Variant report

Variant	esv1842873
Chromosome Location	chr4:20361842-20399168
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	BACH1	chr4:20372120-20372177	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:20382652-20383001	HepG2	liver:	n/a	chr4:20382826-20382837
3	CEBPB	chr4:20382644-20383018	H1-hESC	embryonic stem cell:	n/a	chr4:20382826-20382837
4	CEBPB	chr4:20382713-20382943	Hela-S3	cervix:	n/a	chr4:20382826-20382837
5	CEBPB	chr4:20382715-20383056	ECC-1	luminal epithelium:	n/a	chr4:20382826-20382837
6	CEBPB	chr4:20367156-20367378	H1-hESC	embryonic stem cell:	n/a	chr4:20367242-20367253
7	CEBPB	chr4:20382650-20383016	IMR90	lung:	n/a	chr4:20382826-20382837
8	CEBPB	chr4:20382674-20382986	ECC-1	luminal epithelium:	n/a	chr4:20382826-20382837
9	CEBPB	chr4:20367189-20367412	HepG2	liver:	n/a	chr4:20367242-20367253
10	CEBPB	chr4:20382680-20382932	A549	lung:	n/a	chr4:20382826-20382837
11	CEBPB	chr4:20382662-20383018	K562	blood:	n/a	chr4:20382826-20382837
12	CTCF	chr4:20396880-20397078	GM19239	blood:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
13	CTCF	chr4:20370940-20371090	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr4:20396880-20397030	K562	blood:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
15	CTCF	chr4:20396920-20397070	HCT-116	colon:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
16	CTCF	chr4:20396767-20397202	GM12878	blood:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
17	CTCF	chr4:20396900-20397050	Caco-2	colon:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
18	CTCF	chr4:20396960-20397110	NHDF-neo	bronchial:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
19	CTCF	chr4:20396844-20397083	A549	lung:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
20	CTCF	chr4:20396920-20397070	AG04449	skin:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
21	CTCF	chr4:20396880-20397030	SAEC	small airway:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
22	CTCF	chr4:20396960-20397110	K562	blood:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
23	CTCF	chr4:20396940-20397090	HCM	heart:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
24	CTCF	chr4:20396940-20397090	GM12872	blood:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
25	CTCF	chr4:20396900-20397050	AG09319	gingival:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
26	CTCF	chr4:20396960-20397110	HCT-116	colon:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
27	CTCF	chr4:20396900-20397050	HPAF	blood vessel:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
28	CTCF	chr4:20396897-20397081	GM12892	blood:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
29	CTCF	chr4:20396920-20397070	AoAF	blood vessel:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
30	CTCF	chr4:20396784-20397094	SK-N-SH_RA	brain:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
31	CTCF	chr4:20396900-20397050	BJ	skin:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
32	CTCF	chr4:20396880-20397030	HEK293	kidney:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
33	CTCF	chr4:20396876-20397082	Pancreas_OC	pancreas:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
34	CTCF	chr4:20396849-20397054	SK-N-SH_RA	brain:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
35	CTCF	chr4:20396860-20397010	GM12864	blood:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
36	CTCF	chr4:20396756-20397136	H1-hESC	embryonic stem cell:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
37	CTCF	chr4:20396880-20397030	HBMEC	blood vessel:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
38	CTCF	chr4:20396960-20397110	GM12866	blood:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
39	CTCF	chr4:20396900-20397050	AG04449	skin:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
40	CTCF	chr4:20396775-20397129	MCF-7	breast:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
41	CTCF	chr4:20396900-20397050	MCF-7	breast:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
42	CTCF	chr4:20396880-20397030	SK-N-SH_RA	brain:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
43	CTCF	chr4:20396920-20397070	HCPEpiC	choroid plexus:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
44	CTCF	chr4:20396755-20397194	A549	lung:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
45	CTCF	chr4:20396940-20397090	BE2_C	brain:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
46	CTCF	chr4:20397284-20397330	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr4:20396920-20397070	AG04450	lung:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
48	CTCF	chr4:20396850-20397103	Hela-S3	cervix:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
49	CTCF	chr4:20396940-20397090	HBMEC	blood vessel:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998
50	CTCF	chr4:20396900-20397050	AG09309	skin:	n/a	chr4:20396984-20397005 chr4:20396984-20396992 chr4:20396982-20397000 chr4:20396985-20396998

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20393304-20393354	AG09309	skin:	n/a
2	chr4:20393304-20393354	AG09309	skin:	n/a
3	chr4:20396867-20396917	NB4	blood:	n/a
4	chr4:20393304-20393354	ovcar-3	ovarian:	n/a
5	chr4:20393304-20393354	LNCaP	prostate:	n/a
6	chr4:20396867-20396917	HEK293	kidney:	embryo
7	chr4:20393304-20393354	PrEC	prostate:	n/a
