6:150455452..150457364,2	K562	blood:
22	chr6:150401711..150402469-chr6:150716292..150716821,2	K562	blood:
23	chr6:150430115..150432623-chr6:150435184..150437434,2	K562	blood:
24	chr6:150427042..150429216-chr6:150430762..150432440,2	K562	blood:
25	chr6:150499104..150501184-chr6:150507779..150510819,3	K562	blood:
26	chr6:150450031..150451577-chr6:150457314..150459716,2	MCF-7	breast:
27	chr6:150428307..150430967-chr6:150432896..150435130,3	K562	blood:
28	chr6:150394796..150396864-chr6:150397633..150400539,2	MCF-7	breast:
29	chr6:150475010..150477072-chr6:150477573..150480562,2	K562	blood:
30	chr6:150428307..150430967-chr6:150432896..150435130,3	K562	blood:
31	chr6:150418965..150420517-chr6:150430533..150432429,2	K562	blood:
32	chr6:150401704..150402247-chr6:150654478..150655258,3	MCF-7	breast:
33	chr6:150427042..150429216-chr6:150430762..150432440,2	K562	blood:
34	chr6:150426417..150429410-chr6:150487738..150490654,2	K562	blood:
35	chr6:150489133..150490702-chr6:150526456..150528096,2	K562	blood:
36	chr6:150401453..150402381-chr6:150464218..150464794,3	MCF-7	breast:
37	chr6:150451217..150453033-chr6:150459059..150461141,2	MCF-7	breast:
38	chr6:150471157..150474765-chr6:150475895..150479622,5	K562	blood:
39	chr6:150448969..150450613-chr6:150472579..150475543,2	K562	blood:
40	chr6:150421701..150424614-chr6:150433615..150435705,2	K562	blood:
41	chr6:150495241..150496949-chr6:150500349..150502096,2	MCF-7	breast:
42	chr6:150401196..150403539-chr6:150662242..150665059,2	K562	blood:
43	chr6:150401151..150402465-chr6:150656027..150656922,6	MCF-7	breast:
44	chr6:150472260..150480045-chr6:150481720..150491899,15	K562	blood:
45	chr6:150420929..150422703-chr6:150428326..150430256,2	K562	blood:
46	chr14:68653597..68656597-chr6:150487153..150490564,3	K562	blood:
47	chr6:150487734..150491272-chr6:150592346..150595301,4	K562	blood:
48	chr6:150418965..150420517-chr6:150430533..150432429,2	K562	blood:
49	chr6:150489261..150490775-chr6:150576809..150578342,2	K562	blood:
50	chr6:150404252..150405212-chr6:150654023..150654852,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000238594	TF binding region
PPP1R14C	TF binding region
ENSG00000238594	CpG island
PPP1R14C	CpG island
ENSG00000173821	chromatin interactions
ENSG00000131019	chromatin interactions
ENSG00000198729	chromatin interactions
ENSG00000238594	chromatin interactions

Extended variants
information (count: 4473 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4473 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2343271	chr6:150395424-150395425	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540474659	chr6:150395491-150395492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186995197	chr6:150395521-150395522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1324589	chr6:150395527-150395528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543026247	chr6:150395543-150395544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542331040	chr6:150395559-150395560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1853662	chr6:150395565-150395566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1853661	chr6:150395595-150395596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1853660	chr6:150395625-150395626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4038366	chr6:150395631-150395632	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs141125893	chr6:150395699-150395700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375465232	chr6:150395727-150395728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531835660	chr6:150395729-150395730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571169136	chr6:150395773-150395774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs59602990	chr6:150395782-150395783	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs546823062	chr6:150395783-150395784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368352980	chr6:150395786-150395787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371966152	chr6:150395799-150395800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566206354	chr6:150395874-150395875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535146842	chr6:150395900-150395901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368580040	chr6:150395912-150395913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545566457	chr6:150395919-150395920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537895134	chr6:150395925-150395926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73004058	chr6:150395929-150395930	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs578025820	chr6:150395935-150395936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540407947	chr6:150395948-150395949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553981337	chr6:150395979-150395980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527924582	chr6:150396003-150396004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541917945	chr6:150396015-150396016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562214731	chr6:150396048-150396049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113019071	chr6:150396069-150396070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544633764	chr6:150396082-150396083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567969042	chr6:150396112-150396113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11321850	chr6:150396113-150396114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113196449	chr6:150396125-150396126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113023582	chr6:150396137-150396138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117209141	chr6:150396160-150396161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116815785	chr6:150396179-150396180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147960569	chr6:150396261-150396262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1853659	chr6:150396303-150396304	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs369790767	chr6:150396316-150396317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192342009	chr6:150396329-150396330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559170975	chr6:150396358-150396359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141826211	chr6:150396359-150396360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568976506	chr6:150396360-150396361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537429048	chr6:150396423-150396424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538720837	chr6:150396429-150396430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373464173	chr6:150396473-150396474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9479592	chr6:150396574-150396575	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs534047039	chr6:150396608-150396609	Weak transcription Enhancers	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:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150390400-150397200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr6:150390600-150397200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:150390800-150397000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:150390800-150397200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr6:150390800-150397400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr6:150390800-150400800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:150391000-150397200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:150391200-150410000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:150392400-150395800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:150392400-150395800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:150392400-150400600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:150392600-150396200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr6:150392800-150396200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:150393800-150395600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr6:150393800-150396200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:150393800-150396400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr6:150393800-150397200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:150393800-150397200	Weak transcription	HMEC	breast
19	chr6:150393800-150397400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr6:150393800-150400800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:150394000-150396000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:150394000-150401800	Weak transcription	Stomach Mucosa	stomach
23	chr6:150395200-150395600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr6:150395400-150395600	Enhancers	Fetal Brain Female	brain
25	chr6:150395400-150395600	Enhancers	Spleen	Spleen
26	chr6:150395400-150396000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr6:150395400-150396000	Enhancers	Fetal Muscle Trunk	muscle
28	chr6:150395400-150396200	Enhancers	Fetal Stomach	stomach
29	chr6:150395600-150395800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:150395800-150396200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr6:150395800-150396600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:150395800-150398000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:150396000-150396600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr6:150396200-150396400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr6:150396200-150396400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr6:150396200-150396800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:150396200-150397600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:150396400-150397200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr6:150396400-150397400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr6:150396600-150397000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:150396600-150400200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:150396800-150397600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr6:150397000-150397600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr6:150397000-150398000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:150397200-150397400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr6:150397200-150397400	Enhancers	HMEC	breast
47	chr6:150397200-150397600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:150397200-150397600	Enhancers	Primary T cells fromperipheralblood	blood
49	chr6:150397200-150397600	Enhancers	Primary hematopoietic stem cells	blood
50	chr6:150397200-150397600	Bivalent Enhancer	Fetal Thymus	thymus

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