Variant report

Variant	nsv4371
Chromosome Location	chr4:69046637-69081620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:549)
Chromatin interactive
region (count:6)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:86 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr4:69046738-69047214	Hela-S3	cervix:	n/a	n/a
2	CBX3	chr4:69074794-69075040	K562	blood:	n/a	n/a
3	CEBPB	chr4:69046925-69047238	MCF-7	breast:	n/a	n/a
4	CEBPB	chr4:69046723-69047292	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr4:69049103-69049471	HepG2	liver:	n/a	chr4:69049268-69049279
6	CEBPB	chr4:69049105-69049380	A549	lung:	n/a	chr4:69049268-69049279
7	CEBPB	chr4:69049084-69049619	Hela-S3	cervix:	n/a	chr4:69049268-69049279
8	CEBPB	chr4:69046736-69047277	HCT-116	colon:	n/a	n/a
9	CHD2	chr4:69046647-69047188	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr4:69074090-69074132	LNCaP	prostate:	n/a	n/a
11	CTCF	chr4:69048275-69048355	Fibrobl	skin:	n/a	n/a
12	E2F4	chr4:69079381-69079750	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr4:69046596-69046811	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr4:69046809-69047360	ECC-1	luminal epithelium:	n/a	n/a
15	EP300	chr4:69046724-69047277	Hela-S3	cervix:	n/a	n/a
16	EP300	chr4:69049104-69049524	Hela-S3	cervix:	n/a	n/a
17	EP300	chr4:69046742-69047412	ECC-1	luminal epithelium:	n/a	n/a
18	ESR1	chr4:69051178-69051380	T-47D	breast:	n/a	n/a
19	ESR1	chr4:69051083-69051344	T-47D	breast:	n/a	n/a
20	ESR1	chr4:69051046-69051355	T-47D	breast:	n/a	n/a
21	FOS	chr4:69049230-69049530	MCF10A-Er-Src	breast:	n/a	chr4:69049450-69049460
22	FOS	chr4:69046607-69047219	MCF10A-Er-Src	breast:	n/a	chr4:69047007-69047016
23	FOS	chr4:69046570-69047308	MCF10A-Er-Src	breast:	n/a	chr4:69047007-69047016
24	FOS	chr4:69049253-69049599	MCF10A-Er-Src	breast:	n/a	chr4:69049450-69049460
25	FOS	chr4:69049233-69049535	MCF10A-Er-Src	breast:	n/a	chr4:69049450-69049460
26	FOS	chr4:69046573-69047258	MCF10A-Er-Src	breast:	n/a	chr4:69047007-69047016
27	FOS	chr4:69046652-69047284	MCF10A-Er-Src	breast:	n/a	chr4:69047007-69047016
28	FOSL2	chr4:69046793-69047283	A549	lung:	n/a	chr4:69047007-69047016
29	FOXA1	chr4:69050707-69051016	T-47D	breast:	n/a	n/a
30	FOXA2	chr4:69060058-69060523	A549	lung:	n/a	n/a
31	GATA3	chr4:69074527-69074719	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr4:69051056-69051593	MCF-7	breast:	n/a	n/a
33	GATA3	chr4:69050943-69051653	MCF-7	breast:	n/a	n/a
34	GATA3	chr4:69051216-69051374	MCF-7	breast:	n/a	n/a
35	JUN	chr4:69077787-69077958	K562	blood:	n/a	n/a
36	JUND	chr4:69046571-69047177	Hela-S3	cervix:	n/a	chr4:69047007-69047016
37	KAP1	chr4:69074668-69075268	K562	blood:	n/a	n/a
38	MAFF	chr4:69058968-69059260	HepG2	liver:	n/a	chr4:69059110-69059124 chr4:69059111-69059129
39	MAFF	chr4:69059001-69059282	K562	blood:	n/a	chr4:69059110-69059124 chr4:69059111-69059129
40	MAFF	chr4:69049114-69049419	HepG2	liver:	n/a	n/a
41	MAFK	chr4:69058977-69059269	HepG2	liver:	n/a	chr4:69059109-69059125 chr4:69059113-69059123 chr4:69059110-69059124 chr4:69059107-69059127
42	MAFK	chr4:69049211-69049336	IMR90	lung:	n/a	n/a
43	MAFK	chr4:69049131-69049533	HepG2	liver:	n/a	n/a
44	MAFK	chr4:69059002-69059252	K562	blood:	n/a	chr4:69059109-69059125 chr4:69059113-69059123 chr4:69059110-69059124 chr4:69059107-69059127
45	MAFK	chr4:69058957-69059288	IMR90	lung:	n/a	chr4:69059109-69059125 chr4:69059113-69059123 chr4:69059110-69059124 chr4:69059107-69059127
46	MAFK	chr4:69058948-69059296	HepG2	liver:	n/a	chr4:69059109-69059125 chr4:69059113-69059123 chr4:69059110-69059124 chr4:69059107-69059127
47	MAFK	chr4:69049130-69049419	HepG2	liver:	n/a	n/a
48	MAZ	chr4:69046655-69046775	Hela-S3	cervix:	n/a	n/a
49	MYC	chr4:69046958-69047218	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr4:69046815-69047230	MCF10A-Er-Src	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69048335-69048385	HEEpiC	esophagus:	n/a
2	chr4:69052173-69052223	HMEC	breast:	n/a
3	chr4:69046856-69046906	HEEpiC	esophagus:	n/a
4	chr4:69048233-69048283	HCT-116	colon:	n/a
5	chr4:69048156-69048206	HEEpiC	esophagus:	n/a
6	chr4:69048233-69048283	SK-N-MC	brain:	n/a
7	chr4:69048156-69048206	AG09309	skin:	n/a
8	chr4:69046856-69046906	SK-N-MC	brain:	n/a
9	chr4:69047758-69047808	GM19239	blood:	n/a
10	chr4:69047758-69047808	AG04450	lung:	fetal
11	chr4:69048233-69048283	IMR90	lung:	fetal
12	chr4:69048156-69048206	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:69052173-69052223	HCT-116	colon:	n/a
14	chr4:69046856-69046906	SK-N-SH	brain:	n/a
15	chr4:69048430-69048480	Hepatocyte	liver:	n/a
16	chr4:69048430-69048480	SK-N-MC	brain:	n/a
17	chr4:69054755-69054805	LNCaP	prostate:	n/a
