Variant report

Variant	nsv1005395
Chromosome Location	chr4:69338552-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1233)
CpG islands
(count:793)
Chromatin interactive
region (count:10)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
8	ATF1	chr4:69559343-69559671	K562	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	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
12	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
13	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
14	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
15	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
18	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
19	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
20	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
23	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
24	CEBPB	chr4:69580237-69580432	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
26	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
28	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
29	CEBPB	chr4:69574361-69574618	HepG2	liver:	n/a	chr4:69574511-69574522
30	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
32	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
33	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
34	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
36	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
37	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
38	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
40	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
41	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
42	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:69574389-69574642	A549	lung:	n/a	chr4:69574511-69574522
44	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
45	CHD1	chr4:69583916-69583936	GM12878	blood:	n/a	n/a
46	CTCF	chr4:69418635-69418772	HepG2	liver:	n/a	n/a
47	CTCF	chr4:69364131-69364550	IMR90	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
48	CTCF	chr4:69538990-69539148	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr4:69419858-69419933	Gliobla	brain:	n/a	n/a
50	CTCF	chr4:69538880-69539030	GM12864	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69381368-69381418	HL-60	blood:	n/a
2	chr4:69381368-69381418	NB4	blood:	n/a
3	chr4:69522639-69522689	GM12891	blood:	n/a
4	chr4:69435601-69435651	HepG2	liver:	n/a
5	chr4:69435593-69435643	HepG2	liver:	n/a
6	chr4:69537589-69537639	HRE	kidney:	n/a
7	chr4:69355121-69355171	HL-60	blood:	n/a
8	chr4:69435601-69435651	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:69435250-69435300	HUVEC	blood vessel:	n/a
10	chr4:69434475-69434525	Caco-2	colon:	n/a
11	chr4:69434475-69434525	NH-A	brain:	n/a
12	chr4:69537806-69537856	ovcar-3	ovarian:	n/a
13	chr4:69435601-69435651	PrEC	prostate:	n/a
14	chr4:69522639-69522689	GM19239	blood:	n/a
15	chr4:69355121-69355171	Jurkat	blood:	n/a
16	chr4:69435593-69435643	GM19239	blood:	n/a
17	chr4:69355121-69355171	HRE	kidney:	n/a
18	chr4:69537589-69537639	HepG2	liver:	n/a
19	chr4:69355121-69355171	PFSK-1	brain:	n/a
20	chr4:69536319-69536369	AG04449	skin:	fetal
21	chr4:69435250-69435300	AG10803	skin:	n/a
22	chr4:69381368-69381418	AG04449	skin:	fetal
23	chr4:69434475-69434525	Jurkat	blood:	n/a
24	chr4:69537826-69537876	HNPCEpiC	eye:	n/a
25	chr4:69435593-69435643	PANC-1	pancreas:	n/a
26	chr4:69340916-69340966	HEK293	kidney:	embryo
27	chr4:69434475-69434525	NHBE	bronchial:	n/a
28	chr4:69514031-69514081	HRE	kidney:	n/a
29	chr4:69355121-69355171	MCF10A-Er-Src	breast:	n/a
30	chr4:69435250-69435300	BE2_C	brain:	n/a
31	chr4:69514031-69514081	ovcar-3	ovarian:	n/a
32	chr4:69522639-69522689	SK-N-MC	brain:	n/a
33	chr4:69434475-69434525	AG04450	lung:	fetal
34	chr4:69381368-69381418	HCT-116	colon:	n/a
35	chr4:69514031-69514081	MCF-7	breast:	n/a
36	chr4:69381368-69381418	HEK293	kidney:	embryo
37	chr4:69537826-69537876	NH-A	brain:	n/a
38	chr4:69537589-69537639	SK-N-MC	brain:	n/a
39	chr4:69340916-69340966	HCF	heart:	n/a
40	chr4:69522639-69522689	GM12878	blood:	n/a
41	chr4:69435601-69435651	AoSMC	blood vessel:	n/a
42	chr4:69434475-69434525	SK-N-SH_RA	brain:	n/a
43	chr4:69537826-69537876	SK-N-SH	brain:	n/a
44	chr4:69355121-69355171	K562	blood:	n/a
45	chr4:69355121-69355171	GM12892	blood:	n/a
46	chr4:69434475-69434525	HNPCEpiC	eye:	n/a
47	chr4:69537806-69537856	Hela-S3	cervix:	n/a
48	chr4:69435601-69435651	LNCaP	prostate:	n/a
49	chr4:69537806-69537856	RPTEC	kidney:	n/a
50	chr4:69435601-69435651	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
2	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
3	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
4	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
5	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
6	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
7	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
8	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
9	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
10	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 6744 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6744 , 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	rs565913649	chr4:69338636-69338637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535270388	chr4:69338663-69338664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62317558	chr4:69338666-69338667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191838510	chr4:69338687-69338688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537000341	chr4:69338733-69338734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62317559	chr4:69338734-69338735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184298881	chr4:69338782-69338783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539915614	chr4:69338787-69338788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146202028	chr4:69338795-69338796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188993055	chr4:69338846-69338847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542015114	chr4:69338861-69338862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372280513	chr4:69338866-69338867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377138449	chr4:69338955-69338956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139043682	chr4:69338996-69338997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71193518	chr4:69339018-69339019	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs543827536	chr4:69339027-69339028	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143870611	