Variant report

Variant	nsv879001
Chromosome Location	chr4:46823634-46893766
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	chr4:46839805-46840062	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:46891431-46891841	HepG2	liver:	n/a	chr4:46891740-46891756 chr4:46891741-46891757
3	ARID3A	chr4:46846361-46846708	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:46846410-46846771	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:46877475-46877675	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:46856358-46856637	HepG2	liver:	n/a	chr4:46856496-46856507
7	CEBPB	chr4:46851181-46851393	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:46837106-46837429	A549	lung:	n/a	chr4:46837309-46837320
9	CEBPB	chr4:46881514-46881734	HepG2	liver:	n/a	chr4:46881621-46881632 chr4:46881619-46881632 chr4:46881619-46881630
10	CEBPB	chr4:46837117-46837445	HepG2	liver:	n/a	chr4:46837309-46837320
11	CEBPB	chr4:46881445-46881657	IMR90	lung:	n/a	chr4:46881621-46881632 chr4:46881619-46881632 chr4:46881619-46881630
12	CEBPB	chr4:46839806-46839908	HepG2	liver:	n/a	n/a
13	CTCF	chr4:46846420-46846570	GM12868	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
14	CTCF	chr4:46888840-46888990	BE2_C	brain:	n/a	n/a
15	CTCF	chr4:46846480-46846630	HEEpiC	esophagus:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
16	CTCF	chr4:46846500-46846650	HMF	breast:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
17	CTCF	chr4:46846460-46846610	GM12873	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
18	CTCF	chr4:46846420-46846570	HepG2	liver:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
19	CTCF	chr4:46846420-46846570	HVMF	connective:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
20	CTCF	chr4:46888778-46889095	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr4:46846451-46846612	GM13976	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
22	CTCF	chr4:46846520-46846670	GM12865	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
23	CTCF	chr4:46846393-46846706	Medullo	brain:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
24	CTCF	chr4:46888860-46889010	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr4:46890686-46890724	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr4:46888860-46889010	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr4:46888908-46888995	GM13977	blood:	n/a	n/a
28	CTCF	chr4:46846434-46846628	MCF-7	breast:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
29	CTCF	chr4:46846440-46846590	GM12867	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
30	CTCF	chr4:46846460-46846610	GM12878	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
31	CTCF	chr4:46846420-46846570	WERI-Rb-1	eye:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
32	CTCF	chr4:46846407-46846657	GM10266	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
33	CTCF	chr4:46846460-46846610	BE2_C	brain:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
34	CTCF	chr4:46846411-46846654	MCF-7	breast:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
35	CTCF	chr4:46888860-46889010	RPTEC	kidney:	n/a	n/a
36	CTCF	chr4:46846460-46846610	GM06990	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
37	CTCF	chr4:46846407-46846657	GM13977	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
38	CTCF	chr4:46888880-46889030	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr4:46846416-46846575	A549	lung:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
40	CTCF	chr4:46846460-46846610	HPF	lung:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
41	CTCF	chr4:46888840-46888990	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr4:46846480-46846630	AG04449	skin:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
43	CTCF	chr4:46846420-46846570	MCF-7	breast:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
44	CTCF	chr4:46846400-46846550	A549	lung:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
45	CTCF	chr4:46846440-46846590	HRPEpiC	eye:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
46	CTCF	chr4:46888900-46889050	GM12870	blood:	n/a	n/a
47	CTCF	chr4:46888846-46889031	Medullo	brain:	n/a	n/a
48	CTCF	chr4:46846440-46846590	SK-N-SH_RA	brain:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
49	CTCF	chr4:46846480-46846630	AG10803	skin:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
50	CTCF	chr4:46888820-46888970	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:46848264-46848314	CMK	blood:	n/a
2	chr4:46848264-46848314	CMK	blood:	n/a
3	chr4:46848264-46848314	GM06990	blood:	n/a
4	chr4:46848264-46848314	ovcar-3	ovarian:	n/a
5	chr4:46874750-46874800	BJ	skin:	n/a
6	chr4:46874750-46874800	T-47D	breast:	n/a
7	chr4:46874750-46874800	AG04450	lung:	fetal
8	chr4:46848264-46848314	HRE	kidney:	n/a
9	chr4:46874750-46874800	K562	blood:	n/a
10	chr4:46848264-46848314	GM12878	blood:	n/a
11	chr4:46848264-46848314	MCF-7	breast:	n/a
12	chr4:46848264-46848314	BJ	skin:	n/a
13	chr4:46874750-46874800	MCF10A-Er-Src	breast:	n/a
14	chr4:46874750-46874800	HEEpiC	esophagus:	n/a
15	chr4:46848264-46848314	HRCEpiC	kidney:	n/a
16	chr4:46848264-46848314	H1-hESC	embryonic stem cell:	embryo
