Variant report

Variant	nsv916737
Chromosome Location	chr4:121589793-121748847
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	chr4:121614174-121614541	HepG2	liver:	n/a	n/a
2	ATF2	chr4:121670498-121670947	GM12878	blood:	n/a	n/a
3	BACH1	chr4:121594017-121594053	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:121640212-121640444	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:121642846-121642911	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:121686870-121687098	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:121670672-121671060	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:121651232-121651259	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr4:121644141-121644145	GM12878	blood:	n/a	n/a
10	BRCA1	chr4:121690199-121690775	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:121635451-121636206	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:121614129-121614531	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:121645169-121646234	Hela-S3	cervix:	n/a	chr4:121645385-121645402 chr4:121645889-121645902 chr4:121645891-121645902 chr4:121645891-121645900
14	CEBPB	chr4:121690345-121690783	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:121631112-121631528	IMR90	lung:	n/a	chr4:121631295-121631306
16	CEBPB	chr4:121676743-121677031	HepG2	liver:	n/a	chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676920-121676929 chr4:121676918-121676929
17	CEBPB	chr4:121614054-121614540	A549	lung:	n/a	n/a
18	CEBPB	chr4:121631141-121631341	HepG2	liver:	n/a	chr4:121631295-121631306
19	CEBPB	chr4:121645254-121645513	IMR90	lung:	n/a	chr4:121645385-121645402
20	CEBPB	chr4:121631130-121631448	Hela-S3	cervix:	n/a	chr4:121631295-121631306
21	CEBPB	chr4:121640171-121640485	MCF-7	breast:	n/a	chr4:121640181-121640192
22	CEBPB	chr4:121592716-121593068	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:121613598-121613728	A549	lung:	n/a	n/a
24	CEBPB	chr4:121606918-121607260	IMR90	lung:	n/a	chr4:121607082-121607093
25	CEBPB	chr4:121614121-121614530	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr4:121606955-121607205	Hela-S3	cervix:	n/a	chr4:121607082-121607093
27	CEBPB	chr4:121606961-121607243	H1-hESC	embryonic stem cell:	n/a	chr4:121607082-121607093
28	CEBPB	chr4:121606939-121607247	HepG2	liver:	n/a	chr4:121607082-121607093
29	CEBPB	chr4:121617954-121618297	Hela-S3	cervix:	n/a	chr4:121617999-121618011
30	CEBPB	chr4:121606969-121607255	A549	lung:	n/a	chr4:121607082-121607093
31	CEBPB	chr4:121614175-121614520	A549	lung:	n/a	n/a
32	CEBPB	chr4:121614196-121614485	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:121643338-121643603	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:121614204-121614449	MCF-7	breast:	n/a	n/a
35	CEBPB	chr4:121704092-121704827	IMR90	lung:	n/a	chr4:121704325-121704338 chr4:121704325-121704338 chr4:121704196-121704209
36	CEBPZ	chr4:121610364-121610412	HepG2	liver:	n/a	n/a
37	CHD2	chr4:121655980-121656247	GM12878	blood:	n/a	n/a
38	CHD2	chr4:121690442-121690766	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr4:121670552-121671041	GM12878	blood:	n/a	n/a
40	CTCF	chr4:121640171-121640419	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr4:121730809-121730874	GM13977	blood:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
42	CTCF	chr4:121601853-121601916	GM20000	blood:	n/a	n/a
43	CTCF	chr4:121730800-121730950	GM12872	blood:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
44	CTCF	chr4:121730780-121730930	AG09319	gingival:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
45	CTCF	chr4:121730700-121730850	GM12872	blood:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
46	CTCF	chr4:121730840-121730990	WI-38	lung:	n/a	n/a
47	CTCF	chr4:121730720-121730870	HL-60	blood:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
48	CTCF	chr4:121730800-121730950	AG09319	gingival:	n/a	chr4:121730831-121730849 chr4:121730826-121730847
49	CTCF	chr4:121640220-121640370	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr4:121640220-121640370	HPF	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:121613795-121613845	HEK293	kidney:	embryo
2	chr4:121613795-121613845	Caco-2	colon:	n/a
3	chr4:121613795-121613845	T-47D	breast:	n/a
4	chr4:121613795-121613845	IMR90	lung:	fetal
5	chr4:121613795-121613845	HIPEpiC	eye:	n/a
6	chr4:121613795-121613845	SKMC	muscle:	n/a
7	chr4:121613795-121613845	BJ	skin:	n/a
8	chr4:121613795-121613845	CMK	blood:	n/a
9	chr4:121613795-121613845	HL-60	blood:	n/a
10	chr4:121613795-121613845	NHDF-neo	bronchial:	n/a
11	chr4:121613795-121613845	HRE	kidney:	n/a
12	chr4:121613795-121613845	AG09309	skin:	n/a
13	chr4:121613795-121613845	SK-N-SH_RA	brain:	n/a
14	chr4:121613795-121613845	HAEpiC	amniotic membrane:	n/a
15	chr4:121613795-121613845	HCM	heart:	n/a
16	chr4:121613795-121613845	H1-hESC	embryonic stem cell:	embryo
17	chr4:121613795-121613845	LNCaP	prostate:	n/a
18	chr4:121613795-121613845	PFSK-1	brain:	n/a
19	chr4:121613795-121613845	BE2_C	brain:	n/a
20	chr4:121613795-121613845	NH-A	brain:	n/a
21	chr4:121613795-121613845	MCF10A-Er-Src	breast:	n/a
22	chr4:121613795-121613845	HCF	heart:	n/a
23	chr4:121613795-121613845	HCT-116	colon:	n/a
24	chr4:121613795-121613845	PrEC	prostate:	n/a
25	chr4:121613795-121613845	Hepatocyte	liver:	n/a
