Variant report

Variant	nsv878999
Chromosome Location	chr4:46565663-46860626
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	chr4:46846361-46846708	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:46839805-46840062	HepG2	liver:	n/a	n/a
3	BATF	chr4:46604467-46604700	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:46846410-46846771	GM12878	blood:	n/a	n/a
5	BRCA1	chr4:46757106-46757116	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:46813754-46813779	GM12878	blood:	n/a	n/a
7	CCNT2	chr4:46711119-46711313	K562	blood:	n/a	n/a
8	CEBPB	chr4:46837106-46837429	A549	lung:	n/a	chr4:46837309-46837320
9	CEBPB	chr4:46608580-46608751	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:46787591-46787693	HepG2	liver:	n/a	chr4:46787614-46787627
11	CEBPB	chr4:46611326-46611653	HepG2	liver:	n/a	chr4:46611479-46611488
12	CEBPB	chr4:46611345-46611641	IMR90	lung:	n/a	chr4:46611479-46611488
13	CEBPB	chr4:46650166-46650506	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr4:46856358-46856637	HepG2	liver:	n/a	chr4:46856496-46856507
15	CEBPB	chr4:46769948-46770292	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:46670599-46670937	HepG2	liver:	n/a	chr4:46670759-46670772 chr4:46670759-46670772 chr4:46670760-46670771
17	CEBPB	chr4:46837117-46837445	HepG2	liver:	n/a	chr4:46837309-46837320
18	CEBPB	chr4:46769957-46770292	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:46769999-46770252	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:46839806-46839908	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:46670606-46670927	A549	lung:	n/a	chr4:46670759-46670772 chr4:46670759-46670772 chr4:46670760-46670771
22	CEBPB	chr4:46670638-46670838	Hela-S3	cervix:	n/a	chr4:46670759-46670772 chr4:46670759-46670772 chr4:46670760-46670771
23	CEBPB	chr4:46770004-46770192	A549	lung:	n/a	n/a
24	CEBPB	chr4:46630064-46630372	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:46770005-46770242	K562	blood:	n/a	n/a
26	CEBPB	chr4:46851181-46851393	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:46670619-46670896	H1-hESC	embryonic stem cell:	n/a	chr4:46670759-46670772 chr4:46670759-46670772 chr4:46670760-46670771
28	CHD2	chr4:46678461-46678551	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr4:46846440-46846590	HFF	foreskin:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
30	CTCF	chr4:46717620-46717770	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr4:46846480-46846630	HMEC	breast:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
32	CTCF	chr4:46650280-46650430	NHEK	skin:	n/a	n/a
33	CTCF	chr4:46846420-46846570	Hela-S3	cervix:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
34	CTCF	chr4:46650300-46650450	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:46650260-46650410	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr4:46846270-46846705	HepG2	liver:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
37	CTCF	chr4:46846408-46846670	GM12878	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
38	CTCF	chr4:46650247-46650482	HepG2	liver:	n/a	n/a
39	CTCF	chr4:46717620-46717770	BE2_C	brain:	n/a	n/a
40	CTCF	chr4:46846520-46846670	HMEC	breast:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
41	CTCF	chr4:46650260-46650410	GM06990	blood:	n/a	n/a
42	CTCF	chr4:46846500-46846650	GM12865	blood:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
43	CTCF	chr4:46698861-46698902	GM20000	blood:	n/a	n/a
44	CTCF	chr4:46846433-46846615	A549	lung:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
45	CTCF	chr4:46650620-46650770	GM12865	blood:	n/a	n/a
46	CTCF	chr4:46846420-46846570	MCF-7	breast:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
47	CTCF	chr4:46650260-46650410	BE2_C	brain:	n/a	n/a
48	CTCF	chr4:46846440-46846590	NHDF-neo	bronchial:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
49	CTCF	chr4:46846434-46846628	MCF-7	breast:	n/a	chr4:46846525-46846535 chr4:46846521-46846537 chr4:46846523-46846536 chr4:46846520-46846538 chr4:46846522-46846543
50	CTCF	chr4:46650220-46650370	GM12875	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:46737312-46737362	HL-60	blood:	n/a
2	chr4:46737312-46737362	HL-60	blood:	n/a
3	chr4:46737408-46737458	SK-N-SH_RA	brain:	n/a
4	chr4:46806296-46806346	AG10803	skin:	n/a
5	chr4:46737408-46737458	K562	blood:	n/a
6	chr4:46848264-46848314	MCF10A-Er-Src	breast:	n/a
7	chr4:46783754-46783804	Hela-S3	cervix:	n/a
8	chr4:46725938-46725988	ProgFib	skin:	n/a
9	chr4:46725938-46725988	HCF	heart:	n/a
10	chr4:46737408-46737458	HAEpiC	amniotic membrane:	n/a
11	chr4:46726121-46726171	HEEpiC	esophagus:	n/a
12	chr4:46806296-46806346	NHDF-neo	bronchial:	n/a
13	chr4:46783754-46783804	LNCaP	prostate:	n/a
14	chr4:46783754-46783804	NHDF-neo	bronchial:	n/a
15	chr4:46848264-46848314	HUVEC	blood vessel:	n/a
16	chr4:46725938-46725988	MCF-7	breast:	n/a
17	chr4:46848264-46848314	GM12891	blood:	n/a
18	chr4:46738197-46738247	Jurkat	blood:	n/a
19	chr4:46806296-46806346	BE2_C	brain:	n/a
20	chr4:46726121-46726171	GM06990	blood:	n/a
21	chr4:46737408-46737458	SAEC	small airway:	n/a
22	chr4:46738197-46738247	Hepatocyte	liver:	n/a
