Variant report

Variant	nsv593468
Chromosome Location	chr4:3760093-3769130
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:795)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:3768564-3769140	H1-hESC	embryonic stem cell:	n/a	chr4:3768787-3768801
2	BACH1	chr4:3768715-3769081	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr4:3767173-3768168	K562	blood:	n/a	chr4:3768060-3768069
4	CEBPD	chr4:3767448-3767956	HepG2	liver:	n/a	n/a
5	CEBPD	chr4:3768042-3768292	HepG2	liver:	n/a	n/a
6	CHD2	chr4:3767139-3767236	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr4:3768617-3769097	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr4:3768574-3769520	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr4:3767600-3767750	AG04449	skin:	n/a	n/a
10	CTCF	chr4:3768020-3768170	HepG2	liver:	n/a	n/a
11	CTCF	chr4:3767380-3767530	GM12867	blood:	n/a	n/a
12	CTCF	chr4:3767320-3767470	HFF-Myc	foreskin:	n/a	n/a
13	CTCF	chr4:3767328-3767507	Fibrobl	skin:	n/a	n/a
14	CTCF	chr4:3767340-3767490	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr4:3767320-3767470	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr4:3767680-3767830	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr4:3767418-3767487	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr4:3767340-3767490	HepG2	liver:	n/a	n/a
19	CTCF	chr4:3767660-3767810	GM12875	blood:	n/a	n/a
20	CTCF	chr4:3767180-3767330	GM12867	blood:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
21	CTCF	chr4:3767676-3767764	Fibrobl	skin:	n/a	n/a
22	CTCF	chr4:3767380-3767524	GM13977	blood:	n/a	n/a
23	CTCF	chr4:3767340-3767490	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:3767320-3767470	GM12869	blood:	n/a	n/a
25	CTCF	chr4:3768840-3768990	HRE	kidney:	n/a	n/a
26	CTCF	chr4:3767400-3767550	SAEC	small airway:	n/a	n/a
27	CTCF	chr4:3767636-3767851	HepG2	liver:	n/a	n/a
28	CTCF	chr4:3767405-3767496	GM12892	blood:	n/a	n/a
29	CTCF	chr4:3768840-3768990	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr4:3768915-3769051	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr4:3767300-3767450	HBMEC	blood vessel:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
32	CTCF	chr4:3767360-3767510	GM12870	blood:	n/a	n/a
33	CTCF	chr4:3768840-3768990	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr4:3767637-3767799	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr4:3767365-3767537	A549	lung:	n/a	n/a
36	CTCF	chr4:3767642-3767733	LNCaP	prostate:	n/a	n/a
37	CTCF	chr4:3767300-3767450	AG09309	skin:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
38	CTCF	chr4:3767321-3767554	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr4:3767320-3767470	K562	blood:	n/a	n/a
40	CTCF	chr4:3767300-3767450	BJ	skin:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
41	CTCF	chr4:3767375-3767474	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr4:3768104-3768160	Fibrobl	skin:	n/a	n/a
43	CTCF	chr4:3767360-3767510	BE2_C	brain:	n/a	n/a
44	CTCF	chr4:3767300-3767450	HepG2	liver:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
45	CTCF	chr4:3767657-3767787	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr4:3767660-3767810	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr4:3768824-3769041	ProgFib	skin:	n/a	n/a
48	CTCF	chr4:3767326-3767549	K562	blood:	n/a	n/a
49	CTCF	chr4:3768860-3769010	BJ	skin:	n/a	n/a
50	CTCF	chr4:3767332-3767536	MCF-7	breast:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3768458-3768508	HCF	heart:	n/a
2	chr4:3765047-3765097	LNCaP	prostate:	n/a
3	chr4:3768458-3768508	HCF	heart:	n/a
4	chr4:3765047-3765097	LNCaP	prostate:	n/a
5	chr4:3767402-3767452	H1-hESC	embryonic stem cell:	embryo
6	chr4:3768458-3768508	CMK	blood:	n/a
7	chr4:3768078-3768128	SKMC	muscle:	n/a
8	chr4:3767169-3767219	MCF-7	breast:	n/a
9	chr4:3768078-3768128	AG09309	skin:	n/a
10	chr4:3768458-3768508	Hela-S3	cervix:	n/a
11	chr4:3766656-3766706	SAEC	small airway:	n/a
12	chr4:3768097-3768147	AG10803	skin:	n/a
13	chr4:3768081-3768131	NHDF-neo	bronchial:	n/a
14	chr4:3768081-3768131	BE2_C	brain:	n/a
15	chr4:3768078-3768128	RPTEC	kidney:	n/a
16	chr4:3768458-3768508	HRCEpiC	kidney:	n/a
17	chr4:3766656-3766706	ovcar-3	ovarian:	n/a
18	chr4:3767169-3767219	HCPEpiC	choroid plexus:	n/a
19	chr4:3768078-3768128	CMK	blood:	n/a
20	chr4:3768555-3768605	HCPEpiC	choroid plexus:	n/a
21	chr4:3768097-3768147	HCF	heart:	n/a
22	chr4:3766151-3766201	HRCEpiC	kidney:	n/a
23	chr4:3767169-3767219	GM12892	blood:	n/a
24	chr4:3768081-3768131	GM12892	blood:	n/a
25	chr4:3768555-3768605	HRE	kidney:	n/a
26	chr4:3767073-3767123	Jurkat	blood:	n/a
27	chr4:3767169-3767219	HCF	heart:	n/a
28	chr4:3768555-3768605	HCM	heart:	n/a
29	chr4:3765047-3765097	A549	lung:	n/a
30	chr4:3768458-3768508	AG10803	skin:	n/a
31	chr4:3768097-3768147	CMK	blood:	n/a
32	chr4:3768638-3768688	SK-N-SH_RA	brain:	n/a
33	chr4:3767402-3767452	PANC-1	pancreas:	n/a
34	chr4:3767169-3767219	SK-N-SH	brain:	n/a
