Variant report

Variant	nsv820137
Chromosome Location	chr4:69299117-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1417)
CpG islands
(count:977)
Chromatin interactive
region (count:23)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1417 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
8	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
9	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
11	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
12	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
13	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
14	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
15	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
16	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
17	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
20	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
21	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
22	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
25	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
27	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
28	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
29	CEBPB	chr4:69300033-69300365	HepG2	liver:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
30	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
32	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
34	CEBPB	chr4:69308568-69308582	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:69300028-69300381	IMR90	lung:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
36	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
37	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr4:69580237-69580432	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
40	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
41	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
42	CEBPB	chr4:69310875-69311174	IMR90	lung:	n/a	chr4:69310996-69311009 chr4:69310996-69311009 chr4:69310996-69311007
43	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
44	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:69312976-69313282	MCF-7	breast:	n/a	n/a
46	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
47	CEBPB	chr4:69574389-69574642	A549	lung:	n/a	chr4:69574511-69574522
48	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
50	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69340916-69340966	IMR90	lung:	fetal
2	chr4:69340916-69340966	IMR90	lung:	fetal
3	chr4:69340916-69340966	PrEC	prostate:	n/a
4	chr4:69514031-69514081	SK-N-SH_RA	brain:	n/a
5	chr4:69522639-69522689	HIPEpiC	eye:	n/a
6	chr4:69435593-69435643	SK-N-MC	brain:	n/a
7	chr4:69537589-69537639	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:69381368-69381418	Jurkat	blood:	n/a
9	chr4:69313197-69313247	HRCEpiC	kidney:	n/a
10	chr4:69435601-69435651	Hepatocyte	liver:	n/a
11	chr4:69434475-69434525	PrEC	prostate:	n/a
12	chr4:69537826-69537876	GM06990	blood:	n/a
13	chr4:69522639-69522689	HRCEpiC	kidney:	n/a
14	chr4:69537826-69537876	HRE	kidney:	n/a
15	chr4:69537826-69537876	HRPEpiC	eye:	n/a
16	chr4:69434475-69434525	MCF10A-Er-Src	breast:	n/a
17	chr4:69537589-69537639	T-47D	breast:	n/a
18	chr4:69355121-69355171	Jurkat	blood:	n/a
19	chr4:69313197-69313247	NHDF-neo	bronchial:	n/a
20	chr4:69435250-69435300	GM19239	blood:	n/a
21	chr4:69355121-69355171	CMK	blood:	n/a
22	chr4:69340916-69340966	AG04450	lung:	fetal
23	chr4:69381368-69381418	HMEC	breast:	n/a
24	chr4:69522639-69522689	LNCaP	prostate:	n/a
25	chr4:69340916-69340966	K562	blood:	n/a
26	chr4:69312514-69312564	HRPEpiC	eye:	n/a
27	chr4:69435601-69435651	ECC-1	luminal epithelium:	n/a
28	chr4:69435593-69435643	BE2_C	brain:	n/a
29	chr4:69435601-69435651	AG04449	skin:	fetal
30	chr4:69435593-69435643	Hela-S3	cervix:	n/a
31	chr4:69536319-69536369	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:69312514-69312564	Caco-2	colon:	n/a
33	chr4:69537589-69537639	RPTEC	kidney:	n/a
34	chr4:69537589-69537639	HRPEpiC	eye:	n/a
35	chr4:69355121-69355171	AoSMC	blood vessel:	n/a
36	chr4:69514031-69514081	CMK	blood:	n/a
37	chr4:69536319-69536369	PANC-1	pancreas:	n/a
38	chr4:69435250-69435300	AG04449	skin:	fetal
39	chr4:69312514-69312564	Hepatocyte	liver:	n/a
40	chr4:69381368-69381418	NH-A	brain:	n/a
41	chr4:69435250-69435300	BE2_C	brain:	n/a
42	chr4:69355121-69355171	GM19239	blood:	n/a
43	chr4:69434475-69434525	Jurkat	blood:	n/a
44	chr4:69355121-69355171	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:69340916-69340966	ProgFib	skin:	n/a
46	chr4:69312514-69312564	GM12878	blood:	n/a
47	chr4:69537806-69537856	HCT-116	colon:	n/a
48	chr4:69340916-69340966	NHBE	bronchial:	n/a
49	chr4:69537589-69537639	GM12878	blood:	n/a
50	chr4:69537826-69537876	LNCaP	prostate:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
2	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
3	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
4	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
5	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
6	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
7	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
8	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
9	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
10	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
11	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
12	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
13	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
14	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
15	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
16	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
17	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
18	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
19	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
20	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
21	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
22	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
23	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
2	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
3	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
4	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
5	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
6	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000248635	TF binding region
TMPRSS11E	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
UGT2B29P	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000248635	CpG island
TMPRSS11E	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island
ENSG00000272626	chromatin interactions
ENSG00000249985	chromatin interactions
ENSG00000087128	chromatin interactions
ENSG00000083896	chromatin interactions

Extended variants
