Variant report

Variant	nsv1013336
Chromosome Location	chr4:69320945-69540013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1224)
CpG islands
(count:793)
Chromatin interactive
region (count:14)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1224 , 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	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
8	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
9	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
10	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
11	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
12	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
13	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
14	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
17	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
18	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
21	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
22	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
23	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
24	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
25	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
26	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
27	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
29	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
31	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
33	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
34	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
36	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
37	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
38	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
39	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
40	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
41	CTCF	chr4:69384723-69384880	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:69364200-69364350	GM12871	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
43	CTCF	chr4:69364108-69364552	GM12878	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
44	CTCF	chr4:69443380-69443530	GM12871	blood:	n/a	n/a
45	CTCF	chr4:69434820-69434970	K562	blood:	n/a	n/a
46	CTCF	chr4:69538966-69539127	K562	blood:	n/a	n/a
47	CTCF	chr4:69364193-69364448	GM13977	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
48	CTCF	chr4:69538940-69539090	HRE	kidney:	n/a	n/a
49	CTCF	chr4:69364156-69364459	Medullo	brain:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
50	CTCF	chr4:69538965-69539235	A549	lung:	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	chr4:69537589-69537639	SK-N-SH_RA	brain:	n/a
2	chr4:69435601-69435651	AG04450	lung:	fetal
3	chr4:69435250-69435300	AG04450	lung:	fetal
4	chr4:69435601-69435651	NHDF-neo	bronchial:	n/a
5	chr4:69537826-69537876	AG04450	lung:	fetal
6	chr4:69381368-69381418	HRCEpiC	kidney:	n/a
7	chr4:69435250-69435300	HCF	heart:	n/a
8	chr4:69435250-69435300	H1-hESC	embryonic stem cell:	embryo
9	chr4:69435593-69435643	AG04449	skin:	fetal
10	chr4:69381368-69381418	AG09309	skin:	n/a
11	chr4:69514031-69514081	GM12892	blood:	n/a
12	chr4:69537806-69537856	NB4	blood:	n/a
13	chr4:69537806-69537856	HCF	heart:	n/a
14	chr4:69435601-69435651	SK-N-SH	brain:	n/a
15	chr4:69340916-69340966	HRE	kidney:	n/a
16	chr4:69514031-69514081	T-47D	breast:	n/a
17	chr4:69537826-69537876	GM19239	blood:	n/a
18	chr4:69435601-69435651	HCF	heart:	n/a
19	chr4:69536319-69536369	MCF-7	breast:	n/a
20	chr4:69537589-69537639	ovcar-3	ovarian:	n/a
21	chr4:69435593-69435643	AG09319	gingival:	n/a
22	chr4:69435593-69435643	HRPEpiC	eye:	n/a
23	chr4:69355121-69355171	U87	brain:	n/a
24	chr4:69355121-69355171	GM12892	blood:	n/a
25	chr4:69537589-69537639	Caco-2	colon:	n/a
26	chr4:69355121-69355171	NHDF-neo	bronchial:	n/a
27	chr4:69536319-69536369	NT2-D1	testis:	n/a
28	chr4:69537589-69537639	SKMC	muscle:	n/a
29	chr4:69435593-69435643	PrEC	prostate:	n/a
30	chr4:69537826-69537876	SK-N-MC	brain:	n/a
31	chr4:69381368-69381418	RPTEC	kidney:	n/a
32	chr4:69514031-69514081	HAEpiC	amniotic membrane:	n/a
33	chr4:69522639-69522689	HUVEC	blood vessel:	n/a
34	chr4:69537826-69537876	NB4	blood:	n/a
35	chr4:69522639-69522689	NB4	blood:	n/a
36	chr4:69537826-69537876	HCF	heart:	n/a
37	chr4:69537826-69537876	CMK	blood:	n/a
38	chr4:69435593-69435643	ProgFib	skin:	n/a
39	chr4:69340916-69340966	HL-60	blood:	n/a
40	chr4:69537826-69537876	GM06990	blood:	n/a
41	chr4:69435593-69435643	U87	brain:	n/a
42	chr4:69537806-69537856	HepG2	liver:	n/a
43	chr4:69340916-69340966	AoSMC	blood vessel:	n/a
44	chr4:69434475-69434525	MCF10A-Er-Src	breast:	n/a
45	chr4:69536319-69536369	K562	blood:	n/a
46	chr4:69434475-69434525	CMK	blood:	n/a
47	chr4:69537806-69537856	H1-hESC	embryonic stem cell:	embryo
48	chr4:69434475-69434525	PFSK-1	brain:	n/a
49	chr4:69537589-69537639	HIPEpiC	eye:	n/a
50	chr4:69434475-69434525	AG04450	lung:	fetal