chr4:69339100-69339101	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181760764	chr4:69339126-69339127	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539938160	chr4:69339159-69339160	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62317860	chr4:69339177-69339178	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185528097	chr4:69339236-69339237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538623618	chr4:69339256-69339257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34872892	chr4:69339257-69339258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs568633856	chr4:69339265-69339266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147410815	chr4:69339281-69339282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139629202	chr4:69339285-69339286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570853525	chr4:69339288-69339289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190684956	chr4:69339291-69339292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180671918	chr4:69339308-69339309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567291989	chr4:69339338-69339339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145458940	chr4:69339349-69339350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555552582	chr4:69339370-69339371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147681575	chr4:69339372-69339373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544474377	chr4:69339383-69339384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557677873	chr4:69339393-69339394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569902168	chr4:69339447-69339448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377132767	chr4:69339453-69339454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537381222	chr4:69339502-69339503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186162190	chr4:69339579-69339580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189964187	chr4:69339595-69339596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555585616	chr4:69339646-69339647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs202088337	chr4:69339689-69339690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367559238	chr4:69339694-69339695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140989609	chr4:69339735-69339736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531055394	chr4:69339767-69339768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181135368	chr4:69339792-69339793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566700193	chr4:69339796-69339797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573909081	chr4:69339819-69339820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185578152	chr4:69339833-69339834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190483283	chr4:69339858-69339859	Weak transcription	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:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69326200-69348800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:69333200-69349400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:69335000-69339000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:69339000-69339200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
5	chr4:69339600-69355000	Weak transcription	Esophagus	oesophagus
6	chr4:69341400-69342600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:69341600-69342000	Enhancers	NHDF-Ad	bronchial
8	chr4:69342000-69342200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:69345600-69346000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:69345600-69346000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr4:69345600-69346200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:69345600-69346400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:69348800-69349000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr4:69350400-69358000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr4:69355000-69355400	ZNF genes & repeats	Esophagus	oesophagus
16	chr4:69355200-69355400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr4:69355200-69355400	ZNF genes & repeats	Pancreas	Pancrea
18	chr4:69355200-69355800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:69355400-69362000	Weak transcription	Esophagus	oesophagus
20	chr4:69357600-69358400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:69359400-69360800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr4:69359800-69360600	Enhancers	Duodenum Mucosa	Duodenum
23	chr4:69359800-69360800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr4:69360000-69360400	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr4:69360000-69360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:69360000-69360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:69360200-69360600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:69360200-69360600	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr4:69360200-69360600	Enhancers	GM12878-XiMat	blood
30	chr4:69360200-69360800	Enhancers	Primary B cells from peripheral blood	blood
31	chr4:69360200-69360800	Enhancers	Primary hematopoietic stem cells	blood
32	chr4:69360200-69360800	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr4:69360400-69360800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:69360400-69360800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:69360400-69360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:69360400-69361000	Enhancers	Primary T cells from cord blood	blood
37	chr4:69360800-69364400	Weak transcription	Primary hematopoietic stem cells	blood
38	chr4:69361800-69362000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:69363600-69364000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr4:69363600-69364000	Enhancers	Fetal Kidney	kidney
41	chr4:69363600-69364200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:69363600-69365000	Enhancers	A549	lung
43	chr4:69363600-69365600	Enhancers	HepG2	liver
44	chr4:69364000-69364400	Enhancers	Fetal Intestine Large	intestine
45	chr4:69364000-69364600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr4:69364000-69365200	Enhancers	Liver	Liver
47	chr4:69364200-69364600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:69364400-69364600	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr4:69364400-69364800	Enhancers	Primary hematopoietic stem cells	blood
50	chr4:69364400-69364800	Active TSS	Rectal Mucosa Donor 29	rectum

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