information (count: 8163 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:8163 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377111135	chr4:69299126-69299127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138993124	chr4:69299129-69299130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573646393	chr4:69299171-69299172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201131611	chr4:69299192-69299193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533285305	chr4:69299213-69299214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374194994	chr4:69299224-69299225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542324416	chr4:69299247-69299248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560081687	chr4:69299308-69299309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561897737	chr4:69299312-69299313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373079293	chr4:69299313-69299314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369771872	chr4:69299322-69299323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575453552	chr4:69299407-69299408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544469196	chr4:69299414-69299415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188990707	chr4:69299437-69299438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28656111	chr4:69299472-69299473	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs375849757	chr4:69299477-69299478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541401966	chr4:69299517-69299518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558496852	chr4:69299524-69299525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560573889	chr4:69299571-69299572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs578237842	chr4:69299585-69299586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145840471	chr4:69299603-69299604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112524095	chr4:69299613-69299614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563768026	chr4:69299614-69299615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569040993	chr4:69299647-69299648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529471195	chr4:69299711-69299712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368523803	chr4:69299738-69299739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10635469	chr4:69299744-69299745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541585489	chr4:69299745-69299746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561414661	chr4:69299789-69299790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376057514	chr4:69299823-69299824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527302383	chr4:69299828-69299829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372554139	chr4:69299832-69299833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571448257	chr4:69299837-69299838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534136734	chr4:69299838-69299839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553449482	chr4:69299844-69299845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181762188	chr4:69299854-69299855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186420200	chr4:69299919-69299920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555854694	chr4:69299925-69299926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370512742	chr4:69299942-69299943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191079030	chr4:69299983-69299984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544374964	chr4:69299984-69299985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35923720	chr4:69299993-69299994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567943249	chr4:69300048-69300049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150738386	chr4:69300063-69300064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139047978	chr4:69300104-69300105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34764645	chr4:69300160-69300161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80089997	chr4:69300168-69300169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529323443	chr4:69300172-69300173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549865012	chr4:69300205-69300206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562951463	chr4:69300215-69300216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69296400-69300400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr4:69296400-69300600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr4:69296600-69312000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:69298800-69300400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr4:69299400-69299600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:69299400-69299800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr4:69299800-69300200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr4:69300200-69303400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:69300400-69301000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:69300400-69301800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:69300400-69302800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr4:69300400-69303400	Enhancers	Primary T cells from cord blood	blood
13	chr4:69300400-69303400	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr4:69300400-69303400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr4:69300600-69300800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr4:69300600-69300800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr4:69300600-69301000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:69300600-69302600	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr4:69300600-69302800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr4:69300600-69303400	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr4:69300600-69303400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr4:69300600-69303400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr4:69300800-69301800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr4:69301000-69305800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:69301800-69302000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
26	chr4:69301800-69303200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr4:69301800-69303400	Enhancers	Primary T cells fromperipheralblood	blood
28	chr4:69301800-69307400	Enhancers	Primary B cells from peripheral blood	blood
29	chr4:69302000-69302200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr4:69302200-69302400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr4:69302400-69303400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr4:69302600-69304600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr4:69302800-69303200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr4:69302800-69304800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr4:69302800-69312000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:69303200-69303400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr4:69303200-69303400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr4:69303200-69304600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr4:69303400-69304600	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr4:69303400-69304600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr4:69303400-69304600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr4:69303400-69304600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr4:69303400-69304600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr4:69303400-69304600	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr4:69303400-69304800	Weak transcription	Primary T cells from cord blood	blood
46	chr4:69303400-69304800	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr4:69303400-69304800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr4:69303400-69305600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr4:69303600-69304600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr4:69304600-69305000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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