Variant report

Variant	nsv969292
Chromosome Location	chr6:29604881-29612154
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:29611477-29611680	K562	blood:	n/a	n/a
2	CEBPB	chr6:29611654-29611716	A549	lung:	n/a	n/a
3	EP300	chr6:29610680-29610688	GM12878	blood:	n/a	n/a
4	FOS	chr6:29609245-29609587	MCF10A-Er-Src	breast:	n/a	chr6:29609284-29609298 chr6:29609408-29609416 chr6:29609408-29609415 chr6:29609408-29609417
5	FOS	chr6:29609252-29609597	MCF10A-Er-Src	breast:	n/a	chr6:29609284-29609298 chr6:29609408-29609416 chr6:29609408-29609415 chr6:29609408-29609417
6	FOS	chr6:29609271-29609598	MCF10A-Er-Src	breast:	n/a	chr6:29609284-29609298 chr6:29609408-29609416 chr6:29609408-29609415 chr6:29609408-29609417
7	FOS	chr6:29609286-29609574	MCF10A-Er-Src	breast:	n/a	chr6:29609408-29609416 chr6:29609408-29609415 chr6:29609408-29609417
8	JUND	chr6:29609306-29609546	HepG2	liver:	n/a	chr6:29609408-29609416 chr6:29609408-29609415 chr6:29609408-29609417 chr6:29609406-29609417
9	MAX	chr6:29609642-29609866	K562	blood:	n/a	n/a
10	MAZ	chr6:29609590-29609927	K562	blood:	n/a	n/a
11	MYC	chr6:29609663-29609733	MCF10A-Er-Src	breast:	n/a	n/a
12	MYC	chr6:29609559-29609922	K562	blood:	n/a	n/a
13	NFYA	chr6:29611828-29611993	GM12878	blood:	n/a	n/a
14	POLR2A	chr6:29609757-29609771	K562	blood:	n/a	n/a
15	POLR2A	chr6:29609628-29609750	K562	blood:	n/a	n/a
16	POLR2A	chr6:29610841-29611065	ProgFib	skin:	n/a	n/a
17	RCOR1	chr6:29609593-29610017	K562	blood:	n/a	n/a
18	RFX5	chr6:29609754-29609773	Hela-S3	cervix:	n/a	n/a
19	TBL1XR1	chr6:29607053-29607059	K562	blood:	n/a	n/a
20	TBP	chr6:29607616-29607987	H1-hESC	embryonic stem cell:	n/a	n/a
21	TBP	chr6:29609688-29609847	K562	blood:	n/a	n/a
22	YY1	chr6:29609638-29609858	K562	blood:	n/a	n/a
23	ZNF143	chr6:29609631-29609948	K562	blood:	n/a	n/a
24	ZNF143	chr6:29612064-29612117	H1-hESC	embryonic stem cell:	n/a	n/a
25	ZNF263	chr6:29609297-29609896	HEK293-T-REx	kidney:	n/a	n/a
26	ZNF384	chr6:29606875-29606984	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29607758-29607808	Jurkat	blood:	n/a
2	chr6:29607758-29607808	IMR90	lung:	fetal
3	chr6:29607758-29607808	AG09319	gingival:	n/a
4	chr6:29607758-29607808	AG10803	skin:	n/a
5	chr6:29607758-29607808	HCPEpiC	choroid plexus:	n/a
6	chr6:29607758-29607808	GM12891	blood:	n/a
7	chr6:29607758-29607808	Hepatocyte	liver:	n/a
8	chr6:29607758-29607808	HRE	kidney:	n/a
9	chr6:29607758-29607808	SK-N-MC	brain:	n/a
10	chr6:29607758-29607808	ECC-1	luminal epithelium:	n/a
11	chr6:29607758-29607808	MCF-7	breast:	n/a
12	chr6:29607758-29607808	GM12892	blood:	n/a
13	chr6:29607758-29607808	NB4	blood:	n/a
14	chr6:29607758-29607808	A549	lung:	n/a
15	chr6:29607758-29607808	GM19239	blood:	n/a
16	chr6:29607758-29607808	PANC-1	pancreas:	n/a
17	chr6:29607758-29607808	HRPEpiC	eye:	n/a