23	chr4:46737408-46737458	NH-A	brain:	n/a
24	chr4:46737312-46737362	HRE	kidney:	n/a
25	chr4:46737312-46737362	HUVEC	blood vessel:	n/a
26	chr4:46726121-46726171	HNPCEpiC	eye:	n/a
27	chr4:46725938-46725988	T-47D	breast:	n/a
28	chr4:46737408-46737458	HCM	heart:	n/a
29	chr4:46806296-46806346	BJ	skin:	n/a
30	chr4:46783754-46783804	ECC-1	luminal epithelium:	n/a
31	chr4:46726121-46726171	BJ	skin:	n/a
32	chr4:46725938-46725988	LNCaP	prostate:	n/a
33	chr4:46737408-46737458	ovcar-3	ovarian:	n/a
34	chr4:46806296-46806346	HCPEpiC	choroid plexus:	n/a
35	chr4:46726121-46726171	PFSK-1	brain:	n/a
36	chr4:46725938-46725988	Jurkat	blood:	n/a
37	chr4:46738197-46738247	CMK	blood:	n/a
38	chr4:46737408-46737458	HUVEC	blood vessel:	n/a
39	chr4:46725938-46725988	HCPEpiC	choroid plexus:	n/a
40	chr4:46806296-46806346	Hepatocyte	liver:	n/a
41	chr4:46737312-46737362	HCT-116	colon:	n/a
42	chr4:46783754-46783804	GM12891	blood:	n/a
43	chr4:46738197-46738247	SAEC	small airway:	n/a
44	chr4:46848264-46848314	HCM	heart:	n/a
45	chr4:46738197-46738247	NB4	blood:	n/a
46	chr4:46783754-46783804	T-47D	breast:	n/a
47	chr4:46737312-46737362	HCM	heart:	n/a
48	chr4:46726121-46726171	AG09309	skin:	n/a
49	chr4:46806296-46806346	HCT-116	colon:	n/a
50	chr4:46737408-46737458	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:46809130..46811667-chr4:46812436..46814342,2	K562	blood:
2	chr4:46847631..46849555-chr4:46863205..46865317,2	K562	blood:
3	chr4:46846116..46847033-chr4:47034348..47035254,4	MCF-7	breast:
4	chr4:46745874..46747839-chr4:46749414..46751916,2	MCF-7	breast:
5	chr4:46845685..46846601-chr4:47385587..47386221,2	MCF-7	breast:
6	chr4:46733082..46735429-chr4:46735919..46738940,3	K562	blood:
7	chr4:46809130..46811667-chr4:46812436..46814342,2	K562	blood:
8	chr4:46846275..46847133-chr4:47386047..47386599,2	K562	blood:
9	chr4:46733082..46735429-chr4:46735919..46738940,3	K562	blood:
10	chr4:46745874..46747839-chr4:46749414..46751916,2	MCF-7	breast:
11	chr4:46846051..46846972-chr4:46888430..46889502,3	MCF-7	breast:

Variant related genes	Relation type
RAC1P2	TF binding region
RAC1P2	CpG island

Extended variants
information (count: 2323 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536903050	chr4:46587615-46587616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549775935	chr4:46587629-46587630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76931306	chr4:46587640-46587641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576884374	chr4:46587644-46587645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77474120	chr4:46587705-46587706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116235960	chr4:46587714-46587715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539659161	chr4:46587719-46587720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142263299	chr4:46587738-46587739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187583992	chr4:46587785-46587786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146228714	chr4:46587796-46587797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190737239	chr4:46587818-46587819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573725474	chr4:46587819-46587820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4695162	chr4:46587823-46587824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559200037	chr4:46587830-46587831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533018277	chr4:46587832-46587833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370754950	chr4:46587863-46587864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555500640	chr4:46587869-46587870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560417298	chr4:46587884-46587885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563307928	chr4:46587928-46587929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182973704	chr4:46587994-46587995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187326090	chr4:46588044-46588045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530612710	chr4:46588048-46588049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77152000	chr4:46588054-46588055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567203790	chr4:46588349-46588350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191779064	chr4:46588379-46588380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs151189493	chr4:46588414-46588415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544308276	chr4:46588418-46588419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576045266	chr4:46588429-46588430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140269589	chr4:46588452-46588453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150354255	chr4:46588468-46588469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530847550	chr4:46588558-46588559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374202939	chr4:46588616-46588617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573417278	chr4:46588723-46588724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138764269	