Variant report

Variant	esv3380231
Chromosome Location	chr4:1216752-1220050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:109)
CpG islands
(count:489)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:109 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr4:1219641-1219707	K562	blood:	n/a	n/a
2	CTCF	chr4:1217540-1217690	GM12869	blood:	n/a	n/a
3	CTCF	chr4:1218013-1218014	GM19239	blood:	n/a	n/a
4	CTCF	chr4:1218019-1218053	GM19239	blood:	n/a	n/a
5	MAX	chr4:1217932-1218160	NB4	blood:	n/a	chr4:1218043-1218059 chr4:1218041-1218051
6	MTA3	chr4:1217893-1218449	GM12878	blood:	n/a	n/a
7	MYC	chr4:1218096-1218105	MCF-7	breast:	n/a	n/a
8	MYC	chr4:1218053-1218092	HUVEC	blood vessel:	n/a	n/a
9	POLR2A	chr4:1218100-1218812	ECC-1	luminal epithelium:	n/a	n/a
10	POLR2A	chr4:1218617-1218732	A549	lung:	n/a	n/a
11	POLR2A	chr4:1219542-1219643	GM12878	blood:	n/a	n/a
12	POLR2A	chr4:1217247-1218733	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr4:1218766-1218794	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr4:1218321-1218330	MCF-7	breast:	n/a	n/a
15	POLR2A	chr4:1215246-1219565	K562	blood:	n/a	n/a
16	POLR2A	chr4:1217792-1218717	HepG2	liver:	n/a	n/a
17	POLR2A	chr4:1216625-1219322	HL-60	blood:	n/a	n/a
18	POLR2A	chr4:1217956-1218050	GM12878	blood:	n/a	n/a
19	POLR2A	chr4:1217024-1217373	GM12878	blood:	n/a	n/a
20	POLR2A	chr4:1218172-1218178	MCF-7	breast:	n/a	n/a
21	POLR2A	chr4:1216278-1216807	K562	blood:	n/a	n/a
22	POLR2A	chr4:1216561-1217007	K562	blood:	n/a	n/a
23	POLR2A	chr4:1217518-1217578	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr4:1217236-1217267	GM12878	blood:	n/a	n/a
25	POLR2A	chr4:1219194-1219577	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr4:1218009-1218204	A549	lung:	n/a	n/a
27	POLR2A	chr4:1219011-1219086	ProgFib	skin:	n/a	n/a
28	POLR2A	chr4:1217883-1218071	K562	blood:	n/a	n/a
29	POLR2A	chr4:1217229-1219247	K562	blood:	n/a	n/a
30	POLR2A	chr4:1215486-1219186	SK-N-MC	brain:	n/a	n/a
31	POLR2A	chr4:1218427-1218449	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr4:1217580-1217656	A549	lung:	n/a	n/a
33	POLR2A	chr4:1218841-1218866	MCF-7	breast:	n/a	n/a
34	POLR2A	chr4:1216858-1216937	K562	blood:	n/a	n/a
35	POLR2A	chr4:1219515-1220098	GM12878	blood:	n/a	n/a
36	POLR2A	chr4:1218070-1218381	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr4:1218186-1218916	GM12891	blood:	n/a	n/a
38	POLR2A	chr4:1219391-1219669	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr4:1217684-1219117	GM12878	blood:	n/a	n/a
40	POLR2A	chr4:1218914-1219383	A549	lung:	n/a	n/a
41	POLR2A	chr4:1217802-1218942	PFSK-1	brain:	n/a	n/a
42	POLR2A	chr4:1217887-1217985	A549	lung:	n/a	n/a
43	POLR2A	chr4:1218207-1218467	A549	lung:	n/a	n/a
44	POLR2A	chr4:1219178-1219300	GM12878	blood:	n/a	n/a
45	POLR2A	chr4:1218291-1218311	MCF-7	breast:	n/a	n/a
46	POLR2A	chr4:1218978-1218997	ProgFib	skin:	n/a	n/a
47	POLR2A	chr4:1217751-1218372	HCT-116	colon:	n/a	n/a
48	POLR2A	chr4:1218358-1218364	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr4:1217962-1218510	GM12892	blood:	n/a	n/a