26	chr4:121613795-121613845	HepG2	liver:	n/a
27	chr4:121613795-121613845	GM12892	blood:	n/a
28	chr4:121613795-121613845	HEEpiC	esophagus:	n/a
29	chr4:121613795-121613845	ovcar-3	ovarian:	n/a
30	chr4:121613795-121613845	Hela-S3	cervix:	n/a
31	chr4:121613795-121613845	AoSMC	blood vessel:	n/a
32	chr4:121613795-121613845	MCF-7	breast:	n/a
33	chr4:121613795-121613845	A549	lung:	n/a
34	chr4:121613795-121613845	SK-N-MC	brain:	n/a
35	chr4:121613795-121613845	RPTEC	kidney:	n/a
36	chr4:121613795-121613845	ProgFib	skin:	n/a
37	chr4:121613795-121613845	AG04450	lung:	fetal
38	chr4:121613795-121613845	GM12891	blood:	n/a
39	chr4:121613795-121613845	GM12878	blood:	n/a
40	chr4:121613795-121613845	K562	blood:	n/a
41	chr4:121613795-121613845	HNPCEpiC	eye:	n/a
42	chr4:121613795-121613845	AG09319	gingival:	n/a
43	chr4:121613795-121613845	PANC-1	pancreas:	n/a
44	chr4:121613795-121613845	SAEC	small airway:	n/a
45	chr4:121613795-121613845	HMEC	breast:	n/a
46	chr4:121613795-121613845	NB4	blood:	n/a
47	chr4:121613795-121613845	GM19239	blood:	n/a
48	chr4:121613795-121613845	HCPEpiC	choroid plexus:	n/a
49	chr4:121613795-121613845	HRCEpiC	kidney:	n/a
50	chr4:121613795-121613845	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:121622815..121625386-chr4:121625794..121628188,2	K562	blood:
2	chr4:121396849..121398573-chr4:121700140..121702182,2	K562	blood:
3	chr4:121077068..121077961-chr4:121639964..121640817,3	MCF-7	breast:
4	chr4:121622815..121625386-chr4:121625794..121628188,2	K562	blood:
5	chr4:121650109..121652030-chr4:121655352..121657399,2	K562	blood:
6	chr4:121593641..121594483-chr9:126875138..126875779,2	MCF-7	breast:
7	chr4:121651698..121654667-chr4:121660319..121662690,2	MCF-7	breast:
8	chr4:121650109..121652030-chr4:121655352..121657399,2	K562	blood:
9	chr4:121646983..121649694-chr4:121650404..121652066,2	K562	blood:
10	chr4:121646983..121649694-chr4:121650404..121652066,2	K562	blood:
11	chr4:121745652..121748462-chr4:121750150..121752192,2	MCF-7	breast:
12	chr4:121639899..121640642-chr4:121840005..121841112,3	MCF-7	breast:
13	chr4:121633676..121636146-chr4:121637384..121639291,2	K562	blood:
14	chr4:121651698..121654667-chr4:121660319..121662690,2	MCF-7	breast:
15	chr4:121633676..121636146-chr4:121637384..121639291,2	K562	blood:

Variant related genes	Relation type
PRDM5	TF binding region
RNU6-550P	TF binding region
PRDM5	CpG island
RNU6-550P	CpG island

Extended variants
information (count: 6274 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6274 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201046382	chr4:121589798-121589799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556300843	chr4:121589808-121589809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10024244	chr4:121589810-121589811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs376318969	chr4:121589846-121589847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72676335	chr4:121589847-121589848	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs548925118	chr4:121589897-121589898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139785196	chr4:121589908-121589909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs180745329	chr4:121589945-121589946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76026682	chr4:121589961-121589962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553915060	chr4:121589971-121589972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145280915	chr4:121589986-121589987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147140315	chr4:121590057-121590058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74608978	chr4:121590065-121590066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs80306675	chr4:121590158-121590159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531794716	chr4:121590160-121590161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545248564	chr4:121590208-121590209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10015102	chr4:121590225-121590226	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs577315029	chr4:121590370-121590371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34776884	chr4:121590406-121590407	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs76820397	chr4:121590424-121590425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184784020	chr4:121590515-121590516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374810004	chr4:121590531-121590532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529767723	chr4:121590543-121590544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189691154	chr4:121590612-121590613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12510719	chr4:121590630-121590631	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs113883954	chr4:121590643-121590644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140253239	chr4:121590733-121590734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78255532	chr4:121590751-121590752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538835460	chr4:121590752-121590753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181888665	chr4:121590810-121590811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371943001	chr4:121590845-121590846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551528258	