18	chr6:29607758-29607808	U87	brain:	n/a
19	chr6:29607758-29607808	NHBE	bronchial:	n/a
20	chr6:29607758-29607808	T-47D	breast:	n/a
21	chr6:29607758-29607808	LNCaP	prostate:	n/a
22	chr6:29607758-29607808	MCF10A-Er-Src	breast:	n/a
23	chr6:29607758-29607808	HEK293	kidney:	embryo
24	chr6:29607758-29607808	SK-N-SH	brain:	n/a
25	chr6:29607758-29607808	HL-60	blood:	n/a
26	chr6:29607758-29607808	H1-hESC	embryonic stem cell:	embryo
27	chr6:29607758-29607808	NH-A	brain:	n/a
28	chr6:29607758-29607808	Caco-2	colon:	n/a
29	chr6:29607758-29607808	HNPCEpiC	eye:	n/a
30	chr6:29607758-29607808	Hela-S3	cervix:	n/a
31	chr6:29607758-29607808	RPTEC	kidney:	n/a
32	chr6:29607758-29607808	AG09309	skin:	n/a
33	chr6:29607758-29607808	HCF	heart:	n/a
34	chr6:29607758-29607808	HCM	heart:	n/a
35	chr6:29607758-29607808	GM06990	blood:	n/a
36	chr6:29607758-29607808	PrEC	prostate:	n/a
37	chr6:29607758-29607808	ProgFib	skin:	n/a
38	chr6:29607758-29607808	NT2-D1	testis:	n/a
39	chr6:29607758-29607808	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:29607758-29607808	HIPEpiC	eye:	n/a
41	chr6:29607758-29607808	HRCEpiC	kidney:	n/a
42	chr6:29607758-29607808	HepG2	liver:	n/a
43	chr6:29607758-29607808	PFSK-1	brain:	n/a
44	chr6:29607758-29607808	HAEpiC	amniotic membrane:	n/a
45	chr6:29607758-29607808	CMK	blood:	n/a
46	chr6:29607758-29607808	AoSMC	blood vessel:	n/a
47	chr6:29607758-29607808	HEEpiC	esophagus:	n/a
48	chr6:29607758-29607808	ovcar-3	ovarian:	n/a
49	chr6:29607758-29607808	HMEC	breast:	n/a
50	chr6:29607758-29607808	SK-N-SH_RA	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29608179..29609839-chr6:29617502..29619488,2	K562	blood:
2	chr6:29609719..29612322-chr6:29612804..29614354,2	K562	blood:
3	chr6:29608179..29610477-chr6:29617988..29619609,2	K562	blood:
4	chr6:29598626..29603210-chr6:29607516..29611410,5	K562	blood:
5	chr6:29599418..29601085-chr6:29610262..29612133,2	K562	blood:
6	chr6:29584985..29587112-chr6:29604597..29606396,2	K562	blood:
7	chr6:29588373..29590141-chr6:29604757..29606337,2	K562	blood:
8	chr6:29609140..29610048-chr6:29673773..29674677,2	MCF-7	breast:
9	chr6:29610699..29612322-chr6:29612804..29615708,2	K562	blood:
10	chr6:29607170..29608695-chr6:29718053..29720757,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MOG-1	chr6:29607836-29607913	NONHSAT108535
2	lnc-MOG-1	chr6:29605232-29605340	NONHSAT108535
3	lnc-MOG-1	chr6:29606808-29609323	ucscGeneNc_uc003nmn_2
4	lnc-MOG-1	chr6:29606808-29606924	NONHSAT108535
5	lnc-MOG-1	chr6:29605705-29605799	NONHSAT108535
6	lnc-MOG-1	chr6:29606808-29609324	NONHSAT108534
7	lnc-MOG-1	chr6:29605176-29605340	NONHSAT108534
8	lnc-MOG-1	chr6:29605705-29605799	NONHSAT108534
9	lnc-MOG-1	chr6:29605705-29605799	ucscGeneNc_uc003nmn_2
10	lnc-MOG-1	chr6:29605176-29605340	ucscGeneNc_uc003nmn_2