18	chr4:69048335-69048385	GM12878	blood:	n/a
19	chr4:69048233-69048283	HCM	heart:	n/a
20	chr4:69047758-69047808	AoSMC	blood vessel:	n/a
21	chr4:69047758-69047808	H1-hESC	embryonic stem cell:	embryo
22	chr4:69048335-69048385	HCF	heart:	n/a
23	chr4:69048335-69048385	SK-N-SH_RA	brain:	n/a
24	chr4:69048335-69048385	IMR90	lung:	fetal
25	chr4:69048001-69048051	SK-N-MC	brain:	n/a
26	chr4:69048335-69048385	HRPEpiC	eye:	n/a
27	chr4:69048001-69048051	K562	blood:	n/a
28	chr4:69054755-69054805	HCPEpiC	choroid plexus:	n/a
29	chr4:69048156-69048206	GM12891	blood:	n/a
30	chr4:69048001-69048051	ECC-1	luminal epithelium:	n/a
31	chr4:69048001-69048051	PrEC	prostate:	n/a
32	chr4:69046856-69046906	Jurkat	blood:	n/a
33	chr4:69048430-69048480	GM06990	blood:	n/a
34	chr4:69048001-69048051	CMK	blood:	n/a
35	chr4:69048335-69048385	CMK	blood:	n/a
36	chr4:69054755-69054805	A549	lung:	n/a
37	chr4:69046856-69046906	HCF	heart:	n/a
38	chr4:69054755-69054805	MCF-7	breast:	n/a
39	chr4:69048430-69048480	PANC-1	pancreas:	n/a
40	chr4:69048233-69048283	U87	brain:	n/a
41	chr4:69054755-69054805	SKMC	muscle:	n/a
42	chr4:69047758-69047808	MCF-7	breast:	n/a
43	chr4:69052173-69052223	HL-60	blood:	n/a
44	chr4:69048233-69048283	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:69048430-69048480	Caco-2	colon:	n/a
46	chr4:69046856-69046906	HMEC	breast:	n/a
47	chr4:69048001-69048051	A549	lung:	n/a
48	chr4:69048233-69048283	HEEpiC	esophagus:	n/a
49	chr4:69048430-69048480	PFSK-1	brain:	n/a
50	chr4:69048335-69048385	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
2	chr4:69078600..69080157-chr4:69085569..69088456,2	MCF-7	breast:
3	chr4:69052749..69055570-chr4:69072267..69074922,2	MCF-7	breast:
4	chr4:69052749..69055570-chr4:69072267..69074922,2	MCF-7	breast:
5	chr4:69050039..69052225-chr4:69055143..69056998,2	K562	blood:
6	chr4:68794157..68794866-chr4:69050816..69051359,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS11BNL-1	chr4:69078080-69078195	NONHSAT096727
2	lnc-TMPRSS11E-5	chr4:69048010-69049221	NR_015446
3	lnc-TMPRSS11BNL-1	chr4:69054121-69054474	NONHSAT096726
4	lnc-TMPRSS11E-5	chr4:69051478-69051601	NR_015446
5	lnc-TMPRSS11BNL-1	chr4:69071594-69071815	NONHSAT096726
6	lnc-TMPRSS11BNL-1	chr4:69056739-69057034	NONHSAT096727
7	lnc-TMPRSS11E-5	chr4:69078024-69078188	NR_015446
8	lnc-TMPRSS11BNL-1	chr4:69071753-69071815	NONHSAT096727

No data

Variant related genes	Relation type
FTLP10	TF binding region
ENSG00000250026	TF binding region
FTLP10	CpG island
ENSG00000250026	CpG island
ENSG00000250026	chromatin interactions

Extended variants
information (count: 450 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554009700	chr4:69046654-69046655	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs573403202	chr4:69046665-69046666	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs373218725	chr4:69046672-69046673	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs12507309	chr4:69046711-69046712	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs575570019	chr4:69046743-69046744	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs544547897	chr4:69046821-69046822	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs532314710	chr4:69046856-69046857	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs564633581	chr4:69046866-69046867	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs73823627	chr4:69046998-69046999	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552301477	chr4:69047031-69047032	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs199615851	chr4:69047052-69047053	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs17089132	chr4:69047064-69047065	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs560289395	chr4:69047077-69047078	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs140721136	chr4:69047103-69047104	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs548818622	chr4:69047119-69047120	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs373262555	chr4:69047172-69047173	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs28519542	chr4:69047215-69047216	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551350048	chr4:69047234-69047235	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs571618696	chr4:69047308-69047309	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs386675558	chr4:69047311-69047312	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs548735465	chr4:69047381-69047382	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs184346418	chr4:69047411-69047412	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs145363561	chr4:69047438-69047439	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs567486156	