Variant report

Variant	nsv970176
Chromosome Location	chr6:150319173-150343329
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	chr6:150338070-150338270	HepG2	liver:	n/a	n/a
2	ATF1	chr6:150326501-150326880	K562	blood:	n/a	n/a
3	ATF1	chr6:150336933-150337019	K562	blood:	n/a	n/a
4	ATF2	chr6:150325436-150325936	GM12878	blood:	n/a	n/a
5	ATF2	chr6:150328091-150328518	GM12878	blood:	n/a	n/a
6	ATF2	chr6:150322388-150322974	GM12878	blood:	n/a	n/a
7	ATF2	chr6:150328002-150328596	GM12878	blood:	n/a	n/a
8	ATF2	chr6:150325826-150326122	GM12878	blood:	n/a	n/a
9	ATF2	chr6:150322221-150322969	GM12878	blood:	n/a	n/a
10	ATF3	chr6:150326345-150326945	H1-hESC	embryonic stem cell:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
11	ATF3	chr6:150326273-150326742	GM12878	blood:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
12	ATF3	chr6:150326327-150326877	K562	blood:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
13	ATF3	chr6:150326347-150326676	HepG2	liver:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
14	ATF3	chr6:150326401-150326606	GM12878	blood:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
15	ATF3	chr6:150326376-150326975	H1-hESC	embryonic stem cell:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
16	BACH1	chr6:150326284-150326697	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr6:150328116-150328490	GM12878	blood:	n/a	n/a
18	BATF	chr6:150322436-150322848	GM12878	blood:	n/a	n/a
19	BATF	chr6:150322224-150323107	GM12878	blood:	n/a	n/a
20	BATF	chr6:150328171-150328476	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:150328061-150328481	GM12878	blood:	n/a	chr6:150328226-150328235 chr6:150328420-150328429
22	BCL11A	chr6:150322565-150322831	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:150322320-150322928	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:150328125-150328471	GM12878	blood:	n/a	chr6:150328226-150328235 chr6:150328420-150328429
25	BCL3	chr6:150328101-150328407	GM12878	blood:	n/a	chr6:150328226-150328235
26	BCLAF1	chr6:150325804-150326446	GM12878	blood:	n/a	chr6:150326058-150326067
27	BCLAF1	chr6:150328046-150328455	GM12878	blood:	n/a	chr6:150328226-150328235 chr6:150328420-150328429
28	BCLAF1	chr6:150322320-150322863	GM12878	blood:	n/a	n/a
29	BCLAF1	chr6:150322393-150322790	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:150329735-150330023	K562	blood:	n/a	n/a
31	BHLHE40	chr6:150328197-150328464	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:150326114-150327095	HepG2	liver:	n/a	chr6:150326500-150326509 chr6:150326499-150326508 chr6:150326500-150326509 chr6:150326501-150326510 chr6:150326498-150326511 chr6:150326494-150326515
33	BHLHE40	chr6:150325516-150326816	GM12878	blood:	n/a	chr6:150326500-150326509 chr6:150326499-150326508 chr6:150326500-150326509 chr6:150326501-150326510 chr6:150326498-150326511 chr6:150326494-150326515
34	BHLHE40	chr6:150336771-150337140	K562	blood:	n/a	n/a
35	BHLHE40	chr6:150334502-150334672	K562	blood:	n/a	n/a
36	BHLHE40	chr6:150326209-150326949	K562	blood:	n/a	chr6:150326500-150326509 chr6:150326499-150326508 chr6:150326500-150326509 chr6:150326501-150326510 chr6:150326498-150326511 chr6:150326494-150326515
37	BHLHE40	chr6:150322425-150323112	GM12878	blood:	n/a	n/a
38	BRCA1	chr6:150326274-150326876	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr6:150326801-150326903	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr6:150326263-150326443	H1-hESC	embryonic stem cell:	n/a	n/a
41	CBX3	chr6:150336795-150337204	K562	blood:	n/a	n/a
42	CBX3	chr6:150326784-150327232	K562	blood:	n/a	n/a
43	CBX3	chr6:150325861-150326760	K562	blood:	n/a	n/a
44	CCNT2	chr6:150336957-150337116	K562	blood:	n/a	n/a
45	CCNT2	chr6:150326066-150326830	K562	blood:	n/a	chr6:150326773-150326782
46	CEBPB	chr6:150338050-150338338	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:150328064-150328586	GM12878	blood:	n/a	n/a
48	CEBPB	chr6:150339733-150339933	Hela-S3	cervix:	n/a	chr6:150339786-150339797
49	CEBPB	chr6:150338074-150338240	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr6:150322619-150322812	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150329845-150329895	AG09309	skin:	n/a
2	chr6:150329845-150329895	AG09309	skin:	n/a
3	chr6:150338421-150338471	GM12878	blood:	n/a
4	chr6:150326596-150326646	Caco-2	colon:	n/a
5	chr6:150326316-150326366	HCM	heart:	n/a
6	chr6:150331562-150331612	HL-60	blood:	n/a
7	chr6:150327687-150327737	SK-N-SH	brain:	n/a
8	chr6:150327115-150327165	ECC-1	luminal epithelium:	n/a
9	chr6:150326323-150326373	HEK293	kidney:	embryo
10	chr6:150326316-150326366	RPTEC	kidney:	n/a
11	chr6:150326762-150326812	Caco-2	colon:	n/a
12	chr6:150336054-150336104	NHBE	bronchial:	n/a
13	chr6:150326732-150326782	HUVEC	blood vessel:	n/a
14	chr6:150326762-150326812	SK-N-SH	brain:	n/a
15	chr6:150326596-150326646	LNCaP	prostate:	n/a
16	chr6:150326596-150326646	NHDF-neo	bronchial:	n/a
17	chr6:150326596-150326646	HAEpiC	amniotic membrane:	n/a
18	chr6:150327687-150327737	RPTEC	kidney:	n/a
19	chr6:150335849-150335899	HCM	heart:	n/a
20	chr6:150326316-150326366	GM12891	blood:	n/a
21	chr6:150325970-150326020	SAEC	small airway:	n/a
22	chr6:150326389-150326439	AG04450	lung:	fetal
23	chr6:150335849-150335899	GM12878	blood:	n/a
24	chr6:150325970-150326020	SKMC	muscle:	n/a
25	chr6:150326323-150326373	ECC-1	luminal epithelium:	n/a
26	chr6:150329845-150329895	SAEC	small airway:	n/a
27	chr6:150326776-150326826	HCM	heart:	n/a