No data

Variant related genes	Relation type
SUMO2P1	TF binding region
GABBR1	TF binding region
SUMO2P1	CpG island
GABBR1	CpG island
ENSG00000204681	chromatin interactions
ENSG00000235821	chromatin interactions
ENSG00000272236	chromatin interactions
ENSG00000199290	chromatin interactions

Extended variants
information (count: 236 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:236 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531472026	chr6:29604891-29604892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551189561	chr6:29604945-29604946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576700376	chr6:29604948-29604949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182686992	chr6:29604980-29604981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144387752	chr6:29604981-29604982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553404155	chr6:29605013-29605014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147833153	chr6:29605111-29605112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538624336	chr6:29605120-29605121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558562770	chr6:29605220-29605221	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs575326483	chr6:29605255-29605256	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs113914990	chr6:29605306-29605307	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs187062863	chr6:29605383-29605384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574557441	chr6:29605384-29605385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142743386	chr6:29605407-29605408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532467265	chr6:29605425-29605426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191483136	chr6:29605434-29605435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562512100	chr6:29605464-29605465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549129337	chr6:29605520-29605521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182704320	chr6:29605532-29605533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs367580222	chr6:29605561-29605562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530252202	chr6:29605628-29605629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541499701	chr6:29605657-29605658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563582004	chr6:29605667-29605668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187772312	chr6:29605705-29605706	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs193147229	chr6:29605708-29605709	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs185638684	chr6:29605749-29605750	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs188964323	chr6:29605820-29605821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs444189	chr6:29605935-29605936	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs552315868	chr6:29605938-29605939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11330818	chr6:29605958-29605959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371725590	chr6:29605961-29605962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11351446	chr6:29605966-29605967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116113406	chr6:29605974-29605975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140941628	chr6:29606020-29606021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191983386	chr6:29606096-29606097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540032982	chr6:29606135-29606136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553969427	chr6:29606140-29606141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577203460	chr6:29606143-29606144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3095269	chr6:29606145-29606146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs146809058	chr6:29606161-29606162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140628386	chr6:29606182-29606183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184057453	chr6:29606194-29606195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561604389	chr6:29606195-29606196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188687779	chr6:29606203-29606204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145782904	chr6:29606236-29606237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560785493	chr6:29606248-29606249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138448452	chr6:29606267-29606268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114183654	chr6:29606280-29606281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149205637	chr6:29606301-29606302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537872770	chr6:29606321-29606322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
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
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
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
Hodgkin''s lymphoma	17606441	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
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29601800-29608600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr6:29602400-29607200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:29602600-29607000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr6:29602600-29607000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr6:29602600-29607000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:29602600-29607000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:29602600-29609200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:29602600-29609200	Weak transcription	HMEC	breast
9	chr6:29602800-29607200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr6:29602800-29609200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:29603000-29606800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:29603000-29607000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:29603000-29607200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr6:29603000-29608400	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr6:29604200-29609200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr6:29606800-29607800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr6:29607000-29607400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:29607000-29607400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr6:29607000-29607600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr6:29607000-29607600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr6:29607000-29608400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:29607200-29607600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:29607200-29607600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr6:29607200-29608000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr6:29607400-29609200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr6:29607400-29609400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr6:29607600-29608600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr6:29607600-29609200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr6:29607600-29609200	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:29607600-29609400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr6:29607800-29609200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr6:29608200-29609400	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr6:29608400-29609400	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr6:29608400-29609400	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr6:29608400-29609600	Enhancers	Primary T cells from cord blood	blood
36	chr6:29608400-29610600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr6:29608400-29610800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr6:29608400-29611000	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr6:29608400-29611600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr6:29608400-29616400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:29608600-29609600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr6:29608600-29610000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:29608600-29610200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr6:29608600-29610400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr6:29608800-29609600	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr6:29608800-29609600	Enhancers	K562	blood
47	chr6:29608800-29610400	Enhancers	Primary T cells fromperipheralblood	blood
48	chr6:29608800-29611200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr6:29609200-29609400	Enhancers	H9 Cell Line	embryonic stem cell
50	chr6:29609200-29609400	Enhancers	Monocytes-CD14+_RO01746	blood

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