17	chr4:46848264-46848314	HEEpiC	esophagus:	n/a
18	chr4:46874750-46874800	HAEpiC	amniotic membrane:	n/a
19	chr4:46848264-46848314	SK-N-SH_RA	brain:	n/a
20	chr4:46848264-46848314	HCPEpiC	choroid plexus:	n/a
21	chr4:46848264-46848314	BE2_C	brain:	n/a
22	chr4:46848264-46848314	HAEpiC	amniotic membrane:	n/a
23	chr4:46848264-46848314	PANC-1	pancreas:	n/a
24	chr4:46874750-46874800	SK-N-SH_RA	brain:	n/a
25	chr4:46874750-46874800	PANC-1	pancreas:	n/a
26	chr4:46848264-46848314	AG09309	skin:	n/a
27	chr4:46848264-46848314	AoSMC	blood vessel:	n/a
28	chr4:46848264-46848314	SK-N-SH	brain:	n/a
29	chr4:46874750-46874800	ovcar-3	ovarian:	n/a
30	chr4:46848264-46848314	Jurkat	blood:	n/a
31	chr4:46874750-46874800	PrEC	prostate:	n/a
32	chr4:46848264-46848314	IMR90	lung:	fetal
33	chr4:46848264-46848314	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:46848264-46848314	GM12892	blood:	n/a
35	chr4:46874750-46874800	HCF	heart:	n/a
36	chr4:46848264-46848314	SAEC	small airway:	n/a
37	chr4:46874750-46874800	IMR90	lung:	fetal
38	chr4:46874750-46874800	Caco-2	colon:	n/a
39	chr4:46874750-46874800	HepG2	liver:	n/a
40	chr4:46874750-46874800	GM12892	blood:	n/a
41	chr4:46874750-46874800	HRCEpiC	kidney:	n/a
42	chr4:46848264-46848314	AG04450	lung:	fetal
43	chr4:46874750-46874800	HIPEpiC	eye:	n/a
44	chr4:46848264-46848314	PrEC	prostate:	n/a
45	chr4:46874750-46874800	AoSMC	blood vessel:	n/a
46	chr4:46874750-46874800	MCF-7	breast:	n/a
47	chr4:46874750-46874800	HRE	kidney:	n/a
48	chr4:46848264-46848314	AG04449	skin:	fetal
49	chr4:46874750-46874800	AG09309	skin:	n/a
50	chr4:46848264-46848314	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:46330783..46331886-chr4:46888450..46889607,5	MCF-7	breast:
2	chr4:46846051..46846972-chr4:46888430..46889502,3	MCF-7	breast:
3	chr4:46846051..46846972-chr4:46888430..46889502,3	MCF-7	breast:
4	chr4:46847631..46849555-chr4:46863205..46865317,2	K562	blood:
5	chr4:46847631..46849555-chr4:46863205..46865317,2	K562	blood:
6	chr4:46845685..46846601-chr4:47385587..47386221,2	MCF-7	breast:
7	chr4:46846275..46847133-chr4:47386047..47386599,2	K562	blood:
8	chr4:46846116..46847033-chr4:47034348..47035254,4	MCF-7	breast:

Variant related genes	Relation type
COX7B2	TF binding region
COX7B2	CpG island

Extended variants
information (count: 1046 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571390541	chr4:46832810-46832811	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs149084143	chr4:46832822-46832823	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs143145336	chr4:46832827-46832828	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs151059665	chr4:46832828-46832829	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs114570038	chr4:46832882-46832883	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs112702347	chr4:46832904-46832905	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs532490916	chr4:46832917-46832918	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs553546187	chr4:46832918-46832919	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs186252683	chr4:46832923-46832924	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs189107367	chr4:46832924-46832925	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs530282724	chr4:46832926-46832927	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs548935463	chr4:46832935-46832936	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs142399036	chr4:46832938-46832939	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs181676169	chr4:46832940-46832941	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs116068748	chr4:46832946-46832947	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs186689913	chr4:46832957-46832958	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs191275964	chr4:46832966-46832967	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs536063685	chr4:46832969-46832970	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs532582168	chr4:46832988-46832989	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs114272077	chr4:46832995-46832996	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs11735590	chr4:46833044-46833045	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs535254416	chr4:46833079-46833080	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs553675790	chr4:46833080-46833081	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs183140025	chr4:46833149-46833150	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs534238382	chr4:46833160-46833161	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs558689242	chr4:46833173-46833174	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs185319314	chr4:46833174-46833175	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs367716823	chr4:46833184-46833185	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs544395736	chr4:46833195-46833196	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs112455403	chr4:46833231-46833232	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs112554083	chr4:46833240-46833241	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs113590085	chr4:46833241-46833242	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs545008869	