Variant report

Variant	nsv1017787
Chromosome Location	chr4:188840159-188974472
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:838)
CpG islands
(count:2627)
Chromatin interactive
region (count:15)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:838 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:188915055-188915396	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:188926433-188926974	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:188850148-188850549	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:188916764-188917071	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:188953244-188953886	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:188916749-188917170	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:188917657-188917951	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:188916526-188917174	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:188952989-188953975	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:188964645-188964695	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:188936288-188936488	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr4:188896133-188896354	GM12878	blood:	n/a	chr4:188896272-188896283
13	BCL11A	chr4:188953306-188953649	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr4:188929455-188929456	HepG2	liver:	n/a	n/a
15	BHLHE40	chr4:188923505-188923772	K562	blood:	n/a	n/a
16	BRCA1	chr4:188936021-188936859	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr4:188909297-188909449	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr4:188917816-188917938	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr4:188923496-188923905	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:188898167-188898421	HepG2	liver:	n/a	chr4:188898278-188898291 chr4:188898279-188898290
21	CEBPB	chr4:188936139-188936670	A549	lung:	n/a	n/a
22	CEBPB	chr4:188936287-188936507	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr4:188929383-188929936	A549	lung:	n/a	n/a
24	CEBPB	chr4:188873517-188873689	Hela-S3	cervix:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
25	CEBPB	chr4:188972503-188972708	K562	blood:	n/a	chr4:188972610-188972621
26	CEBPB	chr4:188936268-188936828	A549	lung:	n/a	n/a
27	CEBPB	chr4:188972446-188972753	IMR90	lung:	n/a	chr4:188972610-188972621
28	CEBPB	chr4:188875779-188875862	H1-hESC	embryonic stem cell:	n/a	chr4:188875825-188875836
29	CEBPB	chr4:188873586-188873809	IMR90	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
30	CEBPB	chr4:188972434-188972808	A549	lung:	n/a	chr4:188972610-188972621
31	CEBPB	chr4:188929269-188929961	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:188875669-188875935	HepG2	liver:	n/a	chr4:188875825-188875836
33	CEBPB	chr4:188972436-188972883	HepG2	liver:	n/a	chr4:188972610-188972621
34	CEBPB	chr4:188929371-188929912	A549	lung:	n/a	n/a
35	CEBPB	chr4:188929463-188929848	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:188936053-188937221	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:188873512-188873759	A549	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
38	CEBPB	chr4:188923470-188923960	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:188916852-188917179	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr4:188936262-188936771	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:188873544-188873823	HepG2	liver:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
42	CEBPB	chr4:188972564-188972701	H1-hESC	embryonic stem cell:	n/a	chr4:188972610-188972621
43	CHD1	chr4:188916853-188919438	H1-hESC	embryonic stem cell:	n/a	chr4:188918682-188918692 chr4:188918099-188918109
44	CHD1	chr4:188919719-188919955	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr4:188952977-188953947	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr4:188929422-188929870	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr4:188937818-188938313	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:188923470-188923823	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr4:188952861-188953856	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr4:188914155-188915309	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2627 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188913931-188913981	ovcar-3	ovarian:	n/a