35	chr4:3766656-3766706	Hepatocyte	liver:	n/a
36	chr4:3767169-3767219	Jurkat	blood:	n/a
37	chr4:3766875-3766925	PANC-1	pancreas:	n/a
38	chr4:3767073-3767123	HIPEpiC	eye:	n/a
39	chr4:3765047-3765097	Jurkat	blood:	n/a
40	chr4:3768081-3768131	PANC-1	pancreas:	n/a
41	chr4:3768078-3768128	MCF10A-Er-Src	breast:	n/a
42	chr4:3766656-3766706	Hela-S3	cervix:	n/a
43	chr4:3765047-3765097	HCPEpiC	choroid plexus:	n/a
44	chr4:3768078-3768128	HCF	heart:	n/a
45	chr4:3766151-3766201	GM12891	blood:	n/a
46	chr4:3768078-3768128	GM19239	blood:	n/a
47	chr4:3766656-3766706	U87	brain:	n/a
48	chr4:3768458-3768508	HepG2	liver:	n/a
49	chr4:3766875-3766925	PrEC	prostate:	n/a
50	chr4:3768081-3768131	GM12878	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3767078..3767943-chr4:3882124..3882913,2	MCF-7	breast:
2	chr4:3532933..3534970-chr4:3765784..3768236,2	MCF-7	breast:
3	chr4:3750111..3752894-chr4:3765280..3767505,2	MCF-7	breast:
4	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
5	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
6	chr4:3766468..3768028-chr4:3774128..3775785,2	MCF-7	breast:
7	chr4:3754576..3757273-chr4:3765729..3767791,3	MCF-7	breast:
8	chr4:3741522..3743412-chr4:3768536..3771001,2	MCF-7	breast:
9	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
10	chr19:54974695..54977436-chr4:3766258..3768919,2	MCF-7	breast:
11	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
12	chr4:3769000..3769555-chr4:3785283..3786137,2	MCF-7	breast:
13	chr4:3754355..3758397-chr4:3760571..3763729,4	K562	blood:
14	chr4:3768745..3771580-chr4:3802446..3805073,2	MCF-7	breast:
15	chr4:3767262..3767834-chr4:3882421..3882953,2	K562	blood:
16	chr4:3767101..3767926-chr4:3787451..3788371,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRPAP1-3	chr4:3761872-3765117	XLOC_003862
2	lnc-LRPAP1-3	chr4:3760475-3761753	XLOC_003862

No data

Variant related genes	Relation type
ENSG00000250986	TF binding region
ADRA2C	TF binding region
ENSG00000250986	CpG island
ADRA2C	CpG island
ENSG00000182909	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000216560	chromatin interactions
ENSG00000250986	chromatin interactions

Extended variants
information (count: 403 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3935655	chr4:3760093-3760094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7683372	chr4:3760191-3760192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567797579	chr4:3760207-3760208	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143101309	chr4:3760208-3760209	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112693394	chr4:3760219-3760220	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144751475	chr4:3760228-3760229	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376326460	chr4:3760258-3760259	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148554484	chr4:3760267-3760268	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113893031	chr4:3760286-3760287	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537088798	chr4:3760312-3760313	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567906525	chr4:3760325-3760326	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112844780	chr4:3760326-3760327	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573253447	chr4:3760357-3760358	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76757384	chr4:3760386-3760387	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550262753	chr4:3760440-3760441	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558996330	chr4:3760443-3760444	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141930019	chr4:3760453-3760454	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75215735	chr4:3760461-3760462	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116596941	chr4:3760463-3760464	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560710499	chr4:3760525-3760526	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs188670614	chr4:3760533-3760534	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs73198489	chr4:3760544-3760545	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs551210974	chr4:3760547-3760548	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs369259453	chr4:3760556-3760557	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs561136856	chr4:3760642-3760643	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs553911373	chr4:3760665-3760666	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs192846193	chr4:3760674-3760675	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs572789493	chr4:3760692-3760693	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs547136305	chr4:3760693-3760694	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs566946294	chr4:3760741-3760742	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs184936950	chr4:3760753-3760754	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs533878242	chr4:3760825-3760826	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs115182240	