chr4:121590902-121590903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12507476	chr4:121590926-121590927	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs145510707	chr4:121590996-121590997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573267964	chr4:121591000-121591001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561662236	chr4:121591012-121591013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536707806	chr4:121591048-121591049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556240064	chr4:121591051-121591052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs36132252	chr4:121591059-121591060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs547680608	chr4:121591094-121591095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186968749	chr4:121591106-121591107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79459751	chr4:121591122-121591123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs3085745	chr4:121591123-121591124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148028000	chr4:121591124-121591125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72526515	chr4:121591125-121591126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs397709000	chr4:121591126-121591127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370180707	chr4:121591127-121591128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375691299	chr4:121591129-121591130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374303474	chr4:121591138-121591139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375506278	chr4:121591152-121591153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121585800-121594400	Weak transcription	Pancreas	Pancrea
2	chr4:121589200-121594000	Weak transcription	Aorta	Aorta
3	chr4:121589800-121593000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:121590000-121594400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:121591200-121620600	Weak transcription	Left Ventricle	heart
6	chr4:121592400-121593200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:121592400-121593400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr4:121592400-121594800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr4:121592800-121593200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:121592800-121593200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:121592800-121593200	Enhancers	Fetal Muscle Leg	muscle
12	chr4:121593000-121593200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:121593000-121593400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:121593000-121593400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:121593000-121593800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:121593200-121593400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:121593200-121593800	Weak transcription	Fetal Muscle Leg	muscle
18	chr4:121593200-121594400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:121593400-121594200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr4:121593400-121594400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:121593800-121594200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:121593800-121595400	ZNF genes & repeats	Fetal Muscle Leg	muscle
23	chr4:121594000-121594600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:121594000-121595400	ZNF genes & repeats	Aorta	Aorta
25	chr4:121594000-121596200	Weak transcription	Brain Substantia Nigra	brain
26	chr4:121594200-121594400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:121594200-121594800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:121594200-121595000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:121594200-121595200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:121594200-121595800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
31	chr4:121594200-121595800	ZNF genes & repeats	Lung	lung
32	chr4:121594400-121594800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:121594400-121595000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:121594400-121595400	ZNF genes & repeats	Fetal Lung	lung
35	chr4:121594400-121595400	ZNF genes & repeats	Pancreas	Pancrea
36	chr4:121594400-121595800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:121594400-121595800	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr4:121594600-121594800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:121594600-121595000	Enhancers	Fetal Muscle Trunk	muscle
40	chr4:121594600-121595400	ZNF genes & repeats	Ovary	ovary
41	chr4:121595000-121596000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:121595200-121595600	ZNF genes & repeats	Stomach Smooth Muscle	stomach
43	chr4:121595200-121596000	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr4:121595400-121595800	ZNF genes & repeats	Fetal Intestine Large	intestine
45	chr4:121595400-121598200	Weak transcription	Fetal Lung	lung
46	chr4:121595400-121602600	Weak transcription	Ovary	ovary
47	chr4:121595800-121596200	ZNF genes & repeats	Aorta	Aorta
48	chr4:121603800-121604600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr4:121604000-121604200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr4:121604000-121604400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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