chr4:69047443-69047444	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs536420969	chr4:69047450-69047451	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs77163928	chr4:69047467-69047468	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs4860283	chr4:69047516-69047517	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs547765807	chr4:69047559-69047560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143520230	chr4:69047597-69047598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2874105	chr4:69047603-69047604	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs568582725	chr4:69047646-69047647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375638276	chr4:69047758-69047759	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs577943382	chr4:69047767-69047768	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs540507523	chr4:69047828-69047829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6835461	chr4:69047910-69047911	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs137907332	chr4:69047920-69047921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543168759	chr4:69047930-69047931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547774921	chr4:69047982-69047983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17089133	chr4:69048026-69048027	ZNF genes & repeats Enhancers Weak transcription	CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs141916273	chr4:69048045-69048046	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs571087921	chr4:69048066-69048067	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs374578208	chr4:69048089-69048090	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs115051210	chr4:69048097-69048098	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs368186529	chr4:69048154-69048155	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs527245889	chr4:69048168-69048169	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs547737628	chr4:69048186-69048187	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs567519030	chr4:69048192-69048193	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs73823628	chr4:69048219-69048220	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs556313069	chr4:69048232-69048233	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs569299752	chr4:69048248-69048249	ZNF genes & repeats Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Breast cancer	20369283	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
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Ollier disease	21235737	CNVD
Autism	21865298	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69046600-69047200	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr4:69046600-69047400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:69046600-69047400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:69046600-69047400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:69046600-69047400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:69046600-69047400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr4:69046600-69047400	Enhancers	HMEC	breast
8	chr4:69046600-69047400	Enhancers	NHEK	skin
9	chr4:69046600-69047800	Enhancers	Hela-S3	cervix
10	chr4:69046800-69047200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:69046800-69047400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:69046800-69047400	Enhancers	A549	lung
13	chr4:69046800-69047800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:69047400-69048800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:69047800-69048800	Weak transcription	Hela-S3	cervix
16	chr4:69048000-69048400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:69048000-69048400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:69048000-69048600	Enhancers	Esophagus	oesophagus
19	chr4:69048600-69054400	Weak transcription	Esophagus	oesophagus
20	chr4:69048800-69049200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:69048800-69050000	Enhancers	Hela-S3	cervix
22	chr4:69080200-69081000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:69080400-69084200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:69080800-69081000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr4:69080800-69081000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr4:69081000-69082000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr4:69081000-69082000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr4:69081000-69082200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr4:69081200-69081400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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