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
2	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
3	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
4	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
5	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
6	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
7	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
8	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
9	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
10	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
11	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
12	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
13	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
14	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 6508 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6508 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187554887	chr4:69320974-69320975	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs561069704	chr4:69320990-69320991	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529463068	chr4:69321040-69321041	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549641645	chr4:69321043-69321044	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192600844	chr4:69321060-69321061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140517487	chr4:69321147-69321148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184178284	chr4:69321179-69321180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149706254	chr4:69321181-69321182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534225956	chr4:69321193-69321194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553595301	chr4:69321198-69321199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189405032	chr4:69321218-69321219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570612185	chr4:69321235-69321236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574117348	chr4:69321242-69321243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192424225	chr4:69321334-69321335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555940471	chr4:69321347-69321348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1406703	chr4:69321389-69321390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184861018	chr4:69321422-69321423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1406702	chr4:69321453-69321454	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs571927812	chr4:69321458-69321459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541070133	chr4:69321496-69321497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142861750	chr4:69321497-69321498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371239301	chr4:69321501-69321502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146554889	chr4:69321520-69321521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188830313	chr4:69321528-69321529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375001379	chr4:69321611-69321612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532011000	chr4:69321699-69321700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367960746	chr4:69321722-69321723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571953913	chr4:69321764-69321765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181462146	chr4:69321785-69321786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186104057	chr4:69321786-69321787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189349216	chr4:69321824-69321825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182447772	chr4:69321843-69321844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10518052	chr4:69321885-69321886	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs187353246	chr4:69321919-69321920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538476105	chr4:69321954-69321955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191018491	chr4:69321956-69321957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1406701	chr4:69321971-69321972	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs369721275	chr4:69322019-69322020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374152922	chr4:69322020-69322021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554552720	chr4:69322040-69322041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181036135	chr4:69322052-69322053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186345811	chr4:69322126-69322127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369977857	chr4:69322161-69322162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568833285	chr4:69322165-69322166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371510934	chr4:69322187-69322188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190121701	chr4:69322203-69322204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146866066	chr4:69322216-69322217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374030761	chr4:69322250-69322251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566181612	chr4:69322257-69322258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527989760	chr4:69322264-69322265	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:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69311800-69321200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr4:69312000-69321400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:69314400-69321400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:69319000-69325600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:69319600-69335800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:69319800-69325600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:69320800-69321400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:69321400-69325800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:69325600-69326200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:69325600-69326200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr4:69325800-69326600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:69325800-69326600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr4:69326200-69326400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:69326200-69329600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr4:69326200-69329800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr4:69326200-69334200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:69326200-69348800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:69326600-69331000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr4:69326600-69334200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr4:69327400-69327800	Enhancers	NHEK	skin
21	chr4:69327400-69328800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:69327400-69332800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:69327400-69333200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:69327600-69328400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr4:69327600-69333600	Enhancers	HMEC	breast
26	chr4:69327800-69329600	Weak transcription	NHEK	skin
27	chr4:69328400-69329600	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:69328400-69332600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:69328800-69329800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:69329200-69330000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr4:69329400-69332800	Enhancers	NHDF-Ad	bronchial
32	chr4:69329600-69329800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr4:69329600-69329800	Enhancers	HSMMtube	muscle
34	chr4:69329600-69330000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr4:69329600-69330000	Enhancers	Colon Smooth Muscle	Colon
36	chr4:69329600-69330200	Enhancers	A549	lung
37	chr4:69329600-69332800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:69329600-69332800	Enhancers	HSMM	muscle
39	chr4:69329600-69332800	Enhancers	NH-A	brain
40	chr4:69329600-69333000	Enhancers	NHEK	skin
41	chr4:69329800-69330200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr4:69329800-69330600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:69329800-69331200	Weak transcription	HSMMtube	muscle
44	chr4:69329800-69332800	Enhancers	Osteobl	bone
45	chr4:69329800-69333200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:69330000-69331200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:69330000-69331800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr4:69330000-69332800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr4:69330200-69330600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr4:69330200-69332000	Weak transcription	A549	lung

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