2	chr4:188916724-188916774	ovcar-3	ovarian:	n/a
3	chr4:188924717-188924767	GM06990	blood:	n/a
4	chr4:188916709-188916759	IMR90	lung:	fetal
5	chr4:188913931-188913981	ovcar-3	ovarian:	n/a
6	chr4:188916724-188916774	ovcar-3	ovarian:	n/a
7	chr4:188924717-188924767	GM06990	blood:	n/a
8	chr4:188916709-188916759	IMR90	lung:	fetal
9	chr4:188916709-188916759	NHBE	bronchial:	n/a
10	chr4:188963430-188963480	NB4	blood:	n/a
11	chr4:188854221-188854271	HepG2	liver:	n/a
12	chr4:188854221-188854271	HAEpiC	amniotic membrane:	n/a
13	chr4:188918072-188918122	CMK	blood:	n/a
14	chr4:188858971-188859021	H1-hESC	embryonic stem cell:	embryo
15	chr4:188953586-188953636	HNPCEpiC	eye:	n/a
16	chr4:188895390-188895440	HCM	heart:	n/a
17	chr4:188953586-188953636	HAEpiC	amniotic membrane:	n/a
18	chr4:188953527-188953577	SKMC	muscle:	n/a
19	chr4:188953527-188953577	HepG2	liver:	n/a
20	chr4:188916726-188916776	HCF	heart:	n/a
21	chr4:188953092-188953142	HCPEpiC	choroid plexus:	n/a
22	chr4:188858971-188859021	HUVEC	blood vessel:	n/a
23	chr4:188963324-188963374	HRPEpiC	eye:	n/a
24	chr4:188917251-188917301	HEK293	kidney:	embryo
25	chr4:188953178-188953228	HEK293	kidney:	embryo
26	chr4:188916496-188916546	GM12892	blood:	n/a
27	chr4:188953092-188953142	HEEpiC	esophagus:	n/a
28	chr4:188843522-188843572	AoSMC	blood vessel:	n/a
29	chr4:188918931-188918981	NHDF-neo	bronchial:	n/a
30	chr4:188858709-188858759	PrEC	prostate:	n/a
31	chr4:188915407-188915457	CMK	blood:	n/a
32	chr4:188916875-188916925	CMK	blood:	n/a
33	chr4:188917173-188917223	Hepatocyte	liver:	n/a
34	chr4:188953178-188953228	HCT-116	colon:	n/a
35	chr4:188916814-188916864	ProgFib	skin:	n/a
36	chr4:188963324-188963374	RPTEC	kidney:	n/a
37	chr4:188915407-188915457	HRPEpiC	eye:	n/a
38	chr4:188916724-188916774	HMEC	breast:	n/a
39	chr4:188858709-188858759	HCM	heart:	n/a
40	chr4:188924612-188924662	Jurkat	blood:	n/a
41	chr4:188895421-188895471	PFSK-1	brain:	n/a
42	chr4:188953586-188953636	GM12878	blood:	n/a
43	chr4:188917856-188917906	K562	blood:	n/a
44	chr4:188916865-188916915	Hela-S3	cervix:	n/a
45	chr4:188924717-188924767	HCPEpiC	choroid plexus:	n/a
46	chr4:188843522-188843572	HRE	kidney:	n/a
47	chr4:188895390-188895440	SK-N-MC	brain:	n/a
48	chr4:188917251-188917301	HRPEpiC	eye:	n/a
49	chr4:188916875-188916925	HepG2	liver:	n/a
50	chr4:188858709-188858759	BJ	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188914670..188915671-chr4:189167438..189168869,4	MCF-7	breast:
2	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
3	chr4:188936272..188938284-chr4:188943091..188945323,2	MCF-7	breast:
4	chr4:188955745..188958212-chr4:188967134..188969834,2	K562	blood:
5	chr4:188914697..188915636-chr4:189293778..189294511,3	MCF-7	breast:
6	chr4:188959730..188961356-chr4:188968354..188971076,2	MCF-7	breast:
7	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
8	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
9	chr4:188914709..188915626-chr4:189293756..189294718,5	MCF-7	breast:
10	chr4:188936272..188938284-chr4:188943091..188945323,2	MCF-7	breast:
11	chr4:188955745..188958212-chr4:188967134..188969834,2	K562	blood:
12	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
13	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
14	chr4:188959730..188961356-chr4:188968354..188971076,2	MCF-7	breast:
15	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-8	chr4:188863112-188863571	l_2822_chr4:188790794-188818331_testes
2	lnc-TRIML2-2	chr4:188881751-188881835	NONHSAT099725
3	lnc-ZFP42-8	chr4:188869892-188870239	l_2822_chr4:188790794-188818331_testes
4	lnc-TRIML2-2	chr4:188866788-188867016	XLOC_004222
5	lnc-TRIML2-2	chr4:188881466-188881648	XLOC_004222
6	lnc-TRIML2-2	chr4:188908697-188908733	NONHSAT099726
7	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099726
8	lnc-TRIML2-2	chr4:188881466-188881649	NONHSAT099725
9	lnc-TRIML2-2	chr4:188866817-188867016	NONHSAT099725
10	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099725