chr4:46833257-46833258	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs28396265	chr4:46833294-46833295	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs183538957	chr4:46833301-46833302	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs560808821	chr4:46833315-46833316	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs577328070	chr4:46833333-46833334	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs528003112	chr4:46833338-46833339	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs552792170	chr4:46833349-46833350	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs567496471	chr4:46833352-46833353	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs374445373	chr4:46833366-46833367	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs563945970	chr4:46833387-46833388	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs531299158	chr4:46833388-46833389	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187832016	chr4:46833400-46833401	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs551267030	chr4:46837309-46837310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377305832	chr4:46837313-46837314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536238187	chr4:46837353-46837354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535833029	chr4:46837357-46837358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554733262	chr4:46837366-46837367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566435720	chr4:46837375-46837376	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	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
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46832800-46833400	Active TSS	Spleen	Spleen
2	chr4:46837200-46840800	Enhancers	Liver	Liver
3	chr4:46839000-46841600	Enhancers	HepG2	liver
4	chr4:46839400-46839600	Enhancers	Brain Hippocampus Middle	brain
5	chr4:46839600-46840600	Weak transcription	Brain Hippocampus Middle	brain
6	chr4:46840000-46843000	Enhancers	Brain Substantia Nigra	brain
7	chr4:46840400-46841600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr4:46840400-46842200	Enhancers	Brain Angular Gyrus	brain
9	chr4:46840400-46842600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr4:46840600-46840800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr4:46840600-46841200	Enhancers	Brain Hippocampus Middle	brain
12	chr4:46840600-46841800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:46840600-46842200	Enhancers	Brain Cingulate Gyrus	brain
14	chr4:46840600-46842200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr4:46840800-46841200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr4:46840800-46841400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:46840800-46841400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr4:46840800-46841600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:46841000-46841400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr4:46841000-46841600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:46841200-46841600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr4:46841200-46841600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr4:46841200-46841600	Flanking Active TSS	Brain Hippocampus Middle	brain
24	chr4:46841400-46842200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr4:46841600-46843400	Enhancers	Brain Hippocampus Middle	brain
26	chr4:46842200-46842800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr4:46842200-46846400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr4:46842600-46848400	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr4:46842800-46843000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr4:46845600-46846800	Enhancers	Adipose Nuclei	Adipose
31	chr4:46846400-46846800	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr4:46846600-46846800	Enhancers	Fetal Lung	lung
33	chr4:46846800-46847200	Enhancers	Fetal Brain Male	brain
34	chr4:46847200-46849400	Weak transcription	Fetal Brain Male	brain
35	chr4:46849400-46850000	Enhancers	Fetal Brain Male	brain
36	chr4:46851600-46852800	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr4:46852800-46853200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr4:46852800-46853200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:46852800-46853200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr4:46852800-46853200	Enhancers	Fetal Intestine Large	intestine
41	chr4:46853000-46853200	Bivalent Enhancer	Fetal Lung	lung
42	chr4:46853200-46853400	Enhancers	Fetal Lung	lung
43	chr4:46854800-46855000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:46854800-46855000	Enhancers	Aorta	Aorta
45	chr4:46858200-46858600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:46858400-46860000	Enhancers	Adipose Nuclei	Adipose
47	chr4:46858800-46860000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr4:46863600-46864400	Enhancers	Fetal Brain Male	brain
49	chr4:46865800-46866400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:46866000-46866600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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