28	chr6:150326316-150326366	NH-A	brain:	n/a
29	chr6:150335849-150335899	HEEpiC	esophagus:	n/a
30	chr6:150327115-150327165	HEEpiC	esophagus:	n/a
31	chr6:150326394-150326444	HIPEpiC	eye:	n/a
32	chr6:150326453-150326503	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:150336015-150336065	HCM	heart:	n/a
34	chr6:150326762-150326812	BJ	skin:	n/a
35	chr6:150326762-150326812	NHBE	bronchial:	n/a
36	chr6:150336524-150336574	HCM	heart:	n/a
37	chr6:150336054-150336104	AG10803	skin:	n/a
38	chr6:150326762-150326812	HRE	kidney:	n/a
39	chr6:150326323-150326373	HEEpiC	esophagus:	n/a
40	chr6:150327115-150327165	ProgFib	skin:	n/a
41	chr6:150335849-150335899	MCF-7	breast:	n/a
42	chr6:150327687-150327737	PFSK-1	brain:	n/a
43	chr6:150325970-150326020	HEK293	kidney:	embryo
44	chr6:150326323-150326373	NB4	blood:	n/a
45	chr6:150326596-150326646	RPTEC	kidney:	n/a
46	chr6:150325970-150326020	ECC-1	luminal epithelium:	n/a
47	chr6:150335849-150335899	HUVEC	blood vessel:	n/a
48	chr6:150326732-150326782	BJ	skin:	n/a
49	chr6:150325970-150326020	HRCEpiC	kidney:	n/a
50	chr6:150326334-150326384	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:150274811..150275321-chr6:150336040..150336549,2	MCF-7	breast:
2	chr6:150320978..150322963-chr6:150324763..150326329,2	K562	blood:
3	chr6:150283785..150286352-chr6:150326807..150328312,2	MCF-7	breast:
4	chr6:150328123..150330822-chr6:150332783..150334807,2	MCF-7	breast:
5	chr6:150328123..150330822-chr6:150332783..150334807,2	MCF-7	breast:
6	chr6:150283429..150285848-chr6:150336024..150337757,2	MCF-7	breast:
7	chr6:150154861..150155845-chr6:150337730..150338274,2	K562	blood:
8	chr6:150311706..150314148-chr6:150319764..150322563,2	K562	blood:
9	chr6:150246157..150249113-chr6:150336737..150339289,2	K562	blood:
10	chr6:150255064..150255979-chr6:150337750..150338789,5	K562	blood:
11	chr6:150323301..150326870-chr6:150337464..150339739,3	MCF-7	breast:
12	chr6:150286573..150288463-chr6:150317408..150319689,2	K562	blood:
13	chr6:150258514..150260378-chr6:150337573..150339969,2	MCF-7	breast:
14	chr6:150250322..150251340-chr6:150337738..150338572,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAET1L-2	chr6:150321202-150321330	NONHSAT115529
2	lnc-RAET1L-2	chr6:150326209-150326280	NONHSAT115529
3	lnc-RAET1L-2	chr6:150321989-150322804	NONHSAT115529
4	lnc-RAET1L-2	chr6:150319155-150320020	NONHSAT115529

Variant related genes	Relation type
RAET1K	TF binding region
RAET1K	CpG island
ENSG00000216621	chromatin interactions
ENSG00000111981	chromatin interactions
ENSG00000218358	chromatin interactions

Extended variants
information (count: 1332 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1332 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559859040	chr6:150319203-150319204	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs573349135	chr6:150319221-150319222	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs114226548	chr6:150319241-150319242	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs189296369	chr6:150319384-150319385	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs142381729	chr6:150319393-150319394	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs146372634	chr6:150319405-150319406	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs563925926	chr6:150319478-150319479	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs138996562	chr6:150319589-150319590	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs181150213	chr6:150319671-150319672	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs566804045	chr6:150319735-150319736	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs535621672	chr6:150319748-150319749	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs113358666	chr6:150319763-150319764	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs73779747	chr6:150319773-150319774	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs543990032	chr6:150319782-150319783	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs373970545	chr6:150319784-150319785	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs557276522	chr6:150319802-150319803	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs138057510	chr6:150319833-150319834	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs563682016	chr6:150319879-150319880	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs539863672	chr6:150319898-150319899	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs553389725	chr6:150319954-150319955	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs33997518	chr6:150320018-150320019	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs542006210	chr6:150320047-150320048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555559551	chr6:150320055-150320056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114936578	chr6:150320089-150320090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532646369	chr6:150320120-150320121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543908961	chr6:150320151-150320152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145985791	chr6:150320152-150320153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376719318	chr6:150320198-150320199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540250396	chr6:150320202-150320203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560171340	chr6:150320280-150320281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377177625	