8	chr4:20396867-20396917	HRCEpiC	kidney:	n/a
9	chr4:20393304-20393354	BJ	skin:	n/a
10	chr4:20396867-20396917	SK-N-SH	brain:	n/a
11	chr4:20396867-20396917	MCF-7	breast:	n/a
12	chr4:20393304-20393354	HRE	kidney:	n/a
13	chr4:20396867-20396917	NHBE	bronchial:	n/a
14	chr4:20396867-20396917	HMEC	breast:	n/a
15	chr4:20393304-20393354	T-47D	breast:	n/a
16	chr4:20396867-20396917	NH-A	brain:	n/a
17	chr4:20393304-20393354	HCF	heart:	n/a
18	chr4:20396867-20396917	AG10803	skin:	n/a
19	chr4:20396867-20396917	K562	blood:	n/a
20	chr4:20393304-20393354	AG04450	lung:	fetal
21	chr4:20393304-20393354	ProgFib	skin:	n/a
22	chr4:20393304-20393354	HCT-116	colon:	n/a
23	chr4:20396867-20396917	HIPEpiC	eye:	n/a
24	chr4:20396867-20396917	HCPEpiC	choroid plexus:	n/a
25	chr4:20393304-20393354	HMEC	breast:	n/a
26	chr4:20396867-20396917	IMR90	lung:	fetal
27	chr4:20396867-20396917	Hepatocyte	liver:	n/a
28	chr4:20393304-20393354	A549	lung:	n/a
29	chr4:20396867-20396917	HepG2	liver:	n/a
30	chr4:20393304-20393354	NHDF-neo	bronchial:	n/a
31	chr4:20396867-20396917	PANC-1	pancreas:	n/a
32	chr4:20393304-20393354	HRCEpiC	kidney:	n/a
33	chr4:20393304-20393354	U87	brain:	n/a
34	chr4:20396867-20396917	AG09309	skin:	n/a
35	chr4:20393304-20393354	CMK	blood:	n/a
36	chr4:20393304-20393354	PANC-1	pancreas:	n/a
37	chr4:20396867-20396917	SKMC	muscle:	n/a
38	chr4:20396867-20396917	RPTEC	kidney:	n/a
39	chr4:20393304-20393354	IMR90	lung:	fetal
40	chr4:20393304-20393354	HepG2	liver:	n/a
41	chr4:20396867-20396917	BE2_C	brain:	n/a
42	chr4:20396867-20396917	ECC-1	luminal epithelium:	n/a
43	chr4:20393304-20393354	Caco-2	colon:	n/a
44	chr4:20393304-20393354	NB4	blood:	n/a
45	chr4:20396867-20396917	HUVEC	blood vessel:	n/a
46	chr4:20393304-20393354	HNPCEpiC	eye:	n/a
47	chr4:20396867-20396917	HCT-116	colon:	n/a
48	chr4:20396867-20396917	A549	lung:	n/a
49	chr4:20396867-20396917	MCF10A-Er-Src	breast:	n/a
50	chr4:20396867-20396917	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20396690..20397420-chr7:28961135..28962065,2	MCF-7	breast:
2	chr4:20396516..20397430-chr4:20546057..20546973,2	K562	blood:
3	chr4:20394669..20396479-chr4:20401763..20404703,2	MCF-7	breast:
4	chr4:20386359..20388328-chr4:20392211..20395189,2	K562	blood:
5	chr4:19310650..19311557-chr4:20396987..20397490,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-1	chr4:20393812-20393886	ENSG00000248228.1
2	lnc-PACRGL-1	chr4:20394973-20395076	ENSG00000248228.1
3	lnc-PACRGL-1	chr4:20396152-20396479	ENSG00000248228.1
4	lnc-PACRGL-1	chr4:20395189-20395282	ENSG00000248228.1

Variant related genes	Relation type
SLIT2-IT1	TF binding region
SLIT2-IT1	CpG island
ENSG00000248228	chromatin interactions

Extended variants
information (count: 1510 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1510 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6447958	chr4:20361842-20361843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114471436	chr4:20361873-20361874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562632210	chr4:20361910-20361911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145318104	chr4:20361977-20361978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527400557	chr4:20362017-20362018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570403756	chr4:20362040-20362041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533923246	chr4:20362054-20362055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551866548	chr4:20362059-20362060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540676492	chr4:20362124-20362125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4368605	chr4:20362183-20362184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145075037	chr4:20362241-20362242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537587494	chr4:20362246-20362247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs398107063	chr4:20362247-20362248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556450472	chr4:20362307-20362308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574647905	chr4:20362310-20362311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535685347	chr4:20362370-20362371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554376751	chr4:20362395-20362396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538000045	chr4:20362417-20362418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572425067	chr4:20362421-20362422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147655605	chr4:20362430-20362431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79249439	chr4:20362457-20362458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140724808	chr4:20362461-20362462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149789384	chr4:20362462-20362463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562790983	chr4:20362514-20362515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145773115	chr4:20362526-20362527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79782125	chr4:20362542-20362543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148963086	chr4:20362555-20362556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189340664	chr4:20362620-20362621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181957150	chr4:20362631-20362632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570075790	