chr4:3760851-3760852	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs571563756	chr4:3760888-3760889	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs150671042	chr4:3760907-3760908	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs189495820	chr4:3760947-3760948	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs557178627	chr4:3760966-3760967	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs566945848	chr4:3761000-3761001	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs200732134	chr4:3761017-3761018	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs535825191	chr4:3761082-3761083	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs552684014	chr4:3761093-3761094	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs572595409	chr4:3761107-3761108	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs545632585	chr4:3761137-3761138	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs558890990	chr4:3761173-3761174	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs575755041	chr4:3761174-3761175	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs544596655	chr4:3761182-3761183	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs180965979	chr4:3761188-3761189	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs530143181	chr4:3761193-3761194	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs540613004	chr4:3761196-3761197	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs560606821	chr4:3761198-3761199	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3750000-3763200	Weak transcription	Pancreas	Pancrea
2	chr4:3756200-3764000	Weak transcription	Fetal Kidney	kidney
3	chr4:3757600-3762000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:3758000-3760200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:3758600-3761000	Weak transcription	Aorta	Aorta
6	chr4:3759600-3761400	Weak transcription	Spleen	Spleen
7	chr4:3760200-3761400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:3760800-3761200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr4:3761000-3762000	Strong transcription	Aorta	Aorta
10	chr4:3761400-3762200	ZNF genes & repeats	Spleen	Spleen
11	chr4:3761400-3762600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:3761800-3766600	Weak transcription	HSMM	muscle
13	chr4:3762000-3762200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr4:3762000-3763000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:3762000-3765800	Weak transcription	Aorta	Aorta
16	chr4:3762200-3762400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:3762200-3762600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr4:3762200-3765400	Weak transcription	Spleen	Spleen
19	chr4:3762400-3763200	Enhancers	Fetal Brain Male	brain
20	chr4:3762400-3766800	Weak transcription	Right Atrium	heart
21	chr4:3762600-3763000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:3762600-3763800	Bivalent Enhancer	Fetal Stomach	stomach
23	chr4:3762600-3765400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr4:3763000-3763200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr4:3763000-3763200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:3763000-3763200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr4:3763000-3765400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:3763000-3766800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr4:3763200-3764000	Enhancers	Pancreas	Pancrea
30	chr4:3763200-3765200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:3763800-3764000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:3764000-3764200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr4:3764000-3764400	ZNF genes & repeats	Fetal Kidney	kidney
34	chr4:3764000-3766000	Weak transcription	Pancreas	Pancrea
35	chr4:3764400-3764600	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
36	chr4:3764400-3767400	Weak transcription	Fetal Kidney	kidney
37	chr4:3764600-3766000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr4:3764800-3765800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:3765000-3765400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:3765200-3765400	Bivalent Enhancer	Fetal Stomach	stomach
41	chr4:3765200-3766000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:3765400-3765600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:3765400-3765800	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr4:3765400-3766000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:3765400-3766000	Enhancers	Spleen	Spleen
46	chr4:3765400-3766800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
47	chr4:3765800-3766000	Enhancers	Aorta	Aorta
48	chr4:3765800-3766000	Enhancers	Brain Anterior Caudate	brain
49	chr4:3765800-3766200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr4:3765800-3766200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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