chr6:150320295-150320296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552216774	chr6:150320299-150320300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113138016	chr6:150320322-150320323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139871478	chr6:150320341-150320342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549170668	chr6:150320356-150320357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569076196	chr6:150320358-150320359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530987052	chr6:150320394-150320395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185633451	chr6:150320403-150320404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141601578	chr6:150320410-150320411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146189247	chr6:150320411-150320412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553368164	chr6:150320416-150320417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566791186	chr6:150320417-150320418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190493760	chr6:150320450-150320451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555497617	chr6:150320488-150320489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148397110	chr6:150320503-150320504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370857775	chr6:150320566-150320567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377583459	chr6:150320579-150320580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182724785	chr6:150320637-150320638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539811820	chr6:150320638-150320639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375726939	chr6:150320656-150320657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150315000-150324800	Weak transcription	Dnd41	blood
2	chr6:150316800-150320800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:150317600-150319600	Strong transcription	Fetal Thymus	thymus
4	chr6:150318200-150325400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:150319000-150322600	Weak transcription	Thymus	Thymus
6	chr6:150319600-150321600	Weak transcription	Fetal Thymus	thymus
7	chr6:150319800-150325600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:150320800-150322400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:150320800-150324200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr6:150321000-150322000	Enhancers	GM12878-XiMat	blood
11	chr6:150321200-150321400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:150321200-150321600	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr6:150321400-150322400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chr6:150321400-150325200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:150321600-150322000	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr6:150321600-150323200	Enhancers	Fetal Thymus	thymus
17	chr6:150321600-150325400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:150321800-150322000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
19	chr6:150321800-150322200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
20	chr6:150321800-150322600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr6:150321800-150322800	Enhancers	Primary T cells from cord blood	blood
22	chr6:150322000-150322200	Bivalent Enhancer	Fetal Stomach	stomach
23	chr6:150322000-150322400	Flanking Active TSS	GM12878-XiMat	blood
24	chr6:150322000-150322600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr6:150322000-150322800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr6:150322000-150323200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr6:150322000-150323200	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr6:150322000-150323200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr6:150322000-150323400	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr6:150322200-150322800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr6:150322200-150323000	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr6:150322200-150323400	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr6:150322200-150323400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr6:150322400-150323400	Enhancers	GM12878-XiMat	blood
35	chr6:150322400-150323600	Enhancers	Primary T cells fromperipheralblood	blood
36	chr6:150322400-150325000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:150322600-150323000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr6:150322600-150323000	Enhancers	Thymus	Thymus
39	chr6:150322800-150325200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr6:150322800-150325200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr6:150323000-150323200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr6:150323000-150325200	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr6:150323000-150325200	Weak transcription	Thymus	Thymus
44	chr6:150323200-150324800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr6:150323200-150324800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr6:150323200-150325200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr6:150323200-150325400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr6:150323400-150324400	ZNF genes & repeats	GM12878-XiMat	blood
49	chr6:150323400-150325200	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr6:150323400-150325400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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