Variant report

Variant	nsv1003200
Chromosome Location	chr4:69294787-69521397
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	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
6	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
7	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
9	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
10	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
11	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
14	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
16	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
17	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
18	CEBPB	chr4:69300021-69300356	K562	blood:	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
19	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
20	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
21	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
22	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
23	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
24	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
25	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
26	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:69310875-69311174	IMR90	lung:	n/a	chr4:69310996-69311009 chr4:69310996-69311009 chr4:69310996-69311007
28	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:69312976-69313282	MCF-7	breast:	n/a	n/a
30	CEBPB	chr4:69300055-69300288	A549	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
31	CEBPB	chr4:69300096-69300253	H1-hESC	embryonic stem cell:	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
32	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
33	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
35	CEBPB	chr4:69308568-69308582	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
37	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
38	CTCF	chr4:69364240-69364390	HBMEC	blood vessel:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
39	CTCF	chr4:69364240-69364390	HRE	kidney:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
40	CTCF	chr4:69443453-69443599	GM10248	blood:	n/a	n/a
41	CTCF	chr4:69431314-69431346	Medullo	brain:	n/a	n/a
42	CTCF	chr4:69443340-69443490	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr4:69419680-69419830	GM12872	blood:	n/a	n/a
44	CTCF	chr4:69384731-69384849	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr4:69364144-69364498	T-47D	breast:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
46	CTCF	chr4:69364280-69364430	HRE	kidney:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
47	CTCF	chr4:69364180-69364330	NHEK	skin:	n/a	chr4:69364310-69364328 chr4:69364311-69364327
48	CTCF	chr4:69364194-69364446	GM10248	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
49	CTCF	chr4:69364220-69364370	AG09309	skin:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
50	CTCF	chr4:69364160-69364310	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69435601-69435651	GM12892	blood:	n/a
2	chr4:69434475-69434525	BE2_C	brain:	n/a
3	chr4:69313197-69313247	HAEpiC	amniotic membrane:	n/a
4	chr4:69435601-69435651	GM12892	blood:	n/a
5	chr4:69434475-69434525	BE2_C	brain:	n/a
6	chr4:69313197-69313247	HAEpiC	amniotic membrane:	n/a
7	chr4:69340916-69340966	SAEC	small airway:	n/a
8	chr4:69381368-69381418	HCM	heart:	n/a
9	chr4:69381368-69381418	HEK293	kidney:	embryo
10	chr4:69381368-69381418	HUVEC	blood vessel:	n/a
11	chr4:69514031-69514081	MCF10A-Er-Src	breast:	n/a
12	chr4:69435250-69435300	HCF	heart:	n/a
13	chr4:69435250-69435300	BJ	skin:	n/a
14	chr4:69312514-69312564	HCM	heart:	n/a
15	chr4:69340916-69340966	H1-hESC	embryonic stem cell:	embryo
16	chr4:69355121-69355171	SK-N-SH	brain:	n/a
17	chr4:69435250-69435300	NH-A	brain:	n/a
18	chr4:69435593-69435643	GM12891	blood:	n/a
19	chr4:69340916-69340966	HAEpiC	amniotic membrane:	n/a
20	chr4:69435601-69435651	NHDF-neo	bronchial:	n/a
21	chr4:69435593-69435643	CMK	blood:	n/a
22	chr4:69435250-69435300	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:69312104-69312154	AG04450	lung:	fetal
24	chr4:69340916-69340966	AG04450	lung:	fetal
25	chr4:69514031-69514081	HEK293	kidney:	embryo
26	chr4:69340916-69340966	K562	blood:	n/a
27	chr4:69514031-69514081	T-47D	breast:	n/a
28	chr4:69355121-69355171	Jurkat	blood:	n/a
29	chr4:69434475-69434525	ECC-1	luminal epithelium:	n/a
30	chr4:69435593-69435643	SAEC	small airway:	n/a
31	chr4:69381368-69381418	HL-60	blood:	n/a
32	chr4:69313197-69313247	ovcar-3	ovarian:	n/a
33	chr4:69434475-69434525	CMK	blood:	n/a
34	chr4:69312104-69312154	SAEC	small airway:	n/a
35	chr4:69313197-69313247	HCT-116	colon:	n/a
36	chr4:69381368-69381418	HEEpiC	esophagus:	n/a
37	chr4:69313197-69313247	NH-A	brain:	n/a
38	chr4:69313197-69313247	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:69340916-69340966	RPTEC	kidney:	n/a
40	chr4:69381368-69381418	GM12892	blood:	n/a
41	chr4:69514031-69514081	SK-N-MC	brain:	n/a
42	chr4:69435601-69435651	MCF10A-Er-Src	breast:	n/a
43	chr4:69340916-69340966	BJ	skin:	n/a
44	chr4:69313197-69313247	HepG2	liver:	n/a
45	chr4:69355121-69355171	NB4	blood:	n/a
46	chr4:69435593-69435643	GM12892	blood:	n/a
47	chr4:69312514-69312564	Hepatocyte	liver:	n/a
48	chr4:69434475-69434525	MCF-7	breast:	n/a
49	chr4:69514031-69514081	A549	lung:	n/a
50	chr4:69312514-69312564	U87	brain:	n/a