chr4:46588792-46588793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184372932	chr4:46588830-46588831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537637329	chr4:46588839-46588840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187727754	chr4:46588854-46588855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75624746	chr4:46588858-46588859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374784561	chr4:46588860-46588861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150387274	chr4:46588920-46588921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540693646	chr4:46588929-46588930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368074279	chr4:46589021-46589022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs193114841	chr4:46589068-46589069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540642725	chr4:46589073-46589074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185577267	chr4:46589208-46589209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528093229	chr4:46589216-46589217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563043179	chr4:46589258-46589259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142043533	chr4:46589309-46589310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189244762	chr4:46589311-46589312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145638571	chr4:46589404-46589405	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Cancer	20164919	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46587600-46588800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:46588400-46589000	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr4:46588400-46589600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:46588600-46589000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:46588600-46589000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:46594000-46594400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:46603600-46604000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:46604000-46605000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:46605000-46605400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:46634400-46634800	Active TSS	Fetal Heart	heart
11	chr4:46649600-46649800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:46649600-46650200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr4:46649800-46650200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:46649800-46650200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:46649800-46650200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:46650000-46650200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:46650000-46650200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:46655600-46656000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:46657400-46659800	Enhancers	Fetal Intestine Large	intestine
20	chr4:46657800-46659600	Enhancers	Fetal Intestine Small	intestine
21	chr4:46658000-46658800	Enhancers	Fetal Kidney	kidney
22	chr4:46658200-46658800	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr4:46659600-46660600	Weak transcription	Fetal Intestine Small	intestine
24	chr4:46660600-46661400	Enhancers	Fetal Intestine Small	intestine
25	chr4:46670600-46671200	Enhancers	Dnd41	blood
26	chr4:46676000-46677200	Enhancers	Fetal Brain Male	brain
27	chr4:46678200-46678800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:46678800-46679000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:46679000-46679400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:46691200-46691600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:46691600-46692000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr4:46700600-46701000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:46700600-46701200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:46700800-46701400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:46701400-46701600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr4:46707400-46708600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr4:46708600-46711200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr4:46711200-46712000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr4:46720200-46720600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr4:46720200-46720800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:46720200-46720800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr4:46720400-46720800	Enhancers	Fetal Brain Male	brain
43	chr4:46720400-46721200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:46720800-46722600	Weak transcription	Fetal Brain Male	brain
45	chr4:46722600-46723200	Enhancers	Fetal Brain Male	brain
46	chr4:46744600-46745400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr4:46748200-46749000	Enhancers	Brain Hippocampus Middle	brain
48	chr4:46766400-46770000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:46767400-46768200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:46770000-46770200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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