50	POLR2A	chr4:1218145-1218381	A549	lung:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1217317-1217367	SK-N-SH_RA	brain:	n/a
2	chr4:1217317-1217367	SK-N-SH_RA	brain:	n/a
3	chr4:1219707-1219757	HAEpiC	amniotic membrane:	n/a
4	chr4:1219498-1219548	Hela-S3	cervix:	n/a
5	chr4:1217392-1217442	ovcar-3	ovarian:	n/a
6	chr4:1217317-1217367	LNCaP	prostate:	n/a
7	chr4:1219707-1219757	T-47D	breast:	n/a
8	chr4:1218386-1218436	SK-N-MC	brain:	n/a
9	chr4:1217221-1217271	NHDF-neo	bronchial:	n/a
10	chr4:1218386-1218436	HAEpiC	amniotic membrane:	n/a
11	chr4:1217221-1217271	GM12878	blood:	n/a
12	chr4:1217221-1217271	PANC-1	pancreas:	n/a
13	chr4:1217317-1217367	Caco-2	colon:	n/a
14	chr4:1217392-1217442	LNCaP	prostate:	n/a
15	chr4:1217755-1217805	HIPEpiC	eye:	n/a
16	chr4:1217317-1217367	HCF	heart:	n/a
17	chr4:1217392-1217442	NHDF-neo	bronchial:	n/a
18	chr4:1217221-1217271	MCF-7	breast:	n/a
19	chr4:1218386-1218436	SK-N-SH_RA	brain:	n/a
20	chr4:1219008-1219058	BE2_C	brain:	n/a
21	chr4:1217755-1217805	SKMC	muscle:	n/a
22	chr4:1217317-1217367	RPTEC	kidney:	n/a
23	chr4:1217755-1217805	GM19239	blood:	n/a
24	chr4:1219498-1219548	NB4	blood:	n/a
25	chr4:1217317-1217367	Jurkat	blood:	n/a
26	chr4:1217317-1217367	GM19239	blood:	n/a
27	chr4:1217755-1217805	LNCaP	prostate:	n/a
28	chr4:1219498-1219548	SK-N-SH_RA	brain:	n/a
29	chr4:1217392-1217442	AG09319	gingival:	n/a
30	chr4:1217221-1217271	HRE	kidney:	n/a
31	chr4:1217221-1217271	HMEC	breast:	n/a
32	chr4:1217317-1217367	AG10803	skin:	n/a
33	chr4:1219498-1219548	H1-hESC	embryonic stem cell:	embryo
34	chr4:1217755-1217805	NB4	blood:	n/a
35	chr4:1219498-1219548	HRPEpiC	eye:	n/a
36	chr4:1219008-1219058	BJ	skin:	n/a
37	chr4:1219498-1219548	NT2-D1	testis:	n/a
38	chr4:1217221-1217271	RPTEC	kidney:	n/a
39	chr4:1217392-1217442	Hepatocyte	liver:	n/a
40	chr4:1217392-1217442	SK-N-SH_RA	brain:	n/a
41	chr4:1217221-1217271	NT2-D1	testis:	n/a
42	chr4:1217755-1217805	AG09309	skin:	n/a
43	chr4:1217221-1217271	SAEC	small airway:	n/a
44	chr4:1217392-1217442	AG09309	skin:	n/a
45	chr4:1219498-1219548	HepG2	liver:	n/a
46	chr4:1217317-1217367	GM12891	blood:	n/a
47	chr4:1219707-1219757	GM12892	blood:	n/a
48	chr4:1217317-1217367	CMK	blood:	n/a
49	chr4:1217221-1217271	ovcar-3	ovarian:	n/a
50	chr4:1217392-1217442	Jurkat	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1216435..1221821-chr4:1240439..1244617,5	MCF-7	breast:
2	chr4:1215769..1218494-chr4:1233904..1236705,2	MCF-7	breast:
3	chr4:1218830..1221524-chr4:1242783..1244802,2	MCF-7	breast:
4	chr4:1215555..1220351-chr4:1239288..1242893,7	K562	blood:
5	chr4:1215883..1221793-chr4:1233494..1238232,6	K562	blood:
6	chr4:1211126..1212834-chr4:1216389..1218243,2	K562	blood:
7	chr4:1217670..1219491-chr4:1243014..1244747,2	K562	blood:
8	chr4:1201225..1203014-chr4:1216163..1217887,2	MCF-7	breast:
9	chr4:1209494..1211546-chr4:1218177..1220594,3	MCF-7	breast:
10	chr4:1209168..1212626-chr4:1216430..1218433,3	K562	blood:
11	chr4:1219143..1221497-chr4:1224349..1226849,2	MCF-7	breast:

No data

Variant related genes	Relation type
CTBP1	TF binding region
CTBP1	CpG island
ENSG00000159692	chromatin interactions
ENSG00000159674	chromatin interactions
ENSG00000196810	chromatin interactions

Extended variants
information (count: 206 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:206 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545972496	chr4:1216767-1216768	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs558265916	chr4:1216780-1216781	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs576337754	chr4:1216783-1216784	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs543813356	chr4:1216793-1216794	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs180715791	chr4:1216798-1216799	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs368747629	chr4:1216804-1216805	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs529163393	chr4:1216809-1216810	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs575122873	chr4:1216815-1216816	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs541338545	chr4:1216822-1216823	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs113150506	chr4:1216828-1216829	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs533191907	chr4:1216848-1216849	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs551171117	chr4:1216857-1216858	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs199626206	chr4:1216865-1216866	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs372335949	chr4:1216867-1216868	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs3755949	chr4:1216868-1216869	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs371279138	chr4:1216938-1216939	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs548535952	chr4:1216948-1216949	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs2020137	chr4:1216951-1216952	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs2004531	chr4:1217056-1217057	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs185195103	chr4:1217064-1217065	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs73069921	chr4:1217068-1217069	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs115152027	chr4:1217078-1217079	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
23	rs558091566	chr4:1217095-1217096	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs576450417	chr4:1217169-1217170	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs369564288	chr4:1217170-1217171	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs549799875	chr4:1217187-1217188	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs540176828	chr4:1217217-1217218	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs561711088	chr4:1217221-1217222	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs555753061	chr4:1217267-1217268	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs374273580	chr4:1217269-1217270	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs541322073	chr4:1217279-1217280	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs563639252	chr4:1217281-1217282	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs377202315	chr4:1217297-1217298	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs577738572	chr4:1217325-1217326	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs143319802	chr4:1217330-1217331	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs113583935	chr4:1217357-1217358	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs553989992	chr4:1217392-1217393	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs530481976	chr4:1217393-1217394	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs548671287	chr4:1217449-1217450	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs191881324	chr4:1217454-1217455	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs560537532	chr4:1217456-1217457	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs139105198	chr4:1217460-1217461	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs35827214	chr4:1217470-1217471	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs374553460	chr4:1217506-1217507	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs547753412	chr4:1217509-1217510	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs530911157	chr4:1217529-1217530	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs143967795	chr4:1217576-1217577	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs539762476	chr4:1217591-1217592	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs77229204	chr4:1217614-1217615	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs570160924	chr4:1217683-1217684	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20393555	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1202800-1218000	Weak transcription	Fetal Brain Male	brain
2	chr4:1203200-1217800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr4:1203800-1223000	Strong transcription	Osteobl	bone
4	chr4:1204000-1218000	Weak transcription	K562	blood
5	chr4:1204400-1227200	Strong transcription	Fetal Intestine Small	intestine
6	chr4:1204400-1235800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:1204600-1220400	Strong transcription	Liver	Liver
8	chr4:1204600-1236200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:1204800-1226400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:1204800-1237000	Weak transcription	Psoas Muscle	Psoas
11	chr4:1205000-1226200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr4:1205200-1218000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:1205400-1226800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:1205800-1228200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:1206000-1226800	Strong transcription	Fetal Brain Female	brain
16	chr4:1206400-1226800	Strong transcription	Brain Germinal Matrix	brain
17	chr4:1206600-1227600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:1207600-1218200	Weak transcription	Hela-S3	cervix
19	chr4:1208800-1228000	Strong transcription	Muscle Satellite Cultured Cells	--
20	chr4:1209000-1218000	Weak transcription	Stomach Mucosa	stomach
21	chr4:1209800-1218000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr4:1210600-1225200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr4:1210800-1217800	Weak transcription	Fetal Heart	heart
24	chr4:1210800-1218000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr4:1211000-1217800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr4:1211200-1217800	Strong transcription	Skeletal Muscle Male	skeletal muscle
27	chr4:1211400-1219600	Weak transcription	Right Atrium	heart
28	chr4:1211400-1235400	Weak transcription	Small Intestine	intestine
29	chr4:1211600-1217000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:1211600-1217200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:1211600-1217600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:1211600-1235400	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr4:1211800-1217000	Weak transcription	Brain Angular Gyrus	brain
34	chr4:1211800-1217800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr4:1211800-1217800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr4:1212000-1217000	Weak transcription	Colon Smooth Muscle	Colon
37	chr4:1212600-1225200	Strong transcription	Fetal Muscle Leg	muscle
38	chr4:1212600-1237000	Strong transcription	Dnd41	blood
39	chr4:1213200-1217600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:1213400-1217600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:1213400-1218200	Genic enhancers	NHEK	skin
42	chr4:1213400-1218600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr4:1213400-1219600	Strong transcription	Stomach Smooth Muscle	stomach
44	chr4:1213600-1217800	Weak transcription	Fetal Kidney	kidney
45	chr4:1213600-1224200	Strong transcription	Placenta	Placenta
46	chr4:1213800-1217600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr4:1213800-1219000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr4:1213800-1221800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:1214000-1219200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:1214200-1217800	Strong transcription	Primary T cells fromperipheralblood	blood

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