chr4:20362639-20362640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184270746	chr4:20362659-20362660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143756858	chr4:20362680-20362681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4406013	chr4:20362716-20362717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556212140	chr4:20362726-20362727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554066919	chr4:20362733-20362734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145647748	chr4:20362748-20362749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148274149	chr4:20362755-20362756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566303863	chr4:20362777-20362778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189166953	chr4:20362791-20362792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181058311	chr4:20362794-20362795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10694794	chr4:20362885-20362886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs36034375	chr4:20362886-20362887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77835647	chr4:20362891-20362892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114306096	chr4:20362894-20362895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114345971	chr4:20362902-20362903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186299408	chr4:20362922-20362923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574553365	chr4:20362931-20362932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542019897	chr4:20362941-20362942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542154087	chr4:20362961-20362962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113039899	chr4:20362975-20362976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20353400-20369200	Weak transcription	Pancreas	Pancrea
2	chr4:20353600-20369200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:20353800-20375600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:20356200-20363800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:20357000-20368400	Weak transcription	NHDF-Ad	bronchial
6	chr4:20357000-20369000	Weak transcription	Osteobl	bone
7	chr4:20358400-20368200	Weak transcription	NHLF	lung
8	chr4:20358600-20366800	Weak transcription	Fetal Lung	lung
9	chr4:20358600-20371000	Weak transcription	Brain Anterior Caudate	brain
10	chr4:20358800-20365400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr4:20359000-20363600	Weak transcription	Brain Angular Gyrus	brain
12	chr4:20359000-20363600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr4:20359400-20363600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:20359800-20365000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:20360000-20368200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:20361000-20368600	Weak transcription	NHEK	skin
17	chr4:20363600-20364000	Enhancers	Brain Angular Gyrus	brain
18	chr4:20363600-20364000	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr4:20363600-20364200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:20363800-20364000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:20363800-20364000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:20363800-20364000	Enhancers	Aorta	Aorta
23	chr4:20364000-20365400	Weak transcription	Brain Angular Gyrus	brain
24	chr4:20364000-20369400	Weak transcription	Aorta	Aorta
25	chr4:20364000-20370800	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr4:20364000-20375400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:20364200-20364600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:20364600-20365000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr4:20364600-20366200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:20365000-20365200	Enhancers	Brain Cingulate Gyrus	brain
31	chr4:20365000-20367400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:20365200-20365600	Weak transcription	Brain Cingulate Gyrus	brain
33	chr4:20365400-20365800	Active TSS	Brain Angular Gyrus	brain
34	chr4:20365400-20366200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:20365600-20366000	Active TSS	Brain Cingulate Gyrus	brain
36	chr4:20365600-20366000	Active TSS	Brain Hippocampus Middle	brain
37	chr4:20365600-20370800	Weak transcription	Brain Substantia Nigra	brain
38	chr4:20365800-20366000	Enhancers	Brain Angular Gyrus	brain
39	chr4:20366000-20366400	Enhancers	Brain Hippocampus Middle	brain
40	chr4:20366000-20375600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr4:20366200-20369200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:20366400-20366800	Weak transcription	Brain Hippocampus Middle	brain
43	chr4:20366400-20371000	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr4:20366800-20367000	Enhancers	Brain Hippocampus Middle	brain
45	chr4:20366800-20367400	Strong transcription	Fetal Lung	lung
46	chr4:20367000-20367400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:20367000-20370800	Weak transcription	Brain Hippocampus Middle	brain
48	chr4:20367000-20371000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr4:20367400-20368600	Weak transcription	Fetal Lung	lung
50	chr4:20367400-20369200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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