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

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

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

Extended variants
information (count: 6720 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6720 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78955785	chr4:69294825-69294826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138301105	chr4:69294832-69294833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565327775	chr4:69294866-69294867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149639244	chr4:69294917-69294918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368663820	chr4:69294930-69294931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568862979	chr4:69294951-69294952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541521614	chr4:69294974-69294975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560870374	chr4:69294991-69294992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537414586	chr4:69294993-69294994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554863209	chr4:69295076-69295077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144359132	chr4:69295094-69295095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574602731	chr4:69295134-69295135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs36160020	chr4:69295145-69295146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569594438	chr4:69295158-69295159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368180319	chr4:69295224-69295225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139913613	chr4:69295242-69295243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs66499741	chr4:69295244-69295245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182741393	chr4:69295272-69295273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551749596	chr4:69295281-69295282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565681258	chr4:69295313-69295314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534375007	chr4:69295341-69295342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188106575	chr4:69295346-69295347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567726393	chr4:69295351-69295352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192718229	chr4:69295352-69295353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140121183	chr4:69295372-69295373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550888510	chr4:69295373-69295374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576804527	chr4:69295375-69295376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533739497	chr4:69295401-69295402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558638074	chr4:69295425-69295426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564100945	chr4:69295508-69295509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541134378	chr4:69295659-69295660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561447018	chr4:69295663-69295664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371659902	chr4:69295695-69295696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553595339	chr4:69295714-69295715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183548964	chr4:69295724-69295725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543211964	chr4:69295761-69295762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs62317505	chr4:69295794-69295795	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs529935378	chr4:69295818-69295819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188425852	chr4:69295854-69295855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145960035	chr4:69295903-69295904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139820314	chr4:69295925-69295926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192228112	chr4:69295953-69295954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547912592	chr4:69295971-69295972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568127139	chr4:69295977-69295978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562816285	chr4:69295978-69295979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142038651	chr4:69296084-69296085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550387523	chr4:69296139-69296140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541819858	chr4:69296223-69296224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539290311	chr4:69296232-69296233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371791376	chr4:69296272-69296273	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	17289997	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

Chromatin state (count:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69293000-69295800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:69295600-69296000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:69295800-69296600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:69295800-69296600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:69296000-69296400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:69296000-69296400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:69296000-69296600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:69296400-69300400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr4:69296400-69300600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr4:69296600-69312000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:69298200-69298800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr4:69298800-69300400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr4:69299400-69299600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:69299400-69299800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr4:69299800-69300200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr4:69300200-69303400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr4:69300400-69301000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:69300400-69301800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr4:69300400-69302800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr4:69300400-69303400	Enhancers	Primary T cells from cord blood	blood
21	chr4:69300400-69303400	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr4:69300400-69303400	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr4:69300600-69300800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:69300600-69300800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr4:69300600-69301000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:69300600-69302600	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr4:69300600-69302800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr4:69300600-69303400	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr4:69300600-69303400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr4:69300600-69303400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr4:69300800-69301800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr4:69301000-69305800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:69301800-69302000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
34	chr4:69301800-69303200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr4:69301800-69303400	Enhancers	Primary T cells fromperipheralblood	blood
36	chr4:69301800-69307400	Enhancers	Primary B cells from peripheral blood	blood
37	chr4:69302000-69302200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr4:69302200-69302400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
39	chr4:69302400-69303400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr4:69302600-69304600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr4:69302800-69303200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr4:69302800-69304800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr4:69302800-69312000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:69303200-69303400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr4:69303200-69303400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr4:69303200-69304600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr4:69303400-69304600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr4:69303400-69304600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr4:69303400-69304600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr4:69303400-69304600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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