No data

Variant related genes	Relation type
ZFP42	TF binding region
ENSG00000213331	TF binding region
ZFP42	CpG island
ENSG00000213331	CpG island

Extended variants
information (count: 4257 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4257 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373774604	chr4:188842045-188842046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574361757	chr4:188842061-188842062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540150178	chr4:188842067-188842068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560053815	chr4:188842071-188842072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567660475	chr4:188842097-188842098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs386683693	chr4:188842148-188842149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112658681	chr4:188842149-188842150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6813666	chr4:188842150-188842151	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs531466201	chr4:188842160-188842161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186898046	chr4:188842189-188842190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191109643	chr4:188842201-188842202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6813823	chr4:188842209-188842210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569780728	chr4:188842218-188842219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182411511	chr4:188842226-188842227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530380417	chr4:188842331-188842332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375300187	chr4:188842370-188842371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567200884	chr4:188842372-188842373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538646805	chr4:188842380-188842381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558945650	chr4:188842389-188842390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568988451	chr4:188842483-188842484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188290949	chr4:188842490-188842491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558756269	chr4:188842492-188842493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192524512	chr4:188842497-188842498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376324385	chr4:188842555-188842556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574301637	chr4:188842599-188842600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540473493	chr4:188842638-188842639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577012785	chr4:188842680-188842681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs151258898	chr4:188842703-188842704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577105629	chr4:188842718-188842719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545463969	chr4:188842823-188842824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184488209	chr4:188842830-188842831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187321205	chr4:188842945-188842946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78173034	chr4:188842949-188842950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370431437	chr4:188842997-188842998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531402615	chr4:188842999-188843000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535335180	chr4:188843020-188843021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541956585	chr4:188843043-188843044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192626248	chr4:188843055-188843056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140360339	chr4:188843107-188843108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547212967	chr4:188843162-188843163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184784858	chr4:188843200-188843201	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs572366161	chr4:188843213-188843214	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs190254687	chr4:188843291-188843292	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs6553113	chr4:188843305-188843306	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs568925054	chr4:188843314-188843315	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs572029470	chr4:188843352-188843353	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs78891938	chr4:188843356-188843357	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs542221152	chr4:188843364-188843365	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs554646143	chr4:188843397-188843398	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs568261874	chr4:188843407-188843408	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Cognitive impairment	21505072	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188842000-188844400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:188842600-188843600	Enhancers	Brain Germinal Matrix	brain
3	chr4:188843200-188843400	Bivalent Enhancer	Fetal Brain Male	brain
4	chr4:188843400-188843800	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr4:188843400-188843800	Enhancers	Fetal Lung	lung
6	chr4:188843800-188844200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:188849800-188850000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:188850000-188850200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:188850000-188850600	Enhancers	Lung	lung
10	chr4:188850200-188850400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:188850200-188850800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:188850400-188851000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:188850600-188850800	ZNF genes & repeats	Lung	lung
14	chr4:188850600-188850800	Bivalent Enhancer	Right Ventricle	heart
15	chr4:188850600-188851000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:188851000-188851400	ZNF genes & repeats	Fetal Stomach	stomach
17	chr4:188851000-188853200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr4:188851400-188856000	Weak transcription	Fetal Stomach	stomach
19	chr4:188853200-188854800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr4:188854200-188856200	Enhancers	Ovary	ovary
21	chr4:188855800-188856200	Enhancers	Fetal Kidney	kidney
22	chr4:188855800-188856600	Enhancers	Fetal Muscle Leg	muscle
23	chr4:188855800-188856800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr4:188856000-188856800	Enhancers	Fetal Stomach	stomach
25	chr4:188856200-188857000	Weak transcription	Ovary	ovary
26	chr4:188857000-188857200	Enhancers	Ovary	ovary
27	chr4:188860000-188860400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:188860800-188861600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr4:188861400-188861800	Enhancers	Fetal Lung	lung
30	chr4:188863800-188864000	ZNF genes & repeats	Pancreas	Pancrea
31	chr4:188865000-188866200	Enhancers	Brain Hippocampus Middle	brain
32	chr4:188865000-188866400	Enhancers	Brain Substantia Nigra	brain
33	chr4:188865200-188866400	Enhancers	Brain Cingulate Gyrus	brain
34	chr4:188865200-188866600	Enhancers	Brain Angular Gyrus	brain
35	chr4:188879000-188879200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr4:188879200-188879600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:188879400-188879600	ZNF genes & repeats	Right Atrium	heart
38	chr4:188879600-188883800	Weak transcription	Right Atrium	heart
39	chr4:188881800-188882000	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr4:188881800-188884800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:188882000-188882200	Enhancers	Brain Substantia Nigra	brain
42	chr4:188882000-188882800	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr4:188882400-188882600	Enhancers	Brain Hippocampus Middle	brain
44	chr4:188882400-188883600	Weak transcription	Brain Substantia Nigra	brain
45	chr4:188882600-188883800	Weak transcription	Brain Hippocampus Middle	brain
46	chr4:188882800-188883000	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr4:188883000-188883800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr4:188883000-188884000	Enhancers	Fetal Lung	lung
49	chr4:188883600-188883800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr4:188883600-188883800	Enhancers	Fetal Stomach	stomach

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